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Mohammed Mahnashi

Observed names: Mohammed A Mahnashi, Mohammed A. Mahnashi, Mohammed Alhussain Mahnashi
ORCID: 0000-0003-0263-5301
Observed ORCID: 0000-0003-0263-5301
OpenAlex ID: A5021775839
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
2019 · Dorota Monies, Mohammed Abouelhoda, et al. · The American Journal of Human Genetics · 298
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The morbid genome of ciliopathies: an update
2020 · Hanan E. Shamseldin, Ranad Shaheen, et al. · Genetics in Medicine · 111
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
2019 · Dorota Monies, Mohammed Abouelhoda, et al. · The American Journal of Human Genetics · 48
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Recessive, Deleterious Variants in SMG8 Expand the Role of Nonsense-Mediated Decay in Developmental Disorders in Humans
2020 · Fatema Alzahrani, Hiroyuki Kuwahara, et al. · The American Journal of Human Genetics · 31
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Adult genomic medicine: lessons from a multisite study of 2700 patients
2025 · Khadijah Bakur, Halima Hamid, et al. · Genome Medicine · 9
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The morbid genome of ciliopathies: an update
2022 · Hanan E. Shamseldin, Ranad Shaheen, et al. · Genetics in Medicine · 7
Diagnosis and Management of Pompe Disease in Saudi Arabia
2021 · Mohammed Mahnashi, Ali Alshehri, et al. · American Journal of Medicine and Medical Sciences · 3
JAK2 Mutations in Chronic Myeloproliferative Neoplasm; Towards the Application of Personalized Treatments for Saudi Patients
2012 · Mamdooh Gari, Fatin Al-Sayes, et al. · Open Journal of Blood Diseases · 3
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Case report of congenital neutropenia type 4 with glucose‐6‐phosphatase catalytic subunit 3 (G6PC3) deficiency
2024 · Nabil S. Dhayhi, Mohammed A. Mahnashi, et al. · Clinical Case Reports · 2
Ellis-van Creveld Syndrome 2 With Novel Partial Exon 11 Deletion: A Case From Saudi Arabia
2021 · Nouf Alessa, Mohammed A Mahnashi, et al. · Cureus · 2
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Cellulitis Induced by Jellyfish Sting in A 3-Year-Old Boy: A Case Report, Jazan, Saudi Arabia
2024 · Hadi H. Daghreeri, Mohammed Mahnashi, et al. · Saudi Journal of Emergency Medicine · 1
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Biallelic EZH1 Nonsense Novel Variant in Two Siblings with Neurodevelopmental Disorder and Central Precocious Puberty: A Case Report from a Consanguineous Saudi Family
2026 · Mohamed Baity, Khalid Alharbi, et al. · International Journal of Molecular Sciences
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High-throughput evidence generation to support tentative gene–disease relationship from a cohort enriched for autozygosity and founder effect
2026 · Khadijah Bakur, Bader Alhaddad, et al. · Genetics in Medicine
Early-onset lipoprotein lipase deficiency: detailed analysis of severe hypertriglyceridemia and recurrent necrotizing pancreatitis
2025 · Mohammed Alhussain Mahnashi, Ismail Washili, et al. · Journal of Biochemical and Clinical Genetics
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Vitamin D Dependent Rickets Type 1a as a Rare Cause of Rickets: Case Report and Literature Review
2023 · Amer O. AL Ali, Mohammed A. Soeid, et al. · Scholars Journal of Medical Case Reports
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Vitamin D Dependent Rickets Type IB as a Rare Cause of Rickets, Case Report and Literature Review
2022 · Amer O. AL Ali, Mohammed A. Soeid, et al. · Scholars Journal of Medical Case Reports
Gaucher???s Disease: A Case Report
2020 · Haya H Ezadeen, Mohammed Mahnashi, et al. · Current Pediatric Research
Works count: 17
Citation count: 515
H-index: 6
I10-index: 4
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