Salma M. Wakil
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 75 publications
Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population.
Journal: Clinical dysmorphology
Published: February 27, 2024
Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.
Journal: Dose-response : a publication of International Hormesis Society
Published: March 28, 2021
New or vanishing frontiers: LACC1-associated juvenile arthritis.
Journal: International journal of pediatrics & adolescent medicine
Published: June 30, 2020
Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib.
Journal: Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society
Published: April 01, 2020
New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Journal: Omics : a journal of integrative biology
Published: December 20, 2019
Interleukin-8 Dedifferentiates Primary Human Luminal Cells to Multipotent Stem Cells.
Journal: Molecular and cellular biology
Published: October 16, 2019
A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients.
Journal: BMC medical genetics
Published: September 04, 2019
A novel KIT mutation in a family with expanded syndrome of piebaldism.
Journal: JAAD case reports
Published: July 26, 2019
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia.
Journal: BMC medical genetics
Published: March 03, 2019
Familial, long-term pollakisuria as initial manifestation of HSP4 due to the SPAST variant c.683-2A>C.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: February 26, 2019
First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient.
Journal: Molecular cytogenetics
Published: February 13, 2019
Last Updated: 09/26/2026