Ron Schwessinger

Oxford, ENG OX39DS, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 03, 2026

Exploring the size limits of Bionano optical genome mapping to resolve alternative structures of linked interspersed chromosomal duplications.

Exploring the size limits of Bionano optical genome mapping to resolve alternative structures of linked interspersed chromosomal duplications.

Journal: Genome medicine
Published: March 01, 2025

Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locus.

Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locus.

Journal: HGG advances
Published: April 03, 2024

Iron overload induces dysplastic erythropoiesis and features of myelodysplasia in Nrf2-deficient mice.

Iron overload induces dysplastic erythropoiesis and features of myelodysplasia in Nrf2-deficient mice.

Journal: Leukemia
Published: April 28, 2023

Predicting Chromatin Interactions from DNA Sequence Using DeepC.

Predicting Chromatin Interactions from DNA Sequence Using DeepC.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: February 01, 2023

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.

Journal: Genome medicine
Published: December 14, 2022

Direct correction of haemoglobin E β-thalassaemia using base editors.

Direct correction of haemoglobin E β-thalassaemia using base editors.

Journal: Nature communications
Published: July 04, 2022

The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin.

The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin.

Journal: Nature communications
Published: August 27, 2021

Dynamic Runx1 chromatin boundaries affect gene expression in hematopoietic development.

Dynamic Runx1 chromatin boundaries affect gene expression in hematopoietic development.

Journal: Nature communications
Published: June 08, 2021

Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.

Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.

Journal: Nature genetics
Published: April 30, 2021

Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus.

Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus.

Journal: Nature genetics
Published: October 23, 2020

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Journal: Haematologica
Published: May 20, 2020
Showing 1-12 of 19

Last Updated: 09/26/2026