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M. Amin · SciRah

Researcher profile · Semantic Scholar

M. Amin

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M. Amin — researcher profile on SciRah

h-index: 11
Works: 47
Citations: 459

Most-cited papers

The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources
Marina T. DiStefano, Scott Goehringer, L. Babb, F. Alkuraya +42 more
2022medRxiv149 citations Open access
Semantic Scholar
Multiplicity of infection and genetic diversity of Plasmodium falciparum isolates from patients with uncomplicated and severe malaria in Gezira State, Sudan
Muzamil Mahdi Abdel Hamid, Arwa F. Elamin, Musab M. Ali Albsheer, Abdelmohaymin Abdalla +4 more
2016Parasites & Vectors48 citations Open access
Semantic Scholar
Transmission of Plasmodium vivax in Duffy-negative individuals in central Sudan.
M. H. Abdelraheem, Musab M. A. Albsheer, H. S. Mohamed, M. Amin +1 more
2016Transactions of the Royal Society of Tropical Medicine and Hygiene40 citations
Semantic Scholar
Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report
Ashraf Yahia, Liena E. O. Elsayed, Arwa Babai, M. Salih +10 more
2018BMC Neurology19 citations Open access
Semantic Scholar
Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression
M. Amin, J. Ott, D. Gordon, R. Wu +3 more
2022International Journal of Molecular Sciences16 citations Open access
Semantic Scholar
Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
Hazem Kaheel, Andreas Bress, M. Hassan, A. A. Shah +3 more
2018BMC Ear, Nose and Throat Disorders14 citations Open access
Semantic Scholar
Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity
M. Amin, S. Syed, R. Wu, T. Postolache +1 more
2022International Journal of Molecular Sciences13 citations Open access
Semantic Scholar
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +10 more
2018BMC Medical Genetics13 citations Open access
Semantic Scholar
Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data
M. Koko, M. O. Abdallah, M. Amin, M. Ibrahim
2018BMC Genomics13 citations Open access
Semantic Scholar
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
Ashraf Yahia, Ahlam A. A. Hamed, I. Mohamed, Maha A. Elseed +40 more
2023European Journal of Human Genetics12 citations Open access
Semantic Scholar
Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression
M. Amin, J. Ott, R. Wu, T. Postolache +1 more
2022International Journal of Molecular Sciences12 citations Open access
Semantic Scholar
Genetic diversity and multiplicity of Plasmodium falciparum merozoite surface protein 2 in field isolates from Sudan
Shaza O. Mustafa, Muzamil M. Abdel Hamid, M. Aboud, M. Amin +4 more
201711 citations Open access
Semantic Scholar
In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease
Y. Bakhit, M. O. Ibrahim, M. Amin, Y. Mirghani +1 more
2016Adv. Bioinformatics11 citations Open access
Semantic Scholar
Linkage and association of variants in the dopamine receptor 2 gene (DRD2) with polycystic ovary syndrome
M. Amin, Nicholas Horst, Claudia Gragnoli
2023Journal of Ovarian Research10 citations Open access
Semantic Scholar
Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report
M. Amin, Y. Bakhit, M. Koko, M. O. Ibrahim +3 more
2019Acta myologica8 citations
Semantic Scholar
Novel corticotropin-releasing hormone receptor genes (CRHR1 and CRHR2) linkage to and association with polycystic ovary syndrome
M. Amin, Nicholas Horst, R. Wu, Claudia Gragnoli
2023Journal of Ovarian Research7 citations Open access
Semantic Scholar
Novel variants causing megalencephalic leukodystrophy in Sudanese families
M. Amin, Cédric Vignal, Ahlam A. A. Hamed, Inaam N. Mohammed +19 more
2021Journal of Human Genetics7 citations
Semantic Scholar
Novel linkage and association of the mineralocorticoid receptor gene (NR3C2) with familial type 2 diabetes and depression and their comorbidity
M. Amin, S. Syed, R. Wu, T. Postolache +1 more
2023Aspects of Molecular Medicine6 citations Open access
Semantic Scholar
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
M. Amin, Cédric Vignal, Esraa Eltaraifee, Inaam N. Mohammed +12 more
2022BMC Medical Genomics6 citations Open access
Semantic Scholar
Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment
Hazem Kaheel, Andreas Bress, M. Hassan, A. A. Shah +3 more
2017Genetics Research International6 citations Open access
Semantic Scholar
The prolactin receptor (PRLR) gene is linked to and associated with the comorbidity of depression and type 2 diabetes in Italian families
M. Amin, R. Wu, T. Postolache, Claudia Gragnoli
2023Genes and Diseases5 citations Open access
Semantic Scholar
The role of melatonin receptor 1B gene (MTNR1B) in the susceptibility to depression and type 2 diabetes comorbidity
M. Amin, B. Rafla, R. Wu, T. Postolache +1 more
2023Genes and Diseases5 citations Open access
Semantic Scholar
Clinical and Genetic Characteristics of Leukodystrophies in Africa
M. Amin, Liena E. O. Elsayed, A. Ahmed
2017Journal of Neurosciences in Rural Practice5 citations Open access
Semantic Scholar
Novel Risk Variants in the Oxytocin Receptor Gene (OXTR) Possibly Linked to and Associated with Familial Type 2 Diabetes
M. Amin, R. Wu, Claudia Gragnoli
2023International Journal of Molecular Sciences4 citations Open access
Semantic Scholar
Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms
A. Roberts, Marina T. DiStefano, E. Riggs, K. Josephs +22 more
2023medRxiv3 citations Open access
Semantic Scholar
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
M. Amin, Cédric Vignal, A. Hamed, Inaam N. Mohammed +19 more
2022Frontiers in Genetics3 citations Open access
Semantic Scholar
Recombination and purifying and balancing selection determine the evolution of major antigenic protein 1 (map 1) family genes in Ehrlichia ruminantium.
B. Salim, M. Amin, Manabu Igarashi, Kimihito Ito +4 more
2019Gene3 citations Open access
Semantic Scholar
Overdominance Effects between Malaria and Visceral Leishmaniasis in the 5q31 Region
M. Amin, A. Elhassan, K. Rocket, M. Ibrahim
20153 citations Open access
Semantic Scholar
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
M. Koko, Maha A. Elseed, Inaam N. Mohammed, Ahlam A. A. Hamed +23 more
2024European Journal of Human Genetics2 citations Open access
Semantic Scholar
P451: The Gene Curation Coalition works to resolve discrepancies in gene-disease validity assertions
Marina T. DiStefano, J. Amberger, C. Austin-Tse, M. Balzotti +34 more
2023Genetics in Medicine Open1 citations Open access
Semantic Scholar
Genetic Susceptibility to Asthma and Genetic Interactions in the 5q31-q33 and 16p11 Regions in Sudanese Families
A. Osman, M. Amin, Hiba Salah, O. Abdelaziz +1 more
20181 citations Open access
Semantic Scholar
Biochemical Differences in Human Breast Milk Contents According to Infant’s Gender
Salma Dafaallah, M. Amin, Amar S. Mohammed, Eman Kabbara +1 more
2018Anatomy Physiology & Biochemistry International Journal1 citations Open access
Semantic Scholar
Candidate variants in MLC1 gene causing Megalencephalic Leukodystrophy using in silico prediction methods
M. Amin
20181 citations Open access
Semantic Scholar
Computational Analysis of Single Nucleotide Polymorphisms associated with ENAM gene
M. Amin, Sanaa Alsafi, M. Ibrahim
20161 citations
Semantic Scholar
Analysis of the Role of Vitamin C Synthesis Loss in Primates’ Evolution; Solving an Evolutionary Puzzle
M. Amin
20161 citations Open access
Semantic Scholar
Comorbidity of CRHR2 gene variants in type 2 diabetes and depression
M. Amin, J. Ott, R. Wu, T. Postolache +2 more
2022European psychiatry0 citations Open access
Semantic Scholar
ODP258 CRHR1 gene shows extensive linkage to major depression and type 2 diabetes in Italian families
M. Amin, L. del Bosque-Plata, Manuel Gea González, R. Wu +5 more
2022Journal of the Endocrine Society0 citations Open access
Semantic Scholar
Genetic diversity and multiplicity of Plasmodium falciparum merozoite surface protein 2 in field isolates from Sudan [version 1; peer review: 1 not approved]
Shaza O. Mustafa, Muzamil M. Abdel Hamid, M. Aboud, M. Amin +4 more
20200 citations
Semantic Scholar
Preparation of Monolithic Stationary Phase in Capillary and Conventional Columns, their Characterization and Application
M. Amin, Mohmaed El Mukhtar Abdelaziz Supervisor
20190 citations
Semantic Scholar
Malaria and Burkitt’s Lymphoma: An In Silico Analysis of Gene Expression Links between Malaria and Burkitt’s Lymphoma and Potential Anticancer Activity of Artemisinin Derivatives
Inas Elsayed, M. Amin, M. A. Abdel Hamid, Xiao-Sheng Wang +1 more
2018bioRxiv0 citations Open access
Semantic Scholar
Five decades lead in biomedical research: University of Khartoum tops Sudanese universities in PubMed articles
M. Amin, M. O. Abdallah, M. Koko, Y. Bakhit
2017Khartoum Medical Journal0 citations Open access
Semantic Scholar
In silico analysis of Human Endogenous Retrovirus K113 as a Potential vector for gene therapy
M. Amin
20160 citations
Semantic Scholar
Review Population Genetics in Sudan
M. Ibrahim, M. Amin
20160 citations
Semantic Scholar
A bioinformatic panel to interrogate thousands of ExAC variants with minor reference allele that are missed by conventional variant calling
M. Koko, M. O. Abdallah, M. Amin, M. Ibrahim
2016bioRxiv0 citations Open access
Semantic Scholar
Multiplicity of infection and genetic diversity of Plasmodium falciparum isolates from patients with uncomplicated and severe malaria in Gezira State, Sudan
Muzamil Mahdi Abdel Hamid, Arwa F. Elamin, Musab M. Ali Albsheer, Abdelmohaymin Abdalla +4 more
2016Parasites & Vectors0 citations Open access
Semantic Scholar
DuringSatti'stimepopulationgeneticswasafairlynewsciencethen,pioneeredbyoutstandingscientistslikeJ BHaldane-aBritonalsonotoriousofbeinganardentsocialistactivist.Haldanenotonlypioneeredpopulation geneticsbutdemonstratedthefirstexamplesofhumanadaptationthroughhaemoglobinopathiesthatarestill thefavourit
S. M. Ibrahim, M. Amin, M. Ibrahim
20150 citations
Semantic Scholar
The effectiveness of urodynamic evaluation in patients under age of 60 years presented with lower urinary tract symptoms
M. Amin, A. Mohammed, B. Little
20110 citations Open access
Semantic Scholar

Frequent co-authors

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M. Koko×10
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M. Koko — researcher profile on SciRah
Claudia Gragnoli×10
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Claudia Gragnoli — researcher profile on SciRah
R. Wu×9
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R. Wu — researcher profile on SciRah
M. Ibrahim×9
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M. Ibrahim — researcher profile on SciRah

Liena E. O. Elsayed

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Liena E. O. Elsayed — researcher profile on SciRah

T. Postolache×8

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T. Postolache — researcher profile on SciRah

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Y. Bakhit — researcher profile on SciRah

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A. Ahmed — researcher profile on SciRah

Ashraf Yahia×6

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Ashraf Yahia — researcher profile on SciRah

Maha A. Elseed×6

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Maha A. Elseed — researcher profile on SciRah

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Arwa Babai — researcher profile on SciRah

Inaam N. Mohammed×5

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Inaam N. Mohammed — researcher profile on SciRah