For researchers
Is your paper here?
2,671 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.
70 matches for
Evans DM,
showing the first 10.
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
Medina-Gomez C,
Kemp JP,
Estrada K,
Eriksson J,
Liu J,
Reppe S,
Evans DM,
Heppe DH,
Vandenput L,
Herrera L,
Ring SM,
Kruithof CJ
and 16 more — show all
Timpson NJ,
Zillikens MC,
Olstad OK,
Zheng HF,
Richards JB,
St Pourcain B,
Hofman A,
Jaddoe VW,
Smith GD,
Lorentzon M,
Gautvik KM,
Uitterlinden AG,
Brommage R,
Ohlsson C,
Tobias JH,
Rivadeneira F
PLoS genetics · 2012 · PMID 22792070 · open access
1 page
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans
Guggenheim JA,
McMahon G,
Kemp JP,
Akhtar S,
St Pourcain B,
Northstone K,
Ring SM,
Evans DM,
Smith GD,
Timpson NJ,
Williams C
Molecular vision · 2013 · PMID 23401653 · open access
1 page
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence
St Pourcain B,
Skuse DH,
Mandy WP,
Wang K,
Hakonarson H,
Timpson NJ,
Evans DM,
Kemp JP,
Ring SM,
McArdle WL,
Golding J,
Smith GD
Molecular autism · 2014 · PMID 24564958 · open access
1 page
Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis
Robinson PC,
Claushuis TA,
Cortes A,
Martin TM,
Evans DM,
Leo P,
Mukhopadhyay P,
Bradbury LA,
Cremin K,
Harris J,
Maksymowych WP,
Inman RD
and 19 more — show all
Rahman P,
Haroon N,
Gensler L,
Powell JE,
van der Horst-Bruinsma IE,
Hewitt AW,
Craig JE,
Lim LL,
Wakefield D,
McCluskey P,
Voigt V,
Fleming P,
Degli-Esposti M,
Pointon JJ,
Weisman MH,
Wordsworth BP,
Reveille JD,
Rosenbaum JT,
Brown MA
Spondyloarthritis Research Consortium of Canada, Australio-Anglo-American Spondylitis Consortium, International Genetics of Ankylosing Spondylitis Consortium, Wellcome Trust Case Control Study 2, Mariapia Degli-Esposti
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25200001
1 page
A genome-wide association study of body mass index across early life and childhood
Warrington NM,
Howe LD,
Paternoster L,
Kaakinen M,
Herrala S,
Huikari V,
Wu YY,
Kemp JP,
Timpson NJ,
St Pourcain B,
Davey Smith G,
Tilling K
and 6 more — show all
International journal of epidemiology · 2015 · PMID 25953783 · open access
1 page
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Beaumont RN,
Warrington NM,
Cavadino A,
Tyrrell J,
Nodzenski M,
Horikoshi M,
Geller F,
Myhre R,
Richmond RC,
Paternoster L,
Bradfield JP,
Kreiner-Møller E
and 74 more — show all
Huikari V,
Metrustry S,
Lunetta KL,
Painter JN,
Hottenga JJ,
Allard C,
Barton SJ,
Espinosa A,
Marsh JA,
Potter C,
Zhang G,
Ang W,
Berry DJ,
Bouchard L,
Das S,
Hakonarson H,
Heikkinen J,
Helgeland Ø,
Hocher B,
Hofman A,
Inskip HM,
Jones SE,
Kogevinas M,
Lind PA,
Marullo L,
Medland SE,
Murray A,
Murray JC,
Njølstad PR,
Nohr EA,
Reichetzeder C,
Ring SM,
Ruth KS,
Santa-Marina L,
Scholtens DM,
Sebert S,
Sengpiel V,
Tuke MA,
Vaudel M,
Weedon MN,
Willemsen G,
Wood AR,
Yaghootkar H,
Muglia LJ,
Bartels M,
Relton CL,
Pennell CE,
Chatzi L,
Estivill X,
Holloway JW,
Boomsma DI,
Montgomery GW,
Murabito JM,
Spector TD,
Power C,
Järvelin MR,
Bisgaard H,
Grant SFA,
Sørensen TIA,
Jaddoe VW,
Jacobsson B,
Melbye M,
McCarthy MI,
Hattersley AT,
Hayes MG,
Frayling TM,
Hivert MF,
Felix JF,
Hyppönen E,
Lowe WL Jr,
Evans DM,
Lawlor DA,
Feenstra B,
Freathy RM
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis
D'Urso S,
Rajbhandari D,
Peach E,
de Guzman E,
Li Q,
Medland SE,
Gordon SD,
Martin NG,
Ligthart S,
Brown MA,
Powell J,
McArthur C
and 9 more — show all
CHARGE Inflammation Working Group
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2020 · PMID 32755526
1 page
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
and 114 more — show all
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · 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.