List of works - Peter L Nagy

A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3

scientific article

Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regions.

scientific article published on August 2014

The Glc7 phosphatase subunit of the cleavage and polyadenylation factor is essential for transcription termination on snoRNA genes.

scientific article published in March 2008

Analysis of the ABCA4 genomic locus in Stargardt disease

scientific article

Identification of the Bacillus subtilis pur operon repressor

scientific article published on August 1, 1995

LMNA cardiomyopathy: cell biology and genetics meet clinical medicine.

scientific article

DNA-like class R inhibitory oligonucleotides (INH-ODNs) preferentially block autoantigen-induced B-cell and dendritic cell activation in vitro and autoantibody production in lupus-prone MRL-Fas(lpr/lpr) mice in vivo

scientific article published on 28 May 2009

Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations

scientific article published on 23 December 2016

Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation

scientific article

Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1

scientific article

A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder

scientific article

Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposis

scientific article published on September 14, 2010

LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

scientific article published on 20 December 2011

A histone H3K9M mutation traps histone methyltransferase Clr4 to prevent heterochromatin spreading

scientific article

Two genes for de novo purine nucleotide synthesis on human chromosome 4 are closely linked and divergently transcribed

scientific article

Isoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 (SAT1) gene in major depression and suicide

scientific article

Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort.

scientific article

Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiency

scientific article

The proper splicing of RNAi factors is critical for pericentric heterochromatin assembly in fission yeast

scientific article

C9ORF72 repeat expansions not detected in a group of patients with schizophrenia

scientific article published on October 1, 2012

Phenotypic and molecular analyses of primary lateral sclerosis

scientific article published on April 14, 2015

Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion.

scientific article published on 31 August 2016

Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere length.

scientific article

A case study of an integrative genomic and experimental therapeutic approach for rare tumors: identification of vulnerabilities in a pediatric poorly differentiated carcinoma.

scientific article published on 31 October 2016

Characterization of a novel fusion gene EML4-NTRK3 in a case of recurrent congenital fibrosarcoma.

scientific article published on October 2015

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy

scientific article published on 22 February 2019

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

scientific article

The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations.

scientific article published on 22 July 2015

2q24 deletions: Further characterization of clinical findings and their relation to the SCN cluster

scientific article published on 28 September 2012

Inherited selective cobalamin malabsorption in Komondor dogs associated with a CUBN splice site variant

scientific article published on 27 December 2018

Clinical Implementation of Genomic Sequencing in Pediatric Oncology: Identification and Valuation of Resources and Costs Associated with Next-Generation Sequencing

scientific article published on 26 October 2014

Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected SYNGAP1-Related Disorder

scientific article published on 28 August 2018

Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third

scientific article published on 07 July 2020

Brain-Derived Neurotrophic Factor Elevates Activating Transcription Factor 4 (ATF4) in Neurons and Promotes ATF4-Dependent Induction of Sesn2.

scientific article published in March 2018

Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins

scientific article published on 01 January 2018

List of works by Peter L Nagy

A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3

Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regions.

The Glc7 phosphatase subunit of the cleavage and polyadenylation factor is essential for transcription termination on snoRNA genes.

Analysis of the ABCA4 genomic locus in Stargardt disease

Identification of the Bacillus subtilis pur operon repressor

LMNA cardiomyopathy: cell biology and genetics meet clinical medicine.

DNA-like class R inhibitory oligonucleotides (INH-ODNs) preferentially block autoantigen-induced B-cell and dendritic cell activation in vitro and autoantibody production in lupus-prone MRL-Fas(lpr/lpr) mice in vivo

Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations

Comparative anatomy of chromosomal domains with imprinted and non-imprinted allele-specific DNA methylation

Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1

A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder

Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposis

LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle

A histone H3K9M mutation traps histone methyltransferase Clr4 to prevent heterochromatin spreading

Two genes for de novo purine nucleotide synthesis on human chromosome 4 are closely linked and divergently transcribed

Isoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 (SAT1) gene in major depression and suicide

Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort.

Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiency

The proper splicing of RNAi factors is critical for pericentric heterochromatin assembly in fission yeast

C9ORF72 repeat expansions not detected in a group of patients with schizophrenia

Phenotypic and molecular analyses of primary lateral sclerosis

Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion.

Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere length.

A case study of an integrative genomic and experimental therapeutic approach for rare tumors: identification of vulnerabilities in a pediatric poorly differentiated carcinoma.

Characterization of a novel fusion gene EML4-NTRK3 in a case of recurrent congenital fibrosarcoma.

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations.

2q24 deletions: Further characterization of clinical findings and their relation to the SCN cluster

Inherited selective cobalamin malabsorption in Komondor dogs associated with a CUBN splice site variant

Clinical Implementation of Genomic Sequencing in Pediatric Oncology: Identification and Valuation of Resources and Costs Associated with Next-Generation Sequencing

Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected SYNGAP1-Related Disorder

Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third

Brain-Derived Neurotrophic Factor Elevates Activating Transcription Factor 4 (ATF4) in Neurons and Promotes ATF4-Dependent Induction of Sesn2.

Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins