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Coresh J에 대해
36건, 그중 16건 표시.
Genome-wide association study of blood pressure and hypertension
Levy D,
Ehret GB,
Rice K,
Verwoert GC,
Launer LJ,
Dehghan A,
Glazer NL,
Morrison AC,
Johnson AD,
Aspelund T,
Aulchenko Y,
Lumley T
외 32명 — 모두 보기
Köttgen A,
Vasan RS,
Rivadeneira F,
Eiriksdottir G,
Guo X,
Arking DE,
Mitchell GF,
Mattace-Raso FU,
Smith AV,
Taylor K,
Scharpf RB,
Hwang SJ,
Sijbrands EJ,
Bis J,
Harris TB,
Ganesh SK,
O'Donnell CJ,
Hofman A,
Rotter JI,
Coresh J,
Benjamin EJ,
Uitterlinden AG,
Heiss G,
Fox CS,
Witteman JC,
Boerwinkle E,
Wang TJ,
Gudnason V,
Larson MG,
Chakravarti A,
Psaty BM,
van Duijn CM
Nature genetics · 2009 · PMID 19430479
페이지 3개
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
외 81명 — 모두 보기
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
페이지 3개
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
Genetic Variants Associated with Circulating Parathyroid Hormone
Robinson-Cohen C,
Lutsey PL,
Kleber ME,
Nielson CM,
Mitchell BD,
Bis JC,
Eny KM,
Portas L,
Eriksson J,
Lorentzon M,
Koller DL,
Milaneschi Y
외 37명 — 모두 보기
Teumer A,
Pilz S,
Nethander M,
Selvin E,
Tang W,
Weng LC,
Wong HS,
Lai D,
Peacock M,
Hannemann A,
Völker U,
Homuth G,
Nauk M,
Murgia F,
Pattee JW,
Orwoll E,
Zmuda JM,
Riancho JA,
Wolf M,
Williams F,
Penninx B,
Econs MJ,
Ryan KA,
Ohlsson C,
Paterson AD,
Psaty BM,
Siscovick DS,
Rotter JI,
Pirastu M,
Streeten E,
März W,
Fox C,
Coresh J,
Wallaschofski H,
Pankow JS,
de Boer IH,
Kestenbaum B
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
페이지 3개
Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study
Rhee EP,
Surapaneni A,
Zheng Z,
Zhou L,
Dutta D,
Arking DE,
Zhang J,
Duong T,
Chatterjee N,
Luo S,
Schlosser P,
Mehta R
외 14명 — 모두 보기
Waikar SS,
Saraf SL,
Kelly TN,
Hamm LL,
Rao PS,
Mathew AV,
Hsu CY,
Parsa A,
Vasan RS,
Kimmel PL,
Clish CB,
Coresh J,
Feldman HI,
Grams ME
CKD Biomarkers Consortium and the Chronic Renal Insufficiency Cohort (CRIC) Study Investigators
Kidney international · 2022 · PMID 35120996
페이지 3개
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
Dehghan A,
Köttgen A,
Yang Q,
Hwang SJ,
Kao WL,
Rivadeneira F,
Boerwinkle E,
Levy D,
Hofman A,
Astor BC,
Benjamin EJ,
van Duijn CM
외 3명 — 모두 보기
Lancet (London, England) · 2008 · PMID 18834626
페이지 2개
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
외 52명 — 모두 보기
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
페이지 2개
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
외 119명 — 모두 보기
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
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
Multiple loci associated with indices of renal function and chronic kidney disease
Köttgen A,
Glazer NL,
Dehghan A,
Hwang SJ,
Katz R,
Li M,
Yang Q,
Gudnason V,
Launer LJ,
Harris TB,
Smith AV,
Arking DE
외 27명 — 모두 보기
Astor BC,
Boerwinkle E,
Ehret GB,
Ruczinski I,
Scharpf RB,
Chen YD,
de Boer IH,
Haritunians T,
Lumley T,
Sarnak M,
Siscovick D,
Benjamin EJ,
Levy D,
Upadhyay A,
Aulchenko YS,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
van Duijn CM,
Chasman DI,
Paré G,
Ridker PM,
Kao WH,
Witteman JC,
Coresh J,
Shlipak MG,
Fox CS
Nature genetics · 2009 · PMID 19430482
페이지 1개
Common genetic variants associate with serum phosphorus concentration
Kestenbaum B,
Glazer NL,
Köttgen A,
Felix JF,
Hwang SJ,
Liu Y,
Lohman K,
Kritchevsky SB,
Hausman DB,
Petersen AK,
Gieger C,
Ried JS
외 27명 — 모두 보기
Meitinger T,
Strom TM,
Wichmann HE,
Campbell H,
Hayward C,
Rudan I,
de Boer IH,
Psaty BM,
Rice KM,
Chen YD,
Li M,
Arking DE,
Boerwinkle E,
Coresh J,
Yang Q,
Levy D,
van Rooij FJ,
Dehghan A,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Shlipak MG,
Kao WH,
Witteman JC,
Siscovick DS,
Fox CS
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
페이지 1개
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels
O'Seaghdha CM,
Yang Q,
Glazer NL,
Leak TS,
Dehghan A,
Smith AV,
Kao WH,
Lohman K,
Hwang SJ,
Johnson AD,
Hofman A,
Uitterlinden AG
외 12명 — 모두 보기
Chen YD,
Brown EM,
Siscovick DS,
Harris TB,
Psaty BM,
Coresh J,
Gudnason V,
Witteman JC,
Liu YM,
Kestenbaum BR,
Fox CS,
Köttgen A
GEFOS Consortium
Human molecular genetics · 2010 · PMID 20705733
페이지 1개
CUBN is a gene locus for albuminuria
Böger CA,
Chen MH,
Tin A,
Olden M,
Köttgen A,
de Boer IH,
Fuchsberger C,
O'Seaghdha CM,
Pattaro C,
Teumer A,
Liu CT,
Glazer NL
외 103명 — 모두 보기
Li M,
O'Connell JR,
Tanaka T,
Peralta CA,
Kutalik Z,
Luan J,
Zhao JH,
Hwang SJ,
Akylbekova E,
Kramer H,
van der Harst P,
Smith AV,
Lohman K,
de Andrade M,
Hayward C,
Kollerits B,
Tönjes A,
Aspelund T,
Ingelsson E,
Eiriksdottir G,
Launer LJ,
Harris TB,
Shuldiner AR,
Mitchell BD,
Arking DE,
Franceschini N,
Boerwinkle E,
Egan J,
Hernandez D,
Reilly M,
Townsend RR,
Lumley T,
Siscovick DS,
Psaty BM,
Kestenbaum B,
Haritunians T,
Bergmann S,
Vollenweider P,
Waeber G,
Mooser V,
Waterworth D,
Johnson AD,
Florez JC,
Meigs JB,
Lu X,
Turner ST,
Atkinson EJ,
Leak TS,
Aasarød K,
Skorpen F,
Syvänen AC,
Illig T,
Baumert J,
Koenig W,
Krämer BK,
Devuyst O,
Mychaleckyj JC,
Minelli C,
Bakker SJ,
Kedenko L,
Paulweber B,
Coassin S,
Endlich K,
Kroemer HK,
Biffar R,
Stracke S,
Völzke H,
Stumvoll M,
Mägi R,
Campbell H,
Vitart V,
Hastie ND,
Gudnason V,
Kardia SL,
Liu Y,
Polasek O,
Curhan G,
Kronenberg F,
Prokopenko I,
Rudan I,
Arnlöv J,
Hallan S,
Navis G,
Parsa A,
Ferrucci L,
Coresh J,
Shlipak MG,
Bull SB,
Paterson NJ,
Wichmann HE,
Wareham NJ,
Loos RJ,
Rotter JI,
Pramstaller PP,
Cupples LA,
Beckmann JS,
Yang Q,
Heid IM,
Rettig R,
Dreisbach AW,
Bochud M,
Fox CS,
Kao WH
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
페이지 1개
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Huffman JE,
Albrecht E,
Teumer A,
Mangino M,
Kapur K,
Johnson T,
Kutalik Z,
Pirastu N,
Pistis G,
Lopez LM,
Haller T,
Salo P
외 108명 — 모두 보기
Goel A,
Li M,
Tanaka T,
Dehghan A,
Ruggiero D,
Malerba G,
Smith AV,
Nolte IM,
Portas L,
Phipps-Green A,
Boteva L,
Navarro P,
Johansson A,
Hicks AA,
Polasek O,
Esko T,
Peden JF,
Harris SE,
Murgia F,
Wild SH,
Tenesa A,
Tin A,
Mihailov E,
Grotevendt A,
Gislason GK,
Coresh J,
D'Adamo P,
Ulivi S,
Vollenweider P,
Waeber G,
Campbell S,
Kolcic I,
Fisher K,
Viigimaa M,
Metter JE,
Masciullo C,
Trabetti E,
Bombieri C,
Sorice R,
Döring A,
Reischl E,
Strauch K,
Hofman A,
Uitterlinden AG,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Dalbeth N,
Stamp L,
Smit JH,
Kirin M,
Nagaraja R,
Nauck M,
Schurmann C,
Budde K,
Farrington SM,
Theodoratou E,
Jula A,
Salomaa V,
Sala C,
Hengstenberg C,
Burnier M,
Mägi R,
Klopp N,
Kloiber S,
Schipf S,
Ripatti S,
Cabras S,
Soranzo N,
Homuth G,
Nutile T,
Munroe PB,
Hastie N,
Campbell H,
Rudan I,
Cabrera C,
Haley C,
Franco OH,
Merriman TR,
Gudnason V,
Pirastu M,
Penninx BW,
Snieder H,
Metspalu A,
Ciullo M,
Pramstaller PP,
van Duijn CM,
Ferrucci L,
Gambaro G,
Deary IJ,
Dunlop MG,
Wilson JF,
Gasparini P,
Gyllensten U,
Spector TD,
Wright AF,
Hayward C,
Watkins H,
Perola M,
Bochud M,
Kao WH,
Caulfield M,
Toniolo D,
Völzke H,
Gieger C,
Köttgen A,
Vitart V
PloS one · 2015 · PMID 25811787 · open access
페이지 1개
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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.