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성함이나 학술지명, PMID로 찾아보십시오.
DeStefano A에 대해
14건.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
외 35명 — 모두 보기
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) 외 컨소시엄 10곳
Nature genetics · 2014 · PMID 25064009 · open access
페이지 12개+
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
Williams FM,
Carter AM,
Hysi PG,
Surdulescu G,
Hodgkiss D,
Soranzo N,
Traylor M,
Bevan S,
Dichgans M,
Rothwell PM,
Sudlow C,
Farrall M
외 46명 — 모두 보기
Silander K,
Kaunisto M,
Wagner P,
Saarela O,
Kuulasmaa K,
Virtamo J,
Salomaa V,
Amouyel P,
Arveiler D,
Ferrieres J,
Wiklund PG,
Ikram MA,
Hofman A,
Boncoraglio GB,
Parati EA,
Helgadottir A,
Gretarsdottir S,
Thorsteinsdottir U,
Thorleifsson G,
Stefansson K,
Seshadri S,
DeStefano A,
Gschwendtner A,
Psaty B,
Longstreth W,
Mitchell BD,
Cheng YC,
Clarke R,
Ferrario M,
Bis JC,
Levi C,
Attia J,
Holliday EG,
Scott RJ,
Fornage M,
Sharma P,
Furie KL,
Rosand J,
Nalls M,
Meschia J,
Mosely TH,
Evans A,
Palotie A,
Markus HS,
Grant PJ,
Spector TD
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 외 컨소시엄 3곳
Annals of neurology · 2013 · PMID 23381943 · open access
페이지 11개
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,
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Boerwinkle E,
Borroni B,
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Bråthen G,
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Bresner C,
Brodaty H,
Brookes KJ,
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Bûrger K,
Burholt V,
Bush WS,
Calero M,
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Chene G,
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Carracedo Á,
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Escott-Price V,
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Fardo DW,
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Fernández-Fuertes M,
Ferrari R,
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Sanabria Á,
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Juan PS,
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Satizabal CL,
Scamosci M,
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Schneider A,
Schott JM,
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Solomon A,
Song Y,
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Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
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Thalamuthu A,
Thomas T,
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Traykov L,
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Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
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Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
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EADB · GR@ACE 외 컨소시엄 7곳
Nature genetics · 2022 · PMID 35379992 · open access
페이지 9개
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
외 277명 — 모두 보기
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
Koh JY,
Eicher JD,
Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
Abramovic L,
Alhusaini S,
Milaneschi Y,
Papmeyer M,
Axelsson T,
Ehrlich S,
Roiz-Santiañez R,
Kraemer B,
Håberg AK,
Jones HJ,
Pike GB,
Stein DJ,
Stevens A,
Bralten J,
Vernooij MW,
Harris TB,
Filippi I,
Witte AV,
Guadalupe T,
Wittfeld K,
Mosley TH,
Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
Hilal S,
Nho K,
Mirza-Schreiber N,
Arfanakis K,
Becker DM,
Ames D,
Goldman AL,
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Boomsma DI,
Lovestone S,
Giddaluru S,
Le Hellard S,
Mattheisen M,
Bohlken MM,
Kasperaviciute D,
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Agartz I,
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Davies GE,
Shin J,
Ipser JC,
Vinke LN,
Hoogman M,
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Burkhardt R,
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Crivello F,
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Nature genetics · 2019 · PMID 31636452
페이지 8개
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Wain LV,
Verwoert GC,
O'Reilly PF,
Shi G,
Johnson T,
Johnson AD,
Bochud M,
Rice KM,
Henneman P,
Smith AV,
Ehret GB,
Amin N
외 214명 — 모두 보기
Larson MG,
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Bis JC,
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Janssens AC,
Zhao JH,
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Fu J,
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Pichler I,
Jackson AU,
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Zhang F,
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Hottenga JJ,
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Guo X,
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Boban M,
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LifeLines Cohort Study · EchoGen consortium 외 컨소시엄 6곳
Nature genetics · 2011 · PMID 21909110 · open access
페이지 6개
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels
Debette S,
Visvikis-Siest S,
Chen MH,
Ndiaye NC,
Song C,
Destefano A,
Safa R,
Azimi Nezhad M,
Sawyer D,
Marteau JB,
Xanthakis V,
Siest G
외 11명 — 모두 보기
Sullivan L,
Pfister M,
Smith H,
Choi SH,
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Yang Q,
Fitzgerald P,
Ingelsson E,
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Seshadri S
Circulation research · 2011 · PMID 21757650
페이지 5개
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,
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Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
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페이지 4개
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외 71명 — 모두 보기
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Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
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Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
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외 51명 — 모두 보기
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페이지 1개
Common variants at 6q22 and 17q21 are associated with intracranial volume
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외 44명 — 모두 보기
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페이지 1개
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페이지 1개
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
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외 437명 — 모두 보기
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페이지 1개
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
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외 24명 — 모두 보기
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Communications biology · 2022 · PMID 35396452 · open access
페이지 1개
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