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Bell S에 대해
18건.
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Hill WD,
Davies NM,
Ritchie SJ,
Skene NG,
Bryois J,
Bell S,
Di Angelantonio E,
Roberts DJ,
Xueyi S,
Davies G,
Liewald DCM,
Porteous DJ
외 5명 — 모두 보기
Nature communications · 2019 · PMID 31844048 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
Bachmann CG,
Kemlink D,
Sonka K
외 55명 — 모두 보기
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek ZK,
Ibrahim A,
Bergmann M,
Kittke V,
Harrer P,
Dowsett J,
Chenini S,
Ostrowski SR,
Sørensen E,
Erikstrup C,
Pedersen OB,
Topholm Bruun M,
Nielsen KR,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Burchell B,
Furlotte NA,
Nandakumar P,
Earley CJ,
Ondo WG,
Xiong L,
Desautels A,
Perola M,
Vodicka P,
Dina C,
Stoll M,
Franke A,
Lieb W,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rye DB,
Rouleau GA,
Berger K,
Stefansson H,
Ullum H,
Stefansson K,
Hinds DA,
Di Angelantonio E,
Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
외 60명 — 모두 보기
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair B,
Zhao C,
Bell S,
Tilch E,
Salminen AV,
Pütz B,
Dauvilliers Y,
Stefani A,
Högl B,
Poewe W,
Kemlink D,
Sonka K
외 39명 — 모두 보기
Bachmann CG,
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek Z,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Allen RP,
Earley CJ,
Ondo WG,
Xiong L,
Montplaisir J,
Gan-Or Z,
Perola M,
Vodicka P,
Dina C,
Franke A,
Tittmann L,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rouleau GA,
Berger K,
Oexle K,
Di Angelantonio E,
Hinds DA,
Müller-Myhsok B,
Winkelmann J
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
페이지 10개
New loci associated with kidney function and chronic kidney disease
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C,
Olden M,
Glazer NL,
Parsa A,
Gao X,
Yang Q,
Smith AV,
O'Connell JR,
Li M
외 120명 — 모두 보기
Schmidt H,
Tanaka T,
Isaacs A,
Ketkar S,
Hwang SJ,
Johnson AD,
Dehghan A,
Teumer A,
Paré G,
Atkinson EJ,
Zeller T,
Lohman K,
Cornelis MC,
Probst-Hensch NM,
Kronenberg F,
Tönjes A,
Hayward C,
Aspelund T,
Eiriksdottir G,
Launer LJ,
Harris TB,
Rampersaud E,
Mitchell BD,
Arking DE,
Boerwinkle E,
Struchalin M,
Cavalieri M,
Singleton A,
Giallauria F,
Metter J,
de Boer IH,
Haritunians T,
Lumley T,
Siscovick D,
Psaty BM,
Zillikens MC,
Oostra BA,
Feitosa M,
Province M,
de Andrade M,
Turner ST,
Schillert A,
Ziegler A,
Wild PS,
Schnabel RB,
Wilde S,
Munzel TF,
Leak TS,
Illig T,
Klopp N,
Meisinger C,
Wichmann HE,
Koenig W,
Zgaga L,
Zemunik T,
Kolcic I,
Minelli C,
Hu FB,
Johansson A,
Igl W,
Zaboli G,
Wild SH,
Wright AF,
Campbell H,
Ellinghaus D,
Schreiber S,
Aulchenko YS,
Felix JF,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
Imboden M,
Nitsch D,
Brandstätter A,
Kollerits B,
Kedenko L,
Mägi R,
Stumvoll M,
Kovacs P,
Boban M,
Campbell S,
Endlich K,
Völzke H,
Kroemer HK,
Nauck M,
Völker U,
Polasek O,
Vitart V,
Badola S,
Parker AN,
Ridker PM,
Kardia SL,
Blankenberg S,
Liu Y,
Curhan GC,
Franke A,
Rochat T,
Paulweber B,
Prokopenko I,
Wang W,
Gudnason V,
Shuldiner AR,
Coresh J,
Schmidt R,
Ferrucci L,
Shlipak MG,
van Duijn CM,
Borecki I,
Krämer BK,
Rudan I,
Gyllensten U,
Wilson JF,
Witteman JC,
Pramstaller PP,
Rettig R,
Hastie N,
Chasman DI,
Kao WH,
Heid IM,
Fox CS
Nature genetics · 2010 · PMID 20383146
페이지 4개
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
외 148명 — 모두 보기
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
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
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
외 192명 — 모두 보기
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
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Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
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Navis G,
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Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
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Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
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Watkins H,
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Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
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,
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Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
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Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
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Gromicho M,
Chandran S,
Pal S,
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Ratti A,
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Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
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Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
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Calvo A,
Moglia C,
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Canosa A,
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Bell S,
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Dion PA,
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