Identifying Human Disease Genes through Cross-Species Gene Mapping of Evolutionary Conserved Processes

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

(2010) Yasmin Namavar et al.   BRAIN

Corpus Callosum Abnormalities and the Controversy about the Candidate Genes Located in 1q44

(2010) C. Orellana et al.   CYTOGENETIC AND GENOME RESEARCH

Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene

(2010) Almuth Caliebe et al.   European Journal of Medical Genetics

Functional modules, mutational load and human genetic disease

(2010) Norann A. Zaghloul et al.   TRENDS IN GENETICS

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1-qter

(2009) Maria Kirchhoff et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Multiple cysts of the corpus callosum and psychomotor delay in a patient with a 3.1 Mb 15q24.1q24.2 interstitial deletion identified by array-CGH

(2009) Alice Masurel-Paulet et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Interspecies Trait Genetics Reveals Association of Adcy8 with Mouse Avoidance Behavior and a Human Mood Disorder

(2009) Annetrude (J.G.) de Mooij-van Malsen et al.   BIOLOGICAL PSYCHIATRY

Total Brain Volume and Corpus Callosum Size in Medication-Naïve Adolescents and Young Adults with Autism Spectrum Disorder

(2009) Christine M. Freitag et al.   BIOLOGICAL PSYCHIATRY

A developmental and genetic classification for midbrain-hindbrain malformations

(2009) A. J. Barkovich et al.   BRAIN

Genetic dissection of the mouse CNS using magnetic resonance microscopy

(2009) Alexandra Badea et al.   CURRENT OPINION IN NEUROLOGY

Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex

(2009) Martin Poot et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic dissection of the mouse brain using high-field magnetic resonance microscopy

(2009) A. Badea et al.   NEUROIMAGE

Understanding the Mechanisms of Callosal Development Through the Use of Transgenic Mouse Models

(2009) Amber-Lee S. Donahoo et al.   Seminars in Pediatric Neurology

Identification of the UBP1 Locus as a Critical Blood Pressure Determinant Using a Combination of Mouse and Human Genetics

(2009) Hana Koutnikova et al.   PLoS Genetics

Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients

(2008) Chayim Can Schell-Apacik et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features

(2008) Filomena Tiziana Papa et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Neuroimaging techniques offer new perspectives on callosal transfer and interhemispheric communication

(2008) K DORON et al.   CORTEX

Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss

(2008) Sandesh Chakravarthy Sreenath Nagamani et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array

(2008) Joris Andrieux et al.   European Journal of Medical Genetics

AKT3 as a candidate gene for corpus callosum anomalies in patients with 1q44 deletions

(2008) Martin Poot et al.   European Journal of Medical Genetics

Mild mental retardation in a child with a de novo interstitial deletion of 15q21.2q22.1: A comparison with previously described cases

(2008) Sergio Tempesta et al.   European Journal of Medical Genetics

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

(2008) Juliane Najm et al.   NATURE GENETICS

Automated segmentation of the actively stained mouse brain using multi-spectral MR microscopy

(2007) Anjum A. Sharief et al.   NEUROIMAGE