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Publications by Bronwyn Overs
Using Linkage Studies Combined With Whole‐exome Sequencing to Identify Novel Candidate Genes for Familial Colorectal Cancer
International Journal of Cancer
Cancer Research
Oncology
Prevalence and Factors Associated With Parental Concerns About Development Detected by theParents’ Evaluation of Developmental Status (PEDS)at 6-Month, 12-Month and 18-Month Well-Child Checks in a Birth Cohort
BMJ Open
Medicine
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Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
Frontiers in Genetics
Genetics
Molecular Medicine
Exome Sequencing to Identify Novel Genes in Hypertension
Circulation: Cardiovascular Genetics
Using Whole-Exome Sequencing to Identify Variants Inherited From Mosaic Parents
European Journal of Human Genetics
Genetics
Whole Exome Sequencing in Extended Families With Autism Spectrum Disorder Implicates Four Candidate Genes
Human Genetics
Genetics
Annotation of Genes Having Candidate Somatic Mutations in Acute Myeloid Leukemia With Whole-Exome Sequencing Using Concept Lattice Analysis
Genomics and Informatics
Evolution
Ecology
Genetics
Systematics
Health Informatics
Behavior
Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Identification of ADHD Risk Genes in Extended Pedigrees by Combining Linkage Analysis and Whole-Exome Sequencing
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Exome Sequencing and Case-Control Analyses Identify RCC1 as a Candidate Breast Cancer Susceptibility Gene
International Journal of Cancer
Cancer Research
Oncology
