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2,676 papers hold this site up. Every variant and condition page names
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104 matches for
Ng E,
showing the first 20.
A coding variant in <i>FTO</i> confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD
Kim HS,
Cheon JH,
Jung ES,
Park J,
Aum S,
Park SJ,
Eun S,
Lee J,
Rüther U,
Yeo GSH,
Ma M,
Park KS
and 5 more — show all
Gut · 2017 · PMID 27558924
1 page
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
McCormack M,
Gui H,
Ingason A,
Speed D,
Wright GEB,
Zhang EJ,
Secolin R,
Yasuda C,
Kwok M,
Wolking S,
Becker F,
Rau S
and 37 more — show all
Avbersek A,
Heggeli K,
Leu C,
Depondt C,
Sills GJ,
Marson AG,
Auce P,
Brodie MJ,
Francis B,
Johnson MR,
Koeleman BPC,
Striano P,
Coppola A,
Zara F,
Kunz WS,
Sander JW,
Lerche H,
Klein KM,
Weckhuysen S,
Krenn M,
Gudmundsson LJ,
Stefánsson K,
Krause R,
Shear N,
Ross CJD,
Delanty N,
Pirmohamed M,
Carleton BC,
Cendes F,
Lopes-Cendes I,
Liao WP,
O'Brien TJ,
Sisodiya SM,
Cherny S,
Kwan P,
Baum L,
Cavalleri GL
EPIGEN Consortium; · Canadian Pharmacogenomics Network for Drug Safety; and 2 more consortia
Neurology · 2018 · PMID 29288229 · open access
1 page
The nature of nurture: Effects of parental genotypes
Kong A,
Thorleifsson G,
Frigge ML,
Vilhjalmsson BJ,
Young AI,
Thorgeirsson TE,
Benonisdottir S,
Oddsson A,
Halldorsson BV,
Masson G,
Gudbjartsson DF,
Helgason A
and 3 more — show all
Science (New York, N.Y.) · 2018 · PMID 29371463
1 page
Genome-Wide Association Study Confirming a Strong Effect of HLA and Identifying Variants in <i>CSAD/lnc-ITGB7-1</i> on Chromosome 12q13.13 Associated With Susceptibility to Fulminant Type 1 Diabetes
Kawabata Y,
Nishida N,
Awata T,
Kawasaki E,
Imagawa A,
Shimada A,
Osawa H,
Tanaka S,
Takahashi K,
Nagata M,
Yasuda H,
Uchigata Y
and 7 more — show all
Diabetes · 2019 · PMID 30552108
1 page
Genetic architecture of human thinness compared to severe obesity
Riveros-McKay F,
Mistry V,
Bounds R,
Hendricks A,
Keogh JM,
Thomas H,
Henning E,
Corbin LJ,
O'Rahilly S,
Zeggini E,
Wheeler E,
Barroso I
and 1 more — show all
Understanding Society Scientific Group
PLoS genetics · 2019 · PMID 30677029 · open access
1 page
Factors associated with sharing e-mail information and mental health survey participation in large population cohorts
Adams MJ,
Hill WD,
Howard DM,
Dashti HS,
Davis KAS,
Campbell A,
Clarke TK,
Deary IJ,
Hayward C,
Porteous D,
Hotopf M,
McIntosh AM
International journal of epidemiology · 2020 · PMID 31263887 · open access
1 page
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Yan C,
Zhu M,
Ding Y,
Yang M,
Wang M,
Li G,
Ren C,
Huang T,
Yang W,
He B,
Wang M,
Yu F
and 22 more — show all
Wang J,
Zhang R,
Wang T,
Ni J,
Chen J,
Jiang Y,
Dai J,
Zhang E,
Ma H,
Wang Y,
Xu D,
Wang S,
Chen Y,
Xu Z,
Zhou J,
Ji G,
Wang Z,
Zhang Z,
Hu Z,
Wei Q,
Shen H,
Jin G
Gut · 2020 · PMID 31383772
1 page
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Bandres-Ciga S,
Ahmed S,
Sabir MS,
Blauwendraat C,
Adarmes-Gómez AD,
Bernal-Bernal I,
Bonilla-Toribio M,
Buiza-Rueda D,
Carrillo F,
Carrión-Claro M,
Gómez-Garre P,
Jesús S
and 83 more — show all
Labrador-Espinosa MA,
Macias D,
Méndez-Del-Barrio C,
Periñán-Tocino T,
Tejera-Parrado C,
Vargas-González L,
Diez-Fairen M,
Alvarez I,
Tartari JP,
Buongiorno M,
Aguilar M,
Gorostidi A,
Bergareche JA,
Mondragon E,
Vinagre-Aragon A,
Croitoru I,
Ruiz-Martínez J,
Dols-Icardo O,
Kulisevsky J,
Marín-Lahoz J,
Pagonabarraga J,
Pascual-Sedano B,
Ezquerra M,
Cámara A,
Compta Y,
Fernández M,
Fernández-Santiago R,
Muñoz E,
Tolosa E,
Valldeoriola F,
Gonzalez-Aramburu I,
Sanchez Rodriguez A,
Sierra M,
Menéndez-González M,
Blazquez M,
Garcia C,
Suarez-San Martin E,
García-Ruiz P,
Martínez-Castrillo JC,
Vela-Desojo L,
Ruz C,
Barrero FJ,
Escamilla-Sevilla F,
Mínguez-Castellanos A,
Cerdan D,
Tabernero C,
Gomez Heredia MJ,
Perez Errazquin F,
Romero-Acebal M,
Feliz C,
Lopez-Sendon JL,
Mata M,
Martínez Torres I,
Kim JJ,
Dalgard CL,
Brooks J,
Saez-Atienzar S,
Gibbs JR,
Jorda R,
Botia JA,
Bonet-Ponce L,
Morrison KE,
Clarke C,
Tan M,
Morris H,
Edsall C,
Hernandez D,
Simon-Sanchez J,
Nalls MA,
Scholz SW,
Jimenez-Escrig A,
Duarte J,
Vives F,
Duran R,
Hoenicka J,
Alvarez V,
Infante J,
Marti MJ,
Clarimón J,
López de Munain A,
Pastor P,
Mir P,
Singleton A
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
1 page
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy
Hosoda Y,
Miyake M,
Schellevis RL,
Boon CJF,
Hoyng CB,
Miki A,
Meguro A,
Sakurada Y,
Yoneyama S,
Takasago Y,
Hata M,
Muraoka Y
and 22 more — show all
Nakanishi H,
Oishi A,
Ooto S,
Tamura H,
Uji A,
Miyata M,
Takahashi A,
Ueda-Arakawa N,
Tajima A,
Sato T,
Mizuki N,
Shiragami C,
Iida T,
Khor CC,
Wong TY,
Yamada R,
Honda S,
de Jong EK,
Hollander AID,
Matsuda F,
Yamashiro K,
Tsujikawa A
Communications biology · 2019 · PMID 31872073 · open access
1 page
Systematic review and meta-analysis of the moderating effect of rs1799971 in OPRM1, the mu-opioid receptor gene, on response to naltrexone treatment of alcohol use disorder
Hartwell EE,
Feinn R,
Morris PE,
Gelernter J,
Krystal J,
Arias AJ,
Hoffman M,
Petrakis I,
Gueorguieva R,
Schacht JP,
Oslin D,
Anton RF
and 1 more — show all
Addiction (Abingdon, England) · 2020 · PMID 31961981
1 page
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
Foo JN,
Chew EGY,
Chung SJ,
Peng R,
Blauwendraat C,
Nalls MA,
Mok KY,
Satake W,
Toda T,
Chao Y,
Tan LCS,
Tandiono M
and 33 more — show all
Lian MM,
Ng EY,
Prakash KM,
Au WL,
Meah WY,
Mok SQ,
Annuar AA,
Chan AYY,
Chen L,
Chen Y,
Jeon BS,
Jiang L,
Lim JL,
Lin JJ,
Liu C,
Mao C,
Mok V,
Pei Z,
Shang HF,
Shi CH,
Song K,
Tan AH,
Wu YR,
Xu YM,
Xu R,
Yan Y,
Yang J,
Zhang B,
Koh WP,
Lim SY,
Khor CC,
Liu J,
Tan EK
JAMA neurology · 2020 · PMID 32310270
1 page
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Jia X,
Yamamura T,
Gbadegesin R,
McNulty MT,
Song K,
Nagano C,
Hitomi Y,
Lee D,
Aiba Y,
Khor SS,
Ueno K,
Kawai Y
and 33 more — show all
Nagasaki M,
Noiri E,
Horinouchi T,
Kaito H,
Hamada R,
Okamoto T,
Kamei K,
Kaku Y,
Fujimaru R,
Tanaka R,
Shima Y,
Baek J,
Kang HG,
Ha IS,
Han KH,
Yang EM,
Abeyagunawardena A,
Lane B,
Chryst-Stangl M,
Esezobor C,
Solarin A,
Dossier C,
Deschênes G,
Vivarelli M,
Debiec H,
Ishikura K,
Matsuo M,
Nozu K,
Ronco P,
Cheong HI,
Sampson MG,
Tokunaga K,
Iijima K
Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan · Korean Consortium of Hereditary Renal Diseases in Children and 2 more consortia
Kidney international · 2020 · PMID 32554042
1 page
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
and 114 more — show all
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis
Schack LMH,
Naderi E,
Fachal L,
Dorling L,
Luccarini C,
Dunning AM,
Ong EHW,
Chua MLK,
Langendijk JA,
Alizadeh BZ,
Overgaard J,
Eriksen JG
and 2 more — show all
Head and Neck Group of the Radiogenomics Consortium · Danish Head and Neck Cancer Group (DAHANCA)
British journal of cancer · 2022 · PMID 35039627 · open access
1 page
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
1 page
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Joo YY,
Pacheco JA,
Thompson WK,
Rasmussen-Torvik LJ,
Rasmussen LV,
Lin FTJ,
Andrade M,
Borthwick KM,
Bottinger E,
Cagan A,
Carrell DS,
Denny JC
and 13 more — show all
Ellis SB,
Gottesman O,
Linneman JG,
Pathak J,
Peissig PL,
Shang N,
Tromp G,
Veerappan A,
Smith ME,
Chisholm RL,
Gawron AJ,
Hayes MG,
Kho AN
PloS one · 2023 · PMID 37196047 · open access
1 page
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng EO,
Coetzee SG,
Tyrer JP,
Peng PC,
Rosenow W,
Chen S,
Davis BD,
Dezem FS,
Seo JH,
Nameki R,
Reyes AL,
Aben KKH
and 141 more — show all
Anton-Culver H,
Antonenkova NN,
Aravantinos G,
Bandera EV,
Beane Freeman LE,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernardini MQ,
Bjorge L,
Black A,
Bogdanova NV,
Bolton KL,
Brenton JD,
Budzilowska A,
Butzow R,
Cai H,
Campbell I,
Cannioto R,
Chang-Claude J,
Chanock SJ,
Chen K,
Chenevix-Trench G,
Chiew YE,
Cook LS,
DeFazio A,
Dennis J,
Doherty JA,
Dörk T,
du Bois A,
Dürst M,
Eccles DM,
Ene G,
Fasching PA,
Flanagan JM,
Fortner RT,
Fostira F,
Gentry-Maharaj A,
Giles GG,
Goodman MT,
Gronwald J,
Haiman CA,
Håkansson N,
Heitz F,
Hildebrandt MAT,
Høgdall E,
Høgdall CK,
Huang RY,
Jensen A,
Jones ME,
Kang D,
Karlan BY,
Karnezis AN,
Kelemen LE,
Kennedy CJ,
Khusnutdinova EK,
Kiemeney LA,
Kjaer SK,
Kupryjanczyk J,
Labrie M,
Lambrechts D,
Larson MC,
Le ND,
Lester J,
Li L,
Lubiński J,
Lush M,
Marks JR,
Matsuo K,
May T,
McLaughlin JR,
McNeish IA,
Menon U,
Missmer S,
Modugno F,
Moffitt M,
Monteiro AN,
Moysich KB,
Narod SA,
Nguyen-Dumont T,
Odunsi K,
Olsson H,
Onland-Moret NC,
Park SK,
Pejovic T,
Permuth JB,
Piskorz A,
Prokofyeva D,
Riggan MJ,
Risch HA,
Rodríguez-Antona C,
Rossing MA,
Sandler DP,
Setiawan VW,
Shan K,
Song H,
Southey MC,
Steed H,
Sutphen R,
Swerdlow AJ,
Teo SH,
Terry KL,
Thompson PJ,
Vestrheim Thomsen LC,
Titus L,
Trabert B,
Travis R,
Tworoger SS,
Valen E,
Van Nieuwenhuysen E,
Edwards DV,
Vierkant RA,
Webb PM,
Weinberg CR,
Weise RM,
Wentzensen N,
White E,
Winham SJ,
Wolk A,
Woo YL,
Wu AH,
Yan L,
Yannoukakos D,
Zeinomar N,
Zheng W,
Ziogas A,
Berchuck A,
Goode EL,
Huntsman DG,
Pearce CL,
Ramus SJ,
Sellers TA,
Freedman ML,
Lawrenson K,
Schildkraut JM,
Hazelett D,
Plummer JT,
Kar S,
Jones MR,
Pharoah PDP,
Gayther SA
AOCS Group · OPAL Study Group and 1 more consortia
American journal of human genetics · 2024 · PMID 38723632
1 page
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