| Year |
Citation |
Score |
| 2024 |
Sakano Y, Sakano K, Hurrell BP, Helou DG, Shafiei-Jahani P, Kazemi MH, Li X, Shen S, Hilser JR, Hartiala JA, Allayee H, Barbers R, Akbari O. Blocking CD226 regulates ILC2 effector function and alleviates airway hyperreactivity. The Journal of Allergy and Clinical Immunology. PMID 38244725 DOI: 10.1016/j.jaci.2024.01.003 |
0.557 |
|
| 2023 |
Biswas S, Hilser JR, Woodward NC, Wang Z, Gukasyan J, Nemet I, Schwartzman WS, Huang P, Han Y, Fouladian Z, Charugundla S, Spencer NJ, Pan C, Tang WHW, Lusis AJ, ... ... Allayee H, et al. Effect of Genetic and Dietary Perturbation of Glycine Metabolism on Atherosclerosis in Humans and Mice. Medrxiv : the Preprint Server For Health Sciences. PMID 38168321 DOI: 10.1101/2023.12.08.23299748 |
0.662 |
|
| 2022 |
Hilser JR, Hartiala JA, Sriprasert I, Kono N, Cai Z, Karim R, DeYoung J, Mack WJ, Hodis HN, Allayee H. Effect of menopausal hormone therapy on methylation levels in early and late postmenopausal women. Clinical Epigenetics. 14: 90. PMID 35850911 DOI: 10.1186/s13148-022-01311-w |
0.564 |
|
| 2022 |
Schillemans T, Tragante V, Maitusong B, Gigante B, Cresci S, Laguzzi F, Vikström M, Richards M, Pilbrow A, Cameron V, Foco L, Doughty RN, Kuukasjärvi P, Allayee H, Hartiala JA, et al. Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis. Frontiers in Physiology. 13: 909870. PMID 35812313 DOI: 10.3389/fphys.2022.909870 |
0.66 |
|
| 2022 |
Schmidt KA, Jones RB, Rios C, Corona Y, Berger PK, Plows JF, Alderete TL, Fogel J, Hampson H, Hartiala JA, Cai Z, Allayee H, Nayak KS, Sinatra FR, Harlan G, et al. Clinical Intervention to Reduce Dietary Sugar does not Impact Liver Fat in Latino Youth, Regardless of PNPLA3 Genotype: A Randomized Controlled Trial. The Journal of Nutrition. PMID 35218194 DOI: 10.1093/jn/nxac046 |
0.594 |
|
| 2021 |
Hartiala JA, Hilser JR, Biswas S, Lusis AJ, Allayee H. Gene-Environment Interactions for Cardiovascular Disease. Current Atherosclerosis Reports. 23: 75. PMID 34648097 DOI: 10.1007/s11883-021-00974-9 |
0.62 |
|
| 2021 |
Schunk SJ, Kleber ME, März W, Pang S, Zewinger S, Triem S, Ege P, Reichert MC, Krawczyk M, Weber SN, Jaumann I, Schmit D, Sarakpi T, Wagenpfeil S, Kramann R, ... ... Allayee H, et al. Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality. European Heart Journal. PMID 33748830 DOI: 10.1093/eurheartj/ehab107 |
0.623 |
|
| 2021 |
Hilser JR, Han Y, Biswas S, Gukasyan J, Cai Z, Zhu R, Tang WHW, Deb A, Lusis AJ, Hartiala JA, Allayee H. Association of serum HDL cholesterol and apolipoprotein A1 levels with risk of severe SARS-CoV-2 infection. Journal of Lipid Research. 100061. PMID 33667465 DOI: 10.1016/j.jlr.2021.100061 |
0.635 |
|
| 2021 |
Hartiala JA, Han Y, Jia Q, Hilser JR, Huang P, Gukasyan J, Schwartzman WS, Cai Z, Biswas S, Trégouët DA, Smith NL, Seldin M, ... ... Allayee H, et al. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. European Heart Journal. PMID 33532862 DOI: 10.1093/eurheartj/ehaa1040 |
0.632 |
|
| 2020 |
Mahmoodi BK, Tragante V, Kleber ME, Holmes MV, Schmidt AF, McCubrey RO, Howe LJ, Direk K, Allayee H, Baranova EV, Braund PS, Delgado GE, Eriksson N, Gijsberts CM, Gong Y, et al. Association of Factor V Leiden with Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data. Circulation. PMID 32654539 DOI: 10.1161/Circulationaha.119.045526 |
0.658 |
|
| 2020 |
Huda MN, VerHague M, Albright J, Smallwood T, Bell TA, Que E, Miller DR, Roshanravan B, Allayee H, Pardo-Manuel de Villena F, Bennett BJ. Dissecting the Genetic Architecture of Cystatin C in Diversity Outbred Mice. G3 (Bethesda, Md.). PMID 32467129 DOI: 10.1534/G3.120.401275 |
0.366 |
|
| 2020 |
Han Y, Jia Q, Jahani PS, Hurrell BP, Pan C, Huang P, Gukasyan J, Woodward NC, Eskin E, Gilliland FD, Akbari O, Hartiala JA, Allayee H. Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Nature Communications. 11: 1776. PMID 32296059 DOI: 10.1038/S41467-020-15649-3 |
0.649 |
|
| 2019 |
Maazi H, Hartiala JA, Suzuki Y, Crow AL, Shafiei Jahani P, Lam J, Patel N, Rigas D, Han Y, Huang P, Eskin E, Lusis AJ, Gilliland FD, Akbari O, Allayee H. A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity. Plos Genetics. 15: e1008528. PMID 31869344 DOI: 10.1371/Journal.Pgen.1008528 |
0.659 |
|
| 2019 |
Sriprasert I, Mack WJ, Hodis HN, Allayee H, Brinton RD, Karim R. Effect of ApoE4 Genotype on the Association Between Metabolic Phenotype and Subclinical Atherosclerosis in Postmenopausal Women. The American Journal of Cardiology. PMID 31362877 DOI: 10.1016/J.Amjcard.2019.06.022 |
0.309 |
|
| 2019 |
Shih DM, Zhu W, Schugar RC, Meng Y, Jia X, Miikeda A, Wang Z, Zieger M, Lee R, Graham M, Allayee H, Cantor RM, Mueller C, Brown JM, Hazen SL, et al. Genetic Deficiency of Flavin-Containing Monooxygenase-3 ( Fmo3) Protects Against Thrombosis but Has Only a Minor Effect on Plasma Lipid Levels. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA119312592. PMID 31070450 DOI: 10.1161/Atvbaha.119.312592 |
0.313 |
|
| 2019 |
Jia Q, Han Y, Huang P, Woodward NC, Gukasyan J, Kettunen J, Ala-Korpela M, Anufrieva O, Wang Q, Perola M, Raitakari O, Lehtimäki T, Viikari J, Järvelin MR, Boehnke M, ... ... Allayee H, et al. Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. Journal of the American Heart Association. 8: e011922. PMID 31070104 DOI: 10.1161/Jaha.119.011922 |
0.713 |
|
| 2019 |
Patel RS, Schmidt AF, Tragante V, McCubrey RO, Holmes MV, Howe LJ, Direk K, Åkerblom A, Leander K, Virani SS, Kaminski KA, Muehlschlegel JD, Dubé MP, Allayee H, Almgren P, et al. Association of Chromosome 9p21 with Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data. Circulation. Genomic and Precision Medicine. PMID 30897348 DOI: 10.1161/CIRCGEN.119.002471 |
0.648 |
|
| 2019 |
Patel R, Tragante V, Schmidt AF, McCubrey RO, Holmes MV, Howe LJ, Direk K, Åkerblom A, Leander K, Virani SS, Kaminski KA, Muehlschlegel JD, Allayee H, Almgren P, Alver M, et al. Subsequent Event Risk in Individuals with Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium. Circulation. Genomic and Precision Medicine. PMID 30896328 DOI: 10.1161/CIRCGEN.119.002470 |
0.647 |
|
| 2019 |
Woodward NC, Crow AL, Zhang Y, Epstein S, Hartiala J, Johnson R, Kocalis H, Saffari A, Sankaranarayanan I, Akbari O, Ramanathan G, Araujo JA, Finch CE, Bouret SG, Sioutas C, ... ... Allayee H, et al. Exposure to Nanoscale Particulate Matter from Gestation to Adulthood Impairs Metabolic Homeostasis in Mice. Scientific Reports. 9: 1816. PMID 30755631 DOI: 10.1038/S41598-018-37704-2 |
0.617 |
|
| 2018 |
Li XS, Wang Z, Cajka T, Buffa JA, Nemet I, Hurd AG, Gu X, Skye SM, Roberts AB, Wu Y, Li L, Shahen CJ, Wagner MA, Hartiala JA, Kerby RL, ... ... Allayee H, et al. Untargeted metabolomics identifies trimethyllysine, a TMAO-producing nutrient precursor, as a predictor of incident cardiovascular disease risk. Jci Insight. 3. PMID 29563342 DOI: 10.1172/Jci.Insight.99096 |
0.662 |
|
| 2018 |
Barrington WT, Salvador AC, Hartiala JA, De Caterina R, Kohlmeier M, Martinez JA, Kreutzer CB, Heber D, Lusis AJ, Li Z, Allayee H. Proceedings of the 11th Congress of the International Society of Nutrigenetics and Nutrigenomics (ISNN 2017). Journal of Nutrigenetics and Nutrigenomics. 10: 155-162. PMID 29339647 DOI: 10.1159/000485799 |
0.617 |
|
| 2017 |
Ramos-Lopez O, Milagro FI, Allayee H, Chmurzynska A, Choi MS, Curi R, De Caterina R, Ferguson LR, Goni L, Kang JX, Kohlmeier M, Marti A, Moreno LA, Pérusse L, Prasad C, et al. Guide for Current Nutrigenetic, Nutrigenomic, and Nutriepigenetic Approaches for Precision Nutrition Involving the Prevention and Management of Chronic Diseases Associated with Obesity. Journal of Nutrigenetics and Nutrigenomics. 10: 43-62. PMID 28689206 DOI: 10.1159/000477729 |
0.34 |
|
| 2017 |
Zewinger S, Kleber ME, Tragante V, McCubrey RO, Schmidt AF, Direk K, Laufs U, Werner C, Koenig W, Rothenbacher D, Mons U, Breitling LP, Brenner H, Jennings RT, Petrakis I, ... ... Allayee H, et al. Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study. The Lancet. Diabetes & Endocrinology. PMID 28566218 DOI: 10.1016/S2213-8587(17)30096-7 |
0.684 |
|
| 2017 |
Saleheen D, Zhao W, Young R, Nelson CP, Ho WK, Ferguson JF, Rasheed A, Ou K, Nurnberg ST, Bauer RC, Goel A, Do R, Stewart AFR, Hartiala J, Zhang W, ... ... Allayee H, et al. Loss of Cardio-Protective Effects at the ADAMTS7 Locus Due to Gene-Smoking Interactions. Circulation. PMID 28461624 DOI: 10.1161/Circulationaha.116.022069 |
0.659 |
|
| 2017 |
Hartiala J, Schwartzman WS, Gabbay J, Ghazalpour A, Bennett BJ, Allayee H. The Genetic Architecture of Coronary Artery Disease: Current Knowledge and Future Opportunities. Current Atherosclerosis Reports. 19: 6. PMID 28130654 DOI: 10.1007/S11883-017-0641-6 |
0.647 |
|
| 2016 |
Salehi P, Myint A, Kim YJ, Ge MX, Lavinsky J, Ho MK, Crow AL, Cruz C, Monges-Hernadez M, Wang J, Hartiala J, Zhang LI, Allayee H, Lusis AJ, Ohyama T, et al. Genome-Wide Association Analysis Identifies Dcc as an Essential Factor in the Innervation of the Peripheral Vestibular System in Inbred Mice. Journal of the Association For Research in Otolaryngology : Jaro. PMID 27539716 DOI: 10.1007/S10162-016-0578-4 |
0.65 |
|
| 2016 |
Lavinsky J, Ge M, Crow AL, Pan C, Wang J, Dermanaki PS, Myint A, Eskin E, Allayee H, Lusis AJ, Friedman RA. The Genetic Architecture of Noise-induced Hearing Loss: Evidence for a Gene-by-Environment Interaction. G3 (Bethesda, Md.). PMID 27520957 DOI: 10.1534/G3.116.032516 |
0.343 |
|
| 2016 |
Horvath S, Gurven M, Levine ME, Trumble BC, Kaplan H, Allayee H, Ritz BR, Chen B, Lu AT, Rickabaugh TM, Jamieson BD, Sun D, Li S, Chen W, Quintana-Murci L, et al. An epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease. Genome Biology. 17: 171. PMID 27511193 DOI: 10.1186/S13059-016-1030-0 |
0.302 |
|
| 2016 |
Hartiala J, Breton CV, Tang WH, Lurmann F, Hazen SL, Gilliland FD, Allayee H. Ambient Air Pollution Is Associated With the Severity of Coronary Atherosclerosis and Incident Myocardial Infarction in Patients Undergoing Elective Cardiac Evaluation. Journal of the American Heart Association. 5. PMID 27468926 DOI: 10.1161/Jaha.116.003947 |
0.637 |
|
| 2016 |
Kohlmeier M, De Caterina R, Ferguson LR, Görman U, Allayee H, Prasad C, Kang JX, Nicoletti CF, Martinez JA. Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalized Nutrition: Part 2 - Ethics, Challenges and Endeavors of Precision Nutrition. Journal of Nutrigenetics and Nutrigenomics. 9: 28-46. PMID 27286972 DOI: 10.1159/000446347 |
0.343 |
|
| 2016 |
Ferguson LR, De Caterina R, Görman U, Allayee H, Kohlmeier M, Prasad C, Choi MS, Curi R, de Luis DA, Gil Á, Kang JX, Martin RL, Milagro FI, Nicoletti CF, Nonino CB, et al. Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalised Nutrition: Part 1 - Fields of Precision Nutrition. Journal of Nutrigenetics and Nutrigenomics. 9: 12-27. PMID 27169401 DOI: 10.1159/000445350 |
0.334 |
|
| 2016 |
Lusis AJ, Seldin M, Allayee H, Bennett BJ, Civelek M, Davis RC, Eskin E, Farber C, Hui ST, Mehrabian M, Norheim F, Pan C, Parks B, Rau C, Smith DJ, et al. The Hybrid Mouse Diversity Panel: A Resource for Systems Genetics Analyses of Metabolic and Cardiovascular Traits. Journal of Lipid Research. PMID 27099397 DOI: 10.1194/Jlr.R066944 |
0.386 |
|
| 2016 |
Ferguson JF, Allayee H, Gerszten RE, Ideraabdullah F, Kris-Etherton PM, Ordovás JM, Rimm EB, Wang TJ, Bennett BJ. Nutrigenomics, the Microbiome, and Gene-Environment Interactions: New Directions in Cardiovascular Disease Research, Prevention, and Treatment: A Scientific Statement From the American Heart Association. Circulation. Cardiovascular Genetics. PMID 27095829 DOI: 10.1161/Hcg.0000000000000030 |
0.369 |
|
| 2016 |
Hartiala JA, Tang WH, Wang Z, Crow AL, Stewart AF, Roberts R, McPherson R, Erdmann J, Willenborg C, Hazen SL, Allayee H. Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. Nature Communications. 7: 10558. PMID 26822151 DOI: 10.1038/Ncomms10558 |
0.699 |
|
| 2015 |
Smallwood T, Allayee H, Bennett BJ. Choline metabolites: gene by diet interactions. Current Opinion in Lipidology. PMID 26655287 DOI: 10.1097/Mol.0000000000000259 |
0.387 |
|
| 2015 |
Kato N, Loh M, Takeuchi F, Verweij N, Wang X, Zhang W, Kelly TN, Saleheen D, Lehne B, Mateo Leach I, Drong AW, Abbott J, Wahl S, Tan ST, Scott WR, ... ... Allayee H, et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nature Genetics. 47: 1282-93. PMID 26390057 DOI: 10.1038/Ng.3405 |
0.646 |
|
| 2015 |
Crow AL, Ohmen J, Wang J, Lavinsky J, Hartiala J, Li Q, Li X, Salehide P, Eskin E, Pan C, Lusis AJ, Allayee H, Friedman RA. The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency Specific Genetic Determinants. G3 (Bethesda, Md.). PMID 26342000 DOI: 10.1534/G3.115.021592 |
0.659 |
|
| 2015 |
Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Sconberg JL, Schmidt LC, Volk HE, Tassone F. Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study. Early Human Development. 91: 483-489. PMID 26073892 DOI: 10.1016/J.Earlhumdev.2015.05.008 |
0.653 |
|
| 2015 |
Zhou X, Crow AL, Hartiala J, Spindler TJ, Ghazalpour A, Barsky LW, Bennett BB, Parks BW, Eskin E, Jain R, Epstein JA, Lusis AJ, Adams GB, Allayee H. The Genetic Landscape of Hematopoietic Stem Cell Frequency in Mice. Stem Cell Reports. PMID 26050929 DOI: 10.1016/J.Stemcr.2015.05.008 |
0.653 |
|
| 2015 |
Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA. Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss. Plos Genetics. 11: e1005094. PMID 25880434 DOI: 10.1371/Journal.Pgen.1005094 |
0.363 |
|
| 2015 |
Jeong S, Patel N, Edlund CK, Hartiala J, Hazelett DJ, Itakura T, Wu PC, Avery RL, Davis JL, Flynn HW, Lalwani G, Puliafito CA, Wafapoor H, Hijikata M, Keicho N, ... ... Allayee H, et al. Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension. Investigative Ophthalmology & Visual Science. 56: 2737-48. PMID 25813999 DOI: 10.1167/Iovs.14-14803 |
0.625 |
|
| 2015 |
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, ... ... Allayee H, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/Nature13917 |
0.654 |
|
| 2014 |
Ren J, Xiang AH, Trigo E, Takayanagi M, Beale E, Lawrence JM, Hartiala J, Richey JM, Allayee H, Buchanan TA, Watanabe RM. Genetic variation in MTNR1B is associated with gestational diabetes mellitus and contributes only to the absolute level of beta cell compensation in Mexican Americans. Diabetologia. 57: 1391-9. PMID 24728128 DOI: 10.1007/S00125-014-3239-3 |
0.627 |
|
| 2014 |
Hartiala J, Bennett BJ, Tang WH, Wang Z, Stewart AF, Roberts R, McPherson R, Lusis AJ, Hazen SL, Allayee H. Comparative genome-wide association studies in mice and humans for trimethylamine N-oxide, a proatherogenic metabolite of choline and L-carnitine. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1307-13. PMID 24675659 DOI: 10.1161/Atvbaha.114.303252 |
0.655 |
|
| 2014 |
Gyllenhammer LE, Alderete TL, Mahurka S, Allayee H, Goran MI. Adipose tissue 11βHSD1 gene expression, βcell function and ectopic fat in obese African Americans versus Hispanics. Obesity (Silver Spring, Md.). 22: 14-8. PMID 23836520 DOI: 10.1002/Oby.20571 |
0.305 |
|
| 2013 |
Walker RW, Sinatra F, Hartiala J, Weigensberg M, Spruijt-Metz D, Alderete TL, Goran MI, Allayee H. Genetic and clinical markers of elevated liver fat content in overweight and obese Hispanic children. Obesity (Silver Spring, Md.). 21: E790-7. PMID 23804528 DOI: 10.1002/Oby.20523 |
0.645 |
|
| 2013 |
Fan M, Dandona S, McPherson R, Allayee H, Hazen SL, Wells GA, Roberts R, Stewart AF. Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk. Circulation. Cardiovascular Genetics. 6: 372-80. PMID 23729007 DOI: 10.1161/Circgenetics.113.000104 |
0.398 |
|
| 2013 |
Reiner AP, Hartiala J, Zeller T, Bis JC, Dupuis J, Fornage M, Baumert J, Kleber ME, Wild PS, Baldus S, Bielinski SJ, Fontes JD, Illig T, Keating BJ, Lange LA, ... ... Allayee H, et al. Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Human Molecular Genetics. 22: 3381-93. PMID 23620142 DOI: 10.1093/Hmg/Ddt189 |
0.689 |
|
| 2013 |
Zhou G, Marathe GK, Hartiala J, Hazen SL, Allayee H, Tang WH, McIntyre TM. Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2). The Journal of Biological Chemistry. 288: 11940-8. PMID 23508960 DOI: 10.1074/Jbc.M112.427674 |
0.633 |
|
| 2013 |
Chan K, Patel RS, Newcombe P, Nelson CP, Qasim A, Epstein SE, Burnett S, Vaccarino VL, Zafari AM, Shah SH, Anderson JL, Carlquist JF, Hartiala J, Allayee H, Hinohara K, et al. Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. Journal of the American College of Cardiology. 61: 957-70. PMID 23352782 DOI: 10.1016/J.Jacc.2012.10.051 |
0.653 |
|
| 2013 |
Bennett BJ, de Aguiar Vallim TQ, Wang Z, Shih DM, Meng Y, Gregory J, Allayee H, Lee R, Graham M, Crooke R, Edwards PA, Hazen SL, Lusis AJ. Trimethylamine-N-oxide, a metabolite associated with atherosclerosis, exhibits complex genetic and dietary regulation. Cell Metabolism. 17: 49-60. PMID 23312283 DOI: 10.1016/J.Cmet.2012.12.011 |
0.345 |
|
| 2013 |
Chan K, Patel RS, Newcombe P, Nelson CP, Qasim A, Epstein SE, Burnett S, Vaccarino VL, Zafari AM, Shah SH, Anderson JL, Carlquist JF, Hartiala J, Allayee H, Hinohara K, et al. 126 CHROMOSOME 9P21 LOCUS AND ANGIOGRAPHIC CORONARY ARTERY DISEASE BURDEN: A COLLABORATIVE META-ANALYSIS Heart. 99: A75.1-A75. DOI: 10.1136/Heartjnl-2013-304019.126 |
0.687 |
|
| 2012 |
Beitelshees AL, Aquilante CL, Allayee H, Langaee TY, Welder GJ, Schofield RS, Zineh I. CXCL5 polymorphisms are associated with variable blood pressure in cardiovascular disease-free adults. Human Genomics. 6: 9. PMID 23245743 DOI: 10.1186/1479-7364-6-9 |
0.329 |
|
| 2012 |
van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, et al. Seventy-five genetic loci influencing the human red blood cell. Nature. 492: 369-75. PMID 23222517 DOI: 10.1038/Nature11677 |
0.659 |
|
| 2012 |
Tang WH, Hartiala J, Fan Y, Wu Y, Stewart AF, Erdmann J, Kathiresan S, Roberts R, McPherson R, Allayee H, Hazen SL. Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk. Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 2803-12. PMID 22982463 DOI: 10.1161/Atvbaha.112.253930 |
0.653 |
|
| 2012 |
Ghazalpour A, Rau CD, Farber CR, Bennett BJ, Orozco LD, van Nas A, Pan C, Allayee H, Beaven SW, Civelek M, Davis RC, Drake TA, Friedman RA, Furlotte N, Hui ST, et al. Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 680-92. PMID 22892838 DOI: 10.1007/S00335-012-9411-5 |
0.302 |
|
| 2012 |
Patel RS, Sun YV, Hartiala J, Veledar E, Su S, Sher S, Liu YX, Rahman A, Patel R, Rab ST, Vaccarino V, Zafari AM, Samady H, Tang WH, Allayee H, et al. Association of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography. Circulation. Cardiovascular Genetics. 5: 441-9. PMID 22767652 DOI: 10.1161/Circgenetics.111.960229 |
0.688 |
|
| 2012 |
Armstrong P, Kelley DS, Newman JW, Staggers FE, Hartiala J, Allayee H, Stephensen CB. Arachidonate 5-lipoxygenase gene variants affect response to fish oil supplementation by healthy African Americans. The Journal of Nutrition. 142: 1417-28. PMID 22739369 DOI: 10.3945/Jn.112.159814 |
0.337 |
|
| 2012 |
Schmidt RJ, Tancredi DJ, Ozonoff S, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tassone F, Hertz-Picciotto I. Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study. The American Journal of Clinical Nutrition. 96: 80-9. PMID 22648721 DOI: 10.3945/Ajcn.110.004416 |
0.636 |
|
| 2012 |
Goran MI, Walker R, Allayee H. Genetic-related and carbohydrate-related factors affecting liver fat accumulation. Current Opinion in Clinical Nutrition and Metabolic Care. 15: 392-6. PMID 22617559 DOI: 10.1097/Mco.0B013E3283544477 |
0.316 |
|
| 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, 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 |
0.329 |
|
| 2012 |
Hartiala J, Gilliam E, Vikman S, Campos H, Allayee H. Association of PLA2G4A with myocardial infarction is modulated by dietary PUFAs. The American Journal of Clinical Nutrition. 95: 959-65. PMID 22378731 DOI: 10.3945/Ajcn.111.032094 |
0.671 |
|
| 2012 |
Tang WH, Wu Y, Hartiala J, Fan Y, Stewart AF, Roberts R, McPherson R, Fox PL, Allayee H, Hazen SL. Clinical and genetic association of serum ceruloplasmin with cardiovascular risk. Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 516-22. PMID 22075249 DOI: 10.1161/Atvbaha.111.237040 |
0.662 |
|
| 2011 |
Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y, Lopez LM, Mägi R, Meacham S, Okada Y, Pirastu N, ... ... Allayee H, et al. New gene functions in megakaryopoiesis and platelet formation. Nature. 480: 201-8. PMID 22139419 DOI: 10.1038/Nature10659 |
0.638 |
|
| 2011 |
Morgan TM, House JA, Cresci S, Jones P, Allayee H, Hazen SL, Patel Y, Patel RS, Eapen DJ, Waddy SP, Quyyumi AA, Kleber ME, März W, Winkelmann BR, Boehm BO, et al. Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome. Bmc Medical Genetics. 12: 127. PMID 21957892 DOI: 10.1186/1471-2350-12-127 |
0.36 |
|
| 2011 |
Vasunilashorn S, Finch CE, Crimmins EM, Vikman SA, Stieglitz J, Gurven M, Kaplan H, Allayee H. Inflammatory gene variants in the Tsimane, an indigenous Bolivian population with a high infectious load. Biodemography and Social Biology. 57: 33-52. PMID 21845926 DOI: 10.1080/19485565.2011.564475 |
0.308 |
|
| 2011 |
Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tancredi DJ, Tassone F, Hertz-Picciotto I. Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism. Epidemiology (Cambridge, Mass.). 22: 476-85. PMID 21610500 DOI: 10.1097/Ede.0B013E31821D0E30 |
0.661 |
|
| 2011 |
Wang Z, Klipfell E, Bennett BJ, Koeth R, Levison BS, Dugar B, Feldstein AE, Britt EB, Fu X, Chung YM, Wu Y, Schauer P, Smith JD, Allayee H, Tang WH, et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature. 472: 57-63. PMID 21475195 DOI: 10.1038/Nature09922 |
0.371 |
|
| 2011 |
Mendoza-Fandino GA, Gee JM, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers RM, Leal SM, Allayee H, Patel PI. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Clinical Genetics. 80: 265-72. PMID 21443745 DOI: 10.1111/J.1399-0004.2010.01529.X |
0.616 |
|
| 2011 |
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, Absher D, Aherrahrou Z, Allayee H, Altshuler D, Anand SS, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nature Genetics. 43: 333-8. PMID 21378990 DOI: 10.1038/Ng.784 |
0.451 |
|
| 2011 |
Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, Benjamin EJ, Bennett F, Bowden DW, Chakravarti A, Dreisbach A, Farlow DN, Folsom AR, Fornage M, Forrester T, Fox E, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Plos Genetics. 7: e1001300. PMID 21347282 DOI: 10.1371/Journal.Pgen.1001300 |
0.695 |
|
| 2011 |
Stephensen CB, Armstrong P, Newman JW, Pedersen TL, Legault J, Schuster GU, Kelley D, Vikman S, Hartiala J, Nassir R, Seldin MF, Allayee H. ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation. Journal of Lipid Research. 52: 991-1003. PMID 21296957 DOI: 10.1194/Jlr.P012864 |
0.648 |
|
| 2011 |
Hartiala J, Li D, Conti DV, Vikman S, Patel Y, Tang WH, Brennan ML, Newman JW, Stephensen CB, Armstrong P, Hazen SL, Allayee H. Genetic contribution of the leukotriene pathway to coronary artery disease. Human Genetics. 129: 617-27. PMID 21293878 DOI: 10.1007/S00439-011-0963-3 |
0.694 |
|
| 2011 |
Qi L, Ma J, Qi Q, Hartiala J, Allayee H, Campos H. Genetic risk score and risk of myocardial infarction in Hispanics. Circulation. 123: 374-80. PMID 21242481 DOI: 10.1161/Circulationaha.110.976613 |
0.688 |
|
| 2011 |
Reilly MP, Li M, He J, Ferguson JF, Stylianou IM, Mehta NN, Burnett MS, Devaney JM, Knouff CW, Thompson JR, Horne BD, Stewart AF, Assimes TL, Wild PS, Allayee H, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet. 377: 383-92. PMID 21239051 DOI: 10.1016/S0140-6736(10)61996-4 |
0.362 |
|
| 2010 |
Davis JN, Lê KA, Walker RW, Vikman S, Spruijt-Metz D, Weigensberg MJ, Allayee H, Goran MI. Increased hepatic fat in overweight Hispanic youth influenced by interaction between genetic variation in PNPLA3 and high dietary carbohydrate and sugar consumption. The American Journal of Clinical Nutrition. 92: 1522-7. PMID 20962157 DOI: 10.3945/Ajcn.2010.30185 |
0.323 |
|
| 2010 |
Goran MI, Walker R, Le KA, Mahurkar S, Vikman S, Davis JN, Spruijt-Metz D, Weigensberg MJ, Allayee H. Effects of PNPLA3 on liver fat and metabolic profile in Hispanic children and adolescents. Diabetes. 59: 3127-30. PMID 20852027 DOI: 10.2337/Db10-0554 |
0.319 |
|
| 2010 |
Nicholls SJ, Tang WH, Scoffone H, Brennan DM, Hartiala J, Allayee H, Hazen SL. Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy. Journal of Lipid Research. 51: 3055-61. PMID 20601648 DOI: 10.1194/Jlr.M008961 |
0.641 |
|
| 2009 |
Allayee H, Roth N, Hodis HN. Polyunsaturated fatty acids and cardiovascular disease: implications for nutrigenetics. Journal of Nutrigenetics and Nutrigenomics. 2: 140-8. PMID 19776641 DOI: 10.1159/000235562 |
0.358 |
|
| 2009 |
Li X, Shu YH, Xiang AH, Trigo E, Kuusisto J, Hartiala J, Swift AJ, Kawakubo M, Stringham HM, Bonnycastle LL, Lawrence JM, Laakso M, Allayee H, Buchanan TA, Watanabe RM. Additive effects of genetic variation in GCK and G6PC2 on insulin secretion and fasting glucose. Diabetes. 58: 2946-53. PMID 19741163 DOI: 10.2337/Db09-0228 |
0.605 |
|
| 2009 |
Vikman S, Brena RM, Armstrong P, Hartiala J, Stephensen CB, Allayee H. Functional analysis of 5-lipoxygenase promoter repeat variants. Human Molecular Genetics. 18: 4521-9. PMID 19717473 DOI: 10.1093/Hmg/Ddp414 |
0.648 |
|
| 2009 |
Shu YH, Hartiala J, Xiang AH, Trigo E, Lawrence JM, Allayee H, Buchanan TA, Bottini N, Watanabe RM. Evidence for sex-specific associations between variation in acid phosphatase locus 1 (ACP1) and insulin sensitivity in Mexican-Americans. The Journal of Clinical Endocrinology and Metabolism. 94: 4094-102. PMID 19622628 DOI: 10.1210/Jc.2008-2751 |
0.611 |
|
| 2009 |
Schentrup AM, Allayee H, Lima JJ, Johnson JA, Langaee TY. Genotyping the GGGCGG tandem repeat promoter polymorphism in the 5-lipoxygenase enzyme gene (ALOX5) by pyrosequencing assay. Genetic Testing and Molecular Biomarkers. 13: 361-5. PMID 19473080 DOI: 10.1089/Gtmb.2008.0103 |
0.344 |
|
| 2009 |
Li X, Allayee H, Xiang AH, Trigo E, Hartiala J, Lawrence JM, Buchanan TA, Watanabe RM. Variation in IGF2BP2 interacts with adiposity to alter insulin sensitivity in Mexican Americans. Obesity (Silver Spring, Md.). 17: 729-36. PMID 19148120 DOI: 10.1038/Oby.2008.593 |
0.655 |
|
| 2009 |
Orrú V, Tsai SJ, Rueda B, Fiorillo E, Stanford SM, Dasgupta J, Hartiala J, Zhao L, Ortego-Centeno N, D'Alfonso S, Arnett FC, Wu H, Gonzalez-Gay MA, Tsao BP, ... ... Allayee H, et al. A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus. Human Molecular Genetics. 18: 569-79. PMID 18981062 DOI: 10.1093/Hmg/Ddn363 |
0.653 |
|
| 2008 |
Allayee H, Baylin A, Hartiala J, Wijesuriya H, Mehrabian M, Lusis AJ, Campos H. Nutrigenetic association of the 5-lipoxygenase gene with myocardial infarction. The American Journal of Clinical Nutrition. 88: 934-40. PMID 18842779 DOI: 10.1093/Ajcn/88.4.934 |
0.662 |
|
| 2008 |
Allayee H. Non-conventional genetic risk factors for cardiovascular disease. World Review of Nutrition and Dietetics. 98: 62-76. PMID 18806462 DOI: 10.1159/000152922 |
0.433 |
|
| 2008 |
Mehrabian M, Schulthess FT, Nebohacova M, Castellani LW, Zhou Z, Hartiala J, Oberholzer J, Lusis AJ, Maedler K, Allayee H. Identification of ALOX5 as a gene regulating adiposity and pancreatic function. Diabetologia. 51: 978-88. PMID 18421434 DOI: 10.1007/S00125-008-1002-3 |
0.645 |
|
| 2008 |
Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, et al. Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Human Genetics. 123: 399-408. PMID 18369664 DOI: 10.1007/S00439-008-0489-5 |
0.693 |
|
| 2008 |
Bhattacharyya T, Nicholls SJ, Topol EJ, Zhang R, Yang X, Schmitt D, Fu X, Shao M, Brennan DM, Ellis SG, Brennan ML, Allayee H, Lusis AJ, Hazen SL. Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk. Jama. 299: 1265-76. PMID 18349088 DOI: 10.1001/Jama.299.11.1265 |
0.327 |
|
| 2008 |
Chang AJ, Kline MM, Currie Y, Perez MO, Hartiala J, Wijesuriya H, Buchanan TA, Watanabe RM, Allayee H. Allgrove syndrome in a Mexican American family is caused by an ancestral mutation derived from North Africa. Clinical Genetics. 73: 385-7. PMID 18261130 DOI: 10.1111/J.1399-0004.2008.00965.X |
0.592 |
|
| 2008 |
Pemberton TJ, Mehta NU, Witonsky D, Di Rienzo A, Allayee H, Conti DV, Patel PI. Prevalence of common disease-associated variants in Asian Indians. Bmc Genetics. 9: 13. PMID 18248681 DOI: 10.1186/1471-2156-9-13 |
0.376 |
|
| 2008 |
Black MH, Fingerlin TE, Allayee H, Zhang W, Xiang AH, Trigo E, Hartiala J, Lehtinen AB, Haffner SM, Bergman RN, McEachin RC, Kjos SL, Lawrence JM, Buchanan TA, Watanabe RM. Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans. Diabetes. 57: 1048-56. PMID 18162503 DOI: 10.2337/Db07-0848 |
0.65 |
|
| 2007 |
Allayee H, Hartiala J, Lee W, Mehrabian M, Irvin CG, Conti DV, Lima JJ. The effect of montelukast and low-dose theophylline on cardiovascular disease risk factors in asthmatics. Chest. 132: 868-74. PMID 17646220 DOI: 10.1378/Chest.07-0831 |
0.645 |
|
| 2007 |
Watanabe RM, Black MH, Xiang AH, Allayee H, Lawrence JM, Buchanan TA. Genetics of gestational diabetes mellitus and type 2 diabetes. Diabetes Care. 30: S134-40. PMID 17596461 DOI: 10.2337/Dc07-S205 |
0.33 |
|
| 2007 |
Watanabe RM, Allayee H, Xiang AH, Trigo E, Hartiala J, Lawrence JM, Buchanan TA. Transcription factor 7-like 2 (TCF7L2) is associated with gestational diabetes mellitus and interacts with adiposity to alter insulin secretion in Mexican Americans. Diabetes. 56: 1481-5. PMID 17317761 DOI: 10.2337/Db06-1682 |
0.62 |
|
| 2007 |
Mendoza G, Pemberton TJ, Lee K, Scarel-Caminaga R, Mehrian-Shai R, Gonzalez-Quevedo C, Ninis V, Hartiala J, Allayee H, Snead ML, Leal SM, Line SR, Patel PI. A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Human Genetics. 120: 653-62. PMID 17024372 DOI: 10.1007/S00439-006-0246-6 |
0.646 |
|
| 2006 |
Tymchuk CN, Hartiala J, Patel PI, Mehrabian M, Allayee H. Nonconventional genetic risk factors for cardiovascular disease. Current Atherosclerosis Reports. 8: 184-92. PMID 16640955 DOI: 10.1007/s11883-006-0072-2 |
0.671 |
|
| 2006 |
Allayee H, Andalibi A, Mehrabian M. Using inbred mouse strains to identify genes for complex diseases. Frontiers in Bioscience : a Journal and Virtual Library. 11: 1216-26. PMID 16368507 DOI: 10.2741/1874 |
0.386 |
|
| 2005 |
Mehrabian M, Allayee H, Stockton J, Lum PY, Drake TA, Castellani LW, Suh M, Armour C, Edwards S, Lamb J, Lusis AJ, Schadt EE. Integrating genotypic and expression data in a segregating mouse population to identify 5-lipoxygenase as a susceptibility gene for obesity and bone traits. Nature Genetics. 37: 1224-33. PMID 16200066 DOI: 10.1038/Ng1619 |
0.355 |
|
| 2004 |
Churchill GA, Airey DC, Allayee H, Angel JM, Attie AD, Beatty J, Beavis WD, Belknap JK, Bennett B, Berrettini W, Bleich A, Bogue M, Broman KW, Buck KJ, Buckler E, et al. The Collaborative Cross, a community resource for the genetic analysis of complex traits. Nature Genetics. 36: 1133-7. PMID 15514660 DOI: 10.1038/Ng1104-1133 |
0.334 |
|
| 2004 |
Cantor RM, de Bruin T, Kono N, Napier S, van Nas A, Allayee H, Lusis AJ. Quantitative trait loci for apolipoprotein B, cholesterol, and triglycerides in familial combined hyperlipidemia pedigrees. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1935-41. PMID 15308552 DOI: 10.1161/01.Atv.0000142358.46276.A7 |
0.365 |
|
| 2004 |
Dwyer JH, Allayee H, Dwyer KM, Fan J, Wu H, Mar R, Lusis AJ, Mehrabian M. Arachidonate 5-lipoxygenase promoter genotype, dietary arachidonic acid, and atherosclerosis. The New England Journal of Medicine. 350: 29-37. PMID 14702425 DOI: 10.1016/J.Jvs.2004.03.014 |
0.373 |
|
| 2003 |
Mehrabian M, Allayee H. 5-lipoxygenase and atherosclerosis. Current Opinion in Lipidology. 14: 447-57. PMID 14501583 DOI: 10.1097/00041433-200310000-00005 |
0.338 |
|
| 2003 |
Allayee H, Ghazalpour A, Lusis AJ. Using mice to dissect genetic factors in atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1501-9. PMID 12920046 DOI: 10.1161/01.Atv.0000090886.40027.Dc |
0.396 |
|
| 2003 |
Allayee H, Castellani LW, Cantor RM, de Bruin TW, Lusis AJ. Biochemical and genetic association of plasma apolipoprotein A-II levels with familial combined hyperlipidemia. Circulation Research. 92: 1262-7. PMID 12738753 DOI: 10.1161/01.Res.0000075600.87675.16 |
0.31 |
|
| 2003 |
Pajukanta P, Allayee H, Krass KL, Kuraishy A, Soro A, Lilja HE, Mar R, Taskinen MR, Nuotio I, Laakso M, Rotter JI, de Bruin TW, Cantor RM, Lusis AJ, Peltonen L. Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. American Journal of Human Genetics. 72: 903-17. PMID 12638083 DOI: 10.1086/374177 |
0.363 |
|
| 2002 |
Allayee H, Krass KL, Pajukanta P, Cantor RM, van der Kallen CJ, Mar R, Rotter JI, de Bruin TW, Peltonen L, Lusis AJ. Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia. Circulation Research. 90: 926-31. PMID 11988495 DOI: 10.1161/01.Res.0000015885.27134.F0 |
0.377 |
|
| 2002 |
Sheth SS, Deluna A, Allayee H, Lusis AJ. Understanding atherosclerosis through mouse genetics. Current Opinion in Lipidology. 13: 181-9. PMID 11891421 DOI: 10.1097/00041433-200204000-00010 |
0.326 |
|
| 2001 |
Allayee H, de Bruin TW, Michelle Dominguez K, Cheng LS, Ipp E, Cantor RM, Krass KL, Keulen ET, Aouizerat BE, Lusis AJ, Rotter JI. Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p. Hypertension. 38: 773-8. PMID 11641285 DOI: 10.1161/Hy1001.092617 |
0.362 |
|
| 2000 |
Van Der Kallen CJH, Cantor RM, Van Greevenbroek MMJ, Geurts JMW, Bouwman FG, Aouizerat BE, Allayee H, Buurman WA, Lusis AJ, Rotter JI, De Bruin TWA. Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A International Journal of Obesity. 24: 1381-1391. PMID 11126332 DOI: 10.1038/Sj.Ijo.0801412 |
0.332 |
|
| 2000 |
Geurts JMW, Janssen RGJH, Van Greevenbroek MMJ, Van Der Kallen CJH, Cantor RM, Bu XD, Aouizerat BE, Allayee H, Rotter JI, De Bruin TWA. Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia Human Molecular Genetics. 9: 2067-2074. PMID 10958645 DOI: 10.1093/Hmg/9.14.2067 |
0.315 |
|
| 1999 |
Aouizerat BE, Allayee H, Cantor RM, Dallinga-Thie GM, Lanning CD, De Bruin TWA, Lusis AJ, Rotter JI. Linkage of a candidate gene locus to familial combined hyperlipidemia - Lecithin: Cholesterol acyltransferase on 16q Arteriosclerosis, Thrombosis, and Vascular Biology. 19: 2730-2736. PMID 10559018 DOI: 10.1161/01.Atv.19.11.2730 |
0.395 |
|
| 1999 |
Aouizerat BE, Allayee H, Cantor RM, Davis RC, Lanning CD, Wen PZ, Dallinga-Thie GM, de Bruin TW, Rotter JI, Lusis AJ. A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. American Journal of Human Genetics. 65: 397-412. PMID 10417282 DOI: 10.1086/302490 |
0.328 |
|
| 1999 |
Aouizerat BE, Allayee H, Bodnar J, Krass KL, Peltonen L, de Bruin TW, Rotter JI, Lusis AJ. Novel genes for familial combined hyperlipidemia. Current Opinion in Lipidology. 10: 113-22. PMID 10327279 DOI: 10.1097/00041433-199904000-00005 |
0.349 |
|
| 1998 |
Allayee H, Aouizerat BE, Cantor RM, Dallinga-Thie GM, Krauss RM, Lanning CD, Rotter JI, Lusis AJ, de Bruin TW. Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype. American Journal of Human Genetics. 63: 577-85. PMID 9683614 DOI: 10.1086/301983 |
0.352 |
|
| 1994 |
Liao F, Andalibi A, Qiao JH, Allayee H, Fogelman AM, Lusis AJ. Genetic evidence for a common pathway mediating oxidative stress, inflammatory gene induction, and aortic fatty streak formation in mice Journal of Clinical Investigation. 94: 877-884. PMID 8040344 DOI: 10.1172/Jci117409 |
0.305 |
|
| Show low-probability matches. |