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Author

Idris Mohammed

Observed names: Mohammed I, Mohammed, Idris Omer
ORCID: 0000-0002-8983-0929
Observed ORCID: 0000-0002-8983-0929
OpenAlex ID: A5002941696
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar
2019 · Sara Al‐Khawaga, Idris Mohammed, et al. · Molecular Genetics & Genomic Medicine · 30
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Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar
2021 · Basma Haris, Ikhlak Ahmed, et al. · Scientific Reports · 28
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Understanding the Genetics of Early-Onset Obesity in a Cohort of Children From Qatar
2023 · Idris Mohammed, Basma Haris, et al. · The Journal of Clinical Endocrinology & Metabolism · 25
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Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review
2021 · Amal Elfatih, Idris Mohammed, et al. · Physiological Genomics · 25
A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency
2019 · Sara Al-Khawaga, Jehan AlRayahi, et al. · Frontiers in Pediatrics · 19
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Maturity‐onset diabetes of the young (MODY) due to PDX1 mutation in a sib‐pair diabetes family from Qatar
2021 · Basma Haris, Idris Mohammed, et al. · Clinical Case Reports · 13
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Functional Characterization of Novel MC4R Variants Identified in Two Unrelated Patients with Morbid Obesity in Qatar
2023 · Idris Mohammed, Senthil Selvaraj, et al. · International Journal of Molecular Sciences · 10
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A Novel Homozygous MC2R Variant Leading to Type-1 Familial Glucocorticoid Deficiency
2022 · Idris Mohammed, Basma Haris, et al. · Journal of the Endocrine Society · 9
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Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype
2020 · Idris Mohammed, Sara Al‐Khawaga, et al. · Molecular Genetics & Genomic Medicine · 8
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Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient
2022 · Sanaa Sharari, Mustapha Aouida, et al. · Frontiers in Endocrinology · 7
Analysis of incidental findings in Qatar genome participants reveals novel functional variants in LMNA and DSP
2022 · Amal Elfatih, Sahar I Da’as, et al. · Human Molecular Genetics · 7
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Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome
2022 · Sanaa Sharari, Basirudeen Kabeer, et al. · Biomedicines · 6
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Novel SIM1 Variants Expanding the Spectrum of SIM1-Related Obesity
2026 · Idris Mohammed, Wesam S. Ahmed, et al. · International Journal of Molecular Sciences · 4
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Efficacy of Semaglutide in Pediatric Patients With Bardet-Biedl Syndrome and Alström Syndrome
2025 · Hajar Dauleh, Idris Mohammed, et al. · JCEM Case Reports · 4
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Functional Evaluation of a Novel Homozygous ADCY3 Variant Causing Childhood Obesity
2024 · Idris Mohammed, Senthil Selvaraj, et al. · International Journal of Molecular Sciences · 4
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Management of Childhood Obesity
2026 · Hoda Gad, Hajar Dauleh, et al. · International Journal of Molecular Sciences · 2
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Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation
2022 · Iman Hawari, Basma Haris, et al. · Journal of Clinical and Translational Endocrinology Case Reports · 2
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Functional characterization and cAMP-mediated rescue of a novel truncating AVPR2 mutation causing nephrogenic diabetes insipidus
2025 · Diogo Manoel, Idris Mohammed, et al. · American Journal of Physiology-Endocrinology and Metabolism · 1
Impact of Somatic Gene Mutations on Prognosis Prediction in De Novo AML: Unraveling Insights from a Systematic Review and Meta-Analysis
2025 · Amal Elfatih, Nisar Ahmed, et al. · Cancers · 1
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Permanent Congenital Hypothyroidism due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis
2025 · Ghassan Mohamadsalih, Khalid Al Bureshad, et al. · Case Reports in Medicine · 1
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Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene
2023 · Basma Haris, Idris Mohammed, et al. · Journal of Clinical Research in Pediatric Endocrinology · 1
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A Novel SLC2A2 Mutation Implicated in Fanconi Bickel Syndrome and Dysglycemia
2019 · Sanaa Sharari, Mustapha Aouida, et al. · 58th Annual ESPE Meeting (ESPE 2019) · 1
MLH1 p. His112Arg Variant Is Associated With Increased Cancer Susceptibility
2026 · Amal Elfatih, Issam Tout, et al. · International Journal of Cancer
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Correction: Gad et al. Management of Childhood Obesity. Int. J. Mol. Sci. 2026, 27, 3528
2026 · Hoda Gad, Hajar Dauleh, et al. · International Journal of Molecular Sciences
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Variable Expressivity and Incomplete Penetrance in Monogenic Diabetes
2025 · Shiga Rappai Chirayath, Idris Mohammed, et al. · Annals of Case Reports
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Works count: 30
Citation count: 208
H-index: 8
I10-index: 7
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