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2,660 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.
7 matches for
Esparza-Gordillo J.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
Tachmazidou I,
Hatzikotoulas K,
Southam L,
Esparza-Gordillo J,
Haberland V,
Zheng J,
Johnson T,
Koprulu M,
Zengini E,
Steinberg J,
Wilkinson JM,
Bhatnagar S
and 9 more — show all
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
12 pages+
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
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira MA,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
van Dongen J,
Lu Y,
Rüschendorf F
and 54 more — show all
Esparza-Gordillo J,
Medway CW,
Mountjoy E,
Burrows K,
Hummel O,
Grosche S,
Brumpton BM,
Witte JS,
Hottenga JJ,
Willemsen G,
Zheng J,
Rodríguez E,
Hotze M,
Franke A,
Revez JA,
Beesley J,
Matheson MC,
Dharmage SC,
Bain LM,
Fritsche LG,
Gabrielsen ME,
Balliu B,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Arnold A,
Homuth G,
Schmidt CO,
Thompson PJ,
Martin NG,
Duffy DL,
Novak N,
Schulz H,
Karrasch S,
Gieger C,
Strauch K,
Melles RB,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PKE,
Jansen R,
Jorgenson E,
Lee YA,
Boomsma DI,
Almqvist C,
Karlsson R,
Koppelman GH,
Paternoster L
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 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
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
Baurecht H,
Hotze M,
Brand S,
Büning C,
Cormican P,
Corvin A,
Ellinghaus D,
Ellinghaus E,
Esparza-Gordillo J,
Fölster-Holst R,
Franke A,
Gieger C
and 26 more — show all
Hubner N,
Illig T,
Irvine AD,
Kabesch M,
Lee YA,
Lieb W,
Marenholz I,
McLean WH,
Morris DW,
Mrowietz U,
Nair R,
Nöthen MM,
Novak N,
O'Regan GM,
Schreiber S,
Smith C,
Strauch K,
Stuart PE,
Trembath R,
Tsoi LC,
Weichenthal M,
Barker J,
Elder JT,
Weidinger S,
Cordell HJ,
Brown SJ
Psoriasis Association Genetics Extension
American journal of human genetics · 2015 · PMID 25574825 · open access
5 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
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.