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2,657 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.
8 matches for
Williams FMK.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Medina-Gomez C,
Kemp JP,
Trajanoska K,
Luan J,
Chesi A,
Ahluwalia TS,
Mook-Kanamori DO,
Ham A,
Hartwig FP,
Evans DS,
Joro R,
Nedeljkovic I
and 77 more — show all
Zheng HF,
Zhu K,
Atalay M,
Liu CT,
Nethander M,
Broer L,
Porleifsson G,
Mullin BH,
Handelman SK,
Nalls MA,
Jessen LE,
Heppe DHM,
Richards JB,
Wang C,
Chawes B,
Schraut KE,
Amin N,
Wareham N,
Karasik D,
Van der Velde N,
Ikram MA,
Zemel BS,
Zhou Y,
Carlsson CJ,
Liu Y,
McGuigan FE,
Boer CG,
Bønnelykke K,
Ralston SH,
Robbins JA,
Walsh JP,
Zillikens MC,
Langenberg C,
Li-Gao R,
Williams FMK,
Harris TB,
Akesson K,
Jackson RD,
Sigurdsson G,
den Heijer M,
van der Eerden BCJ,
van de Peppel J,
Spector TD,
Pennell C,
Horta BL,
Felix JF,
Zhao JH,
Wilson SG,
de Mutsert R,
Bisgaard H,
Styrkársdóttir U,
Jaddoe VW,
Orwoll E,
Lakka TA,
Scott R,
Grant SFA,
Lorentzon M,
van Duijn CM,
Wilson JF,
Stefansson K,
Psaty BM,
Kiel DP,
Ohlsson C,
Ntzani E,
van Wijnen AJ,
Forgetta V,
Ghanbari M,
Logan JG,
Williams GR,
Bassett JHD,
Croucher PI,
Evangelou E,
Uitterlinden AG,
Ackert-Bicknell CL,
Tobias JH,
Evans DM,
Rivadeneira F
American journal of human genetics · 2018 · PMID 29304378
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 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 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
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
Suri P,
Palmer MR,
Tsepilov YA,
Freidin MB,
Boer CG,
Yau MS,
Evans DS,
Gelemanovic A,
Bartz TM,
Nethander M,
Arbeeva L,
Karssen L
and 25 more — show all
Neogi T,
Campbell A,
Mellstrom D,
Ohlsson C,
Marshall LM,
Orwoll E,
Uitterlinden A,
Rotter JI,
Lauc G,
Psaty BM,
Karlsson MK,
Lane NE,
Jarvik GP,
Polasek O,
Hochberg M,
Jordan JM,
Van Meurs JBJ,
Jackson R,
Nielson CM,
Mitchell BD,
Smith BH,
Hayward C,
Smith NL,
Aulchenko YS,
Williams FMK
PLoS genetics · 2018 · PMID 30261039 · open access
1 page
Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Sharapov SZ,
Tsepilov YA,
Klaric L,
Mangino M,
Thareja G,
Shadrina AS,
Simurina M,
Dagostino C,
Dmitrieva J,
Vilaj M,
Vuckovic F,
Pavic T
and 20 more — show all
Stambuk J,
Stambuk J,
Trbojevic-Akmacic I,
Kristic J,
Simunovic J,
Momcilovic A,
Campbell H,
Doherty M,
Dunlop MG,
Farrington SM,
Pucic-Bakovic M,
Gieger C,
Allegri M,
Louis E,
Georges M,
Suhre K,
Spector T,
Williams FMK,
Lauc G,
Aulchenko YS
Human molecular genetics · 2019 · PMID 31163085
1 page
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
Nagtegaal AP,
Broer L,
Zilhao NR,
Jakobsdottir J,
Bishop CE,
Brumat M,
Christiansen MW,
Cocca M,
Gao Y,
Heard-Costa NL,
Evans DS,
Pankratz N
and 30 more — show all
Pratt SR,
Price TR,
Spankovich C,
Stimson MR,
Valle K,
Vuckovic D,
Wells H,
Eiriksdottir G,
Fransen E,
Ikram MA,
Li CM,
Longstreth WT Jr,
Steves C,
Van Camp G,
Correa A,
Cruickshanks KJ,
Gasparini P,
Girotto G,
Kaplan RC,
Nalls M,
Schweinfurth JM,
Seshadri S,
Sotoodehnia N,
Tranah GJ,
Uitterlinden AG,
Wilson JG,
Gudnason V,
Hoffman HJ,
Williams FMK,
Goedegebure A
Scientific reports · 2019 · PMID 31645637 · 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.