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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.
3 matches for
Cookson M.
APOE-stratified genome-wide association analyses provide insights into the genetic etiology of Alzheimers's disease
Thomassen JQ,
Leonard H,
Ulms B,
Grenier-Boley B,
Heikkinen S,
Garcia-González P,
Castillo-Morales A,
Kikuchi M,
Gim J,
Cao H,
Küçükali F,
Amin N
and 121 more — show all
Yoon D,
de Rojas I,
Alvarez Jerez P,
Alvarez V,
Arosio B,
Bellenguez C,
Bergh S,
Billingsley K,
Blauwendraat C,
Boada M,
Borroni B,
Bossù P,
Bullido MJ,
Daniele A,
Carracedo Á,
de Mendonça A,
Cookson M,
Deckert J,
Dichgans M,
Djurovic S,
Dols-Icardo O,
Dufouil C,
Düzel E,
Escott-Price V,
Fladby T,
Fratiglioni L,
Fu AKY,
Galimberti D,
García-Alberca JM,
Giedraitis V,
Garcia-Ribas G,
Graff C,
Grimmer T,
Grünblatt E,
Hanon O,
Hausner L,
Heilmann-Heimbach S,
Hort J,
Jessen F,
Jensen K,
Jonson C,
Kim Y,
Kuznetsov N,
Leinonen V,
Lipponen A,
Luo J,
Makarious M,
Martiskainen H,
Masullo C,
Mecocci P,
Mehrabian S,
Mir P,
Miyashita A,
Moebus S,
Mok KY,
Molina Porcel L,
Moreno F,
Nacmias B,
Parnetti L,
Pastor P,
Pérez-Tur J,
Peters O,
Pijnenburg YAL,
Piñol-Ripoll G,
Popp J,
Rainero I,
Real LM,
Riedel-Heller S,
Rodriguez-Rodriguez E,
Rongve A,
Rossi G,
Royo JL,
Rujescu D,
Saltvedt I,
Sáez ME,
Sánchez-Valle R,
Sanchez-Garcia F,
Sandau N,
Scarmeas N,
Scheffler K,
Scherbaum N,
Schneider A,
Selbæk G,
Seripa D,
Solfrizzi V,
Spallazzi M,
Squassina A,
Stordal E,
Tesi N,
Tremolizzo L,
Tripathi KP,
van der Flier WM,
Williams J,
Wiltfang J,
Aarsland D,
Singleton AB,
Amouyel P,
Debette S,
Tsolaki M,
Nicolas G,
van der Lee S,
Holstege H,
Fernandez MV,
Kehoe PG,
Sleegers K,
Ingelsson M,
Ghidoni R,
Andreassen OA,
Holmans PA,
Sánchez-Juan P,
Sims R,
Ip NY,
Lee KH,
Ikeuchi T,
Ramirez A,
Ruiz A,
Hiltunen M,
Lambert JC,
van Duijn C,
Nalls M,
Frikke-Schmidt R
Nature genetics · 2026 · PMID 42736378 · open access
8 pages
Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment
Jiang Y,
Meyers TJ,
Emeka AA,
Cooley LF,
Cooper PR,
Lancki N,
Helenowski I,
Kachuri L,
Lin DW,
Stanford JL,
Newcomb LF,
Kolb S
and 85 more — show all
Finelli A,
Fleshner NE,
Komisarenko M,
Eastham JA,
Ehdaie B,
Benfante N,
Logothetis CJ,
Gregg JR,
Perez CA,
Garza S,
Kim J,
Marks LS,
Delfin M,
Barsa D,
Vesprini D,
Klotz LH,
Loblaw A,
Mamedov A,
Goldenberg SL,
Higano CS,
Spillane M,
Wu E,
Carter HB,
Pavlovich CP,
Mamawala M,
Landis T,
Carroll PR,
Chan JM,
Cooperberg MR,
Cowan JE,
Morgan TM,
Siddiqui J,
Martin R,
Klein EA,
Brittain K,
Gotwald P,
Barocas DA,
Dallmer JR,
Gordetsky JB,
Steele P,
Kundu SD,
Stockdale J,
Roobol MJ,
Venderbos LDF,
Sanda MG,
Arnold R,
Patil D,
Evans CP,
Dall'Era MA,
Vij A,
Costello AJ,
Chow K,
Corcoran NM,
Rais-Bahrami S,
Phares C,
Scherr DS,
Flynn T,
Karnes RJ,
Koch M,
Dhondt CR,
Nelson JB,
McBride D,
Cookson MS,
Stratton KL,
Farriester S,
Hemken E,
Stadler WM,
Pera T,
Banionyte D,
Bianco FJ Jr,
Lopez IH,
Loeb S,
Taneja SS,
Byrne N,
Amling CL,
Martinez A,
Boileau L,
Gaylis FD,
Petkewicz J,
Kirwen N,
Helfand BT,
Xu J,
Scholtens DM,
Catalona WJ,
Witte JS
HGG advances · 2022 · PMID 34993496 · open access
2 pages
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez J,
Schulte C,
Bras JM,
Sharma M,
Gibbs JR,
Berg D,
Paisan-Ruiz C,
Lichtner P,
Scholz SW,
Hernandez DG,
Krüger R,
Federoff M
and 35 more — show all
Klein C,
Goate A,
Perlmutter J,
Bonin M,
Nalls MA,
Illig T,
Gieger C,
Houlden H,
Steffens M,
Okun MS,
Racette BA,
Cookson MR,
Foote KD,
Fernandez HH,
Traynor BJ,
Schreiber S,
Arepalli S,
Zonozi R,
Gwinn K,
van der Brug M,
Lopez G,
Chanock SJ,
Schatzkin A,
Park Y,
Hollenbeck A,
Gao J,
Huang X,
Wood NW,
Lorenz D,
Deuschl G,
Chen H,
Riess O,
Hardy JA,
Singleton AB,
Gasser T
Nature genetics · 2009 · PMID 19915575 · 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.