List of works - Eberhard Schneider

A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices.

scientific article published on 19 January 2012

A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression.

scientific article

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

scientific article

Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices

scientific article

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

scientific article published on 04 October 2013

Epigenetic Dysregulation in the Prefrontal Cortex of Suicide Completers.

scientific article published on 4 July 2015

Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcome.

scientific article

Epigenetic information from ancient DNA provides new insights into human evolution. Commentary on Gokhman D et al. (2014): Reconstructing the DNA methylation maps of the Neanderthal and the Denisovan. Science 344:523-527.

scientific article

Epigenetics and life-long consequences of an adverse nutritional and diabetic intrauterine environment

scientific article

Extreme methylation values of imprinted genes in human abortions and stillbirths

scientific article

Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome.

scientific article published in August 2010

Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.

scientific article published on 4 September 2009

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

scientific article

Humans and chimpanzees differ in their cellular response to DNA damage and non-coding sequence elements of DNA repair-associated genes.

scientific article published on 18 December 2008

Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus.

scientific article published on 3 December 2012

Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices.

scientific article published on 24 March 2012

Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.

scientific article published on 4 February 2011

Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.

scientific article

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

scientific article

Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzees

scientific article

List of works by Eberhard Schneider

A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices.

A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression.

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss.

Epigenetic Dysregulation in the Prefrontal Cortex of Suicide Completers.

Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcome.

Epigenetic information from ancient DNA provides new insights into human evolution. Commentary on Gokhman D et al. (2014): Reconstructing the DNA methylation maps of the Neanderthal and the Denisovan. Science 344:523-527.

Epigenetics and life-long consequences of an adverse nutritional and diabetic intrauterine environment

Extreme methylation values of imprinted genes in human abortions and stillbirths

Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome.

Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

Humans and chimpanzees differ in their cellular response to DNA damage and non-coding sequence elements of DNA repair-associated genes.

Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus.

Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices.

Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.

Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception.

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

Widespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzees