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Is your paper here?
2,663 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.
5 matches for
Marks GB.
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
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Grosche S,
Marenholz I,
Esparza-Gordillo J,
Arnau-Soler A,
Pairo-Castineira E,
Rüschendorf F,
Ahluwalia TS,
Almqvist C,
Arnold A,
Baurecht H,
Bisgaard H,
Bønnelykke K
and 50 more — show all
Brown SJ,
Bustamante M,
Curtin JA,
Custovic A,
Dharmage SC,
Esplugues A,
Falchi M,
Fernandez-Orth D,
Ferreira MAR,
Franke A,
Gerdes S,
Gieger C,
Hakonarson H,
Holt PG,
Homuth G,
Hubner N,
Hysi PG,
Jarvelin MR,
Karlsson R,
Koppelman GH,
Lau S,
Lutz M,
Magnusson PKE,
Marks GB,
Müller-Nurasyid M,
Nöthen MM,
Paternoster L,
Pennell CE,
Peters A,
Rawlik K,
Robertson CF,
Rodriguez E,
Sebert S,
Simpson A,
Sleiman PMA,
Standl M,
Stölzl D,
Strauch K,
Szwajda A,
Tenesa A,
Thompson PJ,
Ullemar V,
Visconti A,
Vonk JM,
Wang CA,
Weidinger S,
Wielscher M,
Worth CL,
Xu CJ,
Lee YA
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 pages
Meta-analysis identifies seven susceptibility loci involved in the atopic march
Marenholz I,
Esparza-Gordillo J,
Rüschendorf F,
Bauerfeind A,
Strachan DP,
Spycher BD,
Baurecht H,
Margaritte-Jeannin P,
Sääf A,
Kerkhof M,
Ege M,
Baltic S
and 61 more — show all
Matheson MC,
Li J,
Michel S,
Ang WQ,
McArdle W,
Arnold A,
Homuth G,
Demenais F,
Bouzigon E,
Söderhäll C,
Pershagen G,
de Jongste JC,
Postma DS,
Braun-Fahrländer C,
Horak E,
Ogorodova LM,
Puzyrev VP,
Bragina EY,
Hudson TJ,
Morin C,
Duffy DL,
Marks GB,
Robertson CF,
Montgomery GW,
Musk B,
Thompson PJ,
Martin NG,
James A,
Sleiman P,
Toskala E,
Rodriguez E,
Fölster-Holst R,
Franke A,
Lieb W,
Gieger C,
Heinzmann A,
Rietschel E,
Keil T,
Cichon S,
Nöthen MM,
Pennell CE,
Sly PD,
Schmidt CO,
Matanovic A,
Schneider V,
Heinig M,
Hübner N,
Holt PG,
Lau S,
Kabesch M,
Weidinger S,
Hakonarson H,
Ferreira MAR,
Laprise C,
Freidin MB,
Genuneit J,
Koppelman GH,
Melén E,
Dizier MH,
Henderson AJ,
Lee YA
Nature communications · 2015 · PMID 26542096 · open access
3 pages
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA
Ramasamy A,
Kuokkanen M,
Vedantam S,
Gajdos ZK,
Couto Alves A,
Lyon HN,
Ferreira MA,
Strachan DP,
Zhao JH,
Abramson MJ,
Brown MA,
Coin L
and 34 more — show all
Dharmage SC,
Duffy DL,
Haahtela T,
Heath AC,
Janson C,
Kähönen M,
Khaw KT,
Laitinen J,
Le Souef P,
Lehtimäki T,
Madden PA,
Marks GB,
Martin NG,
Matheson MC,
Palmer CD,
Palotie A,
Pouta A,
Robertson CF,
Viikari J,
Widen E,
Wjst M,
Jarvis DL,
Montgomery GW,
Thompson PJ,
Wareham N,
Eriksson J,
Jousilahti P,
Laitinen T,
Pekkanen J,
Raitakari OT,
O'Connor GT,
Salomaa V,
Jarvelin MR,
Hirschhorn JN
Australian Asthma Genetics Consortium Collaborators
PloS one · 2012 · PMID 23028483 · open access
2 pages
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
Ferreira MA,
Matheson MC,
Duffy DL,
Marks GB,
Hui J,
Le Souëf P,
Danoy P,
Baltic S,
Nyholt DR,
Jenkins M,
Hayden C,
Willemsen G
and 28 more — show all
Ang W,
Kuokkanen M,
Beilby J,
Cheah F,
de Geus EJ,
Ramasamy A,
Vedantam S,
Salomaa V,
Madden PA,
Heath AC,
Hopper JL,
Visscher PM,
Musk B,
Leeder SR,
Jarvelin MR,
Pennell C,
Boomsma DI,
Hirschhorn JN,
Walters H,
Martin NG,
James A,
Jones G,
Abramson MJ,
Robertson CF,
Dharmage SC,
Brown MA,
Montgomery GW,
Thompson PJ
Australian Asthma Genetics Consortium
Lancet (London, England) · 2011 · PMID 21907864
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.