List of works - Chris Hahn

A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia

scientific article published on 18 July 2017

A four-gene LincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients.

scientific article

A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia

scientific article published on 28 March 2019

A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm.

scientific article

A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability

scientific article published on 03 June 2020

ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II).

scientific article published on 12 October 2017

Chronic increases in sphingosine kinase-1 activity induce a pro-inflammatory, pro-angiogenic phenotype in endothelial cells.

scientific article published on 23 February 2009

Clinical implications of transient myeloproliferative disorder in a neonate without Down syndrome features

scientific article published on 04 July 2017

Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis

scientific article published on 24 October 2019

Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes

scientific article published on 23 June 2017

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

scientific article published on 19 April 2018

Genomic subtyping and therapeutic targeting of acute erythroleukemia

scientific article published on 29 March 2019

Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6

scientific article published on 14 November 2019

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

scientific article published on 15 October 2009

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies

scientific journal article

Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes

scientific article published on 29 April 2010

Regulation of vascular leak and recovery from ischemic injury by general and VE-cadherin-restricted miRNA antagonists of miR-27.

scientific article published on 5 September 2013

Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient.

scientific article published on 29 September 2017

Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis.

scientific article published on 6 August 2010

Spliceosome mutations in hematopoietic malignancies ⬇️

scientific article published on December 27, 2011

Stress-induced premature senescence mediated by a novel gene, SENEX, results in an anti-inflammatory phenotype in endothelial cells

scientific article published on 27 July 2010

T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ.

scientific article published on 15 March 2017

The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution

scientific article published on 14 May 2019

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

scientific article

List of works by Chris Hahn

A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia

A four-gene LincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients.

A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia

A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm.

A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability

ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II).

Chronic increases in sphingosine kinase-1 activity induce a pro-inflammatory, pro-angiogenic phenotype in endothelial cells.

Clinical implications of transient myeloproliferative disorder in a neonate without Down syndrome features

Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis

Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

Genomic subtyping and therapeutic targeting of acute erythroleukemia

Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies

Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes

Regulation of vascular leak and recovery from ischemic injury by general and VE-cadherin-restricted miRNA antagonists of miR-27.

Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient.

Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis.

Spliceosome mutations in hematopoietic malignancies ⬇️

Stress-induced premature senescence mediated by a novel gene, SENEX, results in an anti-inflammatory phenotype in endothelial cells

T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ.

The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.