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2,665 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.
27 matches for
Ellinghaus D,
showing the first 7.
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Schröder J,
Chegwidden L,
Maj C,
Gehlen J,
Speller J,
Böhmer AC,
Borisov O,
Hess T,
Kreuser N,
Venerito M,
Alakus H,
May A
and 56 more — show all
Gerges C,
Schmidt T,
Thieme R,
Heider D,
Hillmer AM,
Reingruber J,
Lyros O,
Dietrich A,
Hoffmeister A,
Mehdorn M,
Lordick F,
Stocker G,
Hohaus M,
Reim D,
Kandler J,
Müller M,
Ebigbo A,
Fuchs C,
Bruns CJ,
Hölscher AH,
Lang H,
Grimminger PP,
Dakkak D,
Vashist Y,
May S,
Görg S,
Franke A,
Ellinghaus D,
Galavotti S,
Veits L,
Weismüller J,
Dommermuth J,
Benner U,
Rösch T,
Messmann H,
Schumacher B,
Neuhaus H,
Schmidt C,
Wissinowski TT,
Nöthen MM,
Dong J,
Ong JS,
Buas MF,
Thrift AP,
Vaughan TL,
Tomlinson I,
Whiteman DC,
Fitzgerald RC,
Jankowski J,
Vieth M,
Mayr A,
Gharahkhani P,
MacGregor S,
Gockel I,
Palles C,
Schumacher J
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 pages
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
Ellinghaus E,
Ellinghaus D,
Stuart PE,
Nair RP,
Debrus S,
Raelson JV,
Belouchi M,
Fournier H,
Reinhard C,
Ding J,
Li Y,
Tejasvi T
and 21 more — show all
Gudjonsson J,
Stoll SW,
Voorhees JJ,
Lambert S,
Weidinger S,
Eberlein B,
Kunz M,
Rahman P,
Gladman DD,
Gieger C,
Wichmann HE,
Karlsen TH,
Mayr G,
Albrecht M,
Kabelitz D,
Mrowietz U,
Abecasis GR,
Elder JT,
Schreiber S,
Weichenthal M,
Franke A
Nature genetics · 2010 · PMID 20953188
1 page
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
Ellinghaus E,
Stanulla M,
Richter G,
Ellinghaus D,
te Kronnie G,
Cario G,
Cazzaniga G,
Horstmann M,
Panzer Grümayer R,
Cavé H,
Trka J,
Cinek O
and 15 more — show all
Teigler-Schlegel A,
ElSharawy A,
Häsler R,
Nebel A,
Meissner B,
Bartram T,
Lescai F,
Franceschi C,
Giordan M,
Nürnberg P,
Heinzow B,
Zimmermann M,
Schreiber S,
Schrappe M,
Franke A
Leukemia · 2012 · PMID 22076464 · open access
1 page
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4
Ellinghaus D,
Folseraas T,
Holm K,
Ellinghaus E,
Melum E,
Balschun T,
Laerdahl JK,
Shiryaev A,
Gotthardt DN,
Weismüller TJ,
Schramm C,
Wittig M
and 25 more — show all
Bergquist A,
Björnsson E,
Marschall HU,
Vatn M,
Teufel A,
Rust C,
Gieger C,
Wichmann HE,
Runz H,
Sterneck M,
Rupp C,
Braun F,
Weersma RK,
Wijmenga C,
Ponsioen CY,
Mathew CG,
Rutgeerts P,
Vermeire S,
Schrumpf E,
Hov JR,
Manns MP,
Boberg KM,
Schreiber S,
Franke A,
Karlsen TH
Hepatology (Baltimore, Md.) · 2013 · PMID 22821403
1 page
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
Fischer A,
Ellinghaus D,
Nutsua M,
Hofmann S,
Montgomery CG,
Iannuzzi MC,
Rybicki BA,
Petrek M,
Mrazek F,
Pabst S,
Grohé C,
Grunewald J
and 23 more — show all
Ronninger M,
Eklund A,
Padyukov L,
Mihailovic-Vucinic V,
Jovanovic D,
Sterclova M,
Homolka J,
Nöthen MM,
Herms S,
Gieger C,
Strauch K,
Winkelmann J,
Boehm BO,
Brand S,
Büning C,
Schürmann M,
Ellinghaus E,
Baurecht H,
Lieb W,
Nebel A,
Müller-Quernheim J,
Franke A,
Schreiber S
GenPhenReSa Consortium
American journal of respiratory and critical care medicine · 2015 · PMID 26051272
1 page
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex
Clay-Gilmour AI,
Hahn T,
Preus LM,
Onel K,
Skol A,
Hungate E,
Zhu Q,
Haiman CA,
Stram DO,
Pooler L,
Sheng X,
Yan L
and 21 more — show all
Liu Q,
Hu Q,
Liu S,
Battaglia S,
Zhu X,
Block AW,
Sait SNJ,
Karaesmen E,
Rizvi A,
Weisdorf DJ,
Ambrosone CB,
Tritchler D,
Ellinghaus E,
Ellinghaus D,
Stanulla M,
Clavel J,
Orsi L,
Spellman S,
Pasquini MC,
McCarthy PL,
Sucheston-Campbell LE
Blood advances · 2017 · PMID 29296818
1 page
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
Ellinghaus D,
Degenhardt F,
Bujanda L,
Buti M,
Albillos A,
Invernizzi P,
Fernández J,
Prati D,
Baselli G,
Asselta R,
Grimsrud MM,
Milani C
and 136 more — show all
Aziz F,
Kässens J,
May S,
Wendorff M,
Wienbrandt L,
Uellendahl-Werth F,
Zheng T,
Yi X,
de Pablo R,
Chercoles AG,
Palom A,
Garcia-Fernandez AE,
Rodriguez-Frias F,
Zanella A,
Bandera A,
Protti A,
Aghemo A,
Lleo A,
Biondi A,
Caballero-Garralda A,
Gori A,
Tanck A,
Carreras Nolla A,
Latiano A,
Fracanzani AL,
Peschuck A,
Julià A,
Pesenti A,
Voza A,
Jiménez D,
Mateos B,
Nafria Jimenez B,
Quereda C,
Paccapelo C,
Gassner C,
Angelini C,
Cea C,
Solier A,
Pestaña D,
Muñiz-Diaz E,
Sandoval E,
Paraboschi EM,
Navas E,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Blasi F,
Téllez L,
Blanco-Grau A,
Hemmrich-Stanisak G,
Grasselli G,
Costantino G,
Cardamone G,
Foti G,
Aneli S,
Kurihara H,
ElAbd H,
My I,
Galván-Femenia I,
Martín J,
Erdmann J,
Erdmann J,
Ferrusquía-Acosta J,
Garcia-Etxebarria K,
Izquierdo-Sanchez L,
Bettini LR,
Sumoy L,
Terranova L,
Moreira L,
Santoro L,
Scudeller L,
Mesonero F,
Roade L,
Rühlemann MC,
Schaefer M,
Carrabba M,
Riveiro-Barciela M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Acosta-Herrera M,
D'Angiò M,
Baldini M,
Cazzaniga M,
Schulzky M,
Cecconi M,
Wittig M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Montano N,
Braun N,
Sacchi N,
Martínez N,
Özer O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
Blandino Ortiz A,
de Cid R,
Ferrer R,
Gualtierotti R,
Nieto R,
Goerg S,
Badalamenti S,
Marsal S,
Matullo G,
Pelusi S,
Juzenas S,
Aliberti S,
Monzani V,
Moreno V,
Wesse T,
Lenz TL,
Pumarola T,
Rimoldi V,
Bosari S,
Albrecht W,
Peter W,
Romero-Gómez M,
D'Amato M,
D'Amato M,
Duga S,
Banales JM,
Hov JR,
Folseraas T,
Valenti L,
Franke A,
Karlsen TH
Severe Covid-19 GWAS Group
The New England journal of medicine · 2020 · PMID 32558485 · 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.