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2,673 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.
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10 matches for
Kaufmann T.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
van der Meer D,
Rokicki J,
Kaufmann T,
Córdova-Palomera A,
Moberget T,
Alnæs D,
Bettella F,
Frei O,
Doan NT,
Sønderby IE,
Smeland OB,
Agartz I
and 42 more — show all
Bertolino A,
Bralten J,
Brandt CL,
Buitelaar JK,
Djurovic S,
van Donkelaar M,
Dørum ES,
Espeseth T,
Faraone SV,
Fernández G,
Fisher SE,
Franke B,
Haatveit B,
Hartman CA,
Hoekstra PJ,
Håberg AK,
Jönsson EG,
Kolskår KK,
Le Hellard S,
Lund MJ,
Lundervold AJ,
Lundervold A,
Melle I,
Monereo Sánchez J,
Norbom LC,
Nordvik JE,
Nyberg L,
Oosterlaan J,
Papalino M,
Papassotiropoulos A,
Pergola G,
de Quervain DJF,
Richard G,
Sanders AM,
Selvaggi P,
Shumskaya E,
Steen VM,
Tønnesen S,
Ulrichsen KM,
Zwiers MP,
Andreassen OA,
Westlye LT
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
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+
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
Shadrin AA,
Kaufmann T,
van der Meer D,
Palmer CE,
Makowski C,
Loughnan R,
Jernigan TL,
Seibert TM,
Hagler DJ,
Smeland OB,
Motazedi E,
Chu Y
and 10 more — show all
NeuroImage · 2021 · PMID 34560273
12 pages+
The genetic architecture of human cortical folding
van der Meer D,
Kaufmann T,
Shadrin AA,
Makowski C,
Frei O,
Roelfs D,
Monereo-Sánchez J,
Linden DEJ,
Rokicki J,
Alnæs D,
de Leeuw C,
Thompson WK
and 5 more — show all
Science advances · 2021 · PMID 34910505 · open access
12 pages+
The Genetic Architecture of Amygdala Nuclei
Mufford MS,
van der Meer D,
Kaufmann T,
Frei O,
Ramesar R,
Thompson PM,
Jahanshad N,
Morey RA,
Andreassen OA,
Stein DJ,
Dalvie S
Biological psychiatry · 2024 · PMID 37391117 · open access
12 pages+
The genetic architecture of human cerebellar morphology supports a key role for the cerebellum in human evolution and psychopathology
Moberget T,
van der Meer D,
Bahrami S,
Roelfs D,
Frei O,
Kaufmann T,
Fernandez-Cabello S,
Kim M,
Wolfers T,
Diedrichsen J,
Smeland OB,
Shadrin A
and 3 more — show all
Communications biology · 2026 · PMID 41703085 · open access
12 pages+
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
van der Meer D,
Gurholt TP,
Sønderby IE,
Shadrin AA,
Hindley G,
Rahman Z,
de Lange AG,
Frei O,
Leinhard OD,
Linge J,
Simon R,
Beck D
and 6 more — show all
Communications biology · 2022 · PMID 36402844 · open access
11 pages
The genetic landscape of basal ganglia and implications for common brain disorders
Bahrami S,
Nordengen K,
Rokicki J,
Shadrin AA,
Rahman Z,
Smeland OB,
Jaholkowski PP,
Parker N,
Parekh P,
O'Connell KS,
Elvsåshagen T,
Toft M
and 5 more — show all
Nature communications · 2024 · PMID 39353893 · open access
7 pages
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
Gurholt TP,
Elvsåshagen T,
Bahrami S,
Rahman Z,
Shadrin A,
Askeland-Gjerde DE,
van der Meer D,
Frei O,
Kaufmann T,
Sønderby IE,
Halvorsen S,
Westlye LT
and 1 more — show all
HGG advances · 2025 · PMID 39663699 · open access
7 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.