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성함이나 학술지명, PMID로 찾아보십시오.
Ng B에 대해
149건, 그중 20건 표시.
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
Liu N,
Zhang L,
Tian T,
Cheng J,
Zhang B,
Qiu S,
Geng Z,
Cui G,
Zhang Q,
Liao W,
Yu Y,
Zhang H
외 32명 — 모두 보기
Gao B,
Xu X,
Han T,
Yao Z,
Qin W,
Liu F,
Liang M,
Xu Q,
Fu J,
Xu J,
Zhu W,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Li J,
Zhang J,
Wang D,
Shen W,
Miao Y,
Xian J,
Gao JH,
Zhang X,
Li MJ,
Xu K,
Zuo XN,
Wang M,
Ye Z,
Yu C
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
페이지 12개+
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Wu X,
Yang C,
Zou Y,
Jones SE,
Zhao X,
Zhang L,
Han Z,
Hao Y,
Xiao J,
Xiao C,
Zhang W,
Yan P
외 10명 — 모두 보기
Journal of sleep research · 2024 · PMID 37380357
페이지 12개+
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Als TD,
Kurki MI,
Grove J,
Voloudakis G,
Therrien K,
Tasanko E,
Nielsen TT,
Naamanka J,
Veerapen K,
Levey DF,
Bendl J,
Bybjerg-Grauholm J
외 31명 — 모두 보기
Zeng B,
Demontis D,
Rosengren A,
Athanasiadis G,
Bækved-Hansen M,
Qvist P,
Bragi Walters G,
Thorgeirsson T,
Stefánsson H,
Musliner KL,
Rajagopal VM,
Farajzadeh L,
Thirstrup J,
Vilhjálmsson BJ,
McGrath JJ,
Mattheisen M,
Meier S,
Agerbo E,
Stefánsson K,
Nordentoft M,
Werge T,
Hougaard DM,
Mortensen PB,
Stein MB,
Gelernter J,
Hovatta I,
Roussos P,
Daly MJ,
Mors O,
Palotie A,
Børglum AD
Nature medicine · 2023 · PMID 37464041
페이지 12개+
Cross-ancestry genome-wide association studies of brain imaging phenotypes
Fu J,
Zhang Q,
Wang J,
Wang M,
Zhang B,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
외 32명 — 모두 보기
Gao B,
Xu X,
Han T,
Yao Z,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Li J,
Shen W,
Miao Y,
Wang D,
Xian J,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Cheng J,
Li MJ,
Yu C
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
페이지 12개+
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
Gorman BR,
Voloudakis G,
Igo RP Jr,
Kinzy T,
Halladay CW,
Bigdeli TB,
Zeng B,
Venkatesh S,
Cooke Bailey JN,
Crawford DC,
Markianos K,
Dong F
외 26명 — 모두 보기
Schreiner PA,
Zhang W,
Hadi T,
Anger MD,
Stockwell A,
Melles RB,
Yin J,
Choquet H,
Kaye R,
Patasova K,
Patel PJ,
Yaspan BL,
Jorgenson E,
Hysi PG,
Lotery AJ,
Gaziano JM,
Tsao PS,
Fliesler SJ,
Sullivan JM,
Greenberg PB,
Wu WC,
Assimes TL,
Pyarajan S,
Roussos P,
Peachey NS,
Iyengar SK
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
페이지 12개+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
외 145명 — 모두 보기
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 40050429
페이지 12개+
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
Ji Y,
Liu N,
Yang Y,
Wang M,
Cheng J,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
외 33명 — 모두 보기
Gao B,
Xu X,
Han T,
Yao Z,
Zhang Q,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Fu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Shen W,
Miao Y,
Wang D,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Li MJ,
Xian J,
Zhang B,
Yu C
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
페이지 12개+
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Bujnis MN,
Sterenborg RBTM,
Li Y,
Åsvold BO,
Brčić L,
Boraska Perica V,
Babbar A,
Denny JC,
Fritsche LG,
Kanai M,
Konrade I,
Leese G
외 22명 — 모두 보기
Marouli E,
Metspalu A,
Moksnes MR,
Mukherjee B,
Okada Y,
Palmer CNA,
Papadopoulou A,
Peculis R,
Rovite V,
Sauer PJ,
Soto-Pedre E,
Srinivasan S,
Steinbrenner I,
Teder-Laving M,
Wang B,
Weihs A,
Zeng C,
Zhou J,
Song X,
Jorde LB,
Medici M,
Teumer A
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
페이지 12개+
Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis
Zhang H,
Liu L,
Ni JJ,
Wei XT,
Feng GJ,
Yang XL,
Xu Q,
Zhang ZJ,
Hai R,
Tian Q,
Shen H,
Deng HW
외 2명 — 모두 보기
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2020 · PMID 32314116
페이지 11개
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
Jiang MZ,
Gaynor SM,
Li X,
Van Buren E,
Stilp A,
Stilp A,
Buth E,
Wang FF,
Manansala R,
Gogarten SM,
Li Z,
Polfus LM
외 35명 — 모두 보기
Salimi S,
Bis JC,
Pankratz N,
Yanek LR,
Durda P,
Tracy RP,
Rich SS,
Rotter JI,
Mitchell BD,
Lewis JP,
Psaty BM,
Pratte KA,
Silverman EK,
Kaplan RC,
Avery C,
North KE,
Mathias RA,
Faraday N,
Lin H,
Wang B,
Carson AP,
Norwood AF,
Gibbs RA,
Kooperberg C,
Lundin J,
Peters U,
Dupuis J,
Hou L,
Fornage M,
Benjamin EJ,
Reiner AP,
Bowler RP,
Lin X,
Auer PL,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Inflammation Working Group
Human molecular genetics · 2024 · PMID 38747556
페이지 11개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Miller FW,
Chen W,
O'Hanlon TP,
Cooper RG,
Vencovsky J,
Rider LG,
Danko K,
Wedderburn LR,
Lundberg IE,
Pachman LM,
Reed AM,
Ytterberg SR
외 13명 — 모두 보기
Padyukov L,
Selva-O'Callaghan A,
Radstake TR,
Isenberg DA,
Chinoy H,
Ollier WE,
Scheet P,
Peng B,
Lee A,
Byun J,
Lamb JA,
Gregersen PK,
Amos CI
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
페이지 9개
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Liu C,
Kraja AT,
Smith JA,
Brody JA,
Franceschini N,
Bis JC,
Rice K,
Morrison AC,
Lu Y,
Weiss S,
Guo X,
Palmas W
외 83명 — 모두 보기
Martin LW,
Chen YD,
Surendran P,
Drenos F,
Cook JP,
Auer PL,
Chu AY,
Giri A,
Zhao W,
Jakobsdottir J,
Lin LA,
Stafford JM,
Amin N,
Mei H,
Yao J,
Voorman A,
Larson MG,
Grove ML,
Smith AV,
Hwang SJ,
Chen H,
Huan T,
Kosova G,
Stitziel NO,
Kathiresan S,
Samani N,
Schunkert H,
Deloukas P,
Li M,
Fuchsberger C,
Pattaro C,
Gorski M,
Kooperberg C,
Papanicolaou GJ,
Rossouw JE,
Faul JD,
Kardia SL,
Bouchard C,
Raffel LJ,
Uitterlinden AG,
Franco OH,
Vasan RS,
O'Donnell CJ,
Taylor KD,
Liu K,
Bottinger EP,
Gottesman O,
Daw EW,
Giulianini F,
Ganesh S,
Salfati E,
Harris TB,
Launer LJ,
Dörr M,
Felix SB,
Rettig R,
Völzke H,
Kim E,
Lee WJ,
Lee IT,
Sheu WH,
Tsosie KS,
Edwards DR,
Liu Y,
Correa A,
Weir DR,
Völker U,
Ridker PM,
Boerwinkle E,
Gudnason V,
Reiner AP,
van Duijn CM,
Borecki IB,
Edwards TL,
Chakravarti A,
Rotter JI,
Psaty BM,
Loos RJ,
Fornage M,
Ehret GB,
Newton-Cheh C,
Levy D,
Chasman DI
CHD Exome+ Consortium · ExomeBP Consortium 외 컨소시엄 4곳
Nature genetics · 2016 · PMID 27618448
페이지 9개
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
외 391명 — 모두 보기
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
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외 9명 — 모두 보기
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페이지 7개
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페이지 7개
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