Monis B. Shamsi
Medina, 42353, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 17 publications
Identification of a Protein-truncating Variant in SCAPER Gene Causing Syndromic form of Intellectual Disability.
Journal: Current medicinal chemistry
Published: November 08, 2024
Prevalence and clinical considerations of Y chromosome microdeletions in azoospermic and oligozoopsermic infertile men from Al Madinah Al Munawarah, Saudi Arabia.
Journal: Saudi medical journal
Published: September 09, 2024
KMT2C Polymorphism in Familial Hypospadias.
Journal: Indian journal of pediatrics
Published: August 14, 2024
Identification of a novel candidate HSD3B2 gene variant for familial hypospadias by whole-exome sequencing.
Journal: Frontiers in genetics
Published: November 24, 2022
Negatively charged food additive dye "Allura Red" rapidly induces SDS-soluble amyloid fibril in beta-lactoglobulin protein.
Journal: International journal of biological macromolecules
Published: June 10, 2017
Teratozoospermia and asthenozoospermia are associated with specific epigenetic signatures.
Journal: Andrology
Published: January 08, 2016
Decreased fecundity and sperm DNA methylation patterns.
Journal: Fertility and sterility
Published: May 11, 2015
Paternal influence of sperm DNA integrity on early embryonic development.
Journal: Human reproduction (Oxford, England)
Published: September 11, 2014
Y chromosome microdeletions in infertile men: prevalence, phenotypes and screening markers for the Indian population.
Journal: Journal of assisted reproduction and genetics
Published: December 03, 2012
Mitochondrial DNA variations in ova and blastocyst: implications in assisted reproduction.
Journal: Mitochondrion
Published: October 01, 2012
Last Updated: 09/26/2026