연구자에게
내 논문이 여기 있나요?
논문 2,683편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Nalls MA에 대해
80건, 그중 20건 표시.
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn L,
Heilbron K,
Blauwendraat C,
Reynolds RH,
Yu E,
Senkevich K,
Rudakou U,
Estiar MA,
Gustavsson EK,
Brolin K,
Ruskey JA,
Freeman K
외 46명 — 모두 보기
Asayesh F,
Chia R,
Arnulf I,
Hu MTM,
Montplaisir JY,
Gagnon JF,
Desautels A,
Dauvilliers Y,
Gigli GL,
Valente M,
Janes F,
Bernardini A,
Högl B,
Stefani A,
Ibrahim A,
Šonka K,
Kemlink D,
Oertel W,
Janzen A,
Plazzi G,
Biscarini F,
Antelmi E,
Figorilli M,
Puligheddu M,
Mollenhauer B,
Trenkwalder C,
Sixel-Döring F,
Cochen De Cock V,
Monaca CC,
Heidbreder A,
Ferini-Strambi L,
Dijkstra F,
Viaene M,
Abril B,
Boeve BF,
Scholz SW,
Ryten M,
Bandres-Ciga S,
Noyce A,
Cannon P,
Pihlstrøm L,
Nalls MA,
Singleton AB,
Rouleau GA,
Postuma RB,
Gan-Or Z
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
페이지 2개
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
Reich D,
Nalls MA,
Kao WH,
Akylbekova EL,
Tandon A,
Patterson N,
Mullikin J,
Hsueh WC,
Cheng CY,
Coresh J,
Boerwinkle E,
Li M
외 12명 — 모두 보기
Waliszewska A,
Neubauer J,
Li R,
Leak TS,
Ekunwe L,
Files JC,
Hardy CL,
Zmuda JM,
Taylor HA,
Ziv E,
Harris TB,
Wilson JG
PLoS genetics · 2009 · PMID 19180233 · open access
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
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
Laaksovirta H,
Peuralinna T,
Schymick JC,
Scholz SW,
Lai SL,
Myllykangas L,
Sulkava R,
Jansson L,
Hernandez DG,
Gibbs JR,
Nalls MA,
Heckerman D
외 2명 — 모두 보기
The Lancet. Neurology · 2010 · PMID 20801718
페이지 1개
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Fornage M,
Debette S,
Bis JC,
Schmidt H,
Ikram MA,
Dufouil C,
Sigurdsson S,
Lumley T,
DeStefano AL,
Fazekas F,
Vrooman HA,
Shibata DK
외 51명 — 모두 보기
Maillard P,
Zijdenbos A,
Smith AV,
Gudnason H,
de Boer R,
Cushman M,
Mazoyer B,
Heiss G,
Vernooij MW,
Enzinger C,
Glazer NL,
Beiser A,
Knopman DS,
Cavalieri M,
Niessen WJ,
Harris TB,
Petrovic K,
Lopez OL,
Au R,
Lambert JC,
Hofman A,
Gottesman RF,
Garcia M,
Heckbert SR,
Atwood LD,
Catellier DJ,
Uitterlinden AG,
Yang Q,
Smith NL,
Aspelund T,
Romero JR,
Rice K,
Taylor KD,
Nalls MA,
Rotter JI,
Sharrett R,
van Duijn CM,
Amouyel P,
Wolf PA,
Gudnason V,
van der Lugt A,
Boerwinkle E,
Psaty BM,
Seshadri S,
Tzourio C,
Breteler MM,
Mosley TH,
Schmidt R,
Longstreth WT,
DeCarli C,
Launer LJ
Annals of neurology · 2011 · PMID 21681796
페이지 1개
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram MA,
Fornage M,
Smith AV,
Seshadri S,
Schmidt R,
Debette S,
Vrooman HA,
Sigurdsson S,
Ropele S,
Taal HR,
Mook-Kanamori DO,
Coker LH
외 44명 — 모두 보기
Longstreth WT Jr,
Niessen WJ,
DeStefano AL,
Beiser A,
Zijdenbos AP,
Struchalin M,
Jack CR Jr,
Rivadeneira F,
Uitterlinden AG,
Knopman DS,
Hartikainen AL,
Pennell CE,
Thiering E,
Steegers EA,
Hakonarson H,
Heinrich J,
Palmer LJ,
Jarvelin MR,
McCarthy MI,
Grant SF,
St Pourcain B,
Timpson NJ,
Smith GD,
Sovio U,
Nalls MA,
Au R,
Hofman A,
Gudnason H,
van der Lugt A,
Harris TB,
Meeks WM,
Vernooij MW,
van Buchem MA,
Catellier D,
Jaddoe VW,
Gudnason V,
Windham BG,
Wolf PA,
van Duijn CM,
Mosley TH Jr,
Schmidt H,
Launer LJ,
Breteler MM,
DeCarli C
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
페이지 1개
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
외 68명 — 모두 보기
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
페이지 1개
Impact of ancestry and common genetic variants on QT interval in African Americans
Smith JG,
Avery CL,
Evans DS,
Nalls MA,
Meng YA,
Smith EN,
Palmer C,
Tanaka T,
Mehra R,
Butler AM,
Young T,
Buxbaum SG
외 39명 — 모두 보기
Kerr KF,
Berenson GS,
Schnabel RB,
Li G,
Ellinor PT,
Magnani JW,
Chen W,
Bis JC,
Curb JD,
Hsueh WC,
Rotter JI,
Liu Y,
Newman AB,
Limacher MC,
North KE,
Reiner AP,
Quibrera PM,
Schork NJ,
Singleton AB,
Psaty BM,
Soliman EZ,
Solomon AJ,
Srinivasan SR,
Alonso A,
Wallace R,
Redline S,
Zhang ZM,
Post WS,
Zonderman AB,
Taylor HA,
Murray SS,
Ferrucci L,
Arking DE,
Evans MK,
Fox ER,
Sotoodehnia N,
Heckbert SR,
Whitsel EA,
Newton-Cheh C
CARe and COGENT consortia
Circulation. Cardiovascular genetics · 2012 · PMID 23166209
페이지 1개
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Lambert JC,
Ibrahim-Verbaas CA,
Harold D,
Naj AC,
Sims R,
Bellenguez C,
DeStafano AL,
Bis JC,
Beecham GW,
Grenier-Boley B,
Russo G,
Thorton-Wells TA
외 160명 — 모두 보기
Jones N,
Smith AV,
Chouraki V,
Thomas C,
Ikram MA,
Zelenika D,
Vardarajan BN,
Kamatani Y,
Lin CF,
Gerrish A,
Gerrish A,
Schmidt H,
Kunkle B,
Dunstan ML,
Ruiz A,
Bihoreau MT,
Choi SH,
Reitz C,
Pasquier F,
Cruchaga C,
Craig D,
Amin N,
Berr C,
Lopez OL,
De Jager PL,
Deramecourt V,
Johnston JA,
Evans D,
Lovestone S,
Letenneur L,
Morón FJ,
Rubinsztein DC,
Eiriksdottir G,
Sleegers K,
Goate AM,
Fiévet N,
Huentelman MW,
Gill M,
Brown K,
Kamboh MI,
Keller L,
Barberger-Gateau P,
McGuiness B,
Larson EB,
Green R,
Myers AJ,
Dufouil C,
Todd S,
Wallon D,
Love S,
Rogaeva E,
Gallacher J,
St George-Hyslop P,
Clarimon J,
Lleo A,
Bayer A,
Tsuang DW,
Yu L,
Tsolaki M,
Bossù P,
Spalletta G,
Proitsi P,
Collinge J,
Sorbi S,
Sanchez-Garcia F,
Fox NC,
Hardy J,
Deniz Naranjo MC,
Bosco P,
Clarke R,
Brayne C,
Galimberti D,
Mancuso M,
Matthews F,
Moebus S,
Mecocci P,
Del Zompo M,
Maier W,
Hampel H,
Pilotto A,
Bullido M,
Panza F,
Caffarra P,
Nacmias B,
Gilbert JR,
Mayhaus M,
Lannefelt L,
Hakonarson H,
Pichler S,
Carrasquillo MM,
Ingelsson M,
Beekly D,
Alvarez V,
Zou F,
Valladares O,
Younkin SG,
Coto E,
Hamilton-Nelson KL,
Gu W,
Razquin C,
Pastor P,
Mateo I,
Owen MJ,
Faber KM,
Jonsson PV,
Combarros O,
O'Donovan MC,
Cantwell LB,
Soininen H,
Blacker D,
Mead S,
Mosley TH Jr,
Bennett DA,
Harris TB,
Fratiglioni L,
Holmes C,
de Bruijn RF,
Passmore P,
Montine TJ,
Bettens K,
Rotter JI,
Brice A,
Morgan K,
Foroud TM,
Kukull WA,
Hannequin D,
Powell JF,
Nalls MA,
Ritchie K,
Lunetta KL,
Kauwe JS,
Boerwinkle E,
Riemenschneider M,
Boada M,
Hiltuenen M,
Martin ER,
Schmidt R,
Rujescu D,
Wang LS,
Dartigues JF,
Mayeux R,
Tzourio C,
Hofman A,
Nöthen MM,
Graff C,
Psaty BM,
Jones L,
Haines JL,
Holmans PA,
Lathrop M,
Pericak-Vance MA,
Launer LJ,
Farrer LA,
van Duijn CM,
Van Broeckhoven C,
Moskvina V,
Seshadri S,
Williams J,
Schellenberg GD,
Amouyel P
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease 외 컨소시엄 2곳
Nature genetics · 2013 · PMID 24162737
페이지 1개
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Musani SK,
Fox ER,
Kraja A,
Bidulescu A,
Lieb W,
Lin H,
Beecham A,
Chen MH,
Felix JF,
Fox CS,
Kao WH,
Kardia SL
외 11명 — 모두 보기
Liu CT,
Nalls MA,
Rundek T,
Sacco RL,
Smith J,
Sun YV,
Wilson G,
Zhang Z,
Mosley TH,
Taylor HA,
Vasan RS
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
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
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
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
외 290명 — 모두 보기
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30926973 · open access
페이지 1개
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Bandres-Ciga S,
Ahmed S,
Sabir MS,
Blauwendraat C,
Adarmes-Gómez AD,
Bernal-Bernal I,
Bonilla-Toribio M,
Buiza-Rueda D,
Carrillo F,
Carrión-Claro M,
Gómez-Garre P,
Jesús S
외 83명 — 모두 보기
Labrador-Espinosa MA,
Macias D,
Méndez-Del-Barrio C,
Periñán-Tocino T,
Tejera-Parrado C,
Vargas-González L,
Diez-Fairen M,
Alvarez I,
Tartari JP,
Buongiorno M,
Aguilar M,
Gorostidi A,
Bergareche JA,
Mondragon E,
Vinagre-Aragon A,
Croitoru I,
Ruiz-Martínez J,
Dols-Icardo O,
Kulisevsky J,
Marín-Lahoz J,
Pagonabarraga J,
Pascual-Sedano B,
Ezquerra M,
Cámara A,
Compta Y,
Fernández M,
Fernández-Santiago R,
Muñoz E,
Tolosa E,
Valldeoriola F,
Gonzalez-Aramburu I,
Sanchez Rodriguez A,
Sierra M,
Menéndez-González M,
Blazquez M,
Garcia C,
Suarez-San Martin E,
García-Ruiz P,
Martínez-Castrillo JC,
Vela-Desojo L,
Ruz C,
Barrero FJ,
Escamilla-Sevilla F,
Mínguez-Castellanos A,
Cerdan D,
Tabernero C,
Gomez Heredia MJ,
Perez Errazquin F,
Romero-Acebal M,
Feliz C,
Lopez-Sendon JL,
Mata M,
Martínez Torres I,
Kim JJ,
Dalgard CL,
Brooks J,
Saez-Atienzar S,
Gibbs JR,
Jorda R,
Botia JA,
Bonet-Ponce L,
Morrison KE,
Clarke C,
Tan M,
Morris H,
Edsall C,
Hernandez D,
Simon-Sanchez J,
Nalls MA,
Scholz SW,
Jimenez-Escrig A,
Duarte J,
Vives F,
Duran R,
Hoenicka J,
Alvarez V,
Infante J,
Marti MJ,
Clarimón J,
López de Munain A,
Pastor P,
Mir P,
Singleton A
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
페이지 1개
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
Foo JN,
Chew EGY,
Chung SJ,
Peng R,
Blauwendraat C,
Nalls MA,
Mok KY,
Satake W,
Toda T,
Chao Y,
Tan LCS,
Tandiono M
외 33명 — 모두 보기
Lian MM,
Ng EY,
Prakash KM,
Au WL,
Meah WY,
Mok SQ,
Annuar AA,
Chan AYY,
Chen L,
Chen Y,
Jeon BS,
Jiang L,
Lim JL,
Lin JJ,
Liu C,
Mao C,
Mok V,
Pei Z,
Shang HF,
Shi CH,
Song K,
Tan AH,
Wu YR,
Xu YM,
Xu R,
Yan Y,
Yang J,
Zhang B,
Koh WP,
Lim SY,
Khor CC,
Liu J,
Tan EK
JAMA neurology · 2020 · PMID 32310270
페이지 1개
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Keene KL,
Hyacinth HI,
Bis JC,
Kittner SJ,
Mitchell BD,
Cheng YC,
Pare G,
Chong M,
O'Donnell M,
Meschia JF,
Chen WM,
Sale MM
외 35명 — 모두 보기
Rich SS,
Nalls MA,
Zonderman AB,
Evans MK,
Wilson JG,
Correa A,
Markus HS,
Traylor M,
Lewis CM,
Carty CL,
Reiner A,
Haessler J,
Langefeld CD,
Gottesman R,
Mosley TH,
Woo D,
Yaffe K,
Liu Y,
Longstreth WT,
Psaty BM,
Kooperberg C,
Lange LA,
Sacco R,
Rundek T,
Lee JM,
Cruchaga C,
Furie KL,
Arnett DK,
Benavente OR,
Grewal RP,
Peddareddygari LR,
Dichgans M,
Malik R,
Worrall BB,
Fornage M
COMPASS, SiGN, and METASTROKE Consortia
Stroke · 2020 · PMID 32693751
페이지 1개
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Yaghootkar H,
Zhang Y,
Spracklen CN,
Karaderi T,
Huang LO,
Bradfield J,
Schurmann C,
Fine RS,
Preuss MH,
Kutalik Z,
Wittemans LBL,
Lu Y
외 104명 — 모두 보기
Metz S,
Willems SM,
Li-Gao R,
Grarup N,
Wang S,
Molnos S,
Sandoval-Zárate AA,
Nalls MA,
Lange LA,
Haesser J,
Guo X,
Lyytikäinen LP,
Feitosa MF,
Sitlani CM,
Venturini C,
Mahajan A,
Kacprowski T,
Wang CA,
Chasman DI,
Amin N,
Broer L,
Robertson N,
Young KL,
Allison M,
Auer PL,
Blüher M,
Borja JB,
Bork-Jensen J,
Carrasquilla GD,
Christofidou P,
Demirkan A,
Doege CA,
Garcia ME,
Graff M,
Guo K,
Hakonarson H,
Hong J,
Ida Chen YD,
Jackson R,
Jakupović H,
Jousilahti P,
Justice AE,
Kähönen M,
Kizer JR,
Kriebel J,
LeDuc CA,
Li J,
Lind L,
Luan J,
Mackey DA,
Mangino M,
Männistö S,
Martin Carli JF,
Medina-Gomez C,
Mook-Kanamori DO,
Morris AP,
de Mutsert R,
Nauck M,
Prokic I,
Pennell CE,
Pradhan AD,
Psaty BM,
Raitakari OT,
Scott RA,
Skaaby T,
Strauch K,
Taylor KD,
Teumer A,
Uitterlinden AG,
Wu Y,
Yao J,
Walker M,
North KE,
Kovacs P,
Ikram MA,
van Duijn CM,
Ridker PM,
Lye S,
Homuth G,
Ingelsson E,
Spector TD,
McKnight B,
Province MA,
Lehtimäki T,
Adair LS,
Rotter JI,
Reiner AP,
Wilson JG,
Harris TB,
Ripatti S,
Grallert H,
Meigs JB,
Salomaa V,
Hansen T,
Willems van Dijk K,
Wareham NJ,
Grant SFA,
Langenberg C,
Frayling TM,
Lindgren CM,
Mohlke KL,
Leibel RL,
Loos RJF,
Kilpeläinen TO
Diabetes · 2020 · PMID 32917775
페이지 1개
Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits
Gouveia MH,
Bentley AR,
Leonard H,
Meeks KAC,
Ekoru K,
Chen G,
Nalls MA,
Simonsick EM,
Tarazona-Santos E,
Lima-Costa MF,
Adeyemo A,
Shriner D
외 1명 — 모두 보기
Scientific reports · 2021 · PMID 33603002 · open access
페이지 1개
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Lahti J,
Tuominen S,
Yang Q,
Pergola G,
Ahmad S,
Amin N,
Armstrong NJ,
Beiser A,
Bey K,
Bis JC,
Boerwinkle E,
Bressler J
외 112명 — 모두 보기
Campbell A,
Campbell H,
Chen Q,
Corley J,
Cox SR,
Davies G,
De Jager PL,
Derks EM,
Faul JD,
Fitzpatrick AL,
Fohner AE,
Ford I,
Fornage M,
Gerring Z,
Grabe HJ,
Grodstein F,
Gudnason V,
Simonsick E,
Holliday EG,
Joshi PK,
Kajantie E,
Kaprio J,
Karell P,
Kleineidam L,
Knol MJ,
Kochan NA,
Kwok JB,
Leber M,
Lam M,
Lee T,
Li S,
Loukola A,
Luck T,
Marioni RE,
Mather KA,
Medland S,
Mirza SS,
Nalls MA,
Nho K,
O'Donnell A,
Oldmeadow C,
Painter J,
Pattie A,
Reppermund S,
Risacher SL,
Rose RJ,
Sadashivaiah V,
Scholz M,
Satizabal CL,
Schofield PW,
Schraut KE,
Scott RJ,
Simino J,
Smith AV,
Smith JA,
Stott DJ,
Surakka I,
Teumer A,
Thalamuthu A,
Trompet S,
Turner ST,
van der Lee SJ,
Villringer A,
Völker U,
Wilson RS,
Wittfeld K,
Vuoksimaa E,
Xia R,
Yaffe K,
Yu L,
Zare H,
Zhao W,
Zhao W,
Ames D,
Attia J,
Bennett DA,
Brodaty H,
Chasman DI,
Goldman AL,
Hayward C,
Ikram MA,
Jukema JW,
Kardia SLR,
Lencz T,
Loeffler M,
Mattay VS,
Palotie A,
Psaty BM,
Ramirez A,
Ridker PM,
Riedel-Heller SG,
Sachdev PS,
Saykin AJ,
Scherer M,
Schofield PR,
Sidney S,
Starr JM,
Trollor J,
Ulrich W,
Wagner M,
Weir DR,
Wilson JF,
Wright MJ,
Weinberger DR,
Debette S,
Eriksson JG,
Mosley TH Jr,
Launer LJ,
van Duijn CM,
Deary IJ,
Seshadri S,
Räikkönen K
Molecular psychiatry · 2022 · PMID 35974141 · open access
페이지 1개
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Pan H,
Liu Z,
Ma J,
Li Y,
Zhao Y,
Zhou X,
Xiang Y,
Wang Y,
Zhou X,
He R,
Xie Y,
Zhou Q
외 48명 — 모두 보기
Yuan K,
Xu Q,
Sun Q,
Wang J,
Yan X,
Zhang H,
Wang C,
Lei L,
Liu W,
Wang X,
Ding X,
Wang T,
Xue Z,
Zhang Z,
Chen L,
Wang Q,
Liu Y,
Tang J,
Zhang X,
Peng S,
Wang C,
Ding J,
Liu C,
Wang L,
Chen H,
Shen L,
Jiang H,
Wu X,
Tan H,
Luo D,
Xiao S,
Chen X,
Tan J,
Hu Z,
Chen C,
Xia K,
Zhang Z,
Foo JN,
Blauwendraat C,
Nalls MA,
Singleton AB,
Liu J,
Chan P,
Zheng H,
Li J,
Guo J,
Yang J,
Tang B
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
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.