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Ma P에 대해
43건, 그중 20건 표시.
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
Li HJ,
Zhang C,
Hui L,
Zhou DS,
Li Y,
Zhang CY,
Wang C,
Wang L,
Li W,
Yang Y,
Qu N,
Tang J
외 37명 — 모두 보기
He Y,
Zhou J,
Yang Z,
Li X,
Cai J,
Yang L,
Chen J,
Fan W,
Tang W,
Tang W,
Jia QF,
Liu W,
Zhuo C,
Song X,
Liu F,
Bai Y,
Zhong BL,
Zhang SF,
Chen J,
Xia B,
Lv L,
Liu Z,
Hu S,
Li XY,
Liu JW,
Cai X,
Yao YG,
Zhang Y,
Yan H,
Chang S,
Zhao JP,
Yue WH,
Luo XJ,
Chen X,
Xiao X,
Fang Y,
Li M
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
페이지 4개
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
외 25명 — 모두 보기
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
페이지 4개
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
Barnes DR,
Tyrer JP,
Dennis J,
Leslie G,
Bolla MK,
Lush M,
Aeilts AM,
Aittomäki K,
Andrieu N,
Andrulis IL,
Anton-Culver H,
Arason A
외 156명 — 모두 보기
Arun BK,
Balmaña J,
Bandera EV,
Barkardottir RB,
Berger LPV,
Berrington de Gonzalez A,
Berthet P,
Białkowska K,
Bjørge L,
Blanco AM,
Blok MJ,
Bobolis KA,
Bogdanova NV,
Brenton JD,
Butz H,
Buys SS,
Caligo MA,
Campbell I,
Castillo C,
Claes KBM,
Colonna SV,
Cook LS,
Daly MB,
Dansonka-Mieszkowska A,
de la Hoya M,
deFazio A,
DePersia A,
Ding YC,
Doherty JA,
Domchek SM,
Dörk T,
Einbeigi Z,
Engel C,
Evans DG,
Foretova L,
Fortner RT,
Fostira F,
Foti MC,
Friedman E,
Frone MN,
Ganz PA,
Gentry-Maharaj A,
Glendon G,
Godwin AK,
González-Neira A,
Greene MH,
Gronwald J,
Guerrieri-Gonzaga A,
Hamann U,
Hansen TVO,
Harris HR,
Hauke J,
Heitz F,
Hogervorst FBL,
Hooning MJ,
Hopper JL,
Huff CD,
Huntsman DG,
Imyanitov EN,
Izatt L,
Jakubowska A,
James PA,
Janavicius R,
John EM,
Kar S,
Karlan BY,
Kennedy CJ,
Kiemeney LALM,
Konstantopoulou I,
Kupryjanczyk J,
Laitman Y,
Lavie O,
Lawrenson K,
Lester J,
Lesueur F,
Lopez-Pleguezuelos C,
Mai PL,
Manoukian S,
May T,
McNeish IA,
Menon U,
Milne RL,
Modugno F,
Mongiovi JM,
Montagna M,
Moysich KB,
Neuhausen SL,
Nielsen FC,
Noguès C,
Oláh E,
Olopade OI,
Osorio A,
Papi L,
Pathak H,
Pearce CL,
Pedersen IS,
Peixoto A,
Pejovic T,
Peng PC,
Peshkin BN,
Peterlongo P,
Powell CB,
Prokofyeva D,
Pujana MA,
Radice P,
Rashid MU,
Rennert G,
Richenberg G,
Sandler DP,
Sasamoto N,
Setiawan VW,
Sharma P,
Sieh W,
Singer CF,
Snape K,
Sokolenko AP,
Soucy P,
Southey MC,
Stoppa-Lyonnet D,
Sutphen R,
Sutter C,
Tan YY,
Teixeira MR,
Terry KL,
Thomsen LCV,
Tischkowitz M,
Toland AE,
Van Gorp T,
Vega A,
Velez Edwards DR,
Webb PM,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Winham SJ,
Wu AH,
Yadav S,
Yu Y,
Ziogas A,
Berchuck A,
Couch FJ,
Goode EL,
Goodman MT,
Monteiro AN,
Offit K,
Ramus SJ,
Risch HA,
Schildkraut JM,
Thomassen M,
Simard J,
Easton DF,
Jones MR,
Chenevix-Trench G,
Gayther SA,
Antoniou AC,
Pharoah PDP
NPJ genomic medicine · 2025 · PMID 41266372 · open access
페이지 4개
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Köttgen A,
Albrecht E,
Teumer A,
Vitart V,
Krumsiek J,
Hundertmark C,
Pistis G,
Ruggiero D,
O'Seaghdha CM,
Haller T,
Yang Q,
Tanaka T
외 214명 — 모두 보기
Johnson AD,
Kutalik Z,
Smith AV,
Shi J,
Struchalin M,
Middelberg RP,
Brown MJ,
Gaffo AL,
Pirastu N,
Li G,
Hayward C,
Zemunik T,
Huffman J,
Yengo L,
Zhao JH,
Demirkan A,
Feitosa MF,
Liu X,
Malerba G,
Lopez LM,
van der Harst P,
Li X,
Kleber ME,
Hicks AA,
Nolte IM,
Johansson A,
Murgia F,
Wild SH,
Bakker SJ,
Peden JF,
Dehghan A,
Steri M,
Tenesa A,
Lagou V,
Salo P,
Mangino M,
Rose LM,
Lehtimäki T,
Woodward OM,
Okada Y,
Tin A,
Müller C,
Oldmeadow C,
Putku M,
Czamara D,
Kraft P,
Frogheri L,
Thun GA,
Grotevendt A,
Gislason GK,
Harris TB,
Launer LJ,
McArdle P,
Shuldiner AR,
Boerwinkle E,
Coresh J,
Schmidt H,
Schallert M,
Martin NG,
Montgomery GW,
Kubo M,
Nakamura Y,
Tanaka T,
Munroe PB,
Samani NJ,
Jacobs DR Jr,
Liu K,
D'Adamo P,
Ulivi S,
Rotter JI,
Psaty BM,
Vollenweider P,
Waeber G,
Campbell S,
Devuyst O,
Navarro P,
Kolcic I,
Hastie N,
Balkau B,
Froguel P,
Esko T,
Salumets A,
Khaw KT,
Langenberg C,
Wareham NJ,
Isaacs A,
Kraja A,
Zhang Q,
Wild PS,
Scott RJ,
Holliday EG,
Org E,
Org E,
Viigimaa M,
Bandinelli S,
Metter JE,
Lupo A,
Trabetti E,
Sorice R,
Döring A,
Lattka E,
Strauch K,
Theis F,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Bruinenberg M,
Stolk RP,
Kooner JS,
Zhang W,
Winkelmann BR,
Boehm BO,
Lucae S,
Penninx BW,
Smit JH,
Curhan G,
Mudgal P,
Plenge RM,
Portas L,
Persico I,
Kirin M,
Wilson JF,
Mateo Leach I,
van Gilst WH,
Goel A,
Ongen H,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Imboden M,
von Eckardstein A,
Cucca F,
Nagaraja R,
Piras MG,
Nauck M,
Schurmann C,
Budde K,
Ernst F,
Farrington SM,
Theodoratou E,
Prokopenko I,
Stumvoll M,
Jula A,
Perola M,
Salomaa V,
Shin SY,
Spector TD,
Sala C,
Ridker PM,
Kähönen M,
Viikari J,
Hengstenberg C,
Nelson CP,
Meschia JF,
Nalls MA,
Sharma P,
Singleton AB,
Kamatani N,
Zeller T,
Burnier M,
Attia J,
Laan M,
Klopp N,
Hillege HL,
Kloiber S,
Choi H,
Pirastu M,
Tore S,
Probst-Hensch NM,
Völzke H,
Gudnason V,
Parsa A,
Schmidt R,
Whitfield JB,
Fornage M,
Gasparini P,
Siscovick DS,
Polašek O,
Campbell H,
Rudan I,
Bouatia-Naji N,
Metspalu A,
Loos RJ,
van Duijn CM,
Borecki IB,
Ferrucci L,
Gambaro G,
Deary IJ,
Wolffenbuttel BH,
Chambers JC,
März W,
Pramstaller PP,
Snieder H,
Gyllensten U,
Wright AF,
Navis G,
Watkins H,
Witteman JC,
Sanna S,
Schipf S,
Dunlop MG,
Tönjes A,
Ripatti S,
Soranzo N,
Toniolo D,
Chasman DI,
Raitakari O,
Kao WH,
Ciullo M,
Fox CS,
Caulfield M,
Bochud M,
Gieger C
LifeLines Cohort Study · CARDIoGRAM Consortium 외 컨소시엄 3곳
Nature genetics · 2013 · PMID 23263486
페이지 3개
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
외 106명 — 모두 보기
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
페이지 3개
A genome- and phenome-wide association study of plasma procalcitonin concentrations in individuals of European ancestry
Zhang W,
van der Most PJ,
Wang S,
Kamali Z,
Giontella A,
Enhörning S,
Gansevoort RT,
van der Harst P,
Bakker SJL,
Melander O,
Keus F,
Lunter G
외 1명 — 모두 보기
EBioMedicine · 2026 · PMID 41406505 · open access
페이지 3개
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation
Lauc G,
Essafi A,
Huffman JE,
Hayward C,
Knežević A,
Kattla JJ,
Polašek O,
Gornik O,
Vitart V,
Abrahams JL,
Pučić M,
Novokmet M
외 14명 — 모두 보기
Redžić I,
Campbell S,
Wild SH,
Borovečki F,
Wang W,
Kolčić I,
Zgaga L,
Gyllensten U,
Wilson JF,
Wright AF,
Hastie ND,
Campbell H,
Rudd PM,
Rudan I
PLoS genetics · 2010 · PMID 21203500 · open access
페이지 2개
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Lemaitre RN,
Tanaka T,
Tang W,
Manichaikul A,
Foy M,
Kabagambe EK,
Nettleton JA,
King IB,
Weng LC,
Bhattacharya S,
Bandinelli S,
Bis JC
외 23명 — 모두 보기
Rich SS,
Jacobs DR Jr,
Cherubini A,
McKnight B,
Liang S,
Gu X,
Rice K,
Laurie CC,
Lumley T,
Browning BL,
Psaty BM,
Chen YD,
Friedlander Y,
Djousse L,
Wu JH,
Siscovick DS,
Uitterlinden AG,
Arnett DK,
Ferrucci L,
Fornage M,
Tsai MY,
Mozaffarian D,
Steffen LM
PLoS genetics · 2011 · PMID 21829377 · open access
페이지 2개
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium
Wu JH,
Lemaitre RN,
Manichaikul A,
Guan W,
Tanaka T,
Foy M,
Kabagambe EK,
Djousse L,
Siscovick D,
Fretts AM,
Johnson C,
King IB
외 16명 — 모두 보기
Psaty BM,
McKnight B,
Rich SS,
Chen YD,
Nettleton JA,
Tang W,
Bandinelli S,
Jacobs DR Jr,
Browning BL,
Laurie CC,
Gu X,
Tsai MY,
Steffen LM,
Ferrucci L,
Fornage M,
Mozaffarian D
Circulation. Cardiovascular genetics · 2013 · PMID 23362303
페이지 2개
Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression
Zhou H,
Polimanti R,
Yang BZ,
Wang Q,
Han S,
Sherva R,
Nuñez YZ,
Zhao H,
Farrer LA,
Kranzler HR,
Gelernter J
JAMA psychiatry · 2017 · PMID 29071344
페이지 2개
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease
Yao C,
Chen G,
Song C,
Keefe J,
Mendelson M,
Huan T,
Sun BB,
Laser A,
Maranville JC,
Wu H,
Ho JE,
Courchesne P
외 12명 — 모두 보기
Lyass A,
Larson MG,
Gieger C,
Graumann J,
Johnson AD,
Danesh J,
Runz H,
Hwang SJ,
Liu C,
Butterworth AS,
Suhre K,
Levy D
Nature communications · 2018 · PMID 30111768 · open access
페이지 2개
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
외 261명 — 모두 보기
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
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Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
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Parsons MT,
Peissel B,
Peixoto A,
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Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators 외 컨소시엄 2곳
Nature genetics · 2020 · PMID 32424353 · open access
페이지 2개
Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans
Kimbrel NA,
Ashley-Koch AE,
Qin XJ,
Lindquist JH,
Garrett ME,
Dennis MF,
Hair LP,
Huffman JE,
Jacobson DA,
Madduri RK,
Trafton JA,
Coon H
외 9명 — 모두 보기
Million Veteran Program Suicide Exemplar Workgroup, the International Suicide Genetics Consortium, the Veterans Affairs Mid-Atlantic Mental Illness Research, Education, and Clinical Center Workgroup, and the Veterans Affairs Million Veteran Program
JAMA psychiatry · 2023 · PMID 36515925
페이지 2개
A comprehensive family-based replication study of schizophrenia genes
Aberg KA,
Liu Y,
Bukszár J,
McClay JL,
Khachane AN,
Andreassen OA,
Blackwood D,
Corvin A,
Djurovic S,
Gurling H,
Ophoff R,
Pato CN
외 15명 — 모두 보기
Pato MT,
Riley B,
Webb T,
Kendler K,
O'Donovan M,
Craddock N,
Kirov G,
Owen M,
Rujescu D,
St Clair D,
Werge T,
Hultman CM,
Delisi LE,
Sullivan P,
van den Oord EJ
JAMA psychiatry · 2013 · PMID 23894747
페이지 1개
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Dichgans M,
Malik R,
König IR,
Rosand J,
Clarke R,
Gretarsdottir S,
Thorleifsson G,
Mitchell BD,
Assimes TL,
Levi C,
O'Donnell CJ,
Fornage M
외 27명 — 모두 보기
Thorsteinsdottir U,
Psaty BM,
Hengstenberg C,
Seshadri S,
Erdmann J,
Bis JC,
Peters A,
Boncoraglio GB,
März W,
Meschia JF,
Kathiresan S,
Ikram MA,
McPherson R,
Stefansson K,
Sudlow C,
Reilly MP,
Thompson JR,
Sharma P,
Hopewell JC,
Chambers JC,
Watkins H,
Rothwell PM,
Roberts R,
Markus HS,
Samani NJ,
Farrall M,
Schunkert H
METASTROKE Consortium · CARDIoGRAM Consortium 외 컨소시엄 2곳
Stroke · 2014 · PMID 24262325
페이지 1개
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels
Ma Q,
Ozel AB,
Ramdas S,
McGee B,
Khoriaty R,
Siemieniak D,
Li HD,
Guan Y,
Brody LC,
Mills JL,
Molloy AM,
Ginsburg D
외 2명 — 모두 보기
Blood · 2014 · PMID 25208887
페이지 1개
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients
Ziv E,
Dean E,
Hu D,
Martino A,
Serie D,
Curtin K,
Campa D,
Aftab B,
Bracci P,
Buda G,
Zhao Y,
Caswell-Jin J
외 27명 — 모두 보기
Diasio R,
Dumontet C,
Dudziński M,
Fejerman L,
Greenberg A,
Huntsman S,
Jamroziak K,
Jurczyszyn A,
Kumar S,
Atanackovic D,
Glenn M,
Cannon-Albright LA,
Jones B,
Lee A,
Marques H,
Martin T,
Martinez-Lopez J,
Martinez-Lopez J,
Rajkumar V,
Sainz J,
Vangsted AJ,
Wątek M,
Wolf J,
Slager S,
Camp NJ,
Canzian F,
Vachon C
Nature communications · 2015 · PMID 26198393
페이지 1개
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
외 55명 — 모두 보기
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
페이지 1개
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