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Is your paper here?
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.
4 matches for
Cotlarciuc I.
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease
van Meurs JB,
Pare G,
Schwartz SM,
Hazra A,
Tanaka T,
Vermeulen SH,
Cotlarciuc I,
Yuan X,
Mälarstig A,
Bandinelli S,
Bis JC,
Blom H
and 46 more — show all
Brown MJ,
Chen C,
Chen YD,
Clarke RJ,
Dehghan A,
Erdmann J,
Ferrucci L,
Hamsten A,
Hofman A,
Hunter DJ,
Goel A,
Johnson AD,
Kathiresan S,
Kampman E,
Kiel DP,
Kiemeney LA,
Chambers JC,
Kraft P,
Lindemans J,
McKnight B,
Nelson CP,
O'Donnell CJ,
Psaty BM,
Ridker PM,
Rivadeneira F,
Rose LM,
Seedorf U,
Siscovick DS,
Schunkert H,
Selhub J,
Ueland PM,
Vollenweider P,
Waeber G,
Waterworth DM,
Watkins H,
Witteman JC,
den Heijer M,
Jacques P,
Uitterlinden AG,
Kooner JS,
Rader DJ,
Reilly MP,
Mooser V,
Chasman DI,
Samani NJ,
Ahmadi KR
The American journal of clinical nutrition · 2013 · PMID 23824729
8 pages
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
and 96 more — show all
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
Genetic loci influencing kidney function and chronic kidney disease
Chambers JC,
Zhang W,
Lord GM,
van der Harst P,
Lawlor DA,
Sehmi JS,
Gale DP,
Wass MN,
Ahmadi KR,
Bakker SJ,
Beckmann J,
Bilo HJ
and 82 more — show all
Bochud M,
Brown MJ,
Caulfield MJ,
Connell JM,
Cook HT,
Cotlarciuc I,
Davey Smith G,
de Silva R,
Deng G,
Devuyst O,
Dikkeschei LD,
Dimkovic N,
Dockrell M,
Dominiczak A,
Ebrahim S,
Eggermann T,
Farrall M,
Ferrucci L,
Floege J,
Forouhi NG,
Gansevoort RT,
Han X,
Hedblad B,
Homan van der Heide JJ,
Hepkema BG,
Hernandez-Fuentes M,
Hypponen E,
Johnson T,
de Jong PE,
Kleefstra N,
Lagou V,
Lapsley M,
Li Y,
Loos RJ,
Luan J,
Luttropp K,
Maréchal C,
Melander O,
Munroe PB,
Nordfors L,
Parsa A,
Peltonen L,
Penninx BW,
Perucha E,
Pouta A,
Prokopenko I,
Roderick PJ,
Ruokonen A,
Samani NJ,
Sanna S,
Schalling M,
Schlessinger D,
Schlieper G,
Seelen MA,
Shuldiner AR,
Sjögren M,
Smit JH,
Snieder H,
Soranzo N,
Spector TD,
Stenvinkel P,
Sternberg MJ,
Swaminathan R,
Tanaka T,
Ubink-Veltmaat LJ,
Uda M,
Vollenweider P,
Wallace C,
Waterworth D,
Zerres K,
Waeber G,
Wareham NJ,
Maxwell PH,
McCarthy MI,
Jarvelin MR,
Mooser V,
Abecasis GR,
Lightstone L,
Scott J,
Navis G,
Elliott P,
Kooner JS
Nature genetics · 2010 · PMID 20383145
1 page
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
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.