Sameera Sogaty
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Hearing, Cochlea, Tinnitus, Genetics, RNA modifications and cancer
Most-Cited Works
- → Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families(2014)467 cited
- → Genomic analysis of primordial dwarfism reveals novel disease genes(2014)163 cited
- → The genetic landscape of familial congenital hydrocephalus(2017)146 cited
- → The morbid genome of ciliopathies: an update(2020)103 cited
- → Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes(2012)71 cited
- → Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy(2020)38 cited
- → A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population(2011)29 cited
- → Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population(2019)29 cited
- → Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly(2021)21 cited
- → Microcephaly‐capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing(2016)21 cited