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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.
6 matches for
Montplaisir J.
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair B,
Zhao C,
Bell S,
Tilch E,
Salminen AV,
Pütz B,
Dauvilliers Y,
Stefani A,
Högl B,
Poewe W,
Kemlink D,
Sonka K
and 39 more — show all
Bachmann CG,
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek Z,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Allen RP,
Earley CJ,
Ondo WG,
Xiong L,
Montplaisir J,
Gan-Or Z,
Perola M,
Vodicka P,
Dina C,
Franke A,
Tittmann L,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rouleau GA,
Berger K,
Oexle K,
Di Angelantonio E,
Hinds DA,
Müller-Myhsok B,
Winkelmann J
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
10 pages
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
Winkelmann J,
Schormair B,
Lichtner P,
Ripke S,
Xiong L,
Jalilzadeh S,
Fulda S,
Pütz B,
Eckstein G,
Hauk S,
Trenkwalder C,
Zimprich A
and 15 more — show all
Stiasny-Kolster K,
Oertel W,
Bachmann CG,
Paulus W,
Peglau I,
Eisensehr I,
Montplaisir J,
Turecki G,
Rouleau G,
Gieger C,
Illig T,
Wichmann HE,
Holsboer F,
Müller-Myhsok B,
Meitinger T
Nature genetics · 2007 · PMID 17637780
4 pages
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1
Winkelmann J,
Czamara D,
Schormair B,
Knauf F,
Schulte EC,
Trenkwalder C,
Dauvilliers Y,
Polo O,
Högl B,
Berger K,
Fuhs A,
Gross N
and 45 more — show all
Stiasny-Kolster K,
Oertel W,
Bachmann CG,
Paulus W,
Xiong L,
Montplaisir J,
Rouleau GA,
Fietze I,
Vávrová J,
Kemlink D,
Sonka K,
Nevsimalova S,
Lin SC,
Wszolek Z,
Vilariño-Güell C,
Farrer MJ,
Gschliesser V,
Frauscher B,
Falkenstetter T,
Poewe W,
Allen RP,
Earley CJ,
Ondo WG,
Le WD,
Spieler D,
Kaffe M,
Zimprich A,
Kettunen J,
Perola M,
Silander K,
Cournu-Rebeix I,
Francavilla M,
Fontenille C,
Fontaine B,
Vodicka P,
Prokisch H,
Lichtner P,
Peppard P,
Faraco J,
Mignot E,
Gieger C,
Illig T,
Wichmann HE,
Müller-Myhsok B,
Meitinger T
PLoS genetics · 2011 · PMID 21779176 · open access
2 pages
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn L,
Heilbron K,
Blauwendraat C,
Reynolds RH,
Yu E,
Senkevich K,
Rudakou U,
Estiar MA,
Gustavsson EK,
Brolin K,
Ruskey JA,
Freeman K
and 46 more — show all
Asayesh F,
Chia R,
Arnulf I,
Hu MTM,
Montplaisir JY,
Gagnon JF,
Desautels A,
Dauvilliers Y,
Gigli GL,
Valente M,
Janes F,
Bernardini A,
Högl B,
Stefani A,
Ibrahim A,
Šonka K,
Kemlink D,
Oertel W,
Janzen A,
Plazzi G,
Biscarini F,
Antelmi E,
Figorilli M,
Puligheddu M,
Mollenhauer B,
Trenkwalder C,
Sixel-Döring F,
Cochen De Cock V,
Monaca CC,
Heidbreder A,
Ferini-Strambi L,
Dijkstra F,
Viaene M,
Abril B,
Boeve BF,
Scholz SW,
Ryten M,
Bandres-Ciga S,
Noyce A,
Cannon P,
Pihlstrøm L,
Nalls MA,
Singleton AB,
Rouleau GA,
Postuma RB,
Gan-Or Z
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
2 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
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Schormair B,
Kemlink D,
Roeske D,
Eckstein G,
Xiong L,
Lichtner P,
Ripke S,
Trenkwalder C,
Zimprich A,
Stiasny-Kolster K,
Oertel W,
Bachmann CG
and 20 more — show all
Paulus W,
Högl B,
Frauscher B,
Gschliesser V,
Poewe W,
Peglau I,
Vodicka P,
Vávrová J,
Sonka K,
Nevsimalova S,
Montplaisir J,
Turecki G,
Rouleau G,
Gieger C,
Illig T,
Wichmann HE,
Holsboer F,
Müller-Myhsok B,
Meitinger T,
Winkelmann J
Nature genetics · 2008 · PMID 18660810
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.