List of works - Sylvie Odent

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

scientific article

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria

scientific article

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

scientific article

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

scientific article

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

scientific article

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

scientific article

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

scientific article

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum

scientific article (publication date: 15 July 2003)

New insights into genotype-phenotype correlation for GLI3 mutations

scientific article

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

scientific article

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations

scientific article (publication date: February 2003)

Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

scientific article

Variants in CUL4B are associated with cerebral malformations

scientific article

Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5.

scientific article published on 8 December 2017

Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X-linked intellectual disability with distinctive facial appearance

scientific article

Not all floating-harbor syndrome cases are due to mutations in exon 34 of SRCAP.

scientific article published on 16 October 2012

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy

scientific article

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

scientific article published on February 9, 2016

Corrigendum: BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

scholarly article published in Nature Genetics

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations

scientific article published on 30 July 2020

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome

scientific article published on 09 November 2020

List of works by Sylvie Odent

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum

New insights into genotype-phenotype correlation for GLI3 mutations

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations

Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

Variants in CUL4B are associated with cerebral malformations

Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5.

Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X-linked intellectual disability with distinctive facial appearance

Not all floating-harbor syndrome cases are due to mutations in exon 34 of SRCAP.

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

Corrigendum: BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome