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Is your paper here?
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.
6 matches for
Glass D.
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
and 140 more — show all
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
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
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms
Zhai G,
Teumer A,
Stolk L,
Perry JR,
Vandenput L,
Coviello AD,
Koster A,
Bell JT,
Bhasin S,
Eriksson J,
Eriksson A,
Ernst F
and 34 more — show all
Ferrucci L,
Frayling TM,
Glass D,
Grundberg E,
Haring R,
Hedman AK,
Hofman A,
Kiel DP,
Kroemer HK,
Liu Y,
Lunetta KL,
Maggio M,
Lorentzon M,
Mangino M,
Melzer D,
Miljkovic I,
Nica A,
Penninx BW,
Vasan RS,
Rivadeneira F,
Small KS,
Soranzo N,
Uitterlinden AG,
Völzke H,
Wilson SG,
Xi L,
Zhuang WV,
Harris TB,
Murabito JM,
Ohlsson C,
Murray A,
de Jong FH,
Spector TD,
Wallaschofski H
MuTHER Consortium
PLoS genetics · 2011 · PMID 21533175 · open access
2 pages
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Hinks A,
Cobb J,
Marion MC,
Prahalad S,
Sudman M,
Bowes J,
Martin P,
Comeau ME,
Sajuthi S,
Andrews R,
Brown M,
Chen WM
and 27 more — show all
Concannon P,
Deloukas P,
Edkins S,
Eyre S,
Gaffney PM,
Guthery SL,
Guthridge JM,
Hunt SE,
James JA,
Keddache M,
Moser KL,
Nigrovic PA,
Onengut-Gumuscu S,
Onslow ML,
Rosé CD,
Rich SS,
Steel KJ,
Wakeland EK,
Wallace CA,
Wedderburn LR,
Woo P,
Bohnsack JF,
Haas JP,
Glass DN,
Langefeld CD,
Thomson W,
Thompson SD
Boston Children's JIA Registry · British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group and 7 more consortia
Nature genetics · 2013 · PMID 23603761 · open access
2 pages
IRF4 variants have age-specific effects on nevus count and predispose to melanoma
Duffy DL,
Iles MM,
Glass D,
Zhu G,
Barrett JH,
Höiom V,
Zhao ZZ,
Sturm RA,
Soranzo N,
Hammond C,
Kvaskoff M,
Whiteman DC
and 9 more — show all
GenoMEL
American journal of human genetics · 2010 · PMID 20602913
1 page
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
Liu F,
Visser M,
Duffy DL,
Hysi PG,
Jacobs LC,
Lao O,
Zhong K,
Walsh S,
Chaitanya L,
Wollstein A,
Zhu G,
Montgomery GW
and 14 more — show all
Henders AK,
Mangino M,
Glass D,
Bataille V,
Sturm RA,
Rivadeneira F,
Hofman A,
van IJcken WF,
Uitterlinden AG,
Palstra RJ,
Spector TD,
Martin NG,
Nijsten TE,
Kayser M
Human genetics · 2015 · PMID 25963972 · 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.