For researchers
Is your paper here?
3,082 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.
4 matches for
Chibnik L.
Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways
Sherva R,
Gross A,
Mukherjee S,
Koesterer R,
Amouyel P,
Bellenguez C,
Dufouil C,
Bennett DA,
Chibnik L,
Cruchaga C,
Del-Aguila J,
Farrer LA
and 8 more — show all
Alzheimer's Disease Genetics Consortium
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2020 · PMID 32573913
7 pages
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Bis JC,
DeCarli C,
Smith AV,
van der Lijn F,
Crivello F,
Fornage M,
Debette S,
Shulman JM,
Schmidt H,
Srikanth V,
Schuur M,
Yu L
and 71 more — show all
Choi SH,
Sigurdsson S,
Verhaaren BF,
DeStefano AL,
Lambert JC,
Jack CR Jr,
Struchalin M,
Stankovich J,
Ibrahim-Verbaas CA,
Fleischman D,
Zijdenbos A,
den Heijer T,
Mazoyer B,
Coker LH,
Enzinger C,
Danoy P,
Amin N,
Arfanakis K,
van Buchem MA,
de Bruijn RF,
Beiser A,
Dufouil C,
Huang J,
Cavalieri M,
Thomson R,
Niessen WJ,
Chibnik LB,
Gislason GK,
Hofman A,
Pikula A,
Pikula A,
Amouyel P,
Freeman KB,
Phan TG,
Oostra BA,
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Wright MJ,
Franke B,
Martin NG,
Thompson PM,
Nalls MA,
Uitterlinden AG,
Au R,
Elbaz A,
Beare RJ,
van Swieten JC,
Lopez OL,
Harris TB,
Chouraki V,
Breteler MM,
De Jager PL,
Becker JT,
Vernooij MW,
Knopman D,
Fazekas F,
Wolf PA,
van der Lugt A,
Gudnason V,
Longstreth WT Jr,
Brown MA,
Bennett DA,
van Duijn CM,
Mosley TH,
Schmidt R,
Tzourio C,
Launer LJ,
Ikram MA,
Seshadri S
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium
Debette S,
Ibrahim Verbaas CA,
Bressler J,
Schuur M,
Smith A,
Bis JC,
Davies G,
Wolf C,
Gudnason V,
Chibnik LB,
Yang Q,
deStefano AL
and 114 more — show all
de Quervain DJ,
Srikanth V,
Lahti J,
Grabe HJ,
Smith JA,
Priebe L,
Yu L,
Karbalai N,
Hayward C,
Wilson JF,
Campbell H,
Petrovic K,
Fornage M,
Chauhan G,
Yeo R,
Boxall R,
Becker J,
Stegle O,
Mather KA,
Chouraki V,
Sun Q,
Rose LM,
Resnick S,
Oldmeadow C,
Kirin M,
Wright AF,
Jonsdottir MK,
Au R,
Becker A,
Amin N,
Nalls MA,
Turner ST,
Kardia SL,
Oostra B,
Windham G,
Coker LH,
Zhao W,
Knopman DS,
Heiss G,
Griswold ME,
Gottesman RF,
Vitart V,
Hastie ND,
Zgaga L,
Rudan I,
Polasek O,
Holliday EG,
Schofield P,
Schofield P,
Choi SH,
Tanaka T,
An Y,
Perry RT,
Kennedy RE,
Sale MM,
Wang J,
Wadley VG,
Liewald DC,
Ridker PM,
Gow AJ,
Pattie A,
Starr JM,
Porteous D,
Liu X,
Thomson R,
Armstrong NJ,
Eiriksdottir G,
Assareh AA,
Kochan NA,
Widen E,
Palotie A,
Hsieh YC,
Eriksson JG,
Vogler C,
van Swieten JC,
Shulman JM,
Beiser A,
Rotter J,
Schmidt CO,
Hoffmann W,
Nöthen MM,
Ferrucci L,
Attia J,
Uitterlinden AG,
Amouyel P,
Dartigues JF,
Amieva H,
Räikkönen K,
Garcia M,
Wolf PA,
Hofman A,
Longstreth WT Jr,
Psaty BM,
Boerwinkle E,
DeJager PL,
Sachdev PS,
Schmidt R,
Breteler MM,
Teumer A,
Lopez OL,
Cichon S,
Chasman DI,
Grodstein F,
Müller-Myhsok B,
Tzourio C,
Papassotiropoulos A,
Bennett DA,
Ikram MA,
Deary IJ,
van Duijn CM,
Launer L,
Fitzpatrick AL,
Seshadri S,
Mosley TH Jr
Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Biological psychiatry · 2015 · PMID 25648963
2 pages
Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies
Chibnik LB,
White CC,
Mukherjee S,
Raj T,
Yu L,
Larson EB,
Montine TJ,
Keene CD,
Sonnen J,
Schneider JA,
Crane PK,
Shulman JM
and 2 more — show all
Molecular psychiatry · 2018 · PMID 28322283 · 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.