For researchers
Is your paper here?
2,655 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.
9 matches for
Ollila HM.
Genetics of 35 blood and urine biomarkers in the UK Biobank
Sinnott-Armstrong N,
Tanigawa Y,
Amar D,
Mars N,
Benner C,
Aguirre M,
Venkataraman GR,
Wainberg M,
Ollila HM,
Kiiskinen T,
Havulinna AS,
Pirruccello JP
and 11 more — show all
Qian J,
Shcherbina A,
Rodriguez F,
Assimes TL,
Agarwala V,
Tibshirani R,
Hastie T,
Ripatti S,
Pritchard JK,
Daly MJ,
Rivas MA
FinnGen
Nature genetics · 2021 · PMID 33462484 · open access
12 pages+
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
and 2 more — show all
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
12 pages+
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Scammell BH,
Tchio C,
Song Y,
Nishiyama T,
Louie TL,
Dashti HS,
Nakatochi M,
Zee PC,
Daghlas I,
Momozawa Y,
Cai J,
Ollila HM
and 6 more — show all
Human molecular genetics · 2023 · PMID 37384397
11 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
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
Han F,
Faraco J,
Dong XS,
Ollila HM,
Lin L,
Li J,
An P,
Wang S,
Jiang KW,
Gao ZC,
Zhao L,
Yan H
and 13 more — show all
Liu YN,
Li QH,
Zhang XZ,
Hu Y,
Wang JY,
Lu YH,
Lu CJ,
Zhou W,
Hallmayer J,
Huang YS,
Strohl KP,
Pollmächer T,
Mignot E
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
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
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.