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Is your paper here?
2,675 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.
6 matches for
Mori H.
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect
Ikeda M,
Takahashi A,
Kamatani Y,
Momozawa Y,
Saito T,
Kondo K,
Shimasaki A,
Kawase K,
Sakusabe T,
Iwayama Y,
Toyota T,
Wakuda T
and 20 more — show all
Kikuchi M,
Kanahara N,
Yamamori H,
Yasuda Y,
Watanabe Y,
Hoya S,
Aleksic B,
Kushima I,
Arai H,
Takaki M,
Hattori K,
Kunugi H,
Okahisa Y,
Ohnuma T,
Ozaki N,
Someya T,
Hashimoto R,
Yoshikawa T,
Kubo M,
Iwata N
Schizophrenia bulletin · 2019 · PMID 30285260
12 pages+
The genetic architecture of the human cerebral cortex
Grasby KL,
Jahanshad N,
Painter JN,
Colodro-Conde L,
Bralten J,
Hibar DP,
Lind PA,
Pizzagalli F,
Ching CRK,
McMahon MAB,
Shatokhina N,
Zsembik LCP
and 348 more — show all
Thomopoulos SI,
Zhu AH,
Strike LT,
Agartz I,
Alhusaini S,
Almeida MAA,
Alnæs D,
Amlien IK,
Andersson M,
Ard T,
Armstrong NJ,
Ashley-Koch A,
Atkins JR,
Bernard M,
Brouwer RM,
Buimer EEL,
Bülow R,
Bürger C,
Cannon DM,
Chakravarty M,
Chen Q,
Cheung JW,
Couvy-Duchesne B,
Dale AM,
Dalvie S,
de Araujo TK,
de Zubicaray GI,
de Zwarte SMC,
den Braber A,
Doan NT,
Dohm K,
Ehrlich S,
Engelbrecht HR,
Erk S,
Fan CC,
Fedko IO,
Foley SF,
Ford JM,
Fukunaga M,
Garrett ME,
Ge T,
Giddaluru S,
Goldman AL,
Green MJ,
Groenewold NA,
Grotegerd D,
Gurholt TP,
Gutman BA,
Hansell NK,
Harris MA,
Harrison MB,
Haswell CC,
Hauser M,
Herms S,
Heslenfeld DJ,
Ho NF,
Hoehn D,
Hoffmann P,
Holleran L,
Hoogman M,
Hottenga JJ,
Ikeda M,
Janowitz D,
Jansen IE,
Jia T,
Jockwitz C,
Kanai R,
Karama S,
Kasperaviciute D,
Kaufmann T,
Kelly S,
Kikuchi M,
Klein M,
Knapp M,
Knodt AR,
Krämer B,
Lam M,
Lancaster TM,
Lee PH,
Lett TA,
Lewis LB,
Lopes-Cendes I,
Luciano M,
Macciardi F,
Marquand AF,
Mathias SR,
Melzer TR,
Milaneschi Y,
Mirza-Schreiber N,
Moreira JCV,
Mühleisen TW,
Müller-Myhsok B,
Najt P,
Nakahara S,
Nho K,
Olde Loohuis LM,
Orfanos DP,
Pearson JF,
Pitcher TL,
Pütz B,
Quidé Y,
Ragothaman A,
Rashid FM,
Reay WR,
Redlich R,
Reinbold CS,
Repple J,
Richard G,
Riedel BC,
Risacher SL,
Rocha CS,
Mota NR,
Salminen L,
Saremi A,
Saykin AJ,
Schlag F,
Schmaal L,
Schofield PR,
Secolin R,
Shapland CY,
Shen L,
Shin J,
Shumskaya E,
Sønderby IE,
Sprooten E,
Tansey KE,
Teumer A,
Thalamuthu A,
Tordesillas-Gutiérrez D,
Turner JA,
Uhlmann A,
Vallerga CL,
van der Meer D,
van Donkelaar MMJ,
van Eijk L,
van Erp TGM,
van Haren NEM,
van Rooij D,
van Tol MJ,
Veldink JH,
Verhoef E,
Walton E,
Wang M,
Wang Y,
Wardlaw JM,
Wen W,
Westlye LT,
Whelan CD,
Witt SH,
Wittfeld K,
Wolf C,
Wolfers T,
Wu JQ,
Yasuda CL,
Zaremba D,
Zhang Z,
Zwiers MP,
Artiges E,
Assareh AA,
Ayesa-Arriola R,
Belger A,
Brandt CL,
Brown GG,
Cichon S,
Curran JE,
Davies GE,
Degenhardt F,
Dennis MF,
Dietsche B,
Djurovic S,
Doherty CP,
Espiritu R,
Garijo D,
Gil Y,
Gowland PA,
Green RC,
Häusler AN,
Heindel W,
Ho BC,
Hoffmann WU,
Holsboer F,
Homuth G,
Hosten N,
Jack CR Jr,
Jang M,
Jansen A,
Kimbrel NA,
Kolskår K,
Koops S,
Krug A,
Lim KO,
Luykx JJ,
Mathalon DH,
Mather KA,
Mattay VS,
Matthews S,
Mayoral Van Son J,
McEwen SC,
Melle I,
Morris DW,
Mueller BA,
Nauck M,
Nordvik JE,
Nöthen MM,
O'Leary DS,
Opel N,
Martinot MP,
Pike GB,
Preda A,
Quinlan EB,
Rasser PE,
Ratnakar V,
Reppermund S,
Steen VM,
Tooney PA,
Torres FR,
Veltman DJ,
Voyvodic JT,
Whelan R,
White T,
Yamamori H,
Adams HHH,
Bis JC,
Debette S,
Decarli C,
Fornage M,
Gudnason V,
Hofer E,
Ikram MA,
Launer L,
Longstreth WT,
Lopez OL,
Mazoyer B,
Mosley TH,
Roshchupkin GV,
Satizabal CL,
Schmidt R,
Seshadri S,
Yang Q,
Alvim MKM,
Ames D,
Anderson TJ,
Andreassen OA,
Arias-Vasquez A,
Bastin ME,
Baune BT,
Beckham JC,
Blangero J,
Boomsma DI,
Brodaty H,
Brunner HG,
Buckner RL,
Buitelaar JK,
Bustillo JR,
Cahn W,
Cairns MJ,
Calhoun V,
Carr VJ,
Caseras X,
Caspers S,
Cavalleri GL,
Cendes F,
Corvin A,
Crespo-Facorro B,
Dalrymple-Alford JC,
Dannlowski U,
de Geus EJC,
Deary IJ,
Delanty N,
Depondt C,
Desrivières S,
Donohoe G,
Espeseth T,
Fernández G,
Fisher SE,
Flor H,
Forstner AJ,
Francks C,
Franke B,
Glahn DC,
Gollub RL,
Grabe HJ,
Gruber O,
Håberg AK,
Hariri AR,
Hartman CA,
Hashimoto R,
Heinz A,
Henskens FA,
Hillegers MHJ,
Hoekstra PJ,
Holmes AJ,
Hong LE,
Hopkins WD,
Hulshoff Pol HE,
Jernigan TL,
Jönsson EG,
Kahn RS,
Kennedy MA,
Kircher TTJ,
Kochunov P,
Kwok JBJ,
Le Hellard S,
Loughland CM,
Martin NG,
Martinot JL,
McDonald C,
McMahon KL,
Meyer-Lindenberg A,
Michie PT,
Morey RA,
Mowry B,
Nyberg L,
Oosterlaan J,
Ophoff RA,
Pantelis C,
Paus T,
Pausova Z,
Penninx BWJH,
Polderman TJC,
Posthuma D,
Rietschel M,
Roffman JL,
Rowland LM,
Sachdev PS,
Sämann PG,
Schall U,
Schumann G,
Scott RJ,
Sim K,
Sisodiya SM,
Smoller JW,
Sommer IE,
St Pourcain B,
Stein DJ,
Toga AW,
Trollor JN,
Van der Wee NJA,
van 't Ent D,
Völzke H,
Walter H,
Weber B,
Weinberger DR,
Wright MJ,
Zhou J,
Stein JL,
Thompson PM,
Medland SE
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
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
4 pages
Common variants at 1p36 are associated with superior frontal gyrus volume
Hashimoto R,
Ikeda M,
Yamashita F,
Ohi K,
Yamamori H,
Yasuda Y,
Fujimoto M,
Fukunaga M,
Nemoto K,
Takahashi T,
Tochigi M,
Onitsuka T
and 8 more — show all
Translational psychiatry · 2014 · PMID 25335168 · 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.