For researchers
Is your paper here?
2,652 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.
10 matches for
Rämö J.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
Tabassum R,
Rämö JT,
Ripatti P,
Koskela JT,
Kurki M,
Karjalainen J,
Palta P,
Hassan S,
Nunez-Fontarnau J,
Kiiskinen TTJ,
Söderlund S,
Matikainen N
and 16 more — show all
Gerl MJ,
Surma MA,
Klose C,
Stitziel NO,
Laivuori H,
Havulinna AS,
Service SK,
Salomaa V,
Pirinen M,
Jauhiainen M,
Daly MJ,
Freimer NB,
Palotie A,
Taskinen MR,
Simons K,
Ripatti S
FinnGen Project
Nature communications · 2019 · PMID 31551469 · open access
12 pages+
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
and 54 more — show all
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
The Genetic Determinants of Aortic Distention
Pirruccello JP,
Rämö JT,
Choi SH,
Chaffin MD,
Kany S,
Nekoui M,
Chou EL,
Jurgens SJ,
Friedman SF,
Juric D,
Stone JR,
Batra P
and 4 more — show all
Journal of the American College of Cardiology · 2023 · PMID 37019578
12 pages+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
Kany S,
Rämö JT,
Hou C,
Jurgens SJ,
Khurshid S,
Nauffal V,
Cunningham JW,
Lau ES,
Koyama S,
Ho JE,
Olgin JE,
Elmariah S
and 4 more — show all
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation
Saarentaus EC,
Karjalainen J,
Rämö JT,
Kiiskinen T,
Havulinna AS,
Mehtonen J,
Hautakangas H,
Ruotsalainen S,
Tamlander M,
Mars N,
Toppila-Salmi S,
Pirinen M
and 6 more — show all
FINNGEN
Nature communications · 2023 · PMID 36653354 · open access
10 pages
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure
Rämö JT,
Kiiskinen T,
Seist R,
Krebs K,
Kanai M,
Karjalainen J,
Kurki M,
Hämäläinen E,
Häppölä P,
Havulinna AS,
Hautakangas H,
Mägi R
and 11 more — show all
Palta P,
Esko T,
Metspalu A,
Pirinen M,
Karczewski KJ,
Ripatti S,
Milani L,
Stankovic KM,
Mäkitie A,
Daly MJ,
Palotie A
FinnGen
Nature communications · 2023 · PMID 36653343 · open access
5 pages
Deep learning of left atrial structure and function provides link to atrial fibrillation risk
Pirruccello JP,
Di Achille P,
Choi SH,
Rämö JT,
Khurshid S,
Nekoui M,
Jurgens SJ,
Nauffal V,
Kany S,
Ng K,
Friedman SF,
Batra P
and 6 more — show all
FinnGen
Nature communications · 2024 · PMID 38773065 · open access
4 pages
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Jurgens SJ,
Rämö JT,
Kramarenko DR,
Wijdeveld LFJM,
Haas J,
Chaffin MD,
Garnier S,
Gaziano L,
Weng LC,
Lipov A,
Zheng SL,
Henry A
and 46 more — show all
Huffman JE,
Challa S,
Rühle F,
Verdugo CD,
Krijger Juárez C,
Kany S,
van Orsouw CA,
Biddinger K,
Poel E,
Elliott AL,
Wang X,
Francis C,
Ruan R,
Koyama S,
Beekman L,
Zimmerman DS,
Deleuze JF,
Villard E,
Trégouët DA,
Isnard R,
Boomsma DI,
de Geus EJC,
Tadros R,
Pinto YM,
Wilde AAM,
Hottenga JJ,
Sinisalo J,
Niiranen T,
Walsh R,
Schmidt AF,
Choi SH,
Chang KM,
Tsao PS,
Matthews PM,
Ware JS,
Lumbers RT,
van der Crabben S,
Laukkanen J,
Palotie A,
Amin AS,
Charron P,
Meder B,
Ellinor PT,
Daly M,
Aragam KG,
Bezzina CR
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Rämö JT,
Kany S,
Hou CR,
Friedman SF,
Roselli C,
Nauffal V,
Koyama S,
Karjalainen J,
Maddah M,
Palotie A,
Ellinor PT,
Pirruccello JP
FinnGen
JAMA cardiology · 2024 · PMID 38477908
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.