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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.
32 matches for
Lin J,
showing the first 12.
A type 1 diabetes genetic risk score discriminates between type 1 diabetes and type 2 diabetes in a Chinese population
Hu J,
Jiang G,
Qin J,
Luo S,
Fan B,
Xie Z,
Wan R,
Li X,
Tam CHT,
Wang Z,
Ding J,
Xia Y
and 16 more — show all
Yang Y,
Lin J,
Yu G,
Jin P,
Lim CKP,
Luk AOY,
So WY,
Chan JCN,
Wang C,
Huang J,
Weedon MN,
Hagopian WA,
Oram RA,
Ma RCW,
Xiao Y,
Zhou Z
Hong Kong Diabetes Biobank Study Group
Diabetologia · 2025 · PMID 40569436 · open access
2 pages
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Ferreira MA,
O'Donovan MC,
Meng YA,
Jones IR,
Ruderfer DM,
Jones L,
Fan J,
Kirov G,
Perlis RH,
Green EK,
Smoller JW,
Grozeva D
and 50 more — show all
Stone J,
Nikolov I,
Chambert K,
Hamshere ML,
Nimgaonkar VL,
Moskvina V,
Thase ME,
Caesar S,
Sachs GS,
Franklin J,
Gordon-Smith K,
Ardlie KG,
Gabriel SB,
Fraser C,
Blumenstiel B,
Defelice M,
Breen G,
Gill M,
Morris DW,
Elkin A,
Muir WJ,
McGhee KA,
Williamson R,
MacIntyre DJ,
MacLean AW,
St CD,
Robinson M,
Van Beck M,
Pereira AC,
Kandaswamy R,
McQuillin A,
Collier DA,
Bass NJ,
Young AH,
Lawrence J,
Ferrier IN,
Anjorin A,
Farmer A,
Curtis D,
Scolnick EM,
McGuffin P,
Daly MJ,
Corvin AP,
Holmans PA,
Blackwood DH,
Gurling HM,
Owen MJ,
Purcell SM,
Sklar P,
Craddock N
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18711365
1 page
Genome-wide association meta-analysis for total serum bilirubin levels
Johnson AD,
Kavousi M,
Smith AV,
Chen MH,
Dehghan A,
Aspelund T,
Lin JP,
van Duijn CM,
Harris TB,
Cupples LA,
Uitterlinden AG,
Launer L
and 7 more — show all
Human molecular genetics · 2009 · PMID 19414484
1 page
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
Landi MT,
Chatterjee N,
Yu K,
Goldin LR,
Goldstein AM,
Rotunno M,
Mirabello L,
Jacobs K,
Wheeler W,
Yeager M,
Bergen AW,
Li Q
and 56 more — show all
Consonni D,
Pesatori AC,
Wacholder S,
Thun M,
Diver R,
Oken M,
Virtamo J,
Albanes D,
Wang Z,
Burdette L,
Doheny KF,
Pugh EW,
Laurie C,
Brennan P,
Hung R,
Gaborieau V,
McKay JD,
Lathrop M,
McLaughlin J,
Wang Y,
Tsao MS,
Spitz MR,
Wang Y,
Krokan H,
Vatten L,
Skorpen F,
Arnesen E,
Benhamou S,
Bouchard C,
Metspalu A,
Metsapalu A,
Vooder T,
Nelis M,
Välk K,
Field JK,
Chen C,
Goodman G,
Sulem P,
Thorleifsson G,
Rafnar T,
Eisen T,
Sauter W,
Rosenberger A,
Bickeböller H,
Risch A,
Chang-Claude J,
Wichmann HE,
Stefansson K,
Houlston R,
Amos CI,
Fraumeni JF Jr,
Savage SA,
Bertazzi PA,
Tucker MA,
Chanock S,
Caporaso NE
American journal of human genetics · 2009 · PMID 19836008
1 page
A variant in MCF2L is associated with osteoarthritis
Day-Williams AG,
Southam L,
Panoutsopoulou K,
Rayner NW,
Esko T,
Estrada K,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Kerkhof HJ
and 33 more — show all
Thorleifsson G,
Arden NK,
Carr A,
Chapman K,
Deloukas P,
Loughlin J,
McCaskie A,
Ollier WE,
Ralston SH,
Spector TD,
Wallis GA,
Wilkinson JM,
Aslam N,
Birell F,
Carluke I,
Joseph J,
Rai A,
Reed M,
Walker K,
Doherty SA,
Jonsdottir I,
Maciewicz RA,
Muir KR,
Metspalu A,
Rivadeneira F,
Stefansson K,
Styrkarsdottir U,
Uitterlinden AG,
van Meurs JB,
Zhang W,
Valdes AM,
Doherty M,
Zeggini E
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
1 page
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Zeggini E,
Panoutsopoulou K,
Southam L,
Rayner NW,
Day-Williams AG,
Lopes MC,
Boraska V,
Esko T,
Evangelou E,
Hoffman A,
Houwing-Duistermaat JJ,
Ingvarsson T
and 64 more — show all
Jonsdottir I,
Jonnson H,
Kerkhof HJ,
Kloppenburg M,
Bos SD,
Mangino M,
Metrustry S,
Slagboom PE,
Thorleifsson G,
Raine EV,
Ratnayake M,
Ricketts M,
Beazley C,
Blackburn H,
Bumpstead S,
Elliott KS,
Hunt SE,
Potter SC,
Shin SY,
Yadav VK,
Zhai G,
Sherburn K,
Dixon K,
Arden E,
Aslam N,
Battley PK,
Carluke I,
Doherty S,
Gordon A,
Joseph J,
Keen R,
Koller NC,
Mitchell S,
O'Neill F,
Paling E,
Reed MR,
Rivadeneira F,
Swift D,
Walker K,
Watkins B,
Wheeler M,
Birrell F,
Ioannidis JP,
Meulenbelt I,
Metspalu A,
Rai A,
Salter D,
Stefansson K,
Stykarsdottir U,
Uitterlinden AG,
van Meurs JB,
Chapman K,
Deloukas P,
Ollier WE,
Wallis GA,
Arden N,
Carr A,
Doherty M,
McCaskie A,
Willkinson JM,
Ralston SH,
Valdes AM,
Spector TD,
Loughlin J
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
1 page
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
Tanskanen T,
van den Berg L,
Välimäki N,
Aavikko M,
Ness-Jensen E,
Hveem K,
Wettergren Y,
Bexe Lindskog E,
Tõnisson N,
Metspalu A,
Silander K,
Orlando G
and 48 more — show all
Law PJ,
Tuupanen S,
Gylfe AE,
Hänninen UA,
Cajuso T,
Kondelin J,
Sarin AP,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
Järvinen H,
Renkonen-Sinisalo L,
Lepistö A,
Böhm J,
Mecklin JP,
Al-Tassan NA,
Palles C,
Martin L,
Barclay E,
Tenesa A,
Farrington SM,
Timofeeva MN,
Meyer BF,
Wakil SM,
Campbell H,
Smith CG,
Idziaszczyk S,
Maughan TS,
Kaplan R,
Kerr R,
Kerr D,
Buchanan DD,
Win AK,
Hopper J,
Jenkins MA,
Newcomb PA,
Gallinger S,
Conti D,
Schumacher FR,
Casey G,
Cheadle JP,
Dunlop MG,
Tomlinson IP,
Houlston RS,
Palin K,
Aaltonen LA
International journal of cancer · 2018 · PMID 28960316
1 page
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
Foo JN,
Chew EGY,
Chung SJ,
Peng R,
Blauwendraat C,
Nalls MA,
Mok KY,
Satake W,
Toda T,
Chao Y,
Tan LCS,
Tandiono M
and 33 more — show all
Lian MM,
Ng EY,
Prakash KM,
Au WL,
Meah WY,
Mok SQ,
Annuar AA,
Chan AYY,
Chen L,
Chen Y,
Jeon BS,
Jiang L,
Lim JL,
Lin JJ,
Liu C,
Mao C,
Mok V,
Pei Z,
Shang HF,
Shi CH,
Song K,
Tan AH,
Wu YR,
Xu YM,
Xu R,
Yan Y,
Yang J,
Zhang B,
Koh WP,
Lim SY,
Khor CC,
Liu J,
Tan EK
JAMA neurology · 2020 · PMID 32310270
1 page
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene
Boer CG,
Yau MS,
Rice SJ,
Coutinho de Almeida R,
Cheung K,
Styrkarsdottir U,
Southam L,
Broer L,
Wilkinson JM,
Uitterlinden AG,
Zeggini E,
Felson D
and 5 more — show all
Annals of the rheumatic diseases · 2021 · PMID 33055079 · open access
1 page
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
Adlam D,
Berrandou TE,
Georges A,
Nelson CP,
Giannoulatou E,
Henry J,
Ma L,
Blencowe M,
Turley TN,
Yang ML,
Chopade S,
Finan C
and 40 more — show all
Braund PS,
Sadeg-Sayoud I,
Iismaa SE,
Kosel ML,
Zhou X,
Hamby SE,
Cheng J,
Liu L,
Tarr I,
Muller DWM,
d'Escamard V,
King A,
Brunham LR,
Baranowska-Clarke AA,
Debette S,
Amouyel P,
Olin JW,
Patil S,
Hesselson SE,
Junday K,
Kanoni S,
Aragam KG,
Butterworth AS,
Tweet MS,
Gulati R,
Combaret N,
Kadian-Dodov D,
Kalman JM,
Fatkin D,
Hingorani AD,
Saw J,
Webb TR,
Hayes SN,
Yang X,
Ganesh SK,
Olson TM,
Kovacic JC,
Graham RM,
Samani NJ,
Bouatia-Naji N
CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia
Nature genetics · 2023 · PMID 37248441 · open access
1 page
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng EO,
Coetzee SG,
Tyrer JP,
Peng PC,
Rosenow W,
Chen S,
Davis BD,
Dezem FS,
Seo JH,
Nameki R,
Reyes AL,
Aben KKH
and 141 more — show all
Anton-Culver H,
Antonenkova NN,
Aravantinos G,
Bandera EV,
Beane Freeman LE,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernardini MQ,
Bjorge L,
Black A,
Bogdanova NV,
Bolton KL,
Brenton JD,
Budzilowska A,
Butzow R,
Cai H,
Campbell I,
Cannioto R,
Chang-Claude J,
Chanock SJ,
Chen K,
Chenevix-Trench G,
Chiew YE,
Cook LS,
DeFazio A,
Dennis J,
Doherty JA,
Dörk T,
du Bois A,
Dürst M,
Eccles DM,
Ene G,
Fasching PA,
Flanagan JM,
Fortner RT,
Fostira F,
Gentry-Maharaj A,
Giles GG,
Goodman MT,
Gronwald J,
Haiman CA,
Håkansson N,
Heitz F,
Hildebrandt MAT,
Høgdall E,
Høgdall CK,
Huang RY,
Jensen A,
Jones ME,
Kang D,
Karlan BY,
Karnezis AN,
Kelemen LE,
Kennedy CJ,
Khusnutdinova EK,
Kiemeney LA,
Kjaer SK,
Kupryjanczyk J,
Labrie M,
Lambrechts D,
Larson MC,
Le ND,
Lester J,
Li L,
Lubiński J,
Lush M,
Marks JR,
Matsuo K,
May T,
McLaughlin JR,
McNeish IA,
Menon U,
Missmer S,
Modugno F,
Moffitt M,
Monteiro AN,
Moysich KB,
Narod SA,
Nguyen-Dumont T,
Odunsi K,
Olsson H,
Onland-Moret NC,
Park SK,
Pejovic T,
Permuth JB,
Piskorz A,
Prokofyeva D,
Riggan MJ,
Risch HA,
Rodríguez-Antona C,
Rossing MA,
Sandler DP,
Setiawan VW,
Shan K,
Song H,
Southey MC,
Steed H,
Sutphen R,
Swerdlow AJ,
Teo SH,
Terry KL,
Thompson PJ,
Vestrheim Thomsen LC,
Titus L,
Trabert B,
Travis R,
Tworoger SS,
Valen E,
Van Nieuwenhuysen E,
Edwards DV,
Vierkant RA,
Webb PM,
Weinberg CR,
Weise RM,
Wentzensen N,
White E,
Winham SJ,
Wolk A,
Woo YL,
Wu AH,
Yan L,
Yannoukakos D,
Zeinomar N,
Zheng W,
Ziogas A,
Berchuck A,
Goode EL,
Huntsman DG,
Pearce CL,
Ramus SJ,
Sellers TA,
Freedman ML,
Lawrenson K,
Schildkraut JM,
Hazelett D,
Plummer JT,
Kar S,
Jones MR,
Pharoah PDP,
Gayther SA
AOCS Group · OPAL Study Group and 1 more consortia
American journal of human genetics · 2024 · PMID 38723632
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.