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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.
5 matches for
Rye D.
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
Bachmann CG,
Kemlink D,
Sonka K
and 55 more — show all
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek ZK,
Ibrahim A,
Bergmann M,
Kittke V,
Harrer P,
Dowsett J,
Chenini S,
Ostrowski SR,
Sørensen E,
Erikstrup C,
Pedersen OB,
Topholm Bruun M,
Nielsen KR,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Burchell B,
Furlotte NA,
Nandakumar P,
Earley CJ,
Ondo WG,
Xiong L,
Desautels A,
Perola M,
Vodicka P,
Dina C,
Stoll M,
Franke A,
Lieb W,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rye DB,
Rouleau GA,
Berger K,
Stefansson H,
Ullum H,
Stefansson K,
Hinds DA,
Di Angelantonio E,
Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
12 pages+
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Skuladottir AT,
Stefansdottir L,
Halldorsson GH,
Stefansson OA,
Bjornsdottir A,
Jonsson P,
Palmadottir V,
Thorgeirsson TE,
Walters GB,
Gisladottir RS,
Bjornsdottir G,
Jonsdottir GA
and 20 more — show all
Sulem P,
Gudbjartsson DF,
Knowlton KU,
Jones DA,
Ottas A,
Pedersen OB,
Didriksen M,
Brunak S,
Banasik K,
Hansen TF,
Erikstrup C,
Haavik J,
Andreassen OA,
Rye D,
Igland J,
Ostrowski SR,
Milani LA,
Nadauld LD,
Stefansson H,
Stefansson K
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
7 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
A genetic risk factor for periodic limb movements in sleep
Stefansson H,
Rye DB,
Hicks A,
Petursson H,
Ingason A,
Thorgeirsson TE,
Palsson S,
Sigmundsson T,
Sigurdsson AP,
Eiriksdottir I,
Soebech E,
Bliwise D
and 14 more — show all
Beck JM,
Rosen A,
Waddy S,
Trotti LM,
Iranzo A,
Thambisetty M,
Hardarson GA,
Kristjansson K,
Gudmundsson LJ,
Thorsteinsdottir U,
Kong A,
Gulcher JR,
Gudbjartsson D,
Stefansson K
The New England journal of medicine · 2007 · PMID 17634447
1 page
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Didriksen M,
Nawaz MS,
Dowsett J,
Bell S,
Erikstrup C,
Pedersen OB,
Sørensen E,
Jennum PJ,
Burgdorf KS,
Burchell B,
Butterworth AS,
Soranzo N
and 22 more — show all
Rye DB,
Trotti LM,
Saini P,
Stefansdottir L,
Magnusson SH,
Thorleifsson G,
Sigmundsson T,
Sigurdsson AP,
Van Den Hurk K,
Quee F,
Tanck MWT,
Ouwehand WH,
Roberts DJ,
Earley EJ,
Busch MP,
Mast AE,
Page GP,
Danesh J,
Di Angelantonio E,
Stefansson H,
Ullum H,
Stefansson K
Communications biology · 2020 · PMID 33239738 · 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.