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Publications by Mohammad Ali Farazi Fard
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
American Journal of Human Genetics
Genetics
A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
A Novel Splice Site Mutation in WAS Gene in Patient With Wiskott-Aldrich Syndrome and Chronic Colitis: A Case Report
BMC Medical Genetics
Genetics
Pre-Implantation Genetic Diagnosis in an Iranian Family With a Novel Mutation in MUT Gene
BMC Medical Genetics
Genetics
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Sequencing Studies in Human Genetics: Design and Interpretation
Nature Reviews Genetics
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Evolution of Genetic and Genomic Features Unique to the Human Lineage
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Recent Human Adaptation: Genomic Approaches, Interpretation and Insights
Nature Reviews Genetics
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ChIP–seq and Beyond: New and Improved Methodologies to Detect and Characterize Protein–DNA Interactions
Nature Reviews Genetics
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Sex and the Singular DM Domain: Insights Into Sexual Regulation, Evolution and Plasticity
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Putting Gene Essentiality Into Context
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Promoter-Proximal Pausing of RNA Polymerase II: Emerging Roles in Metazoans
Nature Reviews Genetics
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Stress and the Epigenetic Landscape: A Link to the Pathobiology of Human Diseases?
Nature Reviews Genetics
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Autoimmune Diseases — Connecting Risk Alleles With Molecular Traits of the Immune System
Nature Reviews Genetics
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Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
Nature Reviews Genetics
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