For researchers
Is your paper here?
2,662 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.
2 matches for
Patil V.
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, 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.