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.
3 matches for
Lemmens R.
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
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
and 55 more — show all
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies
Traylor M,
Persyn E,
Tomppo L,
Klasson S,
Abedi V,
Bakker MK,
Torres N,
Li L,
Bell S,
Rutten-Jacobs L,
Tozer DJ,
Griessenauer CJ
and 29 more — show all
Zhang Y,
Pedersen A,
Sharma P,
Jimenez-Conde J,
Rundek T,
Grewal RP,
Lindgren A,
Meschia JF,
Salomaa V,
Havulinna A,
Kourkoulis C,
Crawford K,
Marini S,
Mitchell BD,
Kittner SJ,
Rosand J,
Dichgans M,
Jern C,
Strbian D,
Fernandez-Cadenas I,
Zand R,
Ruigrok Y,
Rost N,
Lemmens R,
Rothwell PM,
Anderson CD,
Wardlaw J,
Lewis CM,
Markus HS
Helsinki Stroke, Study Dutch Parelsnoer Institute-Cerebrovascular Accident (CVA) Study Group · National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network and 2 more consortia
The Lancet. Neurology · 2021 · PMID 33773637 · 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.