For researchers
Is your paper here?
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.
3 matches for
Thomson R.
Cerebral small vessel disease genomics and its implications across the lifespan
Sargurupremraj M,
Suzuki H,
Jian X,
Sarnowski C,
Evans TE,
Bis JC,
Eiriksdottir G,
Sakaue S,
Terzikhan N,
Habes M,
Zhao W,
Zhao W
and 105 more — show all
Armstrong NJ,
Hofer E,
Yanek LR,
Hagenaars SP,
Kumar RB,
van den Akker EB,
McWhirter RE,
Trompet S,
Mishra A,
Saba Y,
Satizabal CL,
Beaudet G,
Petit L,
Tsuchida A,
Zago L,
Schilling S,
Sigurdsson S,
Gottesman RF,
Lewis CE,
Aggarwal NT,
Lopez OL,
Smith JA,
Valdés Hernández MC,
van der Grond J,
Wright MJ,
Knol MJ,
Dörr M,
Thomson RJ,
Bordes C,
Le Grand Q,
Duperron MG,
Smith AV,
Knopman DS,
Schreiner PJ,
Evans DA,
Rotter JI,
Beiser AS,
Maniega SM,
Beekman M,
Trollor J,
Stott DJ,
Vernooij MW,
Wittfeld K,
Niessen WJ,
Soumaré A,
Boerwinkle E,
Sidney S,
Turner ST,
Davies G,
Thalamuthu A,
Völker U,
van Buchem MA,
Bryan RN,
Dupuis J,
Bastin ME,
Ames D,
Teumer A,
Amouyel P,
Kwok JB,
Bülow R,
Deary IJ,
Schofield PR,
Brodaty H,
Jiang J,
Tabara Y,
Setoh K,
Miyamoto S,
Yoshida K,
Nagata M,
Kamatani Y,
Matsuda F,
Psaty BM,
Bennett DA,
De Jager PL,
Mosley TH,
Sachdev PS,
Schmidt R,
Warren HR,
Evangelou E,
Trégouët DA,
Ikram MA,
Wen W,
DeCarli C,
Srikanth VK,
Jukema JW,
Slagboom EP,
Kardia SLR,
Okada Y,
Mazoyer B,
Wardlaw JM,
Nyquist PA,
Mather KA,
Grabe HJ,
Schmidt H,
Van Duijn CM,
Gudnason V,
Longstreth WT Jr,
Launer LJ,
Lathrop M,
Seshadri S,
Tzourio C,
Adams HH,
Matthews PM,
Fornage M,
Debette S
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 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
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Matteini AM,
Tanaka T,
Karasik D,
Atzmon G,
Chou WC,
Eicher JD,
Johnson AD,
Arnold AM,
Callisaya ML,
Davies G,
Evans DS,
Holtfreter B
and 55 more — show all
Lohman K,
Lunetta KL,
Mangino M,
Smith AV,
Smith JA,
Teumer A,
Yu L,
Arking DE,
Buchman AS,
Chibinik LB,
De Jager PL,
Evans DA,
Faul JD,
Garcia ME,
Gillham-Nasenya I,
Gudnason V,
Hofman A,
Hsu YH,
Ittermann T,
Lahousse L,
Liewald DC,
Liu Y,
Lopez L,
Rivadeneira F,
Rotter JI,
Siggeirsdottir K,
Starr JM,
Thomson R,
Tranah GJ,
Uitterlinden AG,
Völker U,
Völzke H,
Weir DR,
Yaffe K,
Zhao W,
Zhuang WV,
Zmuda JM,
Bennett DA,
Cummings SR,
Deary IJ,
Ferrucci L,
Harris TB,
Kardia SL,
Kocher T,
Kritchevsky SB,
Psaty BM,
Seshadri S,
Spector TD,
Srikanth VK,
Windham BG,
Zillikens MC,
Newman AB,
Walston JD,
Kiel DP,
Murabito JM
Aging cell · 2016 · PMID 27325353 · open access
2 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.