Wei Chen - Publications

Affiliations: 
Biostatistics University of Michigan, Ann Arbor, Ann Arbor, MI 

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

Year Citation  Score
2022 Wielscher M, Mandaviya PR, Kuehnel B, Joehanes R, Mustafa R, Robinson O, Zhang Y, Bodinier B, Walton E, Mishra PP, Schlosser P, Wilson R, Tsai PC, Palaniswamy S, Marioni RE, ... ... Chen W, et al. DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases. Nature Communications. 13: 2408. PMID 35504910 DOI: 10.1038/s41467-022-29792-6  0.461
2021 Si J, Yang S, Sun D, Yu C, Guo Y, Lin Y, Millwood I, Walters R, Yang L, Chen Y, Du H, Hua Y, Liu J, Chen J, Chen Z, ... Chen W, et al. Epigenome-wide analysis of DNA methylation and coronary heart disease: a nested case-control study. Elife. 10. PMID 34515027 DOI: 10.7554/eLife.68671  0.426
2021 Jhun MA, Mendelson M, Wilson R, Gondalia R, Joehanes R, Salfati E, Zhao X, Braun KVE, Do AN, Hedman ÅK, Zhang T, Carnero-Montoro E, Shen J, Bartz TM, Brody JA, ... ... Chen W, et al. Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids. Nature Communications. 12: 4256. PMID 34230475 DOI: 10.1038/s41467-021-24600-z  0.429
2021 Jhun MA, Mendelson M, Wilson R, Gondalia R, Joehanes R, Salfati E, Zhao X, Braun KVE, Do AN, Hedman ÅK, Zhang T, Carnero-Montoro E, Shen J, Bartz TM, Brody JA, ... ... Chen W, et al. A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids. Nature Communications. 12: 3987. PMID 34183656 DOI: 10.1038/s41467-021-23899-y  0.489
2020 Landi MT, Bishop DT, MacGregor S, Machiela MJ, Stratigos AJ, Ghiorzo P, Brossard M, Calista D, Choi J, Fargnoli MC, Zhang T, Rodolfo M, Trower AJ, Menin C, Martinez J, ... ... Chen WV, et al. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics. PMID 32341527 DOI: 10.1038/S41588-020-0611-8  0.522
2019 Lu AT, Seeboth A, Tsai PC, Sun D, Quach A, Reiner AP, Kooperberg C, Ferrucci L, Hou L, Baccarelli AA, Li Y, Harris SE, Corley J, Taylor A, Deary IJ, ... ... Chen W, et al. DNA methylation-based estimator of telomere length. Aging. PMID 31422385 DOI: 10.18632/aging.102173  0.312
2018 Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, et al. Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration. Plos One. 13: e0209943. PMID 30571798 DOI: 10.1371/Journal.Pone.0209943  0.374
2018 Yan Q, Ding Y, Liu Y, Sun T, Fritsche LG, Clemons T, Ratnapriya R, Klein ML, Cook RJ, Liu Y, Fan R, Wei L, Abecasis GR, Swaroop A, Chew EY, ... ... Chen W, et al. Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Human Molecular Genetics. PMID 29346644 DOI: 10.1093/Hmg/Ddy002  0.519
2017 Ding Y, Liu Y, Yan Q, Fritsche LG, Cook RJ, Clemons T, Ratnapriya R, Klein ML, Abecasis GR, Swaroop A, Chew EY, Weeks DE, Chen W. Bivariate Analysis of Age-Related Macular Degeneration Progression Using Genetic Risk Scores. Genetics. PMID 28341650 DOI: 10.1534/Genetics.116.196998  0.443
2017 Haycock PC, Burgess S, Nounu A, Zheng J, Okoli GN, Bowden J, Wade KH, Timpson NJ, Evans DM, Willeit P, Aviv A, Gaunt TR, Hemani G, Mangino M, ... ... Chen WV, et al. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. Jama Oncology. PMID 28241208 DOI: 10.1001/Jamaoncol.2016.5945  0.416
2017 Chen W, Wang T, Pino-Yanes M, Forno E, Liang L, Yan Q, Hu D, Weeks DE, Baccarelli A, Acosta-Perez E, Eng C, Han YY, Boutaoui N, Laprise C, Davies GA, et al. An epigenome-wide association study of total serum immunoglobulin E in Hispanic children. The Journal of Allergy and Clinical Immunology. PMID 28069425 DOI: 10.1016/J.Jaci.2016.11.030  0.598
2016 Vaysse A, Fang S, Brossard M, Wei Q, Chen WV, Mohamdi H, Vincent-Fetita L, Margaritte-Jeannin P, Lavielle N, Maubec E, Lathrop M, Avril MF, Amos CI, Lee JE, Demenais F. A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants. International Journal of Cancer. PMID 27347659 DOI: 10.1002/Ijc.30245  0.318
2016 Wu C, Demerath EW, Pankow JS, Bressler J, Fornage M, Grove ML, Chen W, Guan W. Imputation of Missing Covariate Values in Epigenome-Wide Analysis of DNA Methylation Data. Epigenetics. 0. PMID 26890800 DOI: 10.1080/15592294.2016.1145328  0.475
2015 Fan R, Wang Y, Chiu CY, Chen W, Ren H, Li Y, Boehnke M, Amos CI, Moore JH, Xiong M. Meta-analysis of Complex Diseases at Gene Level by Generalized Functional Linear Models. Genetics. PMID 26715663 DOI: 10.1534/Genetics.115.180869  0.391
2015 Lenz TL, Deutsch AJ, Han B, Hu X, Okada Y, Eyre S, Knapp M, Zhernakova A, Huizinga TW, Abecasis G, Becker J, Boeckxstaens GE, Chen WM, Franke A, Gladman DD, et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nature Genetics. PMID 26258845 DOI: 10.1038/Ng.3379  0.43
2015 Law MH, Bishop DT, Lee JE, Brossard M, Martin NG, Moses EK, Song F, Barrett JH, Kumar R, Easton DF, Pharoah PD, Swerdlow AJ, Kypreou KP, Taylor JC, Harland M, ... ... Chen WV, et al. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics. PMID 26237428 DOI: 10.1038/Ng.3373  0.317
2015 Fan R, Wang Y, Boehnke M, Chen W, Li Y, Ren H, Lobach I, Xiong M. Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models. Genetics. PMID 26058849 DOI: 10.1534/Genetics.115.178343  0.385
2015 Wang T, Guan W, Lin J, Boutaoui N, Canino G, Luo J, Celedón JC, Chen W. A systematic study of normalization methods for Infinium 450K methylation data using whole-genome bisulfite sequencing data. Epigenetics : Official Journal of the Dna Methylation Society. 10: 662-669. PMID 26036609 DOI: 10.1080/15592294.2015.1057384  0.441
2015 Xu Z, Duan Q, Yan S, Chen W, Li M, Lange E, Li Y. DISSCO: direct imputation of summary statistics allowing covariates. Bioinformatics (Oxford, England). PMID 25810429 DOI: 10.1093/Bioinformatics/Btv168  0.553
2015 Mangino M, Christiansen L, Stone R, Hunt SC, Horvath K, Eisenberg DT, Kimura M, Petersen I, Kark JD, Herbig U, Reiner AP, Benetos A, Codd V, Nyholt DR, Sinnreich R, ... ... Chen W, et al. DCAF4, a novel gene associated with leucocyte telomere length. Journal of Medical Genetics. 52: 157-62. PMID 25624462 DOI: 10.1136/Jmedgenet-2014-102681  0.31
2014 Zhang Y, Yi P, Chen W, Ming J, Zhu B, Li Z, Shen N, Shi W, Ke J, Zhao Q, Lu X, Xun X, Liu L, Song R, Guo H, et al. Association between polymorphisms within the susceptibility region 8q24 and breast cancer in a Chinese population. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. 35: 2649-54. PMID 24414391 DOI: 10.1007/S13277-013-1348-0  0.474
2014 Ozel AB, Moroi SE, Reed DM, Nika M, Schmidt CM, Akbari S, Scott K, Rozsa F, Pawar H, Musch DC, Lichter PR, Gaasterland D, Branham K, Gilbert J, Garnai SJ, ... Chen W, et al. Genome-wide association study and meta-analysis of intraocular pressure. Human Genetics. 133: 41-57. PMID 24002674 DOI: 10.1007/S00439-013-1349-5  0.531
2013 Li Y, Chen W, Liu EY, Zhou YH. Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data. Statistics in Biosciences. 5: 3-25. PMID 24489615 DOI: 10.1007/s12561-012-9067-4  0.371
2013 Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, ... ... Chen WM, ... ... Chen W, et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. American Journal of Human Genetics. 93: 545-54. PMID 23972371 DOI: 10.1016/J.Ajhg.2013.07.010  0.382
2013 Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578  0.528
2013 Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, ... ... Chen W, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Human Molecular Genetics. 22: 1663-78. PMID 23303523 DOI: 10.1093/Hmg/Dds555  0.416
2013 Chen W, Li B, Zeng Z, Sanna S, Sidore C, Busonero F, Kang HM, Li Y, Abecasis GR. Genotype calling and haplotyping in parent-offspring trios. Genome Research. 23: 142-51. PMID 23064751 DOI: 10.1101/Gr.142455.112  0.511
2013 Li Y, Chen W, Liu EY, Zhou YH. Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data Statistics in Biosciences. 5: 3-25. DOI: 10.1007/S12561-012-9067-4  0.379
2012 Smith JG, Avery CL, Evans DS, Nalls MA, Meng YA, Smith EN, Palmer C, Tanaka T, Mehra R, Butler AM, Young T, Buxbaum SG, Kerr KF, Berenson GS, Schnabel RB, ... ... Chen W, et al. Impact of ancestry and common genetic variants on QT interval in African Americans. Circulation. Cardiovascular Genetics. 5: 647-55. PMID 23166209 DOI: 10.1161/Circgenetics.112.962787  0.312
2012 Butler AM, Yin X, Evans DS, Nalls MA, Smith EN, Tanaka T, Li G, Buxbaum SG, Whitsel EA, Alonso A, Arking DE, Benjamin EJ, Berenson GS, Bis JC, Chen W, et al. Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circulation. Cardiovascular Genetics. 5: 639-46. PMID 23139255 DOI: 10.1161/Circgenetics.112.963991  0.425
2012 Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Chen W, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/J.Ajhg.2012.08.032  0.534
2012 Li B, Chen W, Zhan X, Busonero F, Sanna S, Sidore C, Cucca F, Kang HM, Abecasis GR. A likelihood-based framework for variant calling and de novo mutation detection in families. Plos Genetics. 8: e1002944. PMID 23055937 DOI: 10.1371/journal.pgen.1002944  0.426
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, 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  0.321
2011 Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, et al. A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. Plos One. 6: e25598. PMID 22022419 DOI: 10.1371/Journal.Pone.0025598  0.494
2011 McKay GJ, Patterson CC, Chakravarthy U, Dasari S, Klaver CC, Vingerling JR, Ho L, de Jong PT, Fletcher AE, Young IS, Seland JH, Rahu M, Soubrane G, Tomazzoli L, Topouzis F, ... ... Chen W, et al. Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies. Human Mutation. 32: 1407-16. PMID 21882290 DOI: 10.1002/Humu.21577  0.449
2011 McKay GJ, Silvestri G, Chakravarthy U, Dasari S, Fritsche LG, Weber BH, Keilhauer CN, Klein ML, Francis PJ, Klaver CC, Vingerling JR, Ho L, De Jong PT, Dean M, Sawitzke J, ... ... Chen W, et al. Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. American Journal of Epidemiology. 173: 1357-64. PMID 21498624 DOI: 10.1093/Aje/Kwr015  0.451
2011 Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Chen W, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007  0.598
2010 Ding J, Gudjonsson JE, Liang L, Stuart PE, Li Y, Chen W, Weichenthal M, Ellinghaus E, Franke A, Cookson W, Nair RP, Elder JT, Abecasis GR. Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals. American Journal of Human Genetics. 87: 779-89. PMID 21129726 DOI: 10.1016/J.Ajhg.2010.10.024  0.684
2010 Smith EN, Chen W, Kähönen M, Kettunen J, Lehtimäki T, Peltonen L, Raitakari OT, Salem RM, Schork NJ, Shaw M, Srinivasan SR, Topol EJ, Viikari JS, Berenson GS, Murray SS. Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. Plos Genetics. 6: e1001094. PMID 20838585 DOI: 10.1371/journal.pgen.1001094  0.308
2010 Baratz KH, Tosakulwong N, Ryu E, Brown WL, Branham K, Chen W, Tran KD, Schmid-Kubista KE, Heckenlively JR, Swaroop A, Abecasis G, Bailey KR, Edwards AO. E2-2 protein and Fuchs's corneal dystrophy. The New England Journal of Medicine. 363: 1016-24. PMID 20825314 DOI: 10.1056/Nejmoa1007064  0.5
2010 Kanda A, Stambolian D, Chen W, Curcio CA, Abecasis GR, Swaroop A. Age-related macular degeneration-associated variants at chromosome 10q26 do not significantly alter ARMS2 and HTRA1 transcript levels in the human retina. Molecular Vision. 16: 1317-23. PMID 20664794  0.477
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, 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  0.322
2010 Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/Pnas.0912702107  0.562
2010 Strunnikova NV, Maminishkis A, Barb JJ, Wang F, Zhi C, Sergeev Y, Chen W, Edwards AO, Stambolian D, Abecasis G, Swaroop A, Munson PJ, Miller SS. Transcriptome analysis and molecular signature of human retinal pigment epithelium. Human Molecular Genetics. 19: 2468-86. PMID 20360305 DOI: 10.1093/Hmg/Ddq129  0.434
2010 Terracciano A, Sanna S, Uda M, Deiana B, Usala G, Busonero F, Maschio A, Scally M, Patriciu N, Chen WM, Distel MA, Slagboom EP, Boomsma DI, Villafuerte S, Sliwerska E, et al. Genome-wide association scan for five major dimensions of personality. Molecular Psychiatry. 15: 647-56. PMID 18957941 DOI: 10.1038/Mp.2008.113  0.506
2009 Wu CC, Shete S, Chen WV, Peng B, Lee AT, Ma J, Gregersen PK, Amos CI. Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis. Human Genetics. 126: 303-15. PMID 19415332 DOI: 10.1007/s00439-009-0672-3  0.311
2009 Liang L, Chen WM, Sham PC, Abecasis GR. Variance components linkage analysis with repeated measurements. Human Heredity. 67: 237-47. PMID 19172083 DOI: 10.1159/000194977  0.532
2009 Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler E, ... ... Chen WM, et al. Variants in MTNR1B influence fasting glucose levels. Nature Genetics. 41: 77-81. PMID 19060907 DOI: 10.1038/Ng.290  0.49
2009 Chen W, Liang L, Abecasis GR. GWAS GUI: graphical browser for the results of whole-genome association studies with high-dimensional phenotypes. Bioinformatics (Oxford, England). 25: 284-5. PMID 19028721 DOI: 10.1093/Bioinformatics/Btn600  0.58
2008 Chen WM, Erdos MR, Jackson AU, Saxena R, Sanna S, Silver KD, Timpson NJ, Hansen T, Orrù M, Grazia Piras M, Bonnycastle LL, Willer CJ, Lyssenko V, Shen H, Kuusisto J, et al. Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. The Journal of Clinical Investigation. 118: 2620-8. PMID 18521185 DOI: 10.1172/Jci34566  0.464
2008 Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, et al. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. Proceedings of the National Academy of Sciences of the United States of America. 105: 1620-5. PMID 18245381 DOI: 10.1073/Pnas.0711566105  0.486
2008 Sanna S, Jackson AU, Nagaraja R, Willer CJ, Chen WM, Bonnycastle LL, Shen H, Timpson N, Lettre G, Usala G, Chines PS, Stringham HM, Scott LJ, Dei M, Lai S, et al. Common variants in the GDF5-UQCC region are associated with variation in human height. Nature Genetics. 40: 198-203. PMID 18193045 DOI: 10.1038/Ng.74  0.517
2008 Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, ... ... Chen WM, et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nature Genetics. 40: 161-9. PMID 18193043 DOI: 10.1038/Ng.76  0.54
2007 Li S, Sanna S, Maschio A, Busonero F, Usala G, Mulas A, Lai S, Dei M, Orrù M, Albai G, Bandinelli S, Schlessinger D, Lakatta E, Scuteri A, Najjar SS, ... ... Chen WM, et al. The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. Plos Genetics. 3: e194. PMID 17997608 DOI: 10.1371/Journal.Pgen.0030194  0.48
2007 Chen WM, Abecasis GR. Family-based association tests for genomewide association scans American Journal of Human Genetics. 81: 913-926. PMID 17924335 DOI: 10.1086/521580  0.524
2007 Swaroop A, Branham KEH, Chen W, Abecasis G. Genetic susceptibility to age-related macular degeneration: A paradigm for dissecting complex disease traits Human Molecular Genetics. 16. PMID 17911160 DOI: 10.1093/Hmg/Ddm212  0.504
2007 Kanda A, Chen W, Othman M, Branham KE, Brooks M, Khanna R, He S, Lyons R, Abecasis GR, Swaroop A. A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 104: 16227-32. PMID 17884985 DOI: 10.1073/Pnas.0703933104  0.493
2007 Dixon AL, Liang L, Moffatt MF, Chen W, Heath S, Wong KC, Taylor J, Burnett E, Gut I, Farrall M, Lathrop GM, Abecasis GR, Cookson WO. A genome-wide association study of global gene expression. Nature Genetics. 39: 1202-7. PMID 17873877 DOI: 10.1038/Ng2109  0.686
2007 Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orrú M, Usala G, Dei M, Lai S, Maschio A, Busonero F, Mulas A, et al. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. Plos Genetics. 3: e115. PMID 17658951 DOI: 10.1371/Journal.Pgen.0030115  0.509
2006 Pilia G, Chen WM, Scuteri A, Orrú M, Albai G, Dei M, Lai S, Usala G, Lai M, Loi P, Mameli C, Vacca L, Deiana M, Olla N, Masala M, et al. Heritability of cardiovascular and personality traits in 6,148 Sardinians. Plos Genetics. 2: e132. PMID 16934002 DOI: 10.1371/Journal.Pgen.0020132  0.46
2006 Burdick JT, Chen WM, Abecasis GR, Cheung VG. In silico method for inferring genotypes in pedigrees. Nature Genetics. 38: 1002-4. PMID 16921375 DOI: 10.1038/Ng1863  0.465
2006 Chen WM, Abecasis GR. Estimating the power of variance component linkage analysis in large pedigrees Genetic Epidemiology. 30: 471-484. PMID 16685720 DOI: 10.1002/gepi.20160  0.433
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