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Hussein Sheikh Ali Mohamoud

BRAF gene: From human cancers to developmental syndromes
2014 · Muhammad Ramzan Manwar Hussain, Mukhtiar Baig, et al. · Saudi Journal of Biological Sciences · 120
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Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis
2017 · Chunbo Yang, Yaobo Xu, et al. · Human Molecular Genetics · 65
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A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalities
2019 · Musharraf Jelani, Hannah C. Dooley, et al. · Brain · 50
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Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3
2015 · Saleem Ahmed, Musharraf Jelani, et al. · Journal of the Neurological Sciences · 43
A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features
2018 · Hussein Sheikh Mohamoud, Saleem Ahmed, et al. · Scientific Reports · 37
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Novel nonsense mutation in the PTRF gene underlies congenital generalized lipodystrophy in a consanguineous Saudi family
2015 · Musharraf Jelani, Saleem Ahmed, et al. · European Journal of Medical Genetics · 35
A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family
2016 · Musharraf Jelani, Changsoo Kang, et al. · Archives of Oral Biology · 29
First ComprehensiveIn SilicoAnalysis of the Functional and Structural Consequences of SNPs in HumanGalNAc-T1Gene
2014 · Hussein Sheikh Ali Mohamoud, Muhammad Ramzan Manwar Hussain, et al. · Computational and Mathematical Methods in Medicine · 29
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
2016 · Fatma Dursun, Hussein Sheikh Ali Mohamoud, et al. · Journal of Clinical Research in Pediatric Endocrinology · 27
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The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family
2016 · Nuha Alrayes, Hussein Sheikh Ali Mohamoud, et al. · Journal of the Neurological Sciences · 23
Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
2015 · Nuha Alrayes, Hussein Sheikh Ali Mohamoud, et al. · BMC Research Notes · 21
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Case of Sjögren–Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis
2015 · Nagwa E. A. Gaboon, Musharraf Jelani, et al. · The Journal of Dermatology · 17
Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH)
2018 · Fehmida Bibi, Isse Ali, et al. · PLoS ONE · 16
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Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family
2015 · Yaser Mohammad Alkhiary, Musharraf Jelani, et al. · Saudi Journal of Biological Sciences · 8
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The Microbial Pathology of Neu5Ac and Gal Epitopes
2013 · Muhammad Ramzan Manwar Hussain, Hani Asfour, et al. · Journal of Carbohydrate Chemistry · 7
Identification of Two Homozygous Sequence Variants in the COL7A1 Gene Underlying Dystrophic Epidermolysis Bullosa by Whole‐Exome Analysis in a Consanguineous Family
2015 · Rehab Serafi, Musharraf Jelani, et al. · Annals of Human Genetics · 4
From Genes to Health – Challenges and Opportunities
2014 · Muhammad Ramzan Manwar Hussain, Asifullah Khan, et al. · Frontiers in Pediatrics · 3
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Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia
2018 · Hams S. Al‐Zahrani, Saeed Al‐Tala, et al. · Congenital Anomalies · 1
An identification and prediction methods for feature-subsets of CpG islands methylation based on human peripheral blood leukocytes of chromosome 21q
2011 · I. Ali, H. S. A. Mohamoud · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · 1
Whole exome sequencing reveals a homozygous SGCB variant in a Pakhtun family with limb girdle muscular dystrophy (LGMDR4) phenotype
2020 · Muhammad Tariq, Muhammad Latif, et al. · Gene Reports
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Additional file 2: of Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
2015 · Alrayes, Nuha, Mohamoud, Hussein, et al. · Figshare
Additional file 1: of Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)
2015 · Alrayes, Nuha, Mohamoud, Hussein, et al. · Figshare
P2: Finetuning of the genotype-phenotype correlation in Cri du Chat syndrome using array CGH
2005 · Adri Mul, Hai-Yen Man, et al. · European Journal of Medical Genetics
Works count: 26
Citation count: 536
H-index: 13
I10-index: 13
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