연구자에게
내 논문이 여기 있나요?
논문 2,676편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Li S에 대해
108건, 그중 20건 표시.
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
Tapper W,
Jones AV,
Kralovics R,
Harutyunyan AS,
Zoi K,
Leung W,
Godfrey AL,
Guglielmelli P,
Callaway A,
Ward D,
Aranaz P,
White HE
외 38명 — 모두 보기
Waghorn K,
Lin F,
Chase A,
Baxter EJ,
Maclean C,
Nangalia J,
Chen E,
Evans P,
Short M,
Jack A,
Wallis L,
Oscier D,
Duncombe AS,
Schuh A,
Mead AJ,
Griffiths M,
Ewing J,
Gale RE,
Schnittger S,
Haferlach T,
Stegelmann F,
Döhner K,
Grallert H,
Strauch K,
Tanaka T,
Bandinelli S,
Giannopoulos A,
Pieri L,
Mannarelli C,
Gisslinger H,
Barosi G,
Cazzola M,
Reiter A,
Harrison C,
Campbell P,
Green AR,
Vannucchi A,
Cross NC
Nature communications · 2015 · PMID 25849990 · open access
페이지 2개
Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Li M,
Foo JN,
Wang JQ,
Low HQ,
Tang XQ,
Toh KY,
Yin PR,
Khor CC,
Goh YF,
Irwan ID,
Xu RC,
Andiappan AK
외 29명 — 모두 보기
Bei JX,
Rotzschke O,
Chen MH,
Cheng CY,
Sun LD,
Jiang GR,
Wong TY,
Lin HL,
Aung T,
Liao YH,
Saw SM,
Ye K,
Ebstein RP,
Chen QK,
Shi W,
Chew SH,
Chen J,
Zhang FR,
Li SP,
Xu G,
Shyong Tai E,
Wang L,
Chen N,
Zhang XJ,
Zeng YX,
Zhang H,
Liu ZH,
Yu XQ,
Liu JJ
Nature communications · 2015 · PMID 26028593 · open access
페이지 2개
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Dai Y,
Chen Y,
Huang H,
Zhou W,
Niu Y,
Zhang M,
Bin P,
Dong H,
Jia Q,
Huang J,
Yi J,
Liao Q
외 26명 — 모두 보기
Li H,
Teng Y,
Zang D,
Zhai Q,
Duan H,
Shen J,
He J,
Meng T,
Sha Y,
Shen M,
Ye M,
Jia X,
Xiang Y,
Huang H,
Wu Q,
Shi M,
Huang X,
Yang H,
Luo L,
Li S,
Li L,
Zhao J,
Li L,
Wang J,
Wang J,
Zheng Y
Scientific reports · 2015 · PMID 26190474 · open access
페이지 2개
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection
Takeuchi F,
Kukimoto I,
Li Z,
Li S,
Li N,
Hu Z,
Takahashi A,
Inoue S,
Yokoi S,
Chen J,
Hang D,
Kuroda M
외 10명 — 모두 보기
Human molecular genetics · 2019 · PMID 30412241
페이지 2개
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Armstrong NJ,
Mather KA,
Sargurupremraj M,
Knol MJ,
Malik R,
Satizabal CL,
Yanek LR,
Wen W,
Gudnason VG,
Dueker ND,
Elliott LT,
Hofer E
외 74명 — 모두 보기
Bis J,
Jahanshad N,
Li S,
Logue MA,
Luciano M,
Scholz M,
Smith AV,
Trompet S,
Vojinovic D,
Xia R,
Alfaro-Almagro F,
Ames D,
Amin N,
Amouyel P,
Beiser AS,
Brodaty H,
Deary IJ,
Fennema-Notestine C,
Gampawar PG,
Gottesman R,
Griffanti L,
Jack CR Jr,
Jenkinson M,
Jiang J,
Kral BG,
Kwok JB,
Lampe L,
C M Liewald D,
Maillard P,
Marchini J,
Bastin ME,
Mazoyer B,
Pirpamer L,
Rafael Romero J,
Roshchupkin GV,
Schofield PR,
Schroeter ML,
Stott DJ,
Thalamuthu A,
Trollor J,
Tzourio C,
van der Grond J,
Vernooij MW,
Witte VA,
Wright MJ,
Yang Q,
Morris Z,
Siggurdsson S,
Psaty B,
Villringer A,
Schmidt H,
Haberg AK,
van Duijn CM,
Jukema JW,
Dichgans M,
Sacco RL,
Wright CB,
Kremen WS,
Becker LC,
Thompson PM,
Mosley TH,
Wardlaw JM,
Ikram MA,
Adams HHH,
Seshadri S,
Sachdev PS,
Smith SM,
Launer L,
Longstreth W,
DeCarli C,
Schmidt R,
Fornage M,
Debette S,
Nyquist PA
Stroke · 2020 · PMID 32517579
페이지 2개
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
외 53명 — 모두 보기
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
페이지 2개
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Yu HP,
Xiang BD,
Qian J,
Liu H,
Li YF,
Lin Q,
Liu S,
Wei J,
Zhan S,
Jiang B,
Dai J,
Ma L
외 20명 — 모두 보기
Zhang L,
Liu Y,
Wen Q,
Gong W,
Li S,
Jiang Y,
Zheng J,
Zhu T,
Zhou Z,
Zeng X,
Wang Z,
Wang JA,
Guo R,
Yang Y,
Wei Q,
Zhou G,
Qiu XQ,
Tang W,
Wang M,
Zhang R
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
페이지 2개
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Willer CJ,
Speliotes EK,
Loos RJ,
Li S,
Lindgren CM,
Heid IM,
Berndt SI,
Elliott AL,
Jackson AU,
Lamina C,
Lettre G,
Lim N
외 133명 — 모두 보기
Lyon HN,
McCarroll SA,
Papadakis K,
Qi L,
Randall JC,
Roccasecca RM,
Sanna S,
Scheet P,
Weedon MN,
Wheeler E,
Zhao JH,
Jacobs LC,
Prokopenko I,
Soranzo N,
Tanaka T,
Timpson NJ,
Almgren P,
Bennett A,
Bergman RN,
Bingham SA,
Bonnycastle LL,
Brown M,
Burtt NP,
Chines P,
Coin L,
Collins FS,
Connell JM,
Cooper C,
Smith GD,
Dennison EM,
Deodhar P,
Elliott P,
Erdos MR,
Estrada K,
Evans DM,
Gianniny L,
Gieger C,
Gillson CJ,
Guiducci C,
Hackett R,
Hadley D,
Hall AS,
Havulinna AS,
Hebebrand J,
Hofman A,
Isomaa B,
Jacobs KB,
Johnson T,
Jousilahti P,
Jovanovic Z,
Khaw KT,
Kraft P,
Kuokkanen M,
Kuusisto J,
Laitinen J,
Lakatta EG,
Luan J,
Luben RN,
Mangino M,
McArdle WL,
Meitinger T,
Mulas A,
Munroe PB,
Narisu N,
Ness AR,
Northstone K,
O'Rahilly S,
Purmann C,
Rees MG,
Ridderstråle M,
Ring SM,
Rivadeneira F,
Ruokonen A,
Sandhu MS,
Saramies J,
Scott LJ,
Scuteri A,
Silander K,
Sims MA,
Song K,
Stephens J,
Stevens S,
Stringham HM,
Tung YC,
Valle TT,
Van Duijn CM,
Vimaleswaran KS,
Vollenweider P,
Waeber G,
Wallace C,
Watanabe RM,
Waterworth DM,
Watkins N,
Witteman JC,
Zeggini E,
Zhai G,
Zillikens MC,
Altshuler D,
Caulfield MJ,
Chanock SJ,
Farooqi IS,
Ferrucci L,
Guralnik JM,
Hattersley AT,
Hu FB,
Jarvelin MR,
Laakso M,
Mooser V,
Ong KK,
Ouwehand WH,
Salomaa V,
Samani NJ,
Spector TD,
Tuomi T,
Tuomilehto J,
Uda M,
Uitterlinden AG,
Wareham NJ,
Deloukas P,
Frayling TM,
Groop LC,
Hayes RB,
Hunter DJ,
Mohlke KL,
Peltonen L,
Schlessinger D,
Strachan DP,
Wichmann HE,
McCarthy MI,
Boehnke M,
Barroso I,
Abecasis GR,
Hirschhorn JN
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
페이지 1개
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study
Ferrucci L,
Perry JR,
Matteini A,
Perola M,
Tanaka T,
Silander K,
Rice N,
Melzer D,
Murray A,
Cluett C,
Fried LP,
Albanes D
외 9명 — 모두 보기
American journal of human genetics · 2009 · PMID 19185284
페이지 1개
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez J,
Schulte C,
Bras JM,
Sharma M,
Gibbs JR,
Berg D,
Paisan-Ruiz C,
Lichtner P,
Scholz SW,
Hernandez DG,
Krüger R,
Federoff M
외 35명 — 모두 보기
Klein C,
Goate A,
Perlmutter J,
Bonin M,
Nalls MA,
Illig T,
Gieger C,
Houlden H,
Steffens M,
Okun MS,
Racette BA,
Cookson MR,
Foote KD,
Fernandez HH,
Traynor BJ,
Schreiber S,
Arepalli S,
Zonozi R,
Gwinn K,
van der Brug M,
Lopez G,
Chanock SJ,
Schatzkin A,
Park Y,
Hollenbeck A,
Gao J,
Huang X,
Wood NW,
Lorenz D,
Deuschl G,
Chen H,
Riess O,
Hardy JA,
Singleton AB,
Gasser T
Nature genetics · 2009 · PMID 19915575 · open access
페이지 1개
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
Shi Y,
Qu J,
Zhang D,
Zhao P,
Zhang Q,
Tam POS,
Sun L,
Zuo X,
Zhou X,
Xiao X,
Hu J,
Li Y
외 30명 — 모두 보기
Cai L,
Liu X,
Lu F,
Liao S,
Chen B,
He F,
Gong B,
Lin H,
Ma S,
Cheng J,
Zhang J,
Chen Y,
Zhao F,
Yang X,
Chen Y,
Yang C,
Lam DSC,
Li X,
Shi F,
Wu Z,
Lin Y,
Yang J,
Li S,
Ren Y,
Xue A,
Fan Y,
Li D,
Pang CP,
Zhang X,
Yang Z
American journal of human genetics · 2011 · PMID 21640322
페이지 1개
New loci associated with chronic hepatitis B virus infection in Han Chinese
Hu Z,
Liu Y,
Zhai X,
Dai J,
Jin G,
Wang L,
Zhu L,
Yang Y,
Liu J,
Chu M,
Wen J,
Xie K
외 16명 — 모두 보기
Du G,
Wang Q,
Zhou Y,
Cao M,
Liu L,
He Y,
Wang Y,
Zhou G,
Jia W,
Lu J,
Li S,
Liu J,
Yang H,
Shi Y,
Zhou W,
Shen H
Nature genetics · 2013 · PMID 24162738
페이지 1개
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
Hek K,
Chen TH,
Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
Warby SC,
Bandinelli S,
Cherkas L,
Evans DS,
Grabe HJ
외 74명 — 모두 보기
Lahti J,
Li M,
Lehtimäki T,
Lumley T,
Marciante KD,
Pérusse L,
Psaty BM,
Robbins J,
Tranah GJ,
Vink JM,
Wilk JB,
Stafford JM,
Bellis C,
Biffar R,
Bouchard C,
Cade B,
Curhan GC,
Eriksson JG,
Ewert R,
Ferrucci L,
Fülöp T,
Gehrman PR,
Goodloe R,
Harris TB,
Heath AC,
Hernandez D,
Hofman A,
Hottenga JJ,
Hunter DJ,
Jensen MK,
Johnson AD,
Kähönen M,
Kao L,
Kraft P,
Larkin EK,
Lauderdale DS,
Luik AI,
Medici M,
Montgomery GW,
Palotie A,
Patel SR,
Pistis G,
Porcu E,
Quaye L,
Raitakari O,
Redline S,
Rimm EB,
Rotter JI,
Smith AV,
Spector TD,
Teumer A,
Uitterlinden AG,
Vohl MC,
Widen E,
Willemsen G,
Young T,
Zhang X,
Liu Y,
Blangero J,
Boomsma DI,
Gudnason V,
Hu F,
Mangino M,
Martin NG,
O'Connor GT,
Stone KL,
Tanaka T,
Viikari J,
Gharib SA,
Punjabi NM,
Räikkönen K,
Völzke H,
Mignot E,
Tiemeier H
Molecular psychiatry · 2015 · PMID 25469926 · open access
페이지 1개
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study
Renauer PA,
Saruhan-Direskeneli G,
Coit P,
Adler A,
Aksu K,
Keser G,
Alibaz-Oner F,
Aydin SZ,
Kamali S,
Inanc M,
Carette S,
Cuthbertson D
외 43명 — 모두 보기
Hoffman GS,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Langford CA,
Maksimowicz-McKinnon K,
McAlear CA,
Ozbalkan Z,
Ates A,
Karaaslan Y,
Duzgun N,
Monach PA,
Ozer HT,
Erken E,
Ozturk MA,
Yazici A,
Cefle A,
Onat AM,
Kisacik B,
Pagnoux C,
Kasifoglu T,
Seyahi E,
Fresko I,
Seo P,
Sreih AG,
Warrington KJ,
Ytterberg SR,
Cobankara V,
Cunninghame-Graham DS,
Vyse TJ,
Pamuk ON,
Tunc SE,
Dalkilic E,
Bicakcigil M,
Yentur SP,
Wren JD,
Merkel PA,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25604533
페이지 1개
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
외 138명 — 모두 보기
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
페이지 1개
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Wen W,
Kato N,
Hwang JY,
Guo X,
Tabara Y,
Li H,
Dorajoo R,
Yang X,
Tsai FJ,
Li S,
Wu Y,
Wu T
외 64명 — 모두 보기
Kim S,
Guo X,
Liang J,
Shungin D,
Adair LS,
Akiyama K,
Allison M,
Cai Q,
Chang LC,
Chen CH,
Chen YT,
Cho YS,
Choi BY,
Gao Y,
Go MJ,
Gu D,
Han BG,
He M,
Hixson JE,
Hu Y,
Huang T,
Isono M,
Jung KJ,
Kang D,
Kim YJ,
Kita Y,
Lee J,
Lee NR,
Lee J,
Wang Y,
Liu JJ,
Long J,
Moon S,
Nakamura Y,
Nakatochi M,
Ohnaka K,
Rao D,
Shi J,
Sull JW,
Tan A,
Ueshima H,
Wu C,
Xiang YB,
Yamamoto K,
Yao J,
Ye X,
Yokota M,
Zhang X,
Zheng Y,
Qi L,
Rotter JI,
Jee SH,
Lin D,
Mohlke KL,
He J,
Mo Z,
Wu JY,
Tai ES,
Lin X,
Miki T,
Kim BJ,
Takeuchi F,
Zheng W,
Shu XO
Scientific reports · 2016 · PMID 26785701 · open access
페이지 1개
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Li Y,
Si L,
Zhai Y,
Hu Y,
Hu Z,
Bei JX,
Xie B,
Ren Q,
Cao P,
Yang F,
Song Q,
Bao Z
외 38명 — 모두 보기
Zhang H,
Han Y,
Wang Z,
Chen X,
Xia X,
Yan H,
Wang R,
Zhang Y,
Gao C,
Meng J,
Tu X,
Liang X,
Cui Y,
Liu Y,
Wu X,
Li Z,
Wang H,
Li Z,
Hu B,
He M,
Gao Z,
Xu X,
Ji H,
Yu C,
Sun Y,
Xing B,
Yang X,
Zhang H,
Tan A,
Wu C,
Jia W,
Li S,
Zeng YX,
Shen H,
He F,
Mo Z,
Zhang H,
Zhou G
Nature communications · 2016 · PMID 27244555 · open access
페이지 1개
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Hu Y,
Tanaka T,
Zhu J,
Guan W,
Wu JHY,
Psaty BM,
McKnight B,
King IB,
Sun Q,
Richard M,
Manichaikul A,
Frazier-Wood AC
외 21명 — 모두 보기
Kabagambe EK,
Hopkins PN,
Ordovas JM,
Ferrucci L,
Bandinelli S,
Arnett DK,
Chen YI,
Liang S,
Siscovick DS,
Tsai MY,
Rich SS,
Fornage M,
Hu FB,
Rimm EB,
Jensen MK,
Lemaitre RN,
Mozaffarian D,
Steffen LM,
Morris AP,
Li H,
Lin X
Journal of lipid research · 2017 · PMID 28298293 · open access
페이지 1개
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
외 204명 — 모두 보기
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28436984
페이지 1개
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
Badarinarayan N,
Jakobsdottir J,
Kunkle BW,
Boland A,
Raybould R,
Bis JC,
Martin ER,
Grenier-Boley B
외 437명 — 모두 보기
Heilmann-Heimbach S,
Chouraki V,
Kuzma AB,
Sleegers K,
Vronskaya M,
Ruiz A,
Graham RR,
Olaso R,
Hoffmann P,
Grove ML,
Vardarajan BN,
Hiltunen M,
Nöthen MM,
White CC,
Hamilton-Nelson KL,
Epelbaum J,
Maier W,
Choi SH,
Beecham GW,
Dulary C,
Herms S,
Smith AV,
Funk CC,
Derbois C,
Forstner AJ,
Ahmad S,
Li H,
Bacq D,
Harold D,
Satizabal CL,
Valladares O,
Squassina A,
Thomas R,
Brody JA,
Qu L,
Sánchez-Juan P,
Morgan T,
Wolters FJ,
Zhao Y,
Garcia FS,
Denning N,
Fornage M,
Malamon J,
Naranjo MCD,
Majounie E,
Mosley TH,
Dombroski B,
Wallon D,
Lupton MK,
Dupuis J,
Whitehead P,
Fratiglioni L,
Medway C,
Jian X,
Mukherjee S,
Keller L,
Brown K,
Lin H,
Cantwell LB,
Panza F,
McGuinness B,
Moreno-Grau S,
Burgess JD,
Solfrizzi V,
Proitsi P,
Adams HH,
Allen M,
Seripa D,
Pastor P,
Cupples LA,
Price ND,
Hannequin D,
Frank-García A,
Levy D,
Chakrabarty P,
Caffarra P,
Giegling I,
Beiser AS,
Giedraitis V,
Hampel H,
Garcia ME,
Wang X,
Lannfelt L,
Mecocci P,
Eiriksdottir G,
Crane PK,
Pasquier F,
Boccardi V,
Henández I,
Barber RC,
Scherer M,
Tarraga L,
Adams PM,
Leber M,
Chen Y,
Albert MS,
Riedel-Heller S,
Emilsson V,
Beekly D,
Braae A,
Schmidt R,
Blacker D,
Masullo C,
Schmidt H,
Doody RS,
Spalletta G,
Longstreth WT Jr,
Fairchild TJ,
Bossù P,
Lopez OL,
Frosch MP,
Sacchinelli E,
Ghetti B,
Yang Q,
Huebinger RM,
Jessen F,
Li S,
Kamboh MI,
Morris J,
Sotolongo-Grau O,
Katz MJ,
Corcoran C,
Dunstan M,
Braddel A,
Thomas C,
Meggy A,
Marshall R,
Gerrish A,
Chapman J,
Aguilar M,
Taylor S,
Hill M,
Fairén MD,
Hodges A,
Vellas B,
Soininen H,
Kloszewska I,
Daniilidou M,
Uphill J,
Patel Y,
Hughes JT,
Lord J,
Turton J,
Hartmann AM,
Cecchetti R,
Fenoglio C,
Serpente M,
Arcaro M,
Caltagirone C,
Orfei MD,
Ciaramella A,
Pichler S,
Mayhaus M,
Gu W,
Lleó A,
Fortea J,
Blesa R,
Barber IS,
Brookes K,
Cupidi C,
Maletta RG,
Carrell D,
Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
Bosco P,
Todd S,
Craig D,
Johnston J,
Gill M,
Lawlor B,
Lynch A,
Fox NC,
Hardy J,
Albin RL,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Bigio EH,
Bird TD,
Boeve BF,
Bowen JD,
Boxer A,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Carroll SL,
Diaz CC,
Chui HC,
Clark DG,
Cribbs DH,
Crocco EA,
DeCarli C,
Dick M,
Duara R,
Evans DA,
Faber KM,
Fallon KB,
Fardo DW,
Farlow MR,
Ferris S,
Foroud TM,
Galasko DR,
Gearing M,
Geschwind DH,
Gilbert JR,
Graff-Radford NR,
Green RC,
Growdon JH,
Hamilton RL,
Harrell LE,
Honig LS,
Huentelman MJ,
Hulette CM,
Hyman BT,
Jarvik GP,
Abner E,
Jin LW,
Jun G,
Karydas A,
Kaye JA,
Kim R,
Kowall NW,
Kramer JH,
LaFerla FM,
Lah JJ,
Leverenz JB,
Levey AI,
Li G,
Lieberman AP,
Lunetta KL,
Lyketsos CG,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Morris JC,
Murrell JR,
Myers AJ,
O'Bryant S,
Olichney JM,
Pankratz VS,
Parisi JE,
Paulson HL,
Perry W,
Peskind E,
Pierce A,
Poon WW,
Potter H,
Quinn JF,
Raj A,
Raskind M,
Reisberg B,
Reitz C,
Ringman JM,
Roberson ED,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Sager MA,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Smith AG,
Sonnen JA,
Spina S,
Stern RA,
Swerdlow RH,
Tanzi RE,
Thornton-Wells TA,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Van Eldik LJ,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Wilhelmsen KC,
Williamson J,
Wingo TS,
Woltjer RL,
Wright CB,
Yu CE,
Yu L,
Garzia F,
Golamaully F,
Septier G,
Engelborghs S,
Vandenberghe R,
De Deyn PP,
Fernadez CM,
Benito YA,
Thonberg H,
Forsell C,
Lilius L,
Kinhult-Stählbom A,
Kilander L,
Brundin R,
Concari L,
Helisalmi S,
Koivisto AM,
Haapasalo A,
Dermecourt V,
Fievet N,
Hanon O,
Dufouil C,
Brice A,
Ritchie K,
Dubois B,
Himali JJ,
Keene CD,
Tschanz J,
Fitzpatrick AL,
Kukull WA,
Norton M,
Aspelund T,
Larson EB,
Munger R,
Rotter JI,
Lipton RB,
Bullido MJ,
Hofman A,
Montine TJ,
Coto E,
Boerwinkle E,
Petersen RC,
Alvarez V,
Rivadeneira F,
Reiman EM,
Gallo M,
O'Donnell CJ,
Reisch JS,
Bruni AC,
Royall DR,
Dichgans M,
Sano M,
Galimberti D,
St George-Hyslop P,
Scarpini E,
Tsuang DW,
Mancuso M,
Bonuccelli U,
Winslow AR,
Daniele A,
Wu CK,
Peters O,
Nacmias B,
Riemenschneider M,
Heun R,
Brayne C,
Rubinsztein DC,
Bras J,
Guerreiro R,
Al-Chalabi A,
Shaw CE,
Collinge J,
Mann D,
Tsolaki M,
Clarimón J,
Sussams R,
Lovestone S,
O'Donovan MC,
Owen MJ,
Behrens TW,
Mead S,
Goate AM,
Uitterlinden AG,
Holmes C,
Cruchaga C,
Ingelsson M,
Bennett DA,
Powell J,
Golde TE,
Graff C,
De Jager PL,
Morgan K,
Ertekin-Taner N,
Combarros O,
Psaty BM,
Passmore P,
Younkin SG,
Berr C,
Gudnason V,
Rujescu D,
Dickson DW,
Dartigues JF,
DeStefano AL,
Ortega-Cubero S,
Hakonarson H,
Campion D,
Boada M,
Kauwe JK,
Farrer LA,
Van Broeckhoven C,
Ikram MA,
Jones L,
Haines JL,
Tzourio C,
Launer LJ,
Escott-Price V,
Mayeux R,
Deleuze JF,
Amin N,
Holmans PA,
Pericak-Vance MA,
Amouyel P,
van Duijn CM,
Ramirez A,
Wang LS,
Lambert JC,
Seshadri S,
Williams J,
Schellenberg GD
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
페이지 1개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.