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Publications by Amirthagowri Ambalavanan
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals
PLoS ONE
Multidisciplinary
Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant With Autistic-Like Features
BMC Medical Genetics
Genetics
Related publications
The Rate of De Novo CNVs in Healthy Controls
Elevated Germline Mutation Rate in Teenage Fathers
Proceedings of the Royal Society B: Biological Sciences
Genetics
Molecular Biology
Environmental Science
Biochemistry
Microbiology
Immunology
Biological Sciences
Medicine
Agricultural
Germline Mutation of RET Codon 883 in Two Cases of De Novo MEN 2B
Oncogene
Cancer Research
Genetics
Molecular Biology
A Germline or De Novo Mutation in Two Families With Gaucher Disease: Implications for Recessive Disorders
European Journal of Human Genetics
Genetics
De Novo VHL Germline Mutation Detected in a Patient With Mild Clinical Phenotype of Von Hippel-Lindau Disease
Journal of Neurosurgery
Surgery
Neurology
Toward Understanding De Novo Germline Mutations in Mammals
Genes and Genetic Systems
Medicine
Genetics
Molecular Biology
P53 Deficiency Does Not Affect Mutation Rate in the Mouse Germline
Oncogene
Cancer Research
Genetics
Molecular Biology
A Human De Novo Mutation inMYH10phenocopies the Loss of Function Mutation in Mice
Rare Diseases
8-Oxoguanine Causes Spontaneous De Novo Germline Mutations in Mice
Scientific Reports
Multidisciplinary
