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An P에 대해
373건, 그중 20건 표시.
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,
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Chapman J,
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Fenoglio C,
Serpente M,
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Caltagirone C,
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Ciaramella A,
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Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
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Todd S,
Craig D,
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Lynch A,
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Hardy J,
Albin RL,
Apostolova LG,
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Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
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Becker JT,
Bigio EH,
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Bowen JD,
Boxer A,
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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,
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Faber KM,
Fallon KB,
Fardo DW,
Farlow MR,
Ferris S,
Foroud TM,
Galasko DR,
Gearing M,
Geschwind DH,
Gilbert JR,
Graff-Radford NR,
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Growdon JH,
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Harrell LE,
Honig LS,
Huentelman MJ,
Hulette CM,
Hyman BT,
Jarvik GP,
Abner E,
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Jun G,
Karydas A,
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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,
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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,
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Weintraub S,
Welsh-Bohmer KA,
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Forsell C,
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Schellenberg GD
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
페이지 1개
Genome-wide association analysis identifies common variants influencing infant brain volumes
Xia K,
Zhang J,
Ahn M,
Jha S,
Crowley JJ,
Szatkiewicz J,
Li T,
Zou F,
Zhu H,
Hibar D,
Thompson P,
Sullivan PF
외 3명 — 모두 보기
ENIGMA Consortium
Translational psychiatry · 2017 · PMID 28763065 · open access
페이지 1개
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
Tanskanen T,
van den Berg L,
Välimäki N,
Aavikko M,
Ness-Jensen E,
Hveem K,
Wettergren Y,
Bexe Lindskog E,
Tõnisson N,
Metspalu A,
Silander K,
Orlando G
외 48명 — 모두 보기
Law PJ,
Tuupanen S,
Gylfe AE,
Hänninen UA,
Cajuso T,
Kondelin J,
Sarin AP,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
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Lepistö A,
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Kerr D,
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Win AK,
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Conti D,
Schumacher FR,
Casey G,
Cheadle JP,
Dunlop MG,
Tomlinson IP,
Houlston RS,
Palin K,
Aaltonen LA
International journal of cancer · 2018 · PMID 28960316
페이지 1개
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
McCormack M,
Gui H,
Ingason A,
Speed D,
Wright GEB,
Zhang EJ,
Secolin R,
Yasuda C,
Kwok M,
Wolking S,
Becker F,
Rau S
외 37명 — 모두 보기
Avbersek A,
Heggeli K,
Leu C,
Depondt C,
Sills GJ,
Marson AG,
Auce P,
Brodie MJ,
Francis B,
Johnson MR,
Koeleman BPC,
Striano P,
Coppola A,
Zara F,
Kunz WS,
Sander JW,
Lerche H,
Klein KM,
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Krenn M,
Gudmundsson LJ,
Stefánsson K,
Krause R,
Shear N,
Ross CJD,
Delanty N,
Pirmohamed M,
Carleton BC,
Cendes F,
Lopes-Cendes I,
Liao WP,
O'Brien TJ,
Sisodiya SM,
Cherny S,
Kwan P,
Baum L,
Cavalleri GL
EPIGEN Consortium; · Canadian Pharmacogenomics Network for Drug Safety; 외 컨소시엄 2곳
Neurology · 2018 · PMID 29288229 · open access
페이지 1개
Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals
Coleman JRI,
Bryois J,
Gaspar HA,
Jansen PR,
Savage JE,
Skene N,
Plomin R,
Muñoz-Manchado AB,
Linnarsson S,
Crawford G,
Hjerling-Leffler J,
Sullivan PF
외 2명 — 모두 보기
Molecular psychiatry · 2019 · PMID 29520040
페이지 1개
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
외 69명 — 모두 보기
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
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Maria A,
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Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
페이지 1개
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour
Jones SE,
van Hees VT,
Mazzotti DR,
Marques-Vidal P,
Sabia S,
van der Spek A,
Dashti HS,
Engmann J,
Kocevska D,
Tyrrell J,
Beaumont RN,
Hillsdon M
외 20명 — 모두 보기
Ruth KS,
Tuke MA,
Yaghootkar H,
Sharp SA,
Ji Y,
Harrison JW,
Freathy RM,
Murray A,
Luik AI,
Amin N,
Lane JM,
Saxena R,
Rutter MK,
Tiemeier H,
Kutalik Z,
Kumari M,
Frayling TM,
Weedon MN,
Gehrman PR,
Wood AR
Nature communications · 2019 · PMID 30952852 · open access
페이지 1개
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
외 74명 — 모두 보기
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
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Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
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Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
페이지 1개
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
외 96명 — 모두 보기
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
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Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
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Easton DF,
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European journal of human genetics : EJHG · 2019 · PMID 31231134
페이지 1개
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
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외 198명 — 모두 보기
Yao S,
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Davis OSP,
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Dina C,
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Docampo E,
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Egberts K,
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Escaramís G,
Esko T,
Estivill X,
Farmer A,
Favaro A,
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Fichter MM,
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Forzan M,
Franklin CS,
Gallinger S,
Giegling I,
Giuranna J,
Gonidakis F,
Gorwood P,
Mayora MG,
Guillaume S,
Guo Y,
Hakonarson H,
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외 80명 — 모두 보기
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외 72명 — 모두 보기
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Nature communications · 2019 · PMID 31413261 · open access
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Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
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외 6명 — 모두 보기
VA Million Veteran Program
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The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
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외 108명 — 모두 보기
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Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
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외 15명 — 모두 보기
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Million Veteran Program
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Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
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외 41명 — 모두 보기
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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
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외 81명 — 모두 보기
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NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
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페이지 1개
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