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Na J,
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Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial
Ekenberg C,
Tang MH,
Zucco AG,
Murray DD,
MacPherson CR,
Hu X,
Sherman BT,
Losso MH,
Wood R,
Paredes R,
Molina JM,
Helleberg M
and 7 more — show all
The Journal of infectious diseases · 2019 · PMID 31219150
12 pages+
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Gharahkhani P,
Jorgenson E,
Hysi P,
Khawaja AP,
Pendergrass S,
Han X,
Ong JS,
Hewitt AW,
Segrè AV,
Rouhana JM,
Hamel AR,
Igo RP Jr
and 67 more — show all
Choquet H,
Qassim A,
Josyula NS,
Cooke Bailey JN,
Bonnemaijer PWM,
Iglesias A,
Siggs OM,
Young TL,
Vitart V,
Thiadens AAHJ,
Karjalainen J,
Uebe S,
Melles RB,
Nair KS,
Luben R,
Simcoe M,
Amersinghe N,
Cree AJ,
Hohn R,
Poplawski A,
Chen LJ,
Rong SS,
Aung T,
Vithana EN,
Tamiya G,
Shiga Y,
Yamamoto M,
Nakazawa T,
Currant H,
Birney E,
Wang X,
Auton A,
Lupton MK,
Martin NG,
Ashaye A,
Olawoye O,
Williams SE,
Akafo S,
Ramsay M,
Hashimoto K,
Kamatani Y,
Akiyama M,
Momozawa Y,
Foster PJ,
Khaw PT,
Morgan JE,
Strouthidis NG,
Kraft P,
Kang JH,
Pang CP,
Pasutto F,
Mitchell P,
Lotery AJ,
Palotie A,
van Duijn C,
Haines JL,
Hammond C,
Pasquale LR,
Klaver CCW,
Hauser M,
Khor CC,
Mackey DA,
Kubo M,
Cheng CY,
Craig JE,
MacGregor S,
Wiggs JL
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord F,
Klarin D,
Brody JA,
Chen MH,
Levin MG,
Chasman DI,
Goode EL,
Hveem K,
Teder-Laving M,
Martinez-Perez A,
Aïssi D,
Daian-Bacq D
and 76 more — show all
Ito K,
Natarajan P,
Lutsey PL,
Nadkarni GN,
de Vries PS,
Cuellar-Partida G,
Wolford BN,
Pattee JW,
Kooperberg C,
Braekkan SK,
Li-Gao R,
Saut N,
Sept C,
Germain M,
Judy RL,
Wiggins KL,
Ko D,
O'Donnell CJ,
Taylor KD,
Giulianini F,
De Andrade M,
Nøst TH,
Boland A,
Empana JP,
Koyama S,
Gilliland T,
Do R,
Huffman JE,
Wang X,
Wang X,
Zhou W,
Manuel Soria J,
Carlos Souto J,
Pankratz N,
Haessler J,
Hindberg K,
Rosendaal FR,
Turman C,
Olaso R,
Kember RL,
Bartz TM,
Lynch JA,
Heckbert SR,
Armasu SM,
Brumpton B,
Smadja DM,
Jouven X,
Komuro I,
Clapham KR,
Loos RJF,
Willer CJ,
Sabater-Lleal M,
Pankow JS,
Reiner AP,
Morelli VM,
Ridker PM,
Vlieg AVH,
Deleuze JF,
Kraft P,
Rader DJ,
Min Lee K,
Psaty BM,
Heidi Skogholt A,
Emmerich J,
Suchon P,
Rich SS,
Vy HMT,
Tang W,
Jackson RD,
Hansen JB,
Morange PE,
Kabrhel C,
Trégouët DA,
Damrauer SM,
Johnson AD,
Smith NL
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Lagou V,
Jiang L,
Ulrich A,
Zudina L,
González KSG,
Balkhiyarova Z,
Faggian A,
Maina JG,
Chen S,
Todorov PV,
Sharapov S,
David A
and 84 more — show all
Marullo L,
Mägi R,
Rujan RM,
Ahlqvist E,
Thorleifsson G,
Gao Η,
Εvangelou Ε,
Benyamin B,
Scott RA,
Isaacs A,
Zhao JH,
Willems SM,
Johnson T,
Gieger C,
Grallert H,
Meisinger C,
Müller-Nurasyid M,
Strawbridge RJ,
Goel A,
Rybin D,
Albrecht E,
Jackson AU,
Stringham HM,
Corrêa IR Jr,
Farber-Eger E,
Steinthorsdottir V,
Uitterlinden AG,
Munroe PB,
Brown MJ,
Schmidberger J,
Holmen O,
Thorand B,
Hveem K,
Wilsgaard T,
Mohlke KL,
Wang Z,
Shmeliov A,
den Hoed M,
Loos RJF,
Kratzer W,
Haenle M,
Koenig W,
Boehm BO,
Tan TM,
Tomas A,
Salem V,
Barroso I,
Tuomilehto J,
Boehnke M,
Florez JC,
Hamsten A,
Watkins H,
Njølstad I,
Wichmann HE,
Caulfield MJ,
Khaw KT,
van Duijn CM,
Hofman A,
Wareham NJ,
Langenberg C,
Whitfield JB,
Martin NG,
Montgomery G,
Scapoli C,
Tzoulaki I,
Elliott P,
Thorsteinsdottir U,
Stefansson K,
Brittain EL,
McCarthy MI,
Froguel P,
Sexton PM,
Wootten D,
Groop L,
Dupuis J,
Meigs JB,
Deganutti G,
Demirkan A,
Pers TH,
Reynolds CA,
Aulchenko YS,
Kaakinen MA,
Jones B,
Prokopenko I
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Ghouse J,
Sveinbjörnsson G,
Vujkovic M,
Seidelin AS,
Gellert-Kristensen H,
Ahlberg G,
Tragante V,
Rand SA,
Brancale J,
Vilarinho S,
Lundegaard PR,
Sørensen E
and 39 more — show all
Erikstrup C,
Bruun MT,
Jensen BA,
Brunak S,
Banasik K,
Ullum H,
Verweij N,
Lotta L,
Baras A,
Mirshahi T,
Carey DJ,
Kaplan DE,
Lynch J,
Morgan T,
Schwantes-An TH,
Dochtermann DR,
Pyarajan S,
Tsao PS,
Laisk T,
Mägi R,
Kozlitina J,
Tybjærg-Hansen A,
Jones D,
Knowlton KU,
Nadauld L,
Ferkingstad E,
Björnsson ES,
Ulfarsson MO,
Sturluson Á,
Sulem P,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Stefansson K,
Olesen MS,
Chang KM,
Holm H,
Bundgaard H,
Stender S
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Western D,
Timsina J,
Wang L,
Wang C,
Yang C,
Phillips B,
Wang Y,
Liu M,
Ali M,
Beric A,
Gorijala P,
Kohlfeld P
and 28 more — show all
Budde J,
Levey AI,
Morris JC,
Perrin RJ,
Ruiz A,
Marquié M,
Boada M,
de Rojas I,
Rutledge J,
Oh H,
Wilson EN,
Le Guen Y,
Reus LM,
Tijms B,
Visser PJ,
van der Lee SJ,
Pijnenburg YAL,
Teunissen CE,
Del Campo Milan M,
Alvarez I,
Aguilar M,
Greicius MD,
Pastor P,
Pulford DJ,
Ibanez L,
Wyss-Coray T,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Wang C,
Yang C,
Western D,
Ali M,
Wang Y,
Phuah CL,
Budde J,
Wang L,
Gorijala P,
Timsina J,
Ruiz A,
Pastor P
and 14 more — show all
Fernandez MV,
Panyard DJ,
Engelman CD,
Deming Y,
Boada M,
Cano A,
Garcia-Gonzalez P,
Graff-Radford NR,
Mori H,
Lee JH,
Perrin RJ,
Ibanez L,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease
Western D,
Yang C,
Timsina J,
Liu M,
Wang C,
Campbell MC,
Kotzbauer P,
Perlmutter JS,
Schindler SE,
Morris JC,
Holtzman DM,
Alvarez I
and 12 more — show all
Pastor P,
Wyss-Coray T,
Marquié M,
Cano A,
Sung YJ,
de Rojas I,
Ruiz A,
Budde J,
Fernandez MV,
Tarawneh R,
Ibanez L,
Cruchaga C
Science translational medicine · 2026 · PMID 42054495
12 pages+
Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor
Litchfield K,
Levy M,
Levy M,
Orlando G,
Loveday C,
Law PJ,
Migliorini G,
Holroyd A,
Broderick P,
Karlsson R,
Haugen TB,
Kristiansen W
and 20 more — show all
Nsengimana J,
Fenwick K,
Assiotis I,
Kote-Jarai Z,
Dunning AM,
Muir K,
Peto J,
Eeles R,
Easton DF,
Dudakia D,
Orr N,
Pashayan N,
Bishop DT,
Reid A,
Huddart RA,
Shipley J,
Grotmol T,
Wiklund F,
Houlston RS,
Turnbull C
UK Testicular Cancer Collaboration · PRACTICAL Consortium
Nature genetics · 2017 · PMID 28604728
8 pages
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
and 106 more — show all
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · 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
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Wang L,
Nykänen NP,
Western D,
Gorijala P,
Timsina J,
Li F,
Wang Z,
Ali M,
Yang C,
Liu M,
Brock W,
Marquié M
and 21 more — show all
Boada M,
Alvarez I,
Aguilar M,
Pastor P,
Ruiz A,
Puerta R,
Orellana A,
Rutledge J,
Oh H,
Greicius MD,
Le Guen Y,
Perrin RJ,
Wyss-Coray T,
Jefferson A,
Hohman TJ,
Graff-Radford N,
Mori H,
Goate A,
Levin J,
Sung YJ,
Cruchaga C
Molecular neurodegeneration · 2024 · PMID 38172904 · open access
4 pages
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Timsina J,
Jiang C,
McCartney DL,
Tao F,
Dalmasso MC,
Najar J,
Anastasi F,
Ohlei O,
Puerta Fuentes R,
Yang C,
Bradley J,
Western D
and 143 more — show all
Ali M,
Wang C,
Yang C,
Wu Y,
Liu M,
Budde J,
Williams J,
Mahoney R,
Castillo Morales A,
Hohman TJ,
Dumitrescu L,
Wang TC,
Tesi N,
Kern S,
Waern M,
Skoog I,
van Harten A,
Pijnenburg YAL,
van der Flier WM,
Sánchez-Juan P,
Rodriguez-Rodriguez E,
Kleineidam L,
Peters O,
Schneider A,
Küçükali F,
Bellenguez C,
Grenier-Boley B,
Heikkinen S,
de Rojas I,
Rujescu D,
Scherbaum N,
Hausner L,
Düzel E,
Grimmer T,
Wiltfang J,
Vandenberghe R,
Engelborghs S,
Heilmann-Heimbach S,
Schmid M,
Tegos T,
Scarmeas N,
Dols-Icardo O,
Moreno F,
Pérez-Tur J,
Bullido MJ,
Sánchez-Valle R,
Álvarez V,
García-González P,
Mir P,
Real LM,
Piñol-Ripoll G,
García-Alberca JM,
Seelaar H,
Ramakers I,
Papma J,
Hulsman M,
Laske C,
Teipel S,
Priller J,
Perneczky R,
Buerger K,
Nöthen MM,
Lewczuk P,
Kornhuber J,
Hampel H,
Giegling I,
Goldhardt O,
Diehl-Schmid J,
Andrade V,
Heneka MM,
Frölich L,
Vogelgsang J,
Graff C,
Thonberg H,
Ullgren A,
Papenberg G,
Deleuze JF,
Dufouil C,
Wagner M,
Jessen F,
Holstege H,
van Duijn C,
Lebouvier T,
Hannon O,
Leinonen V,
Soininen H,
Herukka SK,
Giedraitis V,
Löwenmark M,
Kilander L,
Genius P,
Rodríguez B,
Luckett ES,
Navarro A,
Cano A,
Marquié M,
Blennow K,
Zetterberg H,
Lleo A,
Boada M,
Ruiz A,
Lee VM,
Van Deerlin VM,
Deming Y,
Johnson SC,
Engelman CD,
Pastor P,
Alvarez I,
Peskind ER,
Heslegrave AJ,
Saykin AJ,
Nho K,
Schindler SE,
Morris JC,
Holtzman DM,
McDade E,
Renton AE,
Goate A,
Ibanez L,
Riemenschneider M,
Albert MS,
Laws SM,
Porter T,
O'Brien EK,
Shaw LM,
Tijms BM,
Ingelsson M,
Visser PJ,
Hiltunen M,
Sleegers K,
Ritchie CW,
Sims R,
Belloy M,
Lambert JC,
Vilor-Tejedor N,
Fernández MV,
Li QS,
Nagle MW,
Marioni RE,
Ramirez A,
Bertram L,
van der Lee SJ,
Cruchaga C
Nature communications · 2026 · PMID 42014397 · open access
4 pages
A genome-wide association study of testicular germ cell tumor
Rapley EA,
Turnbull C,
Al Olama AA,
Dermitzakis ET,
Linger R,
Huddart RA,
Renwick A,
Hughes D,
Hines S,
Seal S,
Morrison J,
Nsengimana J
and 5 more — show all
UK Testicular Cancer Collaboration
Nature genetics · 2009 · PMID 19483681
3 pages
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14
Ruark E,
Seal S,
McDonald H,
Zhang F,
Elliot A,
Lau K,
Perdeaux E,
Rapley E,
Eeles R,
Peto J,
Kote-Jarai Z,
Muir K
and 8 more — show all
UK Testicular Cancer Collaboration (UKTCC)
Nature genetics · 2013 · PMID 23666240 · open access
3 pages
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
and 112 more — show all
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
and 180 more — show all
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection
Nicholson G,
Rantalainen M,
Li JV,
Maher AD,
Malmodin D,
Ahmadi KR,
Faber JH,
Barrett A,
Min JL,
Rayner NW,
Toft H,
Krestyaninova M
and 17 more — show all
Viksna J,
Neogi SG,
Dumas ME,
Sarkans U,
Donnelly P,
Illig T,
Adamski J,
Suhre K,
Allen M,
Zondervan KT,
Spector TD,
Nicholson JK,
Lindon JC,
Baunsgaard D,
Holmes E,
McCarthy MI,
Holmes CC
MolPAGE Consortium
PLoS genetics · 2011 · PMID 21931564 · open access
2 pages
Identification of four new susceptibility loci for testicular germ cell tumour
Litchfield K,
Holroyd A,
Lloyd A,
Broderick P,
Nsengimana J,
Eeles R,
Easton DF,
Dudakia D,
Bishop DT,
Reid A,
Huddart RA,
Grotmol T
and 4 more — show all
Nature communications · 2015 · PMID 26503584 · open access
2 pages
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