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2,660 papers hold this site up. Every variant and condition page names
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7 matches for
Invernizzi P.
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
Cordell HJ,
Fryett JJ,
Ueno K,
Darlay R,
Aiba Y,
Hitomi Y,
Kawashima M,
Nishida N,
Khor SS,
Gervais O,
Kawai Y,
Nagasaki M
and 31 more — show all
Tokunaga K,
Tang R,
Shi Y,
Li Z,
Juran BD,
Atkinson EJ,
Gerussi A,
Carbone M,
Asselta R,
Cheung A,
de Andrade M,
Baras A,
Horowitz J,
Ferreira MAR,
Sun D,
Jones DE,
Flack S,
Spicer A,
Mulcahy VL,
Byan J,
Han Y,
Sandford RN,
Lazaridis KN,
Amos CI,
Hirschfield GM,
Seldin MF,
Invernizzi P,
Siminovitch KA,
Ma X,
Nakamura M,
Mells GF
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
9 pages
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
Ji SG,
Juran BD,
Mucha S,
Folseraas T,
Jostins L,
Melum E,
Kumasaka N,
Atkinson EJ,
Schlicht EM,
Liu JZ,
Shah T,
Gutierrez-Achury J
and 58 more — show all
Boberg KM,
Bergquist A,
Vermeire S,
Eksteen B,
Durie PR,
Farkkila M,
Müller T,
Schramm C,
Sterneck M,
Weismüller TJ,
Gotthardt DN,
Ellinghaus D,
Braun F,
Teufel A,
Laudes M,
Lieb W,
Jacobs G,
Beuers U,
Weersma RK,
Wijmenga C,
Marschall HU,
Milkiewicz P,
Pares A,
Kontula K,
Chazouillères O,
Invernizzi P,
Goode E,
Spiess K,
Moore C,
Sambrook J,
Ouwehand WH,
Roberts DJ,
Danesh J,
Floreani A,
Gulamhusein AF,
Eaton JE,
Schreiber S,
Coltescu C,
Bowlus CL,
Luketic VA,
Odin JA,
Chopra KB,
Kowdley KV,
Chalasani N,
Manns MP,
Srivastava B,
Mells G,
Sandford RN,
Alexander G,
Gaffney DJ,
Chapman RW,
Hirschfield GM,
de Andrade M,
Rushbrook SM,
Franke A,
Karlsen TH,
Lazaridis KN,
Anderson CA
UK-PSC Consortium · International IBD Genetics Consortium and 1 more consortia
Nature genetics · 2017 · PMID 27992413 · open access
8 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
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Cordell HJ,
Han Y,
Mells GF,
Li Y,
Hirschfield GM,
Greene CS,
Xie G,
Juran BD,
Zhu D,
Qian DC,
Floyd JA,
Morley KI
and 11 more — show all
Prati D,
Lleo A,
Cusi D,
Gershwin ME,
Anderson CA,
Lazaridis KN,
Invernizzi P,
Seldin MF,
Sandford RN,
Amos CI,
Siminovitch KA
Canadian-US PBC Consortium · Italian PBC Genetics Study Group and 1 more consortia
Nature communications · 2015 · PMID 26394269 · open access
3 pages
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Liu X,
Invernizzi P,
Lu Y,
Kosoy R,
Lu Y,
Bianchi I,
Podda M,
Xu C,
Xie G,
Macciardi F,
Selmi C,
Lupoli S
and 61 more — show all
Shigeta R,
Ransom M,
Lleo A,
Lee AT,
Mason AL,
Myers RP,
Peltekian KM,
Ghent CN,
Bernuzzi F,
Zuin M,
Rosina F,
Borghesio E,
Floreani A,
Lazzari R,
Niro G,
Andriulli A,
Muratori L,
Muratori P,
Almasio PL,
Andreone P,
Margotti M,
Brunetto M,
Coco B,
Alvaro D,
Bragazzi MC,
Marra F,
Pisano A,
Rigamonti C,
Colombo M,
Marzioni M,
Benedetti A,
Fabris L,
Strazzabosco M,
Portincasa P,
Palmieri VO,
Tiribelli C,
Croce L,
Bruno S,
Rossi S,
Vinci M,
Prisco C,
Mattalia A,
Toniutto P,
Picciotto A,
Galli A,
Ferrari C,
Ferrari C,
Colombo S,
Casella G,
Morini L,
Caporaso N,
Colli A,
Spinzi G,
Montanari R,
Gregersen PK,
Heathcote EJ,
Hirschfield GM,
Siminovitch KA,
Amos CI,
Gershwin ME,
Seldin MF
Nature genetics · 2010 · PMID 20639880
2 pages
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
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.