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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.
13 matches for
Palta P.
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+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
and 140 more — show all
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
Salo V,
Määttä J,
Sliz E,
Reimann E,
Mägi R,
Reis K,
Elhanas AG,
Reigo A,
Palta P,
Esko T,
Karppinen J,
Kettunen J
FinnGen · Estonian Biobank Research Team
Nature communications · 2024 · PMID 39511132 · open access
12 pages+
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses
Pujol Gualdo N,
Džigurski J,
Rukins V,
Pajuste FD,
Wolford BN,
Võsa M,
Golob M,
Haug L,
Alver M,
Läll K,
Peters M,
Brumpton BM
and 3 more — show all
Estonian Biobank Research Team
Nature medicine · 2025 · PMID 40069456
12 pages+
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P,
Anttila V,
Winsvold BS,
Palta P,
Esko T,
Pers TH,
Farh KH,
Cuenca-Leon E,
Muona M,
Furlotte NA,
Kurth T,
Ingason A
and 95 more — show all
McMahon G,
Ligthart L,
Terwindt GM,
Kallela M,
Freilinger TM,
Ran C,
Gordon SG,
Stam AH,
Steinberg S,
Borck G,
Koiranen M,
Quaye L,
Adams HH,
Lehtimäki T,
Sarin AP,
Wedenoja J,
Hinds DA,
Buring JE,
Schürks M,
Ridker PM,
Hrafnsdottir MG,
Stefansson H,
Ring SM,
Hottenga JJ,
Penninx BW,
Färkkilä M,
Artto V,
Kaunisto M,
Vepsäläinen S,
Malik R,
Heath AC,
Madden PA,
Martin NG,
Montgomery GW,
Kurki MI,
Kals M,
Mägi R,
Pärn K,
Hämäläinen E,
Huang H,
Byrnes AE,
Franke L,
Huang J,
Stergiakouli E,
Lee PH,
Sandor C,
Webber C,
Cader Z,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Eriksson JG,
Salomaa V,
Heikkilä K,
Loehrer E,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Cherkas L,
Pedersen LM,
Stubhaug A,
Nielsen CS,
Männikkö M,
Mihailov E,
Milani L,
Göbel H,
Esserlind AL,
Christensen AF,
Hansen TF,
Werge T,
Kaprio J,
Aromaa AJ,
Raitakari O,
Ikram MA,
Spector T,
Järvelin MR,
Metspalu A,
Kubisch C,
Strachan DP,
Ferrari MD,
Belin AC,
Dichgans M,
Wessman M,
van den Maagdenberg AM,
Zwart JA,
Boomsma DI,
Smith GD,
Stefansson K,
Eriksson N,
Daly MJ,
Neale BM,
Olesen J,
Chasman DI,
Nyholt DR,
Palotie A
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 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
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
6 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
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
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
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
and 85 more — show all
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene
Rahimov F,
Nieminen P,
Kumari P,
Juuri E,
Nikopensius T,
Paraiso K,
German J,
Karvanen A,
Kals M,
Elnahas AG,
Karjalainen J,
Kurki M
and 16 more — show all
Palotie A,
Heliövaara A,
Esko T,
Jukarainen S,
Palta P,
Ganna A,
Patni AP,
Mar D,
Bomsztyk K,
Mathieu J,
Ruohola-Baker H,
Visel A,
Fakhouri WD,
Schutte BC,
Cornell RA,
Rice DP
FinnGen · Estonian Biobank Research Team
Nature communications · 2024 · PMID 39500877 · open access
2 pages
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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
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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?
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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
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keep in step, because the citation lives on the page that makes the claim.