For researchers
Is your paper here?
2,663 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
18 matches for
Ganesh SK.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
and 50 more — show all
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
Felix JF,
Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
Zheng G,
Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
Launer LJ,
Cupples LA,
Oostra BA,
Zwaginga JJ,
Ouwehand WH,
Thein SL,
Meisinger C,
Deloukas P,
Nauck M,
Spector TD,
Gieger C,
Gudnason V,
van Duijn CM,
Psaty BM,
Ferrucci L,
Chakravarti A,
Greinacher A,
O'Donnell CJ,
Witteman JC,
Furth S,
Cushman M,
Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
12 pages+
New gene functions in megakaryopoiesis and platelet formation
Gieger C,
Radhakrishnan A,
Cvejic A,
Tang W,
Porcu E,
Pistis G,
Serbanovic-Canic J,
Elling U,
Goodall AH,
Labrune Y,
Lopez LM,
Mägi R
and 151 more — show all
Meacham S,
Okada Y,
Pirastu N,
Sorice R,
Teumer A,
Voss K,
Zhang W,
Ramirez-Solis R,
Bis JC,
Ellinghaus D,
Gögele M,
Hottenga JJ,
Langenberg C,
Kovacs P,
O'Reilly PF,
Shin SY,
Esko T,
Hartiala J,
Kanoni S,
Murgia F,
Parsa A,
Stephens J,
van der Harst P,
Ellen van der Schoot C,
Allayee H,
Attwood A,
Balkau B,
Bastardot F,
Basu S,
Baumeister SE,
Biino G,
Bomba L,
Bonnefond A,
Cambien F,
Chambers JC,
Cucca F,
D'Adamo P,
Davies G,
de Boer RA,
de Geus EJ,
Döring A,
Elliott P,
Erdmann J,
Evans DM,
Falchi M,
Feng W,
Folsom AR,
Frazer IH,
Gibson QD,
Glazer NL,
Hammond C,
Hartikainen AL,
Heckbert SR,
Hengstenberg C,
Hersch M,
Illig T,
Loos RJ,
Jolley J,
Khaw KT,
Kühnel B,
Kyrtsonis MC,
Lagou V,
Lloyd-Jones H,
Lumley T,
Mangino M,
Maschio A,
Mateo Leach I,
McKnight B,
Memari Y,
Mitchell BD,
Montgomery GW,
Nakamura Y,
Nauck M,
Navis G,
Nöthlings U,
Nolte IM,
Porteous DJ,
Pouta A,
Pramstaller PP,
Pullat J,
Ring SM,
Rotter JI,
Ruggiero D,
Ruokonen A,
Sala C,
Samani NJ,
Sambrook J,
Schlessinger D,
Schreiber S,
Schunkert H,
Scott J,
Smith NL,
Snieder H,
Starr JM,
Stumvoll M,
Takahashi A,
Tang WH,
Taylor K,
Tenesa A,
Lay Thein S,
Tönjes A,
Uda M,
Ulivi S,
van Veldhuisen DJ,
Visscher PM,
Völker U,
Wichmann HE,
Wiggins KL,
Willemsen G,
Yang TP,
Hua Zhao J,
Zitting P,
Bradley JR,
Dedoussis GV,
Gasparini P,
Hazen SL,
Metspalu A,
Pirastu M,
Shuldiner AR,
Joost van Pelt L,
Zwaginga JJ,
Boomsma DI,
Deary IJ,
Franke A,
Froguel P,
Ganesh SK,
Jarvelin MR,
Martin NG,
Meisinger C,
Psaty BM,
Spector TD,
Wareham NJ,
Akkerman JW,
Ciullo M,
Deloukas P,
Greinacher A,
Jupe S,
Kamatani N,
Khadake J,
Kooner JS,
Penninger J,
Prokopenko I,
Stemple D,
Toniolo D,
Wernisch L,
Sanna S,
Hicks AA,
Rendon A,
Ferreira MA,
Ouwehand WH,
Soranzo N
Nature · 2011 · PMID 22139419
12 pages+
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret GB,
Ferreira T,
Chasman DI,
Jackson AU,
Schmidt EM,
Johnson T,
Thorleifsson G,
Luan J,
Donnelly LA,
Kanoni S,
Petersen AK,
Pihur V
and 301 more — show all
Strawbridge RJ,
Shungin D,
Hughes MF,
Meirelles O,
Kaakinen M,
Bouatia-Naji N,
Kristiansson K,
Shah S,
Kleber ME,
Guo X,
Lyytikäinen LP,
Fava C,
Eriksson N,
Nolte IM,
Magnusson PK,
Salfati EL,
Rallidis LS,
Theusch E,
Smith AJP,
Folkersen L,
Witkowska K,
Pers TH,
Joehanes R,
Kim SK,
Lataniotis L,
Jansen R,
Johnson AD,
Warren H,
Kim YJ,
Zhao W,
Wu Y,
Tayo BO,
Bochud M,
Absher D,
Adair LS,
Amin N,
Arking DE,
Axelsson T,
Baldassarre D,
Balkau B,
Bandinelli S,
Barnes MR,
Barroso I,
Bevan S,
Bis JC,
Bjornsdottir G,
Boehnke M,
Boerwinkle E,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Brown MJ,
Burnier M,
Cabrera CP,
Chambers JC,
Chang IS,
Cheng CY,
Chines PS,
Chung RH,
Collins FS,
Connell JM,
Döring A,
Dallongeville J,
Danesh J,
de Faire U,
Delgado G,
Dominiczak AF,
Doney ASF,
Drenos F,
Edkins S,
Eicher JD,
Elosua R,
Enroth S,
Erdmann J,
Eriksson P,
Esko T,
Evangelou E,
Evans A,
Fall T,
Farrall M,
Felix JF,
Ferrières J,
Ferrucci L,
Fornage M,
Forrester T,
Franceschini N,
Duran OHF,
Franco-Cereceda A,
Fraser RM,
Ganesh SK,
Gao H,
Gertow K,
Gianfagna F,
Gigante B,
Giulianini F,
Goel A,
Goodall AH,
Goodarzi MO,
Gorski M,
Gräßler J,
Groves C,
Gudnason V,
Gyllensten U,
Hallmans G,
Hartikainen AL,
Hassinen M,
Havulinna AS,
Hayward C,
Hercberg S,
Herzig KH,
Hicks AA,
Hingorani AD,
Hirschhorn JN,
Hofman A,
Holmen J,
Holmen OL,
Hottenga JJ,
Howard P,
Hsiung CA,
Hunt SC,
Ikram MA,
Illig T,
Iribarren C,
Jensen RA,
Kähönen M,
Kang H,
Kathiresan S,
Keating BJ,
Khaw KT,
Kim YK,
Kim E,
Kivimaki M,
Klopp N,
Kolovou G,
Komulainen P,
Kooner JS,
Kosova G,
Krauss RM,
Kuh D,
Kutalik Z,
Kuusisto J,
Kvaløy K,
Lakka TA,
Lee NR,
Lee IT,
Lee WJ,
Levy D,
Li X,
Liang KW,
Lin H,
Lin L,
Lindström J,
Lobbens S,
Männistö S,
Müller G,
Müller-Nurasyid M,
Mach F,
Markus HS,
Marouli E,
McCarthy MI,
McKenzie CA,
Meneton P,
Menni C,
Metspalu A,
Mijatovic V,
Moilanen L,
Montasser ME,
Morris AD,
Morrison AC,
Mulas A,
Nagaraja R,
Narisu N,
Nikus K,
O'Donnell CJ,
O'Reilly PF,
Ong KK,
Paccaud F,
Palmer CD,
Parsa A,
Pedersen NL,
Penninx BW,
Perola M,
Peters A,
Poulter N,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rao DC,
Rasheed A,
Rayner NWNWR,
Renström F,
Rettig R,
Rice KM,
Roberts R,
Rose LM,
Rossouw J,
Samani NJ,
Sanna S,
Saramies J,
Schunkert H,
Sebert S,
Sheu WH,
Shin YA,
Sim X,
Smit JH,
Smith AV,
Sosa MX,
Spector TD,
Stančáková A,
Stanton A,
Stirrups KE,
Stringham HM,
Sundstrom J,
Swift AJ,
Syvänen AC,
Tai ES,
Tanaka T,
Tarasov KV,
Teumer A,
Thorsteinsdottir U,
Tobin MD,
Tremoli E,
Uitterlinden AG,
Uusitupa M,
Vaez A,
Vaidya D,
van Duijn CM,
van Iperen EPA,
Vasan RS,
Verwoert GC,
Virtamo J,
Vitart V,
Voight BF,
Vollenweider P,
Wagner A,
Wain LV,
Wareham NJ,
Watkins H,
Weder AB,
Westra HJ,
Wilks R,
Wilsgaard T,
Wilson JF,
Wong TY,
Yang TP,
Yao J,
Yengo L,
Zhang W,
Zhao JH,
Zhu X,
Bovet P,
Cooper RS,
Mohlke KL,
Saleheen D,
Lee JY,
Elliott P,
Gierman HJ,
Willer CJ,
Franke L,
Hovingh GK,
Taylor KD,
Dedoussis G,
Sever P,
Wong A,
Lind L,
Assimes TL,
Njølstad I,
Schwarz PE,
Langenberg C,
Snieder H,
Caulfield MJ,
Melander O,
Laakso M,
Saltevo J,
Rauramaa R,
Tuomilehto J,
Ingelsson E,
Lehtimäki T,
Hveem K,
Palmas W,
März W,
Kumari M,
Salomaa V,
Chen YI,
Rotter JI,
Froguel P,
Jarvelin MR,
Lakatta EG,
Kuulasmaa K,
Franks PW,
Hamsten A,
Wichmann HE,
Palmer CNA,
Stefansson K,
Ridker PM,
Loos RJF,
Chakravarti A,
Deloukas P,
Morris AP,
Newton-Cheh C,
Munroe PB
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
and 215 more — show all
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Wain LV,
Verwoert GC,
O'Reilly PF,
Shi G,
Johnson T,
Johnson AD,
Bochud M,
Rice KM,
Henneman P,
Smith AV,
Ehret GB,
Amin N
and 214 more — show all
Larson MG,
Mooser V,
Hadley D,
Dörr M,
Bis JC,
Aspelund T,
Esko T,
Janssens AC,
Zhao JH,
Heath S,
Laan M,
Fu J,
Pistis G,
Luan J,
Arora P,
Lucas G,
Pirastu N,
Pichler I,
Jackson AU,
Webster RJ,
Zhang F,
Peden JF,
Schmidt H,
Tanaka T,
Campbell H,
Igl W,
Milaneschi Y,
Hottenga JJ,
Vitart V,
Chasman DI,
Trompet S,
Bragg-Gresham JL,
Alizadeh BZ,
Chambers JC,
Guo X,
Lehtimäki T,
Kühnel B,
Lopez LM,
Polašek O,
Boban M,
Nelson CP,
Morrison AC,
Pihur V,
Ganesh SK,
Hofman A,
Kundu S,
Mattace-Raso FU,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Hwang SJ,
Vasan RS,
Wang TJ,
Bergmann S,
Vollenweider P,
Waeber G,
Laitinen J,
Pouta A,
Zitting P,
McArdle WL,
Kroemer HK,
Völker U,
Völzke H,
Glazer NL,
Taylor KD,
Harris TB,
Alavere H,
Haller T,
Keis A,
Tammesoo ML,
Aulchenko Y,
Barroso I,
Khaw KT,
Galan P,
Hercberg S,
Lathrop M,
Eyheramendy S,
Org E,
Org E,
Sõber S,
Lu X,
Nolte IM,
Penninx BW,
Corre T,
Masciullo C,
Sala C,
Groop L,
Voight BF,
Melander O,
O'Donnell CJ,
Salomaa V,
d'Adamo AP,
Fabretto A,
Faletra F,
Ulivi S,
Del Greco F,
Facheris M,
Collins FS,
Bergman RN,
Beilby JP,
Hung J,
Musk AW,
Mangino M,
Shin SY,
Soranzo N,
Watkins H,
Goel A,
Hamsten A,
Gider P,
Loitfelder M,
Zeginigg M,
Hernandez D,
Najjar SS,
Navarro P,
Wild SH,
Corsi AM,
Singleton A,
de Geus EJ,
Willemsen G,
Willemsen G,
Parker AN,
Rose LM,
Buckley B,
Stott D,
Orru M,
Uda M,
van der Klauw MM,
Zhang W,
Li X,
Scott J,
Chen YD,
Burke GL,
Kähönen M,
Viikari J,
Döring A,
Meitinger T,
Davies G,
Starr JM,
Emilsson V,
Plump A,
Lindeman JH,
Hoen PA,
König IR,
Felix JF,
Clarke R,
Hopewell JC,
Ongen H,
Breteler M,
Debette S,
Destefano AL,
Fornage M,
Mitchell GF,
Smith NL,
Holm H,
Stefansson K,
Thorleifsson G,
Thorsteinsdottir U,
Samani NJ,
Preuss M,
Rudan I,
Hayward C,
Deary IJ,
Wichmann HE,
Raitakari OT,
Palmas W,
Kooner JS,
Stolk RP,
Jukema JW,
Wright AF,
Boomsma DI,
Bandinelli S,
Gyllensten UB,
Wilson JF,
Ferrucci L,
Schmidt R,
Farrall M,
Spector TD,
Palmer LJ,
Tuomilehto J,
Pfeufer A,
Gasparini P,
Siscovick D,
Altshuler D,
Loos RJ,
Toniolo D,
Snieder H,
Gieger C,
Meneton P,
Wareham NJ,
Oostra BA,
Metspalu A,
Launer L,
Rettig R,
Strachan DP,
Beckmann JS,
Witteman JC,
Erdmann J,
van Dijk KW,
Boerwinkle E,
Boehnke M,
Ridker PM,
Jarvelin MR,
Chakravarti A,
Abecasis GR,
Gudnason V,
Newton-Cheh C,
Levy D,
Munroe PB,
Psaty BM,
Caulfield MJ,
Rao DC,
Tobin MD,
Elliott P,
van Duijn CM
LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
6 pages
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
Okada Y,
Hirota T,
Kamatani Y,
Takahashi A,
Ohmiya H,
Kumasaka N,
Higasa K,
Yamaguchi-Kabata Y,
Hosono N,
Nalls MA,
Chen MH,
van Rooij FJ
and 19 more — show all
Smith AV,
Tanaka T,
Couper DJ,
Zakai NA,
Ferrucci L,
Longo DL,
Hernandez DG,
Witteman JC,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Tamari M,
Yamamoto K,
Kamatani N
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
Chen P,
Takeuchi F,
Lee JY,
Li H,
Wu JY,
Liang J,
Long J,
Tabara Y,
Goodarzi MO,
Pereira MA,
Kim YJ,
Go MJ
and 59 more — show all
Stram DO,
Vithana E,
Khor CC,
Liu J,
Liao J,
Ye X,
Wang Y,
Lu L,
Young TL,
Lee J,
Thai AC,
Cheng CY,
van Dam RM,
Friedlander Y,
Heng CK,
Koh WP,
Chen CH,
Chang LC,
Pan WH,
Qi Q,
Isono M,
Zheng W,
Zheng W,
Cai Q,
Gao Y,
Yamamoto K,
Ohnaka K,
Takayanagi R,
Kita Y,
Ueshima H,
Hsiung CA,
Cui J,
Sheu WH,
Rotter JI,
Chen YD,
Hsu C,
Okada Y,
Kubo M,
Takahashi A,
Tanaka T,
van Rooij FJ,
Ganesh SK,
Huang J,
Huang T,
Yuan J,
Hwang JY,
Gross MD,
Assimes TL,
Miki T,
Shu XO,
Qi L,
Chen YT,
Lin X,
Aung T,
Wong TY,
Teo YY,
Kim BJ,
Kato N,
Tai ES
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
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
and 32 more — show all
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
3 pages
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
and 81 more — show all
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
3 pages
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
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
and 52 more — show all
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
2 pages
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
Saw J,
Yang ML,
Trinder M,
Tcheandjieu C,
Xu C,
Starovoytov A,
Birt I,
Mathis MR,
Hunker KL,
Schmidt EM,
Jackson L,
Fendrikova-Mahlay N
and 15 more — show all
Zawistowski M,
Brummett CM,
Zoellner S,
Katz A,
Coleman DM,
Swan K,
Swan K,
O'Donnell CJ,
Zhou X,
Li JZ,
Gornik HL,
Assimes TL,
Stanley JC,
Brunham LR,
Ganesh SK
Million Veteran Program
Nature communications · 2020 · PMID 32887874 · open access
1 page
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
Adlam D,
Berrandou TE,
Georges A,
Nelson CP,
Giannoulatou E,
Henry J,
Ma L,
Blencowe M,
Turley TN,
Yang ML,
Chopade S,
Finan C
and 40 more — show all
Braund PS,
Sadeg-Sayoud I,
Iismaa SE,
Kosel ML,
Zhou X,
Hamby SE,
Cheng J,
Liu L,
Tarr I,
Muller DWM,
d'Escamard V,
King A,
Brunham LR,
Baranowska-Clarke AA,
Debette S,
Amouyel P,
Olin JW,
Patil S,
Hesselson SE,
Junday K,
Kanoni S,
Aragam KG,
Butterworth AS,
Tweet MS,
Gulati R,
Combaret N,
Kadian-Dodov D,
Kalman JM,
Fatkin D,
Hingorani AD,
Saw J,
Webb TR,
Hayes SN,
Yang X,
Ganesh SK,
Olson TM,
Kovacic JC,
Graham RM,
Samani NJ,
Bouatia-Naji N
CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia
Nature genetics · 2023 · PMID 37248441 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.