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.
90 matches for
Smith J,
showing the first 20.
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Gudmundsson J,
Sulem P,
Rafnar T,
Bergthorsson JT,
Manolescu A,
Gudbjartsson D,
Agnarsson BA,
Sigurdsson A,
Benediktsdottir KR,
Blondal T,
Jakobsdottir M,
Stacey SN
and 59 more — show all
Kostic J,
Kristinsson KT,
Birgisdottir B,
Ghosh S,
Magnusdottir DN,
Thorlacius S,
Thorleifsson G,
Zheng SL,
Sun J,
Chang BL,
Elmore JB,
Breyer JP,
McReynolds KM,
Bradley KM,
Yaspan BL,
Wiklund F,
Stattin P,
Lindström S,
Adami HO,
McDonnell SK,
Schaid DJ,
Cunningham JM,
Wang L,
Cerhan JR,
St Sauver JL,
Isaacs SD,
Wiley KE,
Partin AW,
Walsh PC,
Polo S,
Ruiz-Echarri M,
Navarrete S,
Fuertes F,
Saez B,
Godino J,
Weijerman PC,
Swinkels DW,
Aben KK,
Witjes JA,
Suarez BK,
Helfand BT,
Frigge ML,
Kristjansson K,
Ober C,
Jonsson E,
Einarsson GV,
Xu J,
Gronberg H,
Smith JR,
Thibodeau SN,
Isaacs WB,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Barkardottir RB,
Gulcher JR,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2008 · PMID 18264098
3 pages
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Blondal T,
Gylfason A,
Agnarsson BA,
Benediktsdottir KR,
Magnusdottir DN,
Orlygsdottir G,
Jakobsdottir M,
Stacey SN,
Sigurdsson A
and 32 more — show all
Wahlfors T,
Tammela T,
Breyer JP,
McReynolds KM,
Bradley KM,
Saez B,
Godino J,
Navarrete S,
Fuertes F,
Murillo L,
Polo E,
Aben KK,
van Oort IM,
Suarez BK,
Helfand BT,
Kan D,
Zanon C,
Frigge ML,
Kristjansson K,
Gulcher JR,
Einarsson GV,
Jonsson E,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Smith JR,
Schleutker J,
Barkardottir RB,
Kong A,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2009 · PMID 19767754
3 pages
Genome-wide association of lipid-lowering response to statins in combined study populations
Barber MJ,
Mangravite LM,
Hyde CL,
Chasman DI,
Smith JD,
McCarty CA,
Li X,
Wilke RA,
Rieder MJ,
Williams PT,
Ridker PM,
Chatterjee A
and 4 more — show all
PloS one · 2010 · PMID 20339536 · open access
3 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
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
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
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
Fernández-Rhodes L,
Graff M,
Buchanan VL,
Justice AE,
Highland HM,
Guo X,
Zhu W,
Chen HH,
Young KL,
Adhikari K,
Palmer ND,
Below JE
and 104 more — show all
Bradfield J,
Pereira AC,
Glover L,
Kim D,
Lilly AG,
Shrestha P,
Thomas AG,
Zhang X,
Chen M,
Chiang CWK,
Pulit S,
Horimoto A,
Krieger JE,
Guindo-Martínez M,
Preuss M,
Schumann C,
Smit RAJ,
Torres-Mejía G,
Acuña-Alonzo V,
Bedoya G,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
González-José R,
Poletti G,
Rothhammer F,
Hakonarson H,
Igo R,
Adler SG,
Iyengar SK,
Nicholas SB,
Gogarten SM,
Isasi CR,
Papnicolaou G,
Stilp AM,
Qi Q,
Kho M,
Smith JA,
Langefeld CD,
Wagenknecht L,
Mckean-Cowdin R,
Gao XR,
Nousome D,
Conti DV,
Feng Y,
Allison MA,
Arzumanyan Z,
Buchanan TA,
Ida Chen YD,
Genter PM,
Goodarzi MO,
Hai Y,
Hsueh W,
Ipp E,
Kandeel FR,
Lam K,
Li X,
Nadler JL,
Raffel LJ,
Roll K,
Sandow K,
Tan J,
Taylor KD,
Xiang AH,
Yao J,
Audirac-Chalifour A,
de Jesus Peralta Romero J,
Hartwig F,
Horta B,
Blangero J,
Curran JE,
Duggirala R,
Lehman DE,
Puppala S,
Fejerman L,
John EM,
Aguilar-Salinas C,
Burtt NP,
Florez JC,
García-Ortíz H,
González-Villalpando C,
Mercader J,
Orozco L,
Tusié-Luna T,
Blanco E,
Gahagan S,
Cox NJ,
Hanis C,
Butte NF,
Cole SA,
Comuzzie AG,
Voruganti VS,
Rohde R,
Wang Y,
Sofer T,
Ziv E,
Grant SFA,
Ruiz-Linares A,
Rotter JI,
Haiman CA,
Parra EJ,
Cruz M,
Loos RJF,
North KE
HGG advances · 2022 · PMID 35399580 · 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
Genome-wide association studies of the PR interval in African Americans
Smith JG,
Magnani JW,
Palmer C,
Meng YA,
Soliman EZ,
Musani SK,
Kerr KF,
Schnabel RB,
Lubitz SA,
Sotoodehnia N,
Redline S,
Pfeufer A
and 16 more — show all
Müller M,
Evans DS,
Nalls MA,
Liu Y,
Newman AB,
Zonderman AB,
Evans MK,
Deo R,
Ellinor PT,
Paltoo DN,
Newton-Cheh C,
Benjamin EJ,
Mehra R,
Alonso A,
Heckbert SR,
Fox ER
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
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
and 94 more — show all
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
2 pages
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
and 470 more — show all
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Matteini AM,
Tanaka T,
Karasik D,
Atzmon G,
Chou WC,
Eicher JD,
Johnson AD,
Arnold AM,
Callisaya ML,
Davies G,
Evans DS,
Holtfreter B
and 55 more — show all
Lohman K,
Lunetta KL,
Mangino M,
Smith AV,
Smith JA,
Teumer A,
Yu L,
Arking DE,
Buchman AS,
Chibinik LB,
De Jager PL,
Evans DA,
Faul JD,
Garcia ME,
Gillham-Nasenya I,
Gudnason V,
Hofman A,
Hsu YH,
Ittermann T,
Lahousse L,
Liewald DC,
Liu Y,
Lopez L,
Rivadeneira F,
Rotter JI,
Siggeirsdottir K,
Starr JM,
Thomson R,
Tranah GJ,
Uitterlinden AG,
Völker U,
Völzke H,
Weir DR,
Yaffe K,
Zhao W,
Zhuang WV,
Zmuda JM,
Bennett DA,
Cummings SR,
Deary IJ,
Ferrucci L,
Harris TB,
Kardia SL,
Kocher T,
Kritchevsky SB,
Psaty BM,
Seshadri S,
Spector TD,
Srikanth VK,
Windham BG,
Zillikens MC,
Newman AB,
Walston JD,
Kiel DP,
Murabito JM
Aging cell · 2016 · PMID 27325353 · open access
2 pages
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
and 76 more — show all
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
2 pages
Genome-wide analysis yields new loci associating with aortic valve stenosis
Helgadottir A,
Thorleifsson G,
Gretarsdottir S,
Stefansson OA,
Tragante V,
Thorolfsdottir RB,
Jonsdottir I,
Bjornsson T,
Steinthorsdottir V,
Verweij N,
Nielsen JB,
Zhou W
and 34 more — show all
Folkersen L,
Martinsson A,
Heydarpour M,
Prakash S,
Oskarsson G,
Gudbjartsson T,
Geirsson A,
Olafsson I,
Sigurdsson EL,
Almgren P,
Melander O,
Franco-Cereceda A,
Hamsten A,
Fritsche L,
Lin M,
Yang B,
Hornsby W,
Guo D,
Brummett CM,
Abecasis G,
Mathis M,
Milewicz D,
Body SC,
Eriksson P,
Willer CJ,
Hveem K,
Newton-Cheh C,
Smith JG,
Danielsen R,
Thorgeirsson G,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
Nature communications · 2018 · PMID 29511194 · open access
2 pages
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
and 77 more — show all
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
2 pages
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
2 pages
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Rajabli F,
Benchek P,
Tosto G,
Kushch N,
Sha J,
Bazemore K,
Zhu C,
Lee WP,
Haut J,
Hamilton-Nelson KL,
Wheeler NR,
Zhao Y
and 274 more — show all
Farrell JJ,
Grunin MA,
Leung YY,
Kuksa PP,
Li D,
da Fonseca EL,
Mez JB,
Palmer EL,
Pillai J,
Sherva RM,
Song YE,
Zhang X,
Ikeuchi T,
Iqbal T,
Pathak O,
Valladares O,
Reyes-Dumeyer D,
Kuzma AB,
Abner E,
Adams LD,
Adams PM,
Aguirre A,
Albert MS,
Albin RL,
Allen M,
Alvarez L,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Auerbach S,
Ayres G,
Baldwin CT,
Barber RC,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Beecham GW,
Beekly D,
Benitez BA,
Bennett D,
Bertelson J,
Bird TD,
Blacker D,
Boeve BF,
Bowen JD,
Boxer A,
Brewer J,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cantwell LB,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Chasse S,
Chesselet MF,
Chin NA,
Chui HC,
Chung J,
Craft S,
Crane PK,
Cribbs DH,
Crocco EA,
Cruchaga C,
Cuccaro ML,
Cullum M,
Darby E,
Davis B,
De Jager PL,
DeCarli C,
DeToledo J,
Dick M,
Dickson DW,
Dombroski BA,
Doody RS,
Duara R,
Ertekin-Taner N,
Evans DA,
Faber KM,
Fairchild TJ,
Fallon KB,
Fardo DW,
Farlow MR,
Fernandez-Hernandez V,
Ferris S,
Friedland RP,
Foroud TM,
Frosch MP,
Fulton-Howard B,
Galasko DR,
Gamboa A,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Go RCP,
Goate AM,
Grabowski TJ,
Graff-Radford NR,
Green RC,
Growdon JH,
Hakonarson H,
Hall J,
Hamilton RL,
Harari O,
Hardy J,
Harrell LE,
Head E,
Henderson VW,
Hernandez M,
Hohman T,
Honig LS,
Huebinger RM,
Huentelman MJ,
Hulette CM,
Hyman BT,
Hynan LS,
Ibanez L,
Jarvik GP,
Jayadev S,
Jin LW,
Johnson K,
Johnson L,
Kamboh MI,
Karydas AM,
Katz MJ,
Kauwe JS,
Kaye JA,
Keene CD,
Khaleeq A,
Kikuchi M,
Kim R,
Knebl J,
Kowall NW,
Kramer JH,
Kukull WA,
LaFerla FM,
Lah JJ,
Larson EB,
Lerner A,
Leverenz JB,
Levey AI,
Lieberman AP,
Lipton RB,
Logue M,
Lopez OL,
Lunetta KL,
Lyketsos CG,
Mains D,
Margaret FE,
Marson DC,
Martin ER,
Martiniuk F,
Mash DC,
Masliah E,
Massman P,
Masurkar A,
McCormick WC,
McCurry SM,
McDavid AN,
McDonough S,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Montine TJ,
Monuki ES,
Morris JC,
Mukherjee S,
Myers AJ,
Nguyen T,
Obisesan T,
O'Bryant S,
Olichney JM,
Ory M,
Palmer R,
Parisi JE,
Paulson HL,
Pavlik V,
Paydarfar D,
Perez V,
Peskind E,
Petersen RC,
Petrovitch H,
Pierce A,
Polk M,
Poon WW,
Potter H,
Qu L,
Quiceno M,
Quinn JF,
Raj A,
Raskind M,
Reiman EM,
Reisberg B,
Reisch JS,
Ringman JM,
Roberson ED,
Rodriguear M,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Royall DR,
Sabbagh M,
Sadovnick AD,
Sager MA,
Sano M,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Slifer SH,
Small S,
Smith AG,
Smith JP,
Sonnen JA,
Spina S,
George-Hyslop PS,
Starks TD,
Stern RA,
Stevens AB,
Strittmatter SM,
Sultzer D,
Swerdlow RH,
Tanzi RE,
Tilson JL,
Trojanowski JQ,
Troncoso JC,
Tsolaki M,
Tsuang DW,
Van Deerlin VM,
van Eldik LJ,
Vance JM,
Vardarajan BN,
Vassar R,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Whitehead PL,
Wijsman EM,
Wilhelmsen KC,
Williams B,
Williamson J,
Wilms H,
Wingo TS,
Wisniewski T,
Woltjer RL,
Woon M,
Wright CB,
Wu CK,
Younkin SG,
Yu CE,
Yu L,
Zhu X,
Kunkle BW,
Bush WS,
Miyashita A,
Byrd GS,
Wang LS,
Farrer LA,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Schellenberg GD,
Jun GR,
Reitz C,
Naj AC
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
and 137 more — show all
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study
Sunderland N,
Asselin G,
Henry A,
Nelson CP,
Lemieux Perreault LP,
Asselbergs FW,
Boersma E,
Cappola TP,
Chazara O,
Chutkow W,
Cyr MC,
Gkatzionis A
and 46 more — show all
Gui H,
Haefliger C,
Hedman ÅK,
Hillege H,
Hyde CL,
Kamanu FK,
Kardys I,
Koekemoer AL,
Kraus WE,
Lang CC,
Malarstig A,
Margulies KB,
Marston NA,
Melloni GEM,
Morley MP,
O'Donoghue ML,
Owens AT,
Paul DS,
Tilling K,
van der Harst P,
van Setten J,
van Vugt M,
Verweij N,
Veluchamy A,
Wallentin L,
Wang X,
Xing H,
Yang Y,
White HD,
Zannad F,
Smith JG,
Brunner-La Rocca HP,
Lanfear DE,
Mann DL,
de Denus S,
Tardif JC,
Voors AA,
Samani NJ,
Ellinor PT,
Ruff CT,
Sabatine MS,
Sattar N,
McMurray JJV,
Paternoster L,
Dubé MP,
Lumbers RT
Journal of the American College of Cardiology · 2026 · PMID 42017882 · open access
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.