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2,661 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
Nagy R.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Nagy R,
Boutin TS,
Marten J,
Huffman JE,
Kerr SM,
Campbell A,
Evenden L,
Gibson J,
Amador C,
Howard DM,
Navarro P,
Morris A
and 13 more — show all
Deary IJ,
Hocking LJ,
Padmanabhan S,
Smith BH,
Joshi P,
Wilson JF,
Hastie ND,
Wright AF,
McIntosh AM,
Porteous DJ,
Haley CS,
Vitart V,
Hayward C
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Masson G,
He H,
Jonasdottir A,
Sigurdsson A,
Stacey SN,
Johannsdottir H,
Helgadottir HT,
Li W
and 35 more — show all
Nagy R,
Ringel MD,
Kloos RT,
de Visser MC,
Plantinga TS,
den Heijer M,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Walters GB,
Bjarnason H,
Tryggvadottir L,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Olafsson I,
Kristjansson K,
Kristvinsson H,
Magnusson OT,
Thorleifsson G,
Gulcher JR,
Kong A,
Kiemeney LA,
Jonsson T,
Hjartarson H,
Mayordomo JI,
Netea-Maier RT,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2012 · PMID 22267200
3 pages
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
and 106 more — show all
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Joshi PK,
Pirastu N,
Kentistou KA,
Fischer K,
Hofer E,
Schraut KE,
Clark DW,
Nutile T,
Barnes CLK,
Timmers PRHJ,
Shen X,
Gandin I
and 101 more — show all
McDaid AF,
Hansen TF,
Gordon SD,
Giulianini F,
Boutin TS,
Abdellaoui A,
Zhao W,
Medina-Gomez C,
Bartz TM,
Trompet S,
Lange LA,
Raffield L,
van der Spek A,
Galesloot TE,
Proitsi P,
Yanek LR,
Bielak LF,
Payton A,
Murgia F,
Concas MP,
Biino G,
Tajuddin SM,
Seppälä I,
Amin N,
Boerwinkle E,
Børglum AD,
Campbell A,
Demerath EW,
Demuth I,
Faul JD,
Ford I,
Gialluisi A,
Gögele M,
Graff M,
Hingorani A,
Hottenga JJ,
Hougaard DM,
Hurme MA,
Ikram MA,
Jylhä M,
Kuh D,
Ligthart L,
Lill CM,
Lindenberger U,
Lumley T,
Mägi R,
Marques-Vidal P,
Medland SE,
Milani L,
Nagy R,
Ollier WER,
Peyser PA,
Pramstaller PP,
Ridker PM,
Rivadeneira F,
Ruggiero D,
Saba Y,
Schmidt R,
Schmidt H,
Slagboom PE,
Smith BH,
Smith JA,
Sotoodehnia N,
Steinhagen-Thiessen E,
van Rooij FJA,
Verbeek AL,
Vermeulen SH,
Vollenweider P,
Wang Y,
Werge T,
Whitfield JB,
Zonderman AB,
Lehtimäki T,
Evans MK,
Pirastu M,
Fuchsberger C,
Bertram L,
Pendleton N,
Kardia SLR,
Ciullo M,
Becker DM,
Wong A,
Psaty BM,
van Duijn CM,
Wilson JG,
Jukema JW,
Kiemeney L,
Uitterlinden AG,
Franceschini N,
North KE,
Weir DR,
Metspalu A,
Boomsma DI,
Hayward C,
Chasman D,
Martin NG,
Sattar N,
Campbell H,
Esko T,
Kutalik Z,
Wilson JF
Nature communications · 2017 · PMID 29030599 · open access
3 pages
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Sigurdsson A,
Bergthorsson JT,
He H,
Blondal T,
Geller F,
Jakobsdottir M,
Magnusdottir DN,
Matthiasdottir S
and 26 more — show all
Stacey SN,
Skarphedinsson OB,
Helgadottir H,
Li W,
Nagy R,
Aguillo E,
Faure E,
Prats E,
Saez B,
Martinez M,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Kristjansson K,
Frigge ML,
Kristvinsson H,
Gulcher JR,
Jonsson T,
Rafnar T,
Hjartarsson H,
Mayordomo JI,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2009 · PMID 19198613
2 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.