| Year |
Citation |
Score |
| 2024 |
Huffman JE, Nicholas J, Hahn J, Heath AS, Raffield LM, Yanek LR, Brody JA, Thibord F, Almasy L, Bartz TM, Bielak LF, Bowler RP, Carrasquilla GD, Chasman DI, Chen MH, et al. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Blood. PMID 39226462 DOI: 10.1182/blood.2023022596 |
0.385 |
|
| 2023 |
Huffman JE, Nicolas J, Hahn J, Heath AS, Raffield LM, Yanek LR, Brody JA, Thibord F, Almasy L, Bartz TM, Bielak LF, Bowler RP, Carrasquilla GD, Chasman DI, Chen MH, et al. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Medrxiv : the Preprint Server For Health Sciences. PMID 37398003 DOI: 10.1101/2023.06.07.23291095 |
0.568 |
|
| 2022 |
Thibord F, Klarin D, Brody JA, Chen MH, Levin MG, Chasman DI, Goode EL, Hveem K, Teder-Laving M, Martinez-Perez A, Aïssi D, Daian-Bacq D, Ito K, Natarajan P, Lutsey PL, et al. Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. Circulation. 101161CIRCULATIONAHA. PMID 36154123 DOI: 10.1161/CIRCULATIONAHA.122.059675 |
0.336 |
|
| 2022 |
Pankratz N, Wei P, Brody JA, Chen MH, Vries PS, Huffman JE, Stimson MR, Auer PL, Boerwinkle E, Cushman M, Maat MPM, Folsom AR, Franco OH, Gibbs RA, Haagenson KK, et al. Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Human Molecular Genetics. PMID 35552711 DOI: 10.1093/hmg/ddac100 |
0.34 |
|
| 2022 |
Thibord F, Chan MV, Chen MH, Johnson AD. A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. Hgg Advances. 3: 100095. PMID 35224516 DOI: 10.1016/j.xhgg.2022.100095 |
0.33 |
|
| 2021 |
Mikhaylova AV, McHugh CP, Polfus LM, Raffield LM, Boorgula MP, Blackwell TW, Brody JA, Broome J, Chami N, Chen MH, Conomos MP, Cox C, Curran JE, Daya M, Ekunwe L, et al. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 34582791 DOI: 10.1016/j.ajhg.2021.08.007 |
0.354 |
|
| 2021 |
Little A, Hu Y, Sun Q, Jain D, Broome J, Chen MH, Thibord F, McHugh C, Surendran P, Blackwell TW, Brody JA, Bhan A, Chami N, Vries PS, Ekunwe L, et al. Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. Human Molecular Genetics. PMID 34553764 DOI: 10.1093/hmg/ddab252 |
0.317 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.355 |
|
| 2020 |
Vuckovic D, Bao EL, Akbari P, Lareau CA, Mousas A, Jiang T, Chen MH, Raffield LM, Tardaguila M, Huffman JE, Ritchie SC, Megy K, Ponstingl H, Penkett CJ, Albers PK, et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11. PMID 32888494 DOI: 10.1016/J.Cell.2020.08.008 |
0.557 |
|
| 2020 |
Chen MH, Raffield LM, Mousas A, Sakaue S, Huffman JE, Moscati A, Trivedi B, Jiang T, Akbari P, Vuckovic D, Bao EL, Zhong X, Manansala R, Laplante V, Chen M, et al. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 182: 1198-1213.e14. PMID 32888493 DOI: 10.1016/J.Cell.2020.06.045 |
0.562 |
|
| 2020 |
Lee DH, Yao C, Bhan A, Schlaeger TM, Keefe J, Rodriguez BA, Hwang SJ, Chen MH, Levy D, Johnson AD. Integrative Genomic Analysis Reveals Four Protein Biomarkers for Platelet Traits. Circulation Research. PMID 32781905 DOI: 10.1161/Circresaha.119.316447 |
0.349 |
|
| 2020 |
Rodriguez BAT, Bhan A, Beswick A, Elwood PC, Niiranen TJ, Salomaa V, Trégouët DA, Morange PE, Civelek M, Ben-Shlomo Y, Schlaeger T, Chen MH, Johnson AD. A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling. American Journal of Human Genetics. PMID 32649856 DOI: 10.1016/J.Ajhg.2020.06.008 |
0.344 |
|
| 2019 |
Lindstrom S, Wang L, Smith EN, Gordon W, van Hylckama Vlieg A, de Andrade M, Brody JA, Pattee JW, Haessler J, Brumpton BM, Chasman DI, Suchon P, Chen MH, Turman C, Germain M, et al. Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Blood. PMID 31420334 DOI: 10.1182/Blood.2019000435 |
0.358 |
|
| 2019 |
Lindström S, Brody JA, Turman C, Germain M, Bartz TM, Smith EN, Chen MH, Puurunen M, Chasman D, Hassler J, Pankratz N, Basu S, Guan W, Gyorgy B, Ibrahim M, et al. A large-scale exome array analysis of venous thromboembolism. Genetic Epidemiology. PMID 30659681 DOI: 10.1002/Gepi.22187 |
0.433 |
|
| 2019 |
de Vries PS, Sabater-Lleal M, Huffman JE, Marten J, Song C, Pankratz N, Bartz TM, de Haan HG, Delgado GE, Eicher JD, Martinez-Perez A, Ward-Caviness CK, Brody JA, Chen MH, de Maat MPM, et al. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Blood. PMID 30642921 DOI: 10.1182/Blood-2018-05-849240 |
0.384 |
|
| 2018 |
Weng LC, Guan W, Steffen LM, Pankow JS, Pankratz N, Chen MH, Cushman M, Basu S, Folsom AR, Tang W. Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variables. Thrombosis Research. 168: 53-59. PMID 29902632 DOI: 10.1016/J.Thromres.2018.05.032 |
0.394 |
|
| 2018 |
Jiang J, Thalamuthu A, Ho JE, Mahajan A, Ek WE, Brown DA, Breit SN, Wang TJ, Gyllensten U, Chen MH, Enroth S, Januzzi JL, Lind L, Armstrong NJ, Kwok JB, et al. A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood. Frontiers in Genetics. 9: 97. PMID 29628937 DOI: 10.3389/Fgene.2018.00097 |
0.34 |
|
| 2017 |
Chen MH, Yanek LR, Backman JD, Eicher JD, Huffman JE, Ben-Shlomo Y, Beswick AD, Yerges-Armstrong LM, Shuldiner AR, O'Connell JR, Mathias RA, Becker DM, Becker LC, Lewis JP, Johnson AD, et al. Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation. Platelets. 1-10. PMID 29185836 DOI: 10.1080/09537104.2017.1384538 |
0.346 |
|
| 2017 |
Mousas A, Ntritsos G, Chen MH, Song C, Huffman JE, Tzoulaki I, Elliott P, Psaty BM, Auer PL, Johnson AD, Evangelou E, Lettre G, Reiner AP. Rare coding variants pinpoint genes that control human hematological traits. Plos Genetics. 13: e1006925. PMID 28787443 DOI: 10.1371/Journal.Pgen.1006925 |
0.41 |
|
| 2017 |
Gorski M, Most PJV, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, ... ... Chen MH, et al. Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific Reports. 7: 46835. PMID 28548086 DOI: 10.1038/Srep46835 |
0.338 |
|
| 2017 |
Gorski M, van der Most PJ, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, ... ... Chen MH, et al. 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific Reports. 7: 45040. PMID 28452372 DOI: 10.1038/Srep45040 |
0.315 |
|
| 2017 |
Wild PS, Felix JF, Schillert A, Teumer A, Chen MH, Leening MJ, Völker U, Großmann V, Brody JA, Irvin MR, Shah SJ, Pramana S, Lieb W, Schmidt R, Stanton AV, et al. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. The Journal of Clinical Investigation. PMID 28394258 DOI: 10.1172/Jci84840 |
0.375 |
|
| 2017 |
Jensen MK, Jensen RA, Mukamal KJ, Guo X, Yao J, Sun Q, Cornelis M, Liu Y, Chen MH, Kizer JR, Djoussé L, Siscovick DS, Psaty BM, Zmuda JM, Rotter JI, et al. Detection of genetic loci associated with plasma fetuin-A: A meta-analysis of genome-wide association studies from the CHARGE Consortium. Human Molecular Genetics. PMID 28379451 DOI: 10.1093/Hmg/Ddx091 |
0.374 |
|
| 2017 |
Eicher JD, Chen MH, Pitsillides AN, Lin H, Veeraraghavan N, Brody JA, Metcalf GA, Muzny DM, Gibbs RA, Becker DM, Becker LC, Faraday N, Mathias RA, Yanek LR, Boerwinkle E, et al. Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation. Thrombosis and Haemostasis. PMID 28300864 DOI: 10.1160/Th16-09-0677 |
0.324 |
|
| 2016 |
Zhu QM, Ko KA, Ture S, Mastrangelo MA, Chen MH, Johnson AD, O'Donnell CJ, Morrell CN, Miano JM, Lowenstein CJ. Novel Thrombotic Function of a Human SNP in STXBP5 Revealed by CRISPR/Cas9 Gene Editing in Mice. Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 28062498 DOI: 10.1161/Atvbaha.116.308614 |
0.345 |
|
| 2016 |
van Rooij FJ, Qayyum R, Smith AV, Zhou Y, Trompet S, Tanaka T, Keller MF, Chang LC, Schmidt H, Yang ML, Chen MH, Hayes J, Johnson AD, Yanek LR, Mueller C, et al. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. American Journal of Human Genetics. PMID 28017375 DOI: 10.1016/J.Ajhg.2016.11.016 |
0.36 |
|
| 2016 |
Zhang W, Jernerén F, Lehne BC, Chen MH, Luben RN, Johnston C, Elshorbagy A, Eppinga RN, Scott WR, Adeyeye E, Scott J, Böger RH, Khaw KT, van der Harst P, Wareham NJ, et al. Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels. Thrombosis and Haemostasis. 116. PMID 27656708 DOI: 10.1160/Th16-02-0151 |
0.397 |
|
| 2016 |
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, Floyd JS, Huang J, Lange L, van Rooij FJ, Gibbs RA, Metcalf G, Muzny D, et al. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 481-488. PMID 27486782 DOI: 10.1016/J.Ajhg.2016.06.016 |
0.423 |
|
| 2016 |
Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill WD, Kacprowski T, Li J, Lyytikäinen LP, Manichaikul A, Mihailov E, O'Donoghue ML, Pankratz N, Pazoki R, ... ... Chen MH, et al. Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases. American Journal of Human Genetics. PMID 27346689 DOI: 10.1016/J.Ajhg.2016.05.003 |
0.314 |
|
| 2016 |
Eicher JD, Chami N, Kacprowski T, Nomura A, Chen MH, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N, Polfus L, Schurmann C, Giri A, Brody JA, Lange LA, et al. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. American Journal of Human Genetics. PMID 27346686 DOI: 10.1016/J.Ajhg.2016.05.005 |
0.306 |
|
| 2016 |
Chami N, Chen MH, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A, Giri A, Lessard S, Brody JA, Schurmann C, Pankratz N, et al. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. American Journal of Human Genetics. PMID 27346685 DOI: 10.1016/J.Ajhg.2016.05.007 |
0.359 |
|
| 2016 |
van Loon J, Dehghan A, Weihong T, Trompet S, McArdle WL, Asselbergs FW, Chen MH, Lopez LM, Huffman JE, Leebeek FW, Basu S, Stott DJ, Rumley A, Gansevoort RT, Davies G, et al. Genome-wide association studies identify genetic loci for low von Willebrand factor levels. European Journal of Human Genetics : Ejhg. 24: 1096. PMID 27307114 DOI: 10.1038/Ejhg.2016.21 |
0.431 |
|
| 2015 |
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V, Hottenga JJ, Trompet S, Müller-Nurasyid M, Zhao JH, Brody JA, et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics. PMID 26561523 DOI: 10.1093/Hmg/Ddv454 |
0.43 |
|
| 2015 |
Chen MH, Yang Q. RVFam: An R Package for Rare Variant Association Analysis with Family Data. Bioinformatics (Oxford, England). PMID 26508760 DOI: 10.1093/Bioinformatics/Btv609 |
0.399 |
|
| 2015 |
van Loon J, Dehghan A, Weihong T, Trompet S, McArdle WL, Asselbergs FF, Chen MH, Lopez LM, Huffman JE, Leebeek FW, Basu S, Stott DJ, Rumley A, Gansevoort RT, Davies G, et al. Genome-wide association studies identify genetic loci for low von Willebrand factor levels. European Journal of Human Genetics : Ejhg. PMID 26486471 DOI: 10.1038/Ejhg.2015.222 |
0.338 |
|
| 2015 |
Dina C, Bouatia-Naji N, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J, Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, et al. Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nature Genetics. PMID 26301497 DOI: 10.1038/Ng.3383 |
0.316 |
|
| 2015 |
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen MH, Guo X, Lin LA, Marioni RE, Müller-Nurasyid M, Yanek LR, Pankratz N, et al. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood. 126: e19-29. PMID 26105150 DOI: 10.1182/Blood-2015-02-624551 |
0.335 |
|
| 2015 |
Musani SK, Fox ER, Kraja A, Bidulescu A, Lieb W, Lin H, Beecham A, Chen MH, Felix JF, Fox CS, Kao WH, Kardia SL, Liu CT, Nalls MA, Rundek T, et al. Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study. Circulation. Cardiovascular Genetics. 8: 122-30. PMID 25561047 DOI: 10.1161/Circgenetics.114.000900 |
0.34 |
|
| 2015 |
Lieb W, Chen MH, Teumer A, de Boer RA, Lin H, Fox ER, Musani SK, Wilson JG, Wang TJ, Völzke H, Petersen AK, Meisinger C, Nauck M, Schlesinger S, Li Y, et al. Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Circulation. Cardiovascular Genetics. 8: 131-40. PMID 25477429 DOI: 10.1161/Circgenetics.114.000613 |
0.415 |
|
| 2014 |
Keller MF, Reiner AP, Okada Y, van Rooij FJ, Johnson AD, Chen MH, Smith AV, Morris AP, Tanaka T, Ferrucci L, Zonderman AB, Lettre G, Harris T, Garcia M, Bandinelli S, et al. Trans-ethnic meta-analysis of white blood cell phenotypes. Human Molecular Genetics. 23: 6944-60. PMID 25096241 DOI: 10.1093/hmg/ddu401 |
0.371 |
|
| 2014 |
Huang J, Huffman JE, Yamakuchi M, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, ... ... Chen MH, et al. Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1093-101. PMID 24578379 DOI: 10.1161/Atvbaha.113.302088 |
0.309 |
|
| 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, 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 |
0.316 |
|
| 2013 |
Ho JE, Chen WY, Chen MH, Larson MG, McCabe EL, Cheng S, Ghorbani A, Coglianese E, Emilsson V, Johnson AD, Walter S, Franceschini N, O'Donnell CJ, et al. Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. The Journal of Clinical Investigation. 123: 4208-18. PMID 23999434 DOI: 10.1172/Jci67119 |
0.334 |
|
| 2013 |
Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S, Rudnicka AR, Trompet S, Mälarstig A, Baumert J, Bis JC, ... ... Chen MH, et al. Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation. 128: 1310-24. PMID 23969696 DOI: 10.1161/Circulationaha.113.002251 |
0.328 |
|
| 2013 |
Rhee EP, Ho JE, Chen MH, Shen D, Cheng S, Larson MG, Ghorbani A, Shi X, Helenius IT, O'Donnell CJ, Souza AL, Deik A, Pierce KA, Bullock K, Walford GA, et al. A genome-wide association study of the human metabolome in a community-based cohort. Cell Metabolism. 18: 130-43. PMID 23823483 DOI: 10.1016/J.Cmet.2013.06.013 |
0.42 |
|
| 2013 |
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, ... Chen MH, et al. Genetic variation associated with circulating monocyte count in the eMERGE Network. Human Molecular Genetics. 22: 2119-27. PMID 23314186 DOI: 10.1093/Hmg/Ddt010 |
0.313 |
|
| 2012 |
Chen MH, Huang J, Chen WM, Larson MG, Fox CS, Vasan RS, Seshadri S, O'Donnell CJ, Yang Q. Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study. Plos One. 7: e51589. PMID 23284720 DOI: 10.1371/Journal.Pone.0051589 |
0.432 |
|
| 2012 |
Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin SY, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD, Smith NL, Williams SM, Ikram MA, Kleber ME, Becker DM, ... ... Chen MH, et al. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood. 120: 4873-81. PMID 22990020 DOI: 10.1182/Blood-2012-06-436188 |
0.328 |
|
| 2011 |
Chen MH, Liu X, Wei F, Larson MG, Fox CS, Vasan RS, Yang Q. A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees. Genetic Epidemiology. 35: 650-7. PMID 21818773 DOI: 10.1002/Gepi.20614 |
0.376 |
|
| 2011 |
Faraday N, Yanek LR, Yang XP, Mathias R, Herrera-Galeano JE, Suktitipat B, Qayyum R, Johnson AD, Chen MH, Tofler GH, Ruczinski I, Friedman AD, Gylfason A, Thorsteinsdottir U, Bray PF, et al. Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. Blood. 118: 3367-75. PMID 21791418 DOI: 10.1182/Blood-2010-11-320788 |
0.403 |
|
| 2011 |
Nalls MA, Couper DJ, Tanaka T, van Rooij FJ, Chen MH, Smith AV, Toniolo D, Zakai NA, Yang Q, Greinacher A, Wood AR, Garcia M, Gasparini P, Liu Y, Lumley T, et al. Multiple loci are associated with white blood cell phenotypes. Plos Genetics. 7: e1002113. PMID 21738480 DOI: 10.1371/Journal.Pgen.1002113 |
0.316 |
|
| 2011 |
Okada Y, Hirota T, Kamatani Y, Takahashi A, Ohmiya H, Kumasaka N, Higasa K, Yamaguchi-Kabata Y, Hosono N, Nalls MA, Chen MH, van Rooij FJ, Smith AV, Tanaka T, Couper DJ, et al. Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. Plos Genetics. 7: e1002067. PMID 21738478 DOI: 10.1371/Journal.Pgen.1002067 |
0.344 |
|
| 2011 |
Smith NL, Huffman JE, Strachan DP, Huang J, Dehghan A, Trompet S, Lopez LM, Shin SY, Baumert J, Vitart V, Bis JC, Wild SH, Rumley A, Yang Q, Uitterlinden AG, ... ... Chen MH, et al. Genetic predictors of fibrin D-dimer levels in healthy adults. Circulation. 123: 1864-72. PMID 21502573 DOI: 10.1161/Circulationaha.110.009480 |
0.406 |
|
| 2010 |
Chen MH, Larson MG, Hsu YH, Peloso GM, Guo CY, Fox CS, Atwood LD, Yang Q. A three-stage approach for genome-wide association studies with family data for quantitative traits. Bmc Genetics. 11: 40. PMID 20470424 DOI: 10.1186/1471-2156-11-40 |
0.397 |
|
| 2010 |
Musunuru K, Lettre G, Young T, Farlow DN, Pirruccello JP, Ejebe KG, Keating BJ, Yang Q, Chen MH, Lapchyk N, Crenshaw A, Ziaugra L, Rachupka A, Benjamin EJ, Cupples LA, et al. Candidate gene association resource (CARe): design, methods, and proof of concept. Circulation. Cardiovascular Genetics. 3: 267-75. PMID 20400780 DOI: 10.1161/Circgenetics.109.882696 |
0.388 |
|
| 2010 |
Smith NL, Chen MH, Dehghan A, Strachan DP, Basu S, Soranzo N, Hayward C, Rudan I, Sabater-Lleal M, Bis JC, de Maat MP, Rumley A, Kong X, Yang Q, Williams FM, et al. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation. 121: 1382-92. PMID 20231535 DOI: 10.1161/Circulationaha.109.869156 |
0.385 |
|
| 2010 |
Chen MH, Yang Q. GWAF: an R package for genome-wide association analyses with family data. Bioinformatics (Oxford, England). 26: 580-1. PMID 20040588 DOI: 10.1093/Bioinformatics/Btp710 |
0.418 |
|
| 2010 |
Chen MH, Van Eerdewegh P, Vincent QB, Alcais A, Abel L, Dupuis J. Evaluation of approaches to identify associated SNPs that explain the linkage evidence in nuclear families with affected siblings. Human Heredity. 69: 104-19. PMID 19996608 DOI: 10.1159/000264448 |
0.563 |
|
| 2009 |
Schnabel RB, Lunetta KL, Larson MG, Dupuis J, Lipinska I, Rong J, Chen MH, Zhao Z, Yamamoto JF, Meigs JB, Nicaud V, Perret C, Zeller T, Blankenberg S, Tiret L, et al. The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations. Circulation. Cardiovascular Genetics. 2: 229-37. PMID 20031590 DOI: 10.1161/Circgenetics.108.804245 |
0.543 |
|
| 2009 |
Dehghan A, Yang Q, Peters A, Basu S, Bis JC, Rudnicka AR, Kavousi M, Chen MH, Baumert J, Lowe GD, McKnight B, Tang W, de Maat M, Larson MG, Eyhermendy S, et al. Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. Circulation. Cardiovascular Genetics. 2: 125-33. PMID 20031576 DOI: 10.1161/Circgenetics.108.825224 |
0.433 |
|
| 2009 |
Ganesh SK, Zakai NA, van Rooij FJ, Soranzo N, Smith AV, Nalls MA, Chen MH, Kottgen A, Glazer NL, Dehghan A, Kuhnel B, Aspelund T, Yang Q, Tanaka T, Jaffe A, et al. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nature Genetics. 41: 1191-8. PMID 19862010 DOI: 10.1038/Ng.466 |
0.347 |
|
| 2009 |
Johnson AD, Kavousi M, Smith AV, Chen MH, Dehghan A, Aspelund T, Lin JP, van Duijn CM, Harris TB, Cupples LA, Uitterlinden AG, Launer L, Hofman A, Rivadeneira F, Stricker B, et al. Genome-wide association meta-analysis for total serum bilirubin levels. Human Molecular Genetics. 18: 2700-10. PMID 19414484 DOI: 10.1093/Hmg/Ddp202 |
0.476 |
|
| 2007 |
Chen MH, Cui J, Guo CY, Cupples LA, Van Eerdewegh P, Dupuis J, Yang Q. Joint modeling of linkage and association using affected sib-pair data. Bmc Proceedings. 1: S38. PMID 18466536 DOI: 10.1186/1753-6561-1-S1-S38 |
0.541 |
|
| 2007 |
Yang Q, Biernacka JM, Chen MH, Houwing-Duistermaat JJ, Bergemann TL, Basu S, Fan R, Liu L, Bourgey M, Clerget-Darpoux F, Lin WY, Elston RC, Cupples LA, Apprey V, Cui J, et al. Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4. Genetic Epidemiology. 31: S34-42. PMID 18046758 DOI: 10.1002/Gepi.20278 |
0.521 |
|
| 2005 |
Chen MH, Van Eerdewegh P, Dupuis J. Identification of polymorphisms explaining a linkage signal: application to the GAW14 simulated data. Bmc Genetics. 6: S88. PMID 16451703 DOI: 10.1186/1471-2156-6-S1-S88 |
0.539 |
|
| Show low-probability matches. |