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Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.
Published in:
International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11509, doi. 10.3390/ijms231911509
By:
- Collins, Stephan C.;
- Vancollie, Valerie E.;
- Mikhaleva, Anna;
- Wagner, Christel;
- Balz, Rebecca;
- Lelliott, Christopher J.;
- Yalcin, Binnaz
Publication type:
Article
Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11431-2
By:
- Wagner, Christel;
- Demeure, Nestor;
- Whitley, Helen;
- Kannan, Meghna;
- Moine, Hervé;
- Collins, Stephan C.;
- Yalcin, Binnaz;
- Mikhaleva, Anna;
- Balz, Rebecca;
- Reymond, Alexandre;
- Vrcelj, Katarina;
- Webber, Caleb;
- Vancollie, Valerie E.;
- Anthony, Lauren F. E.;
- White, Jacqueline K.;
- Adams, David J.;
- Lelliott, Christopher J.;
- Edwards, Andrew
Publication type:
Article
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.
Published in:
Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-03092-8
By:
- Kretz, Perrine F.;
- Wagner, Christel;
- Mikhaleva, Anna;
- Montillot, Charlotte;
- Hugel, Sylvain;
- Morella, Ilaria;
- Kannan, Meghna;
- Fischer, Marie-Christine;
- Milhau, Maxence;
- Yalcin, Ipek;
- Brambilla, Riccardo;
- Selloum, Mohammed;
- Herault, Yann;
- Reymond, Alexandre;
- Collins, Stephan C.;
- Yalcin, Binnaz
Publication type:
Article

Found: 3

Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.

Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis.

Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.