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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.
54 matches for
Hinds D,
showing the first 14.
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
and 27 more — show all
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
3 pages
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Chang D,
Nalls MA,
Hallgrímsdóttir IB,
Hunkapiller J,
van der Brug M,
Cai F,
Kerchner GA,
Ayalon G,
Bingol B,
Sheng M,
Hinds D,
Behrens TW
and 3 more — show all
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides
Kooner JS,
Chambers JC,
Aguilar-Salinas CA,
Hinds DA,
Hyde CL,
Warnes GR,
Gómez Pérez FJ,
Frazer KA,
Elliott P,
Scott J,
Milos PM,
Cox DR
and 1 more — show all
Nature genetics · 2008 · PMID 18193046
2 pages
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Day FR,
Hinds DA,
Tung JY,
Stolk L,
Styrkarsdottir U,
Saxena R,
Bjonnes A,
Broer L,
Dunger DB,
Halldorsson BV,
Lawlor DA,
Laval G
and 15 more — show all
Mathieson I,
McCardle WL,
Louwers Y,
Meun C,
Ring S,
Scott RA,
Sulem P,
Uitterlinden AG,
Wareham NJ,
Thorsteinsdottir U,
Welt C,
Stefansson K,
Laven JSE,
Ong KK,
Perry JRB
Nature communications · 2015 · PMID 26416764 · open access
2 pages
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis
Hinds DA,
Buil A,
Ziemek D,
Martinez-Perez A,
Malik R,
Folkersen L,
Germain M,
Mälarstig A,
Brown A,
Soria JM,
Dichgans M,
Bing N
and 7 more — show all
METASTROKE Consortium, INVENT Consortium
Human molecular genetics · 2016 · PMID 26908601
2 pages
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Zhang G,
Feenstra B,
Bacelis J,
Liu X,
Muglia LM,
Juodakis J,
Miller DE,
Litterman N,
Jiang PP,
Russell L,
Hinds DA,
Hu Y
and 26 more — show all
Weirauch MT,
Chen X,
Chavan AR,
Wagner GP,
Pavličev M,
Nnamani MC,
Maziarz J,
Karjalainen MK,
Rämet M,
Sengpiel V,
Geller F,
Boyd HA,
Palotie A,
Momany A,
Bedell B,
Ryckman KK,
Huusko JM,
Forney CR,
Kottyan LC,
Hallman M,
Teramo K,
Nohr EA,
Davey Smith G,
Melbye M,
Jacobsson B,
Muglia LJ
The New England journal of medicine · 2017 · PMID 28877031 · open access
2 pages
A genomewide association study of skin pigmentation in a South Asian population
Stokowski RP,
Pant PV,
Dadd T,
Fereday A,
Hinds DA,
Jarman C,
Filsell W,
Ginger RS,
Green MR,
van der Ouderaa FJ,
Cox DR
American journal of human genetics · 2007 · PMID 17999355
1 page
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Lo MT,
Hinds DA,
Tung JY,
Franz C,
Fan CC,
Wang Y,
Smeland OB,
Schork A,
Holland D,
Kauppi K,
Sanyal N,
Escott-Price V
and 10 more — show all
Nature genetics · 2017 · PMID 27918536
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
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.