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3 matches for
Wendorff M.
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies
Strippel C,
Herrera-Rivero M,
Wendorff M,
Tietz AK,
Degenhardt F,
Witten A,
Schroeter C,
Nelke C,
Golombeck KS,
Madlener M,
Rüber T,
Ernst L
and 57 more — show all
Racz A,
Baumgartner T,
Widman G,
Doppler K,
Thaler F,
Siebenbrodt K,
Dik A,
Kerin C,
Räuber S,
Gallus M,
Kovac S,
Grauer OM,
Grimm A,
Prüss H,
Wickel J,
Geis C,
Lewerenz J,
Goebels N,
Ringelstein M,
Menge T,
Tackenberg B,
Kellinghaus C,
Bien CG,
Kraft A,
Zettl U,
Ismail FS,
Ayzenberg I,
Urbanek C,
Sühs KW,
Tauber SC,
Mues S,
Körtvélyessy P,
Markewitz R,
Paliantonis A,
Elger CE,
Surges R,
Sommer C,
Kümpfel T,
Gross CC,
Lerche H,
Wellmer J,
Quesada CM,
Then Bergh F,
Wandinger KP,
Becker AJ,
Kunz WS,
Meyer Zu Hörste G,
Malter MP,
Rosenow F,
Wiendl H,
Kuhlenbäumer G,
Leypoldt F,
Lieb W,
Franke A,
Meuth SG,
Stoll M,
Melzer N
German Network for Research on Autoimmune Encephalitis (GENERATE)
Brain : a journal of neurology · 2023 · PMID 35348614 · open access
7 pages
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
Degenhardt F,
Ellinghaus D,
Juzenas S,
Lerga-Jaso J,
Wendorff M,
Maya-Miles D,
Uellendahl-Werth F,
ElAbd H,
Rühlemann MC,
Arora J,
Özer O,
Lenning OB
and 317 more — show all
Myhre R,
Vadla MS,
Wacker EM,
Wienbrandt L,
Blandino Ortiz A,
de Salazar A,
Garrido Chercoles A,
Palom A,
Ruiz A,
Garcia-Fernandez AE,
Blanco-Grau A,
Mantovani A,
Zanella A,
Holten AR,
Mayer A,
Bandera A,
Cherubini A,
Protti A,
Aghemo A,
Gerussi A,
Ramirez A,
Braun A,
Nebel A,
Barreira A,
Lleo A,
Teles A,
Kildal AB,
Biondi A,
Caballero-Garralda A,
Ganna A,
Gori A,
Glück A,
Lind A,
Tanck A,
Hinney A,
Carreras Nolla A,
Fracanzani AL,
Peschuck A,
Cavallero A,
Dyrhol-Riise AM,
Ruello A,
Julià A,
Muscatello A,
Pesenti A,
Voza A,
Rando-Segura A,
Solier A,
Schmidt A,
Cortes B,
Mateos B,
Nafria-Jimenez B,
Schaefer B,
Jensen B,
Bellinghausen C,
Maj C,
Ferrando C,
de la Horra C,
Quereda C,
Skurk C,
Thibeault C,
Scollo C,
Herr C,
Spinner CD,
Gassner C,
Lange C,
Hu C,
Paccapelo C,
Lehmann C,
Angelini C,
Cappadona C,
Azuure C,
Bianco C,
Cea C,
Sancho C,
Hoff DAL,
Galimberti D,
Prati D,
Haschka D,
Jiménez D,
Pestaña D,
Toapanta D,
Muñiz-Diaz E,
Azzolini E,
Sandoval E,
Binatti E,
Scarpini E,
Helbig ET,
Casalone E,
Urrechaga E,
Paraboschi EM,
Pontali E,
Reverter E,
Calderón EJ,
Navas E,
Solligård E,
Contro E,
Arana-Arri E,
Aziz F,
Garcia F,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Kurth F,
Blasi F,
Malvestiti F,
Medrano FJ,
Mesonero F,
Rodriguez-Frias F,
Hanses F,
Müller F,
Hemmrich-Stanisak G,
Bellani G,
Grasselli G,
Pezzoli G,
Costantino G,
Albano G,
Cardamone G,
Bellelli G,
Citerio G,
Foti G,
Lamorte G,
Matullo G,
Baselli G,
Kurihara H,
Neb H,
My I,
Kurth I,
Hernández I,
Pink I,
de Rojas I,
Galván-Femenia I,
Holter JC,
Afset JE,
Heyckendorf J,
Kässens J,
Damås JK,
Rybniker J,
Altmüller J,
Ampuero J,
Martín J,
Erdmann J,
Banales JM,
Badia JR,
Dopazo J,
Schneider J,
Bergan J,
Barretina J,
Walter J,
Hernández Quero J,
Goikoetxea J,
Delgado J,
Guerrero JM,
Fazaal J,
Kraft J,
Schröder J,
Risnes K,
Banasik K,
Müller KE,
Gaede KI,
Garcia-Etxebarria K,
Tonby K,
Heggelund L,
Izquierdo-Sanchez L,
Bettini LR,
Sumoy L,
Sander LE,
Lippert LJ,
Terranova L,
Nkambule L,
Knopp L,
Gustad LT,
Garbarino L,
Santoro L,
Téllez L,
Roade L,
Ostadreza M,
Intxausti M,
Kogevinas M,
Riveiro-Barciela M,
Berger MM,
Schaefer M,
Niemi MEK,
Gutiérrez-Stampa MA,
Carrabba M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Vehreschild MJGT,
Manunta M,
Acosta-Herrera M,
D'Angiò M,
Baldini M,
Cazzaniga M,
Grimsrud MM,
Cornberg M,
Nöthen MM,
Marquié M,
Castoldi M,
Cordioli M,
Cecconi M,
D'Amato M,
Augustin M,
Tomasi M,
Boada M,
Dreher M,
Seilmaier MJ,
Joannidis M,
Wittig M,
Mazzocco M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Imaz Ayo N,
Blay N,
Chueca N,
Montano N,
Braun N,
Ludwig N,
Marx N,
Martínez N,
Cornely OA,
Witzke O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
España PP,
Hoffmann P,
Rosenstiel P,
Schommers P,
Suwalski P,
de Pablo R,
Ferrer R,
Bals R,
Gualtierotti R,
Gallego-Durán R,
Nieto R,
Carpani R,
Morilla R,
Badalamenti S,
Haider S,
Ciesek S,
May S,
Bombace S,
Marsal S,
Pigazzini S,
Klein S,
Pelusi S,
Wilfling S,
Bosari S,
Volland S,
Brunak S,
Raychaudhuri S,
Schreiber S,
Heilmann-Heimbach S,
Aliberti S,
Ripke S,
Dudman S,
Wesse T,
Zheng T,
Bahmer T,
Eggermann T,
Illig T,
Brenner T,
Pumarola T,
Feldt T,
Folseraas T,
Gonzalez Cejudo T,
Landmesser U,
Protzer U,
Hehr U,
Rimoldi V,
Monzani V,
Skogen V,
Keitel V,
Kopfnagel V,
Friaza V,
Andrade V,
Moreno V,
Albrecht W,
Peter W,
Poller W,
Farre X,
Yi X,
Wang X,
Khodamoradi Y,
Karadeniz Z,
Latiano A,
Goerg S,
Bacher P,
Koehler P,
Tran F,
Zoller H,
Schulte EC,
Heidecker B,
Ludwig KU,
Fernández J,
Romero-Gómez M,
Albillos A,
Invernizzi P,
Buti M,
Duga S,
Bujanda L,
Hov JR,
Lenz TL,
Asselta R,
de Cid R,
Valenti L,
Karlsen TH,
Cáceres M,
Franke A
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
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
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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.