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Correction: Corrigendum: Domains of genome-wide gene expression dysregulation in Down’s syndrome

Audrey Letourneau
Federico A. Santoni
Stylianos E. Antonarakis
Amendments and Corrections02 Dec 2015
Nature

Volume: 531, P: 400
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Jean-Louis Blouin
Beth A. Dombroski
Ann E. Pulver
Research01 Sept 1998
Nature Genetics

Volume: 20, P: 70-73
Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

Hamish S. Scott
Jun Kudoh
Stylianos E. Antonarakis
Research01 Jan 2001
Nature Genetics

Volume: 27, P: 59-63
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disease resulting in reduced mucus clearance and impaired lung function. Here, the authors show that mutations in PIH1D3 are responsible for an X-linked form of PCD, affecting assembly of a subset of inner arm dyneins.

Chiara Olcese
Mitali P. Patel
Hannah M. Mitchison
ResearchOpen Access08 Feb 2017
Nature Communications

Volume: 8, P: 1-15
Domains of genome-wide gene expression dysregulation in Down’s syndrome

By studying the transcriptome of fetal cells of monozygotic twins discordant for trisomy 21, this paper finds that differential expression between the twins is organized in domains along all chromosomes; these gene expression dysregulation domains are conserved in the mouse model of Down’s syndrome and correlate with the lamina-associated domains and replication domains.

Audrey Letourneau
Federico A. Santoni
Stylianos E. Antonarakis
Research16 Apr 2014
Nature

Volume: 508, P: 345-350
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma

Sergey Nikolaev, Stylianos Antonarakis and colleagues report exome sequencing of seven melanoma cell lines and matched germline cells. They identify recurring somatic mutations in MAP2K1 and MAP2K2 occurring at an overall frequency of 8%.

Sergey I Nikolaev
Donata Rimoldi
Stylianos E Antonarakis
Research25 Dec 2011
Nature Genetics

Volume: 44, P: 133-139
Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Robert Lyle
Frédérique Béna
Stylianos E Antonarakis
Research12 Nov 2008
European Journal of Human Genetics

Volume: 17, P: 454-466

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Correction: Corrigendum: Domains of genome-wide gene expression dysregulation in Down’s syndrome

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

Domains of genome-wide gene expression dysregulation in Down’s syndrome

Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma

Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

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Correction: Corrigendum: Domains of genome-wide gene expression dysregulation in Down’s syndrome

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

Domains of genome-wide gene expression dysregulation in Down’s syndrome

Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma

Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Search

Quick links