Publications by authors named "Mohammed A Aldahmesh"

Claim this Profile
D
Detection of Chromosomal Aneuploidy Using Exome Sequencing.
Mohamed H Al-Hamed, Sateesh Maddirevula, Nabil Moghrabi, Mohammed A Aldahmesh, Abdullah H Alfalah

Genes (Basel)· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital glaucoma and CYP1B1: an old story revisited.
Hessa S Alsaif, Arif O Khan, Nisha Patel, Hisham Alkuraya, Mais Hashem, Mohammed A Aldahmesh

Hum Genet· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.
Nisha Patel, Deepti Anand, Dorota Monies, Sateesh Maddirevula, Arif O Khan, Mohammed A Aldahmesh

Hum Genet· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Characterizing the morbid genome of ciliopathies.
Ranad Shaheen, Katarzyna Szymanska, Basudha Basu, Nisha Patel, Nour Ewida, Mohammed A Aldahmesh

Genome Biol· November 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital hereditary endothelial dystrophy, not glaucoma, in a child with iris colobomas.
Arif O Khan, Mohammed A Aldahmesh, Fowzan Alkuraya

J AAPOS· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis).
Arif O Khan, Mohammed A Aldahmesh, Fowzan S Alkuraya

Trans Am Ophthalmol Soc· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
Nisha Patel, Mohammed A Aldahmesh, Hisham Alkuraya, Shamsa Anazi, Hadeel Alsharif

Genet Med· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Characterization of LRPAP1-Related Pediatric High Myopia.
Arif O Khan, Mohammed A Aldahmesh, Fowzan S Alkuraya

Ophthalmology· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome-based case-control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy.
Corina Shtir, Mohammed A Aldahmesh, Saad Al-Dahmash, Emad Abboud, Hisham Alkuraya

Hum Genet· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lens subluxation and retinal dysfunction in a girl with homozygous VSX2 mutation.
Arif O Khan, Mohammed A Aldahmesh, Jawaher Noor, Ahmed Salem, Fowzan S Alkuraya

Ophthalmic Genet· March 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recessive mutations in LEPREL1 underlie a recognizable lens subluxation phenotype.
Arif O Khan, Mohammed A Aldahmesh, Hadeel Alsharif, Fowzan S Alkuraya

Ophthalmic Genet· March 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.
Anas M Alazami, Nisha Patel, Hanan E Shamseldin, Shamsa Anazi, Mohammed S Al-Dosari, Mohammed A Aldahmesh

Cell Rep· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutation.
Arif O Khan, Mohammed A Aldahmesh, Leen Abu-Safieh, Fowzan S Alkuraya

Ophthalmic Genet· September 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Complete aniridia with central keratopathy and congenital glaucoma is a CYP1B1-related phenotype.
Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, Hadia Hijazi, Fowzan S Alkuraya

Ophthalmic Genet· September 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome.
Mohammed A Aldahmesh, Yuanyuan Li, Amal Alhashem, Shams Anazi, Hisham Alkuraya

Hum Mol Genet· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Corneal enlargement without optic disk cupping in children with recessive CYP1B1 mutations.
Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, Fowzan S Alkuraya

J AAPOS· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18.
Mohammed A Aldahmesh, Muneera J Alshammari, Arif O Khan, Jawahir Y Mohamed, Fatimah A Alhabib

Hum Mutat· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
No evidence for locus heterogeneity in Knobloch syndrome.
Mohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, Alex V Levin, Wadakarn Wuthisiri

J Med Genet· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in LRPAP1 are associated with severe myopia in humans.
Mohammed A Aldahmesh, Arif O Khan, Hisham Alkuraya, Nouran Adly, Shamsa Anazi

Am J Hum Genet· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus.
Anas M Alazami, Hadia Hijazi, Mohammed S Al-Dosari, Ranad Shaheen, Amal Hashem, Mohammed A Aldahmesh

J Med Genet· July 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
J
Juvenile cataract morphology in 3 siblings not yet diagnosed with cerebrotendinous xanthomatosis.
Arif O Khan, Mohammed A Aldahmesh, Jawaher Y Mohamed, Fowzan S Alkuraya

Ophthalmology· May 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.
Fatema Zahrani, Mohammed A Aldahmesh, Muneera J Alshammari, Selwa A F Al-Hazzaa, Fowzan S Alkuraya

Am J Hum Genet· March 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biometric and molecular characterization of clinically diagnosed posterior microphthalmos.
Sawsan R Nowilaty, Arif O Khan, Mohammed A Aldahmesh, Khalid F Tabbara, Abdullah Al-Amri

Am J Ophthalmol· February 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital glaucoma with acquired peripheral circumferential iris degeneration.
Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, Fowzan S Alkuraya

J AAPOS· February 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CYP1B1 analysis of unilateral primary newborn glaucoma in Saudi children.
Arif O Khan, Mohammed A Aldahmesh, Jawahir Y Mohamed, Hadia Hijazi, Fowzan S Alkuraya

J AAPOS· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis