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Is your paper here?
2,663 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.
47 matches for
Estonian Biobank Research Team,
showing the first 7.
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Braun A,
Shekhar S,
Levey DF,
Straub P,
Kraft J,
Panagiotaropoulou GM,
Heilbron K,
Awasthi S,
Meleka Hanna R,
Hoffmann S,
Stein M,
Lehnerer S
and 28 more — show all
Mergenthaler P,
Elnahas AG,
Topaloudi A,
Koromina M,
Palviainen T,
Asbjornsdottir B,
Stefansson H,
Skuladóttir AT,
Jónsdóttir I,
Stefansson K,
Reis K,
Esko T,
Palotie A,
Leypoldt F,
Stein MB,
Fontanillas P,
Kaprio J,
Gelernter J,
Davis LK,
Paschou P,
Tannemaat MR,
Verschuuren JJGM,
Kuhlenbäumer G,
Gregersen PK,
Huijbers MG,
Stascheit F,
Meisel A,
Ripke S
Estonian Biobank Research Team · 23andMe Research Team
Nature communications · 2024 · PMID 39537604 · open access
2 pages
GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
Ramachandran D,
Wang X,
Laisk T,
Zheng Y,
Ingold N,
Canson DM,
Kho PF,
Naumann BJ,
Chapman CJ,
Bousset K,
Krause AV,
Schürmann P
and 62 more — show all
Wieland B,
Hanel P,
Hülse F,
Häfner N,
Runnebaum I,
Dubrowinskaja N,
Turmanov N,
Yugay T,
Yessimsiitova ZB,
Amant F,
Annibali D,
Beckmann MW,
Bodelon C,
Buchanan DD,
Chen C,
Clarke MA,
Cook LS,
De Vivo I,
De Wispelaere W,
Du M,
Easton DF,
Emons J,
Fasching PA,
Friedenreich CM,
Gallagher G,
Giles GG,
Goode EL,
Harris HR,
Hunter DJ,
Kolin DL,
Kraft P,
Lacey JV,
Lambrechts D,
Lu L,
Mutter GL,
Naduparambil J,
O'Connell K,
Patel AV,
Pharoah PDP,
Rebbeck TR,
Ricceri F,
Risch HA,
Ruebner M,
Sacerdote C,
Scott RJ,
Setiawan VW,
Shu XO,
Southey MC,
Tham E,
Tomlinson I,
Turman C,
Wentzensen N,
Xu W,
Yu H,
Zheng W,
Spurdle AB,
Yarden Y,
Mägi R,
Hillemanns P,
Glubb DM,
Dörk T,
O'Mara TA
Estonian Biobank Research Team
EBioMedicine · 2025 · PMID 40633141 · open access
2 pages
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
Tyrmi JS,
Kaartokallio T,
Lokki AI,
Jääskeläinen T,
Kortelainen E,
Ruotsalainen S,
Karjalainen J,
Ripatti S,
Kivioja A,
Laisk T,
Kettunen J,
Pouta A
and 5 more — show all
FINNPEC Study Group, FinnGen Project, and the Estonian Biobank Research Team
JAMA cardiology · 2023 · PMID 37285119 · open access
1 page
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
and 7 more — show all
Estonian Biobank Research Team · FinnGen and 1 more consortia
BMC genomics · 2024 · PMID 38408933 · open access
1 page
Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity
Tervi A,
Ramste M,
Abner E,
Cheng P,
Lane JM,
Maher M,
Valliere J,
Lammi V,
Strausz S,
Riikonen J,
Nguyen T,
Martyn GE
and 17 more — show all
Sheth MU,
Xia F,
Docampo ML,
Gu W,
Esko T,
Saxena R,
Pirinen M,
Palotie A,
Ripatti S,
Sinnott-Armstrong N,
Daly M,
Engreitz JM,
Rabinovitch M,
Heckman CA,
Quertermous T,
Jones SE,
Ollila HM
FinnGen, Estonian Biobank research team
Cell genomics · 2024 · PMID 39142284 · 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.