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42 matches for
Wang M,
showing the first 20.
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
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
Moon S,
Kim YJ,
Han S,
Hwang MY,
Shin DM,
Park MY,
Lu Y,
Yoon K,
Jang HM,
Kim YK,
Park TJ,
Song DS
and 3 more — show all
Scientific reports · 2019 · PMID 30718733 · open access
6 pages
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate
Sun Y,
Huang Y,
Yin A,
Pan Y,
Wang Y,
Wang C,
Du Y,
Wang M,
Lan F,
Hu Z,
Wang G,
Jiang M
and 17 more — show all
Ma J,
Zhang X,
Ma H,
Ma J,
Zhang W,
Huang Q,
Zhou Z,
Ma L,
Li Y,
Jiang H,
Xie L,
Jiang Y,
Shi B,
Cheng J,
Shen H,
Wang L,
Yang Y
Nature communications · 2015 · PMID 25775280
3 pages
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies
Wang Z,
Dai J,
Hu N,
Miao X,
Abnet CC,
Yang M,
Freedman ND,
Chen J,
Burdette L,
Zhu X,
Chung CC,
Ren C
and 35 more — show all
Dawsey SM,
Wang M,
Ding T,
Du J,
Gao YT,
Zhong R,
Giffen C,
Pan W,
Koh WP,
Dai N,
Liao LM,
Yan C,
Qiao YL,
Jiang Y,
Shu XO,
Chen J,
Wang C,
Ma H,
Su H,
Zhang Z,
Wang L,
Wu C,
Xiang YB,
Hu Z,
Yuan JM,
Xie L,
Zheng W,
Zheng W,
Lin D,
Chanock SJ,
Shi Y,
Goldstein AM,
Jin G,
Taylor PR,
Shen H
Gut · 2017 · PMID 26701879 · open access
3 pages
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
Jin G,
Ma H,
Wu C,
Dai J,
Zhang R,
Shi Y,
Lu J,
Miao X,
Wang M,
Zhou Y,
Chen J,
Li H
and 21 more — show all
Pan S,
Chu M,
Lu F,
Yu D,
Jiang Y,
Dong J,
Hu L,
Chen Y,
Xu L,
Shu Y,
Pan S,
Tan W,
Zhou B,
Lu D,
Wu T,
Zhang Z,
Chen F,
Wang X,
Hu Z,
Lin D,
Shen H
American journal of human genetics · 2012 · PMID 23103227
2 pages
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
He L,
Wu WJ,
Yang JK,
Cheng H,
Zuo XB,
Lai W,
Gao TW,
Ma CL,
Luo N,
Huang JQ,
Lu FY,
Liu YQ
and 22 more — show all
Huang YJ,
Lu QJ,
Zhang HL,
Wang L,
Wang WZ,
Wang MM,
Xiao SX,
Sun Q,
Li CY,
Bai YP,
Li H,
Zhou ZC,
Zhou FS,
Chen G,
Liang B,
Qi J,
Yang XY,
Yang T,
Zheng X,
Sun LD,
Zhang XJ,
Zhang YP
Nature communications · 2014 · PMID 24399259
2 pages
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Hou S,
Du L,
Lei B,
Pang CP,
Zhang M,
Zhuang W,
Zhang M,
Huang L,
Gong B,
Wang M,
Zhang Q,
Hu K
and 17 more — show all
Zhou Q,
Qi J,
Wang C,
Tian Y,
Ye Z,
Liang L,
Yu H,
Li H,
Zhou Y,
Cao Q,
Liu Y,
Bai L,
Liao D,
Kijlstra A,
Xu J,
Yang Z,
Yang P
Nature genetics · 2014 · PMID 25108386
2 pages
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
and 152 more — show all
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
Genome-wide and phenome-wide studies provided insights into brain glymphatic system function and its clinical associations
Ran L,
Fang Y,
Cheng C,
He Y,
Shao Z,
Kong Y,
Huang H,
Xu S,
Luo X,
Wang W,
Hao X,
Wang M
Science advances · 2025 · PMID 39823331 · open access
2 pages
Genome-wide association study provides insights into the genetic basis of Lewy body dementia
Zhu P,
Jin Z,
Wu S,
Gao S,
He Y,
Hu S,
Liu F,
Chen Y,
Wang M,
Wang K,
Liu G
Molecular psychiatry · 2025 · PMID 41068259
2 pages
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Yu HP,
Xiang BD,
Qian J,
Liu H,
Li YF,
Lin Q,
Liu S,
Wei J,
Zhan S,
Jiang B,
Dai J,
Ma L
and 20 more — show all
Zhang L,
Liu Y,
Wen Q,
Gong W,
Li S,
Jiang Y,
Zheng J,
Zhu T,
Zhou Z,
Zeng X,
Wang Z,
Wang JA,
Guo R,
Yang Y,
Wei Q,
Zhou G,
Qiu XQ,
Tang W,
Wang M,
Zhang R
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Lu X,
Wang L,
Chen S,
He L,
Yang X,
Shi Y,
Cheng J,
Zhang L,
Gu CC,
Huang J,
Wu T,
Ma Y
and 68 more — show all
Li J,
Cao J,
Chen J,
Ge D,
Fan Z,
Li Y,
Zhao L,
Li H,
Zhou X,
Chen L,
Liu D,
Chen J,
Duan X,
Hao Y,
Wang L,
Lu F,
Liu Z,
Yao C,
Shen C,
Pu X,
Yu L,
Fang X,
Xu L,
Mu J,
Wu X,
Zheng R,
Wu N,
Zhao Q,
Li Y,
Liu X,
Wang M,
Yu D,
Hu D,
Ji X,
Guo D,
Sun D,
Wang Q,
Yang Y,
Liu F,
Mao Q,
Liang X,
Ji J,
Chen P,
Mo X,
Li D,
Chai G,
Tang Y,
Li X,
Du Z,
Liu X,
Dou C,
Yang Z,
Meng Q,
Wang D,
Wang R,
Yang J,
Schunkert H,
Samani NJ,
Kathiresan S,
Reilly MP,
Erdmann J,
Peng X,
Wu X,
Liu D,
Yang Y,
Chen R,
Qiang B,
Gu D
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Xu J,
Mo Z,
Ye D,
Wang M,
Liu F,
Jin G,
Xu C,
Wang X,
Shao Q,
Chen Z,
Tao Z,
Qi J
and 58 more — show all
Zhou F,
Wang Z,
Fu Y,
He D,
Wei Q,
Guo J,
Wu D,
Gao X,
Yuan J,
Wang G,
Xu Y,
Wang G,
Yao H,
Dong P,
Jiao Y,
Shen M,
Yang J,
Ou-Yang J,
Jiang H,
Zhu Y,
Ren S,
Zhang Z,
Yin C,
Gao X,
Dai B,
Hu Z,
Yang Y,
Wu Q,
Chen H,
Peng P,
Zheng Y,
Zheng X,
Xiang Y,
Long J,
Gong J,
Na R,
Lin X,
Yu H,
Wang Z,
Tao S,
Feng J,
Sun J,
Liu W,
Hsing A,
Rao J,
Ding Q,
Wiklund F,
Gronberg H,
Shu XO,
Zheng W,
Shen H,
Jin L,
Shi R,
Lu D,
Zhang X,
Sun J,
Zheng SL,
Sun Y
Nature genetics · 2012 · PMID 23023329
1 page
Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions
Kim YK,
Kim Y,
Hwang MY,
Shimokawa K,
Won S,
Kato N,
Tabara Y,
Yokota M,
Han BG,
Lee JH,
Kim BJ
BMC medical genetics · 2014 · PMID 24903457 · open access
1 page
Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer
Wang M,
Takahashi A,
Liu F,
Ye D,
Ding Q,
Qin C,
Yin C,
Zhang Z,
Matsuda K,
Kubo M,
Na R,
Lin X
and 11 more — show all
Jiang H,
Ren S,
Sun J,
Zheng SL,
Marchand LL,
Isaacs WB,
Mo Z,
Haiman CA,
Sun Y,
Nakagawa H,
Xu J
Nature communications · 2015 · PMID 26443449 · open access
1 page
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Yan C,
Zhu M,
Ding Y,
Yang M,
Wang M,
Li G,
Ren C,
Huang T,
Yang W,
He B,
Wang M,
Yu F
and 22 more — show all
Wang J,
Zhang R,
Wang T,
Ni J,
Chen J,
Jiang Y,
Dai J,
Zhang E,
Ma H,
Wang Y,
Xu D,
Wang S,
Chen Y,
Xu Z,
Zhou J,
Ji G,
Wang Z,
Zhang Z,
Hu Z,
Wei Q,
Shen H,
Jin G
Gut · 2020 · PMID 31383772
1 page
Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study
Jin G,
Lv J,
Yang M,
Wang M,
Zhu M,
Wang T,
Yan C,
Yu C,
Ding Y,
Li G,
Ren C,
Ni J
and 22 more — show all
Zhang R,
Guo Y,
Bian Z,
Zheng Y,
Zhang N,
Jiang Y,
Chen J,
Wang Y,
Xu D,
Zheng H,
Yang L,
Chen Y,
Walters R,
Millwood IY,
Dai J,
Ma H,
Chen K,
Chen Z,
Hu Z,
Wei Q,
Shen H,
Li L
The Lancet. Oncology · 2020 · PMID 33002439
1 page
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.