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2,660 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.
8 matches for
Young WJ.
Genetically Determined Serum Calcium Levels and Markers of Ventricular Repolarization: A Mendelian Randomization Study in the UK Biobank
Young WJ,
Warren HR,
Mook-Kanamori DO,
Ramírez J,
van Duijvenboden S,
Orini M,
Tinker A,
van Heemst D,
Lambiase PD,
Jukema JW,
Munroe PB,
Noordam R
Circulation. Genomic and precision medicine · 2021 · PMID 33887147
12 pages+
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young WJ,
Lahrouchi N,
Isaacs A,
Duong T,
Foco L,
Ahmed F,
Brody JA,
Salman R,
Noordam R,
Benjamins JW,
Haessler J,
Lyytikäinen LP
and 154 more — show all
Repetto L,
Concas MP,
van den Berg ME,
Weiss S,
Baldassari AR,
Bartz TM,
Cook JP,
Evans DS,
Freudling R,
Hines O,
Isaksen JL,
Lin H,
Mei H,
Moscati A,
Müller-Nurasyid M,
Nursyifa C,
Qian Y,
Richmond A,
Roselli C,
Ryan KA,
Tarazona-Santos E,
Thériault S,
van Duijvenboden S,
Warren HR,
Yao J,
Raza D,
Aeschbacher S,
Ahlberg G,
Alonso A,
Andreasen L,
Bis JC,
Boerwinkle E,
Campbell A,
Catamo E,
Cocca M,
Cutler MJ,
Darbar D,
De Grandi A,
De Luca A,
Ding J,
Ellervik C,
Ellinor PT,
Felix SB,
Froguel P,
Fuchsberger C,
Gögele M,
Graff C,
Graff M,
Guo X,
Hansen T,
Heckbert SR,
Huang PL,
Huikuri HV,
Hutri-Kähönen N,
Ikram MA,
Jackson RD,
Junttila J,
Kavousi M,
Kors JA,
Leal TP,
Lemaitre RN,
Lin HJ,
Lind L,
Linneberg A,
Liu S,
MacFarlane PW,
Mangino M,
Meitinger T,
Mezzavilla M,
Mishra PP,
Mitchell RN,
Mononen N,
Montasser ME,
Morrison AC,
Nauck M,
Nauffal V,
Navarro P,
Nikus K,
Pare G,
Patton KK,
Pelliccione G,
Pittman A,
Porteous DJ,
Pramstaller PP,
Preuss MH,
Raitakari OT,
Reiner AP,
Ribeiro ALP,
Rice KM,
Risch L,
Schlessinger D,
Schotten U,
Schurmann C,
Shen X,
Shoemaker MB,
Sinagra G,
Sinner MF,
Soliman EZ,
Stoll M,
Strauch K,
Tarasov K,
Taylor KD,
Tinker A,
Trompet S,
Uitterlinden A,
Völker U,
Völzke H,
Waldenberger M,
Weng LC,
Whitsel EA,
Wilson JG,
Avery CL,
Conen D,
Correa A,
Cucca F,
Dörr M,
Gharib SA,
Girotto G,
Grarup N,
Hayward C,
Jamshidi Y,
Järvelin MR,
Jukema JW,
Kääb S,
Kähönen M,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lima-Costa MF,
Liu Y,
Loos RJF,
Lubitz SA,
Mook-Kanamori DO,
Morris AP,
O'Connell JR,
Olesen MS,
Orini M,
Padmanabhan S,
Pattaro C,
Peters A,
Psaty BM,
Rotter JI,
Stricker B,
van der Harst P,
van Duijn CM,
Verweij N,
Wilson JF,
Arking DE,
Ramirez J,
Lambiase PD,
Sotoodehnia N,
Mifsud B,
Newton-Cheh C,
Munroe PB
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Young WJ,
Haessler J,
Benjamins JW,
Repetto L,
Yao J,
Isaacs A,
Harper AR,
Ramirez J,
Garnier S,
van Duijvenboden S,
Baldassari AR,
Concas MP
and 82 more — show all
Duong T,
Foco L,
Isaksen JL,
Mei H,
Noordam R,
Nursyifa C,
Richmond A,
Santolalla ML,
Sitlani CM,
Soroush N,
Thériault S,
Trompet S,
Aeschbacher S,
Ahmadizar F,
Alonso A,
Brody JA,
Campbell A,
Correa A,
Darbar D,
De Luca A,
Deleuze JF,
Ellervik C,
Fuchsberger C,
Goel A,
Grace C,
Guo X,
Hansen T,
Heckbert SR,
Jackson RD,
Kors JA,
Lima-Costa MF,
Linneberg A,
Macfarlane PW,
Morrison AC,
Navarro P,
Porteous DJ,
Pramstaller PP,
Reiner AP,
Risch L,
Schotten U,
Shen X,
Sinagra G,
Soliman EZ,
Stoll M,
Tarazona-Santos E,
Tinker A,
Trajanoska K,
Villard E,
Warren HR,
Whitsel EA,
Wiggins KL,
Arking DE,
Avery CL,
Conen D,
Girotto G,
Grarup N,
Hayward C,
Jukema JW,
Mook-Kanamori DO,
Olesen MS,
Padmanabhan S,
Psaty BM,
Pattaro C,
Ribeiro ALP,
Rotter JI,
Stricker BH,
van der Harst P,
van Duijn CM,
Verweij N,
Wilson JG,
Orini M,
Charron P,
Watkins H,
Kooperberg C,
Lin HJ,
Wilson JF,
Kanters JK,
Sotoodehnia N,
Mifsud B,
Lambiase PD,
Tereshchenko LG,
Munroe PB
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
and 135 more — show all
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
Genetic basis of right and left ventricular heart shape
Burns R,
Young WJ,
Aung N,
Lopes LR,
Elliott PM,
Syrris P,
Barriales-Villa R,
Sohrabi C,
Petersen SE,
Ramírez J,
Young A,
Munroe PB
Nature communications · 2024 · PMID 39543113 · 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.