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성함이나 학술지명, PMID로 찾아보십시오.
Wray NR에 대해
25건, 그중 20건 표시.
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
외 26명 — 모두 보기
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
페이지 12개+
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Revez JA,
Lin T,
Qiao Z,
Xue A,
Holtz Y,
Zhu Z,
Zeng J,
Wang H,
Sidorenko J,
Kemper KE,
Vinkhuyzen AAE,
Frater J
외 9명 — 모두 보기
Nature communications · 2020 · PMID 32242144 · open access
페이지 12개+
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Mullins N,
Forstner AJ,
O'Connell KS,
Coombes B,
Coleman JRI,
Qiao Z,
Als TD,
Bigdeli TB,
Børte S,
Bryois J,
Charney AW,
Drange OK
외 305명 — 모두 보기
Gandal MJ,
Hagenaars SP,
Ikeda M,
Kamitaki N,
Kim M,
Krebs K,
Panagiotaropoulou G,
Schilder BM,
Sloofman LG,
Steinberg S,
Trubetskoy V,
Winsvold BS,
Won HH,
Abramova L,
Adorjan K,
Agerbo E,
Al Eissa M,
Albani D,
Alliey-Rodriguez N,
Anjorin A,
Antilla V,
Antoniou A,
Awasthi S,
Baek JH,
Bækvad-Hansen M,
Bass N,
Bauer M,
Beins EC,
Bergen SE,
Birner A,
Bøcker Pedersen C,
Bøen E,
Boks MP,
Bosch R,
Brum M,
Brumpton BM,
Brunkhorst-Kanaan N,
Budde M,
Bybjerg-Grauholm J,
Byerley W,
Cairns M,
Casas M,
Cervantes P,
Clarke TK,
Cruceanu C,
Cuellar-Barboza A,
Cunningham J,
Curtis D,
Czerski PM,
Dale AM,
Dalkner N,
David FS,
Degenhardt F,
Djurovic S,
Dobbyn AL,
Douzenis A,
Elvsåshagen T,
Escott-Price V,
Ferrier IN,
Fiorentino A,
Foroud TM,
Forty L,
Frank J,
Frei O,
Freimer NB,
Frisén L,
Gade K,
Garnham J,
Gelernter J,
Giørtz Pedersen M,
Gizer IR,
Gordon SD,
Gordon-Smith K,
Greenwood TA,
Grove J,
Guzman-Parra J,
Ha K,
Haraldsson M,
Hautzinger M,
Heilbronner U,
Hellgren D,
Herms S,
Hoffmann P,
Holmans PA,
Huckins L,
Jamain S,
Johnson JS,
Kalman JL,
Kamatani Y,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koromina M,
Kranz TM,
Kranzler HR,
Kubo M,
Kupka R,
Kushner SA,
Lavebratt C,
Lawrence J,
Leber M,
Lee HJ,
Lee PH,
Levy SE,
Lewis C,
Liao C,
Lucae S,
Lundberg M,
MacIntyre DJ,
Magnusson SH,
Maier W,
Maihofer A,
Malaspina D,
Maratou E,
Martinsson L,
Mattheisen M,
McCarroll SA,
McGregor NW,
McGuffin P,
McKay JD,
Medeiros H,
Medland SE,
Millischer V,
Montgomery GW,
Moran JL,
Morris DW,
Mühleisen TW,
O'Brien N,
O'Donovan C,
Olde Loohuis LM,
Oruc L,
Papiol S,
Pardiñas AF,
Perry A,
Pfennig A,
Porichi E,
Potash JB,
Quested D,
Raj T,
Rapaport MH,
DePaulo JR,
Regeer EJ,
Rice JP,
Rivas F,
Rivera M,
Roth J,
Roussos P,
Ruderfer DM,
Sánchez-Mora C,
Schulte EC,
Senner F,
Sharp S,
Shilling PD,
Sigurdsson E,
Sirignano L,
Slaney C,
Smeland OB,
Smith DJ,
Sobell JL,
Søholm Hansen C,
Soler Artigas M,
Spijker AT,
Stein DJ,
Strauss JS,
Świątkowska B,
Terao C,
Thorgeirsson TE,
Toma C,
Tooney P,
Tsermpini EE,
Vawter MP,
Vedder H,
Walters JTR,
Witt SH,
Xi S,
Xu W,
Yang JMK,
Young AH,
Young H,
Zandi PP,
Zhou H,
Zillich L,
Adolfsson R,
Agartz I,
Alda M,
Alfredsson L,
Babadjanova G,
Backlund L,
Baune BT,
Bellivier F,
Bengesser S,
Berrettini WH,
Blackwood DHR,
Boehnke M,
Børglum AD,
Breen G,
Carr VJ,
Catts S,
Corvin A,
Craddock N,
Dannlowski U,
Dikeos D,
Esko T,
Etain B,
Ferentinos P,
Frye M,
Fullerton JM,
Gawlik M,
Gershon ES,
Goes FS,
Green MJ,
Grigoroiu-Serbanescu M,
Hauser J,
Henskens F,
Hillert J,
Hong KS,
Hougaard DM,
Hultman CM,
Hveem K,
Iwata N,
Jablensky AV,
Jones I,
Jones LA,
Kahn RS,
Kelsoe JR,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Lochner C,
Loughland C,
Martin NG,
Mathews CA,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Michie P,
Milani L,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Mowry B,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nievergelt CM,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Olsson T,
Owen MJ,
Paciga SA,
Pantelis C,
Pato C,
Pato MT,
Patrinos GP,
Perlis RH,
Posthuma D,
Ramos-Quiroga JA,
Reif A,
Reininghaus EZ,
Ribasés M,
Rietschel M,
Ripke S,
Rouleau GA,
Saito T,
Schall U,
Schalling M,
Schofield PR,
Schulze TG,
Scott LJ,
Scott RJ,
Serretti A,
Shannon Weickert C,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Streit F,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Waldman ID,
Weickert TW,
Werge T,
Wray NR,
Zwart JA,
Biernacka JM,
Nurnberger JI,
Cichon S,
Edenberg HJ,
Stahl EA,
McQuillin A,
Di Florio A,
Ophoff RA,
Andreassen OA
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
페이지 12개+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy V,
Pardiñas AF,
Qi T,
Panagiotaropoulou G,
Awasthi S,
Bigdeli TB,
Bryois J,
Chen CY,
Dennison CA,
Hall LS,
Lam M,
Watanabe K
외 422명 — 모두 보기
Frei O,
Ge T,
Harwood JC,
Koopmans F,
Magnusson S,
Richards AL,
Sidorenko J,
Wu Y,
Zeng J,
Grove J,
Kim M,
Li Z,
Voloudakis G,
Zhang W,
Adams M,
Agartz I,
Atkinson EG,
Agerbo E,
Al Eissa M,
Albus M,
Alexander M,
Alizadeh BZ,
Alptekin K,
Als TD,
Amin F,
Arolt V,
Arrojo M,
Athanasiu L,
Azevedo MH,
Bacanu SA,
Bass NJ,
Begemann M,
Belliveau RA,
Bene J,
Benyamin B,
Bergen SE,
Blasi G,
Bobes J,
Bonassi S,
Braun A,
Bressan RA,
Bromet EJ,
Bruggeman R,
Buckley PF,
Buckner RL,
Bybjerg-Grauholm J,
Cahn W,
Cairns MJ,
Calkins ME,
Carr VJ,
Castle D,
Catts SV,
Chambert KD,
Chan RCK,
Chaumette B,
Cheng W,
Cheung EFC,
Chong SA,
Cohen D,
Consoli A,
Cordeiro Q,
Costas J,
Curtis C,
Davidson M,
Davis KL,
de Haan L,
Degenhardt F,
DeLisi LE,
Demontis D,
Dickerson F,
Dikeos D,
Dinan T,
Djurovic S,
Duan J,
Ducci G,
Dudbridge F,
Eriksson JG,
Fañanás L,
Faraone SV,
Fiorentino A,
Forstner A,
Frank J,
Freimer NB,
Fromer M,
Frustaci A,
Gadelha A,
Genovese G,
Gershon ES,
Giannitelli M,
Giegling I,
Giusti-Rodríguez P,
Godard S,
Goldstein JI,
González Peñas J,
González-Pinto A,
Gopal S,
Gratten J,
Green MF,
Greenwood TA,
Guillin O,
Gülöksüz S,
Gur RE,
Gur RC,
Gutiérrez B,
Hahn E,
Hakonarson H,
Haroutunian V,
Hartmann AM,
Harvey C,
Hayward C,
Henskens FA,
Herms S,
Hoffmann P,
Howrigan DP,
Ikeda M,
Iyegbe C,
Joa I,
Julià A,
Kähler AK,
Kam-Thong T,
Kamatani Y,
Karachanak-Yankova S,
Kebir O,
Keller MC,
Kelly BJ,
Khrunin A,
Kim SW,
Klovins J,
Kondratiev N,
Konte B,
Kraft J,
Kubo M,
Kučinskas V,
Kučinskiene ZA,
Kusumawardhani A,
Kuzelova-Ptackova H,
Landi S,
Lazzeroni LC,
Lee PH,
Legge SE,
Lehrer DS,
Lencer R,
Lerer B,
Li M,
Lieberman J,
Light GA,
Limborska S,
Liu CM,
Lönnqvist J,
Loughland CM,
Lubinski J,
Luykx JJ,
Lynham A,
Macek M Jr,
Mackinnon A,
Magnusson PKE,
Maher BS,
Maier W,
Malaspina D,
Mallet J,
Marder SR,
Marsal S,
Martin AR,
Martorell L,
Mattheisen M,
McCarley RW,
McDonald C,
McGrath JJ,
Medeiros H,
Meier S,
Melegh B,
Melle I,
Mesholam-Gately RI,
Metspalu A,
Michie PT,
Milani L,
Milanova V,
Mitjans M,
Molden E,
Molina E,
Molto MD,
Mondelli V,
Moreno C,
Morley CP,
Muntané G,
Murphy KC,
Myin-Germeys I,
Nenadić I,
Nestadt G,
Nikitina-Zake L,
Noto C,
Nuechterlein KH,
O'Brien NL,
O'Neill FA,
Oh SY,
Olincy A,
Ota VK,
Pantelis C,
Papadimitriou GN,
Parellada M,
Paunio T,
Pellegrino R,
Periyasamy S,
Perkins DO,
Pfuhlmann B,
Pietiläinen O,
Pimm J,
Porteous D,
Powell J,
Quattrone D,
Quested D,
Radant AD,
Rampino A,
Rapaport MH,
Rautanen A,
Reichenberg A,
Roe C,
Roffman JL,
Roth J,
Rothermundt M,
Rutten BPF,
Saker-Delye S,
Salomaa V,
Sanjuan J,
Santoro ML,
Savitz A,
Schall U,
Scott RJ,
Seidman LJ,
Sharp SI,
Shi J,
Siever LJ,
Sigurdsson E,
Sim K,
Skarabis N,
Slominsky P,
So HC,
Sobell JL,
Söderman E,
Stain HJ,
Steen NE,
Steixner-Kumar AA,
Stögmann E,
Stone WS,
Straub RE,
Streit F,
Strengman E,
Stroup TS,
Subramaniam M,
Sugar CA,
Suvisaari J,
Svrakic DM,
Swerdlow NR,
Szatkiewicz JP,
Ta TMT,
Takahashi A,
Terao C,
Thibaut F,
Toncheva D,
Tooney PA,
Torretta S,
Tosato S,
Tura GB,
Turetsky BI,
Üçok A,
Vaaler A,
van Amelsvoort T,
van Winkel R,
Veijola J,
Waddington J,
Walter H,
Waterreus A,
Webb BT,
Weiser M,
Williams NM,
Witt SH,
Wormley BK,
Wu JQ,
Xu Z,
Yolken R,
Zai CC,
Zhou W,
Zhu F,
Zimprich F,
Atbaşoğlu EC,
Ayub M,
Benner C,
Bertolino A,
Black DW,
Bray NJ,
Breen G,
Buccola NG,
Byerley WF,
Chen WJ,
Cloninger CR,
Crespo-Facorro B,
Donohoe G,
Freedman R,
Galletly C,
Gandal MJ,
Gennarelli M,
Hougaard DM,
Hwu HG,
Jablensky AV,
McCarroll SA,
Moran JL,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Neil AL,
Nordentoft M,
Pato MT,
Petryshen TL,
Pirinen M,
Pulver AE,
Schulze TG,
Silverman JM,
Smoller JW,
Stahl EA,
Tsuang DW,
Vilella E,
Wang SH,
Xu S,
Adolfsson R,
Arango C,
Baune BT,
Belangero SI,
Børglum AD,
Braff D,
Bramon E,
Buxbaum JD,
Campion D,
Cervilla JA,
Cichon S,
Collier DA,
Corvin A,
Curtis D,
Forti MD,
Domenici E,
Ehrenreich H,
Escott-Price V,
Esko T,
Fanous AH,
Gareeva A,
Gawlik M,
Gejman PV,
Gill M,
Glatt SJ,
Golimbet V,
Hong KS,
Hultman CM,
Hyman SE,
Iwata N,
Jönsson EG,
Kahn RS,
Kennedy JL,
Khusnutdinova E,
Kirov G,
Knowles JA,
Krebs MO,
Laurent-Levinson C,
Lee J,
Lencz T,
Levinson DF,
Li QS,
Liu J,
Malhotra AK,
Malhotra D,
McIntosh A,
McQuillin A,
Menezes PR,
Morgan VA,
Morris DW,
Mowry BJ,
Murray RM,
Nimgaonkar V,
Nöthen MM,
Ophoff RA,
Paciga SA,
Palotie A,
Pato CN,
Qin S,
Rietschel M,
Riley BP,
Rivera M,
Rujescu D,
Saka MC,
Sanders AR,
Schwab SG,
Serretti A,
Sham PC,
Shi Y,
St Clair D,
Stefánsson H,
Stefansson K,
Tsuang MT,
van Os J,
Vawter MP,
Weinberger DR,
Werge T,
Wildenauer DB,
Yu X,
Yue W,
Holmans PA,
Pocklington AJ,
Roussos P,
Vassos E,
Verhage M,
Visscher PM,
Yang J,
Posthuma D,
Andreassen OA,
Kendler KS,
Owen MJ,
Wray NR,
Daly MJ,
Huang H,
Neale BM,
Sullivan PF,
Ripke S,
Walters JTR,
O'Donovan MC
Indonesia Schizophrenia Consortium · PsychENCODE 외 컨소시엄 3곳
Nature · 2022 · PMID 35396580
페이지 12개+
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Cadby G,
Giles C,
Melton PE,
Huynh K,
Mellett NA,
Duong T,
Nguyen A,
Cinel M,
Smith A,
Olshansky G,
Wang T,
Brozynska M
외 32명 — 모두 보기
Inouye M,
McCarthy NS,
Ariff A,
Hung J,
Hui J,
Beilby J,
Dubé MP,
Watts GF,
Shah S,
Wray NR,
Lim WLF,
Chatterjee P,
Martins I,
Laws SM,
Porter T,
Vacher M,
Bush AI,
Rowe CC,
Villemagne VL,
Ames D,
Masters CL,
Taddei K,
Arnold M,
Kastenmüller G,
Nho K,
Saykin AJ,
Han X,
Kaddurah-Daouk R,
Martins RN,
Blangero J,
Meikle PJ,
Moses EK
Nature communications · 2022 · PMID 35668104 · open access
페이지 12개+
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Borbye-Lorenzen N,
Zhu Z,
Agerbo E,
Albiñana C,
Benros ME,
Bian B,
Børglum AD,
Bulik CM,
Debost JPG,
Grove J,
Hougaard DM,
McRae AF
외 12명 — 모두 보기
Mors O,
Mortensen PB,
Musliner KL,
Nordentoft M,
Petersen LV,
Privé F,
Sidorenko J,
Skogstrand K,
Werge T,
Wray NR,
Vilhjálmsson BJ,
McGrath JJ
Cell genomics · 2023 · PMID 38116117 · open access
페이지 12개+
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Ripke S,
O'Dushlaine C,
Chambert K,
Moran JL,
Kähler AK,
Akterin S,
Bergen SE,
Collins AL,
Crowley JJ,
Fromer M,
Kim Y,
Lee SH
외 176명 — 모두 보기
Lee SH,
Magnusson PK,
Sanchez N,
Stahl EA,
Williams S,
Wray NR,
Xia K,
Bettella F,
Borglum AD,
Bulik-Sullivan BK,
Cormican P,
Craddock N,
de Leeuw C,
Durmishi N,
Gill M,
Golimbet V,
Hamshere ML,
Holmans P,
Hougaard DM,
Kendler KS,
Lin K,
Morris DW,
Mors O,
Mortensen PB,
Neale BM,
O'Neill FA,
Owen MJ,
Milovancevic MP,
Posthuma D,
Powell J,
Richards AL,
Riley BP,
Ruderfer D,
Rujescu D,
Sigurdsson E,
Silagadze T,
Smit AB,
Stefansson H,
Steinberg S,
Suvisaari J,
Tosato S,
Verhage M,
Walters JT,
Levinson DF,
Gejman PV,
Kendler KS,
Laurent C,
Mowry BJ,
O'Donovan MC,
Owen MJ,
Pulver AE,
Riley BP,
Schwab SG,
Wildenauer DB,
Dudbridge F,
Holmans P,
Shi J,
Albus M,
Alexander M,
Campion D,
Cohen D,
Dikeos D,
Duan J,
Eichhammer P,
Godard S,
Hansen M,
Lerer FB,
Liang KY,
Maier W,
Mallet J,
Nertney DA,
Nestadt G,
Norton N,
O'Neill FA,
Papadimitriou GN,
Ribble R,
Sanders AR,
Silverman JM,
Walsh D,
Williams NM,
Wormley B,
Arranz MJ,
Bakker S,
Bender S,
Bramon E,
Collier D,
Crespo-Facorro B,
Hall J,
Iyegbe C,
Jablensky A,
Kahn RS,
Kalaydjieva L,
Lawrie S,
Lewis CM,
Lin K,
Linszen DH,
Mata I,
McIntosh A,
Murray RM,
Ophoff RA,
Powell J,
Rujescu D,
Van Os J,
Walshe M,
Weisbrod M,
Wiersma D,
Donnelly P,
Barroso I,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin AP,
Deloukas P,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Spencer CC,
Band G,
Bellenguez C,
Freeman C,
Hellenthal G,
Giannoulatou E,
Pirinen M,
Pearson RD,
Strange A,
Su Z,
Vukcevic D,
Donnelly P,
Langford C,
Hunt SE,
Edkins S,
Gwilliam R,
Blackburn H,
Bumpstead SJ,
Dronov S,
Gillman M,
Gray E,
Hammond N,
Jayakumar A,
McCann OT,
Liddle J,
Potter SC,
Ravindrarajah R,
Ricketts M,
Tashakkori-Ghanbaria A,
Waller MJ,
Weston P,
Widaa S,
Whittaker P,
Barroso I,
Deloukas P,
Mathew CG,
Blackwell JM,
Brown MA,
Corvin AP,
McCarthy MI,
Spencer CC,
Bramon E,
Corvin AP,
O'Donovan MC,
Stefansson K,
Scolnick E,
Purcell S,
McCarroll SA,
Sklar P,
Hultman CM,
Sullivan PF
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults
Hillary RF,
Trejo-Banos D,
Kousathanas A,
McCartney DL,
Harris SE,
Stevenson AJ,
Patxot M,
Ojavee SE,
Zhang Q,
Liewald DC,
Ritchie CW,
Evans KL
외 7명 — 모두 보기
Genome medicine · 2020 · PMID 32641083 · open access
페이지 7개
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Lu AT,
Xue L,
Salfati EL,
Chen BH,
Ferrucci L,
Levy D,
Joehanes R,
Murabito JM,
Kiel DP,
Tsai PC,
Yet I,
Bell JT
외 27명 — 모두 보기
Mangino M,
Tanaka T,
McRae AF,
Marioni RE,
Visscher PM,
Wray NR,
Deary IJ,
Levine ME,
Quach A,
Assimes T,
Tsao PS,
Absher D,
Stewart JD,
Li Y,
Reiner AP,
Hou L,
Baccarelli AA,
Whitsel EA,
Aviv A,
Cardona A,
Day FR,
Wareham NJ,
Perry JRB,
Ong KK,
Raj K,
Lunetta KL,
Horvath S
Nature communications · 2018 · PMID 29374233 · open access
페이지 6개
Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl EA,
Breen G,
Forstner AJ,
McQuillin A,
Ripke S,
Trubetskoy V,
Mattheisen M,
Wang Y,
Coleman JRI,
Gaspar HA,
de Leeuw CA,
Steinberg S
외 265명 — 모두 보기
Pavlides JMW,
Trzaskowski M,
Byrne EM,
Pers TH,
Holmans PA,
Richards AL,
Abbott L,
Agerbo E,
Akil H,
Albani D,
Alliey-Rodriguez N,
Als TD,
Anjorin A,
Antilla V,
Awasthi S,
Badner JA,
Bækvad-Hansen M,
Barchas JD,
Bass N,
Bauer M,
Belliveau R,
Bergen SE,
Pedersen CB,
Bøen E,
Boks MP,
Boocock J,
Budde M,
Bunney W,
Burmeister M,
Bybjerg-Grauholm J,
Byerley W,
Casas M,
Cerrato F,
Cervantes P,
Chambert K,
Charney AW,
Chen D,
Churchhouse C,
Clarke TK,
Coryell W,
Craig DW,
Cruceanu C,
Curtis D,
Czerski PM,
Dale AM,
de Jong S,
Degenhardt F,
Del-Favero J,
DePaulo JR,
Djurovic S,
Dobbyn AL,
Dumont A,
Elvsåshagen T,
Escott-Price V,
Fan CC,
Fischer SB,
Flickinger M,
Foroud TM,
Forty L,
Frank J,
Fraser C,
Freimer NB,
Frisén L,
Gade K,
Gage D,
Garnham J,
Giambartolomei C,
Pedersen MG,
Goldstein J,
Gordon SD,
Gordon-Smith K,
Green EK,
Green MJ,
Greenwood TA,
Grove J,
Guan W,
Guzman-Parra J,
Hamshere ML,
Hautzinger M,
Heilbronner U,
Herms S,
Hipolito M,
Hoffmann P,
Holland D,
Huckins L,
Jamain S,
Johnson JS,
Juréus A,
Kandaswamy R,
Karlsson R,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koller AC,
Kupka R,
Lavebratt C,
Lawrence J,
Lawson WB,
Leber M,
Lee PH,
Levy SE,
Li JZ,
Liu C,
Lucae S,
Maaser A,
MacIntyre DJ,
Mahon PB,
Maier W,
Martinsson L,
McCarroll S,
McGuffin P,
McInnis MG,
McKay JD,
Medeiros H,
Medland SE,
Meng F,
Milani L,
Montgomery GW,
Morris DW,
Mühleisen TW,
Mullins N,
Nguyen H,
Nievergelt CM,
Adolfsson AN,
Nwulia EA,
O'Donovan C,
Loohuis LMO,
Ori APS,
Oruc L,
Ösby U,
Perlis RH,
Perry A,
Pfennig A,
Potash JB,
Purcell SM,
Regeer EJ,
Reif A,
Reinbold CS,
Rice JP,
Rivas F,
Rivera M,
Roussos P,
Ruderfer DM,
Ryu E,
Sánchez-Mora C,
Schatzberg AF,
Scheftner WA,
Schork NJ,
Shannon Weickert C,
Shehktman T,
Shilling PD,
Sigurdsson E,
Slaney C,
Smeland OB,
Sobell JL,
Søholm Hansen C,
Spijker AT,
St Clair D,
Steffens M,
Strauss JS,
Streit F,
Strohmaier J,
Szelinger S,
Thompson RC,
Thorgeirsson TE,
Treutlein J,
Vedder H,
Wang W,
Watson SJ,
Weickert TW,
Witt SH,
Xi S,
Xu W,
Young AH,
Zandi P,
Zhang P,
Zöllner S,
Adolfsson R,
Agartz I,
Alda M,
Backlund L,
Baune BT,
Bellivier F,
Berrettini WH,
Biernacka JM,
Blackwood DHR,
Boehnke M,
Børglum AD,
Corvin A,
Craddock N,
Daly MJ,
Dannlowski U,
Esko T,
Etain B,
Frye M,
Fullerton JM,
Gershon ES,
Gill M,
Goes F,
Grigoroiu-Serbanescu M,
Hauser J,
Hougaard DM,
Hultman CM,
Jones I,
Jones LA,
Kahn RS,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Martin NG,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Metspalu A,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nimgaonkar V,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Owen MJ,
Paciga SA,
Pato C,
Pato MT,
Posthuma D,
Ramos-Quiroga JA,
Ribasés M,
Rietschel M,
Rouleau GA,
Schalling M,
Schofield PR,
Schulze TG,
Serretti A,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Werge T,
Nurnberger JI,
Wray NR,
Di Florio A,
Edenberg HJ,
Cichon S,
Ophoff RA,
Scott LJ,
Andreassen OA,
Kelsoe J,
Sklar P
eQTLGen Consortium · BIOS Consortium 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31043756 · open access
페이지 6개
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
Willems SM,
Wright DJ,
Day FR,
Trajanoska K,
Joshi PK,
Morris JA,
Matteini AM,
Garton FC,
Grarup N,
Oskolkov N,
Thalamuthu A,
Mangino M
외 64명 — 모두 보기
Liu J,
Demirkan A,
Lek M,
Xu L,
Wang G,
Oldmeadow C,
Gaulton KJ,
Lotta LA,
Miyamoto-Mikami E,
Rivas MA,
White T,
Loh PR,
Aadahl M,
Amin N,
Attia JR,
Austin K,
Benyamin B,
Brage S,
Cheng YC,
Cięszczyk P,
Derave W,
Eriksson KF,
Eynon N,
Linneberg A,
Lucia A,
Massidda M,
Mitchell BD,
Miyachi M,
Murakami H,
Padmanabhan S,
Pandey A,
Papadimitriou I,
Rajpal DK,
Sale C,
Schnurr TM,
Sessa F,
Shrine N,
Tobin MD,
Varley I,
Wain LV,
Wray NR,
Lindgren CM,
MacArthur DG,
Waterworth DM,
McCarthy MI,
Pedersen O,
Khaw KT,
Kiel DP,
Pitsiladis Y,
Fuku N,
Franks PW,
North KN,
van Duijn CM,
Mather KA,
Hansen T,
Hansson O,
Spector T,
Murabito JM,
Richards JB,
Rivadeneira F,
Langenberg C,
Perry JRB,
Wareham NJ,
Scott RA
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
페이지 5개
Genetic signatures of high-altitude adaptation in Tibetans
Yang J,
Jin ZB,
Chen J,
Huang XF,
Li XM,
Liang YB,
Mao JY,
Chen X,
Zheng Z,
Bakshi A,
Zheng DD,
Zheng MQ
외 4명 — 모두 보기
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
페이지 3개
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
외 180명 — 모두 보기
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
페이지 3개
Meta-analysis of genome-wide association studies of anxiety disorders
Otowa T,
Hek K,
Lee M,
Byrne EM,
Mirza SS,
Nivard MG,
Bigdeli T,
Aggen SH,
Adkins D,
Wolen A,
Fanous A,
Keller MC
외 35명 — 모두 보기
Castelao E,
Kutalik Z,
Van der Auwera S,
Homuth G,
Nauck M,
Teumer A,
Milaneschi Y,
Hottenga JJ,
Direk N,
Hofman A,
Uitterlinden A,
Mulder CL,
Henders AK,
Medland SE,
Gordon S,
Heath AC,
Madden PA,
Pergadia ML,
van der Most PJ,
Nolte IM,
van Oort FV,
Hartman CA,
Oldehinkel AJ,
Preisig M,
Grabe HJ,
Middeldorp CM,
Penninx BW,
Boomsma D,
Martin NG,
Montgomery G,
Maher BS,
van den Oord EJ,
Wray NR,
Tiemeier H,
Hettema JM
Molecular psychiatry · 2016 · PMID 26754954 · open access
페이지 2개
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Coleman JRI,
Peyrot WJ,
Purves KL,
Davis KAS,
Rayner C,
Choi SW,
Hübel C,
Gaspar HA,
Kan C,
Van der Auwera S,
Adams MJ,
Lyall DM
외 14명 — 모두 보기
Choi KW,
Dunn EC,
Vassos E,
Danese A,
Maughan B,
Grabe HJ,
Lewis CM,
O'Reilly PF,
McIntosh AM,
Smith DJ,
Wray NR,
Hotopf M,
Eley TC,
Breen G
on the behalf of Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Molecular psychiatry · 2020 · PMID 31969693 · open access
페이지 2개
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