| Year |
Citation |
Score |
| 2023 |
Wang Y, Li H, Hou L, Wang S, Kang X, Yu J, Tian F, Ni W, Deng X, Liu T, You Y, Chen W. Genome-wide association study on coordination and agility in 461 Chinese Han males. Heliyon. 9: e19268. PMID 37654465 DOI: 10.1016/j.heliyon.2023.e19268 |
0.305 |
|
| 2023 |
Do WL, Sun D, Meeks K, Dugué PA, Demerath E, Guan W, Li S, Chen W, Milne R, Adeyemo A, Agyemang C, Nassir R, Manson JE, Shadyab AH, Hou L, et al. Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI. American Journal of Human Genetics. PMID 36649705 DOI: 10.1016/j.ajhg.2022.12.014 |
0.42 |
|
| 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 |
0.453 |
|
| 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 |
0.414 |
|
| 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 |
0.419 |
|
| 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 |
0.482 |
|
| 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 |
0.517 |
|
| 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 |
0.302 |
|
| 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 |
0.369 |
|
| 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 |
0.513 |
|
| 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 |
0.438 |
|
| 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 |
0.412 |
|
| 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 |
0.592 |
|
| 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 |
0.313 |
|
| 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 |
0.466 |
|
| 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 |
0.38 |
|
| 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 |
0.424 |
|
| 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 |
0.312 |
|
| 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 |
0.375 |
|
| 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 |
0.431 |
|
| 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 |
0.542 |
|
| 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 |
0.306 |
|
| 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 |
0.462 |
|
| 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 |
0.526 |
|
| 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 |
0.36 |
|
| 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 |
0.372 |
|
| 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 |
0.522 |
|
| 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 |
0.405 |
|
| 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 |
0.501 |
|
| 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 |
0.368 |
|
| 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 |
0.307 |
|
| 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 |
0.415 |
|
| 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 |
0.523 |
|
| 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 |
0.42 |
|
| 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 |
0.316 |
|
| 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 |
0.487 |
|
| 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 |
0.445 |
|
| 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 |
0.445 |
|
| 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 |
0.587 |
|
| 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 |
0.677 |
|
| 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 |
0.304 |
|
| 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 |
0.493 |
|
| 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 |
0.47 |
|
| 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 |
0.317 |
|
| 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 |
0.554 |
|
| 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 |
0.428 |
|
| 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 |
0.499 |
|
| 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 |
0.306 |
|
| 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 |
0.522 |
|
| 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 |
0.484 |
|
| 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 |
0.571 |
|
| 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 |
0.459 |
|
| 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 |
0.48 |
|
| 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 |
0.511 |
|
| 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 |
0.532 |
|
| 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 |
0.475 |
|
| 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 |
0.519 |
|
| 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 |
0.498 |
|
| 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 |
0.486 |
|
| 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 |
0.679 |
|
| 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 |
0.505 |
|
| 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 |
0.454 |
|
| 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 |
0.459 |
|
| 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 |
0.428 |
|
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