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Lee S에 대해
58건, 그중 18건 표시.
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
외 137명 — 모두 보기
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
페이지 2개
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2
Wright FA,
Strug LJ,
Doshi VK,
Commander CW,
Blackman SM,
Sun L,
Berthiaume Y,
Cutler D,
Cojocaru A,
Collaco JM,
Corey M,
Dorfman R
외 25명 — 모두 보기
Goddard K,
Green D,
Kent JW Jr,
Lange EM,
Lee S,
Li W,
Luo J,
Mayhew GM,
Naughton KM,
Pace RG,
Paré P,
Rommens JM,
Sandford A,
Stonebraker JR,
Sun W,
Taylor C,
Vanscoy LL,
Zou F,
Blangero J,
Zielenski J,
O'Neal WK,
Drumm ML,
Durie PR,
Knowles MR,
Cutting GR
Nature genetics · 2011 · PMID 21602797 · open access
페이지 1개
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Kim HC,
Lee JY,
Sung H,
Choi JY,
Park SK,
Lee KM,
Kim YJ,
Go MJ,
Li L,
Cho YS,
Park M,
Kim DJ
외 27명 — 모두 보기
Oh JH,
Kim JW,
Jeon JP,
Jeon SY,
Min H,
Kim HM,
Park J,
Yoo KY,
Noh DY,
Ahn SH,
Lee MH,
Kim SW,
Lee JW,
Park BW,
Park WY,
Kim EH,
Kim MK,
Han W,
Lee SA,
Matsuo K,
Shen CY,
Wu PE,
Hsiung CN,
Lee JY,
Kim HL,
Han BG,
Kang D
Breast cancer research : BCR · 2012 · PMID 22452962 · open access
페이지 1개
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
Tansey KE,
Buttenschøn HN,
Cohen-Woods S,
Bigdeli T,
Hall LS,
Kutalik Z,
Lee SH,
Ripke S,
Steinberg S,
Teumer A,
Viktorin A
외 64명 — 모두 보기
Wray NR,
Arolt V,
Baune BT,
Boomsma DI,
Børglum AD,
Byrne EM,
Castelao E,
Craddock N,
Craig IW,
Dannlowski U,
Deary IJ,
Degenhardt F,
Forstner AJ,
Gordon SD,
Grabe HJ,
Grove J,
Hamilton SP,
Hayward C,
Heath AC,
Hocking LJ,
Homuth G,
Hottenga JJ,
Kloiber S,
Krogh J,
Landén M,
Lang M,
Levinson DF,
Lichtenstein P,
Lucae S,
MacIntyre DJ,
Madden P,
Magnusson PKE,
Martin NG,
McIntosh AM,
Middeldorp CM,
Milaneschi Y,
Montgomery GW,
Mors O,
Müller-Myhsok B,
Nyholt DR,
Oskarsson H,
Owen MJ,
Padmanabhan S,
Penninx BWJH,
Pergadia ML,
Porteous DJ,
Potash JB,
Preisig M,
Rivera M,
Shi J,
Shyn SI,
Sigurdsson E,
Smit JH,
Smith BH,
Stefansson H,
Stefansson K,
Strohmaier J,
Sullivan PF,
Thomson P,
Thorgeirsson TE,
Van der Auwera S,
Weissman MM,
Breen G,
Lewis CM
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · open access
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
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
Martin J,
Walters RK,
Demontis D,
Mattheisen M,
Lee SH,
Robinson E,
Brikell I,
Ghirardi L,
Larsson H,
Lichtenstein P,
Eriksson N,
Werge T
외 13명 — 모두 보기
Mortensen PB,
Pedersen MG,
Mors O,
Nordentoft M,
Hougaard DM,
Bybjerg-Grauholm J,
Wray NR,
Franke B,
Faraone SV,
O'Donovan MC,
Thapar A,
Børglum AD,
Neale BM
23andMe Research Team · Psychiatric Genomics Consortium: ADHD Subgroup 외 컨소시엄 1곳
Biological psychiatry · 2018 · PMID 29325848 · open access
페이지 1개
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Zhou W,
Nielsen JB,
Fritsche LG,
Dey R,
Gabrielsen ME,
Wolford BN,
LeFaive J,
VandeHaar P,
Gagliano SA,
Gifford A,
Bastarache LA,
Wei WQ
외 7명 — 모두 보기
Nature genetics · 2018 · PMID 30104761 · open access
페이지 1개
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
외 79명 — 모두 보기
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
페이지 1개
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts
Lee JY,
Kim J,
Kim SW,
Park SK,
Ahn SH,
Lee MH,
Suh YJ,
Noh DY,
Son BH,
Cho YU,
Lee SB,
Lee JW
외 2명 — 모두 보기
Scientific reports · 2018 · PMID 30323354 · open access
페이지 1개
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen J,
Evans DS,
Arking DE,
Tesi N,
Nygaard M,
Liu X,
Wojczynski MK,
Biggs ML,
van der Spek A,
Atzmon G,
Ware EB,
Sarnowski C
외 72명 — 모두 보기
Smith AV,
Seppälä I,
Cordell HJ,
Dose J,
Amin N,
Arnold AM,
Ayers KL,
Barzilai N,
Becker EJ,
Beekman M,
Blanché H,
Christensen K,
Christiansen L,
Collerton JC,
Cubaynes S,
Cummings SR,
Davies K,
Debrabant B,
Deleuze JF,
Duncan R,
Faul JD,
Franceschi C,
Galan P,
Gudnason V,
Harris TB,
Huisman M,
Hurme MA,
Jagger C,
Jansen I,
Jylhä M,
Kähönen M,
Karasik D,
Kardia SLR,
Kingston A,
Kirkwood TBL,
Launer LJ,
Lehtimäki T,
Lieb W,
Lyytikäinen LP,
Martin-Ruiz C,
Min J,
Nebel A,
Newman AB,
Nie C,
Nohr EA,
Orwoll ES,
Perls TT,
Province MA,
Psaty BM,
Raitakari OT,
Reinders MJT,
Robine JM,
Rotter JI,
Sebastiani P,
Smith J,
Sørensen TIA,
Taylor KD,
Uitterlinden AG,
van der Flier W,
van der Lee SJ,
van Duijn CM,
van Heemst D,
Vaupel JW,
Weir D,
Ye K,
Zeng Y,
Zheng W,
Holstege H,
Kiel DP,
Lunetta KL,
Slagboom PE,
Murabito JM
Nature communications · 2019 · PMID 31413261 · open access
페이지 1개
An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
Oh JJ,
Shivakumar M,
Miller J,
Verma S,
Lee H,
Hong SK,
Lee SE,
Lee Y,
Lee SJ,
Sung J,
Kim D,
Byun SS
Scientific reports · 2019 · PMID 31748686 · open access
페이지 1개
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children
Lee SHR,
Qian M,
Yang W,
Diedrich JD,
Raetz E,
Yang W,
Dong Q,
Devidas M,
Pei D,
Yeoh A,
Cheng C,
Pui CH
외 7명 — 모두 보기
Journal of the National Cancer Institute · 2021 · PMID 32882024
페이지 1개
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
Surakka I,
Fritsche LG,
Zhou W,
Backman J,
Kosmicki JA,
Lu H,
Brumpton B,
Nielsen JB,
Gabrielsen ME,
Skogholt AH,
Wolford B,
Graham SE
외 14명 — 모두 보기
Chen YE,
Lee S,
Kang HM,
Langhammer A,
Forsmo S,
Åsvold BO,
Styrkarsdottir U,
Holm H,
Gudbjartsson D,
Stefansson K,
Baras A,
Abecasis GR,
Hveem K,
Willer CJ
Regeneron Genetics Center
Nature communications · 2020 · PMID 33097703 · open access
페이지 1개
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
외 21명 — 모두 보기
Lee S,
Kim H,
Dhanasingh I,
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