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90 matches for
North KE,
showing the first 10.
Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
Napier MD,
Franceschini N,
Gondalia R,
Stewart JD,
Méndez-Giráldez R,
Sitlani CM,
Seyerle AA,
Highland HM,
Li Y,
Wilhelmsen KC,
Yan S,
Duan Q
and 21 more — show all
Roach J,
Yao J,
Guo X,
Taylor KD,
Heckbert SR,
Rotter JI,
North KE,
Reiner AP,
Zhang ZM,
Tinker LF,
Liao D,
Laurie CC,
Gogarten SM,
Lin HJ,
Brody JA,
Bartz TM,
Psaty BM,
Sotoodehnia N,
Soliman EZ,
Avery CL,
Whitsel EA
Scientific reports · 2018 · PMID 29618737 · open access
1 page
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE,
Latourelle JC,
Wain LV,
Smith AV,
Grove ML,
Bartz TM,
Obeidat M,
Province MA,
Gao W,
Qaiser B,
Porteous DJ,
Cassano PA
and 95 more — show all
Ahluwalia TS,
Grarup N,
Li J,
Altmaier E,
Marten J,
Harris SE,
Manichaikul A,
Pottinger TD,
Li-Gao R,
Lind-Thomsen A,
Mahajan A,
Lahousse L,
Imboden M,
Teumer A,
Prins B,
Lyytikäinen LP,
Eiriksdottir G,
Franceschini N,
Sitlani CM,
Brody JA,
Bossé Y,
Timens W,
Kraja A,
Loukola A,
Tang W,
Liu Y,
Bork-Jensen J,
Justesen JM,
Linneberg A,
Lange LA,
Rawal R,
Karrasch S,
Huffman JE,
Smith BH,
Davies G,
Burkart KM,
Mychaleckyj JC,
Bonten TN,
Enroth S,
Lind L,
Brusselle GG,
Kumar A,
Stubbe B,
Kähönen M,
Wyss AB,
Psaty BM,
Heckbert SR,
Hao K,
Rantanen T,
Kritchevsky SB,
Lohman K,
Skaaby T,
Pisinger C,
Hansen T,
Schulz H,
Polasek O,
Campbell A,
Starr JM,
Rich SS,
Mook-Kanamori DO,
Johansson Å,
Ingelsson E,
Uitterlinden AG,
Weiss S,
Raitakari OT,
Gudnason V,
North KE,
Gharib SA,
Sin DD,
Taylor KD,
O'Connor GT,
Kaprio J,
Harris TB,
Pederson O,
Vestergaard H,
Wilson JG,
Strauch K,
Hayward C,
Kerr S,
Deary IJ,
Barr RG,
de Mutsert R,
Gyllensten U,
Morris AP,
Ikram MA,
Probst-Hensch N,
Gläser S,
Zeggini E,
Lehtimäki T,
Strachan DP,
Dupuis J,
Morrison AC,
Hall IP,
Tobin MD,
London SJ
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
1 page
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
and 69 more — show all
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
Ansell SM,
Maria A,
Diver WR,
Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
1 page
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
and 290 more — show all
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
and 74 more — show all
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
1 page
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Yaghootkar H,
Zhang Y,
Spracklen CN,
Karaderi T,
Huang LO,
Bradfield J,
Schurmann C,
Fine RS,
Preuss MH,
Kutalik Z,
Wittemans LBL,
Lu Y
and 104 more — show all
Metz S,
Willems SM,
Li-Gao R,
Grarup N,
Wang S,
Molnos S,
Sandoval-Zárate AA,
Nalls MA,
Lange LA,
Haesser J,
Guo X,
Lyytikäinen LP,
Feitosa MF,
Sitlani CM,
Venturini C,
Mahajan A,
Kacprowski T,
Wang CA,
Chasman DI,
Amin N,
Broer L,
Robertson N,
Young KL,
Allison M,
Auer PL,
Blüher M,
Borja JB,
Bork-Jensen J,
Carrasquilla GD,
Christofidou P,
Demirkan A,
Doege CA,
Garcia ME,
Graff M,
Guo K,
Hakonarson H,
Hong J,
Ida Chen YD,
Jackson R,
Jakupović H,
Jousilahti P,
Justice AE,
Kähönen M,
Kizer JR,
Kriebel J,
LeDuc CA,
Li J,
Lind L,
Luan J,
Mackey DA,
Mangino M,
Männistö S,
Martin Carli JF,
Medina-Gomez C,
Mook-Kanamori DO,
Morris AP,
de Mutsert R,
Nauck M,
Prokic I,
Pennell CE,
Pradhan AD,
Psaty BM,
Raitakari OT,
Scott RA,
Skaaby T,
Strauch K,
Taylor KD,
Teumer A,
Uitterlinden AG,
Wu Y,
Yao J,
Walker M,
North KE,
Kovacs P,
Ikram MA,
van Duijn CM,
Ridker PM,
Lye S,
Homuth G,
Ingelsson E,
Spector TD,
McKnight B,
Province MA,
Lehtimäki T,
Adair LS,
Rotter JI,
Reiner AP,
Wilson JG,
Harris TB,
Ripatti S,
Grallert H,
Meigs JB,
Salomaa V,
Hansen T,
Willems van Dijk K,
Wareham NJ,
Grant SFA,
Langenberg C,
Frayling TM,
Lindgren CM,
Mohlke KL,
Leibel RL,
Loos RJF,
Kilpeläinen TO
Diabetes · 2020 · PMID 32917775
1 page
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade BE,
Lee J,
Sofer T,
Wang H,
Zhang M,
Chen H,
Gharib SA,
Gottlieb DJ,
Guo X,
Lane JM,
Liang J,
Lin X
and 27 more — show all
Mei H,
Patel SR,
Purcell SM,
Saxena R,
Shah NA,
Evans DS,
Hanis CL,
Hillman DR,
Mukherjee S,
Palmer LJ,
Stone KL,
Tranah GJ,
Abecasis GR,
Boerwinkle EA,
Correa A,
Cupples LA,
Kaplan RC,
Nickerson DA,
North KE,
Psaty BM,
Rotter JI,
Rich SS,
Tracy RP,
Vasan RS,
Wilson JG,
Zhu X,
Redline S
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Sleep Working Group
Genome medicine · 2021 · PMID 34446064 · open access
1 page
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
and 81 more — show all
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
1 page
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
1 page
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
1 page
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away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
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
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.