For researchers
Is your paper here?
2,673 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.
83 matches for
Ikram MA,
showing the first 20.
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 association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
Sniekers S,
Stringer S,
Watanabe K,
Jansen PR,
Coleman JRI,
Krapohl E,
Taskesen E,
Hammerschlag AR,
Okbay A,
Zabaneh D,
Amin N,
Breen G
and 18 more — show all
Cesarini D,
Chabris CF,
Iacono WG,
Ikram MA,
Johannesson M,
Koellinger P,
Lee JJ,
Magnusson PKE,
McGue M,
Miller MB,
Ollier WER,
Payton A,
Pendleton N,
Plomin R,
Rietveld CA,
Tiemeier H,
van Duijn CM,
Posthuma D
Nature genetics · 2017 · PMID 28530673 · open access
5 pages
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
Warrington NM,
Shevroja E,
Hemani G,
Hysi PG,
Jiang Y,
Auton A,
Boer CG,
Mangino M,
Wang CA,
Kemp JP,
McMahon G,
Medina-Gomez C
and 18 more — show all
Hickey M,
Trajanoska K,
Wolke D,
Ikram MA,
Montgomery GW,
Felix JF,
Wright MJ,
Mackey DA,
Jaddoe VW,
Martin NG,
Tung JY,
Davey Smith G,
Pennell CE,
Spector TD,
van Meurs J,
Rivadeneira F,
Medland SE,
Evans DM
23andMe Research Team
Human molecular genetics · 2018 · PMID 29659830 · open access
5 pages
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Simcoe M,
Valdes A,
Liu F,
Furlotte NA,
Evans DM,
Hemani G,
Ring SM,
Smith GD,
Duffy DL,
Zhu G,
Gordon SD,
Medland SE
and 32 more — show all
Vuckovic D,
Girotto G,
Sala C,
Catamo E,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt A,
Wu W,
Kraft P,
Hammond CJ,
Shi Y,
Chen Y,
Zeng C,
Klaver CCW,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Han J,
Mackey DA,
Martin NG,
Cheng CY,
Hinds DA,
Spector TD,
Kayser M,
Hysi PG
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Verhaaren BF,
Debette S,
Bis JC,
Smith JA,
Ikram MK,
Adams HH,
Beecham AH,
Rajan KB,
Lopez LM,
Barral S,
van Buchem MA,
van der Grond J
and 90 more — show all
Smith AV,
Hegenscheid K,
Aggarwal NT,
de Andrade M,
Atkinson EJ,
Beekman M,
Beiser AS,
Blanton SH,
Boerwinkle E,
Brickman AM,
Bryan RN,
Chauhan G,
Chen CP,
Chouraki V,
de Craen AJ,
Crivello F,
Deary IJ,
Deelen J,
De Jager PL,
Dufouil C,
Elkind MS,
Evans DA,
Freudenberger P,
Gottesman RF,
Guðnason V,
Habes M,
Heckbert SR,
Heiss G,
Hilal S,
Hofer E,
Hofman A,
Ibrahim-Verbaas CA,
Knopman DS,
Lewis CE,
Liao J,
Liewald DC,
Luciano M,
van der Lugt A,
Martinez OO,
Mayeux R,
Mazoyer B,
Nalls M,
Nauck M,
Niessen WJ,
Oostra BA,
Psaty BM,
Rice KM,
Rotter JI,
von Sarnowski B,
Schmidt H,
Schreiner PJ,
Schuur M,
Sidney SS,
Sigurdsson S,
Slagboom PE,
Stott DJ,
van Swieten JC,
Teumer A,
Töglhofer AM,
Traylor M,
Trompet S,
Turner ST,
Tzourio C,
Uh HW,
Uitterlinden AG,
Vernooij MW,
Wang JJ,
Wong TY,
Wardlaw JM,
Windham BG,
Wittfeld K,
Wolf C,
Wright CB,
Yang Q,
Zhao W,
Zijdenbos A,
Jukema JW,
Sacco RL,
Kardia SL,
Amouyel P,
Mosley TH,
Longstreth WT Jr,
DeCarli CC,
van Duijn CM,
Schmidt R,
Launer LJ,
Grabe HJ,
Seshadri SS,
Ikram MA,
Fornage M
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair
Liu F,
Chen Y,
Zhu G,
Hysi PG,
Wu S,
Adhikari K,
Breslin K,
Pospiech E,
Hamer MA,
Peng F,
Muralidharan C,
Acuna-Alonzo V
and 22 more — show all
Canizales-Quinteros S,
Bedoya G,
Gallo C,
Poletti G,
Rothhammer F,
Bortolini MC,
Gonzalez-Jose R,
Zeng C,
Xu S,
Jin L,
Uitterlinden AG,
Ikram MA,
van Duijn CM,
Nijsten T,
Walsh S,
Branicki W,
Wang S,
Ruiz-Linares A,
Spector TD,
Martin NG,
Medland SE,
Kayser M
Human molecular genetics · 2018 · PMID 29220522 · open access
4 pages
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
de las Fuentes L,
Sung YJ,
Noordam R,
Winkler T,
Feitosa MF,
Schwander K,
Bentley AR,
Brown MR,
Guo X,
Manning A,
Chasman DI,
Aschard H
and 211 more — show all
Bartz TM,
Bielak LF,
Campbell A,
Cheng CY,
Dorajoo R,
Hartwig FP,
Horimoto ARVR,
Li C,
Li-Gao R,
Liu Y,
Marten J,
Musani SK,
Ntalla I,
Rankinen T,
Richard M,
Sim X,
Smith AV,
Tajuddin SM,
Tayo BO,
Vojinovic D,
Warren HR,
Xuan D,
Alver M,
Boissel M,
Chai JF,
Chen X,
Christensen K,
Divers J,
Evangelou E,
Gao C,
Girotto G,
Harris SE,
He M,
Hsu FC,
Kühnel B,
Laguzzi F,
Li X,
Lyytikäinen LP,
Nolte IM,
Poveda A,
Rauramaa R,
Riaz M,
Rueedi R,
Shu XO,
Snieder H,
Sofer T,
Takeuchi F,
Verweij N,
Ware EB,
Weiss S,
Yanek LR,
Amin N,
Arking DE,
Arnett DK,
Bergmann S,
Boerwinkle E,
Brody JA,
Broeckel U,
Brumat M,
Burke G,
Cabrera CP,
Canouil M,
Chee ML,
Chen YI,
Cocca M,
Connell J,
de Silva HJ,
de Vries PS,
Eiriksdottir G,
Faul JD,
Fisher V,
Forrester T,
Fox EF,
Friedlander Y,
Gao H,
Gigante B,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt S,
Ikram MA,
Irvin MR,
Kähönen M,
Kavousi M,
Khor CC,
Kilpeläinen TO,
Koh WP,
Komulainen P,
Kraja AT,
Krieger JE,
Langefeld CD,
Li Y,
Liang J,
Liewald DCM,
Liu CT,
Liu J,
Lohman KK,
Mägi R,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mook-Kanamori DO,
Nalls MA,
Nelson CP,
Norris JM,
O'Connell J,
Ogunniyi A,
Padmanabhan S,
Palmer ND,
Pedersen NL,
Perls T,
Peters A,
Petersmann A,
Peyser PA,
Polasek O,
Porteous DJ,
Raffel LJ,
Rice TK,
Rotter JI,
Rudan I,
Rueda-Ochoa OL,
Sabanayagam C,
Salako BL,
Schreiner PJ,
Shikany JM,
Sidney SS,
Sims M,
Sitlani CM,
Smith JA,
Starr JM,
Strauch K,
Swertz MA,
Teumer A,
Tham YC,
Uitterlinden AG,
Vaidya D,
van der Ende MY,
Waldenberger M,
Wang L,
Wang YX,
Wei WB,
Weir DR,
Wen W,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zhao W,
Zonderman AB,
Becker DM,
Bowden DW,
Deary IJ,
Dörr M,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Jonas JB,
Kammerer CM,
Kato N,
Lakka TA,
Leander K,
Lehtimäki T,
Magnusson PKE,
Marques-Vidal P,
Penninx BWJH,
Samani NJ,
van der Harst P,
Wagenknecht LE,
Wu T,
Zheng W,
Zhu X,
Bouchard C,
Cooper RS,
Correa A,
Evans MK,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Kritchevsky SB,
Levy D,
Palmas WR,
Pereira AC,
Province MM,
Psaty BM,
Ridker PM,
Rotimi CN,
Tai ES,
van Dam RM,
van Duijn CM,
Wong TY,
Rice K,
Gauderman WJ,
Morrison AC,
North KE,
Kardia SLR,
Caulfield MJ,
Elliott P,
Munroe PB,
Franks PW,
Rao DC,
Fornage M
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
and 85 more — show all
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Joshi PK,
Pirastu N,
Kentistou KA,
Fischer K,
Hofer E,
Schraut KE,
Clark DW,
Nutile T,
Barnes CLK,
Timmers PRHJ,
Shen X,
Gandin I
and 101 more — show all
McDaid AF,
Hansen TF,
Gordon SD,
Giulianini F,
Boutin TS,
Abdellaoui A,
Zhao W,
Medina-Gomez C,
Bartz TM,
Trompet S,
Lange LA,
Raffield L,
van der Spek A,
Galesloot TE,
Proitsi P,
Yanek LR,
Bielak LF,
Payton A,
Murgia F,
Concas MP,
Biino G,
Tajuddin SM,
Seppälä I,
Amin N,
Boerwinkle E,
Børglum AD,
Campbell A,
Demerath EW,
Demuth I,
Faul JD,
Ford I,
Gialluisi A,
Gögele M,
Graff M,
Hingorani A,
Hottenga JJ,
Hougaard DM,
Hurme MA,
Ikram MA,
Jylhä M,
Kuh D,
Ligthart L,
Lill CM,
Lindenberger U,
Lumley T,
Mägi R,
Marques-Vidal P,
Medland SE,
Milani L,
Nagy R,
Ollier WER,
Peyser PA,
Pramstaller PP,
Ridker PM,
Rivadeneira F,
Ruggiero D,
Saba Y,
Schmidt R,
Schmidt H,
Slagboom PE,
Smith BH,
Smith JA,
Sotoodehnia N,
Steinhagen-Thiessen E,
van Rooij FJA,
Verbeek AL,
Vermeulen SH,
Vollenweider P,
Wang Y,
Werge T,
Whitfield JB,
Zonderman AB,
Lehtimäki T,
Evans MK,
Pirastu M,
Fuchsberger C,
Bertram L,
Pendleton N,
Kardia SLR,
Ciullo M,
Becker DM,
Wong A,
Psaty BM,
van Duijn CM,
Wilson JG,
Jukema JW,
Kiemeney L,
Uitterlinden AG,
Franceschini N,
North KE,
Weir DR,
Metspalu A,
Boomsma DI,
Hayward C,
Chasman D,
Martin NG,
Sattar N,
Campbell H,
Esko T,
Kutalik Z,
Wilson JF
Nature communications · 2017 · PMID 29030599 · open access
3 pages
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Li S,
Weinstein G,
Zare H,
Teumer A,
Völker U,
Friedrich N,
Knol MJ,
Satizabal CL,
Petyuk VA,
Adams HHH,
Launer LJ,
Bennett DA
and 6 more — show all
Brain communications · 2020 · PMID 33345186 · open access
3 pages
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
Duperron MG,
Knol MJ,
Le Grand Q,
Evans TE,
Mishra A,
Tsuchida A,
Roshchupkin G,
Konuma T,
Trégouët DA,
Romero JR,
Frenzel S,
Luciano M
and 76 more — show all
Hofer E,
Bourgey M,
Dueker ND,
Delgado P,
Hilal S,
Tankard RM,
Dubost F,
Shin J,
Saba Y,
Armstrong NJ,
Bordes C,
Bastin ME,
Beiser A,
Brodaty H,
Bülow R,
Carrera C,
Chen C,
Cheng CY,
Deary IJ,
Gampawar PG,
Himali JJ,
Jiang J,
Kawaguchi T,
Li S,
Macalli M,
Marquis P,
Morris Z,
Muñoz Maniega S,
Miyamoto S,
Okawa M,
Paradise M,
Parva P,
Rundek T,
Sargurupremraj M,
Schilling S,
Setoh K,
Soukarieh O,
Tabara Y,
Teumer A,
Thalamuthu A,
Trollor JN,
Valdés Hernández MC,
Vernooij MW,
Völker U,
Wittfeld K,
Wong TY,
Wright MJ,
Zhang J,
Zhao W,
Zhu YC,
Schmidt H,
Sachdev PS,
Wen W,
Yoshida K,
Joutel A,
Satizabal CL,
Sacco RL,
Bourque G,
Lathrop M,
Paus T,
Fernandez-Cadenas I,
Yang Q,
Mazoyer B,
Boutinaud P,
Okada Y,
Grabe HJ,
Mather KA,
Schmidt R,
Joliot M,
Ikram MA,
Matsuda F,
Tzourio C,
Wardlaw JM,
Seshadri S,
Adams HHH,
Debette S
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
Harlow SD,
Holliday E,
Ikram MA,
Kelly T,
Lakka TA,
Lawlor DA,
Li C,
Liu CT,
Mägi R,
Manning AK,
Matsuda F,
Morrison AC,
Nauck M,
North KE,
Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
and 45 more — show all
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
Taylor KD,
Li X,
Iyengar SK,
Xi Q,
Sivakumaran TA,
Mackey DA,
Macgregor S,
Martin NG,
Young TL,
Bis JC,
Wiggins KL,
Heckbert SR,
Hammond CJ,
Andrew T,
Fahy S,
Attia J,
Holliday EG,
Scott RJ,
Islam FM,
Rotter JI,
McAuley AK,
Boerwinkle E,
Tai ES,
Gudnason V,
Siscovick DS,
Vingerling JR,
Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
2 pages
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Bis JC,
DeCarli C,
Smith AV,
van der Lijn F,
Crivello F,
Fornage M,
Debette S,
Shulman JM,
Schmidt H,
Srikanth V,
Schuur M,
Yu L
and 71 more — show all
Choi SH,
Sigurdsson S,
Verhaaren BF,
DeStefano AL,
Lambert JC,
Jack CR Jr,
Struchalin M,
Stankovich J,
Ibrahim-Verbaas CA,
Fleischman D,
Zijdenbos A,
den Heijer T,
Mazoyer B,
Coker LH,
Enzinger C,
Danoy P,
Amin N,
Arfanakis K,
van Buchem MA,
de Bruijn RF,
Beiser A,
Dufouil C,
Huang J,
Cavalieri M,
Thomson R,
Niessen WJ,
Chibnik LB,
Gislason GK,
Hofman A,
Pikula A,
Pikula A,
Amouyel P,
Freeman KB,
Phan TG,
Oostra BA,
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Wright MJ,
Franke B,
Martin NG,
Thompson PM,
Nalls MA,
Uitterlinden AG,
Au R,
Elbaz A,
Beare RJ,
van Swieten JC,
Lopez OL,
Harris TB,
Chouraki V,
Breteler MM,
De Jager PL,
Becker JT,
Vernooij MW,
Knopman D,
Fazekas F,
Wolf PA,
van der Lugt A,
Gudnason V,
Longstreth WT Jr,
Brown MA,
Bennett DA,
van Duijn CM,
Mosley TH,
Schmidt R,
Tzourio C,
Launer LJ,
Ikram MA,
Seshadri S
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Huang J,
Huffman JE,
Yamakuchi M,
Trompet S,
Asselbergs FW,
Sabater-Lleal M,
Trégouët DA,
Chen WM,
Smith NL,
Kleber ME,
Shin SY,
Becker DM
and 81 more — show all
Tang W,
Dehghan A,
Johnson AD,
Truong V,
Folkersen L,
Yang Q,
Oudot-Mellkah T,
Buckley BM,
Moore JH,
Williams FM,
Campbell H,
Silbernagel G,
Vitart V,
Rudan I,
Tofler GH,
Navis GJ,
Destefano A,
Wright AF,
Chen MH,
de Craen AJ,
Worrall BB,
Rudnicka AR,
Rumley A,
Bookman EB,
Psaty BM,
Chen F,
Keene KL,
Franco OH,
Böhm BO,
Uitterlinden AG,
Carter AM,
Jukema JW,
Sattar N,
Bis JC,
Bis JC,
Ikram MA,
Sale MM,
McKnight B,
Fornage M,
Ford I,
Taylor K,
Slagboom PE,
McArdle WL,
Hsu FC,
Franco-Cereceda A,
Goodall AH,
Yanek LR,
Furie KL,
Cushman M,
Hofman A,
Witteman JC,
Folsom AR,
Basu S,
Matijevic N,
van Gilst WH,
Wilson JF,
Westendorp RG,
Kathiresan S,
Reilly MP,
Tracy RP,
Polasek O,
Winkelmann BR,
Grant PJ,
Hillege HL,
Cambien F,
Stott DJ,
Lowe GD,
Spector TD,
Meigs JB,
Marz W,
Eriksson P,
Becker LC,
Morange PE,
Soranzo N,
Williams SM,
Hayward C,
van der Harst P,
Hamsten A,
Lowenstein CJ,
Strachan DP,
O'Donnell CJ
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
and 142 more — show all
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity
de Vries PS,
Boender J,
Sonneveld MA,
Rivadeneira F,
Ikram MA,
Rottensteiner H,
Hofman A,
Uitterlinden AG,
Leebeek FW,
Franco OH,
Dehghan A,
de Maat MP
Blood · 2015 · PMID 25934476
2 pages
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.