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.
1 match for
Jicha GA.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Naj AC,
Jun G,
Beecham GW,
Wang LS,
Vardarajan BN,
Buros J,
Gallins PJ,
Buxbaum JD,
Jarvik GP,
Crane PK,
Larson EB,
Bird TD
and 143 more — show all
Boeve BF,
Graff-Radford NR,
De Jager PL,
Evans D,
Schneider JA,
Carrasquillo MM,
Ertekin-Taner N,
Younkin SG,
Cruchaga C,
Kauwe JS,
Nowotny P,
Kramer P,
Hardy J,
Huentelman MJ,
Myers AJ,
Barmada MM,
Demirci FY,
Baldwin CT,
Green RC,
Rogaeva E,
St George-Hyslop P,
Arnold SE,
Barber R,
Beach T,
Bigio EH,
Bowen JD,
Boxer A,
Burke JR,
Cairns NJ,
Carlson CS,
Carney RM,
Carroll SL,
Chui HC,
Clark DG,
Corneveaux J,
Cotman CW,
Cummings JL,
DeCarli C,
DeKosky ST,
Diaz-Arrastia R,
Dick M,
Dickson DW,
Ellis WG,
Faber KM,
Fallon KB,
Farlow MR,
Ferris S,
Frosch MP,
Galasko DR,
Ganguli M,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Gilman S,
Giordani B,
Glass JD,
Growdon JH,
Hamilton RL,
Harrell LE,
Head E,
Honig LS,
Hulette CM,
Hyman BT,
Jicha GA,
Jin LW,
Johnson N,
Karlawish J,
Karydas A,
Kaye JA,
Kim R,
Koo EH,
Kowall NW,
Lah JJ,
Levey AI,
Lieberman AP,
Lopez OL,
Mack WJ,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Parisi JE,
Perl DP,
Peskind E,
Petersen RC,
Poon WW,
Quinn JF,
Rajbhandary RA,
Raskind M,
Reisberg B,
Ringman JM,
Roberson ED,
Rosenberg RN,
Sano M,
Schneider LS,
Seeley W,
Shelanski ML,
Slifer MA,
Smith CD,
Sonnen JA,
Spina S,
Stern RA,
Tanzi RE,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Williamson J,
Woltjer RL,
Cantwell LB,
Dombroski BA,
Beekly D,
Lunetta KL,
Martin ER,
Kamboh MI,
Saykin AJ,
Reiman EM,
Bennett DA,
Morris JC,
Montine TJ,
Goate AM,
Blacker D,
Tsuang DW,
Hakonarson H,
Kukull WA,
Foroud TM,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Farrer LA,
Schellenberg GD
Nature genetics · 2011 · PMID 21460841 · 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.