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51 matches for
FinnGen,
showing the first 20.
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Bao EL,
Nandakumar SK,
Liao X,
Bick AG,
Karjalainen J,
Tabaka M,
Gan OI,
Havulinna AS,
Kiiskinen TTJ,
Lareau CA,
de Lapuente Portilla AL,
Li B
and 23 more — show all
Emdin C,
Codd V,
Nelson CP,
Walker CJ,
Churchhouse C,
de la Chapelle A,
Klein DE,
Nilsson B,
Wilson PWF,
Cho K,
Pyarajan S,
Gaziano JM,
Samani NJ,
Regev A,
Palotie A,
Neale BM,
Dick JE,
Natarajan P,
O'Donnell CJ,
Daly MJ,
Milyavsky M,
Kathiresan S,
Sankaran VG
FinnGen · 23andMe Research Team
Nature · 2020 · PMID 33057200 · open access
10 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
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
and 391 more — show all
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
MacLeod CA,
Maier W,
Mangialasche F,
Spallazzi M,
Marquié M,
Marshall R,
Martin ER,
Montes AM,
Rodríguez CM,
Masullo C,
Mayeux R,
Mead S,
Mecocci P,
Medina M,
Meggy A,
Mehrabian S,
Mendoza S,
Menéndez-González M,
Mir P,
Moebus S,
Mol M,
Molina-Porcel L,
Montrreal L,
Morelli L,
Moreno F,
Morgan K,
Mosley T,
Nöthen MM,
Muchnik C,
Mukherjee S,
Nacmias B,
Ngandu T,
Nicolas G,
Nordestgaard BG,
Olaso R,
Orellana A,
Orsini M,
Ortega G,
Padovani A,
Paolo C,
Papenberg G,
Parnetti L,
Pasquier F,
Pastor P,
Peloso G,
Pérez-Cordón A,
Pérez-Tur J,
Pericard P,
Peters O,
Pijnenburg YAL,
Pineda JA,
Piñol-Ripoll G,
Pisanu C,
Polak T,
Popp J,
Posthuma D,
Priller J,
Puerta R,
Quenez O,
Quintela I,
Thomassen JQ,
Rábano A,
Rainero I,
Rajabli F,
Ramakers I,
Real LM,
Reinders MJT,
Reitz C,
Reyes-Dumeyer D,
Ridge P,
Riedel-Heller S,
Riederer P,
Roberto N,
Rodriguez-Rodriguez E,
Rongve A,
Allende IR,
Rosende-Roca M,
Royo JL,
Rubino E,
Rujescu D,
Sáez ME,
Sakka P,
Saltvedt I,
Sanabria Á,
Sánchez-Arjona MB,
Sanchez-Garcia F,
Juan PS,
Sánchez-Valle R,
Sando SB,
Sarnowski C,
Satizabal CL,
Scamosci M,
Scarmeas N,
Scarpini E,
Scheltens P,
Scherbaum N,
Scherer M,
Schmid M,
Schneider A,
Schott JM,
Selbæk G,
Seripa D,
Serrano M,
Sha J,
Shadrin AA,
Skrobot O,
Slifer S,
Snijders GJL,
Soininen H,
Solfrizzi V,
Solomon A,
Song Y,
Sorbi S,
Sotolongo-Grau O,
Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
Tárraga L,
Tesí N,
Thalamuthu A,
Thomas T,
Tosto G,
Traykov L,
Tremolizzo L,
Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
Vogelgsang J,
Vyhnalek M,
Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
Pericak-Vance MA,
Amouyel P,
Williams J,
Frikke-Schmidt R,
Clarimon J,
Deleuze JF,
Rossi G,
Seshadri S,
Andreassen OA,
Ingelsson M,
Hiltunen M,
Sleegers K,
Schellenberg GD,
van Duijn CM,
Sims R,
van der Flier WM,
Ruiz A,
Ramirez A,
Lambert JC
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
and 121 more — show all
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
Tyrmi JS,
Karjalainen J,
Venkatesh SS,
Benoit-Pilven C,
Lemmelä SM,
Brunak S,
Aagaard B,
Bruun MT,
Erikstrup C,
Ullum H,
Pedersen OB,
Banasik K
and 19 more — show all
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
Nielsen HS,
Nyegaard M,
Westergaard D,
Rafnar T,
Sulem P,
Stefansson K,
Palta P,
Laisk T,
Tukiainen T,
Lindgren CM,
Daly M,
Havulinna AS,
Laivuori HM
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
Tcheandjieu C,
Xiao K,
Tejeda H,
Lynch JA,
Ruotsalainen S,
Bellomo T,
Palnati M,
Judy R,
Klarin D,
Kember RL,
Verma S,
Palotie A
and 8 more — show all
Regeneron Genetics Center · VA Million Veterans Program and 1 more consortia
Nature genetics · 2022 · PMID 35637384
6 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 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
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Di Lorenzo B,
Camargo Tavares L,
Díaz-Muñoz C,
Heredia-Fernández F,
Bozzarelli I,
Esteban Blanco C,
Wang Z,
Smit RAJ,
Loos RJF,
Hirbo J,
Cox NJ,
Straub P
and 57 more — show all
Favé MJ,
Awadalla P,
Pozdeyev N,
Gignoux CR,
Gudbjartsson DF,
Thorleifsson G,
Jonsdottir I,
Stefansson K,
Abner E,
Palta P,
Williams AT,
Coley K,
Sze G,
John C,
Richmond A,
McCartney D,
Hayward C,
Mulford AJ,
Sanders AR,
Peculis R,
Rovite V,
Dombrovska MS,
Capasso M,
Lo Faro V,
Sinha T,
Lopera Maya EA,
Zhernakova A,
Wang Y,
Martin A,
Vanderwerff B,
Zöllner S,
Ferolito BR,
Pereira AC,
Gaziano JM,
Cho K,
Caruth L,
Guare L,
Kripke CM,
Rader DJ,
Verma SS,
Verma A,
Saad C,
Mbarek H,
Chao PY,
Chen TT,
Lin YF,
Feng YA,
Challa PK,
Khalili H,
Andries A,
Ness-Jensen E,
Brumpton BM,
Grover M,
Lemmelä S,
Sanna S,
Bonfiglio F,
D'Amato M
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
5 pages
The impact of non-additive genetic associations on age-related complex diseases
Guindo-Martínez M,
Amela R,
Bonàs-Guarch S,
Puiggròs M,
Salvoro C,
Miguel-Escalada I,
Carey CE,
Cole JB,
Rüeger S,
Atkinson E,
Leong A,
Sanchez F
and 9 more — show all
FinnGen Consortium
Nature communications · 2021 · PMID 33893285 · open access
4 pages
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer
Koel M,
Võsa U,
Jõeloo M,
Läll K,
Gualdo NP,
Laivuori H,
Lemmelä S,
Daly M,
Palta P,
Mägi R,
Laisk T
Estonian Biobank Research Team; FinnGen
Human molecular genetics · 2023 · PMID 36929174 · open access
4 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
Genetic variants affect diurnal glucose levels throughout the day
Sinnott-Armstrong N,
Strausz S,
Urpa L,
Abner E,
Johnson JP,
Valliere J,
Palumaa T,
Palta P,
Dashti HS,
Chang KM,
Vujkovic M,
Daly M
and 4 more — show all
FinnGen · Estonian Biobank Research Team and 1 more consortia
Nature communications · 2026 · PMID 42173832 · open access
4 pages
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
and 41 more — show all
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
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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.