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60 matches for
Chen W,
showing the first 20.
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
Buxbaum SG,
Alonso A,
Arking DE,
Berenson GS
and 49 more — show all
Bis JC,
Buyske S,
Carty CL,
Chen W,
Chung MK,
Cummings SR,
Deo R,
Eaton CB,
Fox ER,
Heckbert SR,
Heiss G,
Hindorff LA,
Hsueh WC,
Isaacs A,
Jamshidi Y,
Kerr KF,
Liu F,
Liu Y,
Lohman KK,
Magnani JW,
Maher JF,
Mehra R,
Meng YA,
Musani SK,
Newton-Cheh C,
North KE,
Psaty BM,
Redline S,
Rotter JI,
Schnabel RB,
Schork NJ,
Shohet RV,
Singleton AB,
Smith JD,
Soliman EZ,
Srinivasan SR,
Taylor HA Jr,
Van Wagoner DR,
Wilson JG,
Young T,
Zhang ZM,
Zonderman AB,
Evans MK,
Ferrucci L,
Murray SS,
Tranah GJ,
Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
9 pages
Seven new loci associated with age-related macular degeneration
Fritsche LG,
Chen W,
Schu M,
Yaspan BL,
Yu Y,
Thorleifsson G,
Zack DJ,
Arakawa S,
Cipriani V,
Ripke S,
Igo RP Jr,
Buitendijk GH
and 144 more — show all
Sim X,
Weeks DE,
Guymer RH,
Merriam JE,
Francis PJ,
Hannum G,
Agarwal A,
Armbrecht AM,
Audo I,
Aung T,
Barile GR,
Benchaboune M,
Bird AC,
Bishop PN,
Branham KE,
Brooks M,
Brucker AJ,
Cade WH,
Cain MS,
Campochiaro PA,
Chan CC,
Cheng CY,
Chew EY,
Chin KA,
Chowers I,
Clayton DG,
Cojocaru R,
Conley YP,
Cornes BK,
Daly MJ,
Dhillon B,
Edwards AO,
Evangelou E,
Fagerness J,
Ferreyra HA,
Friedman JS,
Geirsdottir A,
George RJ,
Gieger C,
Gupta N,
Hagstrom SA,
Harding SP,
Haritoglou C,
Heckenlively JR,
Holz FG,
Hughes G,
Ioannidis JP,
Ishibashi T,
Joseph P,
Jun G,
Kamatani Y,
Katsanis N,
N Keilhauer C,
Khan JC,
Kim IK,
Kiyohara Y,
Klein BE,
Klein R,
Kovach JL,
Kozak I,
Lee CJ,
Lee KE,
Lichtner P,
Lotery AJ,
Meitinger T,
Mitchell P,
Mohand-Saïd S,
Moore AT,
Morgan DJ,
Morrison MA,
Myers CE,
Naj AC,
Nakamura Y,
Okada Y,
Orlin A,
Ortube MC,
Othman MI,
Pappas C,
Park KH,
Pauer GJ,
Peachey NS,
Poch O,
Priya RR,
Reynolds R,
Richardson AJ,
Ripp R,
Rudolph G,
Ryu E,
Sahel JA,
Schaumberg DA,
Scholl HP,
Schwartz SG,
Scott WK,
Shahid H,
Sigurdsson H,
Silvestri G,
Sivakumaran TA,
Smith RT,
Sobrin L,
Souied EH,
Stambolian DE,
Stefansson H,
Sturgill-Short GM,
Takahashi A,
Tosakulwong N,
Truitt BJ,
Tsironi EE,
Uitterlinden AG,
van Duijn CM,
Vijaya L,
Vingerling JR,
Vithana EN,
Webster AR,
Wichmann HE,
Winkler TW,
Wong TY,
Wright AF,
Zelenika D,
Zhang M,
Zhao L,
Zhang K,
Klein ML,
Hageman GS,
Lathrop GM,
Stefansson K,
Allikmets R,
Baird PN,
Gorin MB,
Wang JJ,
Klaver CC,
Seddon JM,
Pericak-Vance MA,
Iyengar SK,
Yates JR,
Swaroop A,
Weber BH,
Kubo M,
Deangelis MM,
Léveillard T,
Thorsteinsdottir U,
Haines JL,
Farrer LA,
Heid IM,
Abecasis GR
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies
Crouch DJM,
Inshaw JRJ,
Robertson CC,
Ng E,
Zhang JY,
Chen WM,
Onengut-Gumuscu S,
Cutler AJ,
Sidore C,
Cucca F,
Pociot F,
Concannon P
and 2 more — show all
Genetic epidemiology · 2025 · PMID 39749473 · open access
7 pages
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Willer CJ,
Sanna S,
Jackson AU,
Scuteri A,
Bonnycastle LL,
Clarke R,
Heath SC,
Timpson NJ,
Najjar SS,
Stringham HM,
Strait J,
Duren WL
and 38 more — show all
Maschio A,
Busonero F,
Mulas A,
Albai G,
Swift AJ,
Morken MA,
Narisu N,
Bennett D,
Parish S,
Shen H,
Galan P,
Meneton P,
Hercberg S,
Zelenika D,
Chen WM,
Li Y,
Scott LJ,
Scheet PA,
Sundvall J,
Watanabe RM,
Nagaraja R,
Ebrahim S,
Lawlor DA,
Ben-Shlomo Y,
Davey-Smith G,
Shuldiner AR,
Collins R,
Bergman RN,
Uda M,
Tuomilehto J,
Cao A,
Collins FS,
Lakatta E,
Lathrop GM,
Boehnke M,
Schlessinger D,
Mohlke KL,
Abecasis GR
Nature genetics · 2008 · PMID 18193043
5 pages
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
and 76 more — show all
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
Mangino M,
Hwang SJ,
Spector TD,
Hunt SC,
Kimura M,
Fitzpatrick AL,
Christiansen L,
Petersen I,
Elbers CC,
Harris T,
Chen W,
Srinivasan SR
and 27 more — show all
Kark JD,
Benetos A,
El Shamieh S,
Visvikis-Siest S,
Christensen K,
Berenson GS,
Valdes AM,
Viñuela A,
Garcia M,
Arnett DK,
Broeckel U,
Province MA,
Pankow JS,
Kammerer C,
Liu Y,
Nalls M,
Tishkoff S,
Thomas F,
Ziv E,
Psaty BM,
Bis JC,
Rotter JI,
Taylor KD,
Smith E,
Schork NJ,
Levy D,
Aviv A
Human molecular genetics · 2012 · PMID 23001564 · open access
4 pages
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa
Janivara R,
Chen WC,
Hazra U,
Baichoo S,
Agalliu I,
Kachambwa P,
Simonti CN,
Brown LM,
Tambe SP,
Kim MS,
Harlemon M,
Jalloh M
and 48 more — show all
Muzondiwa D,
Naidoo D,
Ajayi OO,
Snyper NY,
Niang L,
Diop H,
Ndoye M,
Mensah JE,
Abrahams AOD,
Biritwum R,
Adjei AA,
Adebiyi AO,
Shittu O,
Ogunbiyi O,
Adebayo S,
Nwegbu MM,
Ajibola HO,
Oluwole OP,
Jamda MA,
Pentz A,
Haiman CA,
Spies PV,
van der Merwe A,
Cook MB,
Chanock SJ,
Berndt SI,
Watya S,
Lubwama A,
Muchengeti M,
Doherty S,
Smyth N,
Lounsbury D,
Fortier B,
Rohan TE,
Jacobson JS,
Neugut AI,
Hsing AW,
Gusev A,
Aisuodionoe-Shadrach OI,
Joffe M,
Adusei B,
Gueye SM,
Fernandez PW,
McBride J,
Andrews C,
Petersen LN,
Lachance J,
Rebbeck TR
Nature genetics · 2024 · PMID 39358599
4 pages
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
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
and 54 more — show all
Kanda A,
Kopplin L,
Li Y,
Augustaitis KJ,
Karoukis AJ,
Scott WK,
Agarwal A,
Kovach JL,
Schwartz SG,
Postel EA,
Brooks M,
Baratz KH,
Brown WL,
Brucker AJ,
Orlin A,
Brown G,
Ho A,
Regillo C,
Donoso L,
Tian L,
Kaderli B,
Hadley D,
Hagstrom SA,
Peachey NS,
Klein R,
Klein BE,
Gotoh N,
Yamashiro K,
Ferris Iii F,
Fagerness JA,
Reynolds R,
Farrer LA,
Kim IK,
Miller JW,
Cortón M,
Carracedo A,
Sanchez-Salorio M,
Pugh EW,
Doheny KF,
Brion M,
Deangelis MM,
Weeks DE,
Zack DJ,
Chew EY,
Heckenlively JR,
Yoshimura N,
Iyengar SK,
Francis PJ,
Katsanis N,
Seddon JM,
Haines JL,
Gorin MB,
Abecasis GR,
Swaroop A
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
3 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
Harlow SD,
Holliday E,
Ikram MA,
Kelly T,
Lakka TA,
Lawlor DA,
Li C,
Liu CT,
Mägi R,
Manning AK,
Matsuda F,
Morrison AC,
Nauck M,
North KE,
Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
Scuteri A,
Sanna S,
Chen WM,
Uda M,
Albai G,
Strait J,
Najjar S,
Nagaraja R,
Orrú M,
Usala G,
Dei M,
Lai S
and 13 more — show all
Maschio A,
Busonero F,
Mulas A,
Ehret GB,
Fink AA,
Weder AB,
Cooper RS,
Galan P,
Chakravarti A,
Schlessinger D,
Cao A,
Lakatta E,
Abecasis GR
PLoS genetics · 2007 · PMID 17658951 · open access
2 pages
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts
Li S,
Sanna S,
Maschio A,
Busonero F,
Usala G,
Mulas A,
Lai S,
Dei M,
Orrù M,
Albai G,
Bandinelli S,
Schlessinger D
and 12 more — show all
Lakatta E,
Scuteri A,
Najjar SS,
Guralnik J,
Naitza S,
Crisponi L,
Cao A,
Abecasis G,
Ferrucci L,
Uda M,
Chen WM,
Nagaraja R
PLoS genetics · 2007 · PMID 17997608 · open access
2 pages
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
Uda M,
Galanello R,
Sanna S,
Lettre G,
Sankaran VG,
Chen W,
Usala G,
Busonero F,
Maschio A,
Albai G,
Piras MG,
Sestu N
and 18 more — show all
Lai S,
Dei M,
Mulas A,
Crisponi L,
Naitza S,
Asunis I,
Deiana M,
Nagaraja R,
Perseu L,
Satta S,
Cipollina MD,
Sollaino C,
Moi P,
Hirschhorn JN,
Orkin SH,
Abecasis GR,
Schlessinger D,
Cao A
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18245381
2 pages
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Monda KL,
Chen GK,
Taylor KC,
Palmer C,
Edwards TL,
Lange LA,
Ng MC,
Adeyemo AA,
Allison MA,
Bielak LF,
Chen G,
Graff M
and 196 more — show all
Irvin MR,
Rhie SK,
Li G,
Liu Y,
Liu Y,
Lu Y,
Nalls MA,
Sun YV,
Wojczynski MK,
Yanek LR,
Aldrich MC,
Ademola A,
Amos CI,
Bandera EV,
Bock CH,
Britton A,
Broeckel U,
Cai Q,
Caporaso NE,
Carlson CS,
Carpten J,
Casey G,
Chen WM,
Chen F,
Chen YD,
Chiang CW,
Coetzee GA,
Demerath E,
Deming-Halverson SL,
Driver RW,
Dubbert P,
Feitosa MF,
Feng Y,
Freedman BI,
Gillanders EM,
Gottesman O,
Guo X,
Haritunians T,
Harris T,
Harris CC,
Hennis AJ,
Hernandez DG,
McNeill LH,
Howard TD,
Howard BV,
Howard VJ,
Johnson KC,
Kang SJ,
Keating BJ,
Kolb S,
Kuller LH,
Kutlar A,
Langefeld CD,
Lettre G,
Lohman K,
Lotay V,
Lyon H,
Manson JE,
Maixner W,
Meng YA,
Monroe KR,
Morhason-Bello I,
Murphy AB,
Mychaleckyj JC,
Nadukuru R,
Nathanson KL,
Nayak U,
N'diaye A,
Nemesure B,
Wu SY,
Leske MC,
Neslund-Dudas C,
Neuhouser M,
Nyante S,
Ochs-Balcom H,
Ogunniyi A,
Ogundiran TO,
Ojengbede O,
Olopade OI,
Palmer JR,
Ruiz-Narvaez EA,
Palmer ND,
Press MF,
Rampersaud E,
Rasmussen-Torvik LJ,
Rodriguez-Gil JL,
Salako B,
Schadt EE,
Schwartz AG,
Shriner DA,
Siscovick D,
Smith SB,
Wassertheil-Smoller S,
Speliotes EK,
Spitz MR,
Sucheston L,
Taylor H,
Tayo BO,
Tucker MA,
Van Den Berg DJ,
Edwards DR,
Wang Z,
Wiencke JK,
Winkler TW,
Witte JS,
Wrensch M,
Wu X,
Yang JJ,
Levin AM,
Young TR,
Zakai NA,
Cushman M,
Zanetti KA,
Zhao JH,
Zhao W,
Zheng Y,
Zhou J,
Ziegler RG,
Zmuda JM,
Fernandes JK,
Gilkeson GS,
Kamen DL,
Hunt KJ,
Spruill IJ,
Ambrosone CB,
Ambs S,
Arnett DK,
Atwood L,
Becker DM,
Berndt SI,
Bernstein L,
Blot WJ,
Borecki IB,
Bottinger EP,
Bowden DW,
Burke G,
Chanock SJ,
Cooper RS,
Ding J,
Duggan D,
Evans MK,
Fox C,
Garvey WT,
Bradfield JP,
Hakonarson H,
Grant SF,
Hsing A,
Chu L,
Hu JJ,
Huo D,
Ingles SA,
John EM,
Jordan JM,
Kabagambe EK,
Kardia SL,
Kittles RA,
Goodman PJ,
Klein EA,
Kolonel LN,
Le Marchand L,
Liu S,
McKnight B,
Millikan RC,
Mosley TH,
Padhukasahasram B,
Williams LK,
Patel SR,
Peters U,
Pettaway CA,
Peyser PA,
Psaty BM,
Redline S,
Rotimi CN,
Rybicki BA,
Sale MM,
Schreiner PJ,
Signorello LB,
Singleton AB,
Stanford JL,
Strom SS,
Thun MJ,
Vitolins M,
Zheng W,
Moore JH,
Williams SM,
Ketkar S,
Zhu X,
Zonderman AB,
Kooperberg C,
Papanicolaou GJ,
Henderson BE,
Reiner AP,
Hirschhorn JN,
Loos RJ,
North KE,
Haiman CA
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Hinks A,
Cobb J,
Marion MC,
Prahalad S,
Sudman M,
Bowes J,
Martin P,
Comeau ME,
Sajuthi S,
Andrews R,
Brown M,
Chen WM
and 27 more — show all
Concannon P,
Deloukas P,
Edkins S,
Eyre S,
Gaffney PM,
Guthery SL,
Guthridge JM,
Hunt SE,
James JA,
Keddache M,
Moser KL,
Nigrovic PA,
Onengut-Gumuscu S,
Onslow ML,
Rosé CD,
Rich SS,
Steel KJ,
Wakeland EK,
Wallace CA,
Wedderburn LR,
Woo P,
Bohnsack JF,
Haas JP,
Glass DN,
Langefeld CD,
Thomson W,
Thompson SD
Boston Children's JIA Registry · British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group and 7 more consortia
Nature genetics · 2013 · PMID 23603761 · open access
2 pages
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
Liu CT,
Monda KL,
Taylor KC,
Lange L,
Demerath EW,
Palmas W,
Wojczynski MK,
Ellis JC,
Vitolins MZ,
Liu S,
Papanicolaou GJ,
Irvin MR
and 81 more — show all
Xue L,
Griffin PJ,
Nalls MA,
Adeyemo A,
Liu J,
Li G,
Ruiz-Narvaez EA,
Chen WM,
Chen F,
Henderson BE,
Millikan RC,
Ambrosone CB,
Strom SS,
Guo X,
Andrews JS,
Sun YV,
Mosley TH,
Yanek LR,
Shriner D,
Haritunians T,
Rotter JI,
Speliotes EK,
Smith M,
Rosenberg L,
Mychaleckyj J,
Nayak U,
Spruill I,
Garvey WT,
Pettaway C,
Nyante S,
Bandera EV,
Britton AF,
Zonderman AB,
Rasmussen-Torvik LJ,
Chen YD,
Ding J,
Lohman K,
Kritchevsky SB,
Zhao W,
Peyser PA,
Kardia SL,
Kabagambe E,
Broeckel U,
Chen G,
Zhou J,
Wassertheil-Smoller S,
Neuhouser ML,
Rampersaud E,
Psaty B,
Kooperberg C,
Manson JE,
Kuller LH,
Ochs-Balcom HM,
Johnson KC,
Sucheston L,
Ordovas JM,
Palmer JR,
Haiman CA,
McKnight B,
Howard BV,
Becker DM,
Bielak LF,
Liu Y,
Allison MA,
Grant SF,
Burke GL,
Patel SR,
Schreiner PJ,
Borecki IB,
Evans MK,
Taylor H,
Sale MM,
Howard V,
Carlson CS,
Rotimi CN,
Cushman M,
Harris TB,
Reiner AP,
Cupples LA,
North KE,
Fox CS
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Franceschini N,
Fox E,
Zhang Z,
Edwards TL,
Nalls MA,
Sung YJ,
Tayo BO,
Sun YV,
Gottesman O,
Adeyemo A,
Johnson AD,
Young JH
and 94 more — show all
Rice K,
Duan Q,
Chen F,
Li Y,
Tang H,
Fornage M,
Keene KL,
Andrews JS,
Smith JA,
Faul JD,
Guangfa Z,
Guo W,
Liu Y,
Murray SS,
Musani SK,
Srinivasan S,
Velez Edwards DR,
Wang H,
Becker LC,
Bovet P,
Bochud M,
Broeckel U,
Burnier M,
Carty C,
Chasman DI,
Ehret G,
Chen WM,
Chen G,
Chen W,
Ding J,
Dreisbach AW,
Evans MK,
Guo X,
Garcia ME,
Jensen R,
Keller MF,
Lettre G,
Lotay V,
Martin LW,
Moore JH,
Morrison AC,
Mosley TH,
Ogunniyi A,
Palmas W,
Papanicolaou G,
Penman A,
Polak JF,
Ridker PM,
Salako B,
Singleton AB,
Shriner D,
Taylor KD,
Vasan R,
Wiggins K,
Williams SM,
Yanek LR,
Zhao W,
Zonderman AB,
Becker DM,
Berenson G,
Boerwinkle E,
Bottinger E,
Cushman M,
Eaton C,
Nyberg F,
Heiss G,
Hirschhron JN,
Howard VJ,
Karczewsk KJ,
Lanktree MB,
Liu K,
Liu Y,
Loos R,
Margolis K,
Snyder M,
Psaty BM,
Schork NJ,
Weir DR,
Rotimi CN,
Sale MM,
Harris T,
Kardia SL,
Hunt SC,
Arnett D,
Redline S,
Cooper RS,
Risch NJ,
Rao DC,
Rotter JI,
Chakravarti A,
Reiner AP,
Levy D,
Keating BJ,
Zhu X
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Huang J,
Huffman JE,
Yamakuchi M,
Trompet S,
Asselbergs FW,
Sabater-Lleal M,
Trégouët DA,
Chen WM,
Smith NL,
Kleber ME,
Shin SY,
Becker DM
and 81 more — show all
Tang W,
Dehghan A,
Johnson AD,
Truong V,
Folkersen L,
Yang Q,
Oudot-Mellkah T,
Buckley BM,
Moore JH,
Williams FM,
Campbell H,
Silbernagel G,
Vitart V,
Rudan I,
Tofler GH,
Navis GJ,
Destefano A,
Wright AF,
Chen MH,
de Craen AJ,
Worrall BB,
Rudnicka AR,
Rumley A,
Bookman EB,
Psaty BM,
Chen F,
Keene KL,
Franco OH,
Böhm BO,
Uitterlinden AG,
Carter AM,
Jukema JW,
Sattar N,
Bis JC,
Bis JC,
Ikram MA,
Sale MM,
McKnight B,
Fornage M,
Ford I,
Taylor K,
Slagboom PE,
McArdle WL,
Hsu FC,
Franco-Cereceda A,
Goodall AH,
Yanek LR,
Furie KL,
Cushman M,
Hofman A,
Witteman JC,
Folsom AR,
Basu S,
Matijevic N,
van Gilst WH,
Wilson JF,
Westendorp RG,
Kathiresan S,
Reilly MP,
Tracy RP,
Polasek O,
Winkelmann BR,
Grant PJ,
Hillege HL,
Cambien F,
Stott DJ,
Lowe GD,
Spector TD,
Meigs JB,
Marz W,
Eriksson P,
Becker LC,
Morange PE,
Soranzo N,
Williams SM,
Hayward C,
van der Harst P,
Hamsten A,
Lowenstein CJ,
Strachan DP,
O'Donnell CJ
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke
Williams SR,
Yang Q,
Chen F,
Liu X,
Keene KL,
Jacques P,
Chen WM,
Weinstein G,
Hsu FC,
Beiser A,
Wang L,
Bookman E
and 9 more — show all
Genomics and Randomized Trials Network · Framingham Heart Study
PLoS genetics · 2014 · PMID 24651765 · open access
2 pages
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans
Carty CL,
Keene KL,
Cheng YC,
Meschia JF,
Chen WM,
Nalls M,
Bis JC,
Kittner SJ,
Rich SS,
Tajuddin S,
Zonderman AB,
Evans MK
and 17 more — show all
Langefeld CD,
Gottesman R,
Mosley TH,
Shahar E,
Woo D,
Yaffe K,
Liu Y,
Sale MM,
Dichgans M,
Malik R,
Longstreth WT Jr,
Mitchell BD,
Psaty BM,
Kooperberg C,
Reiner A,
Worrall BB,
Fornage M
COMPASS and METASTROKE Consortia
Stroke · 2015 · PMID 26089329
2 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
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Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
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Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
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Which pages rest on a paper?
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