Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

 
 
DownloadE-Mail
  Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Sønderby, I. E., Gústafsson, Ó., Doan, N. T., Hibar, D. P., Martin-Brevet, S., Westlye, L. T., et al. (2018). Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry. doi:10.1038/s41380-018-0118-1.

Item is

Basisdaten

einblenden: ausblenden:
Genre: Zeitschriftenartikel

Dateien

einblenden: Dateien
ausblenden: Dateien
:
Sonderby_2018.pdf (Verlagsversion), 2MB
Name:
Sonderby_2018.pdf
Beschreibung:
-
OA-Status:
Sichtbarkeit:
Öffentlich
MIME-Typ / Prüfsumme:
application/pdf / [MD5]
Technische Metadaten:
Copyright Datum:
-
Copyright Info:
-
Lizenz:
-

Externe Referenzen

einblenden:

Urheber

einblenden:
ausblenden:
 Urheber:
Sønderby, Ida Elken1, Autor
Gústafsson, Ómar1, Autor
Doan, Nhat Trung1, Autor
Hibar, Derrek Paul1, Autor
Martin-Brevet, Sandra1, Autor
Westlye, Lars T.1, Autor
Jacquemont, Sébastien1, Autor
Djurovic, Srdjan1, Autor
Stefánsson, Hreinn1, Autor
Stefánsson, Kari1, Autor
Thompson, Paul M.1, Autor
Andreassen, Ole A.1, Autor
Abdellaoui, Abdel1, Autor
Ames, David1, Autor
Amunts, Katrin1, Autor
Andersson, Michael1, Autor
Armstrong, Nicola J.1, Autor
Bernard, Manon1, Autor
Blackburn, Nicholas1, Autor
Blangero, John1, Autor
Boomsma, Dorret I.1, AutorBralten, Janita1, AutorBrattbak, Hans-Richard1, AutorBrodaty, Henry1, AutorBrouwer, Rachel M.1, AutorBülow, Robin1, AutorCalhoun, Vince1, AutorCaspers, Svenja1, AutorCavalleri, Gianpiero1, AutorChen, Chi-Hua1, AutorCichon, Sven1, AutorCiufolini, Simone1, AutorCorvin, Aiden1, AutorCrespo-Facorro, Benedicto1, AutorCurran, Joanne E.1, AutorDale, Anders M1, AutorDalvie, Shareefa1, AutorDazzan, Paola1, Autorde Geus, Eco JC1, Autorde Zubicaray, Greig I.1, Autorde Zwarte, Sonja M.C.1, AutorDelanty, Norman1, Autorden Braber, Anouk1, AutorDesrivières, Sylvane1, AutorDonohoe, Gary1, AutorDraganski, Bogdan1, 2, Autor           Ehrlich, Stefan1, AutorEspeseth, Thomas1, AutorFisher, Simone E.1, AutorFranke, Barbara1, AutorFrouin, Vincent1, AutorFukunaga, Masaki1, AutorGareau, Thomas1, AutorGlahn, David C.1, AutorGrabe, Hans1, AutorGroenewold, Nynke A.1, AutorHaavik, Jan1, AutorHåberg, Asta1, AutorHashimoto, Ryota1, AutorHehir-Kwa, Jayne Y.1, AutorHeinz, Andreas1, AutorHillegers, Manon H.J.1, AutorHoffmann, Per1, AutorHolleran, Laurena1, AutorHottenga, Jouke-Jan1, AutorHulshoff, Hilleke E.1, AutorIkeda, Masashi1, AutorJahanshad, Neda1, AutorJernigan, Terry1, AutorJockwitz, Christiane1, AutorJohansson, Stefan1, AutorJonsdottir, Gudrun A.1, AutorJönsson, Erik G.1, AutorKahn, Rene1, AutorKaufmann, Tobias1, AutorKelly, Sinead1, AutorKikuchi, Masataka1, AutorKnowles, Emma EM.1, AutorKolskår, Knut K.1, AutorKwok, John B.1, AutorLe Hellard, Stephanie1, AutorLeu, Costin1, AutorLiu, Jingyu1, AutorLundervold, Astri J.1, AutorLundervold, Arvid1, AutorMartin, Nicholas G.1, AutorMather, Karen1, AutorMathias, Samuel R.1, AutorMcCormack, Mark1, AutorMcMahon, Katie L.1, AutorMcRae, Allan1, AutorMilaneschi, Yuri1, AutorMoreau, Clara1, AutorMorris, Derek1, AutorMothersill, David1, AutorMühleisen, Thomas W.1, AutorMurray, Robin1, AutorNordvik, Jan E.1, AutorNyberg, Lars1, AutorLoohuis, Loes M. Olde1, AutorOphoff, Roel1, AutorPaus, Tomas1, AutorPausova, Zdenka1, AutorPenninx, Brenda1, AutorPeralta, Juan M.1, AutorPike, Bruce1, AutorPrieto, Carlos1, AutorPudas, Sara1, AutorQuinlan, Erin1, AutorQuintana, Daniel S.1, AutorReinbold, Céline S.1, AutorMarques, Tiago Reis1, AutorReymond, Alexandre1, AutorRichard, Genevieve1, AutorRodriguez-Herreros, Borja1, AutorRoiz-Santiañez, Roberto1, AutorRucker, James1, AutorSachdev, Perminder1, AutorSanders, Anne-Marthe1, AutorSando, Sigrid B.1, AutorSchmaal, Lianne1, AutorSchofield, Peter R.1, AutorSchork, Andrew J.1, AutorSchumann, Gunter1, AutorShin, Jean1, AutorShumskaya, Elena1, AutorSisodiya, Sanjay1, AutorSteen, Vidar M.1, AutorStein, Dan J.1, AutorSteinberg, Stacy1, AutorStrike, Lachlan1, AutorTeumer, Alexander1, AutorThalamuthu, Anbu1, AutorTordesillas-Gutierrez, Diana1, AutorTurner, Jessica1, AutorUeland, Torill1, AutorUhlmann, Anne1, AutorUlfarsson, Magnus O.1, Autorvan Ent, Dennis 't1, Autorvan der Meer, Dennis1, Autorvan Haren, Neeltje E.M.1, AutorVaskinn, Anja1, AutorVassos, Evangelos1, AutorWalters, G. Bragi1, AutorWang, Yunpeng1, AutorWen, Wei1, AutorWhelan, Christopher D.1, AutorWittfeld, Katharina1, AutorWright, Margie1, AutorYamamori, Hidenaga1, AutorZayats, Tetyana1, AutorAgartz, Ingrid1, Autor mehr..
Affiliations:
1External Organizations, ou_persistent22              
2Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              

Inhalt

einblenden:
ausblenden:
Schlagwörter: -
 Zusammenfassung: Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to e.g., autism spectrum disorder and schizophrenia. We compared subcortical brain volumes of 12 16p11.2 distal deletion and 12 duplication carriers to 6882 non-carriers from the large-scale brain Magnetic Resonance Imaging collaboration, ENIGMA-CNV. After stringent CNV calling procedures, and standardized FreeSurfer image analysis, we found negative dose-response associations with copy number on intracranial volume and on regional caudate, pallidum and putamen volumes (β = −0.71 to −1.37; P < 0.0005). In an independent sample, consistent results were obtained, with significant effects in the pallidum (β = −0.95, P = 0.0042). The two data sets combined showed significant negative dose-response for the accumbens, caudate, pallidum, putamen and ICV (P = 0.0032, 8.9 × 10−6, 1.7 × 10−9, 3.5 × 10−12 and 1.0 × 10−4, respectively). Full scale IQ was lower in both deletion and duplication carriers compared to non-carriers. This is the first brain MRI study of the impact of the 16p11.2 distal CNV, and we demonstrate a specific effect on subcortical brain structures, suggesting a neuropathological pattern underlying the neurodevelopmental syndromes

Details

einblenden:
ausblenden:
Sprache(n): eng - English
 Datum: 2018-05-022018-02-122018-05-252018-10-03
 Publikationsstatus: Online veröffentlicht
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1038/s41380-018-0118-1
PMID: 30283035
Anderer: Epub ahead of print
 Art des Abschluß: -

Veranstaltung

einblenden:

Entscheidung

einblenden:

Projektinformation

einblenden:

Quelle 1

einblenden:
ausblenden:
Titel: Molecular Psychiatry
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Houndmills, Hampshire, UK : Stockton Press
Seiten: - Band / Heft: - Artikelnummer: - Start- / Endseite: - Identifikator: ISSN: 1359-4184
CoNE: https://pure.mpg.de/cone/journals/resource/954925619131