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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.
Article dans une revue
inserm-03949413v1
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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⟩
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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.
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.
Article dans une revue
inserm-03949307v1
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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.
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
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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.
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.
Article dans une revue
inserm-03949179v1
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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
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
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.
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.
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.
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.
Article dans une revue
inserm-03949273v1
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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.
Article dans une revue
inserm-04094776v1
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Next-generation sequencing of experimental mouse strains
Binnaz Yalcin
,
David J Adams
,
Jonathan Flint
,
Thomas M Keane
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.
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.
Article dans une revue
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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.
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.
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.
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.
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.
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
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Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth
Médéric Jeanne
,
Marie-Laure Vuillaume
,
Dévina Ung
,
Valerie Vancollie
,
Christel Wagner
,
et al.
Article dans une revue
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Histomorphological Phenotyping of the Adult Mouse Brain
Anna Mikhaleva
,
Meghna Kannan
,
Christel Wagner
,
Binnaz Yalcin
Article dans une revue
hal-03680468v1
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SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2
Anna Niewiadomska-Cimicka
,
Frédéric Doussau
,
Jean-Baptiste Perot
,
Michel Roux
,
Celine Keime
,
et al.
Article dans une revue
hal-03378998v1
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Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects
Anna R Duncan
,
Antonio Vitobello
,
Stephan C Collins
,
Valerie E Vancollie
,
Christopher J Lelliott
,
et al.
Article dans une revue
inserm-03948582v1
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Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice
Binnaz Yalcin
,
Saffron a G Willis-Owen
,
Jan Fullerton
,
Anjela Meesaq
,
Robert M Deacon
,
et al.
Article dans une revue
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