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Mohammad Silawi

Observed name: Silawi, Mohammad
OpenAlex ID: A5017825808
Molecular diagnostic assays for COVID-19: an overview
2021 · Parham Habibzadeh, Mohammad Mofatteh, et al. · Critical Reviews in Clinical Laboratory Sciences · 74
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
2019 · Mohammad Ali Farazi Fard, Adriana P. Rebelo, et al. · The American Journal of Human Genetics · 62
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Expanding the molecular and clinical phenotypes of FUT8‐CDG
2020 · Bobby G. Ng, Hassan Dastsooz, et al. · Journal of Inherited Metabolic Disease · 33
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Genomic prediction for growth using a low-density SNP panel in dromedary camels
2021 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Scientific Reports · 24
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A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment
2019 · Parham Habibzadeh, Soroor Inaloo, et al. · Frontiers in Neurology · 22
Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing
2022 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Animals · 13
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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
2019 · Mohammad Ali Farazi Fard, Adriana P. Rebelo, et al. · The American Journal of Human Genetics · 11
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Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy
2020 · Parham Habibzadeh, Mohammad Silawi, et al. · BMC Gastroenterology · 10
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A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report
2019 · Fateme Ziyaee, Eslam Shorafa, et al. · BMC Medical Genetics · 10
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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
2021 · Daniel L. Polla, Mohammad Ali Farazi Fard, et al. · Genetics in Medicine · 9
Association between rs2303861 polymorphism in CD82 gene and non-alcoholic fatty liver disease: a preliminary case-control study
2019 · Parham Habibzadeh, Behnam Honarvar, et al. · Croatian Medical Journal · 9
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A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report
2018 · Hossein Esmaeilzadeh, Mohammad Reza Bordbar, et al. · BMC Medical Genetics · 8
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Genome-Wide Diversity, Population Structure and Demographic History of Dromedaries in the Central Desert of Iran
2020 · Morteza Bitaraf Sani, Javad Zare Harofte, et al. · Genes · 7
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Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report
2018 · Fatemeh Maghami, Seyed Mohammad Bagher Tabei, et al. · BMC Medical Genetics · 5
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Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations
2017 · Fatemeh Dehghanian, Mohammad Silawi, et al. · Clinical Laboratory · 3
Successful Linkage Analysis in Classical Phenylketonuria Families Followed by Direct Sequencing and Mutation Detection
2016 · Mohammad Silawi, Somayyeh Haqparast, et al. · Clinical Laboratory · 1
Characterization of a Novel Pathogenic Mutation Causing Mitochondrial Neurogastrointestinal Encephalopathy
2019 · Parham Habibzadeh, Mohammad Silawi, et al. · Research Square
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Works count: 20
Citation count: 301
H-index: 9
I10-index: 9
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