For researchers
Is your paper here?
2,677 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.
69 matches for
Franke A,
showing the first 9.
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Juran BD,
Hirschfield GM,
Invernizzi P,
Atkinson EJ,
Li Y,
Xie G,
Kosoy R,
Ransom M,
Sun Y,
Bianchi I,
Schlicht EM,
Lleo A
and 29 more — show all
Coltescu C,
Bernuzzi F,
Podda M,
Lammert C,
Shigeta R,
Chan LL,
Balschun T,
Marconi M,
Cusi D,
Heathcote EJ,
Mason AL,
Myers RP,
Milkiewicz P,
Odin JA,
Luketic VA,
Bacon BR,
Bodenheimer HC Jr,
Liakina V,
Vincent C,
Levy C,
Franke A,
Gregersen PK,
Bossa F,
Gershwin ME,
deAndrade M,
Amos CI,
Lazaridis KN,
Seldin MF,
Siminovitch KA
Italian PBC Genetics Study Group
Human molecular genetics · 2012 · PMID 22936693
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
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Stuart PE,
Nair RP,
Tsoi LC,
Tejasvi T,
Das S,
Kang HM,
Ellinghaus E,
Chandran V,
Callis-Duffin K,
Ike R,
Li Y,
Wen X
and 28 more — show all
Enerbäck C,
Gudjonsson JE,
Kõks S,
Kingo K,
Esko T,
Mrowietz U,
Reis A,
Wichmann HE,
Gieger C,
Hoffmann P,
Nöthen MM,
Winkelmann J,
Kunz M,
Moreta EG,
Mease PJ,
Ritchlin CT,
Bowcock AM,
Krueger GG,
Lim HW,
Weidinger S,
Weichenthal M,
Voorhees JJ,
Rahman P,
Gregersen PK,
Franke A,
Gladman DD,
Abecasis GR,
Elder JT
American journal of human genetics · 2015 · PMID 26626624
1 page
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
Schafmayer C,
Harrison JW,
Buch S,
Lange C,
Reichert MC,
Hofer P,
Cossais F,
Kupcinskas J,
von Schönfels W,
Schniewind B,
Kruis W,
Tepel J
and 51 more — show all
Zobel M,
Rosendahl J,
Jacobi T,
Walther-Berends A,
Schroeder M,
Vogel I,
Sergeev P,
Boedeker H,
Hinrichsen H,
Volk A,
Erk JU,
Burmeister G,
Hendricks A,
Hinz S,
Wolff S,
Böttner M,
Wood AR,
Tyrrell J,
Beaumont RN,
Langheinrich M,
Kucharzik T,
Brezina S,
Huber-Schönauer U,
Pietsch L,
Noack LS,
Brosch M,
Herrmann A,
Thangapandi RV,
Schimming HW,
Zeissig S,
Palm S,
Focke G,
Andreasson A,
Schmidt PT,
Weitz J,
Krawczak M,
Völzke H,
Leeb G,
Michl P,
Lieb W,
Grützmann R,
Franke A,
Lammert F,
Becker T,
Kupcinskas L,
D'Amato M,
Wedel T,
Datz C,
Gsur A,
Weedon MN,
Hampe J
Gut · 2019 · PMID 30661054
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
Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide
Stuart PE,
Tsoi LC,
Nair RP,
Ghosh M,
Kabra M,
Shaiq PA,
Raja GK,
Qamar R,
Thelma BK,
Patrick MT,
Parihar A,
Singh S
and 11 more — show all
Khandpur S,
Kumar U,
Wittig M,
Degenhardt F,
Tejasvi T,
Voorhees JJ,
Weidinger S,
Franke A,
Abecasis GR,
Sharma VK,
Elder JT
HGG advances · 2022 · PMID 34927100 · open access
1 page
GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome
Bonfiglio F,
Liu X,
Smillie C,
Pandit A,
Kurilshikov A,
Bacigalupe R,
Zheng T,
Nim H,
Garcia-Etxebarria K,
Bujanda L,
Andreasson A,
Agreus L
and 15 more — show all
Walter S,
Abecasis G,
Eijsbouts C,
Jostins L,
Parkes M,
Hughes DA,
Timpson N,
Raes J,
Franke A,
Kennedy NA,
Regev A,
Zhernakova A,
Simren M,
Camilleri M,
D'Amato M
Cell genomics · 2021 · PMID 34957435 · open access
1 page
Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset
Homann J,
Osburg T,
Ohlei O,
Dobricic V,
Deecke L,
Bos I,
Vandenberghe R,
Gabel S,
Scheltens P,
Teunissen CE,
Engelborghs S,
Frisoni G
and 26 more — show all
Blin O,
Richardson JC,
Bordet R,
Lleó A,
Alcolea D,
Popp J,
Clark C,
Peyratout G,
Martinez-Lage P,
Tainta M,
Dobson RJB,
Legido-Quigley C,
Sleegers K,
Van Broeckhoven C,
Wittig M,
Franke A,
Lill CM,
Blennow K,
Zetterberg H,
Lovestone S,
Streffer J,
Ten Kate M,
Vos SJB,
Barkhof F,
Visser PJ,
Bertram L
Frontiers in aging neuroscience · 2022 · PMID 35386118 · 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.