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2,662 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.
30 matches for
Lin A,
showing the first 10.
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Chen W,
Stambolian D,
Edwards AO,
Branham KE,
Othman M,
Jakobsdottir J,
Tosakulwong N,
Pericak-Vance MA,
Campochiaro PA,
Klein ML,
Tan PL,
Conley YP
and 54 more — show all
Kanda A,
Kopplin L,
Li Y,
Augustaitis KJ,
Karoukis AJ,
Scott WK,
Agarwal A,
Kovach JL,
Schwartz SG,
Postel EA,
Brooks M,
Baratz KH,
Brown WL,
Brucker AJ,
Orlin A,
Brown G,
Ho A,
Regillo C,
Donoso L,
Tian L,
Kaderli B,
Hadley D,
Hagstrom SA,
Peachey NS,
Klein R,
Klein BE,
Gotoh N,
Yamashiro K,
Ferris Iii F,
Fagerness JA,
Reynolds R,
Farrer LA,
Kim IK,
Miller JW,
Cortón M,
Carracedo A,
Sanchez-Salorio M,
Pugh EW,
Doheny KF,
Brion M,
Deangelis MM,
Weeks DE,
Zack DJ,
Chew EY,
Heckenlively JR,
Yoshimura N,
Iyengar SK,
Francis PJ,
Katsanis N,
Seddon JM,
Haines JL,
Gorin MB,
Abecasis GR,
Swaroop A
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
3 pages
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Blokland GAM,
Grove J,
Chen CY,
Cotsapas C,
Tobet S,
Handa R,
St Clair D,
Lencz T,
Mowry BJ,
Periyasamy S,
Cairns MJ,
Tooney PA
and 118 more — show all
Wu JQ,
Kelly B,
Kirov G,
Sullivan PF,
Corvin A,
Riley BP,
Esko T,
Milani L,
Jönsson EG,
Palotie A,
Ehrenreich H,
Begemann M,
Steixner-Kumar A,
Sham PC,
Iwata N,
Weinberger DR,
Gejman PV,
Sanders AR,
Buxbaum JD,
Rujescu D,
Giegling I,
Konte B,
Hartmann AM,
Bramon E,
Murray RM,
Pato MT,
Lee J,
Melle I,
Molden E,
Ophoff RA,
McQuillin A,
Bass NJ,
Adolfsson R,
Malhotra AK,
Martin NG,
Fullerton JM,
Mitchell PB,
Schofield PR,
Forstner AJ,
Degenhardt F,
Schaupp S,
Comes AL,
Kogevinas M,
Guzman-Parra J,
Reif A,
Streit F,
Sirignano L,
Cichon S,
Grigoroiu-Serbanescu M,
Hauser J,
Lissowska J,
Mayoral F,
Müller-Myhsok B,
Świątkowska B,
Schulze TG,
Nöthen MM,
Rietschel M,
Kelsoe J,
Leboyer M,
Jamain S,
Etain B,
Bellivier F,
Vincent JB,
Alda M,
O'Donovan C,
Cervantes P,
Biernacka JM,
Frye M,
McElroy SL,
Scott LJ,
Stahl EA,
Landén M,
Hamshere ML,
Smeland OB,
Djurovic S,
Vaaler AE,
Andreassen OA,
Baune BT,
Air T,
Preisig M,
Uher R,
Levinson DF,
Weissman MM,
Potash JB,
Shi J,
Knowles JA,
Perlis RH,
Lucae S,
Boomsma DI,
Penninx BWJH,
Hottenga JJ,
de Geus EJC,
Willemsen G,
Milaneschi Y,
Tiemeier H,
Grabe HJ,
Teumer A,
Van der Auwera S,
Völker U,
Hamilton SP,
Magnusson PKE,
Viktorin A,
Mehta D,
Mullins N,
Adams MJ,
Breen G,
McIntosh AM,
Lewis CM,
Hougaard DM,
Nordentoft M,
Mors O,
Mortensen PB,
Werge T,
Als TD,
Børglum AD,
Petryshen TL,
Smoller JW,
Goldstein JM
Schizophrenia Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium and 3 more consortia
Biological psychiatry · 2022 · PMID 34099189
3 pages
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Cichon S,
Mühleisen TW,
Degenhardt FA,
Mattheisen M,
Miró X,
Strohmaier J,
Steffens M,
Meesters C,
Herms S,
Weingarten M,
Priebe L,
Haenisch B
and 64 more — show all
Alexander M,
Vollmer J,
Breuer R,
Schmäl C,
Tessmann P,
Moebus S,
Wichmann HE,
Schreiber S,
Müller-Myhsok B,
Lucae S,
Jamain S,
Leboyer M,
Bellivier F,
Etain B,
Henry C,
Kahn JP,
Heath S,
Hamshere M,
O'Donovan MC,
Owen MJ,
Craddock N,
Schwarz M,
Vedder H,
Kammerer-Ciernioch J,
Reif A,
Sasse J,
Bauer M,
Hautzinger M,
Wright A,
Mitchell PB,
Schofield PR,
Montgomery GW,
Medland SE,
Gordon SD,
Martin NG,
Gustafsson O,
Andreassen O,
Djurovic S,
Sigurdsson E,
Steinberg S,
Stefansson H,
Stefansson K,
Kapur-Pojskic L,
Oruc L,
Rivas F,
Mayoral F,
Chuchalin A,
Babadjanova G,
Tiganov AS,
Pantelejeva G,
Abramova LI,
Grigoroiu-Serbanescu M,
Diaconu CC,
Czerski PM,
Hauser J,
Zimmer A,
Lathrop M,
Schulze TG,
Wienker TF,
Schumacher J,
Maier W,
Propping P,
Rietschel M,
Nöthen MM
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
2 pages
Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans
Chen G,
Bentley A,
Adeyemo A,
Shriner D,
Zhou J,
Doumatey A,
Huang H,
Ramos E,
Erdos M,
Gerry N,
Herbert A,
Christman M
and 1 more — show all
Human molecular genetics · 2012 · PMID 22791750
2 pages
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Buch S,
Stickel F,
Trépo E,
Way M,
Herrmann A,
Nischalke HD,
Brosch M,
Rosendahl J,
Berg T,
Ridinger M,
Rietschel M,
McQuillin A
and 36 more — show all
Frank J,
Kiefer F,
Schreiber S,
Lieb W,
Soyka M,
Semmo N,
Aigner E,
Datz C,
Schmelz R,
Brückner S,
Zeissig S,
Stephan AM,
Wodarz N,
Devière J,
Clumeck N,
Sarrazin C,
Lammert F,
Gustot T,
Deltenre P,
Völzke H,
Lerch MM,
Mayerle J,
Eyer F,
Schafmayer C,
Cichon S,
Nöthen MM,
Nothnagel M,
Ellinghaus D,
Huse K,
Franke A,
Zopf S,
Hellerbrand C,
Moreno C,
Franchimont D,
Morgan MY,
Hampe J
Nature genetics · 2015 · PMID 26482880
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
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis
van Hulzen KJE,
Scholz CJ,
Franke B,
Ripke S,
Klein M,
McQuillin A,
Sonuga-Barke EJ,
Kelsoe JR,
Landén M,
Andreassen OA,
Lesch KP,
Weber H
and 3 more — show all
PGC ADHD Working Group · PGC Bipolar Disorder Working Group
Biological psychiatry · 2017 · PMID 27890468
1 page
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache
O'Connor E,
Fourier C,
Ran C,
Sivakumar P,
Liesecke F,
Southgate L,
Harder AVE,
Vijfhuizen LS,
Yip J,
Giffin N,
Silver N,
Ahmed F
and 28 more — show all
Hostettler IC,
Davies B,
Cader MZ,
Simpson BS,
Sullivan R,
Efthymiou S,
Adebimpe J,
Quinn O,
Campbell C,
Cavalleri GL,
Vikelis M,
Kelderman T,
Paemeleire K,
Kilbride E,
Grangeon L,
Lagrata S,
Danno D,
Trembath R,
Wood NW,
Kockum I,
Winsvold BS,
Steinberg A,
Sjöstrand C,
Waldenlind E,
Vandrovcova J,
Houlden H,
Matharu M,
Belin AC
Annals of neurology · 2021 · PMID 34184781 · open access
1 page
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development
Ghouse J,
Gellert-Kristensen H,
O'Rourke CJ,
Seidelin AS,
Thorleifsson G,
Sveinbjörnsson G,
Tragante V,
Konkwo C,
Brancale J,
Vilarinho S,
Eyrich TM,
Ahlberg G
and 36 more — show all
Bundgaard JS,
Rand SA,
Lundegaard PR,
Sørensen E,
Mikkelsen C,
Træholt J,
Erikstrup C,
Dinh KM,
Bruun MT,
Jensen BA,
Bay JT,
Brunak S,
Banasik K,
Ullum H,
Laisk T,
Mägi R,
Nadauld LD,
Knowlton KU,
Knight S,
Gluud LL,
Vistisen K,
Björnsson ES,
Ulfarsson MO,
Sulem P,
Holm H,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Rafnar T,
Stefansson K,
Lassen U,
Pommergaard HC,
Hillingsø JG,
Andersen JB,
Bundgaard H,
Stender S
DBDS Genomic Consortium, Estonian Biobank Research Team
JHEP reports : innovation in hepatology · 2025 · PMID 40823170 · open access
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.