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2,663 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
8 matches for
van de Vegte YJ.
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
and 175 more — show all
Hayward C,
Marten J,
Cranley JJ,
Concas MP,
Gasparini P,
Boutin T,
Kolcic I,
Polasek O,
Rudan I,
Araujo NM,
Lima-Costa MF,
Ribeiro ALP,
Souza RP,
Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
Foco L,
Gögele M,
Hicks AA,
Cook JP,
Lind L,
Lindgren CM,
Sundström J,
Nelson CP,
Riaz MB,
Samani NJ,
Sinagra G,
Ulivi S,
Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
Montasser ME,
O'Connell JR,
Ryan K,
Shuldiner AR,
Aeschbacher S,
Conen D,
Risch L,
Thériault S,
Hutri-Kähönen N,
Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
Kääb S,
Schramm K,
Sinner MF,
Strauch K,
Cutler MJ,
Fatkin D,
London B,
Olesen M,
Roden DM,
Benjamin Shoemaker M,
Gustav Smith J,
Biggs ML,
Bis JC,
Brody JA,
Psaty BM,
Rice K,
Sotoodehnia N,
De Grandi A,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Ford I,
Wouter Jukema J,
Macfarlane PW,
Trompet S,
Dörr M,
Felix SB,
Völker U,
Weiss S,
Havulinna AS,
Jula A,
Sääksjärvi K,
Salomaa V,
Guo X,
Heckbert SR,
Lin HJ,
Rotter JI,
Taylor KD,
Yao J,
de Mutsert R,
Maan AC,
Mook-Kanamori DO,
Noordam R,
Cucca F,
Ding J,
Lakatta EG,
Qian Y,
Tarasov KV,
Levy D,
Lin H,
Newton-Cheh CH,
Lunetta KL,
Murray AD,
Porteous DJ,
Smith BH,
Stricker BH,
Uitterlinden A,
van den Berg ME,
Haessler J,
Jackson RD,
Kooperberg C,
Peters U,
Reiner AP,
Whitsel EA,
Alonso A,
Arking DE,
Boerwinkle E,
Ehret GB,
Soliman EZ,
Avery CL,
Gogarten SM,
Kerr KF,
Laurie CC,
Seyerle AA,
Stilp A,
Assa S,
Abdullah Said M,
Yldau van der Ende M,
Lambiase PD,
Orini M,
Ramirez J,
Van Duijvenboden S,
Arnar DO,
Gudbjartsson DF,
Holm H,
Sulem P,
Thorleifsson G,
Thorolfsdottir RB,
Thorsteinsdottir U,
Benjamin EJ,
Tinker A,
Stefansson K,
Ellinor PT,
Jamshidi Y,
Lubitz SA,
Munroe PB
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
and 60 more — show all
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration-Brief Report
Said MA,
Yeung MW,
van de Vegte YJ,
Benjamins JW,
Dullaart RPF,
Ruotsalainen S,
Ripatti S,
Natarajan P,
Juarez-Orozco LE,
Verweij N,
van der Harst P
Arteriosclerosis, thrombosis, and vascular biology · 2021 · PMID 33730874
3 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.