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Is your paper here?
2,675 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.
5 matches for
Young E.
Discovery and refinement of loci associated with lipid levels
Willer CJ,
Schmidt EM,
Sengupta S,
Peloso GM,
Gustafsson S,
Kanoni S,
Ganna A,
Chen J,
Buchkovich ML,
Mora S,
Beckmann JS,
Bragg-Gresham JL
and 247 more — show all
Chang HY,
Demirkan A,
Den Hertog HM,
Do R,
Donnelly LA,
Ehret GB,
Esko T,
Feitosa MF,
Ferreira T,
Fischer K,
Fontanillas P,
Fraser RM,
Freitag DF,
Gurdasani D,
Heikkilä K,
Hyppönen E,
Isaacs A,
Jackson AU,
Johansson Å,
Johnson T,
Kaakinen M,
Kettunen J,
Kleber ME,
Li X,
Luan J,
Lyytikäinen LP,
Magnusson PKE,
Mangino M,
Mihailov E,
Montasser ME,
Müller-Nurasyid M,
Nolte IM,
O'Connell JR,
Palmer CD,
Perola M,
Petersen AK,
Sanna S,
Saxena R,
Service SK,
Shah S,
Shungin D,
Sidore C,
Song C,
Strawbridge RJ,
Surakka I,
Tanaka T,
Teslovich TM,
Thorleifsson G,
Van den Herik EG,
Voight BF,
Volcik KA,
Waite LL,
Wong A,
Wu Y,
Zhang W,
Absher D,
Asiki G,
Barroso I,
Been LF,
Bolton JL,
Bonnycastle LL,
Brambilla P,
Burnett MS,
Cesana G,
Dimitriou M,
Doney ASF,
Döring A,
Elliott P,
Epstein SE,
Ingi Eyjolfsson G,
Gigante B,
Goodarzi MO,
Grallert H,
Gravito ML,
Groves CJ,
Hallmans G,
Hartikainen AL,
Hayward C,
Hernandez D,
Hicks AA,
Holm H,
Hung YJ,
Illig T,
Jones MR,
Kaleebu P,
Kastelein JJP,
Khaw KT,
Kim E,
Klopp N,
Komulainen P,
Kumari M,
Langenberg C,
Lehtimäki T,
Lin SY,
Lindström J,
Loos RJF,
Mach F,
McArdle WL,
Meisinger C,
Mitchell BD,
Müller G,
Nagaraja R,
Narisu N,
Nieminen TVM,
Nsubuga RN,
Olafsson I,
Ong KK,
Palotie A,
Papamarkou T,
Pomilla C,
Pouta A,
Rader DJ,
Reilly MP,
Ridker PM,
Rivadeneira F,
Rudan I,
Ruokonen A,
Samani N,
Scharnagl H,
Seeley J,
Silander K,
Stančáková A,
Stirrups K,
Swift AJ,
Tiret L,
Uitterlinden AG,
van Pelt LJ,
Vedantam S,
Wainwright N,
Wijmenga C,
Wild SH,
Willemsen G,
Wilsgaard T,
Wilson JF,
Young EH,
Zhao JH,
Adair LS,
Arveiler D,
Assimes TL,
Bandinelli S,
Bennett F,
Bochud M,
Boehm BO,
Boomsma DI,
Borecki IB,
Bornstein SR,
Bovet P,
Burnier M,
Campbell H,
Chakravarti A,
Chambers JC,
Chen YI,
Collins FS,
Cooper RS,
Danesh J,
Dedoussis G,
de Faire U,
Feranil AB,
Ferrières J,
Ferrucci L,
Freimer NB,
Gieger C,
Groop LC,
Gudnason V,
Gyllensten U,
Hamsten A,
Harris TB,
Hingorani A,
Hirschhorn JN,
Hofman A,
Hovingh GK,
Hsiung CA,
Humphries SE,
Hunt SC,
Hveem K,
Iribarren C,
Järvelin MR,
Jula A,
Kähönen M,
Kaprio J,
Kesäniemi A,
Kivimaki M,
Kooner JS,
Koudstaal PJ,
Krauss RM,
Kuh D,
Kuusisto J,
Kyvik KO,
Laakso M,
Lakka TA,
Lind L,
Lindgren CM,
Martin NG,
März W,
McCarthy MI,
McKenzie CA,
Meneton P,
Metspalu A,
Moilanen L,
Morris AD,
Munroe PB,
Njølstad I,
Pedersen NL,
Power C,
Pramstaller PP,
Price JF,
Psaty BM,
Quertermous T,
Rauramaa R,
Saleheen D,
Salomaa V,
Sanghera DK,
Saramies J,
Schwarz PEH,
Sheu WH,
Shuldiner AR,
Siegbahn A,
Spector TD,
Stefansson K,
Strachan DP,
Tayo BO,
Tremoli E,
Tuomilehto J,
Uusitupa M,
van Duijn CM,
Vollenweider P,
Wallentin L,
Wareham NJ,
Whitfield JB,
Wolffenbuttel BHR,
Ordovas JM,
Boerwinkle E,
Palmer CNA,
Thorsteinsdottir U,
Chasman DI,
Rotter JI,
Franks PW,
Ripatti S,
Cupples LA,
Sandhu MS,
Rich SS,
Boehnke M,
Deloukas P,
Kathiresan S,
Mohlke KL,
Ingelsson E,
Abecasis GR
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
and 39 more — show all
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
Yin X,
Chan LS,
Bose D,
Jackson AU,
VandeHaar P,
Locke AE,
Fuchsberger C,
Stringham HM,
Welch R,
Yu K,
Fernandes Silva L,
Service SK
and 25 more — show all
Zhang D,
Hector EC,
Young E,
Ganel L,
Das I,
Abel H,
Erdos MR,
Bonnycastle LL,
Kuusisto J,
Stitziel NO,
Hall IM,
Wagner GR,
Kang J,
Morrison J,
Burant CF,
Collins FS,
Ripatti S,
Palotie A,
Freimer NB,
Mohlke KL,
Scott LJ,
Wen X,
Fauman EB,
Laakso M,
Boehnke M
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Gurdasani D,
Carstensen T,
Fatumo S,
Chen G,
Franklin CS,
Prado-Martinez J,
Bouman H,
Abascal F,
Haber M,
Tachmazidou I,
Mathieson I,
Ekoru K
and 45 more — show all
DeGorter MK,
Nsubuga RN,
Finan C,
Wheeler E,
Chen L,
Cooper DN,
Schiffels S,
Chen Y,
Ritchie GRS,
Pollard MO,
Fortune MD,
Mentzer AJ,
Garrison E,
Bergström A,
Hatzikotoulas K,
Adeyemo A,
Doumatey A,
Elding H,
Wain LV,
Ehret G,
Auer PL,
Kooperberg CL,
Reiner AP,
Franceschini N,
Maher D,
Montgomery SB,
Kadie C,
Widmer C,
Xue Y,
Seeley J,
Asiki G,
Kamali A,
Young EH,
Pomilla C,
Soranzo N,
Zeggini E,
Pirie F,
Morris AP,
Heckerman D,
Tyler-Smith C,
Motala AA,
Rotimi C,
Kaleebu P,
Barroso I,
Sandhu MS
Cell · 2019 · PMID 31675503
6 pages
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Waterworth DM,
Ricketts SL,
Song K,
Chen L,
Zhao JH,
Ripatti S,
Aulchenko YS,
Zhang W,
Yuan X,
Lim N,
Luan J,
Ashford S
and 54 more — show all
Wheeler E,
Young EH,
Hadley D,
Thompson JR,
Braund PS,
Johnson T,
Struchalin M,
Surakka I,
Luben R,
Khaw KT,
Rodwell SA,
Loos RJ,
Boekholdt SM,
Inouye M,
Deloukas P,
Elliott P,
Schlessinger D,
Sanna S,
Scuteri A,
Jackson A,
Mohlke KL,
Tuomilehto J,
Roberts R,
Stewart A,
Kesäniemi YA,
Mahley RW,
Grundy SM,
McArdle W,
Cardon L,
Waeber G,
Vollenweider P,
Chambers JC,
Boehnke M,
Abecasis GR,
Salomaa V,
Järvelin MR,
Ruokonen A,
Barroso I,
Epstein SE,
Hakonarson HH,
Rader DJ,
Reilly MP,
Witteman JC,
Hall AS,
Samani NJ,
Strachan DP,
Barter P,
van Duijn CM,
Kooner JS,
Peltonen L,
Wareham NJ,
McPherson R,
Mooser V,
Sandhu MS
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
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.