For researchers
Is your paper here?
2,673 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.
50 matches for
Chen Z,
showing the first 20.
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
and 162 more — show all
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
and 73 more — show all
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects
Yang X,
Sun J,
Gao Y,
Tan A,
Zhang H,
Hu Y,
Feng J,
Qin X,
Tao S,
Chen Z,
Kim ST,
Peng T
and 17 more — show all
Liao M,
Lin X,
Zhang Z,
Tang M,
Li L,
Mo L,
Liang Z,
Shi D,
Huang Z,
Huang X,
Liu M,
Liu Q,
Zhang S,
Trent JM,
Zheng SL,
Xu J,
Mo Z
PLoS genetics · 2012 · PMID 23028341 · open access
8 pages
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Chuang LM,
Rotter JI,
Dantoft TM,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
7 pages
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
and 62 more — show all
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Zhu M,
Zhang C,
Han Y,
Jin C,
Miao S,
Zhang J,
Gong L,
Mou Y,
Ji C,
Fu Y,
Zhang E,
Yu C
and 17 more — show all
Sun D,
Jiang Y,
Chen J,
Yang L,
Chen Y,
Du H,
Walters R,
Millwood I,
Dai J,
Chen Z,
Hu Z,
Lv J,
Jin G,
Amos CI,
Shen H,
Li L,
Ma H
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Bradfield JP,
Vogelezang S,
Felix JF,
Chesi A,
Helgeland Ø,
Horikoshi M,
Karhunen V,
Lowry E,
Cousminer DL,
Ahluwalia TS,
Thiering E,
Boh ET
and 87 more — show all
Zafarmand MH,
Vilor-Tejedor N,
Wang CA,
Joro R,
Chen Z,
Gauderman WJ,
Pitkänen N,
Parra EJ,
Fernandez-Rhodes L,
Alyass A,
Monnereau C,
Curtin JA,
Have CT,
McCormack SE,
Hollensted M,
Frithioff-Bøjsøe C,
Valladares-Salgado A,
Peralta-Romero J,
Teo YY,
Standl M,
Leinonen JT,
Holm JC,
Peters T,
Vioque J,
Vrijheid M,
Simpson A,
Custovic A,
Vaudel M,
Canouil M,
Lindi V,
Atalay M,
Kähönen M,
Raitakari OT,
van Schaik BDC,
Berkowitz RI,
Cole SA,
Voruganti VS,
Wang Y,
Highland HM,
Comuzzie AG,
Butte NF,
Justice AE,
Gahagan S,
Blanco E,
Lehtimäki T,
Lakka TA,
Hebebrand J,
Bonnefond A,
Grarup N,
Froguel P,
Lyytikäinen LP,
Cruz M,
Kobes S,
Hanson RL,
Zemel BS,
Hinney A,
Teo KK,
Meyre D,
North KE,
Gilliland FD,
Bisgaard H,
Bustamante M,
Bonnelykke K,
Pennell CE,
Rivadeneira F,
Uitterlinden AG,
Baier LJ,
Vrijkotte TGM,
Heinrich J,
Sørensen TIA,
Saw SM,
Pedersen O,
Hansen T,
Eriksson J,
Widén E,
McCarthy MI,
Njølstad PR,
Power C,
Hyppönen E,
Sebert S,
Brown CD,
Järvelin MR,
Timpson NJ,
Johansson S,
Hakonarson H,
Jaddoe VWV,
Grant SFA
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S,
Voight BF,
Purcell S,
Musunuru K,
Ardissino D,
Mannucci PM,
Anand S,
Engert JC,
Samani NJ,
Schunkert H,
Erdmann J,
Reilly MP
and 174 more — show all
Rader DJ,
Morgan T,
Spertus JA,
Stoll M,
Girelli D,
McKeown PP,
Patterson CC,
Siscovick DS,
O'Donnell CJ,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Melander O,
Altshuler D,
Ardissino D,
Merlini PA,
Berzuini C,
Bernardinelli L,
Peyvandi F,
Tubaro M,
Celli P,
Ferrario M,
Fetiveau R,
Marziliano N,
Casari G,
Galli M,
Ribichini F,
Rossi M,
Bernardi F,
Zonzin P,
Piazza A,
Mannucci PM,
Schwartz SM,
Siscovick DS,
Yee J,
Friedlander Y,
Elosua R,
Marrugat J,
Lucas G,
Subirana I,
Sala J,
Ramos R,
Kathiresan S,
Meigs JB,
Williams G,
Nathan DM,
MacRae CA,
O'Donnell CJ,
Salomaa V,
Havulinna AS,
Peltonen L,
Melander O,
Berglund G,
Voight BF,
Kathiresan S,
Hirschhorn JN,
Asselta R,
Duga S,
Spreafico M,
Musunuru K,
Daly MJ,
Purcell S,
Voight BF,
Purcell S,
Nemesh J,
Korn JM,
McCarroll SA,
Schwartz SM,
Yee J,
Kathiresan S,
Lucas G,
Subirana I,
Elosua R,
Surti A,
Guiducci C,
Gianniny L,
Mirel D,
Parkin M,
Burtt N,
Gabriel SB,
Samani NJ,
Thompson JR,
Braund PS,
Wright BJ,
Balmforth AJ,
Ball SG,
Hall A,
Schunkert H,
Erdmann J,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König I,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Schunkert H,
Samani NJ,
Erdmann J,
Ouwehand W,
Hengstenberg C,
Deloukas P,
Scholz M,
Cambien F,
Reilly MP,
Li M,
Chen Z,
Wilensky R,
Matthai W,
Qasim A,
Hakonarson HH,
Devaney J,
Burnett MS,
Pichard AD,
Kent KM,
Satler L,
Lindsay JM,
Waksman R,
Knouff CW,
Waterworth DM,
Walker MC,
Mooser V,
Epstein SE,
Rader DJ,
Scheffold T,
Berger K,
Stoll M,
Huge A,
Girelli D,
Martinelli N,
Olivieri O,
Corrocher R,
Morgan T,
Spertus JA,
McKeown P,
Patterson CC,
Schunkert H,
Erdmann E,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König IR,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Hólm H,
Thorleifsson G,
Thorsteinsdottir U,
Stefansson K,
Engert JC,
Do R,
Xie C,
Anand S,
Kathiresan S,
Ardissino D,
Mannucci PM,
Siscovick D,
O'Donnell CJ,
Samani NJ,
Melander O,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Altshuler D
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
4 pages
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
and 22 more — show all
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
4 pages
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Shi Y,
Zhao H,
Shi Y,
Cao Y,
Yang D,
Li Z,
Zhang B,
Liang X,
Li T,
Chen J,
Shen J,
Zhao J
and 41 more — show all
You L,
Gao X,
Zhu D,
Zhao X,
Yan Y,
Qin Y,
Li W,
Yan J,
Wang Q,
Zhao J,
Geng L,
Ma J,
Zhao Y,
He G,
Zhang A,
Zou S,
Yang A,
Liu J,
Li W,
Li B,
Wan C,
Qin Y,
Shi J,
Yang J,
Jiang H,
Xu JE,
Qi X,
Sun Y,
Zhang Y,
Hao C,
Ju X,
Zhao D,
Ren CE,
Li X,
Zhang W,
Zhang Y,
Zhang J,
Wu D,
Zhang C,
He L,
Chen ZJ
Nature genetics · 2012 · PMID 22885925
4 pages
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Chen Z,
Tang H,
Qayyum R,
Schick UM,
Nalls MA,
Handsaker R,
Li J,
Lu Y,
Yanek LR,
Keating B,
Meng Y,
van Rooij FJ
and 24 more — show all
Okada Y,
Kubo M,
Rasmussen-Torvik L,
Keller MF,
Lange L,
Evans M,
Bottinger EP,
Linderman MD,
Ruderfer DM,
Hakonarson H,
Papanicolaou G,
Zonderman AB,
Gottesman O,
Thomson C,
Ziv E,
Singleton AB,
Loos RJ,
Sleiman PM,
Ganesh S,
McCarroll S,
Becker DM,
Wilson JG,
Lettre G,
Reiner AP
BioBank Japan Project · CHARGE Consortium
Human molecular genetics · 2013 · PMID 23446634
3 pages
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker KB,
Ramus SJ,
Tyrer J,
Lee A,
Shen HC,
Beesley J,
Lawrenson K,
McGuffog L,
Healey S,
Lee JM,
Spindler TJ,
Lin YG
and 277 more — show all
Pejovic T,
Bean Y,
Li Q,
Coetzee S,
Hazelett D,
Miron A,
Southey M,
Terry MB,
Goldgar DE,
Buys SS,
Janavicius R,
Dorfling CM,
van Rensburg EJ,
Neuhausen SL,
Ding YC,
Hansen TV,
Jønson L,
Gerdes AM,
Ejlertsen B,
Barrowdale D,
Dennis J,
Benitez J,
Osorio A,
Garcia MJ,
Komenaka I,
Weitzel JN,
Ganschow P,
Peterlongo P,
Bernard L,
Viel A,
Bonanni B,
Peissel B,
Manoukian S,
Radice P,
Papi L,
Ottini L,
Fostira F,
Konstantopoulou I,
Garber J,
Frost D,
Perkins J,
Platte R,
Ellis S,
Godwin AK,
Schmutzler RK,
Meindl A,
Engel C,
Sutter C,
Sinilnikova OM,
Damiola F,
Mazoyer S,
Stoppa-Lyonnet D,
Claes K,
De Leeneer K,
Kirk J,
Rodriguez GC,
Piedmonte M,
O'Malley DM,
de la Hoya M,
Caldes T,
Aittomäki K,
Nevanlinna H,
Collée JM,
Rookus MA,
Oosterwijk JC,
Tihomirova L,
Tung N,
Hamann U,
Isaccs C,
Tischkowitz M,
Imyanitov EN,
Caligo MA,
Campbell IG,
Hogervorst FB,
Olah E,
Diez O,
Blanco I,
Brunet J,
Lazaro C,
Pujana MA,
Jakubowska A,
Gronwald J,
Lubinski J,
Sukiennicki G,
Barkardottir RB,
Plante M,
Simard J,
Soucy P,
Montagna M,
Tognazzo S,
Teixeira MR,
Pankratz VS,
Wang X,
Lindor N,
Szabo CI,
Kauff N,
Vijai J,
Aghajanian CA,
Pfeiler G,
Berger A,
Singer CF,
Tea MK,
Phelan CM,
Greene MH,
Mai PL,
Rennert G,
Mulligan AM,
Tchatchou S,
Andrulis IL,
Glendon G,
Toland AE,
Jensen UB,
Kruse TA,
Thomassen M,
Bojesen A,
Zidan J,
Friedman E,
Laitman Y,
Soller M,
Liljegren A,
Arver B,
Einbeigi Z,
Stenmark-Askmalm M,
Olopade OI,
Nussbaum RL,
Rebbeck TR,
Nathanson KL,
Domchek SM,
Lu KH,
Karlan BY,
Walsh C,
Lester J,
Hein A,
Ekici AB,
Beckmann MW,
Fasching PA,
Lambrechts D,
Van Nieuwenhuysen E,
Vergote I,
Lambrechts S,
Dicks E,
Doherty JA,
Wicklund KG,
Rossing MA,
Rudolph A,
Chang-Claude J,
Wang-Gohrke S,
Eilber U,
Moysich KB,
Odunsi K,
Sucheston L,
Lele S,
Wilkens LR,
Goodman MT,
Thompson PJ,
Shvetsov YB,
Runnebaum IB,
Dürst M,
Hillemanns P,
Dörk T,
Antonenkova N,
Bogdanova N,
Leminen A,
Pelttari LM,
Butzow R,
Modugno F,
Kelley JL,
Edwards RP,
Ness RB,
du Bois A,
Heitz F,
Schwaab I,
Harter P,
Matsuo K,
Hosono S,
Orsulic S,
Jensen A,
Kjaer SK,
Hogdall E,
Hasmad HN,
Azmi MA,
Teo SH,
Woo YL,
Fridley BL,
Goode EL,
Cunningham JM,
Vierkant RA,
Bruinsma F,
Giles GG,
Liang D,
Hildebrandt MA,
Wu X,
Levine DA,
Bisogna M,
Berchuck A,
Iversen ES,
Schildkraut JM,
Concannon P,
Weber RP,
Cramer DW,
Terry KL,
Poole EM,
Tworoger SS,
Bandera EV,
Orlow I,
Olson SH,
Krakstad C,
Salvesen HB,
Tangen IL,
Bjorge L,
van Altena AM,
Aben KK,
Kiemeney LA,
Massuger LF,
Kellar M,
Brooks-Wilson A,
Kelemen LE,
Cook LS,
Le ND,
Cybulski C,
Yang H,
Lissowska J,
Brinton LA,
Wentzensen N,
Hogdall C,
Lundvall L,
Nedergaard L,
Baker H,
Song H,
Eccles D,
McNeish I,
Paul J,
Carty K,
Siddiqui N,
Glasspool R,
Whittemore AS,
Rothstein JH,
McGuire V,
Sieh W,
Ji BT,
Zheng W,
Shu XO,
Gao YT,
Rosen B,
Risch HA,
McLaughlin JR,
Narod SA,
Monteiro AN,
Chen A,
Lin HY,
Permuth-Wey J,
Sellers TA,
Tsai YY,
Chen Z,
Ziogas A,
Anton-Culver H,
Gentry-Maharaj A,
Menon U,
Harrington P,
Lee AW,
Wu AH,
Pearce CL,
Coetzee G,
Pike MC,
Dansonka-Mieszkowska A,
Timorek A,
Rzepecka IK,
Kupryjanczyk J,
Freedman M,
Noushmehr H,
Easton DF,
Offit K,
Couch FJ,
Gayther S,
Pharoah PP,
Antoniou AC,
Chenevix-Trench G
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study
Wei X,
Sun D,
Gao J,
Zhang J,
Zhu M,
Yu C,
Ma Z,
Fu Y,
Ji C,
Pei P,
Yang L,
Millwood IY
and 10 more — show all
International journal of cancer · 2024 · PMID 37846649
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 identifies a new ovarian cancer susceptibility locus on 9p22.2
Song H,
Ramus SJ,
Tyrer J,
Bolton KL,
Gentry-Maharaj A,
Wozniak E,
Anton-Culver H,
Chang-Claude J,
Cramer DW,
DiCioccio R,
Dörk T,
Goode EL
and 73 more — show all
Goodman MT,
Schildkraut JM,
Sellers T,
Baglietto L,
Beckmann MW,
Beesley J,
Blaakaer J,
Carney ME,
Chanock S,
Chen Z,
Cunningham JM,
Dicks E,
Doherty JA,
Dürst M,
Ekici AB,
Fenstermacher D,
Fridley BL,
Giles G,
Gore ME,
De Vivo I,
Hillemanns P,
Hogdall C,
Hogdall E,
Iversen ES,
Jacobs IJ,
Jakubowska A,
Li D,
Lissowska J,
Lubiński J,
Lurie G,
McGuire V,
McLaughlin J,
Medrek K,
Moorman PG,
Moysich K,
Narod S,
Phelan C,
Pye C,
Risch H,
Runnebaum IB,
Severi G,
Southey M,
Stram DO,
Thiel FC,
Terry KL,
Tsai YY,
Tworoger SS,
Van Den Berg DJ,
Vierkant RA,
Wang-Gohrke S,
Webb PM,
Wilkens LR,
Wu AH,
Yang H,
Brewster W,
Ziogas A,
Houlston R,
Tomlinson I,
Whittemore AS,
Rossing MA,
Ponder BA,
Pearce CL,
Ness RB,
Menon U,
Kjaer SK,
Gronwald J,
Garcia-Closas M,
Fasching PA,
Easton DF,
Chenevix-Trench G,
Berchuck A,
Pharoah PD,
Gayther SA
Australian Cancer (Ovarian) Study · Australian Ovarian Cancer Study Group and 1 more consortia
Nature genetics · 2009 · PMID 19648919
2 pages
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Shi Y,
Li L,
Hu Z,
Li S,
Wang S,
Liu J,
Wu C,
He L,
Zhou J,
Li Z,
Hu T,
Chen Y
and 72 more — show all
Jia Y,
Wang S,
Wu L,
Cheng X,
Yang Z,
Yang R,
Li X,
Huang K,
Zhang Q,
Zhou H,
Tang F,
Chen Z,
Shen J,
Jiang J,
Ding H,
Xing H,
Zhang S,
Qu P,
Song X,
Lin Z,
Deng D,
Xi L,
Lv W,
Han X,
Tao G,
Yan L,
Han Z,
Li Z,
Miao X,
Pan S,
Shen Y,
Wang H,
Liu D,
Gong E,
Li Z,
Zhou L,
Luan X,
Wang C,
Song Q,
Wu S,
Xu H,
Shen J,
Qiang F,
Ma G,
Liu L,
Chen X,
Liu J,
Wu J,
Shen Y,
Wen Y,
Chu M,
Yu J,
Hu X,
Fan Y,
He H,
Jiang Y,
Lei Z,
Liu C,
Chen J,
Zhang Y,
Yi C,
Chen S,
Li W,
Wang D,
Wang Z,
Di W,
Shen K,
Lin D,
Shen H,
Feng Y,
Xie X,
Ma D
Nature genetics · 2013 · PMID 23817570
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
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.