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The genomic landscape shaped by selection on transposable elements across 18 mouse strains

 Christoffer Nellåker , Thomas Keane , Binnaz Yalcin , Kim Wong , Avigail Agam , et al.
Genome Biology, 2012, 13 (6), pp.R45. ⟨10.1186/gb-2012-13-6-r45⟩
Article dans une revue inserm-03949190v1
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Using Progenitor Strain Information to Identify Quantitative Trait Nucleotides in Outbred Mice

 B Yalcin , J Flint , R Mott
Genetics, 2005, 171, pp.673 - 681. ⟨10.1534/genetics.104.028902⟩
Article dans une revue inserm-03949420v1

The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia

 Stephan C. Collins , Ana Uzquiano , Mohammed Selloum , Olivia Wendling , Marion Gaborit , et al.
Summer Meeting of the Anatomical-Society, Jun 2018, Oxford, United Kingdom. 14 p
Communication dans un congrès hal-02738065v1
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A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.

 Michelle Simon , Simon Greenaway , Jacqueline White , Helmut Fuchs , Valérie Gailus-Durner , et al.
Genome Biology, 2013, 14 (7), pp.R82. ⟨10.1186/gb-2013-14-7-r82⟩
Article dans une revue inserm-00874969v1
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The fine-scale architecture of structural variants in 17 mouse genomes

 Binnaz Yalcin , Kim Wong , Amarjit Bhomra , Martin Goodson , Thomas M Keane , et al.
Genome Biology, 2012, 13 (3), pp.R18. ⟨10.1186/gb-2012-13-3-r18⟩
Article dans une revue inserm-03949179v1
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Human-Mouse Quantitative Trait Locus Concordance and the Dissection of a Human Neuroticism Locus

 Janice M Fullerton , Saffron a G Willis-Owen , Binnaz Yalcin , Sagiv Shifman , Richard R Copley , et al.
Biological Psychiatry, 2008, 63, pp.874 - 883. ⟨10.1016/j.biopsych.2007.10.019⟩
Article dans une revue inserm-03949413v1
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A method for parasagittal sectioning for neuroanatomical quantification of brain structures in the adult mouse

 Stephan Collins , Christel Wagner , Léo Gagliardi , Perrine F. Kretz , Marie-Christine Fischer , et al.
Current Protocols in Mouse Biology, 2018, 8 (3), pp.e48. ⟨10.1002/cpmo.48⟩
Article dans une revue hal-02617690v1
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Mouse genomic variation and its effect on phenotypes and gene regulation

 Thomas M Keane , Leo Goodstadt , Petr Danecek , Michael A White , Kim Wong , et al.
Nature, 2011, 477, pp.289 - 294. ⟨10.1038/nature10413⟩
Article dans une revue inserm-03949307v1

WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy

 Meghna Kannan , Efil Bayam , Christel Wagner , Bruno Rinaldi , Perrine Kretz , et al.
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (44), pp.E9308-E9317. ⟨10.1073/pnas.1713625114⟩
Article dans une revue hal-02378716v1
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Association of the Dopamine D4 Receptor (DRD4) Gene and Approach-Related Personality Traits: Meta-Analysis and New Data

 Marcus R Munafò , Binnaz Yalcin , Saffron A Willis-Owen , Jonathan Flint
Biological Psychiatry, 2008, 63, pp.197 - 206. ⟨10.1016/j.biopsych.2007.04.006⟩
Article dans une revue inserm-03949403v1
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Quantitative Neuroanatomical Phenotyping of the Embryonic Mouse Brain

 Sylvie Nguyen , Meghna Kannan , Marion Gaborit , Stephan C Collins , Binnaz Yalcin
Current Protocols, 2022, 2, pp.e509. ⟨10.1002/cpz1.509⟩
Article dans une revue inserm-03944654v1
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Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci

 Jingtao Lilue , Anthony G. Doran , Ian T. Fiddes , Monica Abrudan , Joel Armstrong , et al.
Nature Genetics, 2018, 50 (11), pp.1574-1583. ⟨10.1038/s41588-018-0223-8⟩
Article dans une revue hal-03448286v1
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A positively-selected MAGEE2 LoF allele is associated with sexual dimorphism in human brain size, and shows similar phenotypes in Magee2 null mice

 Michał Szpak , Stephan Collins , Yan Li , Xiao Liu , Qasim Ayub , et al.
Molecular Biology and Evolution, 2021, 38 (12), pp.5655-5663. ⟨10.1093/molbev/msab243⟩
Article dans une revue hal-03709462v1
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Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy

 Norine Voisin , Rhonda E Schnur , Sofia Douzgou , Susan M Hiatt , Cecilie F Rustad , et al.
American Journal of Human Genetics, 2021, 108, pp.857 - 873. ⟨10.1016/j.ajhg.2021.04.001⟩
Article dans une revue inserm-03948529v1
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Sequence-based characterization of structural variation in the mouse genome

 Binnaz Yalcin , Kim Wong , Avigail Agam , Martin Goodson , Thomas M Keane , et al.
Nature, 2011, 477, pp.326 - 329. ⟨10.1038/nature10432⟩
Article dans une revue inserm-03949273v1
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Next-generation sequencing of experimental mouse strains

 Binnaz Yalcin , David J Adams , Jonathan Flint , Thomas M Keane
Mammalian Genome, 2012, 23, pp.490 - 498. ⟨10.1007/s00335-012-9402-6⟩
Article dans une revue inserm-03949475v1
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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

 Stephan C Collins , Valerie E Vancollie , Anna Mikhaleva , Christel Wagner , Rebecca Balz , et al.
International Journal of Molecular Sciences, 2022, 23 (19), pp.11509. ⟨10.3390/ijms231911509⟩
Article dans une revue inserm-03944621v1
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Dissecting indirect genetic effects from peers in laboratory mice

 Amelie Baud , Francesco Paolo Casale , Amanda M Barkley-Levenson , Nilgoun Farhadi , Charlotte Montillot , et al.
Genome Biology, 2021, 22 (1), pp.216. ⟨10.1186/s13059-021-02415-x⟩
Article dans une revue inserm-03944775v1
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YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse

 Anne-Sophie Denommé-Pichon , Stephan C Collins , Ange-Line Bruel , Anna Mikhaleva , Christel Wagner , et al.
Genetics in Medicine, 2023, pp.100835. ⟨10.1016/j.gim.2023.100835⟩
Article dans une revue inserm-04094776v1

Behavioural characterization of AnkyrinG deficient mice, a model for ANK3 related disorders

 Ilse van Der Werf , Debby van Dam , Stephan Missault , Binnaz Yalcin , Peter de Deyn , et al.
Behavioural Brain Research, 2017, 328, pp.218-226. ⟨10.1016/j.bbr.2017.04.014⟩
Article dans une revue hal-03691184v1
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The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs

 Maria Nicla Loviglio , Thomas Arbogast , Aia Elise Jønch , Stephan C Collins , Konstantin Popadin , et al.
American Journal of Human Genetics, 2017, 101, pp.564 - 577. ⟨10.1016/j.ajhg.2017.08.016⟩
Article dans une revue inserm-03948660v1
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Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny

 Johan G Gilet , Ekaterina Ivanova , Daria Trofimova , Gabrielle Rudolf , Hamid Meziane , et al.
Human Molecular Genetics, 2020, 29 (5), pp.766-784. ⟨10.1093/hmg/ddz316⟩
Article dans une revue inserm-02551504v1
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Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis

 Stephan Collins , Anna Mikhaleva , Katarina Vrcelj , Valerie Vancollie , Christel Wagner , et al.
Nature Communications, 2019, 10 (1), ⟨10.1038/s41467-019-11431-2⟩
Article dans une revue hal-02396037v1
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TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis

 Ekaterina Ivanova , Johan Gilet , Vadym Sulimenko , Arnaud Duchon , Gabrielle Rudolf , et al.
Nature Communications, 2019, 10 (1), pp.100-110. ⟨10.1038/s41467-019-10081-8⟩
Article dans une revue hal-02388602v1
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Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes

 Jacqueline K White , Anna-Karin Gerdin , Natasha A Karp , Ed Ryder , Marija Buljan , et al.
Cell, 2013, 154, pp.452 - 464. ⟨10.1016/j.cell.2013.06.022⟩
Article dans une revue inserm-03948727v1
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Elusive Copy Number Variation in the Mouse Genome

 Avigail Agam , Binnaz Yalcin , Amarjit Bhomra , Matthew Cubin , Caleb Webber , et al.
PLoS ONE, 2010, 5 (9), pp.e12839. ⟨10.1371/journal.pone.0012839⟩
Article dans une revue inserm-03949376v1
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High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues

 Guo-Jen Huang , Sagiv Shifman , William Valdar , Martina Johannesson , Binnaz Yalcin , et al.
Genome Research, 2009, 19, pp.1133 - 1140. ⟨10.1101/gr.088120.108⟩
Article dans une revue inserm-03949391v1
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A knock-in mouse model for KCNQ2 -related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment

 Mathieu Milh , Pierre L. Roubertoux , Najoua Biba , Julie Chavany , Adeline Ghata , et al.
Epilepsia, 2020, 61 (5), pp.868-878. ⟨10.1111/epi.16494⟩
Article dans une revue inserm-02551507v1
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Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity

 Zhengzheng S Liang , Irene Cimino , Binnaz Yalcin , Narayanan Raghupathy , Valerie E Vancollie , et al.
PLoS Genetics, 2020, 16 (9), pp.e1008916. ⟨10.1371/journal.pgen.1008916⟩
Article dans une revue inserm-03948614v1
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Association studies in outbred mice in a new era of full-genome sequencing

 Binnaz Yalcin , Jonathan Flint
Mammalian Genome, 2012, 23, pp.719 - 726. ⟨10.1007/s00335-012-9409-z⟩
Article dans une revue inserm-03949489v1
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