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40 matches for
Grant SF,
showing the first 20.
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Li J,
Glessner JT,
Zhang H,
Hou C,
Wei Z,
Bradfield JP,
Mentch FD,
Guo Y,
Kim C,
Xia Q,
Chiavacci RM,
Thomas KA
and 5 more — show all
Human molecular genetics · 2013 · PMID 23263863
4 pages
Genetic effects on the timing of parturition and links to fetal birth weight
Solé-Navais P,
Flatley C,
Steinthorsdottir V,
Vaudel M,
Juodakis J,
Chen J,
Laisk T,
LaBella AL,
Westergaard D,
Bacelis J,
Brumpton B,
Skotte L
and 73 more — show all
Borges MC,
Helgeland Ø,
Mahajan A,
Wielscher M,
Lin F,
Briggs C,
Wang CA,
Moen GH,
Beaumont RN,
Bradfield JP,
Abraham A,
Thorleifsson G,
Gabrielsen ME,
Ostrowski SR,
Modzelewska D,
Nohr EA,
Hypponen E,
Srivastava A,
Talbot O,
Allard C,
Williams SM,
Menon R,
Shields BM,
Sveinbjornsson G,
Xu H,
Melbye M,
Lowe W Jr,
Bouchard L,
Oken E,
Pedersen OB,
Gudbjartsson DF,
Erikstrup C,
Sørensen E,
Lie RT,
Teramo K,
Hallman M,
Juliusdottir T,
Hakonarson H,
Ullum H,
Hattersley AT,
Sletner L,
Merialdi M,
Rifas-Shiman SL,
Steingrimsdottir T,
Scholtens D,
Power C,
West J,
Nyegaard M,
Capra JA,
Skogholt AH,
Magnus P,
Andreassen OA,
Thorsteinsdottir U,
Grant SFA,
Qvigstad E,
Pennell CE,
Hivert MF,
Hayes GM,
Jarvelin MR,
McCarthy MI,
Lawlor DA,
Nielsen HS,
Mägi R,
Rokas A,
Hveem K,
Stefansson K,
Feenstra B,
Njolstad P,
Muglia LJ,
Freathy RM,
Johansson S,
Zhang G,
Jacobsson B
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Bustamante M,
Standl M,
Bassat Q,
Vilor-Tejedor N,
Medina-Gomez C,
Bonilla C,
Ahluwalia TS,
Bacelis J,
Bradfield JP,
Tiesler CM,
Rivadeneira F,
Ring S
and 27 more — show all
Vissing NH,
Fink NR,
Jugessur A,
Mentch FD,
Ballester F,
Kriebel J,
Kiefte-de Jong JC,
Wolsk HM,
Llop S,
Thiering E,
Beth SA,
Timpson NJ,
Andersen J,
Schulz H,
Jaddoe VW,
Evans DM,
Waage J,
Hakonarson H,
Grant SF,
Jacobsson B,
Bønnelykke K,
Bisgaard H,
Davey Smith G,
Moll HA,
Heinrich J,
Estivill X,
Sunyer J
Human molecular genetics · 2016 · PMID 27559109
3 pages
Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton
Mitchell JA,
Chesi A,
Cousminer DL,
McCormack SE,
Kalkwarf HJ,
Lappe JM,
Gilsanz V,
Oberfield SE,
Shepherd JA,
Kelly A,
Zemel BS,
Grant SF
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2018 · PMID 29240982
3 pages
Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche
Sarnowski C,
Cousminer DL,
Franceschini N,
Raffield LM,
Jia G,
Fernández-Rhodes L,
Grant SFA,
Hakonarson H,
Lange LA,
Long J,
Sofer T,
Tao R
and 13 more — show all
Wallace RB,
Wong Q,
Zirpoli G,
Boerwinkle E,
Bradfield JP,
Correa A,
Kooperberg CL,
North KE,
Palmer JR,
Zemel BS,
Zheng W,
Murabito JM,
Lunetta KL
Human reproduction (Oxford, England) · 2021 · PMID 34021356
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
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakonarson H,
Grant SF,
Bradfield JP,
Marchand L,
Kim CE,
Glessner JT,
Grabs R,
Casalunovo T,
Taback SP,
Frackelton EC,
Lawson ML,
Robinson LJ
and 11 more — show all
Skraban R,
Lu Y,
Chiavacci RM,
Stanley CA,
Kirsch SE,
Rappaport EF,
Orange JS,
Monos DS,
Devoto M,
Qu HQ,
Polychronakos C
Nature · 2007 · PMID 17632545
2 pages
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
Kugathasan S,
Baldassano RN,
Bradfield JP,
Sleiman PM,
Imielinski M,
Guthery SL,
Cucchiara S,
Kim CE,
Frackelton EC,
Annaiah K,
Glessner JT,
Santa E
and 18 more — show all
Willson T,
Eckert AW,
Bonkowski E,
Shaner JL,
Smith RM,
Otieno FG,
Peterson N,
Abrams DJ,
Chiavacci RM,
Grundmeier R,
Mamula P,
Tomer G,
Piccoli DA,
Monos DS,
Annese V,
Denson LA,
Grant SF,
Hakonarson H
Nature genetics · 2008 · PMID 18758464
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
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
and 105 more — show all
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
Jacobsson B,
Jarvelin MR,
Atalay M,
Koppelman GH,
Pennell CE,
Niinikoski H,
Dedoussis GV,
Mccarthy MI,
Frayling TM,
Sunyer J,
Timpson NJ,
Rivadeneira F,
Bønnelykke K,
Jaddoe VW
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites
Chesi A,
Mitchell JA,
Kalkwarf HJ,
Bradfield JP,
Lappe JM,
Cousminer DL,
Roy SM,
McCormack SE,
Gilsanz V,
Oberfield SE,
Hakonarson H,
Shepherd JA
and 3 more — show all
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017 · PMID 28181694
2 pages
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Cousminer DL,
Ahlqvist E,
Mishra R,
Andersen MK,
Chesi A,
Hawa MI,
Davis A,
Hodge KM,
Bradfield JP,
Zhou K,
Guy VC,
Åkerlund M
and 41 more — show all
Wod M,
Fritsche LG,
Vestergaard H,
Snyder J,
Højlund K,
Linneberg A,
Käräjämäki A,
Brandslund I,
Kim CE,
Witte D,
Sørgjerd EP,
Brillon DJ,
Pedersen O,
Beck-Nielsen H,
Grarup N,
Pratley RE,
Rickels MR,
Vella A,
Ovalle F,
Melander O,
Harris RI,
Varvel S,
Grill VER,
Hakonarson H,
Froguel P,
Lonsdale JT,
Mauricio D,
Schloot NC,
Khunti K,
Greenbaum CJ,
Åsvold BO,
Yderstræde KB,
Pearson ER,
Schwartz S,
Voight BF,
Hansen T,
Tuomi T,
Boehm BO,
Groop L,
Leslie RD,
Grant SFA
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
2 pages
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes
Forgetta V,
Manousaki D,
Istomine R,
Ross S,
Tessier MC,
Marchand L,
Li M,
Qu HQ,
Bradfield JP,
Grant SFA,
Hakonarson H,
Paterson AD
and 3 more — show all
DCCT/EDIC Research Group
Diabetes · 2020 · PMID 32005708 · open access
2 pages
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Yang C,
Veenstra J,
Bartz TM,
Pahl MC,
Hallmark B,
Chen YI,
Westra J,
Steffen LM,
Brown CD,
Siscovick D,
Tsai MY,
Wood AC
and 9 more — show all
Communications biology · 2023 · PMID 37587153 · open access
2 pages
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Solé-Navais P,
Juodakis J,
Ytterberg K,
Wu X,
Bradfield JP,
Vaudel M,
LaBella AL,
Helgeland Ø,
Flatley C,
Geller F,
Finel M,
Zhao M
and 11 more — show all
Lazarus P,
Hakonarson H,
Magnus P,
Andreassen OA,
Njølstad PR,
Grant SFA,
Feenstra B,
Muglia LJ,
Johansson S,
Zhang G,
Jacobsson B
Nature communications · 2024 · PMID 39214992 · open access
2 pages
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram MA,
Fornage M,
Smith AV,
Seshadri S,
Schmidt R,
Debette S,
Vrooman HA,
Sigurdsson S,
Ropele S,
Taal HR,
Mook-Kanamori DO,
Coker LH
and 44 more — show all
Longstreth WT Jr,
Niessen WJ,
DeStefano AL,
Beiser A,
Zijdenbos AP,
Struchalin M,
Jack CR Jr,
Rivadeneira F,
Uitterlinden AG,
Knopman DS,
Hartikainen AL,
Pennell CE,
Thiering E,
Steegers EA,
Hakonarson H,
Heinrich J,
Palmer LJ,
Jarvelin MR,
McCarthy MI,
Grant SF,
St Pourcain B,
Timpson NJ,
Smith GD,
Sovio U,
Nalls MA,
Au R,
Hofman A,
Gudnason H,
van der Lugt A,
Harris TB,
Meeks WM,
Vernooij MW,
van Buchem MA,
Catellier D,
Jaddoe VW,
Gudnason V,
Windham BG,
Wolf PA,
van Duijn CM,
Mosley TH Jr,
Schmidt H,
Launer LJ,
Breteler MM,
DeCarli C
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
1 page
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Beaumont RN,
Warrington NM,
Cavadino A,
Tyrrell J,
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Huikari V,
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Grant SFA,
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Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
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Questions about this list
Why is my paper here? I never gave you permission.
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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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