John Blangero - Publications

Affiliations: 
 

500 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Blangero J, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084  0.33
2021 Gao S, Donohue B, Hatch KS, Chen S, Ma T, Ma Y, Kvarta MD, Bruce H, Adhikari BM, Jahanshad N, Thompson PM, Blangero J, Hong LE, Medland SE, Ganjgahi H, et al. Comparing Empirical Kinship Derived Heritability for Imaging Genetics Traits in the UK Biobank and Human Connectome Project. Neuroimage. 118700. PMID 34740793 DOI: 10.1016/j.neuroimage.2021.118700  0.587
2021 Tran NK, Lea RA, Holland S, Nguyen Q, Raghubar AM, Sutherland HG, Benton MC, Haupt LM, Blackburn NB, Curran JE, Blangero J, Mallett AJ, Griffiths LR. Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific Reports. 11: 19425. PMID 34593906 DOI: 10.1038/s41598-021-98935-4  0.309
2021 Blackburn NB, Meikle PJ, Peralta JM, Kumar S, Leandro AC, Bellinger MA, Giles C, Huynh K, Mahaney MC, Göring HHH, VandeBerg JL, Williams-Blangero S, Glahn DC, Duggirala R, Blangero J, et al. Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion in . Circulation. Genomic and Precision Medicine. PMID 33887960 DOI: 10.1161/CIRCGEN.120.003232  0.336
2020 Pizzagalli F, Auzias G, Yang Q, Mathias SR, Faskowitz J, Boyd JD, Amini A, Rivière D, McMahon KL, de Zubicaray GI, Martin NG, Mangin JF, Glahn DC, Blangero J, Wright MJ, et al. The reliability and heritability of cortical folds and their genetic correlations across hemispheres. Communications Biology. 3: 510. PMID 32934300 DOI: 10.1038/s42003-020-01163-1  0.578
2020 Li X, Li Z, Zhou H, Gaynor SM, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Aslibekyan S, Ballantyne CM, Bielak LF, Blangero J, Boerwinkle E, Bowden DW, et al. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale. Nature Genetics. PMID 32839606 DOI: 10.1038/S41588-020-0676-4  0.347
2020 Kochunov P, Zavaliangos-Petropulu A, Jahanshad N, Thompson PM, Ryan MC, Chiappelli J, Chen S, Du X, Hatch K, Adhikari B, Sampath H, Hare S, Kvarta M, Goldwaser E, Yang F, ... ... Blangero J, et al. A White Matter Connection of Schizophrenia and Alzheimer's Disease. Schizophrenia Bulletin. PMID 32681179 DOI: 10.1093/Schbul/Sbaa078  0.503
2020 Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, ... ... Blangero J, et al. The genetic architecture of the human cerebral cortex. Science (New York, N.Y.). 367. PMID 32193296 DOI: 10.1126/Science.Aay6690  0.596
2020 Alexander-Bloch AF, Raznahan A, Vandekar SN, Seidlitz J, Lu Z, Matthias SR, Knowles E, Mollon J, Rodrigue A, Curran JE, Görring HHH, Satterthwaite TD, Gur RE, Bassett DS, Hoftman GD, ... ... Blangero J, et al. Imaging local genetic influences on cortical folding. Proceedings of the National Academy of Sciences of the United States of America. PMID 32170019 DOI: 10.1073/Pnas.1912064117  0.384
2020 Cadby G, Melton PE, McCarthy NS, Giles C, Mellett NA, Huynh K, Hung J, Beilby J, Dubé MP, Watts GF, Blangero J, Meikle PJ, Moses EK. Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study. Journal of Lipid Research. PMID 32060071 DOI: 10.1194/Jlr.Ra119000594  0.36
2020 Mathias SR, Knowles EEM, Mollon J, Rodrigue A, Koenis MMC, Alexander-Bloch AF, Winkler AM, Olvera RL, Duggirala R, Göring HHH, Curran JE, Fox PT, Almasy L, Blangero J, Glahn DC. Minimal Relationship between Local Gyrification and General Cognitive Ability in Humans. Cerebral Cortex (New York, N.Y. : 1991). PMID 32037459 DOI: 10.1093/Cercor/Bhz319  0.317
2020 Mollon J, Curran JE, Mathias SR, Knowles EEM, Carlisle P, Fox PT, Olvera RL, Göring HHH, Rodrigue A, Almasy L, Duggirala R, Blangero J, Glahn DC. Neurocognitive impairment in type 2 diabetes: evidence for shared genetic aetiology. Diabetologia. PMID 32016567 DOI: 10.1007/S00125-020-05101-Y  0.304
2020 Blackburn AN, Blondell L, Kos MZ, Blackburn NB, Peralta JM, Stevens PT, Lehman DM, Blangero J, Göring HHH. Genotype phasing in pedigrees using whole-genome sequence data. European Journal of Human Genetics : Ejhg. PMID 31996801 DOI: 10.1038/S41431-020-0574-3  0.304
2020 Williams-Blangero S, Vandeberg JL, Blangero J, Konigsberg L, Dyke B. Genetic differentiation between baboon subspecies: Relevance for biomedical research. American Journal of Primatology. 20: 67-81. PMID 31963994 DOI: 10.1002/Ajp.1350200202  0.349
2020 Towne B, Blangero J, Mott GE. Genetic analysis of sexual dimorphism in serum apo AI and HDL-C concentrations in baboons. American Journal of Primatology. 27: 107-117. PMID 31948143 DOI: 10.1002/Ajp.1350270206  0.319
2020 Blangero J, Williams-Blangero S, Hixson JE. Assessing the effects of candidate genes on quantitative traits in primate populations. American Journal of Primatology. 27: 119-132. PMID 31948141 DOI: 10.1002/Ajp.1350270207  0.451
2020 Williams-Blangero S, Blangero J. Heritability of age at first birth in captive olive baboons. American Journal of Primatology. 37: 233-239. PMID 31936949 DOI: 10.1002/Ajp.1350370305  0.383
2019 Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C, Barnes KC, Becker LC, Bien SA, Bis JC, Blangero J, et al. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Plos Genetics. 15: e1008500. PMID 31869403 DOI: 10.1371/Journal.Pgen.1008500  0.384
2019 Caballero M, Seidman DN, Qiao Y, Sannerud J, Dyer TD, Lehman DM, Curran JE, Duggirala R, Blangero J, Carmi S, Williams AL. Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives. Plos Genetics. 15: e1007979. PMID 31860654 DOI: 10.1371/Journal.Pgen.1007979  0.335
2019 van der Meer D, Sønderby IE, Kaufmann T, Walters GB, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, et al. Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. Jama Psychiatry. 1-11. PMID 31665216 DOI: 10.1001/Jamapsychiatry.2019.3779  0.315
2019 Sarnowski C, Leong A, Raffield LM, Wu P, de Vries PS, DiCorpo D, Guo X, Xu H, Liu Y, Zheng X, Hu Y, Brody JA, Goodarzi MO, Hidalgo BA, Highland HM, ... ... Blangero J, et al. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American Journal of Human Genetics. PMID 31564435 DOI: 10.1016/J.Ajhg.2019.08.010  0.346
2019 Blackburn NB, Michael LF, Meikle PJ, Peralta JM, Mosior M, McAhren S, Bui HH, Bellinger MA, Giles C, Kumar S, Leandro AC, Almeida M, Weir JM, Mahaney MC, Dyer TD, ... ... Blangero J, et al. Rare variant significantly alters de novo ceramide synthesis pathway. Journal of Lipid Research. PMID 31227640 DOI: 10.1194/Jlr.P094433  0.36
2019 Rodrigue AL, Knowles EE, Mollon J, Mathias SR, Koenis MM, Peralta JM, Leandro AC, Fox PT, Sprooten E, Kochunov P, Olvera RL, Duggirala R, Almasy L, Curran JE, Blangero J, et al. Evidence for genetic correlation between human cerebral white matter microstructure and inflammation. Human Brain Mapping. PMID 31187567 DOI: 10.1002/Hbm.24694  0.586
2019 Johnson MP, Keyho R, Blackburn NB, Laston S, Kumar S, Peralta J, Thapa SS, Towne B, Subedi J, Blangero J, Williams-Blangero S. Glycated Serum Protein Genetics and Pleiotropy with Cardiometabolic Risk Factors. Journal of Diabetes Research. 2019: 2310235. PMID 31089471 DOI: 10.1155/2019/2310235  0.419
2019 Kotkowski E, Price LR, Franklin C, Salazar M, Woolsey M, DeFronzo RA, Blangero J, Glahn DC, Fox PT. A neural signature of metabolic syndrome. Human Brain Mapping. PMID 31062906 DOI: 10.1002/Hbm.24617  0.321
2019 M Knowles EE, Curran JE, Goring HHH, Mathias SR, Mollon J, Rodrigue A, Olvera RL, Leandro A, Duggirala R, Almasy L, Blangero J, Glahn DC. Family-Based Analyses Reveal Novel Genetic Overlap Between Interleukin-8 and Risk for Suicide Attempt. Brain, Behavior, and Immunity. PMID 30953777 DOI: 10.1016/J.Bbi.2019.04.004  0.3
2019 Melton PE, Johnson MP, Gokhale-Agashe D, Rea AJ, Ariff A, Cadby G, Peralta JM, Mcnab TJ, Allcock RJ, Abraham LJ, Blangero J, Brennecke SP, Moses EK. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes. Journal of Hypertension. PMID 30633125 DOI: 10.1097/Hjh.0000000000002023  0.35
2019 LOPEZ-ALVARENGA JC, ARYA R, CHITTOOR G, PAUL SF, PUPPALA SR, FAROOK VS, FOWLER SP, RESENDEZ RG, DIAZ-BADILLO A, LEHMAN D, MUMMIDI S, JENKINSON C, LYNCH JL, DEFRONZO RA, BLANGERO J, et al. 2093-P: Acanthosis Nigricans as a Composite Marker of Cardiometabolic Risk and Its Complex Association with Obesity and Insulin Resistance in Mexican-American Children Diabetes. 68: 2093-P. DOI: 10.2337/Db19-2093-P  0.325
2019 VENKATESAN V, LOPEZ-ALVARENGA JC, ARYA R, KOSHY T, RAVICHANDRAN U, SHARMA S, LODHA S, PONNALA AR, SHARMA KK, SHAIK MV, RESENDEZ RG, RAMU D, VENUGOPAL P, R. P, S. N, ... ... BLANGERO J, et al. 1717-P: Burden of Type 2 Diabetes and Its Genetic Determinants in Indian Populations: Findings from the INDIGENIUS Consortium Diabetes. 68: 1717-P. DOI: 10.2337/Db19-1717-P  0.334
2019 Glahn D, Mollon J, Knowles E, Mathias S, Gur R, Peralta JM, Weiner D, Robinson E, Gur RE, Blangero J, Almasy L. GENETIC INFLUENCE ON NEUROANATOMIC DEVELOPMENT BETWEEN CHILDHOOD AND ADULTHOOD European Neuropsychopharmacology. 29: S1025-S1026. DOI: 10.1016/J.Euroneuro.2018.07.012  0.39
2019 Mollon J, Knowles E, Mathais S, Rodrigue A, Koenis M, Gur R, Peralta JM, Robinson E, Gur R, Blangero J, Almasy L, Glahn D. O55. The Genetic Factors Influencing Externalizing Psychopathology Overlap With Those Influencing Neurocognition and Show Developmental Variation Biological Psychiatry. 85. DOI: 10.1016/J.Biopsych.2019.03.320  0.352
2019 Knowles E, Curran J, Göring H, Mathias S, Mollon J, Rodrigue A, Olvera R, Leandro A, Duggirala R, Almasy L, Blangero J, Glahn D. 45. The Effect of Sex and BMI on the Genetic Overlap Between Plasma-Based Interleukins (-6 and -8) and Suicide Attempt Biological Psychiatry. 85. DOI: 10.1016/J.Biopsych.2019.03.059  0.327
2018 Mollon J, Knowles EEM, Mathias SR, Gur R, Peralta JM, Weiner DJ, Robinson EB, Gur RE, Blangero J, Almasy L, Glahn DC. Genetic influence on cognitive development between childhood and adulthood. Molecular Psychiatry. PMID 30644433 DOI: 10.1038/S41380-018-0277-0  0.348
2018 Chen H, Huffman JE, Brody JA, Wang C, Lee S, Li Z, Gogarten SM, Sofer T, Bielak LF, Bis JC, Blangero J, Bowler RP, Cade BE, Cho MH, Correa A, et al. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30639324 DOI: 10.1016/J.Ajhg.2018.12.012  0.353
2018 Kochunov P, Donohue B, Mitchell BD, Ganjgahi H, Adhikari B, Ryan M, Medland SE, Jahanshad N, Thompson PM, Blangero J, Fieremans E, Novikov DS, Marcus D, Van Essen DC, Glahn DC, et al. Genomic kinship construction to enhance genetic analyses in the human connectome project data. Human Brain Mapping. PMID 30496643 DOI: 10.1002/Hbm.24479  0.617
2018 Blondell L, Blackburn A, Kos MZ, Blangero J, Göring HHH. Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage. Human Heredity. 83: 92-99. PMID 30391948 DOI: 10.1159/000492830  0.391
2018 Knowles EEM, Mathias SR, Mollon J, Rodrigue A, Koenis MMG, Dyer TD, Goring HH, Curran JE, Olvera RL, Duggirala R, Almasy L, Blangero J, Glahn DC. A QTL on chromosome 3q23 influences processing speed in humans. Genes, Brain, and Behavior. e12530. PMID 30379395 DOI: 10.1111/Gbb.12530  0.358
2018 Peralta JM, Blackburn NB, Porto A, Blangero J, Charlesworth J. Genome-wide linkage scan for loci influencing plasma triglyceride levels. Bmc Proceedings. 12: 52. PMID 30275898 DOI: 10.1186/S12919-018-0137-6  0.372
2018 Porto A, Peralta JM, Blackburn NB, Blangero J. Reliability of genomic predictions of complex human phenotypes. Bmc Proceedings. 12: 51. PMID 30275897 DOI: 10.1186/S12919-018-0138-5  0.441
2018 Blackburn NB, Porto A, Peralta JM, Blangero J. Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. Bmc Proceedings. 12: 34. PMID 30263045 DOI: 10.1186/S12919-018-0133-X  0.425
2018 Almeida M, Peralta J, Garcia J, Diego V, Goring H, Williams-Blangero S, Blangero J. Modeling methylation data as an additional genetic variance component. Bmc Proceedings. 12: 29. PMID 30263043 DOI: 10.1186/S12919-018-0128-7  0.363
2018 Ganjgahi H, Winkler AM, Glahn DC, Blangero J, Donohue B, Kochunov P, Nichols TE. Fast and powerful genome wide association of dense genetic data with high dimensional imaging phenotypes. Nature Communications. 9: 3254. PMID 30108209 DOI: 10.1038/S41467-018-05444-6  0.599
2018 Knowles EEM, Curran JE, Meikle PJ, Huynh K, Mathias SR, Göring HHH, VandeBerg JL, Mahaney MC, Jalbrzikowski M, Mosior MK, Michael LF, Olvera RL, Duggirala R, Almasy L, Glahn DC, ... Blangero J, et al. Disentangling the genetic overlap between cholesterol and suicide risk. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 30082891 DOI: 10.1038/S41386-018-0162-1  0.326
2018 Adhikari BM, Jahanshad N, Shukla D, Glahn DC, Blangero J, Fox PT, Reynolds RC, Cox RW, Fieremans E, Veraart J, Novikov DS, Nichols TE, Hong LE, Thompson PM, Kochunov P. Comparison of heritability estimates on resting state fMRI connectivity phenotypes using the ENIGMA analysis pipeline. Human Brain Mapping. PMID 30052318 DOI: 10.1002/Hbm.24331  0.61
2018 Merino J, Dashti HS, Li SX, Sarnowski C, Justice AE, Graff M, Papoutsakis C, Smith CE, Dedoussis GV, Lemaitre RN, Wojczynski MK, Männistö S, Ngwa JS, Kho M, Ahluwalia TS, ... ... Blangero J, et al. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium. Molecular Psychiatry. PMID 29988085 DOI: 10.1038/S41380-018-0079-4  0.436
2018 Glahn DC, Nimgaonkar VL, Raventós H, Contreras J, McIntosh AM, Thomson PA, Jablensky A, McCarthy NS, Charlesworth JC, Blackburn NB, Peralta JM, Knowles EEM, Mathias SR, Ament SA, McMahon FJ, ... ... Blangero J, et al. Rediscovering the value of families for psychiatric genetics research. Molecular Psychiatry. PMID 29955165 DOI: 10.1038/S41380-018-0073-X  0.425
2018 Ramstetter MD, Shenoy SA, Dyer TD, Lehman DM, Curran JE, Duggirala R, Blangero J, Mezey JG, Williams AL. Inferring Identical-by-Descent Sharing of Sample Ancestors Promotes High-Resolution Relative Detection. American Journal of Human Genetics. PMID 29937093 DOI: 10.1016/J.Ajhg.2018.05.008  0.307
2018 Gao C, Tabb KL, Dimitrov LM, Taylor KD, Wang N, Guo X, Long J, Rotter JI, Watanabe RM, Curran JE, Blangero J, Langefeld CD, Bowden DW, Palmer ND. Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS). Scientific Reports. 8: 5603. PMID 29618726 DOI: 10.1038/S41598-018-23727-2  0.388
2018 Arya R, Escalante A, Farook VS, Restrepo JF, Battafarano DF, Almeida M, Kos MZ, Fourcaudot MJ, Mummidi S, Kumar S, Curran JE, Jenkinson CP, Blangero J, Duggirala R, Del Rincon I. Data on genetic associations of carotid atherosclerosis markers in Mexican American and European American rheumatoid arthritis subjects. Data in Brief. 17: 820-829. PMID 29527544 DOI: 10.1016/J.Dib.2018.02.006  0.381
2018 Khan FF, Melton PE, McCarthy NS, Morar B, Blangero J, Moses EK, Jablensky A. Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity. Schizophrenia Research. PMID 29486958 DOI: 10.1016/J.Schres.2018.02.034  0.33
2018 Arya R, Farook VS, Fowler SP, Puppala S, Chittoor G, Resendez RG, Mummidi S, Vanamala J, Almasy L, Curran JE, Comuzzie AG, Lehman DM, Jenkinson CP, Lynch JL, DeFronzo RA, ... Blangero J, et al. Genetic and environmental (physical fitness and sedentary activity) interaction effects on cardiometabolic risk factors in Mexican American children and adolescents. Genetic Epidemiology. PMID 29460292 DOI: 10.1002/Gepi.22114  0.327
2018 Adhikari BM, Jahanshad N, Shukla D, Glahn DC, Blangero J, Reynolds RC, Cox RW, Fieremans E, Veraart J, Novikov DS, Nichols TE, Hong LE, Thompson PM, Kochunov P. Heritability estimates on resting state fMRI data using ENIGMA analysis pipeline. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 23: 307-318. PMID 29218892  0.508
2018 Diego VP, Almeida MA, Luu BW, Haack K, Chitlur MB, Ameri A, Dinh LV, Rajalingam R, Powell JS, Blangero J, Almasy L, Cole S, Howard TE. Genetics of Factor VIII Inhibitor Development in Hemophilia Patients: Novel Statistical Approaches in the PATH Study Blood. 132: 1199-1199. DOI: 10.1182/Blood-2018-99-120021  0.348
2018 Mollon J, Knowles E, Mathias S, Gur R, Peralta JM, Curran J, Gur R, Blangero J, Glahn D. F49. Genetic Basis of Changes in Neurocognition and Psychopathology Between Childhood and Adulthood Biological Psychiatry. 83. DOI: 10.1016/J.Biopsych.2018.02.662  0.321
2018 Glahn D, McIntosh A, Jablensky A, Nimgaonkar V, Gur R, Curran J, Almasy L, Gur R, Blangero J. 106. Genome-Wide Significant Locus on Chromosome 5 Influences Psychosis Risk and General Intellectual Ability Biological Psychiatry. 83: S43-S44. DOI: 10.1016/J.Biopsych.2018.02.124  0.316
2017 Arya R, Escalante A, Farook VS, Restrepo JF, Battafarano DF, Almeida M, Kos MZ, Fourcaudot MJ, Mummidi S, Kumar S, Curran JE, Jenkinson CP, Blangero J, Duggirala R, Del Rincon I. A genetic association study of carotid intima-media thickness (CIMT) and plaque in Mexican Americans and European Americans with rheumatoid arthritis. Atherosclerosis. 271: 92-101. PMID 29482039 DOI: 10.1016/J.Atherosclerosis.2017.11.024  0.339
2017 Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, ... ... Blangero J, et al. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America. PMID 29279374 DOI: 10.1073/Pnas.1705859115  0.423
2017 Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Blangero J, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179  0.355
2017 Alexander-Bloch AF, Mathias SR, Fox PT, Olvera RL, Göring HHH, Duggirala R, Curran JE, Blangero J, Glahn DC. Human Cortical Thickness Organized into Genetically-determined Communities across Spatial Resolutions. Cerebral Cortex (New York, N.Y. : 1991). 1-13. PMID 29190330 DOI: 10.1093/Cercor/Bhx309  0.429
2017 Cadby G, Melton PE, McCarthy NS, Almeida M, Williams-Blangero S, Curran JE, VandeBerg JL, Hui J, Beilby J, Musk AW, James AL, Hung J, Blangero J, Moses EK. Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study. Human Genetics. PMID 29181734 DOI: 10.1007/S00439-017-1856-X  0.423
2017 Jasinska AJ, Zelaya I, Service SK, Peterson CB, Cantor RM, Choi OW, DeYoung J, Eskin E, Fairbanks LA, Fears S, Furterer AE, Huang YS, Ramensky V, Schmitt CA, Svardal H, ... ... Blangero J, et al. Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. Nature Genetics. PMID 29083405 DOI: 10.1038/Ng.3959  0.419
2017 McCarthy NS, Badcock JC, Clark ML, Knowles EEM, Cadby G, Melton PE, Morgan VA, Blangero J, Moses EK, Glahn DC, Jablensky A. Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia. Schizophrenia Bulletin. PMID 29040798 DOI: 10.1093/Schbul/Sbx141  0.372
2017 Mercader JM, Liao RG, Davis A, Dymek Z, Estrada K, Tukiainen T, Huerta-Chagoya A, Moreno-Macías H, Jablonski KA, Hanson RL, Walford GA, Moran I, Chen L, Agarwala V, Ordoñez-Sánchez ML, ... ... Blangero J, et al. A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes. Diabetes. PMID 28838971 DOI: 10.2337/Db17-0187  0.388
2017 Ramstetter MD, Dyer T, Lehman DM, Curran JE, Duggirala R, Blangero J, Mezey JG, Williams AL. Benchmarking Relatedness Inference Methods with Genome-Wide Data from Thousands of Relatives. Genetics. PMID 28739658 DOI: 10.1534/Genetics.117.1122  0.337
2017 Kulkarni H, Mamtani M, Wong G, Weir JM, Barlow CK, Dyer TD, Almasy L, Mahaney MC, Comuzzie AG, Duggirala R, Meikle PJ, Blangero J, Curran JE. Genetic correlation of the plasma lipidome with type 2 diabetes, prediabetes and insulin resistance in Mexican American families. Bmc Genetics. 18: 48. PMID 28525987 DOI: 10.1186/S12863-017-0515-5  0.364
2017 Farook VS, Reddivari L, Mummidi S, Puppala S, Arya R, Lopez-Alvarenga JC, Fowler SP, Chittoor G, Resendez RG, Kumar BM, Comuzzie AG, Curran JE, Lehman DM, Jenkinson CP, Lynch JL, ... ... Blangero J, et al. Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children. The American Journal of Clinical Nutrition. PMID 28515064 DOI: 10.3945/Ajcn.116.144006  0.382
2017 Blackburn NB, Marthick JR, Banks A, Charlesworth JC, Marsden KA, Lowenthal RM, Blangero J, Dickinson JL. Evaluating a CLL susceptibility variant in ITGB2 in families with multiple sub-types of hematological malignancies. Blood. PMID 28490571 DOI: 10.1182/Blood-2017-03-774232  0.329
2017 Graff M, Scott RA, Justice AE, Young KL, Feitosa MF, Barata L, Winkler TW, Chu AY, Mahajan A, Hadley D, Xue L, Workalemahu T, Heard-Costa NL, den Hoed M, Ahluwalia TS, ... ... Blangero J, et al. Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Plos Genetics. 13: e1006528. PMID 28448500 DOI: 10.1371/Journal.Pgen.1006528  0.344
2017 Justice AE, Winkler TW, Feitosa MF, Graff M, Fisher VA, Young K, Barata L, Deng X, Czajkowski J, Hadley D, Ngwa JS, Ahluwalia TS, Chu AY, Heard-Costa NL, Lim E, ... ... Blangero J, et al. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications. 8: 14977. PMID 28443625 DOI: 10.1038/Ncomms14977  0.404
2017 Hodgson K, Carless MA, Kulkarni H, Curran JE, Sprooten E, Knowles EE, Mathias S, Göring HH, Yao N, Olvera RL, Fox PT, Almasy L, Duggirala R, Blangero J, Glahn DC. Epigenetic Age Acceleration Assessed With Human White-Matter Images. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 28385874 DOI: 10.1523/Jneurosci.0177-17.2017  0.34
2017 Knowles EE, Huynh K, Meikle PJ, Göring HH, Olvera RL, Mathias SR, Duggirala R, Almasy L, Blangero J, Curran JE, Glahn DC. The lipidome in major depressive disorder: Shared genetic influence for ether-phosphatidylcholines, a plasma-based phenotype related to inflammation, and disease risk. European Psychiatry : the Journal of the Association of European Psychiatrists. 43: 44-50. PMID 28365467 DOI: 10.1016/J.Eurpsy.2017.02.479  0.312
2017 Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Blangero J, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329  0.333
2017 Knowles EE, Meikle PJ, Huynh K, Göring HH, Olvera RL, Mathias SR, Duggirala R, Almasy L, Blangero J, Curran JE, Glahn DC. Serum phosphatidylinositol as a biomarker for bipolar disorder liability. Bipolar Disorders. PMID 28230325 DOI: 10.1016/J.Euroneuro.2016.09.521  0.32
2017 Hibar DP, Adams HH, Jahanshad N, Chauhan G, Stein JL, Hofer E, Renteria ME, Bis JC, Arias-Vasquez A, Ikram MK, Desrivières S, Vernooij MW, Abramovic L, Alhusaini S, Amin N, ... ... Blangero J, et al. Novel genetic loci associated with hippocampal volume. Nature Communications. 8: 13624. PMID 28098162 DOI: 10.1038/Ncomms13624  0.609
2017 Yao L, Liu Y, Qiu Z, Kumar S, Curran JE, Blangero J, Chen Y, Lehman DM. Molecular profiling of human iPS-derived hypothalamic neurons provides developmental insights to genetic loci for body weight regulation. Journal of Neuroendocrinology. PMID 28071834 DOI: 10.1111/Jne.12455  0.31
2017 Tabb KL, Hellwege JN, Palmer ND, Dimitrov L, Sajuthi S, Taylor KD, Ng MC, Hawkins GA, Chen YI, Brown WM, McWilliams D, Williams A, Lorenzo C, Norris JM, Long J, ... ... Blangero J, et al. Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study. Annals of Human Genetics. PMID 28067407 DOI: 10.1111/Ahg.12184  0.412
2017 Glahn D, Curran J, Knowles E, Mathias S, Hodgson K, Almasy L, Duggirala R, Blangero J. LOCALIZING GENETIC LOCI FOR AFFECTIVE AND PSYCHOTIC DISORDERS WITH ENDOPHENOTYPES European Neuropsychopharmacology. 27: S519-S520. DOI: 10.1016/J.Euroneuro.2016.09.637  0.436
2017 Blangero J. DIRECT ESTIMATION OF GENETIC LIABILITY FOR MENTAL ILLNESS USING ENDOPHENOTYPES European Neuropsychopharmacology. 27: S518-S519. DOI: 10.1016/J.Euroneuro.2016.09.635  0.433
2017 McCarthy N, Clark M, Cadby G, Blangero J, Dragovic M, Melton P, Moses E, Badcock J, Jablensky A. Association Between Polygenic Risk Score for Schizophrenia and Neurocognitive Measures in the Western Australian Family Study of Schizophrenia (Wafss) European Neuropsychopharmacology. 27: S505-S506. DOI: 10.1016/J.Euroneuro.2016.09.611  0.344
2017 Knowles E, Curran J, Meikle P, Huynh K, Goring H, Olvera R, Duggirala R, Almasy L, Blangero J, Glahn D. Disentangling The Shared Genetic Etiology Between Serum Cholesterol And Suicide Risk: A Potential Moderating Role For Cholesterol Efflux European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.588  0.351
2017 Curran J, Knowles E, Huynh K, Meikle P, Goring H, Olvera R, Mathias S, Duggirala R, Almasy L, Blangero J, Glahn D. The Lipidome In Major Depressive Disorder: Shared Genetic Influence For Ether-Phosphatidylcholines, A Plasma-Based Phenotype Related To Inflammation, And Disease Risk European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.500  0.35
2017 Mathias S, Knowles E, Curran J, Goring H, Olvera R, Fox P, Duggirala R, Almasy L, Blangero J, Glahn D. An Exploratory Study of The Genetic Relationships Between Plasma-Based Measures of Inflammation And Brain Anatomy European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.409  0.406
2017 Hodgson K, Carless M, Curran J, Sprooten E, Knowles E, Mathias S, Yao N, Göring H, Olvera R, Fox P, Almasy L, Duggirala R, Blangero J, Glahn D. Epigenetic Age Acceleration Assessed In White-Matter Integrity: Towards A Biomarker of Successfully Brain Aging European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.407  0.322
2017 Alexander-Bloch A, Mathais S, Duggirala R, Curran J, Blangero J, Glahn D. 372. Healthy Developmental and Genetic Brain Modules Influence Maturation Abnormalities in Schizophrenia Biological Psychiatry. 81: S152. DOI: 10.1016/J.Biopsych.2017.02.389  0.327
2016 Quillen EE, Blangero J, Almasy L. A variance component method for integrated pathway analysis of gene expression data. Bmc Proceedings. 10: 337-342. PMID 27980659 DOI: 10.1186/S12919-016-0053-6  0.339
2016 Almeida M, Blondell L, Peralta JM, Kent JW, Jun G, Teslovich TM, Fuchsberger C, Wood AR, Manning AK, Frayling TM, Cingolani PE, Sladek R, Dyer TD, Abecasis G, Duggirala R, ... Blangero J, et al. Independent test assessment using the extreme value distribution theory. Bmc Proceedings. 10: 245-249. PMID 27980644 DOI: 10.1186/S12919-016-0038-5  0.399
2016 Peralta JM, Almeida M, Abraham LJ, Moses E, Blangero J. Finding potential cis-regulatory loci using allele-specific chromatin accessibility as weights in a kernel-based variance component test. Bmc Proceedings. 10: 103-108. PMID 27980619 DOI: 10.1186/S12919-016-0013-1  0.356
2016 Blangero J, Teslovich TM, Sim X, Almeida MA, Jun G, Dyer TD, Johnson M, Peralta JM, Manning A, Wood AR, Fuchsberger C, Kent JW, Aguilar DA, Below JE, Farook VS, et al. Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19. Bmc Proceedings. 10: 71-77. PMID 27980614 DOI: 10.1186/S12919-016-0008-Y  0.398
2016 Zhou H, Blangero J, Dyer TD, Chan KK, Lange K, Sobel EM. Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data. Genetic Epidemiology. PMID 27943406 DOI: 10.1002/Gepi.21988  0.428
2016 McCarthy NS, Melton PE, Ward SV, Allan SM, Dragovic M, Clark ML, Morar B, Rubio JP, Blangero J, Badcock JC, Morgan VA, Moses EK, Jablensky A. Exome array analysis suggests an increased variant burden in families with schizophrenia. Schizophrenia Research. PMID 27939555 DOI: 10.1016/J.Schres.2016.12.007  0.36
2016 Chu AY, Deng X, Fisher VA, Drong A, Zhang Y, Feitosa MF, Liu CT, Weeks O, Choh AC, Duan Q, Dyer TD, Eicher JD, Guo X, Heard-Costa NL, Kacprowski T, ... ... Blangero J, et al. Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Nature Genetics. PMID 27918534 DOI: 10.1038/Ng.3738  0.398
2016 Kulkarni H, Mamtani M, Peralta JM, Diego V, Dyer TD, Goring H, Almasy L, Mahaney MC, Williams-Blangero S, Duggirala R, Curran JE, Blangero J. Lack of Association between SLC30A8 Variants and Type 2 Diabetes in Mexican American Families. Journal of Diabetes Research. 2016: 6463214. PMID 27896278 DOI: 10.1155/2016/6463214  0.36
2016 Ried JS, Jeff M J, Chu AY, Bragg-Gresham JL, van Dongen J, Huffman JE, Ahluwalia TS, Cadby G, Eklund N, Eriksson J, Esko T, Feitosa MF, Goel A, Gorski M, Hayward C, ... ... Blangero J, et al. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nature Communications. 7: 13357. PMID 27876822 DOI: 10.1038/Ncomms13357  0.412
2016 Hodgson K, Poldrack RA, Curran JE, Knowles EE, Mathias S, Göring HH, Yao N, Olvera RL, Fox PT, Almasy L, Duggirala R, Barch DM, Blangero J, Glahn DC. Shared Genetic Factors Influence Head Motion During MRI and Body Mass Index. Cerebral Cortex (New York, N.Y. : 1991). PMID 27744290 DOI: 10.1093/Cercor/Bhw321  0.326
2016 Guadalupe T, Mathias SR, vanErp TG, Whelan CD, Zwiers MP, Abe Y, Abramovic L, Agartz I, Andreassen OA, Arias-Vásquez A, Aribisala BS, Armstrong NJ, Arolt V, Artiges E, Ayesa-Arriola R, ... ... Blangero J, et al. Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior. PMID 27738994 DOI: 10.1007/S11682-016-9629-Z  0.38
2016 Adams HH, Hibar DP, Chouraki V, Stein JL, Nyquist PA, Rentería ME, Trompet S, Arias-Vasquez A, Seshadri S, Desrivières S, Beecham AH, Jahanshad N, Wittfeld K, Van der Lee SJ, Abramovic L, ... ... Blangero J, et al. Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. PMID 27694991 DOI: 10.1038/Nn.4398  0.616
2016 Thameem F, Puppala S, Farook VS, Kasinath BS, Blangero J, Duggirala R, Abboud HE. Genetic Variants in Toll-Like Receptor 4 Gene and Their Association Analysis with Estimated Glomerular Filtration Rate in Mexican American Families. Cardiorenal Medicine. 6: 301-6. PMID 27648011 DOI: 10.1159/000445754  0.356
2016 Ali O, Cerjak D, Kent JW, James R, Blangero J, Carless MA, Zhang Y. Methylation of SOCS3 is Inversely Associated with Metabolic Syndrome in an Epigenome-Wide Association Study of Obesity. Epigenetics. 0. PMID 27564309 DOI: 10.1080/15592294.2016.1216284  0.326
2016 Hodgson K, Almasy L, Knowles EE, Kent JW, Curran JE, Dyer TD, Göring HH, Olvera RL, Woolsey MD, Duggirala R, Fox PT, Blangero J, Glahn DC. The genetic basis of the comorbidity between cannabis use and major depression. Addiction (Abingdon, England). PMID 27517884 DOI: 10.1111/add.13558  0.327
2016 Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Blangero J, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642  0.375
2016 Nicholson AM, Finch NA, Almeida M, Perkerson RB, van Blitterswijk M, Wojtas A, Cenik B, Rotondo S, Inskeep V, Almasy L, Dyer T, Peralta J, Jun G, Wood AR, Frayling TM, ... ... Blangero J, et al. Prosaposin is a regulator of progranulin levels and oligomerization. Nature Communications. 7: 11992. PMID 27356620 DOI: 10.1038/Ncomms11992  0.317
2016 Hanson RL, Leti F, Tsinajinnie D, Kobes S, Puppala S, Curran JE, Almasy L, Lehman DM, Blangero J, Duggirala R, DiStefano JK. The Arg59Trp variant in ANGPTL8 (betatrophin) is associated with total and HDL-cholesterol in American Indians and Mexican Americans and differentially affects cleavage of ANGPTL3. Molecular Genetics and Metabolism. PMID 27117576 DOI: 10.1016/J.Ymgme.2016.04.007  0.352
2016 Jenkinson CP, Göring HH, Arya R, Blangero J, Duggirala R, DeFronzo RA. Transcriptomics in type 2 diabetes: Bridging the gap between genotype and phenotype. Genomics Data. 8: 25-36. PMID 27114903 DOI: 10.1016/J.Gdata.2015.12.001  0.445
2016 Chittoor G, Kent JW, Almeida M, Puppala S, Farook VS, Cole SA, Haack K, Göring HH, MacCluer JW, Curran JE, Carless MA, Johnson MP, Moses EK, Almasy L, Mahaney MC, ... ... Blangero J, et al. GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans. Bmc Genomics. 17: 276. PMID 27039371 DOI: 10.1186/S12864-016-2594-5  0.358
2016 Horikoshi M, Pasquali L, Wiltshire S, Huyghe JR, Mahajan A, Asimit JL, Ferreira T, Locke AE, Robertson NR, Wang X, Sim X, Fujita H, Hara K, Young R, Zhang W, ... ... Blangero J, et al. Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. Human Molecular Genetics. PMID 26911676 DOI: 10.1093/Hmg/Ddw048  0.387
2016 Yerges-Armstrong LM, Chai S, O'Connell JR, Curran JE, Blangero J, Mitchell BD, Shuldiner AR, Damcott CM. Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 26896383 DOI: 10.1093/Gerona/Glv212  0.374
2016 Lu Y, Day FR, Gustafsson S, Buchkovich ML, Na J, Bataille V, Cousminer DL, Dastani Z, Drong AW, Esko T, Evans DM, Falchi M, Feitosa MF, Ferreira T, Hedman ÅK, ... ... Blangero J, et al. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nature Communications. 7: 10495. PMID 26833246 DOI: 10.1038/Ncomms10495  0.388
2016 Kilpeläinen TO, Carli JF, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW, Hayes JE, Zhao J, Pers TH, Schick U, Grarup N, Kutalik Z, Trompet S, ... ... Blangero J, et al. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nature Communications. 7: 10494. PMID 26833098 DOI: 10.1038/Ncomms10494  0.364
2016 Mamtani M, Kulkarni H, Dyer TD, Göring HH, Neary JL, Cole SA, Kent JW, Kumar S, Glahn DC, Mahaney MC, Comuzzie AG, Almasy L, Curran JE, Duggirala R, Blangero J, et al. Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families. Clinical Epigenetics. 8: 6. PMID 26798409 DOI: 10.1186/S13148-016-0173-X  0.406
2016 Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Blangero J, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448  0.435
2016 Blangero J. Update to Blangero et al.'s "Quantitative trait nucleotide analysis using Bayesian model selection" (2005): from QTL localization to functional variant identification. Human Biology. 81: 849-52. PMID 20504201 DOI: 10.3378/027.081.0626  0.345
2016 Blangero J. Update to Blangero's "Statistical genetic approaches to human adaptability" (1993): a unified theory of genotype x environment interaction. Human Biology. 81: 547-50. PMID 20504180 DOI: 10.3378/027.081.0604  0.325
2016 Blangero J. Statistical genetic approaches to human adaptability. 1993. Human Biology. 81: 523-46. PMID 20504179 DOI: 10.3378/027.081.0603  0.404
2015 Knowles EE, Kent JW, McKay DR, Sprooten E, Mathias SR, Curran JE, Carless MA, de Almeida MA, Harald HH, Dyer TD, Olvera RL, Fox PT, Duggirala R, Almasy L, Blangero J, et al. Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression. Journal of Affective Disorders. 191: 123-131. PMID 26655122 DOI: 10.1016/J.Jad.2015.11.012  0.359
2015 Benton MC, Lea RA, Macartney-Coxson D, Bellis C, Carless MA, Curran JE, Hanna M, Eccles D, Chambers GK, Blangero J, Griffiths LR. Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate. Bmc Genetics. 16: 136. PMID 26628212 DOI: 10.1186/S12863-015-0291-Z  0.406
2015 Clark MM, Blangero J, Dyer TD, Sobel EM, Sinsheimer JS. The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions. Annals of Human Genetics. PMID 26567478 DOI: 10.1111/Ahg.12137  0.39
2015 Arya R, Del Rincon I, Farook VS, Restrepo JF, Winnier DA, Fourcaudot MJ, Battafarano DF, de Almeida M, Kumar S, Curran JE, Jenkinson CP, Blangero J, Duggirala R, Escalante A. Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis. Genetic Epidemiology. PMID 26498133 DOI: 10.1002/Gepi.21938  0.333
2015 Peters MJ, Joehanes R, Pilling LC, Schurmann C, Conneely KN, Powell J, Reinmaa E, Sutphin GL, Zhernakova A, Schramm K, Wilson YA, Kobes S, Tukiainen T, Ramos YF, ... ... Blangero J, et al. The transcriptional landscape of age in human peripheral blood. Nature Communications. 6: 8570. PMID 26490707 DOI: 10.1038/Ncomms9570  0.302
2015 Traurig M, Hanson RL, Marinelarena A, Kobes S, Piaggi P, Cole S, Curran JE, Blangero J, Göring H, Kumar S, Nelson RG, Howard BV, Knowler WC, Baier LJ, Bogardus C. Analysis of SLC16A11 variants in 12,811 American Indians: genotype-obesity interaction for type 2 diabetes and an association with RNASEK expression. Diabetes. PMID 26487785 DOI: 10.2337/Db15-0571  0.322
2015 Mathias SR, Knowles EE, Kent JW, McKay DR, Curran JE, de Almeida MA, Dyer TD, Göring HH, Olvera RL, Duggirala R, Fox PT, Almasy L, Blangero J, Glahn DC. Recurrent major depression and right hippocampal volume: A bivariate linkage and association study. Human Brain Mapping. PMID 26485182 DOI: 10.1002/Hbm.23025  0.391
2015 Benton MC, Lea RA, Macartney-Coxson D, Hanna M, Eccles DA, Carless MA, Chambers GK, Bellis C, Goring HH, Curran JE, Harper JL, Gibson G, Blangero J, Griffiths LR. A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. Plos Genetics. 11: e1005593. PMID 26474483 DOI: 10.1371/Journal.Pgen.1005593  0.44
2015 Sprooten E, Gupta CN, Knowles EE, McKay DR, Mathias SR, Curran JE, Kent JW, Carless MA, Almeida MA, Dyer TD, Göring HH, Olvera RL, Kochunov P, Fox PT, Duggirala R, ... ... Blangero J, et al. Genome-wide significant linkage of schizophrenia-related neuroanatomical trait to 12q24. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 678-86. PMID 26440917 DOI: 10.1002/Ajmg.B.32360  0.591
2015 Winkler TW, Justice AE, Graff M, Barata L, Feitosa MF, Chu S, Czajkowski J, Esko T, Fall T, Kilpeläinen TO, Lu Y, Mägi R, Mihailov E, Pers TH, Rüeger S, ... ... Blangero J, et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Plos Genetics. 11: e1005378. PMID 26426971 DOI: 10.1371/Journal.Pgen.1005378  0.362
2015 Kos MZ, Carless MA, Peralta J, Blackburn A, Almeida M, Roalf D, Pogue-Geile MF, Prasad K, Gur RC, Nimgaonkar V, Curran JE, Duggirala R, Glahn DC, Blangero J, Gur RE, et al. Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk. Schizophrenia Bulletin. PMID 26405221 DOI: 10.1093/Schbul/Sbv135  0.324
2015 Benton MC, Stuart S, Bellis C, Macartney-Coxson D, Eccles D, Curran JE, Chambers G, Blangero J, Lea RA, Grffiths LR. 'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. Investigative Genetics. 6: 11. PMID 26339467 DOI: 10.1186/S13323-015-0028-9  0.345
2015 Diego VP, de Chaves RN, Blangero J, de Souza MC, Santos D, Gomes TN, Dos Santos FK, Garganta R, Katzmarzyk PT, Maia JA. Sex-specific genetic effects in physical activity: results from a quantitative genetic analysis. Bmc Medical Genetics. 16: 58. PMID 26231751 DOI: 10.1186/S12881-015-0207-9  0.388
2015 Rodriguez-Acevedo AJ, Ferreira MA, Benton MC, Carless MA, Goring HH, Curran JE, Blangero J, Lea RA, Griffiths LR. Common polygenic variation contributes to risk of migraine in the Norfolk Island population Human Genetics. 134: 1079-1087. PMID 26220684 DOI: 10.1007/S00439-015-1587-9  0.382
2015 Fox AS, Oler JA, Shackman AJ, Shelton SE, Raveendran M, McKay DR, Converse AK, Alexander A, Davidson RJ, Blangero J, Rogers J, Kalin NH. Intergenerational neural mediators of early-life anxious temperament. Proceedings of the National Academy of Sciences of the United States of America. PMID 26150480 DOI: 10.1073/Pnas.1508593112  0.304
2015 Rudkowska I, Pérusse L, Bellis C, Blangero J, Després JP, Bouchard C, Vohl MC. Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study Journal of Nutrigenetics and Nutrigenomics. 8: 44-53. PMID 26112879 DOI: 10.1159/000431151  0.333
2015 Kulkarni H, Kos MZ, Neary J, Dyer TD, Kent JW, Göring HH, Cole SA, Comuzzie AG, Almasy L, Mahaney MC, Curran JE, Blangero J, Carless MA. Novel epigenetic determinants of type 2 diabetes in Mexican-American families. Human Molecular Genetics. 24: 5330-44. PMID 26101197 DOI: 10.1093/Hmg/Ddv232  0.315
2015 Huang YS, Ramensky V, Service SK, Jasinska AJ, Jung Y, Choi OW, Cantor RM, Juretic N, Wasserscheid J, Kaplan JR, Jorgensen MJ, Dyer TD, Dewar K, Blangero J, Wilson RK, et al. Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits. Bmc Biology. 13: 41. PMID 26092298 DOI: 10.1186/S12915-015-0152-2  0.336
2015 Thameem F, Voruganti VS, Blangero J, Comuzzie AG, Abboud HE. Evaluation of neurotrophic tyrosine receptor kinase 2 (NTRK2) as a positional candidate gene for variation in estimated glomerular filtration rate (eGFR) in Mexican American participants of San Antonio Family Heart study. Journal of Biomedical Science. 22: 23. PMID 25885044 DOI: 10.1186/S12929-015-0123-5  0.387
2015 Winnier DA, Fourcaudot M, Norton L, Abdul-Ghani MA, Hu SL, Farook VS, Coletta DK, Kumar S, Puppala S, Chittoor G, Dyer TD, Arya R, Carless M, Lehman DM, Curran JE, ... ... Blangero J, et al. Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES). Plos One. 10: e0119941. PMID 25830378 DOI: 10.1371/Journal.Pone.0119941  0.381
2015 Ganjgahi H, Winkler AM, Glahn DC, Blangero J, Kochunov P, Nichols TE. Fast and powerful heritability inference for family-based neuroimaging studies. Neuroimage. 115: 256-68. PMID 25812717 DOI: 10.1016/J.Neuroimage.2015.03.005  0.588
2015 Williams AL, Genovese G, Dyer T, Altemose N, Truax K, Jun G, Patterson N, Myers SR, Curran JE, Duggirala R, Blangero J, Reich D, Przeworski M. Non-crossover gene conversions show strong GC bias and unexpected clustering in humans. Elife. 4. PMID 25806687 DOI: 10.7554/Elife.04637  0.331
2015 Spieker EA, Kochunov P, Rowland LM, Sprooten E, Winkler AM, Olvera RL, Almasy L, Duggirala R, Fox PT, Blangero J, Glahn DC, Curran JE. Shared genetic variance between obesity and white matter integrity in Mexican Americans. Frontiers in Genetics. 6: 26. PMID 25763009 DOI: 10.3389/Fgene.2015.00026  0.608
2015 Rubicz R, Yolken R, Drigalenko E, Carless MA, Dyer TD, Kent J, Curran JE, Johnson MP, Cole SA, Fowler SP, Arya R, Puppala S, Almasy L, Moses EK, Kraig E, ... ... Blangero J, et al. Genome-wide genetic investigation of serological measures of common infections. European Journal of Human Genetics : Ejhg. PMID 25758998 DOI: 10.1038/Ejhg.2015.24  0.382
2015 Kochunov P, Jahanshad N, Marcus D, Winkler A, Sprooten E, Nichols TE, Wright SN, Hong LE, Patel B, Behrens T, Jbabdi S, Andersson J, Lenglet C, Yacoub E, Moeller S, ... ... Blangero J, et al. Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data. Neuroimage. 111: 300-11. PMID 25747917 DOI: 10.1016/J.Neuroimage.2015.02.050  0.635
2015 Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S, Buchkovich ML, Yang J, Croteau-Chonka DC, Esko T, Fall T, Ferreira T, Gustafsson S, ... ... Blangero J, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 518: 197-206. PMID 25673413 DOI: 10.1038/Nature14177  0.338
2015 Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE, Workalemahu T, Wu JM, Buchkovich ML, Heard-Costa NL, Roman TS, ... ... Blangero J, et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 518: 187-96. PMID 25673412 DOI: 10.1038/Nature14132  0.38
2015 Mahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N, Im HK, Cingolani P, Flannick J, Fontanillas P, Fuchsberger C, Gaulton KJ, Teslovich TM, ... ... Blangero J, et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Plos Genetics. 11: e1004876. PMID 25625282 DOI: 10.1371/Journal.Pgen.1004876  0.396
2015 Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, ... ... Blangero J, et al. Common genetic variants influence human subcortical brain structures. Nature. 520: 224-9. PMID 25607358 DOI: 10.1038/Nature14101  0.605
2015 Blackburn A, Almeida M, Dean A, Curran JE, Johnson MP, Moses EK, Abraham LJ, Carless MA, Dyer TD, Kumar S, Almasy L, Mahaney MC, Comuzzie A, Williams-Blangero S, Blangero J, et al. Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans. European Journal of Human Genetics : Ejhg. PMID 25585699 DOI: 10.1038/Ejhg.2014.280  0.347
2015 Toledo RA, Hatakana R, Lourenço DM, Lindsey SC, Camacho CP, Almeida M, Lima JV, Sekiya T, Garralda E, Naslavsky MS, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJ, Lebrao ML, ... ... Blangero J, et al. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility. Endocrine-Related Cancer. 22: 65-76. PMID 25425582 DOI: 10.1530/Erc-14-0491  0.316
2015 Wood AR, Tuke MA, Nalls M, Hernandez D, Gibbs JR, Lin H, Xu CS, Li Q, Shen J, Jun G, Almeida M, Tanaka T, Perry JR, Gaulton K, Rivas M, ... ... Blangero J, et al. Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. Human Molecular Genetics. 24: 1504-12. PMID 25378555 DOI: 10.1093/Hmg/Ddu560  0.372
2015 Blackburn NB, Charlesworth JC, Marthick JR, Tegg EM, Marsden KA, Srikanth V, Blangero J, Lowenthal RM, Foote SJ, Dickinson JL. A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies Study. Oncology Reports. 33: 25-32. PMID 25351806 DOI: 10.3892/Or.2014.3568  0.353
2015 Glahn DC, Williams JT, McKay DR, Knowles EE, Sprooten E, Mathias SR, Curran JE, Kent JW, Carless MA, Göring HH, Dyer TD, Woolsey MD, Winkler AM, Olvera RL, Kochunov P, ... ... Blangero J, et al. Discovering schizophrenia endophenotypes in randomly ascertained pedigrees. Biological Psychiatry. 77: 75-83. PMID 25168609 DOI: 10.1016/J.Biopsych.2014.06.027  0.583
2015 Dager AD, McKay DR, Kent JW, Curran JE, Knowles E, Sprooten E, Göring HH, Dyer TD, Pearlson GD, Olvera RL, Fox PT, Lovallo WR, Duggirala R, Almasy L, Blangero J, et al. Shared genetic factors influence amygdala volumes and risk for alcoholism. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 40: 412-20. PMID 25079289 DOI: 10.1038/Npp.2014.187  0.373
2015 Ali O, Cerjak D, Kent JW, James R, Blangero J, Carless MA, Zhang Y. An epigenetic map of age-associated autosomal loci in northern european families at high risk for the metabolic syndrome Clinical Epigenetics. 7. DOI: 10.1186/S13148-015-0048-6  0.333
2015 Moses E, Melton P, Johnson M, Gokhale-Agashe D, Rea A, Allcock R, Blangero J, Brennecke S. O4. Genome wide sequencing approaches to identify missing heritability of preeclampsia Pregnancy Hypertension: An International Journal of Women's Cardiovascular Health. 5: 209-210. DOI: 10.1016/J.Preghy.2015.07.005  0.376
2015 MacCluer JW, Blangero J, Comuzzie AG, Ebbesson SOE, Howard BV, Cole SA. Genetics of cardiovascular disease in minority populations Genome Mapping and Genomics in Human and Non-Human Primates. 155-179. DOI: 10.1007/978-3-662-46306-2_11  0.332
2014 Løset M, Johnson MP, Melton PE, Ang W, Huang RC, Mori TA, Beilin LJ, Pennell C, Roten LT, Iversen AC, Austgulen R, East CE, Blangero J, Brennecke SP, Moses EK. Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22. Pregnancy Hypertension. 4: 178-85. PMID 26104425 DOI: 10.1016/J.Preghy.2014.03.005  0.334
2014 Koran ME, Thornton-Wells TA, Jahanshad N, Glahn DC, Thompson PM, Blangero J, Nichols TE, Kochunov P, Landman BA. Impact of family structure and common environment on heritability estimation for neuroimaging genetics studies using Sequential Oligogenic Linkage Analysis Routines. Journal of Medical Imaging (Bellingham, Wash.). 1: 014005. PMID 25558465 DOI: 10.1117/1.Jmi.1.1.014005  0.609
2014 Quillen EE, Voruganti VS, Chittoor G, Rubicz R, Peralta JM, Almeida MA, Kent JW, Diego VP, Dyer TD, Comuzzie AG, Göring HH, Duggirala R, Almasy L, Blangero J. Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure. Bmc Proceedings. 8: S66. PMID 25519398 DOI: 10.1186/1753-6561-8-S1-S66  0.462
2014 Peralta JM, Almeida M, Kent JW, Blangero J. A variance component-based gene burden test. Bmc Proceedings. 8: S49. PMID 25519388 DOI: 10.1186/1753-6561-8-S1-S49  0.39
2014 Almeida M, Peralta JM, Farook V, Puppala S, Kent JW, Duggirala R, Blangero J. Pedigree-based random effect tests to screen gene pathways. Bmc Proceedings. 8: S100. PMID 25519354 DOI: 10.1186/1753-6561-8-S1-S100  0.429
2014 Almasy L, Dyer TD, Peralta JM, Jun G, Wood AR, Fuchsberger C, Almeida MA, Kent JW, Fowler S, Blackwell TW, Puppala S, Kumar S, Curran JE, Lehman D, Abecasis G, ... ... Blangero J, et al. Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees. Bmc Proceedings. 8: S2. PMID 25519314 DOI: 10.1186/1753-6561-8-S1-S2  0.4
2014 Gottlieb DJ, Hek K, Chen TH, Watson NF, Eiriksdottir G, Byrne EM, Cornelis M, Warby SC, Bandinelli S, Cherkas L, Evans DS, Grabe HJ, Lahti J, Li M, Lehtimäki T, ... ... Blangero J, et al. Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Molecular Psychiatry. PMID 25469926 DOI: 10.1038/Mp.2014.133  0.337
2014 Bellis C, Kulkarni H, Mamtani M, Kent JW, Wong G, Weir JM, Barlow CK, Diego V, Almeida M, Dyer TD, Göring HH, Almasy L, Mahaney MC, Comuzzie AG, Williams-Blangero S, ... ... Blangero J, et al. Human plasma lipidome is pleiotropically associated with cardiovascular risk factors and death. Circulation. Cardiovascular Genetics. 7: 854-63. PMID 25363705 DOI: 10.1161/Circgenetics.114.000600  0.327
2014 Jones RM, Cadby G, Blangero J, Abraham LJ, Whitehouse AJ, Moses EK. MACROD2 gene associated with autistic-like traits in a general population sample. Psychiatric Genetics. 24: 241-8. PMID 25360606 DOI: 10.1097/Ypg.0000000000000052  0.388
2014 Santos DM, Katzmarzyk PT, Diego VP, Blangero J, Souza MC, Freitas DL, Chaves RN, Gomes TN, Santos FK, Maia JA. Genotype by sex and genotype by age interactions with sedentary behavior: the Portuguese Healthy Family Study. Plos One. 9: e110025. PMID 25302714 DOI: 10.1371/Journal.Pone.0110025  0.398
2014 Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J, Kutalik Z, Amin N, Buchkovich ML, Croteau-Chonka DC, Day FR, Duan Y, ... ... Blangero J, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics. 46: 1173-86. PMID 25282103 DOI: 10.1038/Ng.3097  0.398
2014 Zhang X, Gierman HJ, Levy D, Plump A, Dobrin R, Goring HH, Curran JE, Johnson MP, Blangero J, Kim SK, O'Donnell CJ, Emilsson V, Johnson AD. Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs. Bmc Genomics. 15: 532. PMID 24973796 DOI: 10.1186/1471-2164-15-532  0.342
2014 Rubicz R, Yolken R, Alaedini A, Drigalenko E, Charlesworth JC, Carless MA, Severance EG, Krivogorsky B, Dyer TD, Kent JW, Curran JE, Johnson MP, Cole SA, Almasy L, Moses EK, ... Blangero J, et al. Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens. Genetic Epidemiology. 38: 439-46. PMID 24962563 DOI: 10.1002/Gepi.21817  0.386
2014 Chouinard-Decorte F, McKay DR, Reid A, Khundrakpam B, Zhao L, Karama S, Rioux P, Sprooten E, Knowles E, Kent JW, Curran JE, Göring HH, Dyer TD, Olvera RL, Kochunov P, ... ... Blangero J, et al. Heritable changes in regional cortical thickness with age. Brain Imaging and Behavior. 8: 208-16. PMID 24752552 DOI: 10.1007/S11682-014-9296-X  0.596
2014 Sprooten E, Knowles EE, McKay DR, Göring HH, Curran JE, Kent JW, Carless MA, Dyer TD, Drigalenko EI, Olvera RL, Fox PT, Almasy L, Duggirala R, Kochunov P, Blangero J, et al. Common genetic variants and gene expression associated with white matter microstructure in the human brain. Neuroimage. 97: 252-61. PMID 24736177 DOI: 10.1016/J.Neuroimage.2014.04.021  0.621
2014 Kos MZ, Glahn DC, Carless MA, Olvera R, McKay DR, Quillen EE, Gelernter J, Chen XD, Deng HW, Kent JW, Dyer TD, Göring HH, Curran JE, Duggirala R, Blangero J, et al. Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 294-302. PMID 24692236 DOI: 10.1002/Ajmg.B.32231  0.378
2014 Ali O, Cerjak D, Kent JW, James R, Blangero J, Zhang Y. Obesity, central adiposity and cardiometabolic risk factors in children and adolescents: a family-based study. Pediatric Obesity. 9: e58-e62. PMID 24677702 DOI: 10.1111/J.2047-6310.2014.218.X  0.324
2014 Kochunov P, Jahanshad N, Sprooten E, Nichols TE, Mandl RC, Almasy L, Booth T, Brouwer RM, Curran JE, de Zubicaray GI, Dimitrova R, Duggirala R, Fox PT, Hong LE, Landman BA, ... ... Blangero J, et al. Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling. Neuroimage. 95: 136-50. PMID 24657781 DOI: 10.1016/J.Neuroimage.2014.03.033  0.608
2014 Kulkarni H, Meikle PJ, Mamtani M, Weir JM, Almeida M, Diego V, Peralta JM, Barlow CK, Bellis C, Dyer TD, Almasy L, Mahaney MC, Comuzzie AG, Göring HH, Curran JE, ... Blangero J, et al. Plasma lipidome is independently associated with variability in metabolic syndrome in Mexican American families. Journal of Lipid Research. 55: 939-46. PMID 24627127 DOI: 10.1194/Jlr.M044065  0.348
2014 Flannick J, Thorleifsson G, Beer NL, Jacobs SB, Grarup N, Burtt NP, Mahajan A, Fuchsberger C, Atzmon G, Benediktsson R, Blangero J, Bowden DW, Brandslund I, Brosnan J, Burslem F, et al. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nature Genetics. 46: 357-63. PMID 24584071 DOI: 10.1038/Ng.2915  0.314
2014 Glahn DC, Knowles EE, McKay DR, Sprooten E, Raventós H, Blangero J, Gottesman II, Almasy L. Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 122-30. PMID 24464604 DOI: 10.1002/Ajmg.B.32221  0.431
2014 Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, Toro R, Jahanshad N, Schumann G, Franke B, Wright MJ, Martin NG, Agartz I, Alda M, Alhusaini S, ... ... Blangero J, et al. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 8: 153-82. PMID 24399358 DOI: 10.1007/S11682-013-9269-5  0.597
2014 McKay DR, Knowles EE, Winkler AA, Sprooten E, Kochunov P, Olvera RL, Curran JE, Kent JW, Carless MA, Göring HH, Dyer TD, Duggirala R, Almasy L, Fox PT, Blangero J, et al. Influence of age, sex and genetic factors on the human brain. Brain Imaging and Behavior. 8: 143-52. PMID 24297733 DOI: 10.1007/S11682-013-9277-5  0.608
2014 Knowles EE, Carless MA, de Almeida MA, Curran JE, McKay DR, Sprooten E, Dyer TD, Göring HH, Olvera R, Fox P, Almasy L, Duggirala R, Kent JW, Blangero J, Glahn DC. Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 84-95. PMID 24243780 DOI: 10.1002/Ajmg.B.32211  0.362
2014 Kaskow BJ, Diepeveen LA, Proffitt JM, Rea AJ, Ulgiati D, Blangero J, Moses EK, Abraham LJ. Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1. European Journal of Human Genetics : Ejhg. 22: 688-95. PMID 24045843 DOI: 10.1038/Ejhg.2013.208  0.343
2014 Wey HY, Phillips KA, McKay DR, Laird AR, Kochunov P, Davis MD, Glahn DC, Blangero J, Duong TQ, Fox PT. Multi-region hemispheric specialization differentiates human from nonhuman primate brain function. Brain Structure & Function. 219: 2187-94. PMID 23928747 DOI: 10.1007/S00429-013-0620-9  0.439
2014 Mamtani M, Kulkarni H, Dyer TD, Almasy L, Mahaney MC, Duggirala R, Comuzzie AG, Blangero J, Curran JE. Waist circumference is genetically correlated with incident Type 2 diabetes in Mexican-American families Diabetic Medicine. 31: 31-35. PMID 23796311 DOI: 10.1111/Dme.12266  0.364
2014 Choh AC, Lee M, Kent JW, Diego VP, Johnson W, Curran JE, Dyer TD, Bellis C, Blangero J, Siervogel RM, Towne B, Demerath EW, Czerwinski SA. Gene-by-age effects on BMI from birth to adulthood: the Fels Longitudinal Study. Obesity (Silver Spring, Md.). 22: 875-81. PMID 23794238 DOI: 10.1002/Oby.20517  0.369
2014 Blangero J. Complex rare variation and its role in endophenotypic variation in schizophrenia. Biological Psychiatry. 73: 499-500. PMID 23438633 DOI: 10.1016/J.Biopsych.2013.01.028  0.346
2014 Koran ME, Li B, Jahanshad N, Thornton-Wells TA, Glahn DC, Thompson PM, Blangero J, Nichols TE, Kochunov P, Landman BA. On study design in neuroimaging heritability analyses Progress in Biomedical Optics and Imaging - Proceedings of Spie. 9034. DOI: 10.1117/12.2043565  0.635
2014 Jahanshad N, Kochunov PV, Sprooten E, Mandl RC, Nichols TE, Almasy L, Blangero J, Brouwer RM, Curran JE, de Zubicaray GI, Duggirala R, Fox PT, Hong LE, Landman BA, Martin NG, et al. Corrigendum to Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group [NeuroImage 81 (2013) 455-469] Neuroimage. 90: 470-471. DOI: 10.1016/J.Neuroimage.2013.12.053  0.545
2014 Jahanshad N, Kochunov P, Nichols TE, Sprooten E, Mandl RC, Almasy L, Brouwer RM, Curran JE, De Zubicaray GI, Dimitrova R, Fox PT, Hong LE, Landman BA, Lemaitre H, Lopez L, ... ... Blangero J, et al. Combining Meta- and mega-analytic approaches for multi-site diffusion imaging based genetic studies: From the enigma-DTI working group 2014 Ieee 11th International Symposium On Biomedical Imaging, Isbi 2014. 1234-1238.  0.482
2013 Løset M, Johnson MP, Melton PE, Ang W, Marsh J, Huang RC, Mori T, Beilin L, Pennell C, Roten LT, Iversen AC, Austgulen R, East CE, Blangero J, Brennecke SP, et al. OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits. Pregnancy Hypertension. 3: 63. PMID 26105849 DOI: 10.1016/J.Preghy.2013.04.020  0.41
2013 Voruganti VS, Kent JW, Debnath S, Cole SA, Haack K, Göring HH, Carless MA, Curran JE, Johnson MP, Almasy L, Dyer TD, Maccluer JW, Moses EK, Abboud HE, Mahaney MC, ... Blangero J, et al. Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Frontiers in Genetics. 4: 279. PMID 24379826 DOI: 10.3389/Fgene.2013.00279  0.38
2013 Benton MC, Lea RA, Macartney-Coxson D, Carless MA, Göring HH, Bellis C, Hanna M, Eccles D, Chambers GK, Curran JE, Harper JL, Blangero J, Griffiths LR. Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. American Journal of Human Genetics. 93: 1087-99. PMID 24314549 DOI: 10.1016/J.Ajhg.2013.11.004  0.419
2013 Santos DM, Katzmarzyk PT, Diego VP, Souza MC, Chaves RN, Blangero J, Maia JA. Genotype by energy expenditure interaction with metabolic syndrome traits: the Portuguese healthy family study. Plos One. 8: e80417. PMID 24260389 DOI: 10.1371/Journal.Pone.0080417  0.324
2013 Glahn DC, Kent JW, Sprooten E, Diego VP, Winkler AM, Curran JE, McKay DR, Knowles EE, Carless MA, Göring HH, Dyer TD, Olvera RL, Fox PT, Almasy L, Charlesworth J, ... ... Blangero J, et al. Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging. Proceedings of the National Academy of Sciences of the United States of America. 110: 19006-11. PMID 24191011 DOI: 10.1073/Pnas.1313735110  0.566
2013 Demerath EW, Choh AC, Johnson W, Curran JE, Lee M, Bellis C, Dyer TD, Czerwinski SA, Blangero J, Towne B. The positive association of obesity variants with adulthood adiposity strengthens over an 80-year period: a gene-by-birth year interaction. Human Heredity. 75: 175-85. PMID 24081233 DOI: 10.1159/000351742  0.341
2013 Curran JE, McKay DR, Winkler AM, Olvera RL, Carless MA, Dyer TD, Kent JW, Kochunov P, Sprooten E, Knowles EE, Comuzzie AG, Fox PT, Almasy L, Duggirala R, Blangero J, et al. Identification of pleiotropic genetic effects on obesity and brain anatomy. Human Heredity. 75: 136-43. PMID 24081229 DOI: 10.1159/000353953  0.593
2013 McKay DR, Kochunov P, Cykowski MD, Kent JW, Laird AR, Lancaster JL, Blangero J, Glahn DC, Fox PT. Sulcal depth-position profile is a genetically mediated neuroscientific trait: description and characterization in the central sulcus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 15618-25. PMID 24068828 DOI: 10.1523/Jneurosci.1616-13.2013  0.614
2013 Farook VS, Coletta DK, Puppala S, Schneider J, Chittoor G, Hu SL, Winnier DA, Norton L, Dyer TD, Arya R, Cole SA, Carless M, Göring HH, Almasy L, Mahaney MC, ... ... Blangero J, et al. Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES). Human Heredity. 76: 36-46. PMID 24060607 DOI: 10.1159/000354849  0.355
2013 Carless MA, Kulkarni H, Kos MZ, Charlesworth J, Peralta JM, Göring HH, Curran JE, Almasy L, Dyer TD, Comuzzie AG, Mahaney MC, Blangero J. Genetic effects on DNA methylation and its potential relevance for obesity in Mexican Americans. Plos One. 8: e73950. PMID 24058506 DOI: 10.1371/Journal.Pone.0073950  0.35
2013 Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, ... ... Blangero J, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/Ng.2758  0.328
2013 Weir JM, Wong G, Barlow CK, Greeve MA, Kowalczyk A, Almasy L, Comuzzie AG, Mahaney MC, Jowett JB, Shaw J, Curran JE, Blangero J, Meikle PJ. Plasma lipid profiling in a large population-based cohort. Journal of Lipid Research. 54: 2898-908. PMID 23868910 DOI: 10.1194/Jlr.P035808  0.301
2013 Kulkarni H, Meikle PJ, Mamtani M, Weir JM, Barlow CK, Jowett JB, Bellis C, Dyer TD, Johnson MP, Rainwater DL, Almasy L, Mahaney MC, Comuzzie AG, Blangero J, Curran JE. Plasma lipidomic profile signature of hypertension in Mexican American families: specific role of diacylglycerols. Hypertension. 62: 621-6. PMID 23798346 DOI: 10.1161/Hypertensionaha.113.01396  0.318
2013 Fowler SP, Puppala S, Arya R, Chittoor G, Farook VS, Schneider J, Resendez RG, Upadhayay RP, Vandeberg J, Hunt KJ, Bradshaw B, Cersosimo E, Vandeberg JL, Almasy L, Curran JE, ... ... Blangero J, et al. Genetic epidemiology of cardiometabolic risk factors and their clustering patterns in Mexican American children and adolescents: the SAFARI Study. Human Genetics. 132: 1059-71. PMID 23736306 DOI: 10.1007/S00439-013-1315-2  0.351
2013 Kochunov P, Charlesworth J, Winkler A, Hong LE, Nichols TE, Curran JE, Sprooten E, Jahanshad N, Thompson PM, Johnson MP, Kent JW, Landman BA, Mitchell B, Cole SA, Dyer TD, ... ... Blangero J, et al. Transcriptomics of cortical gray matter thickness decline during normal aging. Neuroimage. 82: 273-83. PMID 23707588 DOI: 10.1016/J.Neuroimage.2013.05.066  0.556
2013 Chittoor G, Farook VS, Puppala S, Fowler SP, Schneider J, Dyer TD, Cole SA, Lynch JL, Curran JE, Almasy L, Maccluer JW, Comuzzie AG, Hale DE, Ramamurthy RS, Dudley DJ, ... ... Blangero J, et al. Localization of a major susceptibility locus influencing preterm birth. Molecular Human Reproduction. 19: 687-96. PMID 23689979 DOI: 10.1093/Molehr/Gat036  0.395
2013 Jahanshad N, Kochunov PV, Sprooten E, Mandl RC, Nichols TE, Almasy L, Blangero J, Brouwer RM, Curran JE, de Zubicaray GI, Duggirala R, Fox PT, Hong LE, Landman BA, Martin NG, et al. Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group. Neuroimage. 81: 455-69. PMID 23629049 DOI: 10.1016/J.Neuroimage.2013.04.061  0.602
2013 Zhang Y, Kent JW, Olivier M, Ali O, Cerjak D, Broeckel U, Abdou RM, Dyer TD, Comuzzie A, Curran JE, Carless MA, Rainwater DL, Göring HH, Blangero J, Kissebah AH. A comprehensive analysis of adiponectin QTLs using SNP association, SNP cis-effects on peripheral blood gene expression and gene expression correlation identified novel metabolic syndrome (MetS) genes with potential role in carcinogenesis and systemic inflammation. Bmc Medical Genomics. 6: 14. PMID 23628382 DOI: 10.1186/1755-8794-6-14  0.34
2013 Zhang Y, Kent JW, Lee A, Cerjak D, Ali O, Diasio R, Olivier M, Blangero J, Carless MA, Kissebah AH. Fatty acid binding protein 3 (fabp3) is associated with insulin, lipids and cardiovascular phenotypes of the metabolic syndrome through epigenetic modifications in a Northern European family population. Bmc Medical Genomics. 6: 9. PMID 23510163 DOI: 10.1186/1755-8794-6-9  0.329
2013 Plourde M, Vohl MC, Bellis C, Carless M, Dyer T, Dolley G, Marette A, Després JP, Bouchard C, Blangero J, Pérusse L. A variant in the LRRFIP1 gene is associated with adiposity and inflammation. Obesity (Silver Spring, Md.). 21: 185-92. PMID 23505185 DOI: 10.1002/Oby.20242  0.361
2013 Melton PE, Carless MA, Curran JE, Dyer TD, Göring HH, Kent JW, Drigalenko E, Johnson MP, Maccluer JW, Moses EK, Comuzzie AG, Mahaney MC, O'Leary DH, Blangero J, Almasy L. Genetic architecture of carotid artery intima-media thickness in Mexican Americans. Circulation. Cardiovascular Genetics. 6: 211-21. PMID 23487405 DOI: 10.1161/Circgenetics.113.000079  0.364
2013 Johnson MP, Brennecke SP, East CE, Dyer TD, Roten LT, Proffitt JM, Melton PE, Fenstad MH, Aalto-Viljakainen T, Mäkikallio K, Heinonen S, Kajantie E, Kere J, Laivuori H, ... ... Blangero J, et al. Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. Molecular Human Reproduction. 19: 423-37. PMID 23420841 DOI: 10.1093/Molehr/Gat011  0.393
2013 Blangero J, Diego VP, Dyer TD, Almeida M, Peralta J, Kent JW, Williams JT, Almasy L, Göring HH. A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees. Advances in Genetics. 81: 1-31. PMID 23419715 DOI: 10.1016/B978-0-12-407677-8.00001-4  0.442
2013 Zhang Y, Kent JW, Olivier M, Ali O, Broeckel U, Abdou RM, Dyer TD, Comuzzie A, Curran JE, Carless MA, Rainwater DL, Göring HHH, Blangero J, Kissebah AH. QTL-based association analyses reveal novel genes influencing pleiotropy of metabolic syndrome (MetS) Obesity. 21: 2099-2111. PMID 23418049 DOI: 10.1002/Oby.20324  0.433
2013 Rubicz R, Yolken R, Drigalenko E, Carless MA, Dyer TD, Bauman L, Melton PE, Kent JW, Harley JB, Curran JE, Johnson MP, Cole SA, Almasy L, Moses EK, Dhurandhar NV, ... ... Blangero J, et al. A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). Plos Genetics. 9: e1003147. PMID 23326239 DOI: 10.1371/Journal.Pgen.1003147  0.349
2013 Johnson W, Choh AC, Curran JE, Czerwinski SA, Bellis C, Dyer TD, Blangero J, Towne B, Demerath EW. Genetic risk for earlier menarche also influences peripubertal body mass index. American Journal of Physical Anthropology. 150: 10-20. PMID 23283660 DOI: 10.1002/Ajpa.22121  0.368
2013 Kochunov P, Glahn DC, Rowland LM, Olvera RL, Winkler A, Yang YH, Sampath H, Carpenter WT, Duggirala R, Curran J, Blangero J, Hong LE. Testing the hypothesis of accelerated cerebral white matter aging in schizophrenia and major depression. Biological Psychiatry. 73: 482-91. PMID 23200529 DOI: 10.1016/J.Biopsych.2012.10.002  0.517
2013 Koller DL, Zheng HF, Karasik D, Yerges-Armstrong L, Liu CT, McGuigan F, Kemp JP, Giroux S, Lai D, Edenberg HJ, Peacock M, Czerwinski SA, Choh AC, McMahon G, St Pourcain B, ... ... Blangero J, et al. Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 547-58. PMID 23074152 DOI: 10.1002/Jbmr.1796  0.334
2013 Blackburn A, Göring HH, Dean A, Carless MA, Dyer T, Kumar S, Fowler S, Curran JE, Almasy L, Mahaney M, Comuzzie A, Duggirala R, Blangero J, Lehman DM. Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans. European Journal of Human Genetics : Ejhg. 21: 404-9. PMID 22909773 DOI: 10.1038/Ejhg.2012.188  0.428
2013 Wey H, Phillips KA, McKay DR, Laird AR, Kochunov P, Davis MD, Glahn DC, Blangero J, Duong TQ, Fox PT. Erratum to: Multi-region hemispheric specialization differentiates human from nonhuman primate brain function Brain Structure and Function. 219: 2195-2195. DOI: 10.1007/S00429-013-0635-2  0.534
2012 Moses E, Johnson M, East C, Dyer T, Roten L, Proffitt J, Fenstad M, Aalto-Viljakainen T, Mäkikallio K, Heinonen S, Kajantie E, Kere J, Laivuori H, Austgulen R, Blangero J, et al. OS077. The chromosome 2q22 preeclampsia susceptibility locus reveals shared novel risk factors for CVD. Pregnancy Hypertension. 2: 219-20. PMID 26105291 DOI: 10.1016/J.Preghy.2012.04.078  0.346
2012 Løset M, Johnson MP, Pennell C, Huang RC, Mori T, Beilin L, Melton P, Roten LT, Iversen AC, Austgulen R, East C, Blangero J, Brennecke SP, Moses EK. OS070. Shared genetic risk factors for preeclampsia and cardiovascular disease. Pregnancy Hypertension. 2: 214-5. PMID 26105283 DOI: 10.1016/J.Preghy.2012.04.071  0.436
2012 Johnson M, Løset M, Brennecke S, Peralta J, Dyer T, East C, Pennell C, Huang RC, Mori T, Beilin L, Blangero J, Moses E. OS049. Exome sequencing identifies likely functional variantsinfluencing preeclampsia and CVD risk. Pregnancy Hypertension. 2: 203-4. PMID 26105263 DOI: 10.1016/J.Preghy.2012.04.050  0.4
2012 Johnson M, Brennecke S, Iversen AC, East C, Olsen G, Kent J, Dyer T, Said J, Roten L, Abraham L, Zwart JA, Winsvold B, Håberg A, Huentelman M, Krokan H, ... ... Blangero J, et al. OS046. Genome-wide association scans identify novel maternalsusceptibility loci for preeclampsia. Pregnancy Hypertension. 2: 202. PMID 26105260 DOI: 10.1016/J.Preghy.2012.04.047  0.386
2012 López S, Buil A, Souto JC, Casademont J, Blangero J, Martinez-Perez A, Fontcuberta J, Lathrop M, Almasy L, Soria JM. Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci. Plos One. 7: e42711. PMID 22916149 DOI: 10.1371/Journal.Pone.0042711  0.403
2012 Kent JW, Göring HH, Charlesworth JC, Drigalenko E, Diego VP, Curran JE, Johnson MP, Dyer TD, Cole SA, Jowett JB, Mahaney MC, Comuzzie AG, Almasy L, Moses EK, Blangero J, et al. Genotype×age interaction in human transcriptional ageing. Mechanisms of Ageing and Development. 133: 581-90. PMID 22871458 DOI: 10.1016/J.Mad.2012.07.005  0.344
2012 Bastarrachea RA, Gallegos-Cabriales EC, Nava-González EJ, Haack K, Voruganti VS, Charlesworth J, Laviada-Molina HA, Veloz-Garza RA, Cardenas-Villarreal VM, Valdovinos-Chavez SB, Gomez-Aguilar P, Meléndez G, López-Alvarenga JC, Göring HH, Cole SA, ... Blangero J, et al. Integrating genomic analysis with the genetic basis of gene expression: preliminary evidence of the identification of causal genes for cardiovascular and metabolic traits related to nutrition in Mexicans. Advances in Nutrition (Bethesda, Md.). 3: 596S-604S. PMID 22797999 DOI: 10.3945/An.112.001925  0.395
2012 Voruganti VS, Higgins PB, Ebbesson SO, Kennish J, Göring HH, Haack K, Laston S, Drigalenko E, Wenger CR, Harris WS, Fabsitz RR, Devereux RB, Maccluer JW, Curran JE, Carless MA, ... ... Blangero J, et al. Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos. Frontiers in Genetics. 3: 86. PMID 22701466 DOI: 10.3389/Fgene.2012.00086  0.365
2012 Liu CT, Estrada K, Yerges-Armstrong LM, Amin N, Evangelou E, Li G, Minster RL, Carless MA, Kammerer CM, Oei L, Zhou Y, Alonso N, Dailiana Z, Eriksson J, García-Giralt N, ... ... Blangero J, et al. Assessment of gene-by-sex interaction effect on bone mineral density. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 27: 2051-64. PMID 22692763 DOI: 10.1002/Jbmr.1679  0.358
2012 Cox HC, Lea RA, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth J, Macgregor S, Nyholt D, Chasman D, Ridker PM, Schürks M, Blangero J, Griffiths LR. A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility. Neurogenetics. 13: 261-6. PMID 22678113 DOI: 10.1007/S10048-012-0325-X  0.429
2012 Maher BH, Lea RA, Benton M, Cox HC, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth JC, Buring JE, Kurth T, Chasman DI, Ridker PM, Schürks M, Blangero J, et al. An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. Plos One. 7: e37903. PMID 22666411 DOI: 10.1371/Journal.Pone.0037903  0.385
2012 Thameem F, Puppala S, Schneider J, Bhandari B, Arya R, Arar NH, Vasylyeva TL, Farook VS, Fowler S, Almasy L, Blangero J, Duggirala R, Abboud HE. The Gly(972)Arg variant of human IRS1 gene is associated with variation in glomerular filtration rate likely through impaired insulin receptor signaling. Diabetes. 61: 2385-93. PMID 22617042 DOI: 10.2337/Db11-1078  0.414
2012 Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, ... ... Blangero J, et al. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics. 44: 659-69. PMID 22581228 DOI: 10.1038/Ng.2274  0.368
2012 Quillen EE, Rainwater DL, Dyer TD, Carless MA, Curran JE, Johnson MP, Göring HH, Cole SA, Rutherford S, Maccluer JW, Moses EK, Blangero J, Almasy L, Mahaney MC. Novel associations of nonstructural Loci with paraoxonase activity. Journal of Lipids. 2012: 189681. PMID 22577559 DOI: 10.1155/2012/189681  0.398
2012 Kochunov P, Glahn DC, Hong LE, Lancaster J, Curran JE, Johnson MP, Winkler AM, Holcomb HH, Kent JW, Mitchell B, Kochunov V, Olvera RL, Cole SA, Dyer TD, Moses EK, ... ... Blangero J, et al. P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans. Frontiers in Genetics. 3: 65. PMID 22558002 DOI: 10.3389/Fgene.2012.00065  0.379
2012 Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, ... ... Blangero J, et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 44: 552-61. PMID 22504417 DOI: 10.1038/Ng.2250  0.585
2012 Farook VS, Puppala S, Schneider J, Fowler SP, Chittoor G, Dyer TD, Allayee H, Cole SA, Arya R, Black MH, Curran JE, Almasy L, Buchanan TA, Jenkinson CP, Lehman DM, ... ... Blangero J, et al. Metabolic syndrome is linked to chromosome 7q21 and associated with genetic variants in CD36 and GNAT3 in Mexican Americans. Obesity (Silver Spring, Md.). 20: 2083-92. PMID 22456541 DOI: 10.1038/Oby.2012.74  0.348
2012 Winkler AM, Sabuncu MR, Yeo BT, Fischl B, Greve DN, Kochunov P, Nichols TE, Blangero J, Glahn DC. Measuring and comparing brain cortical surface area and other areal quantities. Neuroimage. 61: 1428-43. PMID 22446492 DOI: 10.1016/J.Neuroimage.2012.03.026  0.498
2012 Johnson MP, Brennecke SP, East CE, Göring HH, Kent JW, Dyer TD, Said JM, Roten LT, Iversen AC, Abraham LJ, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, ... ... Blangero J, et al. Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. Plos One. 7: e33666. PMID 22432041 DOI: 10.1371/Journal.Pone.0033666  0.371
2012 Williams-Blangero S, Criscione CD, VandeBerg JL, Correa-Oliveira R, Williams KD, Subedi J, Kent JW, Williams J, Kumar S, Blangero J. Host genetics and population structure effects on parasitic disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 367: 887-94. PMID 22312056 DOI: 10.1098/Rstb.2011.0296  0.319
2012 Lee M, Choh AC, Williams KD, Schroeder V, Dyer TD, Blangero J, Cole SA, Chumlea WC, Duren DL, Sherwood RJ, Siervogel RM, Towne B, Czerwinski SA. Genome-wide linkage scan for quantitative trait loci underlying normal variation in heel bone ultrasound measures. The Journal of Nutrition, Health & Aging. 16: 8-13. PMID 22237995 DOI: 10.1007/S12603-011-0080-Y  0.42
2012 Cox HC, Lea RA, Bellis C, Nyholt DR, Dyer TD, Haupt LM, Charlesworth J, Matovinovic E, Blangero J, Griffiths LR. Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. Gene. 494: 119-23. PMID 22197687 DOI: 10.1016/J.Gene.2011.11.056  0.446
2012 Kaskow BJ, Proffitt JM, Michael Proffit J, Blangero J, Moses EK, Abraham LJ. Diverse biological activities of the vascular non-inflammatory molecules - the Vanin pantetheinases. Biochemical and Biophysical Research Communications. 417: 653-8. PMID 22155241 DOI: 10.1016/J.Bbrc.2011.11.099  0.309
2012 Diego VP, Curran JE, Charlesworth J, Peralta JM, Voruganti VS, Cole SA, Dyer TD, Johnson MP, Moses EK, Göring HH, Williams JT, Comuzzie AG, Almasy L, Blangero J, Williams-Blangero S. Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging. Mechanisms of Ageing and Development. 133: 11-9. PMID 22155176 DOI: 10.1016/J.Mad.2011.11.007  0.337
2012 Glahn DC, Curran JE, Winkler AM, Carless MA, Kent JW, Charlesworth JC, Johnson MP, Göring HH, Cole SA, Dyer TD, Moses EK, Olvera RL, Kochunov P, Duggirala R, Fox PT, ... ... Blangero J, et al. High dimensional endophenotype ranking in the search for major depression risk genes. Biological Psychiatry. 71: 6-14. PMID 21982424 DOI: 10.1016/J.Biopsych.2011.08.022  0.573
2012 Cummings N, Shields KA, Curran JE, Bozaoglu K, Trevaskis J, Gluschenko K, Cai G, Comuzzie AG, Dyer TD, Walder KR, Zimmet P, Collier GR, Blangero J, Jowett JB. Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass. International Journal of Obesity (2005). 36: 201-6. PMID 21407171 DOI: 10.1038/Ijo.2011.67  0.339
2012 Kochunov P, Williamson DE, Lancaster J, Fox P, Cornell J, Blangero J, Glahn DC. Fractional anisotropy of water diffusion in cerebral white matter across the lifespan. Neurobiology of Aging. 33: 9-20. PMID 20122755 DOI: 10.1016/J.Neurobiolaging.2010.01.014  0.514
2012 Howard TE, Drigalenko E, Johnson MP, Cole SS, Kim B, Viel KR, Sauna ZE, Curran JE, Blangero J, Almasy LA, Göring HH. Common SNPs within or near Three Immune Response Genes Implicated in the Risk of FVIII Immunogenicity in Hemophilia A Do Not Influence Steady-State Levels of Their Encoded mRNAs Blood. 120: 3366-3366. DOI: 10.1182/Blood.V120.21.3366.3366  0.365
2012 Kim B, Sauna ZE, Carless MA, Curran JE, Viel KR, Cole SS, Raja R, Blangero J, Howard TE. F8 and HLA-II Haplotypes in the Hispanic Population: Implications for Inhibitor Risk Development in Hispanic Hemophilia A Patients Blood. 120: 3365-3365. DOI: 10.1182/Blood.V120.21.3365.3365  0.305
2011 Kent JW, Farook V, Göring HH, Dyer TD, Almasy L, Duggirala R, Blangero J. Do rare variant genotypes predict common variant genotypes? Bmc Proceedings. 5: S87. PMID 22373504 DOI: 10.1186/1753-6561-5-S9-S87  0.427
2011 Almasy L, Dyer TD, Peralta JM, Kent JW, Charlesworth JC, Curran JE, Blangero J. Genetic Analysis Workshop 17 mini-exome simulation. Bmc Proceedings. 5: S2. PMID 22373155 DOI: 10.1186/1753-6561-5-S9-S2  0.42
2011 Melton PE, Kent JW, Dyer TD, Almasy L, Blangero J. Genetic signal maximization using environmental regression. Bmc Proceedings. 5: S72. PMID 22373104 DOI: 10.1186/1753-6561-5-S9-S72  0.416
2011 Ziegler A, Ghosh S, Dyer TD, Blangero J, MacCluer J, Almasy L. Introduction to genetic analysis workshop 17 summaries. Genetic Epidemiology. 35: S1-4. PMID 22128048 DOI: 10.1002/Gepi.20641  0.355
2011 Pinkerton RC, Oriá RB, Kent JW, Kohli A, Abreu C, Bushen O, Lima AA, Blangero J, Williams-Blangero S, Guerrant RL. Evidence for genetic susceptibility to developing early childhood diarrhea among shantytown children living in northeastern Brazil. The American Journal of Tropical Medicine and Hygiene. 85: 893-6. PMID 22049044 DOI: 10.4269/Ajtmh.2011.11-0159  0.413
2011 Cox HC, Lea RA, Bellis C, Carless M, Dyer T, Blangero J, Griffiths LR. Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate. The Journal of Headache and Pain. 12: 603-8. PMID 22030984 DOI: 10.1007/S10194-011-0392-7  0.422
2011 Kochunov P, Glahn DC, Nichols TE, Winkler AM, Hong EL, Holcomb HH, Stein JL, Thompson PM, Curran JE, Carless MA, Olvera RL, Johnson MP, Cole SA, Kochunov V, Kent J, ... Blangero J, et al. Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain. Frontiers in Neuroscience. 5: 120. PMID 22028680 DOI: 10.3389/Fnins.2011.00120  0.631
2011 Rubicz R, Leach CT, Kraig E, Dhurandhar NV, Duggirala R, Blangero J, Yolken R, Göring HH. Genetic factors influence serological measures of common infections. Human Heredity. 72: 133-41. PMID 21996708 DOI: 10.1159/000331220  0.328
2011 Duren DL, Blangero J, Sherwood RJ, Seselj M, Dyer T, Cole SA, Lee M, Choh AC, Chumlea WC, Siervogel RM, Czerwinski SA, Towne B. Cortical bone health shows significant linkage to chromosomes 2p, 3p, and 17q in 10-year-old children. Bone. 49: 1213-8. PMID 21907839 DOI: 10.1016/J.Bone.2011.08.024  0.324
2011 Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. Unifying ideas for non-parametric linkage analysis. Human Heredity. 71: 267-80. PMID 21822022 DOI: 10.1159/000323752  0.385
2011 Williams-Blangero S, VandeBerg JL, Blangero J, Corrêa-Oliveira R. Genetic epidemiology of Chagas disease. Advances in Parasitology. 75: 147-67. PMID 21820555 DOI: 10.1016/B978-0-12-385863-4.00007-1  0.403
2011 Vinson A, Curran JE, Johnson MP, Dyer TD, Moses EK, Blangero J, Cox LA, Rogers J, Havill LM, Vandeberg JL, Mahaney MC. Genetical genomics of Th1 and Th2 immune response in a baboon model of atherosclerosis risk factors. Atherosclerosis. 217: 387-94. PMID 21762917 DOI: 10.1016/J.Atherosclerosis.2011.06.015  0.3
2011 Choh AC, Curran JE, Odegaard AO, Nahhas RW, Czerwinski SA, Blangero J, Towne B, Demerath EW. Differences in the heritability of growth and growth velocity during infancy and associations with FTO variants. Obesity (Silver Spring, Md.). 19: 1847-54. PMID 21720422 DOI: 10.1038/Oby.2011.175  0.391
2011 Kochunov P, Glahn DC, Lancaster J, Thompson PM, Kochunov V, Rogers B, Fox P, Blangero J, Williamson DE. Fractional anisotropy of cerebral white matter and thickness of cortical gray matter across the lifespan. Neuroimage. 58: 41-9. PMID 21640837 DOI: 10.1016/J.Neuroimage.2011.05.050  0.519
2011 Wright FA, Strug LJ, Doshi VK, Commander CW, Blackman SM, Sun L, Berthiaume Y, Cutler D, Cojocaru A, Collaco JM, Corey M, Dorfman R, Goddard K, Green D, Kent JW, ... ... Blangero J, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Nature Genetics. 43: 539-46. PMID 21602797 DOI: 10.1038/Ng.838  0.366
2011 Olvera RL, Bearden CE, Velligan DI, Almasy L, Carless MA, Curran JE, Williamson DE, Duggirala R, Blangero J, Glahn DC. Common genetic influences on depression, alcohol, and substance use disorders in Mexican-American families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 561-8. PMID 21557468 DOI: 10.1002/Ajmg.B.31196  0.329
2011 Freed KA, Blangero J, Howard T, Johnson MP, Curran JE, Garcia YR, Lan HC, Abboud HE, Moses EK. The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells. Journal of Medical Genetics. 48: 563-6. PMID 21546516 DOI: 10.1136/Jmg.2010.083303  0.323
2011 Voruganti VS, Diego VP, Haack K, Cole SA, Blangero J, Göring HH, Laston S, Wenger CR, Ebbesson SO, Fabsitz RR, Devereux RB, Howard BV, Umans JG, MacCluer JW, Comuzzie AG. A QTL for genotype by sex interaction for anthropometric measurements in Alaskan Eskimos (GOCADAN Study) on chromosome 19q12-13. Obesity (Silver Spring, Md.). 19: 1840-6. PMID 21527897 DOI: 10.1038/Oby.2011.78  0.402
2011 Carless MA, Glahn DC, Johnson MP, Curran JE, Bozaoglu K, Dyer TD, Winkler AM, Cole SA, Almasy L, MacCluer JW, Duggirala R, Moses EK, Göring HH, Blangero J. Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. Molecular Psychiatry. 16: 1096-104, 1063. PMID 21483430 DOI: 10.1038/Mp.2011.37  0.307
2011 Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. Linkage analysis without defined pedigrees. Genetic Epidemiology. 35: 360-70. PMID 21465549 DOI: 10.1002/Gepi.20584  0.363
2011 Thameem F, Puppala S, Arar NH, Blangero J, Duggirala R, Abboud HE. Genetic variants in transient receptor potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans. Clinica Chimica Acta; International Journal of Clinical Chemistry. 412: 2058-62. PMID 21439949 DOI: 10.1016/J.Cca.2011.03.024  0.381
2011 Johansson A, Curran JE, Johnson MP, Freed KA, Fenstad MH, Bjørge L, Eide IP, Carless MA, Rainwater DL, Goring HH, Austgulen R, Moses EK, Blangero J. Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease. European Journal of Human Genetics : Ejhg. 19: 796-800. PMID 21343950 DOI: 10.1038/Ejhg.2011.19  0.352
2011 Sherwood RJ, Duren DL, Mahaney MC, Blangero J, Dyer TD, Cole SA, Czerwinski SA, Chumlea WC, Siervogel RM, Choh AC, Nahhas RW, Lee M, Towne B. A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens). Anatomical Record (Hoboken, N.J. : 2007). 294: 664-75. PMID 21328561 DOI: 10.1002/Ar.21337  0.431
2011 Puppala S, Coletta DK, Schneider J, Hu SL, Farook VS, Dyer TD, Arya R, Blangero J, Duggirala R, DeFronzo RA, Jenkinson CP. Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a major susceptibility locus on chromosome 6q14.1. Human Heredity. 71: 1-10. PMID 21293138 DOI: 10.1159/000323143  0.344
2011 Kochunov P, Glahn DC, Lancaster J, Winkler A, Karlsgodt K, Olvera RL, Curran JE, Carless MA, Dyer TD, Almasy L, Duggirala R, Fox PT, Blangero J. Blood pressure and cerebral white matter share common genetic factors in Mexican Americans. Hypertension. 57: 330-5. PMID 21135356 DOI: 10.1161/Hypertensionaha.110.162206  0.605
2011 Johansson A, Løset M, Mundal SB, Johnson MP, Freed KA, Fenstad MH, Moses EK, Austgulen R, Blangero J. Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model. Human Genetics. 129: 25-34. PMID 20931231 DOI: 10.1007/S00439-010-0893-5  0.315
2011 Curran JE, Meikle PJ, Blangero J. New approaches for the discovery of lipid-related genes Clinical Lipidology. 6: 495-500. DOI: 10.2217/Clp.11.45  0.378
2011 Glahn DC, Blangero J. Why endophenotype development requires families Chinese Science Bulletin. 56: 3382-3384. DOI: 10.1007/S11434-011-4740-4  0.369
2010 Diego VP, Almasy L, Rainwater DL, Mahaney MC, Comuzzie AG, Cole SA, Tracy RP, Stern MP, Maccluer JW, Blangero J. A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study. International Journal of Vascular Medicine. 2010: 490241. PMID 21151504 DOI: 10.1155/2010/490241  0.38
2010 Fenstad MH, Johnson MP, Roten LT, Aas PA, Forsmo S, Klepper K, East CE, Abraham LJ, Blangero J, Brennecke SP, Austgulen R, Moses EK. Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q. Plos One. 5. PMID 20927378 DOI: 10.1371/Journal.Pone.0012993  0.327
2010 Kochunov P, Glahn D, Lancaster J, Winkler A, Kent JW, Olvera RL, Cole SA, Dyer TD, Almasy L, Duggirala R, Fox PT, Blangero J. Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses. Stroke; a Journal of Cerebral Circulation. 41: 2137-42. PMID 20724716 DOI: 10.1161/Strokeaha.110.590943  0.607
2010 Oler JA, Fox AS, Shelton SE, Rogers J, Dyer TD, Davidson RJ, Shelledy W, Oakes TR, Blangero J, Kalin NH. Amygdalar and hippocampal substrates of anxious temperament differ in their heritability. Nature. 466: 864-8. PMID 20703306 DOI: 10.1038/Nature09282  0.358
2010 Melton PE, Rutherford S, Voruganti VS, Göring HH, Laston S, Haack K, Comuzzie AG, Dyer TD, Johnson MP, Kent JW, Curran JE, Moses EK, Blangero J, Barac A, Lee ET, et al. Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. Human Molecular Genetics. 19: 3662-71. PMID 20601674 DOI: 10.1093/Hmg/Ddq274  0.405
2010 Cummings N, Dyer TD, Kotea N, Kowlessur S, Chitson P, Zimmet P, Blangero J, Jowett JB. Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate. European Journal of Human Genetics : Ejhg. 18: 1243-7. PMID 20588307 DOI: 10.1038/Ejhg.2010.97  0.413
2010 Karlsgodt KH, Kochunov P, Winkler AM, Laird AR, Almasy L, Duggirala R, Olvera RL, Fox PT, Blangero J, Glahn DC. A multimodal assessment of the genetic control over working memory. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 8197-202. PMID 20554870 DOI: 10.1523/Jneurosci.0359-10.2010  0.554
2010 Almasy L, Blangero J. Variance component methods for analysis of complex phenotypes. Cold Spring Harbor Protocols. 2010: pdb.top77. PMID 20439422 DOI: 10.1101/Pdb.Top77  0.46
2010 Charlesworth J, Kramer PL, Dyer T, Diego V, Samples JR, Craig JE, Mackey DA, Hewitt AW, Blangero J, Wirtz MK. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness. Investigative Ophthalmology & Visual Science. 51: 3509-14. PMID 20237253 DOI: 10.1167/Iovs.09-4786  0.46
2010 Rogers J, Kochunov P, Zilles K, Shelledy W, Lancaster J, Thompson P, Duggirala R, Blangero J, Fox PT, Glahn DC. On the genetic architecture of cortical folding and brain volume in primates. Neuroimage. 53: 1103-8. PMID 20176115 DOI: 10.1016/J.Neuroimage.2010.02.020  0.553
2010 Glahn DC, Winkler AM, Kochunov P, Almasy L, Duggirala R, Carless MA, Curran JC, Olvera RL, Laird AR, Smith SM, Beckmann CF, Fox PT, Blangero J. Genetic control over the resting brain. Proceedings of the National Academy of Sciences of the United States of America. 107: 1223-8. PMID 20133824 DOI: 10.1073/Pnas.0909969107  0.569
2010 Kochunov P, Glahn DC, Lancaster JL, Winkler AM, Smith S, Thompson PM, Almasy L, Duggirala R, Fox PT, Blangero J. Genetics of microstructure of cerebral white matter using diffusion tensor imaging. Neuroimage. 53: 1109-16. PMID 20117221 DOI: 10.1016/J.Neuroimage.2010.01.078  0.611
2010 Prior MJ, Foletta VC, Jowett JB, Segal DH, Carless MA, Curran JE, Dyer TD, Moses EK, McAinch AJ, Konstantopoulos N, Bozaoglu K, Collier GR, Cameron-Smith D, Blangero J, Walder KR. The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome. Metabolism: Clinical and Experimental. 59: 1057-64. PMID 20045148 DOI: 10.1016/J.Metabol.2009.11.002  0.33
2010 Kochunov P, Glahn DC, Fox PT, Lancaster JL, Saleem K, Shelledy W, Zilles K, Thompson PM, Coulon O, Mangin JF, Blangero J, Rogers J. Genetics of primary cerebral gyrification: Heritability of length, depth and area of primary sulci in an extended pedigree of Papio baboons. Neuroimage. 53: 1126-34. PMID 20035879 DOI: 10.1016/J.Neuroimage.2009.12.045  0.593
2010 Jowett JB, Curran JE, Johnson MP, Carless MA, Göring HH, Dyer TD, Cole SA, Comuzzie AG, MacCluer JW, Moses EK, Blangero J. Genetic variation at the FTO locus influences RBL2 gene expression. Diabetes. 59: 726-32. PMID 20009087 DOI: 10.2337/Db09-1277  0.416
2010 Winkler AM, Kochunov P, Blangero J, Almasy L, Zilles K, Fox PT, Duggirala R, Glahn DC. Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. Neuroimage. 53: 1135-46. PMID 20006715 DOI: 10.1016/J.Neuroimage.2009.12.028  0.594
2010 Smith EM, Zhang Y, Baye TM, Gawrieh S, Cole R, Blangero J, Carless MA, Curran JE, Dyer TD, Abraham LJ, Moses EK, Kissebah AH, Martin LJ, Olivier M. INSIG1 influences obesity-related hypertriglyceridemia in humans. Journal of Lipid Research. 51: 701-8. PMID 19965593 DOI: 10.1194/Jlr.M001404  0.371
2010 Calafell F, Almasy L, Sabater-Lleal M, Buil A, Mordillo C, Ramírez-Soriano A, Sikora M, Souto JC, Blangero J, Fontcuberta J, Soria JM. Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. Human Molecular Genetics. 19: 517-25. PMID 19933701 DOI: 10.1093/Hmg/Ddp517  0.449
2010 Cole SA, Butte NF, Voruganti VS, Cai G, Haack K, Kent JW, Blangero J, Comuzzie AG, McPherson JD, Gibbs RA. Evidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children. The American Journal of Clinical Nutrition. 91: 191-9. PMID 19889825 DOI: 10.3945/Ajcn.2009.28514  0.32
2010 Curran JE, Jowett JB, Abraham LJ, Diepeveen LA, Elliott KS, Dyer TD, Kerr-Bayles LJ, Johnson MP, Comuzzie AG, Moses EK, Walder KR, Collier GR, Blangero J, Kissebah AH. Genetic variation in PARL influences mitochondrial content. Human Genetics. 127: 183-90. PMID 19862556 DOI: 10.1007/S00439-009-0756-0  0.365
2010 Macgregor S, Bellis C, Lea RA, Cox H, Dyer T, Blangero J, Visscher PM, Griffiths LR. Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island. European Journal of Human Genetics : Ejhg. 18: 67-72. PMID 19584896 DOI: 10.1038/Ejhg.2009.111  0.37
2010 Jowett JBM, Blangero J. Response to Comment on: Jowett et al. (2010) Genetic Variation at the FTO Locus Influences RBL2 Gene Expression. Diabetes;59:726-732 Diabetes. 59: e10-e10. DOI: 10.2337/Db10-0443  0.335
2010 Howard TE, Viel KR, Drigalenko E, Cole S, Epstein M, Carless M, Hughes R, Kim B, Dyer T, Pratt KP, MacCluer JW, Curran JE, Johnson MP, Moses EK, Blangero J, et al. No Evidence of Cis-Acting SNPs In Immune Response Genes Previously Associated with Factor VIII Inhibitors: The San Antonio Family Heart Study Blood. 116: 4422-4422. DOI: 10.1182/Blood.V116.21.4422.4422  0.359
2009 Soria JM, Almasy L, Souto JC, Sabaterlleal M, Fontcuberta J, Blangero J. The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005. Human Biology. 81: 853-67. PMID 20504202 DOI: 10.3378/027.081.0627  0.408
2009 Charlesworth JC, Peralta JM, Drigalenko E, Göring HH, Almasy L, Dyer TD, Blangero J. Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data. Bmc Proceedings. 3: S92. PMID 20018089 DOI: 10.1186/1753-6561-3-S7-S92  0.333
2009 Kent JW, Peterson CP, Dyer TD, Almasy L, Blangero J. Genome-wide discovery of maternal effect variants. Bmc Proceedings. 3: S19. PMID 20018008 DOI: 10.1186/1753-6561-3-S7-S19  0.372
2009 Kochunov P, Glahn D, Winkler A, Duggirala R, Olvera RL, Cole S, Dyer TD, Almasy L, Fox PT, Blangero J. Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume. Stroke; a Journal of Cerebral Circulation. 40: 3685-90. PMID 19834011 DOI: 10.1161/Strokeaha.109.565390  0.615
2009 Sabater-Lleal M, Chillón M, Mordillo C, Martínez A, Gil E, Mateo J, Blangero J, Almasy L, Fontcuberta J, Soria JM. Combined cis-regulator elements as important mechanism affecting FXII plasma levels. Thrombosis Research. 125: e55-60. PMID 19786295 DOI: 10.1016/J.Thromres.2009.08.019  0.304
2009 Johnson MP, Roten LT, Dyer TD, East CE, Forsmo S, Blangero J, Brennecke SP, Austgulen R, Moses EK. The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations. Human Genetics. 126: 655-66. PMID 19578876 DOI: 10.1007/S00439-009-0714-X  0.401
2009 Thameem F, Puppala S, He X, Arar NH, Stern MP, Blangero J, Duggirala R, Abboud HE. Evaluation of gremlin 1 (GREM1) as a candidate susceptibility gene for albuminuria-related traits in Mexican Americans with type 2 diabetes mellitus. Metabolism: Clinical and Experimental. 58: 1496-502. PMID 19577778 DOI: 10.1016/J.Metabol.2009.04.039  0.421
2009 Thameem F, He X, Voruganti VS, Nath SD, Fanti P, Blangero J, Maccluer JW, Comuzzie AG, Arar NH, Abboud HE. Evaluation of polymorphisms in paraoxonase 2 (PON2) gene and their association with cardiovascular-renal disease risk in Mexican Americans. Kidney & Blood Pressure Research. 32: 200-4. PMID 19546579 DOI: 10.1159/000225943  0.322
2009 Nath SD, He X, Voruganti VS, Blangero J, MacCluer JW, Comuzzie AG, Arar NH, Abboud HE, Thameem F. The 27-bp repeat polymorphism in intron 4 (27 bp-VNTR) of endothelial nitric oxide synthase (eNOS) gene is associated with albumin to creatinine ratio in Mexican Americans. Molecular and Cellular Biochemistry. 331: 201-5. PMID 19468830 DOI: 10.1007/S11010-009-0159-5  0.364
2009 Cox HC, Bellis C, Lea RA, Quinlan S, Hughes R, Dyer T, Charlesworth J, Blangero J, Griffiths LR. Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolate Human Heredity. 68: 55-64. PMID 19339786 DOI: 10.1159/000210449  0.395
2009 Jowett JB, Diego VP, Kotea N, Kowlessur S, Chitson P, Dyer TD, Zimmet P, Blangero J. Genetic influences on type 2 diabetes and metabolic syndrome related quantitative traits in Mauritius. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 12: 44-52. PMID 19210179 DOI: 10.1375/Twin.12.1.44  0.344
2009 Fitzpatrick E, Johnson MP, Dyer TD, Forrest S, Elliott K, Blangero J, Brennecke SP, Moses EK. Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia. Molecular Human Reproduction. 15: 195-204. PMID 19126782 DOI: 10.1093/Molehr/Gap001  0.399
2009 Shaffer JR, Kammerer CM, Bruder JM, Cole SA, Dyer TD, Almasy L, Maccluer JW, Blangero J, Bauer RL, Mitchell BD. Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults. Calcified Tissue International. 84: 75-84. PMID 19067020 DOI: 10.1007/S00223-008-9197-3  0.324
2009 Rainwater DL, Rutherford S, Dyer TD, Rainwater ED, Cole SA, VandeBerg JL, Almasy L, Blangero J, MacCluer JW, Mahaney MC. Determinants of variation in human serum paraoxonase activity Heredity. 102: 147-154. PMID 18971955 DOI: 10.1038/Hdy.2008.110  0.411
2009 Coletta DK, Schneider J, Hu SL, Dyer TD, Puppala S, Farook VS, Arya R, Lehman DM, Blangero J, DeFronzo RA, Duggirala R, Jenkinson CP. Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans Administration Genetic Epidemiology Study. Diabetes. 58: 279-84. PMID 18931038 DOI: 10.2337/Db08-0491  0.394
2009 Roten LT, Johnson MP, Forsmo S, Fitzpatrick E, Dyer TD, Brennecke SP, Blangero J, Moses EK, Austgulen R. Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study). European Journal of Human Genetics : Ejhg. 17: 250-7. PMID 18781190 DOI: 10.1038/Ejhg.2008.158  0.332
2009 Winkler A, Kochunov P, Fox P, Duggirala R, Almasy L, Blangero J, Glahn D. Heritability of Volume, Surface Area and Thickness for Anatomically Defined Cortical Brain Regions Estimated in a Large Extended Pedigree Neuroimage. 47. DOI: 10.1016/S1053-8119(09)71713-6  0.403
2009 Kochunov P, Winkler A, Blangero J, Lancaster J, Almasy L, Fox P, Glahn D. Genetics of DTI-derived parameters of cerebral white matter. A track-based heritability and linkage study in extended pedigree. Neuroimage. 47: S139. DOI: 10.1016/S1053-8119(09)71377-1  0.362
2008 Towne B, Williams KD, Blangero J, Czerwinski SA, Demerath EW, Nahhas RW, Dyer TD, Cole SA, Lee M, Choh AC, Duren DL, Sherwood RJ, Chumlea WC, Siervogel RM. Presentation, heritability, and genome-wide linkage analysis of the midchildhood growth spurt in healthy children from the Fels Longitudinal Study. Human Biology. 80: 623-36. PMID 19728540 DOI: 10.3378/1534-6617-80.6.623  0.303
2008 Thameem F, Voruganti VS, He X, Nath SD, Blangero J, MacCluer JW, Comuzzie AG, Abboud HE, Arar NH. Genetic variants in the renin-angiotensin system genes are associated with cardiovascular-renal-related risk factors in Mexican Americans. Human Genetics. 124: 557-9. PMID 18985387 DOI: 10.1007/S00439-008-0581-X  0.335
2008 Bellis C, Cox HC, Dyer TD, Charlesworth JC, Begley KN, Quinlan S, Lea RA, Heath SC, Blangero J, Griffiths LR. Linkage mapping of CVD risk traits in the isolated Norfolk Island population Human Genetics. 124: 543-552. PMID 18975005 DOI: 10.1007/S00439-008-0580-Y  0.442
2008 Almasy L, Blangero J. Human QTL linkage mapping. Genetica. 136: 333-40. PMID 18668207 DOI: 10.1007/S10709-008-9305-3  0.418
2008 Sabater-Lleal M, Buil A, Souto JC, Alamsy L, Borrell M, Lathrop M, Blangero J, Fontcuberta J, Soria JM. A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels. Human Genetics. 124: 81-8. PMID 18563448 DOI: 10.1007/S00439-008-0527-3  0.441
2008 López S, Buil A, Ordoñez J, Souto JC, Almasy L, Lathrop M, Blangero J, Blanco-Vaca F, Fontcuberta J, Soria JM. Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels. European Journal of Human Genetics : Ejhg. 16: 1372-9. PMID 18560444 DOI: 10.1038/Ejhg.2008.114  0.386
2008 Thameem F, Puppala S, Arar NH, Stern MP, Blangero J, Duggirala R, Abboud HE. Endothelial nitric oxide synthase (eNOS) gene polymorphisms and their association with type 2 diabetes-related traits in Mexican Americans. Diabetes & Vascular Disease Research. 5: 109-13. PMID 18537098 DOI: 10.3132/Dvdr.2008.018  0.405
2008 Samudrala N, Farook VS, Dodd GD, Puppala S, Schneider J, Fowler S, Granato R, Dyer TD, Arya R, Almasy L, Jenkinson CP, Diehl AK, Blangero J, Duggirala R. Autosomal genome-wide linkage analysis to identify loci for gallbladder wall thickness in Mexican Americans. Human Biology. 80: 11-28. PMID 18505042 DOI: 10.3378/1534-6617(2008)80[11:Aglati]2.0.Co;2  0.42
2008 Jenkinson CP, Coletta DK, Flechtner-Mors M, Hu SL, Fourcaudot MJ, Rodriguez LM, Schneider J, Arya R, Stern MP, Blangero J, Duggirala R, DeFronzo RA. Association of genetic variation in ENPP1 with obesity-related phenotypes. Obesity (Silver Spring, Md.). 16: 1708-13. PMID 18464750 DOI: 10.1038/Oby.2008.262  0.415
2008 Tejero ME, Voruganti VS, Proffitt JM, Curran JE, Göring HH, Johnson MP, Dyer TD, Jowett JB, Collier GR, Moses EK, MacCluer JW, Mahaney MC, Blangero J, Comuzzie AG, Cole SA. Cross-species replication of a resistin mRNA QTL, but not QTLs for circulating levels of resistin, in human and baboon. Heredity. 101: 60-6. PMID 18446183 DOI: 10.1038/Hdy.2008.28  0.347
2008 Arar NH, Voruganti VS, Nath SD, Thameem F, Bauer R, Cole SA, Blangero J, MacCluer JW, Comuzzie AG, Abboud HE. A genome-wide search for linkage to chronic kidney disease in a community-based sample: the SAFHS. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 23: 3184-91. PMID 18443212 DOI: 10.1093/Ndt/Gfn215  0.331
2008 Shaffer JR, Kammerer CM, Bruder JM, Cole SA, Dyer TD, Almasy L, MacCluer JW, Blangero J, Bauer RL, Mitchell BD. Genetic influences on bone loss in the San Antonio Family Osteoporosis study Osteoporosis International. 19: 1759-1767. PMID 18414963 DOI: 10.1007/S00198-008-0616-0  0.319
2008 Almasy L, Blangero J. Contemporary model-free methods for linkage analysis. Advances in Genetics. 60: 175-93. PMID 18358321 DOI: 10.1016/S0065-2660(07)00408-7  0.367
2008 Tejero ME, Voruganti VS, Rodríguez-Sánchez IP, Proffitt JM, Blangero J, Cox LA, Mahaney MC, Rogers J, VandeBerg JL, Cole SA, Comuzzie AG. Genetics of variation in adiponectin in pedigreed baboons: evidence for pleiotropic effects on adipocyte volume and serum adiponectin. Heredity. 100: 382-9. PMID 18285814 DOI: 10.1038/Sj.Hdy.6801089  0.379
2008 Voruganti VS, Lopez-Alvarenga JC, Nath SD, Rainwater DL, Bauer R, Cole SA, Maccluer JW, Blangero J, Comuzzie AG. Genetics of variation in HOMA-IR and cardiovascular risk factors in Mexican-Americans. Journal of Molecular Medicine (Berlin, Germany). 86: 303-11. PMID 18204828 DOI: 10.1007/S00109-007-0273-3  0.421
2008 Williams-Blangero S, Vandeberg JL, Subedi J, Jha B, Corrêa-Oliveira R, Blangero J. Localization of multiple quantitative trait loci influencing susceptibility to infection with Ascaris lumbricoides. The Journal of Infectious Diseases. 197: 66-71. PMID 18171287 DOI: 10.1086/524060  0.367
2008 Viel K, Charlesworth J, Tejero E, Dyer T, Cole S, Haack K, MacCluer J, Blangero J, Almasy L. A linkage analysis of cigarette and alcohol consumption in an unselected Mexican American population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 983-6. PMID 18163450 DOI: 10.1002/Ajmg.B.30661  0.325
2008 Bellis C, Cox HC, Ovcaric M, Begley KN, Lea RA, Quinlan S, Burgner D, Heath SC, Blangero J, Griffiths LR. Linkage disequilibrium analysis in the genetically isolated Norfolk Island population Heredity. 100: 366-373. PMID 18091769 DOI: 10.1038/Sj.Hdy.6801083  0.391
2008 Moses EK, Johnson MP, Tømmerdal L, Forsmo S, Curran JE, Abraham LJ, Charlesworth JC, Brennecke SP, Blangero J, Austgulen R. Genetic association of preeclampsia to the inflammatory response gene SEPS1. American Journal of Obstetrics and Gynecology. 198: 336.e1-5. PMID 18068137 DOI: 10.1016/J.Ajog.2007.09.024  0.342
2008 Thameem F, Puppala S, Arar N, Blangero J, Stern MP, Duggirala R, Abboud HE. Genetic polymorphisms in the renin-angiotensin system (RAS) genes and their association analysis with type 2 diabetes and related traits in Mexican Americans. Diabetes Research and Clinical Practice. 79: e14-6. PMID 17936396 DOI: 10.1016/J.Diabres.2007.08.025  0.371
2007 Santamaría A, Diego VP, Almasy L, Rainwater DL, Mahaney MC, Comuzzie AG, Cole SA, Dyer TD, Tracy RP, Stern MP, Maccluer JW, Blangero J. Quantitative trait locus on chromosome 12q14.1 influences variation in plasma plasminogen levels in the San Antonio Family Heart Study Human Biology. 79: 515-523. PMID 18478967 DOI: 10.1353/Hub.2008.0008  0.39
2007 Comuzzie AG, Tejero ME, Funahashi T, Martin LJ, Kissebah A, Takahashi M, Kihara S, Tanaka S, Rainwater DL, Matsuzawa Y, MacCluer JW, Blangero J. The genes influencing adiponectin levels also influence risk factors for metabolic syndrome and type 2 diabetes. Human Biology. 79: 191-200. PMID 18027814 DOI: 10.1353/Hub.2007.0029  0.354
2007 Nath SD, Voruganti VS, Arar NH, Thameem F, Lopez-Alvarenga JC, Bauer R, Blangero J, MacCluer JW, Comuzzie AG, Abboud HE. Genome scan for determinants of serum uric acid variability. Journal of the American Society of Nephrology : Jasn. 18: 3156-63. PMID 17978310 DOI: 10.1681/Asn.2007040426  0.375
2007 Saunders CL, Chiodini BD, Sham P, Lewis CM, Abkevich V, Adeyemo AA, de Andrade M, Arya R, Berenson GS, Blangero J, Boehnke M, Borecki IB, Chagnon YC, Chen W, Comuzzie AG, et al. Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring, Md.). 15: 2263-75. PMID 17890495 DOI: 10.1038/Oby.2007.269  0.329
2007 Göring HH, Curran JE, Johnson MP, Dyer TD, Charlesworth J, Cole SA, Jowett JB, Abraham LJ, Rainwater DL, Comuzzie AG, Mahaney MC, Almasy L, MacCluer JW, Kissebah AH, Collier GR, ... ... Blangero J, et al. Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. Nature Genetics. 39: 1208-16. PMID 17873875 DOI: 10.1038/Ng2119  0.353
2007 Rutherford S, Cai G, Lopez-Alvarenga JC, Kent JW, Voruganti VS, Proffitt JM, Curran JE, Johnson MP, Dyer TD, Jowett JB, Bastarrachea RA, Atwood LD, Goring HH, Maccluer JW, Moses EK, ... Blangero J, et al. A chromosome 11q quantitative-trait locus influences change of blood-pressure measurements over time in Mexican Americans of the San Antonio Family Heart Study. American Journal of Human Genetics. 81: 744-55. PMID 17846999 DOI: 10.1086/521151  0.37
2007 Puppala S, Arya R, Thameem F, Arar NH, Bhandari K, Lehman DM, Schneider J, Fowler S, Farook VS, Diego VP, Almasy L, Blangero J, Stern MP, Duggirala R, Abboud HE. Genotype by diabetes interaction effects on the detection of linkage of glomerular filtration rate to a region on chromosome 2q in Mexican Americans. Diabetes. 56: 2818-28. PMID 17698600 DOI: 10.2337/Db06-0984  0.333
2007 Demerath EW, Choh AC, Czerwinski SA, Lee M, Sun SS, Chumlea WC, Duren D, Sherwood RJ, Blangero J, Towne B, Siervogel RM. Genetic and environmental influences on infant weight and weight change: the Fels Longitudinal Study. American Journal of Human Biology : the Official Journal of the Human Biology Council. 19: 692-702. PMID 17639582 DOI: 10.1002/Ajhb.20660  0.321
2007 Gur RE, Nimgaonkar VL, Almasy L, Calkins ME, Ragland JD, Pogue-Geile MF, Kanes S, Blangero J, Gur RC. Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia. The American Journal of Psychiatry. 164: 813-9. PMID 17475741 DOI: 10.1176/AJP.2007.164.5.813  0.322
2007 Curran JE, Johnson MP, Dyer TD, Göring HH, Kent JW, Charlesworth JC, Borg AJ, Jowett JB, Cole SA, MacCluer JW, Kissebah AH, Moses EK, Blangero J. Genetic determinants of mitochondrial content. Human Molecular Genetics. 16: 1504-14. PMID 17468176 DOI: 10.1093/Hmg/Ddm101  0.319
2007 Glahn DC, Thompson PM, Blangero J. Neuroimaging endophenotypes: strategies for finding genes influencing brain structure and function. Human Brain Mapping. 28: 488-501. PMID 17440953 DOI: 10.1002/Hbm.20401  0.394
2007 Rogers J, Kochunov P, Lancaster J, Shelledy W, Glahn D, Blangero J, Fox P. Heritability of brain volume, surface area and shape: an MRI study in an extended pedigree of baboons. Human Brain Mapping. 28: 576-83. PMID 17437285 DOI: 10.1002/Hbm.20407  0.581
2007 Coletta DK, Schneider J, Stern MP, Blangero J, DeFronzo RA, Duggirala R, Jenkinson CP. Association of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican Americans. Obesity (Silver Spring, Md.). 15: 809-15. PMID 17426313 DOI: 10.1038/Oby.2007.610  0.341
2007 Goodarzi MO, Lehman DM, Taylor KD, Guo X, Cui J, Quiñones MJ, Clee SM, Yandell BS, Blangero J, Hsueh WA, Attie AD, Stern MP, Rotter JI. SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse. Diabetes. 56: 1922-9. PMID 17426289 DOI: 10.2337/Db06-1677  0.326
2007 Arar N, Nath S, Thameem F, Bauer R, Voruganti S, Comuzzie A, Cole S, Blangero J, MacCluer J, Abboud H. Genome-wide scans for microalbuminuria in Mexican Americans: the San Antonio Family Heart Study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 80-7. PMID 17304049 DOI: 10.1097/Gim.0B013E31803068Ec  0.379
2007 Sabater-Lleal M, Chillón M, Howard TE, Gil E, Almasy L, Blangero J, Fontcuberta J, Soria JM. Functional analysis of the genetic variability in the F7 gene promoter. Atherosclerosis. 195: 262-8. PMID 17292373 DOI: 10.1016/J.Atherosclerosis.2006.12.031  0.37
2007 Lehman DM, Richardson DK, Jenkinson CP, Hunt KJ, Dyer TD, Leach RJ, Arya R, Abboud HE, Blangero J, Duggirala R, Stern MP. P2 promoter variants of the hepatocyte nuclear factor 4alpha gene are associated with type 2 diabetes in Mexican Americans. Diabetes. 56: 513-7. PMID 17259399 DOI: 10.2337/Db06-0881  0.345
2007 Lehman DM, Hunt KJ, Leach RJ, Hamlington J, Arya R, Abboud HE, Duggirala R, Blangero J, Göring HH, Stern MP. Haplotypes of transcription factor 7-like 2 (TCF7L2) gene and its upstream region are associated with type 2 diabetes and age of onset in Mexican Americans. Diabetes. 56: 389-93. PMID 17259383 DOI: 10.2337/Db06-0860  0.33
2007 Kent JW, Dyer TD, Göring HH, Blangero J. Type I error rates in association versus joint linkage/association tests in related individuals. Genetic Epidemiology. 31: 173-7. PMID 17219375 DOI: 10.1002/Gepi.20200  0.378
2007 Viel KR, Machiah DK, Warren DM, Khachidze M, Buil A, Fernstrom K, Souto JC, Peralta JM, Smith T, Blangero J, Porter S, Warren ST, Fontcuberta J, Soria JM, Flanders WD, et al. A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels. Blood. 109: 3713-24. PMID 17209060 DOI: 10.1182/Blood-2006-06-026104  0.383
2007 Diego VP, Rainwater DL, Wang XL, Cole SA, Curran JE, Johnson MP, Jowett JB, Dyer TD, Williams JT, Moses EK, Comuzzie AG, Maccluer JW, Mahaney MC, Blangero J. Genotype x adiposity interaction linkage analyses reveal a locus on chromosome 1 for lipoprotein-associated phospholipase A2, a marker of inflammation and oxidative stress. American Journal of Human Genetics. 80: 168-77. PMID 17160904 DOI: 10.1086/510497  0.349
2007 Winnier DA, Rainwater DL, Cole SA, Williams JT, Dyer TD, Blangero J, MacCluer JW, Mahaney MC. Sex-specific QTL effects on variation in paraoxonase 1 (PON1) activity in Mexican Americans. Genetic Epidemiology. 31: 66-74. PMID 17136774 DOI: 10.1002/Gepi.20191  0.392
2007 Kent JW, Mahaney MC, Comuzzie AG, Göring HH, Almasy L, Dyer TD, Cole SA, MacCluer JW, Blangero J. Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans. Atherosclerosis. 195: 367-73. PMID 17112530 DOI: 10.1016/J.Atherosclerosis.2006.10.005  0.436
2007 Johnson MP, Fitzpatrick E, Dyer TD, Jowett JB, Brennecke SP, Blangero J, Moses EK. Identification of two novel quantitative trait loci for pre-eclampsia susceptibility on chromosomes 5q and 13q using a variance components-based linkage approach. Molecular Human Reproduction. 13: 61-7. PMID 17085769 DOI: 10.1093/Molehr/Gal095  0.364
2007 Glahn DC, Almasy L, Blangero J, Burk GM, Estrada J, Peralta JM, Meyenberg N, Castro MP, Barrett J, Nicolini H, Raventós H, Escamilla MA. Adjudicating neurocognitive endophenotypes for schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 242-9. PMID 17034022 DOI: 10.1002/Ajmg.B.30446  0.333
2007 Duren D, Blangero J, Sherwood R, Dyer T, Cole S, Czerwinski S, Chumlea W, Sun S, Demerath E, Siervogel R, Towne B. Childhood bone strength shows genetic linkage to chromosomes 2, 4 and 12: Results from the Fels Longitudinal Study Bone. 40: S42-S43. DOI: 10.1016/J.Bone.2007.04.042  0.344
2006 Winnier DA, Rainwater DL, Cole SA, Dyer TD, Blangero J, Maccluer JW, Mahaney MC. Multiple QTLs influence variation in paraoxonase 1 activity in Mexican Americans. Human Biology. 78: 341-52. PMID 17216806 DOI: 10.1353/Hub.2006.0050  0.37
2006 Warren DM, Cole SA, Dyer TD, Soria JM, Souto JC, Fontcuberta J, Blangero J, Maccluer JW, Almasy L. A locus on chromosome 13 influences levels of TAFI antigen in healthy Mexican Americans. Human Biology. 78: 329-39. PMID 17216805 DOI: 10.1353/Hub.2006.0049  0.431
2006 Feitosa ME, Rice T, Borecki IB, Rankinen T, Leon AS, Skinner JS, Després JP, Blangero J, Bouchard C, Rao DC. Pleiotropic QTL on chromosome 12q23-q24 influences triglyceride and high-density lipoprotein cholesterol levels: the HERITAGE family study. Human Biology. 78: 317-27. PMID 17216804 DOI: 10.1353/Hub.2006.0043  0.372
2006 Bozaoglu K, Curran JE, Elliott KS, Walder KR, Dyer TD, Rainwater DL, VandeBerg JL, Comuzzie AG, Collier GR, Zimmet P, MacCluer JW, Jowett JB, Blangero J. Association of genetic variation within UBL5 with phenotypes of metabolic syndrome. Human Biology. 78: 147-59. PMID 17036923 DOI: 10.1353/Hub.2006.0033  0.447
2006 Richardson DK, Schneider J, Fourcaudot MJ, Rodriguez LM, Arya R, Dyer TD, Almasy L, Blangero J, Stern MP, DeFronzo RA, Duggirala R, Jenkinson CP. Association between variants in the genes for adiponectin and its receptors with insulin resistance syndrome (IRS)-related phenotypes in Mexican Americans Diabetologia. 49: 2317-2328. PMID 16955209 DOI: 10.1007/S00125-006-0384-3  0.33
2006 Williams-Blangero S, Blangero J. Collection of pedigree data for genetic analysis in isolate populations. Human Biology. 78: 89-101. PMID 16900884 DOI: 10.1353/Hub.2006.0023  0.431
2006 Khachidze M, Buil A, Viel KR, Porter S, Warren D, Machiah DK, Soria JM, Souto JC, Ameri A, Lathrop M, Blangero J, Fontcuberta J, Warren ST, Almasy L, Howard TE. Genetic determinants of normal variation in coagulation factor (F) IX levels: Genome-wide scan and examination of the FIX structural gene Journal of Thrombosis and Haemostasis. 4: 1537-1545. PMID 16839351 DOI: 10.1111/J.1538-7836.2006.02024.X  0.421
2006 Moses EK, Fitzpatrick E, Freed KA, Dyer TD, Forrest S, Elliott K, Johnson MP, Blangero J, Brennecke SP. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22. Molecular Human Reproduction. 12: 505-12. PMID 16809377 DOI: 10.1093/Molehr/Gal056  0.397
2006 Diego VP, Göring HH, Cole SA, Almasy L, Dyer TD, Blangero J, Duggirala R, Laston S, Wenger C, Cantu T, Dyke B, North K, Schurr T, Best LG, Devereux RB, et al. Fasting insulin and obesity-related phenotypes are linked to chromosome 2p: the Strong Heart Family Study. Diabetes. 55: 1874-8. PMID 16731856 DOI: 10.2337/Db05-0668  0.361
2006 Sabater-Lleal M, Almasy L, Martínez-Marchán E, Martínez-Sánchez E, Souto R, Blangero J, Souto J, Fontcuberta J, Soria JM. Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assays. Clinical Genetics. 69: 420-8. PMID 16650081 DOI: 10.1111/J.1399-0004.2006.00608.X  0.424
2006 Arya R, Demerath E, Jenkinson CP, Göring HHH, Puppala S, Farook V, Fowler S, Schneider J, Granato R, Resendez RG, Dyer TD, Cole SA, Almasy L, Comuzzie AG, Siervogel RM, ... ... Blangero J, et al. A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies Human Molecular Genetics. 15: 1569-1579. PMID 16611675 DOI: 10.1093/Hmg/Ddl076  0.343
2006 Puppala S, Dodd GD, Fowler S, Arya R, Schneider J, Farook VS, Granato R, Dyer TD, Almasy L, Jenkinson CP, Diehl AK, Stern MP, Blangero J, Duggirala R. A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. American Journal of Human Genetics. 78: 377-92. PMID 16400619 DOI: 10.1086/500274  0.442
2006 Bellis C, Hughes RM, Begley KN, Quinlan S, Lea RA, Heath SC, Blangero J, Griffiths LR. Phenotypical characterisation of the isolated norfolk island population focusing on epidemiological indicators of cardiovascular disease. Human Heredity. 60: 211-9. PMID 16391489 DOI: 10.1159/000090545  0.312
2006 Feitosa MF, Rice T, North KE, Kraja A, Rankinen T, Leon AS, Skinner JS, Blangero J, Bouchard C, Rao DC. Pleiotropic QTL on chromosome 19q13 for triglycerides and adiposity: the HERITAGE Family Study. Atherosclerosis. 185: 426-32. PMID 16046215 DOI: 10.1016/J.Atherosclerosis.2005.06.023  0.376
2005 Blangero J, Goring HH, Kent JW, Williams JT, Peterson CP, Almasy L, Dyer TD. Quantitative trait nucleotide analysis using Bayesian model selection. Human Biology. 77: 541-59. PMID 16596940 DOI: 10.1353/Hub.2006.0003  0.451
2005 Havill LM, Dyer TD, Richardson DK, Mahaney MC, Blangero J. The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification. Bmc Genetics. 6: S91. PMID 16451707 DOI: 10.1186/1471-2156-6-S1-S91  0.399
2005 Peralta JM, Dyer TD, Warren DM, Blangero J, Almasy L. Linkage disequilibrium across two different single-nucleotide polymorphism genome scans. Bmc Genetics. 6: S86. PMID 16451701 DOI: 10.1186/1471-2156-6-S1-S86  0.372
2005 Kent JW, Lease LR, Mahaney MC, Dyer TD, Almasy L, Blangero J. X chromosome effects and their interactions with mitochondrial effects. Bmc Genetics. 6: S157. PMID 16451618 DOI: 10.1186/1471-2156-6-S1-S157  0.37
2005 Warren DM, Dyer TD, Peterson CP, Mahaney MC, Blangero J, Almasy L. A comparison of univariate, bivariate, and trivariate whole-genome linkage screens of genetically correlated electrophysiological endophenotypes. Bmc Genetics. 6: S117. PMID 16451574 DOI: 10.1186/1471-2156-6-S1-S117  0.428
2005 Buil A, Dyer TD, Almasy L, Blangero J. Smoothing of the bivariate LOD score for non-normal quantitative traits Bmc Genetics. 6. PMID 16451568 DOI: 10.1186/1471-2156-6-S1-S111  0.382
2005 Kent JW, Dyer TD, Blangero J. Estimating the additive genetic effect of the X chromosome Genetic Epidemiology. 29: 377-388. PMID 16294301 DOI: 10.1002/Gepi.20093  0.326
2005 Sabater-Lleal M, Soria JM, Bertranpetit J, Almasy L, Blangero J, Fontcuberta J, Calafell F. Human F7 sequence is split into three deep clades that are related to FVII plasma levels. Human Genetics. 118: 741-51. PMID 16292673 DOI: 10.1007/S00439-005-0045-5  0.412
2005 Curran JE, Jowett JB, Elliott KS, Gao Y, Gluschenko K, Wang J, Abel Azim DM, Cai G, Mahaney MC, Comuzzie AG, Dyer TD, Walder KR, Zimmet P, MacCluer JW, Collier GR, ... ... Blangero J, et al. Genetic variation in selenoprotein S influences inflammatory response. Nature Genetics. 37: 1234-41. PMID 16227999 DOI: 10.1038/Ng1655  0.353
2005 Lehman DM, Arya R, Blangero J, Almasy L, Puppala S, Dyer TD, Leach RJ, O'Connell P, Stern MP, Duggirala R. Bivariate linkage analysis of the insulin resistance syndrome phenotypes on chromosome 7q. Human Biology. 77: 231-46. PMID 16201139 DOI: 10.1353/Hub.2005.0040  0.426
2005 Charlesworth JC, Dyer TD, Stankovich JM, Blangero J, Mackey DA, Craig JE, Green CM, Foote SJ, Baird PN, Sale MM. Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree. Investigative Ophthalmology & Visual Science. 46: 3723-9. PMID 16186355 DOI: 10.1167/Iovs.05-0312  0.349
2005 Bauman LE, Almasy L, Blangero J, Duggirala R, Sinsheimer JS, Lange K. Fishing for pleiotropic QTLs in a polygenic sea. Annals of Human Genetics. 69: 590-611. PMID 16138917 DOI: 10.1111/J.1529-8817.2005.00181.X  0.377
2005 Remacha AF, Souto JC, Soria JM, Buil A, Sardà MP, Lathrop M, Blangero J, Almasy L, Fontcuberta J. Genomewide linkage analysis of soluble transferrin receptor plasma levels. Annals of Hematology. 85: 25-8. PMID 16132911 DOI: 10.1007/S00277-005-1092-7  0.457
2005 Hunt KJ, Lehman DM, Arya R, Fowler S, Leach RJ, Göring HH, Almasy L, Blangero J, Dyer TD, Duggirala R, Stern MP. Genome-wide linkage analyses of type 2 diabetes in Mexican Americans: the San Antonio Family Diabetes/Gallbladder Study. Diabetes. 54: 2655-62. PMID 16123354 DOI: 10.2337/Diabetes.54.9.2655  0.347
2005 Almasy L, Rainwater DL, Cole S, Mahaney MC, Vandeberg JL, Hixson JE, Stern MP, MacCluer JW, Blangero J. Joint linkage and association analysis of the hepatic lipase promoter polymorphism and lipoprotein size phenotypes. Human Biology. 77: 17-25. PMID 16114813 DOI: 10.1353/Hub.2005.0025  0.329
2005 Warren DM, Soria JM, Souto JC, Comuzzie A, Fontcuberta J, Blangero J, MacCluer JW, Almasy L. Heritability of hemostasis phenotypes and their correlation with type 2 diabetes status in Mexican Americans. Human Biology. 77: 1-15. PMID 16114812 DOI: 10.1353/Hub.2005.0034  0.415
2005 Souto JC, Blanco-Vaca F, Soria JM, Buil A, Almasy L, Ordoñez-Llanos J, Martín-Campos JM, Lathrop M, Stone W, Blangero J, Fontcuberta J. A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project. American Journal of Human Genetics. 76: 925-33. PMID 15849667 DOI: 10.1086/430409  0.407
2005 Almasy L, Soria JM, Souto JC, Warren DM, Buil A, Borrell M, Muñoz X, Sala N, Lathrop M, Fontcuberta J, Blangero J. A locus on chromosome 2 influences levels of tissue factor pathway inhibitor: results from the GAIT study. Arteriosclerosis, Thrombosis, and Vascular Biology. 25: 1489-92. PMID 15845911 DOI: 10.1161/01.Atv.0000166602.04711.2E  0.366
2005 Lehman DM, Fu DJ, Freeman AB, Hunt KJ, Leach RJ, Johnson-Pais T, Hamlington J, Dyer TD, Arya R, Abboud H, Göring HH, Duggirala R, Blangero J, Konrad RJ, Stern MP. A single nucleotide polymorphism in MGEA5 encoding O-GlcNAc-selective N-acetyl-beta-D glucosaminidase is associated with type 2 diabetes in Mexican Americans. Diabetes. 54: 1214-21. PMID 15793264 DOI: 10.2337/Diabetes.54.4.1214  0.317
2005 Towne B, Czerwinski SA, Demerath EW, Blangero J, Roche AF, Siervogel RM. Heritability of age at menarche in girls from the Fels Longitudinal Study. American Journal of Physical Anthropology. 128: 210-9. PMID 15779076 DOI: 10.1002/Ajpa.20106  0.38
2005 Soria JM, Almasy L, Souto JC, Buil A, Lathrop M, Blangero J, Fontcuberta J. A genome search for genetic determinants that influence plasma fibrinogen levels. Arteriosclerosis, Thrombosis, and Vascular Biology. 25: 1287-92. PMID 15761192 DOI: 10.1161/01.Atv.0000161927.38739.6F  0.4
2005 North KE, Miller MB, Coon H, Martin LJ, Peacock JM, Arnett D, Zhang B, Province M, Oberman A, Blangero J, Almasy L, Ellison RC, Heiss G. Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. Atherosclerosis. 179: 119-25. PMID 15721017 DOI: 10.1016/J.Atherosclerosis.2004.09.009  0.344
2005 Johnson L, Luke A, Adeyemo A, Deng HW, Mitchell BD, Comuzzie AG, Cole SA, Blangero J, Perola M, Teare MD. Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p. International Journal of Obesity (2005). 29: 413-9. PMID 15685251 DOI: 10.1038/Sj.Ijo.0802817  0.366
2005 Johnson L, Luke A, Deng H, Mitchell BD, Comuzzie AG, Cole SA, Blangero J, Perola M, Teare MD. Erratum: Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p International Journal of Obesity. 29: 878-878. DOI: 10.1038/Sj.Ijo.0802966  0.33
2004 Czerwinski SA, Mahaney MC, Rainwater DL, VandeBerg JL, MacCluer JW, Stern MP, Blangero J. Gene by smoking interaction: Evidence for effects on low-density lipoprotein size and plasma levels of triglyceride and high-density lipoprotein cholesterol Human Biology. 76: 863-876. PMID 15974298 DOI: 10.1353/Hub.2005.0014  0.342
2004 Cai G, Cole SA, Freeland-Graves JH, MacCluer JW, Blangero J, Comuzzie AG. Principal component for metabolic syndrome risk maps to chromosome 4p in Mexican Americans: the San Antonio Family Heart Study. Human Biology. 76: 651-65. PMID 15757239 DOI: 10.1353/Hub.2005.0001  0.377
2004 Williams JT, Blangero J. Power of variance component linkage analysis-II. Discrete traits. Annals of Human Genetics. 68: 620-32. PMID 15598220 DOI: 10.1046/J.1529-8817.2004.00128.X  0.384
2004 Kent JW, Comuzzie AG, Mahaney MC, Almasy L, Rainwater DL, VandeBerg JL, MacCluer JW, Blangero J. Intercellular adhesion molecule-1 concentration is genetically correlated with insulin resistance, obesity, and HDL concentration in Mexican Americans. Diabetes. 53: 2691-5. PMID 15448102 DOI: 10.2337/Diabetes.53.10.2691  0.379
2004 Rainwater DL, Mahaney MC, VandeBerg JL, Brush G, Almasy L, Blangero J, Dyke B, Hixson JE, Cole SA, MacCluer JW. A quantitative trait locus influences coordinated variation in measures of ApoB-containing lipoproteins. Atherosclerosis. 176: 379-86. PMID 15380462 DOI: 10.1016/J.Atherosclerosis.2004.06.004  0.409
2004 Jowett JB, Elliott KS, Curran JE, Hunt N, Walder KR, Collier GR, Zimmet PZ, Blangero J. Genetic variation in BEACON influences quantitative variation in metabolic syndrome-related phenotypes. Diabetes. 53: 2467-72. PMID 15331561 DOI: 10.2337/Diabetes.53.9.2467  0.42
2004 Samollow PB, Perez G, Kammerer CM, Finegold D, Zwartjes PW, Havill LM, Comuzzie AG, Mahaney MC, Göring HH, Blangero J, Foley TP, Barmada MM. Genetic and environmental influences on thyroid hormone variation in Mexican Americans. The Journal of Clinical Endocrinology and Metabolism. 89: 3276-84. PMID 15240603 DOI: 10.1210/Jc.2003-031706  0.329
2004 Blangero J. Localization and identification of human quantitative trait loci: king harvest has surely come. Current Opinion in Genetics & Development. 14: 233-40. PMID 15172664 DOI: 10.1016/J.Gde.2004.04.009  0.401
2004 Buil A, Soria JM, Souto JC, Almasy L, Lathrop M, Blangero J, Fontcuberta J. Protein C levels are regulated by a quantitative trait locus on chromosome 16: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1321-5. PMID 15142863 DOI: 10.1161/01.Atv.0000132408.13064.09  0.386
2004 Esparza-Gordillo J, Soria JM, Buil A, Almasy L, Blangero J, Fontcuberta J, Rodríguez de Córdoba S. Genetic and environmental factors influencing the human factor H plasma levels. Immunogenetics. 56: 77-82. PMID 15118848 DOI: 10.1007/S00251-004-0660-7  0.345
2004 Cai G, Cole SA, Freeland-Graves JH, MacCluer JW, Blangero J, Comuzzie AG. Genome-wide scans reveal quantitative trait Loci on 8p and 13q related to insulin action and glucose metabolism: the San Antonio Family Heart Study. Diabetes. 53: 1369-74. PMID 15111508 DOI: 10.2337/Diabetes.53.5.1369  0.322
2004 Martin LJ, Cianflone K, Zakarian R, Nagrani G, Almasy L, Rainwater DL, Cole S, Hixson JE, MacCluer JW, Blangero J, Comuzzie AG. Bivariate linkage between acylation-stimulating protein and BMI and high-density lipoproteins. Obesity Research. 12: 669-78. PMID 15090635 DOI: 10.1038/Oby.2004.77  0.313
2004 Martin LJ, Comuzzie AG, Sonnenberg GE, Myklebust J, James R, Marks J, Blangero J, Kissebah AH. Major quantitative trait locus for resting heart rate maps to a region on chromosome 4. Hypertension (Dallas, Tex. : 1979). 43: 1146-51. PMID 14993199 DOI: 10.1161/01.Hyp.0000122873.42047.17  0.337
2004 North KE, Rose KM, Borecki IB, Oberman A, Hunt SC, Miller MB, Blangero J, Almasy L, Pankow JS. Evidence for a gene on chromosome 13 influencing postural systolic blood pressure change and body mass index. Hypertension. 43: 780-4. PMID 14967843 DOI: 10.1161/01.Hyp.0000118921.66329.Da  0.401
2004 Almasy L, Blangero J. Exploring positional candidate genes: linkage conditional on measured genotype. Behavior Genetics. 34: 173-7. PMID 14755182 DOI: 10.1023/B:Bege.0000013731.03827.69  0.431
2004 Sonnenberg GE, Krakower GR, Martin LJ, Olivier M, Kwitek AE, Comuzzie AG, Blangero J, Kissebah AH. Genetic determinants of obesity-related lipid traits. Journal of Lipid Research. 45: 610-5. PMID 14754912 DOI: 10.1194/Jlr.M300474-Jlr200  0.406
2004 Arya R, Duggirala R, Jenkinson CP, Almasy L, Blangero J, O'Connell P, Stern MP. Evidence of a novel quantitative-trait locus for obesity on chromosome 4p in Mexican Americans. American Journal of Human Genetics. 74: 272-82. PMID 14740316 DOI: 10.1086/381717  0.398
2004 Esparza-Gordillo J, Soria JM, Buil A, Souto JC, Almasy L, Blangero J, de Córdoba SR, Fontcuberta J. Genetic correlation between plasma levels of C4BP isoforms containing beta chains and susceptibility to thrombosis. Journal of Medical Genetics. 41: e5. PMID 14729845 DOI: 10.1136/Jmg.2003.010611  0.459
2004 Sabater M, Soria JM, Khachidze M, Meng X, Almasy L, Souto JC, Fontcuberta J, Blangero J, Howard T. Confirmation of a New Statistical Method for Comprehensively Dissecting QTLs Using In Vitro Transcription, the Model Factor VII Gene and a Novel Modification of the G-Free Cassette. Blood. 104: 4002-4002. DOI: 10.1182/Blood.V104.11.4002.4002  0.392
2003 Martin LJ, North KE, Dyer T, Blangero J, Comuzzie AG, Williams J. Phenotypic, genetic, and genome-wide structure in the metabolic syndrome. Bmc Genetics. 4: S95. PMID 14975163 DOI: 10.1186/1471-2156-4-S1-S95  0.406
2003 Soler JM, Blangero J. Longitudinal familial analysis of blood pressure involving parametric (co)variance functions. Bmc Genetics. S87. PMID 14975155 DOI: 10.1186/1471-2156-4-S1-S87  0.395
2003 Göring HH, Williams JT, Dyer TD, Blangero J. On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis. Bmc Genetics. 4: S72. PMID 14975140 DOI: 10.1186/1471-2156-4-S1-S72  0.321
2003 Arya R, Lehman D, Hunt KJ, Schneider J, Almasy L, Blangero J, Stern MP, Duggirala R. Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study. Bmc Genetics. S52. PMID 14975120 DOI: 10.1186/1471-2156-4-S1-S52  0.373
2003 Comuzzie AG, Mitchell BD, Cole S, Martin LJ, Hsueh WC, Rainwater DL, Almasy L, Stern MP, Hixson J, MacCluer JW, Blangero J. The genetics of obesity in Mexican Americans: the evidence from genome scanning efforts in the San Antonio family heart study. Human Biology. 75: 635-46. PMID 14763601 DOI: 10.1353/Hub.2003.0073  0.375
2003 Kammerer CM, Schneider JL, Cole SA, Hixson JE, Samollow PB, O'Connell JR, Perez R, Dyer TD, Almasy L, Blangero J, Bauer RL, Mitchell BD. Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 2245-52. PMID 14672361 DOI: 10.1359/Jbmr.2003.18.12.2245  0.319
2003 Blangero J, Williams JT, Almasy L. Novel family-based approaches to genetic risk in thrombosis. Journal of Thrombosis and Haemostasis : Jth. 1: 1391-7. PMID 12871272 DOI: 10.1046/J.1538-7836.2003.00310.X  0.446
2003 Cole SA, Martin LJ, Peebles KW, Leland MM, Rice K, VandeBerg JL, Blangero J, Comuzzie AG. Genetics of leptin expression in baboons. International Journal of Obesity. 27: 778-783. PMID 12821961 DOI: 10.1038/Sj.Ijo.0802310  0.318
2003 Walder K, Segal D, Jowett J, Blangero J, Collier GR. Obesity and diabetes gene discovery approaches. Current Pharmaceutical Design. 9: 1357-72. PMID 12769728 DOI: 10.2174/1381612033454739  0.338
2003 Williams-Blangero S, VandeBerg JL, Blangero J, Corrêa-Oliveira R. Genetic epidemiology of Trypanosoma cruzi infection and Chagas' disease. Frontiers in Bioscience : a Journal and Virtual Library. 8: e337-45. PMID 12700060 DOI: 10.2741/1058  0.339
2003 Esparza-Gordillo J, Soria JM, Buil A, Souto JC, Almasy L, Blangero J, Fontcuberta J, de Córdoba SR. Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families. Immunogenetics. 54: 862-6. PMID 12671737 DOI: 10.1007/S00251-003-0537-1  0.341
2003 Almasy L, Soria JM, Souto JC, Coll I, Bacq D, Faure A, Mateo J, Borrell M, Muñoz X, Sala N, Stone WH, Lathrop M, Fontcuberta J, Blangero J. A quantitative trait locus influencing free plasma protein S levels on human chromosome 1q: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) project. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 508-11. PMID 12615682 DOI: 10.1161/01.Atv.0000055740.22563.C5  0.386
2003 Mahaney MC, Almasy L, Rainwater DL, VandeBerg JL, Cole SA, Hixson JE, Blangero J, MacCluer JW. A quantitative trait locus on chromosome 16q influences variation in plasma HDL-C levels in Mexican Americans Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 339-345. PMID 12588781 DOI: 10.1161/01.Atv.0000051406.14162.6A  0.395
2003 Comuzzie AG, Cole SA, Martin L, Carey KD, Mahaney MC, Blangero J, VandeBerg JL. The baboon as a nonhuman primate model for the study of the genetics of obesity. Obesity Research. 11: 75-80. PMID 12529488 DOI: 10.1038/Oby.2003.12  0.321
2003 Souto J, Blanco-Vaca F, Soria JM, Buil A, Ordoñez-Llanos J, Lathrop M, Almasy L, Stone W, Blangero J, Fontcuberta J. A quantitative trait locus on chromosome 11 is the major genetic determinant of homocysteine plasma levels. Results from the GAIT Project Journal of Thrombosis and Haemostasis. 1: OC160-OC160. DOI: 10.1111/J.1538-7836.2003.Tb04541.X  0.376
2003 Buil A, Soria JM, Souto JC, Borell M, Almasy L, Lathrop M, Vallve C, Mateo J, Ortin R, Blangero J, Fontcuberta J. Genetic dissection of thrombin-activatable fibrinolysis inhibitor (TAFI) Journal of Thrombosis and Haemostasis. 1: P0794-P0794. DOI: 10.1111/J.1538-7836.2003.Tb04428.X  0.365
2003 Almasy L, Manuel Soria J, Buil A, Stone W, Lathrop M, Blangero J, Fontcuberta J, Carlos Souto J. Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project Thrombosis and Haemostasis. 89: 468-474. DOI: 10.1055/S-0037-1613375  0.447
2002 Hunt KJ, Duggirala R, Göring HH, Williams JT, Almasy L, Blangero J, O'Leary DH, Stern MP. Genetic basis of variation in carotid artery plaque in the San Antonio Family Heart Study. Stroke; a Journal of Cerebral Circulation. 33: 2775-80. PMID 12468769 DOI: 10.1161/01.Str.0000043827.03966.Ef  0.344
2002 Martin LJ, Comuzzie AG, Dupont S, Vionnet N, Dina C, Gallina S, Houari M, Blangero J, Froguel P. A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French family. Diabetes. 51: 3568-72. PMID 12453915 DOI: 10.2337/Diabetes.51.12.3568  0.368
2002 Bethony J, Williams JT, Blangero J, Kloos H, Gazzinelli A, Soares-Filho B, Coelho L, Alves-Fraga L, Williams-Blangero S, Loverde PT, Correa-Oliveira R. Additive host genetic factors influence fecal egg excretion rates during Schistosoma mansoni infection in a rural area in Brazil. The American Journal of Tropical Medicine and Hygiene. 67: 336-43. PMID 12452486 DOI: 10.4269/Ajtmh.2002.67.336  0.382
2002 Soria JM, Almasy L, Souto JC, Buil A, Martinez-Sanchez E, Mateo J, Borrell M, Stone WH, Lathrop M, Fontcuberta J, Blangero J. A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility. Blood. 101: 163-7. PMID 12393556 DOI: 10.1182/Blood-2002-06-1792  0.437
2002 Merikangas KR, Chakravarti A, Moldin SO, Araj H, Blangero JC, Burmeister M, Crabbe J, Depaulo JR, Foulks E, Freimer NB, Koretz DS, Lichtenstein W, Mignot E, Reiss AL, Risch NJ, et al. Future of genetics of mood disorders research. Biological Psychiatry. 52: 457-77. PMID 12361664 DOI: 10.1016/S0006-3223(02)01471-3  0.418
2002 Duggirala R, Uttley M, Williams K, Arya R, Blangero J, Crawford MH. Genetic determination of biological age in the Mennonites of the Midwestern United States. Genetic Epidemiology. 23: 97-109. PMID 12214304 DOI: 10.1002/Gepi.1126  0.35
2002 Soria JM, Blangero J, Souto JC, Martínez-Sánchez E, Martínez-Marchán E, Coll I, Tirado I, Cercós A, Almasy L, Fontcuberta J. Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties. Human Genetics. 111: 59-65. PMID 12136237 DOI: 10.1007/S00439-002-0746-Y  0.38
2002 Martin LJ, Mahaney MC, Almasy L, Hixson JE, Cole SA, MacCluer JW, Jaquish CE, Blangero J, Comuzzie AG. A quantitative trait locus on chromosome 22 for serum leptin levels adjusted for serum testosterone. Obesity Research. 10: 602-7. PMID 12105281 DOI: 10.1038/Oby.2002.82  0.333
2002 Williams-Blangero S, VandeBerg JL, Subedi J, Aivaliotis MJ, Rai DR, Upadhayay RP, Jha B, Blangero J. Genes on chromosomes 1 and 13 have significant effects on Ascaris infection. Proceedings of the National Academy of Sciences of the United States of America. 99: 5533-8. PMID 11960011 DOI: 10.1073/Pnas.082115999  0.423
2002 Arya R, Blangero J, Williams K, Almasy L, Dyer TD, Leach RJ, O'Connell P, Stern MP, Duggirala R. Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans. Diabetes. 51: 841-7. PMID 11872689 DOI: 10.2337/Diabetes.51.3.841  0.377
2002 Broeckel U, Hengstenberg C, Mayer B, Holmer S, Martin LJ, Comuzzie AG, Blangero J, Nürnberg P, Reis A, Riegger GA, Jacob HJ, Schunkert H. A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nature Genetics. 30: 210-4. PMID 11818963 DOI: 10.1038/Ng827  0.359
2002 Soria JM, Almasy L, Souto JC, Bacq D, Buil A, Faure A, Martínez-Marchán E, Mateo J, Borrell M, Stone W, Lathrop M, Fontcuberta J, Blangero J. A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. American Journal of Human Genetics. 70: 567-74. PMID 11805911 DOI: 10.1086/339259  0.431
2002 Almasy L, Towne B, Peterson C, Blangero J. Detecting genotype x age interaction. Genetic Epidemiology. S819-24. PMID 11793786 DOI: 10.1002/Gepi.2001.21.S1.S819  0.338
2002 Martin LJ, Cole SA, Hixson JE, Mahaney MC, Czerwinski SA, Almasy L, Blangero J, Comuzzie AG. Genotype by smoking interaction for leptin levels in the San Antonio Family Heart Study. Genetic Epidemiology. 22: 105-15. PMID 11788957 DOI: 10.1002/Gepi.0135  0.303
2002 Arya R, Duggirala R, Almasy L, Rainwater DL, Mahaney MC, Cole S, Dyer TD, Williams K, Leach RJ, Hixson JE, MacCluer JW, O'Connell P, Stern MP, Blangero J. Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans. Nature Genetics. 30: 102-5. PMID 11743583 DOI: 10.1038/Ng810  0.354
2002 Almasy L, Borrell M, Stone W, Blanco-Vaca F, Soria J, Blangero J, Fontcuberta J, Souto J. Thromboplastin-thrombomodulin-mediated Time and Serum Folate Levels Are Genetically Correlated with the Risk of Thromboembolic Disease: Results from the GAIT Project Thrombosis and Haemostasis. 87: 68-73. DOI: 10.1055/S-0037-1612945  0.454
2002 Walder K, Segal D, Jowett J, Blangero J, Collier G. Genetic study in psammomys obesus International Journal of Obesity. DOI: 10.1038/Sj.Ijo.0802091  0.413
2001 Martin LJ, Blangero J, Rogers J, Mahaney MC, Hixson JE, Dee Carey K, Comuzzie AG. A quantitative trait locus influencing activin-to-estrogen ratio in pedigreed baboons maps to a region homologous to human chromosome 19 Human Biology. 73: 787-800. PMID 11804195 DOI: 10.1353/Hub.2001.0086  0.403
2001 Williams JT, North KE, Martin LJ, Comuzzie AG, Göring HH, Blangero J. Distribution of lod scores in oligogenic linkage analysis. Genetic Epidemiology. 21: S805-10. PMID 11793782 DOI: 10.1002/Gepi.2001.21.S1.S805  0.41
2001 Martin LJ, Comuzzie AG, North KE, Williams JT, Blangero J. The utility of Bayesian model averaging for detecting known oligogenic effects. Genetic Epidemiology. 21: S789-93. PMID 11793779 DOI: 10.1002/Gepi.2001.21.S1.S789  0.411
2001 Göring HH, Williams JT, Blangero J. Linkage analysis of quantitative traits in randomly ascertained pedigrees: comparison of penetrance-based and variance component analysis. Genetic Epidemiology. 21: S783-8. PMID 11793778 DOI: 10.1002/Gepi.2001.21.S1.S783  0.402
2001 Czerwinski SA, Williams JT, Demerath EW, Towne B, Siervogel RM, Blangero J. Does accounting for mitochondrial genetic variation improve the fit of genetic models? Genetic Epidemiology. 21: S779-82. PMID 11793777 DOI: 10.1002/Gepi.2001.21.S1.S779  0.377
2001 Arya R, Duggirala R, Williams JT, Almasy L, Blangero J. Power to localize the major gene for disease liability is increased after accounting for the effects of related quantitative phenotypes. Genetic Epidemiology. 21: S774-8. PMID 11793776 DOI: 10.1002/Gepi.2001.21.S1.S774  0.409
2001 Hsueh WC, Göring HHH, Blangero J, Mitchell BD. Replication of linkage to quantitative trait loci: Variation in location and magnitude of the lod score Genetic Epidemiology. 21. PMID 11793721 DOI: 10.1002/Gepi.2001.21.S1.S473  0.416
2001 Braxton DM, Hsueh WC, Schneider JL, Blangero J. Using step-wise linear regression to detect "functional" sequence variants: Application to simulated data Genetic Epidemiology. 21: S353-S357. PMID 11793697 DOI: 10.1002/Gepi.2001.21.S1.S353  0.356
2001 Almasy L, Terwilliger JD, Nielsen D, Dyer TD, Zaykin D, Blangero J. GAW12: Simulated genome scan, sequence, and family data for a common disease Genetic Epidemiology. 21. PMID 11793693 DOI: 10.1002/Gepi.2001.21.S1.S332  0.359
2001 Dyer TD, Blangero J, Williams JT, Göring HH, Mahaney MC. The effect of pedigree complexity on quantitative trait linkage analysis. Genetic Epidemiology. 21: S236-43. PMID 11793675 DOI: 10.1002/Gepi.2001.21.S1.S236  0.34
2001 Göring HH, Terwilliger JD, Blangero J. Large upward bias in estimation of locus-specific effects from genomewide scans. American Journal of Human Genetics. 69: 1357-69. PMID 11593451 DOI: 10.1086/324471  0.329
2001 Bethony J, Gazzinelli A, Lopes A, Pereira W, Alves-Oliveira LF, Willams-Blangero S, Blangero J, LoVerde PT, Corrêa-Oliveira R. Genetic Epidemiology of Fecal Egg Excretion during Schistosoma mansoni Infection in an Endemic Area in Minas Gerais, Brazil Memorias Do Instituto Oswaldo Cruz. 96: 49-55. PMID 11586426 DOI: 10.1590/S0074-02762001000900007  0.4
2001 Comuzzie AG, Funahashi T, Sonnenberg G, Martin LJ, Jacob HJ, Black AE, Maas D, Takahashi M, Kihara S, Tanaka S, Matsuzawa Y, Blangero J, Cohen D, Kissebah A. The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. The Journal of Clinical Endocrinology and Metabolism. 86: 4321-5. PMID 11549668 DOI: 10.1210/Jcem.86.9.7878  0.438
2001 Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Adamson J, Schaid DJ, Blangero J, Hutton M, Younkin SG. Heritability of plasma amyloid beta in typical late-onset Alzheimer's disease pedigrees. Genetic Epidemiology. 21: 19-30. PMID 11443731 DOI: 10.1002/Gepi.1015  0.311
2001 Almasy L, Blangero J. Endophenotypes as quantitative risk factors for psychiatric disease: rationale and study design. American Journal of Medical Genetics. 105: 42-4. PMID 11424994 DOI: 10.1002/1096-8628(20010108)105:1<42::Aid-Ajmg1055>3.0.Co;2-9  0.382
2001 Comuzzie AG, Williams JT, Martin LJ, Blangero J. Searching for genes underlying normal variation in human adiposity. Journal of Molecular Medicine (Berlin, Germany). 79: 57-70. PMID 11327104 DOI: 10.1007/S001090100202  0.393
2001 Hsueh WC, Cole SA, Shuldiner AR, Beamer BA, Blangero J, Hixson JE, MacCluer JW, Mitchell BD. Interactions between variants in the β3-adrenergic receptor and peroxisome proliferator-activated receptor-γ2 genes and obesity Diabetes Care. 24: 672-677. PMID 11315829 DOI: 10.2337/Diacare.24.4.672  0.382
2001 Duggirala R, Blangero J, Almasy L, Arya R, Dyer TD, Williams KL, Leach RJ, O'Connell P, Stern MP. A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans American Journal of Human Genetics. 68: 1149-1164. PMID 11283790 DOI: 10.1086/320100  0.332
2001 Iturria SJ, Blangero J. An EM algorithm for obtaining maximum likelihood estimates in the multi-phenotype variance components linkage model. Annals of Human Genetics. 64: 349-62. PMID 11246476 DOI: 10.1017/S0003480000008228  0.329
2001 Martin LJ, Blangero J, Rogers J, Mahaney MC, Hixson JE, Carey KD, Morin PA, Comuzzie AG. A quantitative trait locus influencing estrogen levels maps to a region homologous to human chromosome 20. Physiological Genomics. 5: 75-80. PMID 11242591 DOI: 10.1152/Physiolgenomics.2001.5.2.75  0.391
2001 Almasy L, Porjesz B, Blangero J, Goate A, Edenberg HJ, Chorlian DB, Kuperman S, O'Connor SJ, Rohrbaugh J, Bauer LO, Foroud T, Rice JP, Reich T, Begleiter H. Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism. American Journal of Human Genetics. 68: 128-135. PMID 11102287 DOI: 10.1086/316936  0.396
2001 Blangero J, Williams JT, Almasy L. Variance component methods for detecting complex trait loci. Advances in Genetics. 42: 151-81. PMID 11037320 DOI: 10.1016/S0065-2660(01)42021-9  0.366
2001 Rogers J, Mahaney MC, Almasy L, Comuzzie AG, Blangero J. Quantitative trait linkage mapping in anthropology. American Journal of Physical Anthropology. 127-51. PMID 10601985 DOI: 10.1002/(Sici)1096-8644(1999)110:29+<127::Aid-Ajpa5>3.0.Co;2-T  0.436
2001 Almasy L, Blangero J, Stone W, Borrell M, Urrutia T, Mateo J, Fontcuberta J, Souto JC. Genetic Regulation of Plasma Levels of Vitamin K-dependent Proteins Involved in Hemostasis Thrombosis and Haemostasis. 85: 88-92. DOI: 10.1055/S-0037-1612909  0.4
2000 Kissebah AH, Sonnenberg GE, Myklebust J, Goldstein M, Broman K, James RG, Marks JA, Krakower GR, Jacob HJ, Weber J, Martin L, Blangero J, Comuzzie AG. Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome Proceedings of the National Academy of Sciences of the United States of America. 97: 14478-14483. PMID 11121050 DOI: 10.1073/Pnas.97.26.14478  0.402
2000 Blangero J, Williams JT, Almasy L. Robust LOD scores for variance component-based linkage analysis. Genetic Epidemiology. 19: S8-14. PMID 11055364 DOI: 10.1002/1098-2272(2000)19:1+<::Aid-Gepi2>3.0.Co;2-Y  0.347
2000 Souto JC, Almasy L, Borrell M, Blanco-Vaca F, Mateo J, Soria JM, Coll I, Felices R, Stone W, Fontcuberta J, Blangero J. Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia. American Journal of Human Genetics. 67: 1452-9. PMID 11038326 DOI: 10.1086/316903  0.435
2000 Comuzzie AG, Almasy L, Cole SA, Boss O, Giacobino JP, Muzzin P, Stern MP, MacCluer JW, Blangero J, Hixson JE. Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans International Journal of Obesity. 24: 1065-1068. PMID 10951548 DOI: 10.1038/Sj.Ijo.0801257  0.369
2000 Souto JC, Almasy L, Muñiz-Diaz E, Soria JM, Borrell M, Bayén L, Mateo J, Madoz P, Stone W, Blangero J, Fontcuberta J. Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2024-8. PMID 10938027 DOI: 10.1161/01.Atv.20.8.2024  0.364
2000 Burke JP, Duggirala R, Hale DE, Blangero J, Stern MP. Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes. Human Genetics. 106: 467-72. PMID 10914675 DOI: 10.1007/S004390000274  0.396
2000 Mitchell BD, Cole SA, Hsueh WC, Comuzzie AG, Blangero J, MacCluer JW, Hixson JE. Linkage of serum insulin concentrations to chromosome 3p in Mexican Americans Diabetes. 49: 513-516. PMID 10868977 DOI: 10.2337/Diabetes.49.3.513  0.353
2000 Hixson JE, Blangero J. Genomic searches for genes that influence atherosclerosis and its risk factors Annals of the New York Academy of Sciences. 902: 1-7. PMID 10865820 DOI: 10.1111/J.1749-6632.2000.Tb06295.X  0.407
2000 Cole SA, Mitchell BD, Hsueh WC, Pineda P, Beamer BA, Shuldiner AR, Comuzzie AG, Blangero J, Hixson JE. The Pro12Ala variant of peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with measures of obesity in Mexican Americans International Journal of Obesity. 24: 522-524. PMID 10805513 DOI: 10.1038/Sj.Ijo.0801210  0.364
2000 Mitchell BD, Cole SA, Bauer RL, Iturria SJ, Rodriguez EA, Blangero J, MacCluer JW, Hixson JE. Genes influencing variation in serum osteocalcin concentrations are linked to markers on chromosomes 16q and 20q. The Journal of Clinical Endocrinology and Metabolism. 85: 1362-6. PMID 10770166 DOI: 10.1210/Jcem.85.4.6571  0.372
2000 Nguyen TV, Blangero J, Eisman JA. Genetic epidemiological approaches to the search for osteoporosis genes Journal of Bone and Mineral Research. 15: 392-401. PMID 10750553 DOI: 10.1359/Jbmr.2000.15.3.392  0.402
2000 Souto JC, Almasy L, Borrell M, Garí M, Martínez E, Mateo J, Stone WH, Blangero J, Fontcuberta J. Genetic determinants of hemostasis phenotypes in Spanish families. Circulation. 101: 1546-51. PMID 10747348 DOI: 10.1161/01.Cir.101.13.1546  0.388
2000 Duggirala R, Blangero J, Almasy L, Dyer TD, Williams KL, Leach RJ, O'Connell P, Stern MP. A major susceptibility locus influencing plasma triglyceride concentrations is located chromosome 15q in Mexican Americans American Journal of Human Genetics. 66: 1237-1245. PMID 10729112 DOI: 10.1086/302849  0.438
2000 Towne B, Almasy L, Siervogel RM, Blangero J. Effects of genotype x sex interaction on linkage analysis of visual event-related evoked potentials. Genetic Epidemiology. S355-60. PMID 10597462 DOI: 10.1002/Gepi.1370170760  0.371
2000 Duggirala R, Almasy L, Blangero J. Smoking behavior is under the influence of a major quantitative trait locus on human chromosome 5q. Genetic Epidemiology. S139-44. PMID 10597426 DOI: 10.1002/Gepi.1370170724  0.344
2000 Soria JM, Almasy L, Souto JC, Tirado I, Borell M, Mateo J, Slifer S, Stone W, Blangero J, Fontcuberta J. Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis Blood. 95: 2780-2785. DOI: 10.1182/Blood.V95.9.2780.009K36_2780_2785  0.353
2000 Almasy L, Blangero J. Challenges for genetic analysis in the 21st century: localizing and characterizing genes for common complex diseases and their quantitative risk factors Genescreen. 1: 113-116. DOI: 10.1046/J.1466-9218.2000.00033.X  0.409
1999 Williams JT, Blangero J. Power of variance component linkage analysis to detect quantitative trait loci. Annals of Human Genetics. 63: 545-63. PMID 11246457 DOI: 10.1017/S0003480099007848  0.366
1999 Williams JT, Blangero J. Asymptotic power of likelihood-ratio tests for detecting quantitative trait loci using the COGA data. Genetic Epidemiology. 17: S397-402. PMID 10597469 DOI: 10.1002/Gepi.1370170767  0.367
1999 Iturria SJ, Williams JT, Almasy L, Dyer TD, Blangero J. An empirical test of the significance of an observed quantitative trait locus effect that preserves additive genetic variation. Genetic Epidemiology. 17: S169-73. PMID 10597431 DOI: 10.1002/Gepi.1370170729  0.431
1999 Czerwinski SA, Mahaney MC, Williams JT, Almasy L, Blangero J. Genetic analysis of personality traits and alcoholism using a mixed discrete continuous trait variance component model. Genetic Epidemiology. 17: S121-6. PMID 10597423 DOI: 10.1002/Gepi.1370170721  0.359
1999 Almasy L, Williams JT, Dyer TD, Blangero J. Quantitative trait locus detection using combined linkage/disequilibrium analysis. Genetic Epidemiology. 17: S31-6. PMID 10597408 DOI: 10.1002/Gepi.1370170706  0.37
1999 Hixson JE, Almasy L, Cole S, Birnbaum S, Mitchell BD, Mahaney MC, Stern MP, Maccluer JW, Blangero J, Comuzzie AG. Normal variation in leptin levels is associated with polymorphisms in the proopiomelanocortin gene, POMC Journal of Clinical Endocrinology and Metabolism. 84: 3187-3191. PMID 10487685 DOI: 10.1210/Jcem.84.9.5951  0.416
1999 Williams JT, Begleiter H, Porjesz B, Edenberg HJ, Foroud T, Reich T, Goate A, Van Eerdewegh P, Almasy L, Blangero J. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. American Journal of Human Genetics. 65: 1148-60. PMID 10486334 DOI: 10.1086/302571  0.34
1999 Williams JT, Van Eerdewegh P, Almasy L, Blangero J. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. I. Likelihood formulation and simulation results. American Journal of Human Genetics. 65: 1134-47. PMID 10486333 DOI: 10.1086/302570  0.422
1999 Mitchell BD, Cole SA, Comuzzie AG, Almasy L, Blangero J, MacCluer JW, Hixson JE. A quantitative trait locus influencing BMI maps to the region of the adrenergic receptor Diabetes. 48: 1863-1867. PMID 10480620 DOI: 10.2337/Diabetes.48.9.1863  0.389
1999 Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J. Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. American Journal of Human Genetics. 65: 531-44. PMID 10417295 DOI: 10.1086/302487  0.362
1999 Williams-Blangero S, Subedi J, Upadhayay RP, Manral DB, Rai DR, Jha B, Robinson ES, Blangero J. Genetic analysis of susceptibility to infection with Ascaris lumbricoides. The American Journal of Tropical Medicine and Hygiene. 60: 921-6. PMID 10403321 DOI: 10.4269/Ajtmh.1999.60.921  0.398
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