For researchers
Is your paper here?
2,660 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
67 matches for
He H,
showing the first 20.
Seventy-five genetic loci influencing the human red blood cell
van der Harst P,
Zhang W,
Mateo Leach I,
Rendon A,
Verweij N,
Sehmi J,
Paul DS,
Elling U,
Allayee H,
Li X,
Radhakrishnan A,
Tan ST
and 183 more — show all
Voss K,
Weichenberger CX,
Albers CA,
Al-Hussani A,
Asselbergs FW,
Ciullo M,
Danjou F,
Dina C,
Esko T,
Evans DM,
Franke L,
Gögele M,
Hartiala J,
Hersch M,
Holm H,
Hottenga JJ,
Kanoni S,
Kleber ME,
Lagou V,
Langenberg C,
Lopez LM,
Lyytikäinen LP,
Melander O,
Murgia F,
Nolte IM,
O'Reilly PF,
Padmanabhan S,
Parsa A,
Pirastu N,
Porcu E,
Portas L,
Prokopenko I,
Ried JS,
Shin SY,
Tang CS,
Teumer A,
Traglia M,
Ulivi S,
Westra HJ,
Yang J,
Zhao JH,
Anni F,
Abdellaoui A,
Attwood A,
Balkau B,
Bandinelli S,
Bastardot F,
Benyamin B,
Boehm BO,
Cookson WO,
Das D,
de Bakker PI,
de Boer RA,
de Geus EJ,
de Moor MH,
Dimitriou M,
Domingues FS,
Döring A,
Engström G,
Eyjolfsson GI,
Ferrucci L,
Fischer K,
Galanello R,
Garner SF,
Genser B,
Gibson QD,
Girotto G,
Gudbjartsson DF,
Harris SE,
Hartikainen AL,
Hastie CE,
Hedblad B,
Illig T,
Jolley J,
Kähönen M,
Kema IP,
Kemp JP,
Liang L,
Lloyd-Jones H,
Loos RJ,
Meacham S,
Medland SE,
Meisinger C,
Memari Y,
Mihailov E,
Miller K,
Moffatt MF,
Nauck M,
Novatchkova M,
Nutile T,
Olafsson I,
Onundarson PT,
Parracciani D,
Penninx BW,
Perseu L,
Piga A,
Pistis G,
Pouta A,
Puc U,
Raitakari O,
Ring SM,
Robino A,
Ruggiero D,
Ruokonen A,
Saint-Pierre A,
Sala C,
Salumets A,
Sambrook J,
Schepers H,
Schmidt CO,
Silljé HH,
Sladek R,
Smit JH,
Starr JM,
Stephens J,
Sulem P,
Tanaka T,
Thorsteinsdottir U,
Tragante V,
van Gilst WH,
van Pelt LJ,
van Veldhuisen DJ,
Völker U,
Whitfield JB,
Willemsen G,
Winkelmann BR,
Wirnsberger G,
Algra A,
Cucca F,
d'Adamo AP,
Danesh J,
Deary IJ,
Dominiczak AF,
Elliott P,
Fortina P,
Froguel P,
Gasparini P,
Greinacher A,
Hazen SL,
Jarvelin MR,
Khaw KT,
Lehtimäki T,
Maerz W,
Martin NG,
Metspalu A,
Mitchell BD,
Montgomery GW,
Moore C,
Navis G,
Pirastu M,
Pramstaller PP,
Ramirez-Solis R,
Schadt E,
Scott J,
Shuldiner AR,
Smith GD,
Smith JG,
Snieder H,
Sorice R,
Spector TD,
Stefansson K,
Stumvoll M,
Tang WH,
Toniolo D,
Tönjes A,
Visscher PM,
Vollenweider P,
Wareham NJ,
Wolffenbuttel BH,
Boomsma DI,
Beckmann JS,
Dedoussis GV,
Deloukas P,
Ferreira MA,
Sanna S,
Uda M,
Hicks AA,
Penninger JM,
Gieger C,
Kooner JS,
Ouwehand WH,
Soranzo N,
Chambers JC
Nature · 2012 · PMID 23222517
12 pages+
Connecting genetic risk to disease end points through the human blood plasma proteome
Suhre K,
Arnold M,
Bhagwat AM,
Cotton RJ,
Engelke R,
Raffler J,
Sarwath H,
Thareja G,
Wahl A,
DeLisle RK,
Gold L,
Pezer M
and 12 more — show all
Lauc G,
El-Din Selim MA,
Mook-Kanamori DO,
Al-Dous EK,
Mohamoud YA,
Malek J,
Strauch K,
Grallert H,
Peters A,
Kastenmüller G,
Gieger C,
Graumann J
Nature communications · 2017 · PMID 28240269 · open access
12 pages+
Genomic atlas of the human plasma proteome
Sun BB,
Maranville JC,
Peters JE,
Stacey D,
Staley JR,
Blackshaw J,
Burgess S,
Jiang T,
Paige E,
Surendran P,
Oliver-Williams C,
Kamat MA
and 21 more — show all
Prins BP,
Wilcox SK,
Zimmerman ES,
Chi A,
Bansal N,
Spain SL,
Wood AM,
Morrell NW,
Bradley JR,
Janjic N,
Roberts DJ,
Ouwehand WH,
Todd JA,
Soranzo N,
Suhre K,
Paul DS,
Fox CS,
Plenge RM,
Danesh J,
Runz H,
Butterworth AS
Nature · 2018 · PMID 29875488
12 pages+
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
and 65 more — show all
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
The genetic architecture of the human cerebral cortex
Grasby KL,
Jahanshad N,
Painter JN,
Colodro-Conde L,
Bralten J,
Hibar DP,
Lind PA,
Pizzagalli F,
Ching CRK,
McMahon MAB,
Shatokhina N,
Zsembik LCP
and 348 more — show all
Thomopoulos SI,
Zhu AH,
Strike LT,
Agartz I,
Alhusaini S,
Almeida MAA,
Alnæs D,
Amlien IK,
Andersson M,
Ard T,
Armstrong NJ,
Ashley-Koch A,
Atkins JR,
Bernard M,
Brouwer RM,
Buimer EEL,
Bülow R,
Bürger C,
Cannon DM,
Chakravarty M,
Chen Q,
Cheung JW,
Couvy-Duchesne B,
Dale AM,
Dalvie S,
de Araujo TK,
de Zubicaray GI,
de Zwarte SMC,
den Braber A,
Doan NT,
Dohm K,
Ehrlich S,
Engelbrecht HR,
Erk S,
Fan CC,
Fedko IO,
Foley SF,
Ford JM,
Fukunaga M,
Garrett ME,
Ge T,
Giddaluru S,
Goldman AL,
Green MJ,
Groenewold NA,
Grotegerd D,
Gurholt TP,
Gutman BA,
Hansell NK,
Harris MA,
Harrison MB,
Haswell CC,
Hauser M,
Herms S,
Heslenfeld DJ,
Ho NF,
Hoehn D,
Hoffmann P,
Holleran L,
Hoogman M,
Hottenga JJ,
Ikeda M,
Janowitz D,
Jansen IE,
Jia T,
Jockwitz C,
Kanai R,
Karama S,
Kasperaviciute D,
Kaufmann T,
Kelly S,
Kikuchi M,
Klein M,
Knapp M,
Knodt AR,
Krämer B,
Lam M,
Lancaster TM,
Lee PH,
Lett TA,
Lewis LB,
Lopes-Cendes I,
Luciano M,
Macciardi F,
Marquand AF,
Mathias SR,
Melzer TR,
Milaneschi Y,
Mirza-Schreiber N,
Moreira JCV,
Mühleisen TW,
Müller-Myhsok B,
Najt P,
Nakahara S,
Nho K,
Olde Loohuis LM,
Orfanos DP,
Pearson JF,
Pitcher TL,
Pütz B,
Quidé Y,
Ragothaman A,
Rashid FM,
Reay WR,
Redlich R,
Reinbold CS,
Repple J,
Richard G,
Riedel BC,
Risacher SL,
Rocha CS,
Mota NR,
Salminen L,
Saremi A,
Saykin AJ,
Schlag F,
Schmaal L,
Schofield PR,
Secolin R,
Shapland CY,
Shen L,
Shin J,
Shumskaya E,
Sønderby IE,
Sprooten E,
Tansey KE,
Teumer A,
Thalamuthu A,
Tordesillas-Gutiérrez D,
Turner JA,
Uhlmann A,
Vallerga CL,
van der Meer D,
van Donkelaar MMJ,
van Eijk L,
van Erp TGM,
van Haren NEM,
van Rooij D,
van Tol MJ,
Veldink JH,
Verhoef E,
Walton E,
Wang M,
Wang Y,
Wardlaw JM,
Wen W,
Westlye LT,
Whelan CD,
Witt SH,
Wittfeld K,
Wolf C,
Wolfers T,
Wu JQ,
Yasuda CL,
Zaremba D,
Zhang Z,
Zwiers MP,
Artiges E,
Assareh AA,
Ayesa-Arriola R,
Belger A,
Brandt CL,
Brown GG,
Cichon S,
Curran JE,
Davies GE,
Degenhardt F,
Dennis MF,
Dietsche B,
Djurovic S,
Doherty CP,
Espiritu R,
Garijo D,
Gil Y,
Gowland PA,
Green RC,
Häusler AN,
Heindel W,
Ho BC,
Hoffmann WU,
Holsboer F,
Homuth G,
Hosten N,
Jack CR Jr,
Jang M,
Jansen A,
Kimbrel NA,
Kolskår K,
Koops S,
Krug A,
Lim KO,
Luykx JJ,
Mathalon DH,
Mather KA,
Mattay VS,
Matthews S,
Mayoral Van Son J,
McEwen SC,
Melle I,
Morris DW,
Mueller BA,
Nauck M,
Nordvik JE,
Nöthen MM,
O'Leary DS,
Opel N,
Martinot MP,
Pike GB,
Preda A,
Quinlan EB,
Rasser PE,
Ratnakar V,
Reppermund S,
Steen VM,
Tooney PA,
Torres FR,
Veltman DJ,
Voyvodic JT,
Whelan R,
White T,
Yamamori H,
Adams HHH,
Bis JC,
Debette S,
Decarli C,
Fornage M,
Gudnason V,
Hofer E,
Ikram MA,
Launer L,
Longstreth WT,
Lopez OL,
Mazoyer B,
Mosley TH,
Roshchupkin GV,
Satizabal CL,
Schmidt R,
Seshadri S,
Yang Q,
Alvim MKM,
Ames D,
Anderson TJ,
Andreassen OA,
Arias-Vasquez A,
Bastin ME,
Baune BT,
Beckham JC,
Blangero J,
Boomsma DI,
Brodaty H,
Brunner HG,
Buckner RL,
Buitelaar JK,
Bustillo JR,
Cahn W,
Cairns MJ,
Calhoun V,
Carr VJ,
Caseras X,
Caspers S,
Cavalleri GL,
Cendes F,
Corvin A,
Crespo-Facorro B,
Dalrymple-Alford JC,
Dannlowski U,
de Geus EJC,
Deary IJ,
Delanty N,
Depondt C,
Desrivières S,
Donohoe G,
Espeseth T,
Fernández G,
Fisher SE,
Flor H,
Forstner AJ,
Francks C,
Franke B,
Glahn DC,
Gollub RL,
Grabe HJ,
Gruber O,
Håberg AK,
Hariri AR,
Hartman CA,
Hashimoto R,
Heinz A,
Henskens FA,
Hillegers MHJ,
Hoekstra PJ,
Holmes AJ,
Hong LE,
Hopkins WD,
Hulshoff Pol HE,
Jernigan TL,
Jönsson EG,
Kahn RS,
Kennedy MA,
Kircher TTJ,
Kochunov P,
Kwok JBJ,
Le Hellard S,
Loughland CM,
Martin NG,
Martinot JL,
McDonald C,
McMahon KL,
Meyer-Lindenberg A,
Michie PT,
Morey RA,
Mowry B,
Nyberg L,
Oosterlaan J,
Ophoff RA,
Pantelis C,
Paus T,
Pausova Z,
Penninx BWJH,
Polderman TJC,
Posthuma D,
Rietschel M,
Roffman JL,
Rowland LM,
Sachdev PS,
Sämann PG,
Schall U,
Schumann G,
Scott RJ,
Sim K,
Sisodiya SM,
Smoller JW,
Sommer IE,
St Pourcain B,
Stein DJ,
Toga AW,
Trollor JN,
Van der Wee NJA,
van 't Ent D,
Völzke H,
Walter H,
Weber B,
Weinberger DR,
Wright MJ,
Zhou J,
Stein JL,
Thompson PM,
Medland SE
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Zhou W,
Brumpton B,
Kabil O,
Gudmundsson J,
Thorleifsson G,
Weinstock J,
Zawistowski M,
Nielsen JB,
Chaker L,
Medici M,
Teumer A,
Naitza S
and 44 more — show all
Sanna S,
Schultheiss UT,
Cappola A,
Karjalainen J,
Kurki M,
Oneka M,
Taylor P,
Fritsche LG,
Graham SE,
Wolford BN,
Overton W,
Rasheed H,
Haug EB,
Gabrielsen ME,
Skogholt AH,
Surakka I,
Davey Smith G,
Pandit A,
Roychowdhury T,
Hornsby WE,
Jonasson JG,
Senter L,
Liyanarachchi S,
Ringel MD,
Xu L,
Kiemeney LA,
He H,
Netea-Maier RT,
Mayordomo JI,
Plantinga TS,
Hrafnkelsson J,
Hjartarson H,
Sturgis EM,
Palotie A,
Daly M,
Citterio CE,
Arvan P,
Brummett CM,
Boehnke M,
de la Chapelle A,
Stefansson K,
Hveem K,
Willer CJ,
Åsvold BO
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
Feofanova EV,
Chen H,
Dai Y,
Jia P,
Grove ML,
Morrison AC,
Qi Q,
Daviglus M,
Cai J,
North KE,
Laurie CC,
Kaplan RC
and 2 more — show all
American journal of human genetics · 2020 · PMID 33031748
12 pages+
Insights into the genetic architecture of the human face
White JD,
Indencleef K,
Naqvi S,
Eller RJ,
Hoskens H,
Roosenboom J,
Lee MK,
Li J,
Mohammed J,
Richmond S,
Quillen EE,
Norton HL
and 11 more — show all
Feingold E,
Swigut T,
Marazita ML,
Peeters H,
Hens G,
Shaffer JR,
Wysocka J,
Walsh S,
Weinberg SM,
Shriver MD,
Claes P
Nature genetics · 2021 · PMID 33288918 · open access
12 pages+
Deep learning enables genetic analysis of the human thoracic aorta
Pirruccello JP,
Chaffin MD,
Chou EL,
Fleming SJ,
Lin H,
Nekoui M,
Khurshid S,
Friedman SF,
Bick AG,
Arduini A,
Weng LC,
Choi SH
and 18 more — show all
Akkad AD,
Batra P,
Tucker NR,
Hall AW,
Roselli C,
Benjamin EJ,
Vellarikkal SK,
Gupta RM,
Stegmann CM,
Juric D,
Stone JR,
Vasan RS,
Ho JE,
Hoffmann U,
Lubitz SA,
Philippakis AA,
Lindsay ME,
Ellinor PT
Nature genetics · 2022 · PMID 34837083 · open access
12 pages+
An Amish founder population reveals rare-population genetic determinants of the human lipidome
Montasser ME,
Aslibekyan S,
Srinivasasainagendra V,
Tiwari HK,
Patki A,
Bagheri M,
Kind T,
Barupal DK,
Fan S,
Perry J,
Ryan KA,
Shuldiner AR
and 4 more — show all
Communications biology · 2022 · PMID 35393526 · open access
12 pages+
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Cadby G,
Giles C,
Melton PE,
Huynh K,
Mellett NA,
Duong T,
Nguyen A,
Cinel M,
Smith A,
Olshansky G,
Wang T,
Brozynska M
and 32 more — show all
Inouye M,
McCarthy NS,
Ariff A,
Hung J,
Hui J,
Beilby J,
Dubé MP,
Watts GF,
Shah S,
Wray NR,
Lim WLF,
Chatterjee P,
Martins I,
Laws SM,
Porter T,
Vacher M,
Bush AI,
Rowe CC,
Villemagne VL,
Ames D,
Masters CL,
Taddei K,
Arnold M,
Kastenmüller G,
Nho K,
Saykin AJ,
Han X,
Kaddurah-Daouk R,
Martins RN,
Blangero J,
Meikle PJ,
Moses EK
Nature communications · 2022 · PMID 35668104 · open access
12 pages+
The X chromosome's influences on the human brain
Jiang Z,
Sullivan PF,
Li T,
Zhao B,
Wang X,
Luo T,
Huang S,
Guan PY,
Chen J,
Yang Y,
Stein JL,
Li Y
and 3 more — show all
Science advances · 2025 · PMID 39854466 · open access
12 pages+
The Genetic Architecture of the Human Corpus Callosum and its Subregions
Bhatt RR,
Gadewar SP,
Shetty A,
Ba Gari I,
Haddad E,
Javid S,
Ramesh A,
Nourollahimoghadam E,
Zhu AH,
de Leeuw C,
Thompson PM,
Medland SE
and 1 more — show all
Nature communications · 2025 · PMID 41188267 · open access
12 pages+
Genetic study identifies novel genes in developmental dysplasia of the hip
Yoshino S,
Chen S,
Yamaguchi R,
Kurakazu T,
Hatzikotoulas K,
Koike Y,
Inoue D,
Kohno Y,
Sasaki K,
Choe H,
Baba S,
Hara T
and 31 more — show all
Ito J,
Okuzu Y,
Shiomoto K,
Nakamura T,
Koyano G,
Shimizu T,
Kinoshita K,
Takahashi E,
Utsunomiya T,
Hara D,
Sato T,
Kawahara S,
Kaneuji A,
Yamamoto T,
Takahashi D,
Jinno T,
Kawano T,
Goto K,
Takagi M,
Mawatari T,
Inaba Y,
Nakamura T,
Kabata T,
Hamai S,
Motomura G,
Southam L,
Wilkinson JM,
Zeggini E,
Ikegawa S,
Nakashima Y,
Terao C
Bone research · 2026 · PMID 41912496 · open access
9 pages
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Soranzo N,
Spector TD,
Mangino M,
Kühnel B,
Rendon A,
Teumer A,
Willenborg C,
Wright B,
Chen L,
Li M,
Salo P,
Voight BF
and 68 more — show all
Burns P,
Laskowski RA,
Xue Y,
Menzel S,
Altshuler D,
Bradley JR,
Bumpstead S,
Burnett MS,
Devaney J,
Döring A,
Elosua R,
Epstein SE,
Erber W,
Falchi M,
Garner SF,
Ghori MJ,
Goodall AH,
Gwilliam R,
Hakonarson HH,
Hall AS,
Hammond N,
Hengstenberg C,
Illig T,
König IR,
Knouff CW,
McPherson R,
Melander O,
Mooser V,
Nauck M,
Nieminen MS,
O'Donnell CJ,
Peltonen L,
Potter SC,
Prokisch H,
Rader DJ,
Rice CM,
Roberts R,
Salomaa V,
Sambrook J,
Schreiber S,
Schunkert H,
Schwartz SM,
Serbanovic-Canic J,
Sinisalo J,
Siscovick DS,
Stark K,
Surakka I,
Stephens J,
Thompson JR,
Völker U,
Völzke H,
Watkins NA,
Wells GA,
Wichmann HE,
Van Heel DA,
Tyler-Smith C,
Thein SL,
Kathiresan S,
Perola M,
Reilly MP,
Stewart AF,
Erdmann J,
Samani NJ,
Meisinger C,
Greinacher A,
Deloukas P,
Ouwehand WH,
Gieger C
Nature genetics · 2009 · PMID 19820697
8 pages
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies
Strippel C,
Herrera-Rivero M,
Wendorff M,
Tietz AK,
Degenhardt F,
Witten A,
Schroeter C,
Nelke C,
Golombeck KS,
Madlener M,
Rüber T,
Ernst L
and 57 more — show all
Racz A,
Baumgartner T,
Widman G,
Doppler K,
Thaler F,
Siebenbrodt K,
Dik A,
Kerin C,
Räuber S,
Gallus M,
Kovac S,
Grauer OM,
Grimm A,
Prüss H,
Wickel J,
Geis C,
Lewerenz J,
Goebels N,
Ringelstein M,
Menge T,
Tackenberg B,
Kellinghaus C,
Bien CG,
Kraft A,
Zettl U,
Ismail FS,
Ayzenberg I,
Urbanek C,
Sühs KW,
Tauber SC,
Mues S,
Körtvélyessy P,
Markewitz R,
Paliantonis A,
Elger CE,
Surges R,
Sommer C,
Kümpfel T,
Gross CC,
Lerche H,
Wellmer J,
Quesada CM,
Then Bergh F,
Wandinger KP,
Becker AJ,
Kunz WS,
Meyer Zu Hörste G,
Malter MP,
Rosenow F,
Wiendl H,
Kuhlenbäumer G,
Leypoldt F,
Lieb W,
Franke A,
Meuth SG,
Stoll M,
Melzer N
German Network for Research on Autoimmune Encephalitis (GENERATE)
Brain : a journal of neurology · 2023 · PMID 35348614 · open access
7 pages
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Scelo G,
Purdue MP,
Brown KM,
Johansson M,
Wang Z,
Eckel-Passow JE,
Ye Y,
Hofmann JN,
Choi J,
Foll M,
Gaborieau V,
Machiela MJ
and 111 more — show all
Colli LM,
Li P,
Sampson JN,
Abedi-Ardekani B,
Besse C,
Blanche H,
Boland A,
Burdette L,
Chabrier A,
Durand G,
Le Calvez-Kelm F,
Prokhortchouk E,
Robinot N,
Skryabin KG,
Wozniak MB,
Yeager M,
Basta-Jovanovic G,
Dzamic Z,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Mukeriya A,
Rascu S,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Szeszenia-Dabrowska N,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Baglietto L,
Boeing H,
Khaw KT,
Weiderpass E,
Ljungberg B,
Sitaram RT,
Bruinsma F,
Jordan SJ,
Severi G,
Winship I,
Hveem K,
Vatten LJ,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Freeman LEB,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Gapstur SM,
Stevens VL,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Buring J,
Lee IM,
Chow WH,
Moore LE,
Wood C,
Eisen T,
Henrion M,
Larkin J,
Barman P,
Leibovich BC,
Choueiri TK,
Mark Lathrop G,
Rothman N,
Deleuze JF,
McKay JD,
Parker AS,
Wu X,
Houlston RS,
Brennan P,
Chanock SJ
Nature communications · 2017 · PMID 28598434 · open access
6 pages
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
Skibola CF,
Berndt SI,
Vijai J,
Conde L,
Wang Z,
Yeager M,
de Bakker PI,
Birmann BM,
Vajdic CM,
Foo JN,
Bracci PM,
Vermeulen RC
and 100 more — show all
Slager SL,
de Sanjose S,
Wang SS,
Linet MS,
Salles G,
Lan Q,
Severi G,
Hjalgrim H,
Lightfoot T,
Melbye M,
Gu J,
Ghesquières H,
Link BK,
Morton LM,
Holly EA,
Smith A,
Tinker LF,
Teras LR,
Kricker A,
Becker N,
Purdue MP,
Spinelli JJ,
Zhang Y,
Giles GG,
Vineis P,
Monnereau A,
Bertrand KA,
Albanes D,
Zeleniuch-Jacquotte A,
Gabbas A,
Chung CC,
Burdett L,
Hutchinson A,
Lawrence C,
Montalvan R,
Liang L,
Huang J,
Ma B,
Liu J,
Adami HO,
Glimelius B,
Ye Y,
Nowakowski GS,
Dogan A,
Thompson CA,
Habermann TM,
Novak AJ,
Liebow M,
Witzig TE,
Weiner GJ,
Schenk M,
Hartge P,
De Roos AJ,
Cozen W,
Zhi D,
Akers NK,
Riby J,
Smith MT,
Lacher M,
Villano DJ,
Maria A,
Roman E,
Kane E,
Jackson RD,
North KE,
Diver WR,
Turner J,
Armstrong BK,
Benavente Y,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
Staines A,
McKay J,
Brooks-Wilson AR,
Zheng T,
Holford TR,
Chamosa S,
Kaaks R,
Kelly RS,
Ohlsson B,
Travis RC,
Weiderpass E,
Clavel J,
Giovannucci E,
Kraft P,
Virtamo J,
Mazza P,
Cocco P,
Ennas MG,
Chiu BC,
Fraumeni JF Jr,
Nieters A,
Offit K,
Wu X,
Cerhan JR,
Smedby KE,
Chanock SJ,
Rothman N
American journal of human genetics · 2014 · PMID 25279986
5 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
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
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
needed four, and "et al." erases that. Twelve names show and the rest are one click
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.