For researchers
Is your paper here?
2,665 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.
8 matches for
McRae AF.
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Xue A,
Wu Y,
Zhu Z,
Zhang F,
Kemper KE,
Zheng Z,
Yengo L,
Lloyd-Jones LR,
Sidorenko J,
Wu Y,
McRae AF,
Visscher PM
and 2 more — show all
eQTLGen Consortium
Nature communications · 2018 · PMID 30054458 · open access
12 pages+
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Borbye-Lorenzen N,
Zhu Z,
Agerbo E,
Albiñana C,
Benros ME,
Bian B,
Børglum AD,
Bulik CM,
Debost JPG,
Grove J,
Hougaard DM,
McRae AF
and 12 more — show all
Mors O,
Mortensen PB,
Musliner KL,
Nordentoft M,
Petersen LV,
Privé F,
Sidorenko J,
Skogstrand K,
Werge T,
Wray NR,
Vilhjálmsson BJ,
McGrath JJ
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults
Hillary RF,
Trejo-Banos D,
Kousathanas A,
McCartney DL,
Harris SE,
Stevenson AJ,
Patxot M,
Ojavee SE,
Zhang Q,
Liewald DC,
Ritchie CW,
Evans KL
and 7 more — show all
Genome medicine · 2020 · PMID 32641083 · open access
7 pages
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Lu AT,
Xue L,
Salfati EL,
Chen BH,
Ferrucci L,
Levy D,
Joehanes R,
Murabito JM,
Kiel DP,
Tsai PC,
Yet I,
Bell JT
and 27 more — show all
Mangino M,
Tanaka T,
McRae AF,
Marioni RE,
Visscher PM,
Wray NR,
Deary IJ,
Levine ME,
Quach A,
Assimes T,
Tsao PS,
Absher D,
Stewart JD,
Li Y,
Reiner AP,
Hou L,
Baccarelli AA,
Whitsel EA,
Aviv A,
Cardona A,
Day FR,
Wareham NJ,
Perry JRB,
Ong KK,
Raj K,
Lunetta KL,
Horvath S
Nature communications · 2018 · PMID 29374233 · open access
6 pages
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
and 180 more — show all
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development
Larsson M,
Duffy DL,
Zhu G,
Liu JZ,
Macgregor S,
McRae AF,
Wright MJ,
Sturm RA,
Mackey DA,
Montgomery GW,
Martin NG,
Medland SE
American journal of human genetics · 2011 · PMID 21835309
2 pages
Common variants in the trichohyalin gene are associated with straight hair in Europeans
Medland SE,
Nyholt DR,
Painter JN,
McEvoy BP,
McRae AF,
Zhu G,
Gordon SD,
Ferreira MA,
Wright MJ,
Henders AK,
Campbell MJ,
Duffy DL
and 6 more — show all
American journal of human genetics · 2009 · PMID 19896111
1 page
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
Mbarek H,
Steinberg S,
Nyholt DR,
Gordon SD,
Miller MB,
McRae AF,
Hottenga JJ,
Day FR,
Willemsen G,
de Geus EJ,
Davies GE,
Martin HC
and 25 more — show all
Penninx BW,
Jansen R,
McAloney K,
Vink JM,
Kaprio J,
Plomin R,
Spector TD,
Magnusson PK,
Reversade B,
Harris RA,
Aagaard K,
Kristjansson RP,
Olafsson I,
Eyjolfsson GI,
Sigurdardottir O,
Iacono WG,
Lambalk CB,
Montgomery GW,
McGue M,
Ong KK,
Perry JRB,
Martin NG,
Stefánsson H,
Stefánsson K,
Boomsma DI
American journal of human genetics · 2016 · PMID 27132594
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.