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Publications by Bohua Wu

Investigating the Effects of Missense Mutations in MSH2 Gene Associated With Lynch Syndrome

Biophysical Journal

Biophysics

2019

English

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Novel Germline MSH2 Mutation in Lynch Syndrome Patient Surviving Multiple Cancers

Hereditary Cancer in Clinical Practice

Oncology

Genetics

2012

English

Late Onset MLD With Normal Nerve Conduction Associated With Two Novel Missense Mutations in the ASA Gene

Journal of Neurology, Neurosurgery and Psychiatry

English

Long-Qt Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel

Circulation

Cardiovascular Medicine

Physiology

Cardiology

2001

English

Recq Helicase, Missense Mutations, Oxidative Stress and BLM Gene Defect in Bloom Syndrome

International Journal of Molecular Biology

2017

English

Predictors and Prevalence of Paraganglioma Syndrome Associated With Mutations of the SDHC Gene

JAMA - Journal of the American Medical Association

Medicine

2005

English

Analyzing Effects of Naturally Occurring Missense Mutations

Computational and Mathematical Methods in Medicine

English

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

American Journal of Human Genetics

Genetics

2018

English

Three Novel Missense Mutations in SLC20A2 Associated With Idiopathic Basal Ganglia Calcification

Journal of the Neurological Sciences

Neurology

2017

English

Functional Characterization of Bestrophin-1 Missense Mutations Associated With Autosomal Recessive Bestrophinopathy

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Bohua Wu

Investigating the Effects of Missense Mutations in MSH2 Gene Associated With Lynch Syndrome

Related publications

Novel Germline MSH2 Mutation in Lynch Syndrome Patient Surviving Multiple Cancers

Late Onset MLD With Normal Nerve Conduction Associated With Two Novel Missense Mutations in the ASA Gene

Long-Qt Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel

Recq Helicase, Missense Mutations, Oxidative Stress and BLM Gene Defect in Bloom Syndrome

Predictors and Prevalence of Paraganglioma Syndrome Associated With Mutations of the SDHC Gene

Analyzing Effects of Naturally Occurring Missense Mutations

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

Three Novel Missense Mutations in SLC20A2 Associated With Idiopathic Basal Ganglia Calcification

Functional Characterization of Bestrophin-1 Missense Mutations Associated With Autosomal Recessive Bestrophinopathy