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Soranzo N에 대해
81건, 그중 20건 표시.
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Akbari P,
Vuckovic D,
Stefanucci L,
Jiang T,
Kundu K,
Kreuzhuber R,
Bao EL,
Collins JH,
Downes K,
Grassi L,
Guerrero JA,
Kaptoge S
외 20명 — 모두 보기
Knight JC,
Meacham S,
Sambrook J,
Seyres D,
Stegle O,
Verboon JM,
Walter K,
Watkins NA,
Danesh J,
Roberts DJ,
Di Angelantonio E,
Sankaran VG,
Frontini M,
Burgess S,
Kuijpers T,
Peters JE,
Butterworth AS,
Ouwehand WH,
Soranzo N,
Astle WJ
Nature communications · 2023 · PMID 37596262 · 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+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
외 366명 — 모두 보기
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
Boes T,
Bonnycastle LL,
Bornstein SR,
Brown MJ,
Buchanan TA,
Busonero F,
Campbell H,
Cappuccio FP,
Cavalcanti-Proença C,
Chen YD,
Chen CM,
Chines PS,
Clarke R,
Coin L,
Connell J,
Day IN,
den Heijer M,
Duan J,
Ebrahim S,
Elliott P,
Elliott P,
Elosua R,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Facheris MF,
Felix SB,
Fischer-Posovszky P,
Folsom AR,
Friedrich N,
Freimer NB,
Fu M,
Gaget S,
Gejman PV,
Geus EJ,
Gieger C,
Gjesing AP,
Goel A,
Goyette P,
Grallert H,
Grässler J,
Greenawalt DM,
Groves CJ,
Gudnason V,
Guiducci C,
Hartikainen AL,
Hassanali N,
Hall AS,
Havulinna AS,
Hayward C,
Heath AC,
Hengstenberg C,
Hicks AA,
Hinney A,
Hofman A,
Homuth G,
Hui J,
Igl W,
Iribarren C,
Isomaa B,
Jacobs KB,
Jarick I,
Jewell E,
John U,
Jørgensen T,
Jousilahti P,
Jula A,
Kaakinen M,
Kajantie E,
Kaplan LM,
Kathiresan S,
Kettunen J,
Kinnunen L,
Knowles JW,
Kolcic I,
König IR,
Koskinen S,
Kovacs P,
Kuusisto J,
Kraft P,
Kvaløy K,
Laitinen J,
Lantieri O,
Lanzani C,
Launer LJ,
Lecoeur C,
Lehtimäki T,
Lettre G,
Liu J,
Lokki ML,
Lorentzon M,
Luben RN,
Ludwig B,
Manunta P,
Marek D,
Marre M,
Martin NG,
McArdle WL,
McCarthy A,
McKnight B,
Meitinger T,
Melander O,
Meyre D,
Midthjell K,
Montgomery GW,
Morken MA,
Morris AP,
Mulic R,
Ngwa JS,
Nelis M,
Neville MJ,
Nyholt DR,
O'Donnell CJ,
O'Rahilly S,
Ong KK,
Oostra B,
Paré G,
Parker AN,
Perola M,
Pichler I,
Pietiläinen KH,
Platou CG,
Polasek O,
Pouta A,
Rafelt S,
Raitakari O,
Rayner NW,
Ridderstråle M,
Rief W,
Ruokonen A,
Robertson NR,
Rzehak P,
Salomaa V,
Sanders AR,
Sandhu MS,
Sanna S,
Saramies J,
Savolainen MJ,
Scherag S,
Schipf S,
Schreiber S,
Schunkert H,
Silander K,
Sinisalo J,
Siscovick DS,
Smit JH,
Soranzo N,
Sovio U,
Stephens J,
Surakka I,
Swift AJ,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teslovich TM,
Thompson JR,
Thomson B,
Tönjes A,
Tuomi T,
van Meurs JB,
van Ommen GJ,
Vatin V,
Viikari J,
Visvikis-Siest S,
Vitart V,
Vogel CI,
Voight BF,
Waite LL,
Wallaschofski H,
Walters GB,
Widen E,
Wiegand S,
Wild SH,
Willemsen G,
Witte DR,
Witteman JC,
Xu J,
Zhang Q,
Zgaga L,
Ziegler A,
Zitting P,
Beilby JP,
Farooqi IS,
Hebebrand J,
Huikuri HV,
James AL,
James AL,
Kähönen M,
Levinson DF,
Macciardi F,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Ridker PM,
Stumvoll M,
Beckmann JS,
Boeing H,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Collins FS,
Cupples LA,
Smith GD,
Erdmann J,
Froguel P,
Grönberg H,
Gyllensten U,
Hall P,
Hansen T,
Harris TB,
Hattersley AT,
Hayes RB,
Heinrich J,
Hu FB,
Hveem K,
Illig T,
Jarvelin MR,
Kaprio J,
Karpe F,
Khaw KT,
Kiemeney LA,
Krude H,
Laakso M,
Lawlor DA,
Metspalu A,
Munroe PB,
Ouwehand WH,
Pedersen O,
Penninx BW,
Peters A,
Pramstaller PP,
Quertermous T,
Reinehr T,
Rissanen A,
Rudan I,
Samani NJ,
Schwarz PE,
Schwarz PE,
Shuldiner AR,
Spector TD,
Tuomilehto J,
Uda M,
Uitterlinden A,
Valle TT,
Wabitsch M,
Waeber G,
Wareham NJ,
Watkins H,
Wilson JF,
Wright AF,
Zillikens MC,
Chatterjee N,
McCarroll SA,
Purcell S,
Schadt EE,
Visscher PM,
Assimes TL,
Borecki IB,
Deloukas P,
Fox CS,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
Mohlke KL,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
van Duijn CM,
Wichmann HE,
Frayling TM,
Thorsteinsdottir U,
Abecasis GR,
Barroso I,
Boehnke M,
Stefansson K,
North KE,
McCarthy MI,
Hirschhorn JN,
Ingelsson E,
Loos RJ
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
페이지 11개
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
외 162명 — 모두 보기
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
페이지 11개
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
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
외 198명 — 모두 보기
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
Nature genetics · 2016 · PMID 27618447 · open access
페이지 11개
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
외 82명 — 모두 보기
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
페이지 10개
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler E,
Leong A,
Liu CT,
Hivert MF,
Strawbridge RJ,
Podmore C,
Li M,
Yao J,
Sim X,
Hong J,
Chu AY,
Zhang W
외 203명 — 모두 보기
Wang X,
Chen P,
Maruthur NM,
Porneala BC,
Sharp SJ,
Jia Y,
Kabagambe EK,
Chang LC,
Chen WM,
Elks CE,
Evans DS,
Fan Q,
Giulianini F,
Go MJ,
Hottenga JJ,
Hu Y,
Jackson AU,
Kanoni S,
Kim YJ,
Kleber ME,
Ladenvall C,
Lecoeur C,
Lim SH,
Lu Y,
Mahajan A,
Marzi C,
Nalls MA,
Navarro P,
Nolte IM,
Rose LM,
Rybin DV,
Sanna S,
Shi Y,
Stram DO,
Takeuchi F,
Tan SP,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Wong A,
Yengo L,
Zhao W,
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EPIC-CVD Consortium · EPIC-InterAct Consortium 외 컨소시엄 1곳
PLoS medicine · 2017 · PMID 28898252 · open access
페이지 10개
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
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외 39명 — 모두 보기
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23andMe Research Team · DESIR study group
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페이지 10개
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
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외 102명 — 모두 보기
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Circulation · 2011 · PMID 21300955
페이지 9개
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
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외 133명 — 모두 보기
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VTE Consortium · STROKE Consortium 외 컨소시엄 3곳
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페이지 9개
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
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외 68명 — 모두 보기
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페이지 8개
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
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외 167명 — 모두 보기
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LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
페이지 8개
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
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외 256명 — 모두 보기
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Global BPgen Consortium · CARDIoGRAM Consortium 외 컨소시엄 4곳
Nature genetics · 2013 · PMID 23583979
페이지 8개
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
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외 155명 — 모두 보기
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