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Is your paper here?
2,673 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.
9 matches for
Ross OA.
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+
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 in essential tremor identifies three new loci
Müller SH,
Girard SL,
Hopfner F,
Merner ND,
Bourassa CV,
Lorenz D,
Clark LN,
Tittmann L,
Soto-Ortolaza AI,
Klebe S,
Hallett M,
Schneider SA
and 37 more — show all
Hodgkinson CA,
Lieb W,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Poewe W,
Ortega-Cubero S,
Seppi K,
Rajput A,
Hussl A,
Rajput AH,
Berg D,
Dion PA,
Wurster I,
Shulman JM,
Srulijes K,
Haubenberger D,
Pastor P,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Ladwig KH,
Dupré N,
Jankovic J,
Strauch K,
Panisset M,
Winkelmann J,
Testa CM,
Reischl E,
Zeuner KE,
Ross OA,
Arzberger T,
Chouinard S,
Deuschl G,
Louis ED,
Kuhlenbäumer G,
Rouleau GA
Brain : a journal of neurology · 2016 · PMID 27797806 · open access
4 pages
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Deelen J,
Beekman M,
Uh HW,
Broer L,
Ayers KL,
Tan Q,
Kamatani Y,
Bennet AM,
Tamm R,
Trompet S,
Guðbjartsson DF,
Flachsbart F
and 75 more — show all
Rose G,
Viktorin A,
Fischer K,
Nygaard M,
Cordell HJ,
Crocco P,
van den Akker EB,
Böhringer S,
Helmer Q,
Nelson CP,
Saunders GI,
Alver M,
Andersen-Ranberg K,
Breen ME,
van der Breggen R,
Caliebe A,
Capri M,
Cevenini E,
Collerton JC,
Dato S,
Davies K,
Ford I,
Gampe J,
Garagnani P,
de Geus EJ,
Harrow J,
van Heemst D,
Heijmans BT,
Heinsen FA,
Hottenga JJ,
Hofman A,
Jeune B,
Jonsson PV,
Lathrop M,
Lechner D,
Martin-Ruiz C,
Mcnerlan SE,
Mihailov E,
Montesanto A,
Mooijaart SP,
Murphy A,
Nohr EA,
Paternoster L,
Postmus I,
Rivadeneira F,
Ross OA,
Salvioli S,
Sattar N,
Schreiber S,
Stefánsson H,
Stott DJ,
Tiemeier H,
Uitterlinden AG,
Westendorp RG,
Willemsen G,
Samani NJ,
Galan P,
Sørensen TI,
Boomsma DI,
Jukema JW,
Rea IM,
Passarino G,
de Craen AJ,
Christensen K,
Nebel A,
Stefánsson K,
Metspalu A,
Magnusson P,
Blanché H,
Christiansen L,
Kirkwood TB,
van Duijn CM,
Franceschi C,
Houwing-Duistermaat JJ,
Slagboom PE
Human molecular genetics · 2014 · PMID 24688116 · open access
2 pages
Identification of genetic modifiers of age-at-onset for familial Parkinson's disease
Hill-Burns EM,
Ross OA,
Wissemann WT,
Soto-Ortolaza AI,
Zareparsi S,
Siuda J,
Lynch T,
Wszolek ZK,
Silburn PA,
Mellick GD,
Ritz B,
Scherzer CR
and 4 more — show all
Human molecular genetics · 2016 · PMID 27402877 · open access
2 pages
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Wang H,
Chang TS,
Dombroski BA,
Cheng PL,
Patil V,
Valiente-Banuet L,
Farrell K,
Mclean C,
Molina-Porcel L,
Rajput A,
De Deyn PP,
Le Bastard N
and 49 more — show all
Gearing M,
Kaat LD,
Van Swieten JC,
Dopper E,
Ghetti BF,
Newell KL,
Troakes C,
de Yébenes JG,
Rábano-Gutierrez A,
Meller T,
Oertel WH,
Respondek G,
Stamelou M,
Arzberger T,
Roeber S,
Müller U,
Hopfner F,
Pastor P,
Brice A,
Durr A,
Le Ber I,
Beach TG,
Serrano GE,
Hazrati LN,
Litvan I,
Rademakers R,
Ross OA,
Galasko D,
Boxer AL,
Miller BL,
Seeley WW,
Van Deerlin VM,
Lee EB,
White CL 3rd,
Morris H,
de Silva R,
Crary JF,
Goate AM,
Friedman JS,
Leung YY,
Coppola G,
Naj AC,
Wang LS,
Dalgard C,
Dickson DW,
Höglinger GU,
Schellenberg GD,
Geschwind DH,
Lee WP
P. S. P. genetics study group
Molecular neurodegeneration · 2024 · PMID 39152475 · open access
2 pages
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Jabbari E,
Koga S,
Valentino RR,
Reynolds RH,
Ferrari R,
Tan MMX,
Rowe JB,
Dalgard CL,
Scholz SW,
Dickson DW,
Warner TT,
Revesz T
and 6 more — show all
PSP Genetics Group
The Lancet. Neurology · 2021 · PMID 33341150
1 page
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Liao C,
Castonguay CE,
Heilbron K,
Vuokila V,
Medeiros M,
Houle G,
Akçimen F,
Ross JP,
Catoire H,
Diez-Fairen M,
Kang J,
Mueller SH
and 36 more — show all
Girard SL,
Hopfner F,
Lorenz D,
Clark LN,
Soto-Beasley AI,
Klebe S,
Hallett M,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Seppi K,
Berg D,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Dupré N,
Jankovic J,
Testa CM,
Ross OA,
Arzberger T,
Chouinard S,
Louis ED,
Mandich P,
Vitale C,
Barone P,
García-Martín E,
Alonso-Navarro H,
Agúndez JAG,
Jiménez-Jiménez FJ,
Pastor P,
Rajput A,
Deuschl G,
Kuhlenbaümer G,
Meijer IA,
Dion PA,
Rouleau GA
23andMe Research Team
JAMA neurology · 2022 · PMID 34982113 · open access
1 page
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Farrell K,
Humphrey J,
Chang T,
Zhao Y,
Leung YY,
Kuksa PP,
Patil V,
Lee WP,
Kuzma AB,
Valladares O,
Cantwell LB,
Wang H
and 37 more — show all
Ravi A,
De Sanctis C,
Han N,
Christie TD,
Afzal R,
Kandoi S,
Whitney K,
Krassner MM,
Ressler H,
Kim S,
Dangoor D,
Iida MA,
Casella A,
Walker RH,
Nirenberg MJ,
Renton AE,
Babrowicz B,
Coppola G,
Raj T,
Höglinger GU,
Müller U,
Golbe LI,
Morris HR,
Hardy J,
Revesz T,
Warner TT,
Jaunmuktane Z,
Mok KY,
Rademakers R,
Dickson DW,
Ross OA,
Wang LS,
Goate A,
Schellenberg G,
Geschwind DH,
Crary JF,
Naj A
PSP Genetics Study Group
Nature communications · 2024 · PMID 39251599 · 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.