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성함이나 학술지명, PMID로 찾아보십시오.
Han M에 대해
19건.
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
Chong M,
Mohammadi-Shemirani P,
Perrot N,
Nelson W,
Morton R,
Narula S,
Lali R,
Khan I,
Khan M,
Judge C,
Machipisa T,
Cawte N
외 4명 — 모두 보기
eLife · 2022 · PMID 35023831 · open access
페이지 12개+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
외 73명 — 모두 보기
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium 외 컨소시엄 4곳
Nature genetics · 2026 · PMID 41644669 · open access
페이지 12개+
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Mells GF,
Floyd JA,
Morley KI,
Cordell HJ,
Franklin CS,
Shin SY,
Heneghan MA,
Neuberger JM,
Donaldson PT,
Day DB,
Ducker SJ,
Muriithi AW
외 8명 — 모두 보기
UK PBC Consortium · Wellcome Trust Case Control Consortium 3
Nature genetics · 2011 · PMID 21399635 · open access
페이지 11개
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
Teslovich TM,
Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
Khan H,
Grallert H,
Mahajan A,
Prokopenko I,
Kang HM
외 192명 — 모두 보기
Dina C,
Esko T,
Fraser RM,
Kanoni S,
Kumar A,
Lagou V,
Langenberg C,
Luan J,
Lindgren CM,
Müller-Nurasyid M,
Pechlivanis S,
Rayner NW,
Scott LJ,
Wiltshire S,
Yengo L,
Kinnunen L,
Rossin EJ,
Raychaudhuri S,
Johnson AD,
Dimas AS,
Loos RJ,
Vedantam S,
Chen H,
Florez JC,
Fox C,
Liu CT,
Rybin D,
Couper DJ,
Kao WH,
Li M,
Cornelis MC,
Kraft P,
Sun Q,
van Dam RM,
Stringham HM,
Chines PS,
Fischer K,
Fontanillas P,
Holmen OL,
Hunt SE,
Jackson AU,
Kong A,
Lawrence R,
Meyer J,
Perry JR,
Platou CG,
Potter S,
Rehnberg E,
Robertson N,
Sivapalaratnam S,
Stančáková A,
Stirrups K,
Thorleifsson G,
Tikkanen E,
Wood AR,
Almgren P,
Atalay M,
Benediktsson R,
Bonnycastle LL,
Burtt N,
Carey J,
Charpentier G,
Crenshaw AT,
Doney AS,
Dorkhan M,
Edkins S,
Emilsson V,
Eury E,
Forsen T,
Gertow K,
Gigante B,
Grant GB,
Groves CJ,
Guiducci C,
Herder C,
Hreidarsson AB,
Hui J,
James A,
Jonsson A,
Rathmann W,
Klopp N,
Kravic J,
Krjutškov K,
Langford C,
Leander K,
Lindholm E,
Lobbens S,
Männistö S,
Mirza G,
Mühleisen TW,
Musk B,
Parkin M,
Rallidis L,
Saramies J,
Sennblad B,
Shah S,
Sigurðsson G,
Silveira A,
Steinbach G,
Thorand B,
Trakalo J,
Veglia F,
Wennauer R,
Winckler W,
Zabaneh D,
Campbell H,
van Duijn C,
Uitterlinden AG,
Hofman A,
Sijbrands E,
Abecasis GR,
Owen KR,
Zeggini E,
Trip MD,
Forouhi NG,
Syvänen AC,
Eriksson JG,
Peltonen L,
Nöthen MM,
Balkau B,
Palmer CN,
Lyssenko V,
Tuomi T,
Isomaa B,
Hunter DJ,
Qi L,
Shuldiner AR,
Roden M,
Barroso I,
Wilsgaard T,
Beilby J,
Hovingh K,
Price JF,
Wilson JF,
Rauramaa R,
Lakka TA,
Lind L,
Dedoussis G,
Njølstad I,
Pedersen NL,
Khaw KT,
Wareham NJ,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Korpi-Hyövälti E,
Saltevo J,
Laakso M,
Kuusisto J,
Metspalu A,
Collins FS,
Mohlke KL,
Bergman RN,
Tuomilehto J,
Boehm BO,
Gieger C,
Hveem K,
Cauchi S,
Froguel P,
Baldassarre D,
Tremoli E,
Humphries SE,
Saleheen D,
Danesh J,
Ingelsson E,
Ripatti S,
Salomaa V,
Erbel R,
Jöckel KH,
Moebus S,
Peters A,
Illig T,
de Faire U,
Hamsten A,
Morris AD,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Boerwinkle E,
Melander O,
Kathiresan S,
Nilsson PM,
Deloukas P,
Thorsteinsdottir U,
Groop LC,
Stefansson K,
Hu F,
Pankow JS,
Dupuis J,
Meigs JB,
Altshuler D,
Boehnke M,
McCarthy MI
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22885922 · open access
페이지 10개
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
Go MJ,
Zhang W,
Below JE,
Gaulton KJ,
Ferreira T,
Horikoshi M,
Johnson AD,
Ng MC,
Prokopenko I,
Saleheen D,
Wang X
외 322명 — 모두 보기
Zeggini E,
Abecasis GR,
Adair LS,
Almgren P,
Atalay M,
Aung T,
Baldassarre D,
Balkau B,
Bao Y,
Barnett AH,
Barroso I,
Basit A,
Been LF,
Beilby J,
Bell GI,
Benediktsson R,
Bergman RN,
Boehm BO,
Boerwinkle E,
Bonnycastle LL,
Burtt N,
Cai Q,
Campbell H,
Carey J,
Cauchi S,
Caulfield M,
Chan JC,
Chang LC,
Chang TJ,
Chang YC,
Charpentier G,
Chen CH,
Chen H,
Chen YT,
Chia KS,
Chidambaram M,
Chines PS,
Cho NH,
Cho YM,
Chuang LM,
Chuang LM,
Collins FS,
Cornelis MC,
Couper DJ,
Crenshaw AT,
van Dam RM,
Danesh J,
Das D,
de Faire U,
Dedoussis G,
Deloukas P,
Dimas AS,
Dina C,
Doney AS,
Donnelly PJ,
Dorkhan M,
van Duijn C,
Dupuis J,
Edkins S,
Elliott P,
Emilsson V,
Erbel R,
Eriksson JG,
Escobedo J,
Esko T,
Eury E,
Florez JC,
Fontanillas P,
Forouhi NG,
Forsen T,
Fox C,
Fraser RM,
Frayling TM,
Froguel P,
Frossard P,
Gao Y,
Gertow K,
Gieger C,
Gigante B,
Grallert H,
Grant GB,
Grrop LC,
Groves CJ,
Grundberg E,
Guiducci C,
Hamsten A,
Han BG,
Hara K,
Hassanali N,
Hattersley AT,
Hayward C,
Hedman AK,
Herder C,
Hofman A,
Holmen OL,
Hovingh K,
Hreidarsson AB,
Hu C,
Hu FB,
Hui J,
Humphries SE,
Hunt SE,
Hunter DJ,
Hveem K,
Hydrie ZI,
Ikegami H,
Illig T,
Ingelsson E,
Islam M,
Isomaa B,
Jackson AU,
Jafar T,
James A,
Jia W,
Jöckel KH,
Jonsson A,
Jowett JB,
Kadowaki T,
Kang HM,
Kanoni S,
Kao WH,
Kathiresan S,
Kato N,
Katulanda P,
Keinanen-Kiukaanniemi KM,
Kelly AM,
Khan H,
Khaw KT,
Khor CC,
Kim HL,
Kim S,
Kim YJ,
Kinnunen L,
Klopp N,
Kong A,
Korpi-Hyövälti E,
Kowlessur S,
Kraft P,
Kravic J,
Kristensen MM,
Krithika S,
Kumar A,
Kumate J,
Kuusisto J,
Kwak SH,
Laakso M,
Lagou V,
Lakka TA,
Langenberg C,
Langford C,
Lawrence R,
Leander K,
Lee JM,
Lee NR,
Li M,
Li X,
Li Y,
Liang J,
Liju S,
Lim WY,
Lind L,
Lindgren CM,
Lindholm E,
Liu CT,
Liu JJ,
Lobbens S,
Long J,
Loos RJ,
Lu W,
Luan J,
Lyssenko V,
Ma RC,
Maeda S,
Mägi R,
Männisto S,
Matthews DR,
Meigs JB,
Melander O,
Metspalu A,
Meyer J,
Mirza G,
Mihailov E,
Moebus S,
Mohan V,
Mohlke KL,
Morris AD,
Mühleisen TW,
Müller-Nurasyid M,
Musk B,
Nakamura J,
Nakashima E,
Navarro P,
Ng PK,
Nica AC,
Nilsson PM,
Njølstad I,
Nöthen MM,
Ohnaka K,
Ong TH,
Owen KR,
Palmer CN,
Pankow JS,
Park KS,
Parkin M,
Pechlivanis S,
Pedersen NL,
Peltonen L,
Perry JR,
Peters A,
Pinidiyapathirage JM,
Platou CG,
Potter S,
Price JF,
Qi L,
Radha V,
Rallidis L,
Rasheed A,
Rathman W,
Rauramaa R,
Raychaudhuri S,
Rayner NW,
Rees SD,
Rehnberg E,
Ripatti S,
Robertson N,
Roden M,
Rossin EJ,
Rudan I,
Rybin D,
Saaristo TE,
Salomaa V,
Saltevo J,
Samuel M,
Sanghera DK,
Saramies J,
Scott J,
Scott LJ,
Scott RA,
Segrè AV,
Sehmi J,
Sennblad B,
Shah N,
Shah S,
Shera AS,
Shu XO,
Shuldiner AR,
Sigurđsson G,
Sijbrands E,
Silveira A,
Sim X,
Sivapalaratnam S,
Small KS,
So WY,
Stančáková A,
Stefansson K,
Steinbach G,
Steinthorsdottir V,
Stirrups K,
Strawbridge RJ,
Stringham HM,
Sun Q,
Suo C,
Syvänen AC,
Takayanagi R,
Takeuchi F,
Tay WT,
Teslovich TM,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tikkanen E,
Trakalo J,
Tremoli E,
Trip MD,
Tsai FJ,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Valladares-Salgado A,
Vedantam S,
Veglia F,
Voight BF,
Wang C,
Wareham NJ,
Wennauer R,
Wickremasinghe AR,
Wilsgaard T,
Wilson JF,
Wiltshire S,
Winckler W,
Wong TY,
Wood AR,
Wu JY,
Wu Y,
Yamamoto K,
Yamauchi T,
Yang M,
Yengo L,
Yokota M,
Young R,
Zabaneh D,
Zhang F,
Zhang R,
Zheng W,
Zheng W,
Zimmet PZ,
Altshuler D,
Bowden DW,
Cho YS,
Cox NJ,
Cruz M,
Hanis CL,
Kooner J,
Lee JY,
Seielstad M,
Teo YY,
Boehnke M,
Parra EJ,
Chambers JC,
Tai ES,
McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium 외 컨소시엄 3곳
Nature genetics · 2014 · PMID 24509480 · open access
페이지 9개
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
외 155명 — 모두 보기
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
페이지 7개
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
Liu JZ,
Almarri MA,
Gaffney DJ,
Mells GF,
Jostins L,
Cordell HJ,
Ducker SJ,
Day DB,
Heneghan MA,
Neuberger JM,
Donaldson PT,
Bathgate AJ
외 7명 — 모두 보기
UK Primary Biliary Cirrhosis (PBC) Consortium · Wellcome Trust Case Control Consortium 3
Nature genetics · 2012 · PMID 22961000 · open access
페이지 6개
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
외 70명 — 모두 보기
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
페이지 4개
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Mingardo E,
Beaman G,
Grote P,
Nordenskjöld A,
Newman W,
Woolf AS,
Eckstein M,
Hilger AC,
Dworschak GC,
Rösch W,
Ebert AK,
Stein R
외 54명 — 모두 보기
Brusco A,
Di Grazia M,
Tamer A,
Torres FM,
Hernandez JL,
Erben P,
Maj C,
Olmos JM,
Riancho JA,
Valero C,
Hostettler IC,
Houlden H,
Werring DJ,
Schumacher J,
Gehlen J,
Giel AS,
Buerfent BC,
Arkani S,
Åkesson E,
Rotstein E,
Ludwig M,
Holmdahl G,
Giorgio E,
Berettini A,
Keene D,
Cervellione RM,
Younsi N,
Ortlieb M,
Oswald J,
Haid B,
Promm M,
Neissner C,
Hirsch K,
Stehr M,
Schäfer FM,
Schmiedeke E,
Boemers TM,
van Rooij IALM,
Feitz WFJ,
Marcelis CLM,
Lacher M,
Nelson J,
Ure B,
Fortmann C,
Gale DP,
Chan MMY,
Ludwig KU,
Nöthen MM,
Heilmann S,
Zwink N,
Jenetzky E,
Odermatt B,
Knapp M,
Reutter H
Communications biology · 2022 · PMID 36352089 · open access
페이지 4개
Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci
Han MR,
Long J,
Choi JY,
Low SK,
Kweon SS,
Zheng Y,
Cai Q,
Shi J,
Guo X,
Matsuo K,
Iwasaki M,
Shen CY
외 19명 — 모두 보기
Kim MK,
Wen W,
Li B,
Takahashi A,
Shin MH,
Xiang YB,
Ito H,
Kasuga Y,
Noh DY,
Matsuda K,
Park MH,
Gao YT,
Iwata H,
Tsugane S,
Park SK,
Kubo M,
Shu XO,
Kang D,
Zheng W
Human molecular genetics · 2016 · PMID 27354352
페이지 3개
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
Noth I,
Zhang Y,
Ma SF,
Flores C,
Barber M,
Huang Y,
Broderick SM,
Wade MS,
Hysi P,
Scuirba J,
Richards TJ,
Juan-Guardela BM
외 9명 — 모두 보기
The Lancet. Respiratory medicine · 2013 · PMID 24429156
페이지 2개
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
Hartiala JA,
Han Y,
Jia Q,
Hilser JR,
Huang P,
Gukasyan J,
Schwartzman WS,
Cai Z,
Biswas S,
Trégouët DA,
Smith NL,
Seldin M
외 47명 — 모두 보기
Pan C,
Mehrabian M,
Lusis AJ,
Bazeley P,
Sun YV,
Liu C,
Quyyumi AA,
Scholz M,
Thiery J,
Delgado GE,
Kleber ME,
März W,
Howe LJ,
Asselbergs FW,
van Vugt M,
Vlachojannis GJ,
Patel RS,
Lyytikäinen LP,
Kähönen M,
Lehtimäki T,
Nieminen TVM,
Kuukasjärvi P,
Laurikka JO,
Chang X,
Heng CK,
Jiang R,
Kraus WE,
Hauser ER,
Ferguson JF,
Reilly MP,
Ito K,
Koyama S,
Kamatani Y,
Komuro I,
Stolze LK,
Romanoski CE,
Khan MD,
Turner AW,
Miller CL,
Aherrahrou R,
Civelek M,
Ma L,
Björkegren JLM,
Kumar SR,
Tang WHW,
Hazen SL,
Allayee H
INVENT Consortium · CHARGE Consortium Hemostasis Working Group 외 컨소시엄 2곳
European heart journal · 2021 · PMID 33532862
페이지 2개
A genome-wide association study identifies two new risk loci for Graves' disease
Chu X,
Pan CM,
Zhao SX,
Liang J,
Gao GQ,
Zhang XM,
Yuan GY,
Li CG,
Xue LQ,
Shen M,
Liu W,
Xie F
외 36명 — 모두 보기
Yang SY,
Wang HF,
Shi JY,
Sun WW,
Du WH,
Zuo CL,
Shi JX,
Liu BL,
Guo CC,
Zhan M,
Gu ZH,
Zhang XN,
Sun F,
Wang ZQ,
Song ZY,
Zou CY,
Sun WH,
Guo T,
Cao HM,
Ma JH,
Han B,
Li P,
Jiang H,
Huang QH,
Liang L,
Liu LB,
Chen G,
Su Q,
Peng YD,
Zhao JJ,
Ning G,
Chen Z,
Chen JL,
Chen SJ,
Huang W,
Song HD
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
페이지 1개
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
Zhan M,
Chen G,
Pan CM,
Gu ZH,
Zhao SX,
Liu W,
Wang HN,
Ye XP,
Xie HJ,
Yu SS,
Liang J,
Gao GQ
외 9명 — 모두 보기
China Consortium for Genetics of Autoimmune Thyroid Disease
Human molecular genetics · 2014 · PMID 24852370
페이지 1개
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Khor CC,
Do T,
Jia H,
Nakano M,
George R,
Abu-Amero K,
Duvesh R,
Chen LJ,
Li Z,
Nongpiur ME,
Perera SA,
Qiao C
외 217명 — 모두 보기
Wong HT,
Sakai H,
Barbosa de Melo M,
Lee MC,
Chan AS,
Azhany Y,
Dao TL,
Ikeda Y,
Perez-Grossmann RA,
Zarnowski T,
Day AC,
Jonas JB,
Tam PO,
Tran TA,
Ayub H,
Akhtar F,
Micheal S,
Chew PT,
Aljasim LA,
Dada T,
Luu TT,
Awadalla MS,
Kitnarong N,
Wanichwecharungruang B,
Aung YY,
Mohamed-Noor J,
Vijayan S,
Sarangapani S,
Husain R,
Jap A,
Baskaran M,
Goh D,
Su DH,
Wang H,
Yong VK,
Yip LW,
Trinh TB,
Makornwattana M,
Nguyen TT,
Leuenberger EU,
Park KH,
Wiyogo WA,
Kumar RS,
Tello C,
Kurimoto Y,
Thapa SS,
Pathanapitoon K,
Salmon JF,
Sohn YH,
Fea A,
Ozaki M,
Lai JS,
Tantisevi V,
Khaing CC,
Mizoguchi T,
Nakano S,
Kim CY,
Tang G,
Fan S,
Wu R,
Meng H,
Nguyen TT,
Tran TD,
Ueno M,
Martinez JM,
Ramli N,
Aung YM,
Reyes RD,
Vernon SA,
Fang SK,
Xie Z,
Chen XY,
Foo JN,
Sim KS,
Wong TT,
Quek DT,
Venkatesh R,
Kavitha S,
Krishnadas SR,
Soumittra N,
Shantha B,
Lim BA,
Ogle J,
de Vasconcellos JP,
Costa VP,
Abe RY,
de Souza BB,
Sng CC,
Aquino MC,
Kosior-Jarecka E,
Fong GB,
Tamanaja VC,
Fujita R,
Jiang Y,
Waseem N,
Low S,
Pham HN,
Al-Shahwan S,
Craven ER,
Khan MI,
Dada R,
Mohanty K,
Faiq MA,
Hewitt AW,
Burdon KP,
Gan EH,
Prutthipongsit A,
Patthanathamrongkasem T,
Catacutan MA,
Felarca IR,
Liao CS,
Rusmayani E,
Istiantoro VW,
Consolandi G,
Pignata G,
Lavia C,
Rojanapongpun P,
Mangkornkanokpong L,
Chansangpetch S,
Chan JC,
Choy BN,
Shum JW,
Than HM,
Oo KT,
Han AT,
Yong VH,
Ng XY,
Goh SR,
Chong YF,
Hibberd ML,
Seielstad M,
Png E,
Dunstan SJ,
Chau NV,
Bei J,
Zeng YX,
Karkey A,
Basnyat B,
Pasutto F,
Paoli D,
Frezzotti P,
Wang JJ,
Mitchell P,
Fingert JH,
Allingham RR,
Hauser MA,
Lim ST,
Chew SH,
Ebstein RP,
Sakuntabhai A,
Park KH,
Ahn J,
Boland G,
Snippe H,
Stead R,
Quino R,
Zaw SN,
Lukasik U,
Shetty R,
Zahari M,
Bae HW,
Oo NL,
Kubota T,
Manassakorn A,
Ho WL,
Dallorto L,
Hwang YH,
Kiire CA,
Kuroda M,
Djamal ZE,
Peregrino JI,
Ghosh A,
Jeoung JW,
Hoan TS,
Srisamran N,
Sandragasu T,
Set SH,
Doan VH,
Bhattacharya SS,
Ho CL,
Tan DT,
Sihota R,
Loon SC,
Mori K,
Kinoshita S,
Hollander AI,
Qamar R,
Wang YX,
Teo YY,
Tai ES,
Hartleben-Matkin C,
Lozano-Giral D,
Saw SM,
Cheng CY,
Zenteno JC,
Pang CP,
Bui HT,
Hee O,
Craig JE,
Edward DP,
Yonahara M,
Neto JM,
Guevara-Fujita ML,
Xu L,
Ritch R,
Liza-Sharmini AT,
Wong TY,
Al-Obeidan S,
Do NH,
Sundaresan P,
Tham CC,
Foster PJ,
Vijaya L,
Tashiro K,
Vithana EN,
Wang N,
Aung T
Nature genetics · 2016 · PMID 27064256
페이지 1개
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
Zhao SX,
Liu W,
Liang J,
Gao GQ,
Zhang XM,
Yao Y,
Wang HN,
Yuan FF,
Xue LQ,
Ma YR,
Zhang LL,
Ye XP
외 25명 — 모두 보기
Zhang QY,
Sun F,
Zhang RJ,
Yang SY,
Zhan M,
Du WH,
Liu BL,
Chen X,
Song ZY,
Li XS,
Li P,
Ru Y,
Zuo CL,
Li SX,
Han B,
Zhu H,
Qiao J,
Xuan M,
Su B,
Sun F,
Ma JH,
Chen JL,
Tian HM,
Chen SJ,
Song HD
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
페이지 1개
Genome-wide association study on coordination and agility in 461 Chinese Han males
Wang Y,
Li H,
Hou L,
Wang S,
Kang X,
Yu J,
Tian F,
Ni W,
Deng X,
Liu T,
You Y,
Chen W
Heliyon · 2023 · PMID 37654465 · open access
페이지 1개
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