For researchers
Is your paper here?
2,647 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.
3 matches for
Perrin RJ.
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Western D,
Timsina J,
Wang L,
Wang C,
Yang C,
Phillips B,
Wang Y,
Liu M,
Ali M,
Beric A,
Gorijala P,
Kohlfeld P
and 28 more — show all
Budde J,
Levey AI,
Morris JC,
Perrin RJ,
Ruiz A,
Marquié M,
Boada M,
de Rojas I,
Rutledge J,
Oh H,
Wilson EN,
Le Guen Y,
Reus LM,
Tijms B,
Visser PJ,
van der Lee SJ,
Pijnenburg YAL,
Teunissen CE,
Del Campo Milan M,
Alvarez I,
Aguilar M,
Greicius MD,
Pastor P,
Pulford DJ,
Ibanez L,
Wyss-Coray T,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Wang C,
Yang C,
Western D,
Ali M,
Wang Y,
Phuah CL,
Budde J,
Wang L,
Gorijala P,
Timsina J,
Ruiz A,
Pastor P
and 14 more — show all
Fernandez MV,
Panyard DJ,
Engelman CD,
Deming Y,
Boada M,
Cano A,
Garcia-Gonzalez P,
Graff-Radford NR,
Mori H,
Lee JH,
Perrin RJ,
Ibanez L,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Wang L,
Nykänen NP,
Western D,
Gorijala P,
Timsina J,
Li F,
Wang Z,
Ali M,
Yang C,
Liu M,
Brock W,
Marquié M
and 21 more — show all
Boada M,
Alvarez I,
Aguilar M,
Pastor P,
Ruiz A,
Puerta R,
Orellana A,
Rutledge J,
Oh H,
Greicius MD,
Le Guen Y,
Perrin RJ,
Wyss-Coray T,
Jefferson A,
Hohman TJ,
Graff-Radford N,
Mori H,
Goate A,
Levin J,
Sung YJ,
Cruchaga C
Molecular neurodegeneration · 2024 · PMID 38172904 · open access
3 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.