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2,657 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.
6 matches for
Cantor RM.
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher CS,
Mäkinen N,
Harris HR,
Rahmioglu N,
Uimari O,
Cook JP,
Shigesi N,
Ferreira T,
Velez-Edwards DR,
Edwards TL,
Mortlock S,
Ruhioglu Z
and 24 more — show all
Day F,
Becker CM,
Karhunen V,
Martikainen H,
Järvelin MR,
Cantor RM,
Ridker PM,
Terry KL,
Buring JE,
Gordon SD,
Medland SE,
Montgomery GW,
Nyholt DR,
Hinds DA,
Tung JY,
Perry JRB,
Lind PA,
Painter JN,
Martin NG,
Morris AP,
Chasman DI,
Missmer SA,
Zondervan KT,
Morton CC
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
Ko A,
Cantor RM,
Weissglas-Volkov D,
Nikkola E,
Reddy PM,
Sinsheimer JS,
Pasaniuc B,
Brown R,
Alvarez M,
Rodriguez A,
Rodriguez-Guillen R,
Bautista IC
and 19 more — show all
Arellano-Campos O,
Muñoz-Hernández LL,
Salomaa V,
Kaprio J,
Jula A,
Jauhiainen M,
Heliövaara M,
Raitakari O,
Lehtimäki T,
Eriksson JG,
Perola M,
Lohmueller KE,
Matikainen N,
Taskinen MR,
Rodriguez-Torres M,
Riba L,
Tusie-Luna T,
Aguilar-Salinas CA,
Pajukanta P
Nature communications · 2014 · PMID 24886709 · open access
5 pages
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci
Weissglas-Volkov D,
Aguilar-Salinas CA,
Nikkola E,
Deere KA,
Cruz-Bautista I,
Arellano-Campos O,
Muñoz-Hernandez LL,
Gomez-Munguia L,
Ordoñez-Sánchez ML,
Reddy PM,
Lusis AJ,
Matikainen N
and 6 more — show all
Journal of medical genetics · 2013 · PMID 23505323
3 pages
Common variants conferring risk of schizophrenia
Stefansson H,
Ophoff RA,
Steinberg S,
Andreassen OA,
Cichon S,
Rujescu D,
Werge T,
Pietiläinen OP,
Mors O,
Mortensen PB,
Sigurdsson E,
Gustafsson O
and 75 more — show all
Nyegaard M,
Tuulio-Henriksson A,
Ingason A,
Hansen T,
Suvisaari J,
Lonnqvist J,
Paunio T,
Børglum AD,
Hartmann A,
Fink-Jensen A,
Nordentoft M,
Hougaard D,
Norgaard-Pedersen B,
Böttcher Y,
Olesen J,
Breuer R,
Möller HJ,
Giegling I,
Rasmussen HB,
Timm S,
Mattheisen M,
Bitter I,
Réthelyi JM,
Magnusdottir BB,
Sigmundsson T,
Olason P,
Masson G,
Gulcher JR,
Haraldsson M,
Fossdal R,
Thorgeirsson TE,
Thorsteinsdottir U,
Ruggeri M,
Tosato S,
Franke B,
Strengman E,
Kiemeney LA,
Melle I,
Djurovic S,
Abramova L,
Kaleda V,
Sanjuan J,
de Frutos R,
Bramon E,
Vassos E,
Fraser G,
Ettinger U,
Picchioni M,
Walker N,
Toulopoulou T,
Need AC,
Ge D,
Yoon JL,
Shianna KV,
Freimer NB,
Cantor RM,
Murray R,
Kong A,
Golimbet V,
Carracedo A,
Arango C,
Costas J,
Jönsson EG,
Terenius L,
Agartz I,
Petursson H,
Nöthen MM,
Rietschel M,
Matthews PM,
Muglia P,
Peltonen L,
St Clair D,
Goldstein DB,
Stefansson K,
Collier DA
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
and 190 more — show all
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
Meisenzahl E,
Melle I,
Moses EK,
Mühleisen TW,
Nauck M,
Nöthen MM,
Olvera RL,
Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
Royle NA,
Rujescu D,
Savitz J,
Schnack HG,
Schnell K,
Seiferth N,
Smith C,
Steen VM,
Valdés Hernández MC,
Van den Heuvel M,
van der Wee NJ,
Van Haren NE,
Veltman JA,
Völzke H,
Walker R,
Westlye LT,
Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
Djurovic S,
Drevets WC,
Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
Sussmann J,
Toga AW,
Veltman DJ,
Walter H,
Weiner MW,
Bis JC,
Ikram MA,
Smith AV,
Gudnason V,
Tzourio C,
Vernooij MW,
Launer LJ,
DeCarli C,
Seshadri S,
Andreassen OA,
Apostolova LG,
Bastin ME,
Blangero J,
Brunner HG,
Buckner RL,
Cichon S,
Coppola G,
de Zubicaray GI,
Deary IJ,
Donohoe G,
de Geus EJ,
Espeseth T,
Fernández G,
Glahn DC,
Grabe HJ,
Hardy J,
Hulshoff Pol HE,
Jenkinson M,
Kahn RS,
McDonald C,
McIntosh AM,
McMahon FJ,
McMahon KL,
Meyer-Lindenberg A,
Morris DW,
Müller-Myhsok B,
Nichols TE,
Ophoff RA,
Paus T,
Pausova Z,
Penninx BW,
Potkin SG,
Sämann PG,
Saykin AJ,
Schumann G,
Smoller JW,
Wardlaw JM,
Weale ME,
Martin NG,
Franke B,
Wright MJ,
Thompson PM
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid
Luykx JJ,
Bakker SC,
Lentjes E,
Neeleman M,
Strengman E,
Mentink L,
DeYoung J,
de Jong S,
Sul JH,
Eskin E,
van Eijk K,
van Setten J
and 12 more — show all
Buizer-Voskamp JE,
Cantor RM,
Lu A,
van Amerongen M,
van Dongen EP,
Keijzers P,
Kappen T,
Borgdorff P,
Bruins P,
Derks EM,
Kahn RS,
Ophoff RA
Molecular psychiatry · 2014 · PMID 23319000
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.