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Relton C에 대해
7건.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou I,
Süveges D,
Min JL,
Ritchie GRS,
Steinberg J,
Walter K,
Iotchkova V,
Schwartzentruber J,
Huang J,
Memari Y,
McCarthy S,
Crawford AA
외 91명 — 모두 보기
Bombieri C,
Cocca M,
Farmaki AE,
Gaunt TR,
Jousilahti P,
Kooijman MN,
Lehne B,
Malerba G,
Männistö S,
Matchan A,
Medina-Gomez C,
Metrustry SJ,
Nag A,
Ntalla I,
Paternoster L,
Rayner NW,
Sala C,
Scott WR,
Shihab HA,
Southam L,
St Pourcain B,
Traglia M,
Trajanoska K,
Zaza G,
Zhang W,
Artigas MS,
Bansal N,
Benn M,
Chen Z,
Danecek P,
Lin WY,
Locke A,
Luan J,
Manning AK,
Mulas A,
Sidore C,
Tybjaerg-Hansen A,
Varbo A,
Zoledziewska M,
Finan C,
Hatzikotoulas K,
Hendricks AE,
Kemp JP,
Moayyeri A,
Panoutsopoulou K,
Szpak M,
Wilson SG,
Boehnke M,
Cucca F,
Di Angelantonio E,
Langenberg C,
Lindgren C,
McCarthy MI,
Morris AP,
Nordestgaard BG,
Scott RA,
Tobin MD,
Wareham NJ,
Burton P,
Chambers JC,
Smith GD,
Dedoussis G,
Felix JF,
Franco OH,
Gambaro G,
Gasparini P,
Hammond CJ,
Hofman A,
Jaddoe VWV,
Kleber M,
Kooner JS,
Perola M,
Relton C,
Ring SM,
Rivadeneira F,
Salomaa V,
Spector TD,
Stegle O,
Toniolo D,
Uitterlinden AG,
Barroso I,
Greenwood CMT,
Perry JRB,
Walker BR,
Butterworth AS,
Xue Y,
Durbin R,
Small KS,
Soranzo N,
Timpson NJ,
Zeggini E
SpiroMeta Consortium · GoT2D Consortium 외 컨소시엄 3곳
American journal of human genetics · 2017 · PMID 28552196 · open access
페이지 12개+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
외 196명 — 모두 보기
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
페이지 12개+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
외 269명 — 모두 보기
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
McCartney DL,
Min JL,
Richmond RC,
Lu AT,
Sobczyk MK,
Davies G,
Broer L,
Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
외 97명 — 모두 보기
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
페이지 12개+
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
외 140명 — 모두 보기
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
페이지 11개
Whole-genome sequence-based analysis of thyroid function
Taylor PN,
Porcu E,
Chew S,
Campbell PJ,
Traglia M,
Brown SJ,
Mullin BH,
Shihab HA,
Min J,
Walter K,
Memari Y,
Huang J
외 38명 — 모두 보기
Barnes MR,
Beilby JP,
Charoen P,
Danecek P,
Dudbridge F,
Forgetta V,
Greenwood C,
Grundberg E,
Johnson AD,
Hui J,
Lim EM,
McCarthy S,
Muddyman D,
Panicker V,
Perry JR,
Bell JT,
Yuan W,
Relton C,
Gaunt T,
Schlessinger D,
Abecasis G,
Cucca F,
Surdulescu GL,
Woltersdorf W,
Zeggini E,
Zheng HF,
Toniolo D,
Dayan CM,
Naitza S,
Walsh JP,
Spector T,
Davey Smith G,
Durbin R,
Richards JB,
Sanna S,
Soranzo N,
Timpson NJ,
Wilson SG
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · open access
페이지 7개
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Beaumont RN,
Warrington NM,
Cavadino A,
Tyrrell J,
Nodzenski M,
Horikoshi M,
Geller F,
Myhre R,
Richmond RC,
Paternoster L,
Bradfield JP,
Kreiner-Møller E
외 74명 — 모두 보기
Huikari V,
Metrustry S,
Lunetta KL,
Painter JN,
Hottenga JJ,
Allard C,
Barton SJ,
Espinosa A,
Marsh JA,
Potter C,
Zhang G,
Ang W,
Berry DJ,
Bouchard L,
Das S,
Hakonarson H,
Heikkinen J,
Helgeland Ø,
Hocher B,
Hofman A,
Inskip HM,
Jones SE,
Kogevinas M,
Lind PA,
Marullo L,
Medland SE,
Murray A,
Murray JC,
Njølstad PR,
Nohr EA,
Reichetzeder C,
Ring SM,
Ruth KS,
Santa-Marina L,
Scholtens DM,
Sebert S,
Sengpiel V,
Tuke MA,
Vaudel M,
Weedon MN,
Willemsen G,
Wood AR,
Yaghootkar H,
Muglia LJ,
Bartels M,
Relton CL,
Pennell CE,
Chatzi L,
Estivill X,
Holloway JW,
Boomsma DI,
Montgomery GW,
Murabito JM,
Spector TD,
Power C,
Järvelin MR,
Bisgaard H,
Grant SFA,
Sørensen TIA,
Jaddoe VW,
Jacobsson B,
Melbye M,
McCarthy MI,
Hattersley AT,
Hayes MG,
Frayling TM,
Hivert MF,
Felix JF,
Hyppönen E,
Lowe WL Jr,
Evans DM,
Lawlor DA,
Feenstra B,
Freathy RM
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
페이지 1개
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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.