| Year |
Citation |
Score |
| 2020 |
Lai CQ, Parnell LD, Smith CE, Guo T, Sayols-Baixeras S, Aslibekyan S, Tiwari HK, Irvin MR, Bender C, Fei D, Hidalgo B, Hopkins PN, Absher DM, Province MA, Elosua R, et al. Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A. The American Journal of Clinical Nutrition. PMID 32930325 DOI: 10.1093/Ajcn/Nqaa233 |
0.306 |
|
| 2020 |
Yaghootkar H, Zhang Y, Spracklen CN, Karaderi T, Huang LO, Bradfield J, Schurmann C, Fine RS, Preuss MH, Kutalik Z, Wittemans LB, Lu Y, Metz S, Willems SM, Li-Gao R, ... ... Province MA, et al. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. Diabetes. PMID 32917775 DOI: 10.2337/Db20-0070 |
0.341 |
|
| 2020 |
Christensen K, Wojczynski MK, Pedersen JK, Larsen LA, Kløjgaard S, Skytthe A, McGue M, Vaupel JW, Province MA. Mechanisms underlying familial aggregation of exceptional health and survival: A three-generation cohort study. Aging Cell. e13228. PMID 32886847 DOI: 10.1111/Acel.13228 |
0.312 |
|
| 2020 |
Hunt SC, Hansen MEB, Verhulst S, McQuillan MA, Beggs W, Lai TP, Mokone GG, Mpoloka SW, Meskel DW, Belay G, Nyambo TB, Abnet CC, Yeager M, Chanock SJ, Province MA, et al. Genetics and Geography of Leukocyte Telomere Length in Sub-Saharan Africans. Human Molecular Genetics. PMID 32821950 DOI: 10.1093/Hmg/Ddaa187 |
0.345 |
|
| 2020 |
Liu Y, Smith CE, Parnell LD, Lee YC, An P, Straka RJ, Tiwari HK, Wood AC, Kabagambe EK, Hidalgo B, Hopkins PN, Province MA, Arnett DK, Tucker KL, Ordovas JM, et al. Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk. Clinical Chemistry. PMID 32337541 DOI: 10.1093/Clinchem/Hvaa072 |
0.302 |
|
| 2020 |
Feitosa MF, Lunetta KL, Wang L, Wojczynski MK, Kammerer CM, Perls T, Schupf N, Christensen K, Murabito JM, Province MA. Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies. Atherosclerosis. 297: 102-110. PMID 32109663 DOI: 10.1016/J.Atherosclerosis.2020.02.005 |
0.328 |
|
| 2020 |
An P, Lu Y, Thyagarajan B, Kuipers AL, Anema JA, Miljkovic I, Daw EW, Province M. 1410-P: Genetics of TG/HDL-C Ratio and Its Change over Time in Nondiabetic Subjects Diabetes. 69. DOI: 10.2337/Db20-1410-P |
0.387 |
|
| 2020 |
Kraja AT, Daw EW, Lenzini P, Wang L, Lin SJ, Williams CA, Wells AB, Lunetta KL, Murabito JM, Sebastiani P, Tosto G, Barral S, Minster RL, Yashin A, Perls T, ... Province MA, et al. A comparison of genetic imputation methods using Long Life Family Study genotypes and sequence data with the 1000 Genome reference panel International Journal of Bioinformatics Research and Applications. 16: 59. DOI: 10.1504/Ijbra.2020.104855 |
0.347 |
|
| 2019 |
Kuipers AL, Wojczynski MK, Barinas-Mitchell E, Minster RL, Wang L, Feitosa MF, Kulminski A, Thyagarajan B, Lee JH, Province MA, Newman AB, Zmuda JM. Genome-wide linkage analysis of carotid artery traits in exceptionally long-lived families. Atherosclerosis. 291: 19-26. PMID 31634740 DOI: 10.1016/J.Atherosclerosis.2019.10.008 |
0.391 |
|
| 2019 |
Spracklen CN, Karaderi T, Yaghootkar H, Schurmann C, Fine RS, Kutalik Z, Preuss MH, Lu Y, Wittemans LBL, Adair LS, Allison M, Amin N, Auer PL, Bartz TM, Blüher M, ... ... Province MA, et al. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. American Journal of Human Genetics. PMID 31178129 DOI: 10.1016/J.Ajhg.2019.05.002 |
0.387 |
|
| 2019 |
Sung YJ, de Las Fuentes L, Winkler TW, Chasman DI, Bentley AR, Kraja AT, Ntalla I, Warren HR, Guo X, Schwander K, Manning AK, Brown MR, Aschard H, Feitosa MF, Franceschini N, ... ... Province MA, et al. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Human Molecular Genetics. PMID 31127295 DOI: 10.1093/Hmg/Ddz070 |
0.348 |
|
| 2019 |
Bentley AR, Sung YJ, Brown MR, Winkler TW, Kraja AT, Ntalla I, Schwander K, Chasman DI, Lim E, Deng X, Guo X, Liu J, Lu Y, Cheng CY, Sim X, ... ... Province MA, et al. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nature Genetics. 51: 636-648. PMID 30926973 DOI: 10.1038/S41588-019-0378-Y |
0.329 |
|
| 2019 |
de Vries PS, Brown MR, Bentley AR, Sung YJ, Winkler TW, Ntalla I, Schwander K, Kraja AT, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Huffman JE, Musani SK, ... ... Province MA, et al. Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. American Journal of Epidemiology. PMID 30698716 DOI: 10.1093/Aje/Kwz005 |
0.345 |
|
| 2019 |
Kilpeläinen TO, Bentley AR, Noordam R, Sung YJ, Schwander K, Winkler TW, Jakupović H, Chasman DI, Manning A, Ntalla I, Aschard H, Brown MR, de Las Fuentes L, Franceschini N, Guo X, ... ... Province MA, et al. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nature Communications. 10: 376. PMID 30670697 DOI: 10.1038/S41467-018-08008-W |
0.334 |
|
| 2019 |
Katzmarzyk PT, Malina RM, Pérusse L, Rice T, Province MA, Rao DC, Bouchard C. Familial resemblance in fatness and fat distribution. American Journal of Human Biology : the Official Journal of the Human Biology Council. 12: 395-404. PMID 11534030 DOI: 10.1002/(Sici)1520-6300(200005/06)12:3<395::Aid-Ajhb10>3.0.Co;2-J |
0.324 |
|
| 2019 |
AN P, THYAGARAJAN B, LEE JH, SCHUPF N, ZMUDA JM, PROVINCE M. 1447-P: Epistatic Interactions of Known Gene Variants for Glycated Hemoglobin: Evidence from the Long Life Family Study Diabetes. 68: 1447-P. DOI: 10.2337/Db19-1447-P |
0.326 |
|
| 2018 |
Arbeeva LS, Hanson HA, Arbeev KG, Kulminski AM, Stallard E, Ukraintseva SV, Wu D, Boudreau RM, Province MA, Smith KR, Yashin AI. How Well Does the Family Longevity Selection Score Work: A Validation Test Using the Utah Population Database. Frontiers in Public Health. 6: 277. PMID 30327761 DOI: 10.3389/Fpubh.2018.00277 |
0.318 |
|
| 2018 |
Kraja AT, An P, Lenzini P, Lin SJ, Williams C, Hicks JE, Warwick Daw E, Province MA. Simulation of a medication and methylation effects on triglycerides in the Genetic Analysis Workshop 20. Bmc Proceedings. 12: 25. PMID 30275880 DOI: 10.1186/S12919-018-0115-Z |
0.316 |
|
| 2018 |
Daw EW, Hicks J, Lenzini P, Lin SJ, Wang J, Williams C, An P, Province MA, Kraja AT. Methods for detecting methylation by SNP interaction in GAW20 simulation. Bmc Proceedings. 12: 37. PMID 30263046 DOI: 10.1186/S12919-018-0140-Y |
0.3 |
|
| 2018 |
Feitosa MF, Kraja AT, Chasman DI, Sung YJ, Winkler TW, Ntalla I, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Marten J, Musani SK, Li C, Bentley AR, ... ... Province MA, et al. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Plos One. 13: e0198166. PMID 29912962 DOI: 10.1371/Journal.Pone.0198166 |
0.34 |
|
| 2018 |
Laville V, Bentley AR, Privé F, Zhu X, Gauderman J, Winkler TW, Province M, Rao DC, Aschard H. VarExp: Estimating variance explained by Genome-Wide GxE summary statistics. Bioinformatics (Oxford, England). PMID 29726908 DOI: 10.1093/Bioinformatics/Bty379 |
0.359 |
|
| 2018 |
Mahajan A, Wessel J, Willems SM, Zhao W, Robertson NR, Chu AY, Gan W, Kitajima H, Taliun D, Rayner NW, Guo X, Lu Y, Li M, Jensen RA, Hu Y, ... ... Province MA, et al. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nature Genetics. 50: 559-571. PMID 29632382 DOI: 10.1038/S41588-018-0084-1 |
0.321 |
|
| 2018 |
Baranski TJ, Kraja AT, Fink JL, Feitosa M, Lenzini PA, Borecki IB, Liu CT, Cupples LA, North KE, Province MA. A high throughput, functional screen of human Body Mass Index GWAS loci using tissue-specific RNAi Drosophila Melanogaster crosses. Plos Genetics. 14: e1007222. PMID 29608557 DOI: 10.1371/Journal.Pgen.1007222 |
0.347 |
|
| 2018 |
Geng X, Irvin MR, Hidalgo B, Aslibekyan S, Srinivasasainagendra V, An P, Frazier-Wood A, Tiwari HK, Dave T, Ryan K, Ordovas JM, Straka RJ, Feitosa MF, Hopkins PN, Borecki I, ... Province MA, et al. An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort. Journal of Lipid Research. PMID 29463568 DOI: 10.1194/Jlr.P080333 |
0.363 |
|
| 2018 |
Sung YJ, Winkler TW, de Las Fuentes L, Bentley AR, Brown MR, Kraja AT, Schwander K, Ntalla I, Guo X, Franceschini N, Lu Y, Cheng CY, Sim X, Vojinovic D, Marten J, ... ... Province MA, et al. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. American Journal of Human Genetics. PMID 29455858 DOI: 10.1016/J.Ajhg.2018.01.015 |
0.38 |
|
| 2017 |
Klingel SL, Roke K, Hidalgo B, Aslibekyan S, Straka RJ, An P, Province MA, Hopkins PN, Arnett DK, Ordovas JM, Lai CQ, Mutch DM. Sex Differences in Blood HDL-c, the Total Cholesterol/HDL-c Ratio, and Palmitoleic Acid are Not Associated with Variants in Common Candidate Genes. Lipids. PMID 29080057 DOI: 10.1007/S11745-017-4307-5 |
0.325 |
|
| 2017 |
Kraja AT, Cook JP, Warren HR, Surendran P, Liu C, Evangelou E, Manning AK, Grarup N, Drenos F, Sim X, Smith AV, Amin N, Blakemore AIF, Bork-Jensen J, Brandslund I, ... ... Province MA, et al. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Circulation. Cardiovascular Genetics. 10. PMID 29030403 DOI: 10.1161/Circgenetics.117.001778 |
0.359 |
|
| 2017 |
Macé A, Tuke MA, Deelen P, Kristiansson K, Mattsson H, Nõukas M, Sapkota Y, Schick U, Porcu E, Rüeger S, McDaid AF, Porteous D, Winkler TW, Salvi E, Shrine N, ... ... Province MA, et al. CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications. 8: 744. PMID 28963451 DOI: 10.1038/S41467-017-00556-X |
0.366 |
|
| 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, ... ... Province MA, 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 |
0.322 |
|
| 2017 |
Aslibekyan S, Irvin MR, Hidalgo BA, Perry RT, Jeyarajah EJ, Garcia E, Shalaurova I, Hopkins PN, Province MA, Tiwari HK, Ordovas JM, Absher DM, Arnett DK. Genome- and CD4+ T-cell methylome-wide association study of circulating trimethylamine-N-oxide in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). Journal of Nutrition & Intermediary Metabolism. 8: 1-7. PMID 28439531 DOI: 10.1016/J.Jnim.2017.03.002 |
0.33 |
|
| 2016 |
Natarajan P, Bis JC, Bielak LF, Cox AJ, Dörr M, Feitosa MF, Franceschini N, Guo X, Hwang SJ, Isaacs A, Jhun MA, Kavousi M, Li-Gao R, Lyytikäinen LP, Marioni RE, ... ... Province MA, et al. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. Circulation. Cardiovascular Genetics. PMID 27872105 DOI: 10.1161/Circgenetics.116.001572 |
0.34 |
|
| 2016 |
Lai CQ, Wojczynski MK, Parnell LD, Hidalgo BA, Irvin MR, Aslibekyan S, Province MA, Absher DM, Arnett DK, Ordovas JM. Epigenome-wide association study of triglyceride postprandial responses to a high-fat dietary challenge. Journal of Lipid Research. PMID 27777315 DOI: 10.1194/Jlr.M069948 |
0.35 |
|
| 2016 |
Liu CT, Raghavan S, Maruthur N, Kabagambe EK, Hong J, Ng MC, Hivert MF, Lu Y, An P, Bentley AR, Drolet AM, Gaulton KJ, Guo X, Armstrong LL, Irvin MR, ... ... Province MA, et al. Trans-ethnic Meta-Analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin. American Journal of Human Genetics. PMID 27321945 DOI: 10.1016/J.Ajhg.2016.05.006 |
0.378 |
|
| 2016 |
Sung YJ, Winkler TW, Manning AK, Aschard H, Gudnason V, Harris TB, Smith AV, Boerwinkle E, Brown MR, Morrison AC, Fornage M, Lin LA, Richard M, Bartz TM, Psaty BM, ... ... Province MA, et al. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group. Genetic Epidemiology. PMID 27230302 DOI: 10.1002/Gepi.21978 |
0.373 |
|
| 2016 |
Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF, Oskarsson S, Pickrell JK, Thom K, Timshel P, de Vlaming R, ... ... Province MA, et al. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 533: 539-42. PMID 27225129 DOI: 10.1038/Nature17671 |
0.36 |
|
| 2016 |
Druley TE, Wang L, Lin SJ, Lee JH, Zhang Q, Daw EW, Abel HJ, Chasnoff SE, Ramos EI, Levinson BT, Thyagarajan B, Newman AB, Christensen K, Mayeux R, Province MA. Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study. Bmc Geriatrics. 16: 80. PMID 27060904 DOI: 10.1186/S12877-016-0253-Y |
0.378 |
|
| 2016 |
Wang S, Zhao JH, An P, Guo X, Jensen RA, Marten J, Huffman JE, Meidtner K, Boeing H, Campbell A, Rice KM, Scott RA, Yao J, Schulze MB, Wareham NJ, ... ... Province MA, et al. General Framework for Meta-Analysis of Haplotype Association Tests. Genetic Epidemiology. 40: 244-252. PMID 27027517 DOI: 10.1002/Gepi.21959 |
0.371 |
|
| 2015 |
Rao TJ, Province MA. A Framework for Interpreting Type I Error Rates from a Product-Term Model of Interaction Applied to Quantitative Traits. Genetic Epidemiology. PMID 26659945 DOI: 10.1002/Gepi.21944 |
0.321 |
|
| 2015 |
Wojczynski MK, Parnell LD, Pollin TI, Lai CQ, Feitosa MF, O'Connell JR, Frazier-Wood AC, Gibson Q, Aslibekyan S, Ryan KA, Province MA, Tiwari HK, Ordovas JM, Shuldiner AR, Arnett DK, et al. Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). Metabolism: Clinical and Experimental. 64: 1359-71. PMID 26256467 DOI: 10.1016/J.Metabol.2015.07.001 |
0.363 |
|
| 2015 |
Honig LS, Kang MS, Cheng R, Eckfeldt JH, Thyagarajan B, Leiendecker-Foster C, Province MA, Sanders JL, Perls T, Christensen K, Lee JH, Mayeux R, Schupf N. Heritability of telomere length in a study of long-lived families. Neurobiology of Aging. PMID 26239175 DOI: 10.1016/J.Neurobiolaging.2015.06.017 |
0.333 |
|
| 2015 |
Gomez F, Wang L, Abel H, Zhang Q, Province MA, Borecki IB. Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study. Bmc Genetics. 16: 42. PMID 25902833 DOI: 10.1186/S12863-015-0196-X |
0.361 |
|
| 2015 |
Minster RL, Sanders JL, Singh J, Kammerer CM, Barmada MM, Matteini AM, Zhang Q, Wojczynski MK, Daw EW, Brody JA, Arnold AM, Lunetta KL, Murabito JM, Christensen K, Perls TT, ... Province MA, et al. Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 25758594 DOI: 10.1093/Gerona/Glv006 |
0.301 |
|
| 2015 |
Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert MF, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, ... ... Province MA, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897. PMID 25631608 DOI: 10.1038/Ncomms6897 |
0.306 |
|
| 2015 |
Kulminski AM, Arbeev KG, Culminskaya I, Ukraintseva SV, Stallard E, Province MA, Yashin AI. Trade-offs in the effects of the apolipoprotein E polymorphism on risks of diseases of the heart, cancer, and neurodegenerative disorders: insights on mechanisms from the Long Life Family Study. Rejuvenation Research. 18: 128-35. PMID 25482294 DOI: 10.1089/Rej.2014.1616 |
0.344 |
|
| 2014 |
Barral S, Cosentino S, Christensen K, Newman AB, Perls TT, Province MA, Mayeux R. Common genetic variants on 6q24 associated with exceptional episodic memory performance in the elderly. Jama Neurology. 71: 1514-9. PMID 25317765 DOI: 10.1001/Jamaneurol.2014.1663 |
0.306 |
|
| 2014 |
Zhang Q, Wang L, Koboldt D, Boreki IB, Province MA. Adjusting family relatedness in data-driven burden test of rare variants. Genetic Epidemiology. 38: 722-7. PMID 25169066 DOI: 10.1002/Gepi.21848 |
0.335 |
|
| 2014 |
Kraja AT, Chasman DI, North KE, Reiner AP, Yanek LR, Kilpeläinen TO, Smith JA, Dehghan A, Dupuis J, Johnson AD, Feitosa MF, Tekola-Ayele F, Chu AY, Nolte IM, Dastani Z, ... ... Province MA, et al. Pleiotropic genes for metabolic syndrome and inflammation. Molecular Genetics and Metabolism. 112: 317-38. PMID 24981077 DOI: 10.1016/J.Ymgme.2014.04.007 |
0.384 |
|
| 2014 |
Feitosa MF, Wojczynski MK, Straka R, Kammerer CM, Lee JH, Kraja AT, Christensen K, Newman AB, Province MA, Borecki IB. Genetic analysis of long-lived families reveals novel variants influencing high density-lipoprotein cholesterol. Frontiers in Genetics. 5: 159. PMID 24917880 DOI: 10.3389/Fgene.2014.00159 |
0.401 |
|
| 2014 |
An P, Straka RJ, Pollin TI, Feitosa MF, Wojczynski MK, Daw EW, O'Connell JR, Gibson Q, Ryan KA, Hopkins PN, Tsai MY, Lai CQ, Province MA, Ordovas JM, Shuldiner AR, et al. Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response. Human Genetics. 133: 919-30. PMID 24604477 DOI: 10.1007/S00439-014-1435-3 |
0.395 |
|
| 2014 |
Kulminski AM, Arbeev KG, Culminskaya I, Arbeeva L, Ukraintseva SV, Stallard E, Christensen K, Schupf N, Province MA, Yashin AI. Age, gender, and cancer but not neurodegenerative and cardiovascular diseases strongly modulate systemic effect of the Apolipoprotein E4 allele on lifespan. Plos Genetics. 10: e1004141. PMID 24497847 DOI: 10.1371/Journal.Pgen.1004141 |
0.311 |
|
| 2014 |
An P, Miljkovic I, Thyagarajan B, Kraja AT, Daw EW, Pankow JS, Selvin E, Kao WH, Maruthur NM, Nalls MA, Liu Y, Harris TB, Lee JH, Borecki IB, Christensen K, ... ... Province MA, et al. Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS). Metabolism: Clinical and Experimental. 63: 461-8. PMID 24405752 DOI: 10.1016/J.Metabol.2013.11.018 |
0.384 |
|
| 2014 |
Miedema MD, Petrone AB, Arnett DK, Dodson JA, Carr JJ, Pankow JS, Hunt SC, Province MA, Kraja A, Gaziano JM, Djousse L. Adult height and prevalence of coronary artery calcium: the National Heart, Lung, and Blood Institute Family Heart Study. Circulation. Cardiovascular Imaging. 7: 52-7. PMID 24336983 DOI: 10.1161/Circimaging.113.000681 |
0.322 |
|
| 2013 |
Lee JH, Cheng R, Honig LS, Feitosa M, Kammerer CM, Kang MS, Schupf N, Lin SJ, Sanders JL, Bae H, Druley T, Perls T, Christensen K, Province M, Mayeux R. Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. Frontiers in Genetics. 4: 310. PMID 24478790 DOI: 10.3389/Fgene.2013.00310 |
0.399 |
|
| 2013 |
Parsa A, Fuchsberger C, Köttgen A, O'Seaghdha CM, Pattaro C, de Andrade M, Chasman DI, Teumer A, Endlich K, Olden M, Chen MH, Tin A, Kim YJ, Taliun D, Li M, ... ... Province M, et al. Common variants in Mendelian kidney disease genes and their association with renal function. Journal of the American Society of Nephrology : Jasn. 24: 2105-17. PMID 24029420 DOI: 10.1681/Asn.2012100983 |
0.367 |
|
| 2013 |
Wojczynski MK, Li M, Bielak LF, Kerr KF, Reiner AP, Wong ND, Yanek LR, Qu L, White CC, Lange LA, Ferguson JF, He J, Young T, Mosley TH, Smith JA, ... ... Province MA, et al. Genetics of coronary artery calcification among African Americans, a meta-analysis. Bmc Medical Genetics. 14: 75. PMID 23870195 DOI: 10.1186/1471-2350-14-75 |
0.38 |
|
| 2013 |
Barral S, Cosentino S, Costa R, Andersen SL, Christensen K, Eckfeldt JH, Newman AB, Perls TT, Province MA, Hadley EC, Rossi WK, Mayeux R. Exceptional memory performance in the Long Life Family Study. Neurobiology of Aging. 34: 2445-8. PMID 23759147 DOI: 10.1016/J.Neurobiolaging.2013.05.002 |
0.304 |
|
| 2013 |
Randall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpeläinen TO, Esko T, Mägi R, Li S, Workalemahu T, Feitosa MF, Croteau-Chonka DC, Day FR, Fall T, ... ... Province MA, et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Plos Genetics. 9: e1003500. PMID 23754948 DOI: 10.1371/Journal.Pgen.1003500 |
0.348 |
|
| 2013 |
Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR, Esko T, Fall T, Ferreira T, Gentilini D, Jackson AU, ... ... Province MA, et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics. 45: 501-12. PMID 23563607 DOI: 10.1038/Ng.2606 |
0.348 |
|
| 2013 |
Divers J, Palmer ND, Lu L, Register TC, Carr JJ, Hicks PJ, Hightower RC, Smith SC, Xu J, Cox AJ, Hruska KA, Bowden DW, Lewis CE, Heiss G, Province MA, et al. Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus. Circulation. Cardiovascular Genetics. 6: 97-105. PMID 23233742 DOI: 10.1161/Circgenetics.112.964114 |
0.371 |
|
| 2013 |
Kraja AT, Borecki IB, Tsai MY, Ordovas JM, Hopkins PN, Lai CQ, Frazier-Wood AC, Straka RJ, Hixson JE, Province MA, Arnett DK. Genetic analysis of 16 NMR-lipoprotein fractions in humans, the GOLDN study. Lipids. 48: 155-65. PMID 23192668 DOI: 10.1007/S11745-012-3740-8 |
0.31 |
|
| 2013 |
Schupf N, Barral S, Perls T, Newman A, Christensen K, Thyagarajan B, Province M, Rossi WK, Mayeux R. Apolipoprotein E and familial longevity. Neurobiology of Aging. 34: 1287-91. PMID 23040522 DOI: 10.1016/J.Neurobiolaging.2012.08.019 |
0.341 |
|
| 2012 |
Ramos E, Levinson BT, Chasnoff S, Hughes A, Young AL, Thornton K, Li A, Vallania FL, Province M, Druley TE. Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing. Bmc Genomics. 13: 683. PMID 23216810 DOI: 10.1186/1471-2164-13-683 |
0.308 |
|
| 2012 |
Mangino M, Hwang SJ, Spector TD, Hunt SC, Kimura M, Fitzpatrick AL, Christiansen L, Petersen I, Elbers CC, Harris T, Chen W, Srinivasan SR, Kark JD, Benetos A, El Shamieh S, ... ... Province MA, et al. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Human Molecular Genetics. 21: 5385-94. PMID 23001564 DOI: 10.1093/Hmg/Dds382 |
0.382 |
|
| 2012 |
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, ... ... Province M, et al. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human Molecular Genetics. 21: 5329-43. PMID 22962313 DOI: 10.1093/Hmg/Dds369 |
0.35 |
|
| 2012 |
Scott RA, Lagou V, Welch RP, Wheeler E, Montasser ME, Luan J, Mägi R, Strawbridge RJ, Rehnberg E, Gustafsson S, Kanoni S, Rasmussen-Torvik LJ, Yengo L, Lecoeur C, Shungin D, ... ... Province MA, et al. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nature Genetics. 44: 991-1005. PMID 22885924 DOI: 10.1038/Ng.2385 |
0.392 |
|
| 2012 |
Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, ... ... Province MA, et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American Journal of Respiratory and Critical Care Medicine. 186: 622-32. PMID 22837378 DOI: 10.1164/Rccm.201202-0366Oc |
0.381 |
|
| 2012 |
Cresci S, Dorn GW, Jones PG, Beitelshees AL, Li AY, Lenzini PA, Province MA, Spertus JA, Lanfear DE. Adrenergic-pathway gene variants influence beta-blocker-related outcomes after acute coronary syndrome in a race-specific manner. Journal of the American College of Cardiology. 60: 898-907. PMID 22703928 DOI: 10.1016/J.Jacc.2012.02.051 |
0.334 |
|
| 2012 |
Billings LK, Hsu YH, Ackerman RJ, Dupuis J, Voight BF, Rasmussen-Torvik LJ, Hercberg S, Lathrop M, Barnes D, Langenberg C, Hui J, Fu M, Bouatia-Naji N, Lecoeur C, An P, ... ... Province MA, et al. Impact of common variation in bone-related genes on type 2 diabetes and related traits. Diabetes. 61: 2176-86. PMID 22698912 DOI: 10.2337/Db11-1515 |
0.358 |
|
| 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, ... ... Province MA, 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 |
0.339 |
|
| 2012 |
Boraska V, Day-Williams A, Franklin CS, Elliott KS, Panoutsopoulou K, Tachmazidou I, Albrecht E, Bandinelli S, Beilin LJ, Bochud M, Cadby G, Ernst F, Evans DM, Hayward C, Hicks AA, ... ... Province MA, et al. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. Plos One. 7: e31369. PMID 22479309 DOI: 10.1371/Journal.Pone.0031369 |
0.375 |
|
| 2012 |
Pattaro C, Köttgen A, Teumer A, Garnaas M, Böger CA, Fuchsberger C, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, ... ... Province M, et al. Genome-wide association and functional follow-up reveals new loci for kidney function. Plos Genetics. 8: e1002584. PMID 22479191 DOI: 10.1371/Journal.Pgen.1002584 |
0.305 |
|
| 2012 |
Kraja AT, Lawson HA, Arnett DK, Borecki IB, Broeckel U, de las Fuentes L, Hunt SC, Province MA, Cheverud J, Rao DC. Obesity-insulin targeted genes in the 3p26-25 region in human studies and LG/J and SM/J mice. Metabolism: Clinical and Experimental. 61: 1129-41. PMID 22386932 DOI: 10.1016/J.Metabol.2012.01.008 |
0.36 |
|
| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... ... Province MA, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.368 |
|
| 2012 |
Mechanic LE, Chen HS, Amos CI, Chatterjee N, Cox NJ, Divi RL, Fan R, Harris EL, Jacobs K, Kraft P, Leal SM, McAllister K, Moore JH, Paltoo DN, Province MA, et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genetic Epidemiology. 36: 22-35. PMID 22147673 DOI: 10.1002/Gepi.20652 |
0.372 |
|
| 2011 |
Kraja AT, Czajkowski J, Feitosa MF, Borecki IB, Province MA. Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data. Bmc Proceedings. 5: S96. PMID 22373254 DOI: 10.1186/1753-6561-5-S9-S96 |
0.366 |
|
| 2011 |
Chung D, Zhang Q, Kraja AT, Borecki IB, Province MA. Distance-based phenotypic association analysis of DNA sequence data. Bmc Proceedings. 5: S54. PMID 22373107 DOI: 10.1186/1753-6561-5-S9-S54 |
0.331 |
|
| 2011 |
Zhang Q, Chung D, Kraja A, Borecki II, Province MA. Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits. Bmc Proceedings. 5: S35. PMID 22373066 DOI: 10.1186/1753-6561-5-S9-S35 |
0.361 |
|
| 2011 |
Hutz JE, Manning WA, Province MA, McLeod HL. Genomewide analysis of inherited variation associated with phosphorylation of PI3K/AKT/mTOR signaling proteins. Plos One. 6: e24873. PMID 21949775 DOI: 10.1371/Journal.Pone.0024873 |
0.77 |
|
| 2011 |
Cresci S, Wu J, Province MA, Spertus JA, Steffes M, McGill JB, Alderman EL, Brooks MM, Kelsey SF, Frye RL, Bach RG. Peroxisome proliferator-activated receptor pathway gene polymorphism associated with extent of coronary artery disease in patients with type 2 diabetes in the bypass angioplasty revascularization investigation 2 diabetes trial. Circulation. 124: 1426-34. PMID 21911782 DOI: 10.1161/Circulationaha.111.029173 |
0.319 |
|
| 2011 |
Zhang Q, Irvin MR, Arnett DK, Province MA, Borecki I. A data-driven method for identifying rare variants with heterogeneous trait effects. Genetic Epidemiology. 35: 679-85. PMID 21818776 DOI: 10.1002/Gepi.20618 |
0.378 |
|
| 2011 |
Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA. Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease. Circulation. Cardiovascular Genetics. 4: 169-78. PMID 21372283 DOI: 10.1161/Circgenetics.110.959296 |
0.315 |
|
| 2011 |
Manning AK, LaValley M, Liu CT, Rice K, An P, Liu Y, Miljkovic I, Rasmussen-Torvik L, Harris TB, Province MA, Borecki IB, Florez JC, Meigs JB, Cupples LA, Dupuis J. Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients. Genetic Epidemiology. 35: 11-8. PMID 21181894 DOI: 10.1002/Gepi.20546 |
0.364 |
|
| 2011 |
Simino J, Shi G, Kume R, Schwander K, Province MA, Gu CC, Kardia S, Chakravarti A, Ehret G, Olshen RA, Turner ST, Ho LT, Zhu X, Jaquish C, Paltoo D, et al. Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program. American Journal of Hypertension. 24: 347-54. PMID 21151011 DOI: 10.1038/Ajh.2010.238 |
0.364 |
|
| 2011 |
Kraja AT, Hunt SC, Rao DC, Dávila-Román VG, Arnett DK, Province MA. Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies. Current Hypertension Reports. 13: 46-54. PMID 21128019 DOI: 10.1007/S11906-010-0174-7 |
0.326 |
|
| 2011 |
Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA. Response to Letter Regarding Article “Chromosome 9p21 Haplotypes and Prognosis in White and Black Patients With Coronary Artery Disease” Circulation-Cardiovascular Genetics. 4. DOI: 10.1161/Circgenetics.111.960807 |
0.32 |
|
| 2010 |
Beitelshees AL, Johnson JA, Hames ML, Gong Y, Cooper-Dehoff RM, Wu J, Cresci S, Ma CX, Pepine CJ, Province MA, Spertus JA, McLeod HL. Aromatase gene polymorphisms are associated with survival among patients with cardiovascular disease in a sex-specific manner. Plos One. 5: e15180. PMID 21170323 DOI: 10.1371/Journal.Pone.0015180 |
0.302 |
|
| 2010 |
Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, ... ... Province MA, et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 467: 832-8. PMID 20881960 DOI: 10.1038/Nature09410 |
0.405 |
|
| 2010 |
Levy D, Neuhausen SL, Hunt SC, Kimura M, Hwang SJ, Chen W, Bis JC, Fitzpatrick AL, Smith E, Johnson AD, Gardner JP, Srinivasan SR, Schork N, Rotter JI, Herbig U, ... ... Province MA, et al. Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Proceedings of the National Academy of Sciences of the United States of America. 107: 9293-8. PMID 20421499 DOI: 10.1073/Pnas.0911494107 |
0.38 |
|
| 2010 |
Monda KL, North KE, Hunt SC, Rao DC, Province MA, Kraja AT. The genetics of obesity and the metabolic syndrome. Endocrine, Metabolic & Immune Disorders Drug Targets. 10: 86-108. PMID 20406164 DOI: 10.2174/187153010791213100 |
0.333 |
|
| 2010 |
Kraja AT, Province MA, Straka RJ, Ordovas JM, Borecki IB, Arnett DK. Fenofibrate and metabolic syndrome. Endocrine, Metabolic & Immune Disorders Drug Targets. 10: 138-48. PMID 20406163 DOI: 10.2174/187153010791213047 |
0.341 |
|
| 2010 |
Köttgen A, Pattaro C, Böger CA, Fuchsberger C, Olden M, Glazer NL, Parsa A, Gao X, Yang Q, Smith AV, O'Connell JR, Li M, Schmidt H, Tanaka T, Isaacs A, ... ... Province M, et al. New loci associated with kidney function and chronic kidney disease. Nature Genetics. 42: 376-84. PMID 20383146 DOI: 10.1038/Ng.568 |
0.308 |
|
| 2010 |
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Province MA, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics. 42: 105-16. PMID 20081858 DOI: 10.1038/Ng.520 |
0.318 |
|
| 2010 |
Junyent M, Parnell LD, Lai CQ, Arnett DK, Tsai MY, Kabagambe EK, Straka RJ, Province M, An P, Smith CE, Lee YC, Borecki I, Ordovás JM. ADAM17_i33708A>G polymorphism interacts with dietary n-6 polyunsaturated fatty acids to modulate obesity risk in the Genetics of Lipid Lowering Drugs and Diet Network study Nutrition, Metabolism and Cardiovascular Diseases. 20: 698-705. PMID 19819120 DOI: 10.1016/J.Numecd.2009.06.011 |
0.328 |
|
| 2010 |
Junyent M, Lee YC, Smith CE, Arnett DK, Tsai MY, Kabagambe EK, Straka RJ, Province M, An P, Lai CQ, Parnell LD, Shen J, Borecki I, Ordovas JM. The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene Nutrition, Metabolism and Cardiovascular Diseases. 20: 34-40. PMID 19364639 DOI: 10.1016/J.Numecd.2009.02.010 |
0.343 |
|
| 2009 |
Daw EW, Plunkett J, Feitosa M, Gao X, Van Brunt A, Ma D, Czajkowski J, Province MA, Borecki I. A framework for analyzing both linkage and association: an analysis of Genetic Analysis Workshop 16 simulated data. Bmc Proceedings. 3: S98. PMID 20018095 DOI: 10.1186/1753-6561-3-S7-S98 |
0.365 |
|
| 2009 |
An P, Feitosa M, Ketkar S, Adelman A, Lin S, Borecki I, Province M. Epistatic interactions of CDKN2B-TCF7L2 for risk of type 2 diabetes and of CDKN2B-JAZF1 for triglyceride/high-density lipoprotein ratio longitudinal change: evidence from the Framingham Heart Study. Bmc Proceedings. 3: S71. PMID 20018066 DOI: 10.1186/1753-6561-3-S7-S71 |
0.378 |
|
| 2009 |
Kraja AT, Culverhouse R, Daw EW, Wu J, Van Brunt A, Province MA, Borecki IB. The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study. Bmc Proceedings. 3: S4. PMID 20018031 DOI: 10.1186/1753-6561-3-S7-S4 |
0.383 |
|
| 2009 |
Park YM, Province MA, Gao X, Feitosa M, Wu J, Ma D, Rao D, Kraja AT. Longitudinal trends in the association of metabolic syndrome with 550 k single-nucleotide polymorphisms in the Framingham Heart Study. Bmc Proceedings. 3: S116. PMID 20017981 DOI: 10.1186/1753-6561-3-S7-S116 |
0.357 |
|
| 2009 |
An P, Mukherjee O, Chanda P, Yao L, Engelman CD, Huang CH, Zheng T, Kovac IP, Dubé MP, Liang X, Li J, de Andrade M, Culverhouse R, Malzahn D, Manning AK, ... ... Province MA, et al. The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16. Genetic Epidemiology. 33: S58-67. PMID 19924703 DOI: 10.1002/Gepi.20474 |
0.32 |
|
| 2009 |
Sebastiani P, Hadley EC, Province M, Christensen K, Rossi W, Perls TT, Ash AS. A family longevity selection score: ranking sibships by their longevity, size, and availability for study. American Journal of Epidemiology. 170: 1555-62. PMID 19910380 DOI: 10.1093/Aje/Kwp309 |
0.331 |
|
| 2009 |
Junyent M, Parnell LD, Lai CQ, Lee YC, Smith CE, Arnett DK, Tsai MY, Kabagambe EK, Straka RJ, Province M, An P, Borecki I, Ordovás JM. Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study. The American Journal of Clinical Nutrition. 90: 686-94. PMID 19605566 DOI: 10.3945/Ajcn.2009.27738 |
0.328 |
|
| 2009 |
Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, ... ... Province MA, et al. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. Plos Genetics. 5: e1000539. PMID 19557197 DOI: 10.1371/Journal.Pgen.1000539 |
0.365 |
|
| 2009 |
Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 2182-9. PMID 19461589 DOI: 10.1038/Oby.2009.141 |
0.404 |
|
| 2009 |
Junyent M, Arnett DK, Tsai MY, Kabagambe EK, Straka RJ, Province M, An P, Lai CQ, Parnell LD, Shen J, Lee YC, Borecki I, Ordovás JM. Genetic variants at the PDZ-interacting domain of the scavenger receptor class B type I interact with diet to influence the risk of metabolic syndrome in obese men and women. The Journal of Nutrition. 139: 842-8. PMID 19321583 DOI: 10.3945/Jn.108.101196 |
0.368 |
|
| 2009 |
Lai CQ, Parnell LD, Arnett DK, GarcÃa-Bailo B, Tsai MY, Kabagambe EK, Straka RJ, Province MA, An P, Borecki IB, Tucker KL, Ordovás JM. WDTC1, the ortholog of Drosophila adipose gene, associates with human obesity, modulated by MUFA intake. Obesity (Silver Spring, Md.). 17: 593-600. PMID 19238144 DOI: 10.1038/Oby.2008.561 |
0.325 |
|
| 2009 |
Wu J, Pankow JS, Tracy RP, North KE, Myers RH, Feitosa ME, Province MA, Borecki IB. A QTL on 12q influencing an inflammation marker and obesity in white women: the NHLBI Family Heart Study. Obesity (Silver Spring, Md.). 17: 525-31. PMID 19238141 DOI: 10.1038/Oby.2008.556 |
0.344 |
|
| 2009 |
Warodomwichit D, Shen J, Arnett DK, Tsai MY, Kabagambe EK, Peacock JM, Hixson JE, Straka RJ, Province MA, An P, Lai CQ, Parnell LD, Borecki IB, Ordovas JM. ADIPOQ polymorphisms, monounsaturated fatty acids, and obesity risk: the GOLDN study. Obesity (Silver Spring, Md.). 17: 510-7. PMID 19238139 DOI: 10.1038/Oby.2008.583 |
0.328 |
|
| 2009 |
Ma D, Feitosa MF, Wilk JB, Laramie JM, Yu K, Leiendecker-Foster C, Myers RH, Province MA, Borecki IB. Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension. 53: 473-9. PMID 19204185 DOI: 10.1161/Hypertensionaha.108.118133 |
0.321 |
|
| 2009 |
Warodomwichit D, Arnett DK, Kabagambe EK, Tsai MY, Hixson JE, Straka RJ, Province M, An P, Lai CQ, Borecki I, Ordovas JM. Polyunsaturated fatty acids modulate the effect of TCF7L2 gene variants on postprandial lipemia. The Journal of Nutrition. 139: 439-46. PMID 19141698 DOI: 10.3945/Jn.108.096461 |
0.348 |
|
| 2009 |
Feitosa MF, Myers RH, Pankow JS, Province MA, Borecki IB. LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. Atherosclerosis. 204: 171-7. PMID 19101670 DOI: 10.1016/J.Atherosclerosis.2008.09.007 |
0.381 |
|
| 2009 |
Perez-Martinez P, Corella D, Shen J, Arnett DK, Yiannakouris N, Tai ES, Orho-Melander M, Tucker KL, Tsai M, Straka RJ, Province M, Chew SK, Perez-Jimenez F, Lai CQ, Lopez-Miranda J, et al. Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states American Journal of Clinical Nutrition. 89: 391-399. PMID 19056598 DOI: 10.3945/Ajcn.2008.26363 |
0.347 |
|
| 2008 |
Kraja AT, Province MA, Huang P, Jarvis JP, Rice T, Cheverud JM, Rao DC. Trends in metabolic syndrome and gene networks in human and rodent models. Endocrine, Metabolic & Immune Disorders Drug Targets. 8: 198-207. PMID 18782016 DOI: 10.2174/187153008785700145 |
0.336 |
|
| 2008 |
Borecki IB, Province MA. Genetic and genomic discovery using family studies. Circulation. 118: 1057-63. PMID 18765388 DOI: 10.1161/Circulationaha.107.714592 |
0.408 |
|
| 2008 |
Hutz JE, Kraja AT, McLeod HL, Province MA. CANDID: a flexible method for prioritizing candidate genes for complex human traits. Genetic Epidemiology. 32: 779-90. PMID 18613097 DOI: 10.1002/Gepi.20346 |
0.765 |
|
| 2008 |
Liu Y, Ordovas JM, Gao G, Province M, Straka RJ, Tsai MY, Lai CQ, Zhang K, Borecki I, Hixson JE, Allison DB, Arnett DK. The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions. Journal of Human Genetics. 53: 709-17. PMID 18542840 DOI: 10.1007/S10038-008-0302-2 |
0.336 |
|
| 2008 |
Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study. Bmc Medical Genetics. 9: 46. PMID 18498660 DOI: 10.1186/1471-2350-9-46 |
0.382 |
|
| 2008 |
Borecki IB, Province MA. Linkage and association: basic concepts. Advances in Genetics. 60: 51-74. PMID 18358316 DOI: 10.1016/S0065-2660(07)00403-8 |
0.376 |
|
| 2008 |
Perez-Martinez P, Yiannakouris N, Lopez-Miranda J, Arnett D, Tsai M, Galan E, Straka R, Delgado-Lista J, Province M, Ruano J, Borecki I, Hixson J, Garcia-Bailo B, Perez-Jimenez F, Ordovas JM. Postprandial triacylglycerol metabolism is modified by the presence of genetic variation at the perilipin (PLIN) locus in 2 white populations. The American Journal of Clinical Nutrition. 87: 744-52. PMID 18326614 DOI: 10.1093/Ajcn/87.3.744 |
0.302 |
|
| 2008 |
Shen J, Arnett DK, Parnell LD, Peacock JM, Lai CQ, Hixson JE, Tsai MY, Province MA, Straka RJ, Ordovas JM. Association of common C-reactive protein (CRP) gene polymorphisms with baseline plasma CRP levels and fenofibrate response: the GOLDN study. Diabetes Care. 31: 910-5. PMID 18285551 DOI: 10.2337/Dc07-1687 |
0.313 |
|
| 2008 |
Zhang Q, Lewis CE, Wagenknecht LE, Myers RH, Pankow JS, Hunt SC, North KE, Hixson JE, Jeffrey Carr J, Shimmin LC, Borecki I, Province MA. Genome-wide admixture mapping for coronary artery calcification in African Americans: the NHLBI Family Heart Study. Genetic Epidemiology. 32: 264-72. PMID 18200599 DOI: 10.1002/Gepi.20301 |
0.378 |
|
| 2007 |
Kraja AT, Corbett J, Ping A, Lin RS, Jacobsen PA, Crosswhite M, Borecki IB, Province MA. Rheumatoid arthritis, item response theory, Blom transformation, and mixed models. Bmc Proceedings. 1: S116. PMID 18466457 DOI: 10.1186/1753-6561-1-S1-S116 |
0.31 |
|
| 2007 |
Weir BA, Woo MS, Getz G, Perner S, Ding L, Beroukhim R, Lin WM, Province MA, Kraja A, Johnson LA, Shah K, Sato M, Thomas RK, Barletta JA, Borecki IB, et al. Characterizing the cancer genome in lung adenocarcinoma. Nature. 450: 893-8. PMID 17982442 DOI: 10.1038/Nature06358 |
0.316 |
|
| 2007 |
Corella D, Arnett DK, Tsai MY, Kabagambe EK, Peacock JM, Hixson JE, Straka RJ, Province M, Lai CQ, Parnell LD, Borecki I, Ordovas JM. The -256T>C polymorphism in the apolipoprotein A-II gene promoter is associated with body mass index and food intake in the genetics of lipid lowering drugs and diet network study. Clinical Chemistry. 53: 1144-52. PMID 17446329 DOI: 10.1373/Clinchem.2006.084863 |
0.305 |
|
| 2007 |
North KE, Franceschini N, Borecki IB, Gu CC, Heiss G, Province MA, Arnett DK, Lewis CE, Miller MB, Myers RH, Hunt SC, Freedman BI. Genotype-by-sex interaction on fasting insulin concentration: the HyperGEN study. Diabetes. 56: 137-42. PMID 17192475 DOI: 10.2337/Db06-0624 |
0.349 |
|
| 2007 |
Feitosa MF, Province MA, Heiss G, Arnett DK, Myers RH, Pankow JS, Hopkins PN, Borecki IB. Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). Atherosclerosis. 190: 232-7. PMID 16529751 DOI: 10.1016/J.Atherosclerosis.2006.02.006 |
0.359 |
|
| 2006 |
Kraja AT, Borecki IB, North K, Tang W, Myers RH, Hopkins PN, Arnett D, Corbett J, Adelman A, Province MA. Longitudinal and age trends of metabolic syndrome and its risk factors: the Family Heart Study. Nutrition & Metabolism. 3: 41. PMID 17147796 DOI: 10.1186/1743-7075-3-41 |
0.31 |
|
| 2006 |
Djoussé L, Pankow JS, Hunt SC, Heiss G, Province MA, Kabagambe EK, Ellison RC. Influence of saturated fat and linolenic acid on the association between intake of dairy products and blood pressure. Hypertension. 48: 335-41. PMID 16801477 DOI: 10.1161/01.Hyp.0000229668.73501.E8 |
0.32 |
|
| 2006 |
Wang Q, Hunt SC, Xu Q, Chen YE, Province MA, Eckfeldt JH, Pankow JS, Song Q. Association study of CRP gene polymorphisms with serum CRP level and cardiovascular risk in the NHLBI Family Heart Study. American Journal of Physiology. Heart and Circulatory Physiology. 291: H2752-7. PMID 16731635 DOI: 10.1152/Ajpheart.01164.2005 |
0.369 |
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| 2006 |
Hopkins PN, Ellison RC, Province MA, Pankow JS, Carr JJ, Arnett DK, Lewis CE, Heiss G, Hunt SC. Association of Coronary Artery Calcified Plaque With Clinical Coronary Heart Disease in the National Heart, Lung, and Blood Institute's Family Heart Study American Journal of Cardiology. 97: 1564-1569. PMID 16728214 DOI: 10.1016/J.Amjcard.2005.12.043 |
0.324 |
|
| 2006 |
Tang W, Arnett DK, Province MA, Lewis CE, North K, Carr JJ, Pankow JS, Hopkins PN, Devereux RB, Wilk JB, Wagenknecht L. Racial differences in the association of coronary calcified plaque with left ventricular hypertrophy: the National Heart, Lung, and Blood Institute Family Heart Study and Hypertension Genetic Epidemiology Network. The American Journal of Cardiology. 97: 1441-8. PMID 16679080 DOI: 10.1016/J.Amjcard.2005.11.076 |
0.304 |
|
| 2006 |
Tang W, Hong Y, Province MA, Rich SS, Hopkins PN, Arnett DK, Pankow JS, Miller MB, Eckfeldt JH. Familial clustering for features of the metabolic syndrome: the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study. Diabetes Care. 29: 631-6. PMID 16505518 DOI: 10.2337/Diacare.29.03.06.Dc05-0679 |
0.36 |
|
| 2006 |
Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A. The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 14: 469-77. PMID 16493446 DOI: 10.1038/Sj.Ejhg.5201582 |
0.362 |
|
| 2006 |
Wu X, Kan D, Province M, Quertermous T, Rao DC, Chang C, Mosley TH, Curb D, Boerwinkle E, Cooper RS. An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP). American Journal of Hypertension. 19: 122-7. PMID 16461203 DOI: 10.1016/J.Amjhyper.2005.07.010 |
0.349 |
|
| 2006 |
Yu K, Gu CC, Xiong C, An P, Province MA. Global transmission/disequilibrium tests based on haplotype sharing in multiple candidate genes. Genetic Epidemiology. 29: 323-35. PMID 16240444 DOI: 10.1002/Gepi.20102 |
0.337 |
|
| 2005 |
Kraja AT, Borecki IB, Province MA. Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data. Bmc Genetics. 6: 1-4. PMID 16451710 DOI: 10.1186/1471-2156-6-S1-S94 |
0.395 |
|
| 2005 |
Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao DC, Province MA. Quantitative trait loci for metabolic syndrome in the Hypertension Genetic Epidemiology Network study. Obesity Research. 13: 1885-90. PMID 16339118 DOI: 10.1038/Oby.2005.231 |
0.345 |
|
| 2005 |
Bielinski SJ, Lynch AI, Miller MB, Weder A, Cooper R, Oberman A, Chen YD, Turner ST, Fornage M, Province M, Arnett DK. Genome-wide linkage analysis for loci affecting pulse pressure: the Family Blood Pressure Program. Hypertension. 46: 1286-93. PMID 16286574 DOI: 10.1161/01.Hyp.0000191706.41980.29 |
0.329 |
|
| 2005 |
Tang W, Arnett DK, Devereux RB, Panagiotou D, Province MA, Miller MB, de Simone G, Gu C, Ferrell RE. Identification of a novel 5-base pair deletion in calcineurin B (PPP3R1) promoter region and its association with left ventricular hypertrophy. American Heart Journal. 150: 845-51. PMID 16209992 DOI: 10.1016/J.Ahj.2004.12.004 |
0.332 |
|
| 2005 |
Kraja AT, Rao DC, Weder AB, Cooper R, Curb JD, Hanis CL, Turner ST, de Andrade M, Hsiung CA, Quertermous T, Zhu X, Province MA. Two major QTLs and several others relate to factors of metabolic syndrome in the family blood pressure program. Hypertension. 46: 751-7. PMID 16172425 DOI: 10.1161/01.Hyp.0000184249.20016.Bb |
0.336 |
|
| 2005 |
Feitosa MF, Rice T, Rankinen T, Province MA, Chagnon YC, Gagnon J, Leon AS, Skinner JS, Wilmore JH, Després JP, Bouchard C, Rao DC, Borecki IB. Evidence of QTLs on chromosomes 13q and 14q for triglycerides before and after 20 weeks of exercise training: the HERITAGE Family Study. Atherosclerosis. 182: 349-60. PMID 16159608 DOI: 10.1016/J.Atherosclerosis.2005.01.052 |
0.308 |
|
| 2005 |
Yu K, Xu J, Rao DC, Province M. Using tree-based recursive partitioning methods to group haplotypes for increased power in association studies. Annals of Human Genetics. 69: 577-89. PMID 16138916 DOI: 10.1111/J.1529-8817.2005.00193.X |
0.35 |
|
| 2005 |
Wangler MF, An P, Feinberg AP, Province M, Debaun MR. Inheritance pattern of Beckwith-Wiedemann syndrome is heterogeneous in 291 families with an affected proband. American Journal of Medical Genetics. Part A. 137: 16-21. PMID 16007611 DOI: 10.1002/Ajmg.A.30827 |
0.337 |
|
| 2005 |
Yu K, Zhang S, Borecki I, Kraja A, Xiong C, Myers R, Province M. A haplotype similarity based transmission/disequilibrium test under founder heterogeneity Annals of Human Genetics. 69: 455-467. PMID 15996173 DOI: 10.1046/J.1529-8817.2005.00168.X |
0.362 |
|
| 2005 |
Djoussé L, Arnett DK, Carr JJ, Eckfeldt JH, Hopkins PN, Province MA, Ellison RC. Dietary linolenic acid is inversely associated with calcified atherosclerotic plaque in the coronary arteries: The National Heart, Lung, and Blood Institute Family Heart Study Circulation. 111: 2921-2926. PMID 15927976 DOI: 10.1161/Circulationaha.104.489534 |
0.324 |
|
| 2005 |
Djoussé L, Rautaharju PM, Hopkins PN, Whitsel EA, Arnett DK, Eckfeldt JH, Province MA, Ellison RC. Dietary linolenic acid and adjusted QT and JT intervals in the national heart, lung, and blood institute family heart study Journal of the American College of Cardiology. 45: 1716-1722. PMID 15893192 DOI: 10.1016/J.Jacc.2005.01.060 |
0.306 |
|
| 2005 |
An P, Freedman BI, Hanis CL, Chen YD, Weder AB, Schork NJ, Boerwinkle E, Province MA, Hsiung CA, Wu X, Quertermous T, Rao DC. Genome-wide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis. Diabetes. 54: 909-14. PMID 15734873 DOI: 10.2337/Diabetes.54.3.909 |
0.32 |
|
| 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 |
0.354 |
|
| 2005 |
Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao D, Province MA. An evaluation of the metabolic syndrome in the HyperGEN study. Nutrition & Metabolism. 2: 2. PMID 15656912 DOI: 10.1186/1743-7075-2-2 |
0.324 |
|
| 2005 |
Djoussé L, Arnett DK, Pankow JS, Hopkins PN, Province MA, Curtis Ellison R. Dietary linolenic acid is associated with a lower prevalence of hypertension in the NHLBI family heart study Hypertension. 45: 368-373. PMID 15655119 DOI: 10.1161/01.Hyp.0000154679.41568.E6 |
0.321 |
|
| 2005 |
Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. Ethnicity and human genetic linkage maps. American Journal of Human Genetics. 76: 276-90. PMID 15627237 DOI: 10.1086/427926 |
0.353 |
|
| 2005 |
Tang H, Quertermous T, Rodriguez B, Kardia SL, Zhu X, Brown A, Pankow JS, Province MA, Hunt SC, Boerwinkle E, Schork NJ, Risch NJ. Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. American Journal of Human Genetics. 76: 268-75. PMID 15625622 DOI: 10.1086/427888 |
0.332 |
|
| 2005 |
Feitosa MF, Borecki IB, Rankinen T, Rice T, Després JP, Chagnon YC, Gagnon J, Leon AS, Skinner JS, Bouchard C, Province MA, Rao DC. Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study. Journal of Lipid Research. 46: 281-6. PMID 15576847 DOI: 10.1194/Jlr.M400252-Jlr200 |
0.329 |
|
| 2005 |
Yu K, Gu CC, Province M, Xiong CJ, Rao DC. Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes. Genetic Epidemiology. 27: 182-91. PMID 15389925 DOI: 10.1002/Gepi.20022 |
0.386 |
|
| 2005 |
Edwin D, Fenske TS, McMahon C, Mathews V, Bogue M, Province M, Cheverud J, McLeod H, Graubert TA. Susceptibility to Alkylator-Induced Cancer Is a Heritable Trait. Blood. 106: 3266-3266. DOI: 10.1182/Blood.V106.11.3266.3266 |
0.331 |
|
| 2004 |
Arnett DK, Miller MB, Coon H, Ellison RC, North KE, Province M, Leppert M, Eckfeldt JH. Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Human Genetics. 115: 468-74. PMID 15375693 DOI: 10.1007/S00439-004-1182-Y |
0.373 |
|
| 2004 |
Wilk JB, Djousse L, Arnett DK, Hunt SC, Province MA, Heiss G, Myers RH. Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study. American Journal of Hypertension. 17: 839-44. PMID 15363829 DOI: 10.1016/J.Amjhyper.2004.06.003 |
0.327 |
|
| 2004 |
Pankow JS, Heiss G, Evans GW, Sholinsky P, Province MA, Coon H, Ellison RC, Miller MB, Qaqish B. Familial aggregation and genome-wide linkage analysis of carotid artery plaque: the NHLBI family heart study. Human Heredity. 57: 80-9. PMID 15192280 DOI: 10.1159/000077545 |
0.333 |
|
| 2004 |
Coon H, Singh N, Dunn D, Eckfeldt JH, Province MA, Hopkins PN, Weiss R, Hunt SC, Leppert MF. TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study Atherosclerosis. 174: 357-362. PMID 15136067 DOI: 10.1016/J.Atherosclerosis.2004.02.004 |
0.4 |
|
| 2004 |
Ellison RC, Zhang Y, Qureshi MM, Knox S, Arnett DK, Province MA. Lifestyle determinants of high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study. American Heart Journal. 147: 529-35. PMID 14999205 DOI: 10.1016/J.Ahj.2003.10.033 |
0.306 |
|
| 2004 |
Djoussé L, Arnett DK, Coon H, Province MA, Moore LL, Ellison RC. Fruit and vegetable consumption and LDL cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study. The American Journal of Clinical Nutrition. 79: 213-7. PMID 14749225 DOI: 10.1093/Ajcn/79.2.213 |
0.322 |
|
| 2004 |
Barkley RA, Chakravarti A, Cooper RS, Ellison RC, Hunt SC, Province MA, Turner ST, Weder AB, Boerwinkle E. Positional identification of hypertension susceptibility genes on chromosome 2. Hypertension. 43: 477-82. PMID 14732741 DOI: 10.1161/01.Hyp.0000111585.76299.F7 |
0.383 |
|
| 2003 |
Corbett J, Kraja A, Borecki IB, Province MA. Use of a random coefficient regression (RCR) model to estimate growth parameters Bmc Genetics. 4: 1-5. PMID 14975073 DOI: 10.1186/1471-2156-4-S1-S5 |
0.316 |
|
| 2003 |
Freedman BI, Beck SR, Rich SS, Heiss G, Lewis CE, Turner S, Province MA, Schwander KL, Arnett DK, Mellen BG. A genome-wide scan for urinary albumin excretion in hypertensive families. Hypertension (Dallas, Tex. : 1979). 42: 291-6. PMID 12925555 DOI: 10.1161/01.Hyp.0000087890.33245.41 |
0.402 |
|
| 2003 |
Hopkins PN, Heiss G, Ellison RC, Province MA, Pankow JS, Eckfeldt JH, Hunt SC. Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: A case-control comparison from the National Heart, Lung, and Blood Institute Family Heart study Circulation. 108: 519-523. PMID 12847072 DOI: 10.1161/01.Cir.0000081777.17879.85 |
0.371 |
|
| 2003 |
Wilk JB, DeStefano AL, Arnett DK, Rich SS, Djousse L, Crapo RO, Leppert MF, Province MA, Cupples LA, Gottlieb DJ, Myers RH. A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Respiratory and Critical Care Medicine. 167: 1528-33. PMID 12637344 DOI: 10.1164/Rccm.200207-755Oc |
0.354 |
|
| 2003 |
Rao DC, Province MA, Leppert MF, Oberman Al, Heiss G, Ellison RC, Arnett DK, Eckfeldt JH, Schwander K, Mockrin SC, Hunt SC. A genome-wide affected sibpair linkage analysis of hypertension: the HyperGEN network. American Journal of Hypertension. 16: 148-50. PMID 12559683 DOI: 10.1016/S0895-7061(02)03247-8 |
0.345 |
|
| 2003 |
Province MA, Kardia SL, Ranade K, Rao DC, Thiel BA, Cooper RS, Risch N, Turner ST, Cox DR, Hunt SC, Weder AB, Boerwinkle E. A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. American Journal of Hypertension. 16: 144-7. PMID 12559682 DOI: 10.1016/S0895-7061(02)03248-X |
0.318 |
|
| 2002 |
Pankow JS, Province MA, Hunt SC, Arnett DK. Regarding "Testing for population subdivision and association in four case-control studies" [2] American Journal of Human Genetics. 71: 1478-1480. PMID 12515254 DOI: 10.1086/344582 |
0.364 |
|
| 2002 |
Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Human Genetics. 111: 263-9. PMID 12215839 DOI: 10.1007/S00439-002-0773-8 |
0.387 |
|
| 2002 |
Argyropoulos G, Rankinen T, Neufeld DR, Rice T, Province MA, Leon AS, Skinner JS, Wilmore JH, Rao DC, Bouchard C. A polymorphism in the human agouti-related protein is associated with late-onset obesity. The Journal of Clinical Endocrinology and Metabolism. 87: 4198-202. PMID 12213871 DOI: 10.1210/Jc.2002-011834 |
0.318 |
|
| 2002 |
Gu CC, Rao DC, Stormo G, Hicks C, Province MA. Role of gene expression microarray analysis in finding complex disease genes. Genetic Epidemiology. 23: 37-56. PMID 12112247 DOI: 10.1002/Gepi.220 |
0.326 |
|
| 2002 |
Hunt SC, Ellison RC, Atwood LD, Pankow JS, Province MA, Leppert MF. Genome scans for blood pressure and hypertension: The National Heart, Lung, and Blood Institute Family Heart Study Hypertension. 40: 1-6. PMID 12105129 DOI: 10.1161/01.Hyp.0000022660.28915.B1 |
0.316 |
|
| 2002 |
Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC. Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. European Journal of Human Genetics : Ejhg. 10: 367-74. PMID 12080388 DOI: 10.1038/Sj.Ejhg.5200818 |
0.377 |
|
| 2002 |
DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study. American Journal of Human Genetics. 71: 204-5. PMID 12068377 DOI: 10.1086/340730 |
0.356 |
|
| 2002 |
Rice T, Rankinen T, Chagnon YC, Province MA, Pérusse L, Leon AS, Skinner JS, Wilmore JH, Bouchard C, Rao DC. Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, and Genetics. Hypertension. 39: 1037-43. PMID 12052838 DOI: 10.1161/01.Hyp.0000018911.46067.6E |
0.377 |
|
| 2002 |
Province MA. Searching for the mountains of the moon: genome scans for atherosclerosis. Current Atherosclerosis Reports. 4: 169-175. PMID 11931713 DOI: 10.1007/S11883-002-0016-4 |
0.322 |
|
| 2002 |
Silverman EK, Palmer LJ, Mosley JD, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, et al. Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. American Journal of Human Genetics. 70: 1229-39. PMID 11914989 DOI: 10.1086/340316 |
0.335 |
|
| 2002 |
Silverman EK, Mosley JD, Palmer LJ, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, et al. Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes. Human Molecular Genetics. 11: 623-32. PMID 11912177 DOI: 10.1093/Hmg/11.6.623 |
0.318 |
|
| 2002 |
Boerwinkle E, Brown CA, Carrejo M, Ferrell R, Hanis C, Hutchinson R, Kardia S, Sing C, Turner S, Weder A, Chakravarti A, Cooper R, Jacob H, NS, Hunt S, ... ... Province M, et al. Multi-center genetic study of hypertension: The Family blood pressure program (FBPP) Hypertension. 39: 3-9. PMID 11799070 DOI: 10.1161/Hy1201.100415 |
0.33 |
|
| 2002 |
Feitosa MF, Borecki IB, Rich SS, Arnett DK, Sholinsky P, Myers RH, Leppert M, Province MA. Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. American Journal of Human Genetics. 70: 72-82. PMID 11713718 DOI: 10.1086/338144 |
0.395 |
|
| 2001 |
Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G. Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1969-76. PMID 11742872 DOI: 10.1161/Hq1201.100228 |
0.378 |
|
| 2001 |
Silverman EK, Mosley JD, Rao DC, Palmer LJ, Province MA, Elston RC, Weiss ST, Campbell EJ. Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases. Human Heredity. 52: 223-32. PMID 11713419 DOI: 10.1159/000053380 |
0.345 |
|
| 2001 |
Province MA. The Significance of Not Finding a Gene American Journal of Human Genetics. 69: 660-663. PMID 11481587 DOI: 10.1086/323316 |
0.334 |
|
| 2001 |
Pérusse L, Gagnon J, Province MA, Rao DC, Wilmore JH, Leon AS, Bouchard C, Skinner JS. Familial aggregation of submaximal aerobic performance in the HERITAGE Family study. Medicine and Science in Sports and Exercise. 33: 597-604. PMID 11283436 DOI: 10.1097/00005768-200104000-00014 |
0.321 |
|
| 2001 |
Shannon WD, Province MA, Rao DC. Tree-based recursive partitioning methods for subdividing sibpairs into relatively more homogeneous subgroups. Genetic Epidemiology. 20: 293-306. PMID 11255239 DOI: 10.1002/Gepi.1 |
0.353 |
|
| 2001 |
Pérusse L, Rice T, Chagnon YC, Després J, Lemieux S, Roy S, Lacaille M, Ho-Kim M, Chagnon M, Province MA, Rao DC, Bouchard C. A genome-wide scan for abdominal fat assessed by computed tomography in the Québec Family Study. Diabetes. 50: 614-621. PMID 11246882 DOI: 10.2337/Diabetes.50.3.614 |
0.352 |
|
| 2001 |
Williams RR, Hunt SC, Heiss G, Province MA, Bensen JT, Higgins M, Chamberlain RM, Ware J, Hopkins PN. Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study). The American Journal of Cardiology. 87: 129-35. PMID 11152826 DOI: 10.1016/S0002-9149(00)01303-5 |
0.315 |
|
| 2001 |
Province MA, Shannon WD, Rao DC. Classification methods for confronting heterogeneity. Advances in Genetics. 42: 273-86. PMID 11037327 DOI: 10.1016/S0065-2660(01)42028-1 |
0.302 |
|
| 2001 |
Gu C, Province MA, Rao DC. Meta-analysis for model-free methods. Advances in Genetics. 42: 255-272. PMID 11037326 DOI: 10.1016/S0065-2660(01)42027-X |
0.366 |
|
| 2001 |
Province MA. 13 Linkage and association with structural relationships Advances in Genetics. 42: 183-190. PMID 11037321 DOI: 10.1016/S0065-2660(01)42022-0 |
0.304 |
|
| 2000 |
Hunt KJ, Heiss G, Sholinsky PD, Province MA. Familial history of metabolic disorders and the multiple metabolic syndrome: The NHLBI Family Heart Study Genetic Epidemiology. 19: 395-409. PMID 11108648 DOI: 10.1002/1098-2272(200012)19:4<395::Aid-Gepi10>3.0.Co;2-3 |
0.332 |
|
| 2000 |
Pankow JS, Rose KM, Oberman A, Hunt SC, Atwood LD, Djoussé L, Province MA, Rao DC. Possible locus on chromosome 18q influencing postural systolic blood pressure changes Hypertension. 36: 471-476. PMID 11040221 DOI: 10.1161/01.Hyp.36.4.471 |
0.328 |
|
| 2000 |
Rice T, Rankinen T, Province MA, Chagnon YC, Pérusse L, Borecki IB, Bouchard C, Rao DC. Genome-wide linkage analysis of systolic and diastolic blood pressure: the Québec Family Study. Circulation. 102: 1956-1963. PMID 11034945 DOI: 10.1161/01.Cir.102.16.1956 |
0.38 |
|
| 2000 |
Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2275-80. PMID 11031215 DOI: 10.1161/01.Atv.20.10.2275 |
0.381 |
|
| 2000 |
Djoussé L, Myers RH, Coon H, Arnett DK, Province MA, Ellison RC. Smoking influences the association between apolipoprotein E and lipids: the National Heart, Lung, and Blood Institute Family Heart Study. Lipids. 35: 827-31. PMID 10984105 DOI: 10.1007/S11745-000-0591-1 |
0.308 |
|
| 2000 |
Williams RR, Rao DC, Ellison RC, Arnett DK, Heiss G, Oberman A, Eckfeldt JH, Leppert MF, Province MA, Mockrin SC, Hunt SC. NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. Annals of Epidemiology. 10: 389-400. PMID 10964005 DOI: 10.1016/S1047-2797(00)00063-6 |
0.304 |
|
| 2000 |
Feitosa MF, Borecki I, Hunt SC, Arnett DK, Rao DC, Province M. Inheritance of the waist-to-hip ratio in the National Heart, Lung, and Blood Institute Family Heart Study. Obesity Research. 8: 294-301. PMID 10933305 DOI: 10.1038/Oby.2000.35 |
0.323 |
|
| 2000 |
Province MA, Boerwinkle E, Chakravarti A, Cooper R, Fornage M, Leppert M, Risch N, Ranade K. Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute. Journal of Hypertension. 18: 867-76. PMID 10930184 DOI: 10.1097/00004872-200018070-00008 |
0.301 |
|
| 2000 |
Province MA, Arnett DK, Hunt SC, Leiendecker-Foster C, Eckfeldt JH, Oberman A, Ellison RC, Heiss G, Mockrin SC, Williams RR. Association between the alpha-adducin gene and hypertension in the HyperGEN Study. American Journal of Hypertension. 13: 710-8. PMID 10912758 DOI: 10.1016/S0895-7061(99)00282-4 |
0.342 |
|
| 2000 |
Wilk JB, Djousse L, Arnett DK, Rich SS, Province MA, Hunt SC, Crapo RO, Higgins M, Myers RH. Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genetic Epidemiology. 19: 81-94. PMID 10861898 DOI: 10.1002/1098-2272(200007)19:1<81::Aid-Gepi6>3.0.Co;2-8 |
0.369 |
|
| 2000 |
Garenc C, Pérusse L, Gagnon J, Chagnon YC, Bergeron J, Després JP, Province MA, Leon AS, Skinner JS, Wilmore JH, Rao DC, Bouchard C. Linkage and association studies of the lipoprotein lipase gene with postheparin plasma lipase activities, body fat, and plasma lipid and lipoprotein concentrations: the HERITAGE Family Study. Metabolism: Clinical and Experimental. 49: 432-9. PMID 10778864 DOI: 10.1016/S0026-0495(00)80004-9 |
0.335 |
|
| 2000 |
Weidner G, Rice T, Knox SS, Ellison RC, Province MA, Rao DC, Higgins MW. Familial Resemblance for Hostility: The National Heart, Lung, and Blood Institute Family Heart Study Psychosomatic Medicine. 62: 197-204. PMID 10772397 DOI: 10.1097/00006842-200003000-00008 |
0.355 |
|
| 2000 |
Li R, Bensen JT, Hutchinson RG, Province MA, Hertz-Picciotto I, Sprafka JM, Tyroler HA. Family risk score of coronary heart disease (CHD) as a predictor of CHD: The atherosclerosis risk in communities (ARIC) study and the NHLBI family heart study Genetic Epidemiology. 18: 236-250. PMID 10723108 DOI: 10.1002/(Sici)1098-2272(200003)18:3<236::Aid-Gepi4>3.0.Co;2-0 |
0.336 |
|
| 2000 |
Bouchard C, Rankinen T, Chagnon YC, Rice T, Pérusse L, Gagnon J, Borecki I, An P, Leon AS, Skinner JS, Wilmore JH, Province M, Rao DC. Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study. Journal of Applied Physiology (Bethesda, Md. : 1985). 88: 551-9. PMID 10658022 DOI: 10.1152/Jappl.2000.88.2.551 |
0.366 |
|
| 1999 |
Gu C, Province M, Rao DC. Meta-analysis of genetic linkage to quantitative trait loci with study-specific covariates: a mixed-effects model. Genetic Epidemiology. 17. PMID 10597499 DOI: 10.1002/Gepi.1370170797 |
0.33 |
|
| 1999 |
Borecki IB, Province MA. The impact of marker allele frequency misspecification in variance components quantitative trait locus analysis using sibship data. Genetic Epidemiology. 17. PMID 10597415 DOI: 10.1002/Gepi.1370170713 |
0.325 |
|
| 1999 |
Bensen JT, Liese AD, Rushing JT, Province M, Folsom AR, Rich SS, Higgins M. Accuracy of proband reported family history: The NHLBI Family Heart Study (FHS) Genetic Epidemiology. 17: 141-150. PMID 10414557 DOI: 10.1002/(Sici)1098-2272(1999)17:2<141::Aid-Gepi4>3.0.Co;2-Q |
0.331 |
|
| 1999 |
Siegmund KD, Todorov AA, Province MA. A frailty approach for modelling diseases with variable age of onset in families: the NHLBI Family Heart Study. Statistics in Medicine. 18: 1517-28. PMID 10398289 DOI: 10.1002/(Sici)1097-0258(19990630)18:12<1517::Aid-Sim132>3.0.Co;2-4 |
0.384 |
|
| 1999 |
Hunt SC, Province MA, Atwood LD, Sholinsky P, Lalouel JM, Rao DC, Williams RR, Leppert MF. No linkage of the lipoprotein lipase locus to hypertension in Caucasians. Journal of Hypertension. 17: 39-43. PMID 10100092 DOI: 10.1097/00004872-199917010-00007 |
0.334 |
|
| 1999 |
Bensen JT, Li R, Hutchinson RG, Province MA, Tyroler HA. Family history of coronary heart disease and pre-clinical carotid artery atherosclerosis in African Americans and whites: The ARIC study Genetic Epidemiology. 16: 165-178. PMID 10030399 DOI: 10.1002/(Sici)1098-2272(1999)16:2<165::Aid-Gepi4>3.0.Co;2-H |
0.33 |
|
| 1998 |
Gu C, Province M, Todorov A, Rao DC. Meta-analysis methodology for combining non-parametric sibpair linkage results: genetic homogeneity and identical markers. Genetic Epidemiology. 15: 609-26. PMID 9811422 DOI: 10.1002/(Sici)1098-2272(1998)15:6<609::Aid-Gepi5>3.0.Co;2-N |
0.37 |
|
| 1998 |
Pankow JS, Folsom AR, Province MA, Rao DC, Williams RR, Eckfeldt J, Sellers TA. Segregation analysis of plasminogen activator inhibitor-1 and fibrinogen levels in the NHLBI family heart study. Arteriosclerosis, Thrombosis, and Vascular Biology. 18: 1559-67. PMID 9763527 DOI: 10.1161/01.Atv.18.10.1559 |
0.383 |
|
| 1998 |
Siegmund KD, Province MA, Higgins M, Williams RR, Keller J, Todorov AA. Modeling disease incidence rates in families. Epidemiology (Cambridge, Mass.). 9: 557-62. PMID 9730037 DOI: 10.1097/00001648-199809000-00015 |
0.377 |
|
| 1998 |
Todorov AA, Vogler GP, Gu C, Province MA, Li Z, Heath AC, Rao DC. Testing causal hypotheses in multivariate linkage analysis of quantitative traits: general formulation and application to sibpair data. Genetic Epidemiology. 15: 263-78. PMID 9593113 DOI: 10.1002/(Sici)1098-2272(1998)15:3<263::Aid-Gepi5>3.0.Co;2-5 |
0.303 |
|
| 1998 |
Borecki IB, Higgins M, Schreiner PJ, Arnett DK, Mayer-Davis E, Hunt SC, Province MA. Evidence for multiple determinants of the body mass index: The national heart, lung, and blood institute family heart study Obesity Research. 6: 107-114. PMID 9545016 DOI: 10.1002/J.1550-8528.1998.Tb00323.X |
0.377 |
|
| 1998 |
Bouchard C, Daw EW, Rice T, Pérusse L, Gagnon J, Province MA, Leon AS, Rao DC, Skinner JS, Wilmore JH. Familial resemblance for VO2max in the sedentary state: the HERITAGE family study. Medicine and Science in Sports and Exercise. 30: 252-8. PMID 9502354 DOI: 10.1097/00005768-199802000-00013 |
0.348 |
|
| 1998 |
Folsom AR, Pankow JS, Williams RR, Evans GW, Province MA, Eckfeldt JH. Fibrinogen, plasminogen activator inhibitor-1, and carotid intima-media wall thickness in the NHLBI Family Heart Study. Thrombosis and Haemostasis. 79: 400-4. PMID 9493598 DOI: 10.1055/S-0037-1614999 |
0.344 |
|
| 1998 |
Pérusse L, Rice T, Després JP, Bergeron J, Province MA, Gagnon J, Leon AS, Rao DC, Skinner JS, Wilmore JH, Bouchard C. Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study. Arteriosclerosis, Thrombosis, and Vascular Biology. 17: 3263-9. PMID 9409321 DOI: 10.1161/01.Atv.17.11.3263 |
0.332 |
|
| 1997 |
El-Moalem HE, Gagnon J, Province M, Bouchard C, Leon AS, Skinner JS, Wilmore JH, Rao DC. Race differences in reproducibilities: The HERITAGE family study. American Journal of Human Biology : the Official Journal of the Human Biology Council. 9: 415-424. PMID 28561281 DOI: 10.1002/(Sici)1520-6300(1997)9:4<415::Aid-Ajhb1>3.0.Co;2-V |
0.31 |
|
| 1997 |
Pankow JS, Folsom AR, Province MA, Rao DC, Eckfeldt J, Heiss G, Shahar E, Wu KK. Family history of coronary heart disease and hemostatic variables in middle-aged adults Thrombosis and Haemostasis. 77: 87-93. DOI: 10.1055/S-0038-1655912 |
0.336 |
|
| 1996 |
Gagnon J, Province MA, Bouchard C, Leon AS, Skinner JS, Wilmore JH, Rao DC. The HERITAGE family study: Quality assurance and quality control Annals of Epidemiology. 6: 520-529. PMID 8978882 DOI: 10.1016/S1047-2797(96)00068-3 |
0.304 |
|
| 1996 |
Higgins M, Province M, Heiss G, Eckfeldt J, Ellison RC, Folsom AR, Rao DC, Sprafka JM, Williams R. NHLBI Family Heart Study: objectives and design. American Journal of Epidemiology. 143: 1219-28. PMID 8651220 DOI: 10.1093/Oxfordjournals.Aje.A008709 |
0.4 |
|
| 1996 |
Inoue H, Ferrer J, Welling CM, Elbein SC, Hoffman M, Mayorga R, Warren-Perry M, Zhang Y, Millns H, Turner R, Province M, Bryan J, Permutt MA, Aguilar-Bryan L. Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians. Diabetes. 45: 825-31. PMID 8635661 DOI: 10.2337/Diab.45.6.825 |
0.316 |
|
| 1994 |
Borecki IB, Province MA, Rao DC. Power of segregation analysis for detection of major gene effects on quantitative traits Genetic Epidemiology. 11: 409-418. PMID 7835687 DOI: 10.1002/Gepi.1370110503 |
0.342 |
|
| 1991 |
Rice T, Province MA, Keller JB, Bouchard C, Higgins MW, Rao DC. Heterogeneity among populations for familial aggregation of blood pressure. American Journal of Human Biology : the Official Journal of the Human Biology Council. 3: 515-523. PMID 28597518 DOI: 10.1002/Ajhb.1310030511 |
0.343 |
|
| 1990 |
Rice T, Vogler GP, Perry TS, Laskarzewski PM, Province MA, Rao DC. Heterogeneity in the familial aggregation of fasting serum uric acid level in five North American populations: the Lipid Research Clinics Family Study. American Journal of Medical Genetics. 36: 219-25. PMID 2368810 DOI: 10.1002/Ajmg.1320360216 |
0.341 |
|
| 1990 |
Silverman EK, Province MA, Campbell EJ, Pierce JA, Rao DC. Biochemical intermediates in α1-antitrypsin deficiency: Residual family resemblance for total α1-antitrypsin, oxidized α-antitrysin and immunoglobulin e after adjustment for the effect of the pi locus Genetic Epidemiology. 7: 137-149. PMID 2338230 DOI: 10.1002/Gepi.1370070204 |
0.334 |
|
| 1990 |
Silverman EK, Province MA, Campbell EJ, Pierce JA, Rao C. Variability of pulmonary function in alpha-l-antitrypsin deficiency: Residual family resemblance beyond the effect of the pi locus Human Heredity. 40: 340-355. PMID 2083948 DOI: 10.1159/000153958 |
0.362 |
|
| 1989 |
Province M, Tishler P, Rao D, Eaves LJ. Repeated-measures model for the investigation of temporal trends using longitudinal family studies: application to systolic blood pressure. Genetic Epidemiology. 6: 333-347. PMID 2721928 DOI: 10.1002/Gepi.1370060204 |
0.313 |
|
| 1988 |
Province MA, Rao DC. Familial aggregation in the presence of temporal trends. Statistics in Medicine. 7: 185-198. PMID 3258435 DOI: 10.1002/Sim.4780070120 |
0.315 |
|
| 1985 |
Province MA, Rao DC, MacCluer JW. A new model for the resolution of cultural and biological inheritance in the presence of temporal trends: Application to systolic blood pressure Genetic Epidemiology. 2: 363-374. PMID 3841327 DOI: 10.1002/Gepi.1370020405 |
0.337 |
|
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