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Sameera Sogaty · SciRah

Researcher profile · Semantic Scholar

Sameera Sogaty

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Sameera Sogaty — researcher profile on SciRah

h-index: 12
Works: 14
Citations: 1,226

Most-cited papers

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.
A. Alazami, N. Patel, H. Shamseldin, S. Anazi +49 more
2015Cell Reports461 citations Open access
Semantic Scholar
Genomic analysis of primordial dwarfism reveals novel disease genes
R. Shaheen, E. Faqeih, Shinu Ansari, G. Abdel-Salam +5 more
2014Genome Research162 citations Open access
Semantic Scholar
IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome.
M. Aldahmesh, Yuan-Yuan Li, A. Alhashem, S. Anazi +11 more
2014Human Molecular Genetics147 citations Open access
Semantic Scholar
The genetic landscape of familial congenital hydrocephalus
R. Shaheen, M. Sebai, N. Patel, N. Ewida +25 more
2017Annals of Neurology127 citations
Semantic Scholar
The morbid genome of ciliopathies: an update
H. Shamseldin, R. Shaheen, N. Ewida, Dalal K Bubshait +37 more
2020Genetics in Medicine95 citations Open access
Semantic Scholar
Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes
R. Shaheen, E. Faqeih, M. Alshammari, Abdulrahman Swaid +10 more
2012European Journal of Human Genetics74 citations Open access
Semantic Scholar
Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy
Z. Al-Hassnan, A. Almesned, S. Tulbah, A. Alakhfash +30 more
2020Circulation Genomic and Precision Medicine43 citations Open access
Semantic Scholar
A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population
F. Imtiaz, K. Taibah, K. Ramzan, Ghada Bin-Khamis +10 more
2011BMC Medical Genetics30 citations Open access
Semantic Scholar
Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly
M. I. Naseer, A. Abdulkareem, O. Muthaffar, Sameera Sogaty +3 more
2021Frontiers in Pediatrics24 citations Open access
Semantic Scholar
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
M. I. Naseer, M. Rasool, Sameera Sogaty, Rukhaa Adeel Chaudhary +4 more
2017Annals of Saudi Medicine22 citations Open access
Semantic Scholar
Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population
K. Ramzan, M. Al-Owain, N. Al-Numair, Sibtain Afzal +11 more
2019American Journal of Medical Genetics Part B: Neuropsychiatric Genetics18 citations
Semantic Scholar
Microcephaly‐capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing
M. I. Naseer, Sameera Sogaty, M. Rasool, A. Chaudhary +8 more
2016American Journal of Medical Genetics. Part A16 citations
Semantic Scholar
Chromosomal Micro-aberration in a Saudi Family with Juvenile Myoclonic Epilepsy.
M. I. Naseer, M. Rasool, A. Chaudhary, Sameera Sogaty +6 more
2017CNS and Neurological Disorders - Drug Targets7 citations
Semantic Scholar
The morbid genome of ciliopathies: an update.
H. Shamseldin, R. Shaheen, N. Ewida, Dalal K Bubshait +37 more
2022Genetics in Medicine2 citations Open access
Semantic Scholar

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