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Matullo G.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 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
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
and 147 more — show all
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
Koutros S,
Kiemeney LA,
Pal Choudhury P,
Milne RL,
Lopez de Maturana E,
Ye Y,
Joseph V,
Florez-Vargas O,
Dyrskjøt L,
Figueroa J,
Dutta D,
Giles GG
and 88 more — show all
Hildebrandt MAT,
Offit K,
Kogevinas M,
Weiderpass E,
McCullough ML,
Freedman ND,
Albanes D,
Kooperberg C,
Cortessis VK,
Karagas MR,
Johnson A,
Schwenn MR,
Baris D,
Furberg H,
Bajorin DF,
Cussenot O,
Cancel-Tassin G,
Benhamou S,
Kraft P,
Porru S,
Carta A,
Bishop T,
Southey MC,
Matullo G,
Fletcher T,
Kumar R,
Taylor JA,
Lamy P,
Prip F,
Kalisz M,
Weinstein SJ,
Hengstler JG,
Selinski S,
Harland M,
Teo M,
Kiltie AE,
Tardón A,
Serra C,
Carrato A,
García-Closas R,
Lloreta J,
Schned A,
Lenz P,
Riboli E,
Brennan P,
Tjønneland A,
Otto T,
Ovsiannikov D,
Volkert F,
Vermeulen SH,
Aben KK,
Galesloot TE,
Turman C,
De Vivo I,
Giovannucci E,
Hunter DJ,
Hohensee C,
Hunt R,
Patel AV,
Huang WY,
Thorleifsson G,
Gago-Dominguez M,
Amiano P,
Golka K,
Stern MC,
Yan W,
Liu J,
Li SA,
Katta S,
Hutchinson A,
Hicks B,
Wheeler WA,
Purdue MP,
McGlynn KA,
Kitahara CM,
Haiman CA,
Greene MH,
Rafnar T,
Chatterjee N,
Chanock SJ,
Wu X,
Real FX,
Silverman DT,
Garcia-Closas M,
Stefansson K,
Prokunina-Olsson L,
Malats N,
Rothman N
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
and 84 more — show all
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · open access
3 pages
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Wu X,
Ye Y,
Kiemeney LA,
Sulem P,
Rafnar T,
Matullo G,
Seminara D,
Yoshida T,
Saeki N,
Andrew AS,
Dinney CP,
Czerniak B
and 36 more — show all
Zhang ZF,
Kiltie AE,
Bishop DT,
Vineis P,
Porru S,
Buntinx F,
Kellen E,
Zeegers MP,
Kumar R,
Rudnai P,
Gurzau E,
Koppova K,
Mayordomo JI,
Sanchez M,
Saez B,
Lindblom A,
de Verdier P,
Steineck G,
Mills GB,
Schned A,
Guarrera S,
Polidoro S,
Chang SC,
Lin J,
Chang DW,
Hale KS,
Majewski T,
Grossman HB,
Thorlacius S,
Thorsteinsdottir U,
Aben KK,
Witjes JA,
Stefansson K,
Amos CI,
Karagas MR,
Gu J
Nature genetics · 2009 · PMID 19648920
2 pages
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Rothman N,
Garcia-Closas M,
Chatterjee N,
Malats N,
Wu X,
Figueroa JD,
Real FX,
Van Den Berg D,
Matullo G,
Baris D,
Thun M,
Kiemeney LA
and 98 more — show all
Vineis P,
De Vivo I,
Albanes D,
Purdue MP,
Rafnar T,
Hildebrandt MA,
Kiltie AE,
Cussenot O,
Golka K,
Kumar R,
Taylor JA,
Mayordomo JI,
Jacobs KB,
Kogevinas M,
Hutchinson A,
Wang Z,
Fu YP,
Prokunina-Olsson L,
Burdett L,
Yeager M,
Wheeler W,
Tardón A,
Serra C,
Carrato A,
García-Closas R,
Lloreta J,
Johnson A,
Schwenn M,
Karagas MR,
Schned A,
Andriole G Jr,
Grubb R 3rd,
Black A,
Jacobs EJ,
Diver WR,
Gapstur SM,
Weinstein SJ,
Virtamo J,
Cortessis VK,
Gago-Dominguez M,
Pike MC,
Stern MC,
Yuan JM,
Hunter DJ,
McGrath M,
Dinney CP,
Czerniak B,
Chen M,
Yang H,
Vermeulen SH,
Aben KK,
Witjes JA,
Makkinje RR,
Sulem P,
Besenbacher S,
Stefansson K,
Riboli E,
Brennan P,
Panico S,
Navarro C,
Allen NE,
Bueno-de-Mesquita HB,
Trichopoulos D,
Caporaso N,
Landi MT,
Canzian F,
Ljungberg B,
Tjonneland A,
Clavel-Chapelon F,
Bishop DT,
Teo MT,
Knowles MA,
Guarrera S,
Polidoro S,
Ricceri F,
Sacerdote C,
Allione A,
Cancel-Tassin G,
Selinski S,
Hengstler JG,
Dietrich H,
Fletcher T,
Rudnai P,
Gurzau E,
Koppova K,
Bolick SC,
Godfrey A,
Xu Z,
Sanz-Velez JI,
D García-Prats M,
Sanchez M,
Valdivia G,
Porru S,
Benhamou S,
Hoover RN,
Fraumeni JF Jr,
Silverman DT,
Chanock SJ
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
and 104 more — show all
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
2 pages
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Jones E,
Hummerich H,
Viré E,
Uphill J,
Dimitriadis A,
Speedy H,
Campbell T,
Norsworthy P,
Quinn L,
Whitfield J,
Linehan J,
Jaunmuktane Z
and 53 more — show all
Brandner S,
Jat P,
Nihat A,
How Mok T,
Ahmed P,
Collins S,
Stehmann C,
Sarros S,
Kovacs GG,
Geschwind MD,
Golubjatnikov A,
Frontzek K,
Budka H,
Aguzzi A,
Karamujić-Čomić H,
van der Lee SJ,
Ibrahim-Verbaas CA,
van Duijn CM,
Sikorska B,
Golanska E,
Liberski PP,
Calero M,
Calero O,
Sanchez-Juan P,
Salas A,
Martinón-Torres F,
Bouaziz-Amar E,
Haïk S,
Laplanche JL,
Brandel JP,
Amouyel P,
Lambert JC,
Parchi P,
Bartoletti-Stella A,
Capellari S,
Poleggi A,
Ladogana A,
Pocchiari M,
Aneli S,
Matullo G,
Knight R,
Zafar S,
Zerr I,
Booth S,
Coulthart MB,
Jansen GH,
Glisic K,
Blevins J,
Gambetti P,
Safar J,
Appleby B,
Collinge J,
Mead S
The Lancet. Neurology · 2020 · PMID 32949544
2 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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