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Srinivasan S에 대해
12건.
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry A,
Mo X,
Finan C,
Chaffin MD,
Speed D,
Issa H,
Denaxas S,
Ware JS,
Zheng SL,
Malarstig A,
Gratton J,
Bond I
외 169명 — 모두 보기
Roselli C,
Miller D,
Chopade S,
Schmidt AF,
Abner E,
Adams L,
Andersson C,
Aragam KG,
Ärnlöv J,
Asselin G,
Raja AA,
Backman JD,
Bartz TM,
Biddinger KJ,
Biggs ML,
Bloom HL,
Boersma E,
Brandimarto J,
Brown MR,
Brunak S,
Bruun MT,
Buckbinder L,
Bundgaard H,
Carey DJ,
Chasman DI,
Chen X,
Cook JP,
Czuba T,
de Denus S,
Dehghan A,
Delgado GE,
Doney AS,
Dörr M,
Dowsett J,
Dudley SC,
Engström G,
Erikstrup C,
Esko T,
Farber-Eger EH,
Felix SB,
Finer S,
Ford I,
Ghanbari M,
Ghasemi S,
Ghouse J,
Giedraitis V,
Giulianini F,
Gottdiener JS,
Gross S,
Guðbjartsson DF,
Gui H,
Gutmann R,
Hägg S,
Haggerty CM,
Hedman ÅK,
Helgadottir A,
Hemingway H,
Hillege H,
Hyde CL,
Aagaard Jensen B,
Jukema JW,
Kardys I,
Karra R,
Kavousi M,
Kizer JR,
Kleber ME,
Køber L,
Koekemoer A,
Kuchenbaecker K,
Lai YP,
Lanfear D,
Langenberg C,
Lin H,
Lind L,
Lindgren CM,
Liu PP,
London B,
Lowery BD,
Luan J,
Lubitz SA,
Magnusson P,
Margulies KB,
Marston NA,
Martin H,
März W,
Melander O,
Mordi IR,
Morley MP,
Morris AP,
Morrison AC,
Morton L,
Nagle MW,
Nelson CP,
Niessner A,
Niiranen T,
Noordam R,
Nowak C,
O'Donoghue ML,
Ostrowski SR,
Owens AT,
Palmer CNA,
Paré G,
Pedersen OB,
Perola M,
Pigeyre M,
Psaty BM,
Rice KM,
Ridker PM,
Romaine SPR,
Rotter JI,
Ruff CT,
Sabatine MS,
Sallah N,
Salomaa V,
Sattar N,
Shalaby AA,
Shekhar A,
Smelser DT,
Smith NL,
Sørensen E,
Srinivasan S,
Stefansson K,
Sveinbjörnsson G,
Svensson P,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teumer A,
Thorgeirsson G,
Thorsteinsdottir U,
Torp-Pedersen C,
Tragante V,
Trompet S,
Uitterlinden AG,
Ullum H,
van der Harst P,
van Heel D,
van Setten J,
van Vugt M,
Veluchamy A,
Verschuuren M,
Verweij N,
Vissing CR,
Völker U,
Voors AA,
Wallentin L,
Wang Y,
Weeke PE,
Wiggins KL,
Williams LK,
Yang Y,
Yu B,
Zannad F,
Zheng C,
Asselbergs FW,
Cappola TP,
Dubé MP,
Dunn ME,
Lang CC,
Samani NJ,
Shah S,
Vasan RS,
Smith JG,
Holm H,
Shah S,
Ellinor PT,
Hingorani AD,
Wells Q,
Lumbers RT
Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 2곳
Nature genetics · 2025 · PMID 40038546 · open access
페이지 12개+
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Bujnis MN,
Sterenborg RBTM,
Li Y,
Åsvold BO,
Brčić L,
Boraska Perica V,
Babbar A,
Denny JC,
Fritsche LG,
Kanai M,
Konrade I,
Leese G
외 22명 — 모두 보기
Marouli E,
Metspalu A,
Moksnes MR,
Mukherjee B,
Okada Y,
Palmer CNA,
Papadopoulou A,
Peculis R,
Rovite V,
Sauer PJ,
Soto-Pedre E,
Srinivasan S,
Steinbrenner I,
Teder-Laving M,
Wang B,
Weihs A,
Zeng C,
Zhou J,
Song X,
Jorde LB,
Medici M,
Teumer A
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
페이지 12개+
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
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Beaumont RN,
Flatley C,
Vaudel M,
Wu X,
Chen J,
Moen GH,
Skotte L,
Helgeland Ø,
Solé-Navais P,
Banasik K,
Albiñana C,
Ronkainen J
외 76명 — 모두 보기
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
Westergaard D,
Srinivasan S,
Sánchez-Soriano C,
Bilbao JR,
Allard C,
Groleau M,
Kuulasmaa T,
Leirer DJ,
White F,
Jacques PÉ,
Cheng H,
Hao K,
Andreassen OA,
Åsvold BO,
Atalay M,
Bhatta L,
Bouchard L,
Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
Elliott P,
Engelbrechtsen L,
Erikstrup C,
Estarlich M,
Franks S,
Gaillard R,
Geller F,
Grove J,
Hougaard DM,
Kajantie E,
Morgen CS,
Nohr EA,
Nyegaard M,
Palmer CNA,
Pedersen OB,
Rivadeneira F,
Sebert S,
Shields BM,
Stoltenberg C,
Surakka I,
Thørner LW,
Ullum H,
Vaarasmaki M,
Vilhjalmsson BJ,
Willer CJ,
Lakka TA,
Gybel-Brask D,
Bustamante M,
Hansen T,
Pearson ER,
Reynolds RM,
Ostrowski SR,
Pennell CE,
Jaddoe VWV,
Felix JF,
Hattersley AT,
Melbye M,
Lawlor DA,
Hveem K,
Werge T,
Nielsen HS,
Magnus P,
Evans DM,
Jacobsson B,
Järvelin MR,
Zhang G,
Hivert MF,
Johansson S,
Freathy RM,
Feenstra B,
Njølstad PR
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
페이지 10개
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
Buxbaum SG,
Alonso A,
Arking DE,
Berenson GS
외 49명 — 모두 보기
Bis JC,
Buyske S,
Carty CL,
Chen W,
Chung MK,
Cummings SR,
Deo R,
Eaton CB,
Fox ER,
Heckbert SR,
Heiss G,
Hindorff LA,
Hsueh WC,
Isaacs A,
Jamshidi Y,
Kerr KF,
Liu F,
Liu Y,
Lohman KK,
Magnani JW,
Maher JF,
Mehra R,
Meng YA,
Musani SK,
Newton-Cheh C,
North KE,
Psaty BM,
Redline S,
Rotter JI,
Schnabel RB,
Schork NJ,
Shohet RV,
Singleton AB,
Smith JD,
Soliman EZ,
Srinivasan SR,
Taylor HA Jr,
Van Wagoner DR,
Wilson JG,
Young T,
Zhang ZM,
Zonderman AB,
Evans MK,
Ferrucci L,
Murray SS,
Tranah GJ,
Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
페이지 9개
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Eeles RA,
Olama AA,
Benlloch S,
Saunders EJ,
Leongamornlert DA,
Tymrakiewicz M,
Ghoussaini M,
Luccarini C,
Dennis J,
Jugurnauth-Little S,
Dadaev T,
Neal DE
외 132명 — 모두 보기
Hamdy FC,
Donovan JL,
Muir K,
Giles GG,
Severi G,
Wiklund F,
Gronberg H,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Lindstrom S,
Kraft P,
Hunter DJ,
Gapstur S,
Chanock SJ,
Berndt SI,
Albanes D,
Andriole G,
Schleutker J,
Weischer M,
Canzian F,
Riboli E,
Key TJ,
Travis RC,
Campa D,
Ingles SA,
John EM,
Hayes RB,
Pharoah PD,
Pashayan N,
Khaw KT,
Stanford JL,
Ostrander EA,
Signorello LB,
Thibodeau SN,
Schaid D,
Maier C,
Vogel W,
Kibel AS,
Cybulski C,
Lubinski J,
Cannon-Albright L,
Brenner H,
Park JY,
Kaneva R,
Batra J,
Spurdle AB,
Clements JA,
Teixeira MR,
Dicks E,
Lee A,
Dunning AM,
Baynes C,
Conroy D,
Maranian MJ,
Ahmed S,
Govindasami K,
Guy M,
Wilkinson RA,
Sawyer EJ,
Morgan A,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As NJ,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatananon A,
Cox A,
Southey MC,
Hopper JL,
English DR,
Aly M,
Adolfsson J,
Xu J,
Zheng SL,
Yeager M,
Kaaks R,
Diver WR,
Gaudet MM,
Stern MC,
Corral R,
Joshi AD,
Shahabi A,
Wahlfors T,
Tammela TL,
Auvinen A,
Virtamo J,
Klarskov P,
Nordestgaard BG,
Røder MA,
Nielsen SF,
Bojesen SE,
Siddiq A,
Fitzgerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Blot WJ,
Zheng W,
Cai Q,
McDonnell SK,
Rinckleb AE,
Drake B,
Colditz G,
Wokolorczyk D,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Sellers TA,
Lin HY,
Slavov C,
Mitev V,
Lose F,
Srinivasan S,
Maia S,
Paulo P,
Lange E,
Cooney KA,
Antoniou AC,
Vincent D,
Bacot F,
Tessier DC,
Kote-Jarai Z,
Easton DF
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource 외 컨소시엄 3곳
Nature genetics · 2013 · PMID 23535732
페이지 7개
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
Mangino M,
Hwang SJ,
Spector TD,
Hunt SC,
Kimura M,
Fitzpatrick AL,
Christiansen L,
Petersen I,
Elbers CC,
Harris T,
Chen W,
Srinivasan SR
외 27명 — 모두 보기
Kark JD,
Benetos A,
El Shamieh S,
Visvikis-Siest S,
Christensen K,
Berenson GS,
Valdes AM,
Viñuela A,
Garcia M,
Arnett DK,
Broeckel U,
Province MA,
Pankow JS,
Kammerer C,
Liu Y,
Nalls M,
Tishkoff S,
Thomas F,
Ziv E,
Psaty BM,
Bis JC,
Rotter JI,
Taylor KD,
Smith E,
Schork NJ,
Levy D,
Aviv A
Human molecular genetics · 2012 · PMID 23001564 · open access
페이지 4개
The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium
Srinivasan S,
Chen L,
Todd J,
Divers J,
Gidding S,
Chernausek S,
Gubitosi-Klug RA,
Kelsey MM,
Shah R,
Black MH,
Wagenknecht LE,
Manning A
외 5명 — 모두 보기
ProDiGY Consortium
Diabetes · 2021 · PMID 33479058 · open access
페이지 3개
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Franceschini N,
Fox E,
Zhang Z,
Edwards TL,
Nalls MA,
Sung YJ,
Tayo BO,
Sun YV,
Gottesman O,
Adeyemo A,
Johnson AD,
Young JH
외 94명 — 모두 보기
Rice K,
Duan Q,
Chen F,
Li Y,
Tang H,
Fornage M,
Keene KL,
Andrews JS,
Smith JA,
Faul JD,
Guangfa Z,
Guo W,
Liu Y,
Murray SS,
Musani SK,
Srinivasan S,
Velez Edwards DR,
Wang H,
Becker LC,
Bovet P,
Bochud M,
Broeckel U,
Burnier M,
Carty C,
Chasman DI,
Ehret G,
Chen WM,
Chen G,
Chen W,
Ding J,
Dreisbach AW,
Evans MK,
Guo X,
Garcia ME,
Jensen R,
Keller MF,
Lettre G,
Lotay V,
Martin LW,
Moore JH,
Morrison AC,
Mosley TH,
Ogunniyi A,
Palmas W,
Papanicolaou G,
Penman A,
Polak JF,
Ridker PM,
Salako B,
Singleton AB,
Shriner D,
Taylor KD,
Vasan R,
Wiggins K,
Williams SM,
Yanek LR,
Zhao W,
Zonderman AB,
Becker DM,
Berenson G,
Boerwinkle E,
Bottinger E,
Cushman M,
Eaton C,
Nyberg F,
Heiss G,
Hirschhron JN,
Howard VJ,
Karczewsk KJ,
Lanktree MB,
Liu K,
Liu Y,
Loos R,
Margolis K,
Snyder M,
Psaty BM,
Schork NJ,
Weir DR,
Rotimi CN,
Sale MM,
Harris T,
Kardia SL,
Hunt SC,
Arnett D,
Redline S,
Cooper RS,
Risch NJ,
Rao DC,
Rotter JI,
Chakravarti A,
Reiner AP,
Levy D,
Keating BJ,
Zhu X
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
페이지 2개
Impact of ancestry and common genetic variants on QT interval in African Americans
Smith JG,
Avery CL,
Evans DS,
Nalls MA,
Meng YA,
Smith EN,
Palmer C,
Tanaka T,
Mehra R,
Butler AM,
Young T,
Buxbaum SG
외 39명 — 모두 보기
Kerr KF,
Berenson GS,
Schnabel RB,
Li G,
Ellinor PT,
Magnani JW,
Chen W,
Bis JC,
Curb JD,
Hsueh WC,
Rotter JI,
Liu Y,
Newman AB,
Limacher MC,
North KE,
Reiner AP,
Quibrera PM,
Schork NJ,
Singleton AB,
Psaty BM,
Soliman EZ,
Solomon AJ,
Srinivasan SR,
Alonso A,
Wallace R,
Redline S,
Zhang ZM,
Post WS,
Zonderman AB,
Taylor HA,
Murray SS,
Ferrucci L,
Arking DE,
Evans MK,
Fox ER,
Sotoodehnia N,
Heckbert SR,
Whitsel EA,
Newton-Cheh C
CARe and COGENT consortia
Circulation. Cardiovascular genetics · 2012 · PMID 23166209
페이지 1개
Genome-wide association study of age at menarche in African-American women
Demerath EW,
Liu CT,
Franceschini N,
Chen G,
Palmer JR,
Smith EN,
Chen CT,
Ambrosone CB,
Arnold AM,
Bandera EV,
Berenson GS,
Bernstein L
외 45명 — 모두 보기
Britton A,
Cappola AR,
Carlson CS,
Chanock SJ,
Chen W,
Chen Z,
Deming SL,
Elks CE,
Evans MK,
Gajdos Z,
Henderson BE,
Hu JJ,
Ingles S,
John EM,
Kerr KF,
Kolonel LN,
Le Marchand L,
Lu X,
Millikan RC,
Musani SK,
Nock NL,
North K,
Nyante S,
Press MF,
Rodriquez-Gil JL,
Ruiz-Narvaez EA,
Schork NJ,
Srinivasan SR,
Woods NF,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman A,
Heiss G,
Gwen Windham B,
Wellons M,
Murray SS,
Nalls M,
Pastinen T,
Rajkovic A,
Hirschhorn J,
Adrienne Cupples L,
Kooperberg C,
Murabito JM,
Haiman CA
Human molecular genetics · 2013 · PMID 23599027
페이지 1개
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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.