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114 matches for
Taylor K,
showing the first 20.
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
Hodonsky CJ,
Jain D,
Schick UM,
Morrison JV,
Brown L,
McHugh CP,
Schurmann C,
Chen DD,
Liu YM,
Auer PL,
Laurie CA,
Taylor KD
and 15 more — show all
Browning BL,
Li Y,
Papanicolaou G,
Rotter JI,
Kurita R,
Nakamura Y,
Browning SR,
Loos RJF,
North KE,
Laurie CC,
Thornton TA,
Pankratz N,
Bauer DE,
Sofer T,
Reiner AP
PLoS genetics · 2017 · PMID 28453575 · open access
4 pages
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Aung N,
Vargas JD,
Yang C,
Fung K,
Sanghvi MM,
Piechnik SK,
Neubauer S,
Manichaikul A,
Rotter JI,
Taylor KD,
Lima JAC,
Bluemke DA
and 3 more — show all
Nature genetics · 2022 · PMID 35697868
4 pages
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
Harley JB,
Alarcón-Riquelme ME,
Criswell LA,
Jacob CO,
Kimberly RP,
Moser KL,
Tsao BP,
Vyse TJ,
Langefeld CD,
Nath SK,
Guthridge JM,
Cobb BL
and 29 more — show all
Mirel DB,
Marion MC,
Williams AH,
Divers J,
Wang W,
Frank SG,
Namjou B,
Gabriel SB,
Lee AT,
Gregersen PK,
Behrens TW,
Taylor KE,
Fernando M,
Zidovetzki R,
Gaffney PM,
Edberg JC,
Rioux JD,
Ojwang JO,
James JA,
Merrill JT,
Gilkeson GS,
Seldin MF,
Yin H,
Baechler EC,
Li QZ,
Wakeland EK,
Bruner GR,
Kaufman KM,
Kelly JA
International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN)
Nature genetics · 2008 · PMID 18204446
3 pages
Genome-wide association study of blood pressure and hypertension
Levy D,
Ehret GB,
Rice K,
Verwoert GC,
Launer LJ,
Dehghan A,
Glazer NL,
Morrison AC,
Johnson AD,
Aspelund T,
Aulchenko Y,
Lumley T
and 32 more — show all
Köttgen A,
Vasan RS,
Rivadeneira F,
Eiriksdottir G,
Guo X,
Arking DE,
Mitchell GF,
Mattace-Raso FU,
Smith AV,
Taylor K,
Scharpf RB,
Hwang SJ,
Sijbrands EJ,
Bis J,
Harris TB,
Ganesh SK,
O'Donnell CJ,
Hofman A,
Rotter JI,
Coresh J,
Benjamin EJ,
Uitterlinden AG,
Heiss G,
Fox CS,
Witteman JC,
Boerwinkle E,
Wang TJ,
Gudnason V,
Larson MG,
Chakravarti A,
Psaty BM,
van Duijn CM
Nature genetics · 2009 · PMID 19430479
3 pages
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
Gateva V,
Sandling JK,
Hom G,
Taylor KE,
Chung SA,
Sun X,
Ortmann W,
Kosoy R,
Ferreira RC,
Nordmark G,
Gunnarsson I,
Svenungsson E
and 24 more — show all
Padyukov L,
Sturfelt G,
Jönsen A,
Bengtsson AA,
Rantapää-Dahlqvist S,
Baechler EC,
Brown EE,
Alarcón GS,
Edberg JC,
Ramsey-Goldman R,
McGwin G Jr,
Reveille JD,
Vilá LM,
Kimberly RP,
Manzi S,
Petri MA,
Lee A,
Gregersen PK,
Seldin MF,
Rönnblom L,
Criswell LA,
Syvänen AC,
Behrens TW,
Graham RR
Nature genetics · 2009 · PMID 19838195
3 pages
Multiple loci are associated with white blood cell phenotypes
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
and 81 more — show all
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Below JE,
Parra EJ,
Gamazon ER,
Torres J,
Krithika S,
Candille S,
Lu Y,
Manichakul A,
Peralta-Romero J,
Duan Q,
Li Y,
Morris AP
and 13 more — show all
Gottesman O,
Bottinger E,
Wang XQ,
Taylor KD,
Ida Chen YD,
Rotter JI,
Rich SS,
Loos RJ,
Tang H,
Cox NJ,
Cruz M,
Hanis CL,
Valladares-Salgado A
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos
Jain D,
Hodonsky CJ,
Schick UM,
Morrison JV,
Minnerath S,
Brown L,
Schurmann C,
Liu Y,
Auer PL,
Laurie CA,
Taylor KD,
Browning BL
and 9 more — show all
Human molecular genetics · 2017 · PMID 28158719
3 pages
Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at <i>ID2</i>
Seyerle AA,
Lin HJ,
Gogarten SM,
Stilp A,
Méndez Giráldez R,
Soliman E,
Baldassari A,
Graff M,
Heckbert S,
Kerr KF,
Kooperberg C,
Rodriguez C
and 8 more — show all
Heart (British Cardiac Society) · 2018 · PMID 29127183
3 pages
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
Franceschini N,
Giambartolomei C,
de Vries PS,
Finan C,
Bis JC,
Huntley RP,
Lovering RC,
Tajuddin SM,
Winkler TW,
Graff M,
Kavousi M,
Dale C
and 146 more — show all
Smith AV,
Hofer E,
van Leeuwen EM,
Nolte IM,
Lu L,
Scholz M,
Sargurupremraj M,
Pitkänen N,
Franzén O,
Joshi PK,
Noordam R,
Marioni RE,
Hwang SJ,
Musani SK,
Schminke U,
Palmas W,
Isaacs A,
Correa A,
Zonderman AB,
Hofman A,
Teumer A,
Cox AJ,
Uitterlinden AG,
Wong A,
Smit AJ,
Newman AB,
Britton A,
Ruusalepp A,
Sennblad B,
Hedblad B,
Pasaniuc B,
Penninx BW,
Langefeld CD,
Wassel CL,
Tzourio C,
Fava C,
Baldassarre D,
O'Leary DH,
Teupser D,
Kuh D,
Tremoli E,
Mannarino E,
Grossi E,
Boerwinkle E,
Schadt EE,
Ingelsson E,
Veglia F,
Rivadeneira F,
Beutner F,
Chauhan G,
Heiss G,
Snieder H,
Campbell H,
Völzke H,
Markus HS,
Deary IJ,
Jukema JW,
de Graaf J,
Price J,
Pott J,
Hopewell JC,
Liang J,
Thiery J,
Engmann J,
Gertow K,
Rice K,
Taylor KD,
Dhana K,
Kiemeney LALM,
Lind L,
Raffield LM,
Launer LJ,
Holdt LM,
Dörr M,
Dichgans M,
Traylor M,
Sitzer M,
Kumari M,
Kivimaki M,
Nalls MA,
Melander O,
Raitakari O,
Franco OH,
Rueda-Ochoa OL,
Roussos P,
Whincup PH,
Amouyel P,
Giral P,
Anugu P,
Wong Q,
Malik R,
Rauramaa R,
Burkhardt R,
Hardy R,
Schmidt R,
de Mutsert R,
Morris RW,
Strawbridge RJ,
Wannamethee SG,
Hägg S,
Shah S,
McLachlan S,
Trompet S,
Seshadri S,
Kurl S,
Heckbert SR,
Ring S,
Harris TB,
Lehtimäki T,
Galesloot TE,
Shah T,
de Faire U,
Plagnol V,
Rosamond WD,
Post W,
Zhu X,
Zhang X,
Guo X,
Saba Y,
Dehghan A,
Seldenrijk A,
Morrison AC,
Hamsten A,
Psaty BM,
van Duijn CM,
Lawlor DA,
Mook-Kanamori DO,
Bowden DW,
Schmidt H,
Wilson JF,
Wilson JG,
Rotter JI,
Wardlaw JM,
Deanfield J,
Halcox J,
Lyytikäinen LP,
Loeffler M,
Evans MK,
Debette S,
Humphries SE,
Völker U,
Gudnason V,
Hingorani AD,
Björkegren JLM,
Casas JP,
O'Donnell CJ
MEGASTROKE Consortium
Nature communications · 2018 · PMID 30510157 · open access
3 pages
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
Swenson BR,
Louie T,
Lin HJ,
Méndez-Giráldez R,
Below JE,
Laurie CC,
Kerr KF,
Highland H,
Thornton TA,
Ryckman KK,
Kooperberg C,
Soliman EZ
and 18 more — show all
Seyerle AA,
Guo X,
Taylor KD,
Yao J,
Heckbert SR,
Darbar D,
Petty LE,
McKnight B,
Cheng S,
Bello NA,
Whitsel EA,
Hanis CL,
Nalls MA,
Evans DS,
Rotter JI,
Sofer T,
Avery CL,
Sotoodehnia N
PloS one · 2019 · PMID 31251759 · open access
3 pages
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
Fernández-Rhodes L,
Graff M,
Buchanan VL,
Justice AE,
Highland HM,
Guo X,
Zhu W,
Chen HH,
Young KL,
Adhikari K,
Palmer ND,
Below JE
and 104 more — show all
Bradfield J,
Pereira AC,
Glover L,
Kim D,
Lilly AG,
Shrestha P,
Thomas AG,
Zhang X,
Chen M,
Chiang CWK,
Pulit S,
Horimoto A,
Krieger JE,
Guindo-Martínez M,
Preuss M,
Schumann C,
Smit RAJ,
Torres-Mejía G,
Acuña-Alonzo V,
Bedoya G,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
González-José R,
Poletti G,
Rothhammer F,
Hakonarson H,
Igo R,
Adler SG,
Iyengar SK,
Nicholas SB,
Gogarten SM,
Isasi CR,
Papnicolaou G,
Stilp AM,
Qi Q,
Kho M,
Smith JA,
Langefeld CD,
Wagenknecht L,
Mckean-Cowdin R,
Gao XR,
Nousome D,
Conti DV,
Feng Y,
Allison MA,
Arzumanyan Z,
Buchanan TA,
Ida Chen YD,
Genter PM,
Goodarzi MO,
Hai Y,
Hsueh W,
Ipp E,
Kandeel FR,
Lam K,
Li X,
Nadler JL,
Raffel LJ,
Roll K,
Sandow K,
Tan J,
Taylor KD,
Xiang AH,
Yao J,
Audirac-Chalifour A,
de Jesus Peralta Romero J,
Hartwig F,
Horta B,
Blangero J,
Curran JE,
Duggirala R,
Lehman DE,
Puppala S,
Fejerman L,
John EM,
Aguilar-Salinas C,
Burtt NP,
Florez JC,
García-Ortíz H,
González-Villalpando C,
Mercader J,
Orozco L,
Tusié-Luna T,
Blanco E,
Gahagan S,
Cox NJ,
Hanis C,
Butte NF,
Cole SA,
Comuzzie AG,
Voruganti VS,
Rohde R,
Wang Y,
Sofer T,
Ziv E,
Grant SFA,
Ruiz-Linares A,
Rotter JI,
Haiman CA,
Parra EJ,
Cruz M,
Loos RJF,
North KE
HGG advances · 2022 · PMID 35399580 · open access
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
A genome-wide association study of carotid atherosclerosis in HIV-infected men
Shrestha S,
Irvin MR,
Taylor KD,
Wiener HW,
Pajewski NM,
Haritunians T,
Delaney JA,
Schambelan M,
Polak JF,
Arnett DK,
Chen YD,
Grunfeld C
AIDS (London, England) · 2010 · PMID 20009918
2 pages
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease
McGovern DP,
Jones MR,
Taylor KD,
Marciante K,
Yan X,
Dubinsky M,
Ippoliti A,
Vasiliauskas E,
Berel D,
Derkowski C,
Dutridge D,
Fleshner P
and 9 more — show all
International IBD Genetics Consortium
Human molecular genetics · 2010 · PMID 20570966
2 pages
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
and 45 more — show all
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
Taylor KD,
Li X,
Iyengar SK,
Xi Q,
Sivakumaran TA,
Mackey DA,
Macgregor S,
Martin NG,
Young TL,
Bis JC,
Wiggins KL,
Heckbert SR,
Hammond CJ,
Andrew T,
Fahy S,
Attia J,
Holliday EG,
Scott RJ,
Islam FM,
Rotter JI,
McAuley AK,
Boerwinkle E,
Tai ES,
Gudnason V,
Siscovick DS,
Vingerling JR,
Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
2 pages
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
Bis JC,
Kavousi M,
Franceschini N,
Isaacs A,
Abecasis GR,
Schminke U,
Post WS,
Smith AV,
Cupples LA,
Markus HS,
Schmidt R,
Huffman JE
and 81 more — show all
Lehtimäki T,
Baumert J,
Münzel T,
Heckbert SR,
Dehghan A,
North K,
Oostra B,
Bevan S,
Stoegerer EM,
Hayward C,
Raitakari O,
Meisinger C,
Schillert A,
Sanna S,
Völzke H,
Cheng YC,
Thorsson B,
Fox CS,
Rice K,
Rivadeneira F,
Nambi V,
Halperin E,
Petrovic KE,
Peltonen L,
Wichmann HE,
Schnabel RB,
Dörr M,
Parsa A,
Aspelund T,
Demissie S,
Kathiresan S,
Reilly MP,
Taylor K,
Uitterlinden A,
Couper DJ,
Sitzer M,
Kähönen M,
Illig T,
Wild PS,
Orru M,
Lüdemann J,
Shuldiner AR,
Eiriksdottir G,
White CC,
Rotter JI,
Hofman A,
Seissler J,
Zeller T,
Usala G,
Ernst F,
Launer LJ,
D'Agostino RB Sr,
O'Leary DH,
Ballantyne C,
Thiery J,
Ziegler A,
Lakatta EG,
Chilukoti RK,
Harris TB,
Wolf PA,
Psaty BM,
Polak JF,
Li X,
Rathmann W,
Uda M,
Boerwinkle E,
Klopp N,
Schmidt H,
Wilson JF,
Viikari J,
Koenig W,
Blankenberg S,
Newman AB,
Witteman J,
Heiss G,
Duijn Cv,
Scuteri A,
Homuth G,
Mitchell BD,
Gudnason V,
O'Donnell CJ
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
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
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
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