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Abdelhamid Bouramtane

Observed names: BOURAMTANE Abdelhamid, Bouramtane Abdelhamid, Bouramtane, Abdelhamid
ORCID: 0009-0002-3618-5396
Observed ORCID: 0009-0002-3618-5396
OpenAlex ID: A5024983515
The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study
2023 · Mohamed Ahakoud, Hanae Daha Belghiti, et al. · Cureus · 5
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A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
2023 · Khawla El Fizazi, Abdelhamid Bouramtane, et al. · American Journal of Medical Genetics Part A · 4
Unveiling a novel AIMP2 c.157 C>T variant in a Moroccan patient with hypomyelinating leukodystrophy type 17: A case report and insights from a literature review
2025 · Amal Ouskri, Abdelhamid Bouramtane, et al. · Medical Reports · 1
Expanding the spectrum of ATP8A2 mutations: a new splicing variant and systematic review of CAMRQ4 syndrome
2025 · Bouramtane Abdelhamid, Elmakhzen Badreddine, et al. · Molecular Biology Reports · 1
P047: Correlation between clinico-biological elements and the type of BCR-ABl transcripts in chronic myeloid leukemia
2023 · Abdelhamid Bouramtane, Hajar El Azami El Idrissi, et al. · Genetics in Medicine Open · 1
Long-Read Nanopore Sequencing Enhances BRCA1/2 Variant Detection Compared with Ion Torrent Analysis.
2026 · EL Makhzen, Nada, El Hejjioui, Brahim, et al. · Open Access CRIS of the University of Bern
Clinical and Genetic Insights into Angelman Syndrome: A Retrospective Study of 26 Cases in Morocco
2026 · Amal Ouskri, Bouramtane Abdelhamid, et al. · Journal of Molecular Neuroscience
Long-Read Nanopore Sequencing Enhances BRCA1/2 Variant Detection Compared with Ion Torrent Analysis
2026 · Nada El Makhzen, Brahim El Hejjioui, et al. · Journal of Molecular Diagnostics
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The importance of family history in indicating HBOC genetic testing in a resource-limited setting.
2026 · Ghita Abou El Jaoud, Abdelhamid Bouramtane, et al. · Journal of Clinical Oncology
Landscape of therapeutically actionable HRR gene variants in Moroccan breast and ovarian cancer: A systematic review and meta-analysis.
2026 · Abdelhamid Bouramtane, Brahim El Hejjioui, et al. · Journal of Clinical Oncology
Germline RET variants in medullary thyroid carcinoma: A single-center experience from 2019 to 2025.
2026 · Kaoutar Madkouri, Abdelhamid Bouramtane, et al. · Journal of Clinical Oncology
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Molecular characterization of ABL kinase domain mutations associated with imatinib resistance in chronic myeloid leukemia patients, including a novel pathogenic D276V variant.
2026 · Soufiyan Rehioui, Brahim El Hejjioui, et al. · Journal of Clinical Oncology
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Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation
2026 · Abdelhamid Bouramtane, Badreddine Elmakhzen, et al. · Epigenomes
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The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatment
2026 · Brahim El Hejjioui, Abdelhamid Bouramtane, et al. · BMC Medical Genomics
Novel Variant in the NLRP12 Gene: Insights From a Case Report and Systematic Review
2025 · Abdelhamid Bouramtane, Badreddine Elmakhzen, et al. · International Journal of Immunogenetics
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Chimerism in Males and Recurrent Miscarriages: A Case Study
2025 · Abdelhamid Bouramtane, Ahmed Lazraq, et al. · Human Biology
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic review
2025 · Amal Ouskri, Abdelhamid Bouramtane, et al. · Clinical Dysmorphology
MCLMR Syndrome: A Case Report and Systematic Review
2025 · Abdelhamid Bouramtane, Omar Askander, et al. · SN Comprehensive Clinical Medicine
Genetic epidemiology of colorectal cancer in Morocco: A systematic review and meta-analysis.
2025 · Abdelhamid Bouramtane, Samia Arifi · Journal of Clinical Oncology
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Chimerism in Males and Recurrent Miscarriages: A Case Study
2023 · Abdelhamid Bouramtane, Ahmed Lazraq, et al. · Human Biology
P046: Involvement of MLH1 and MSH2 genes in hereditary susceptibility to CRC in the Moroccan population
2023 · Abdelhamid Bouramtane, Fatima Zahra Moufid, et al. · Genetics in Medicine Open
P048: Novel frameshift MLH1 germline mutation in a Moroccan Lynch syndrome family
2023 · Abdelhamid Bouramtane, Fatima Zohra Moufid, et al. · Genetics in Medicine Open
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L'apport de la neuronavigation dans la prise en charge des pathologies neurochirurgicales : expérience du service de neurochirurgie au CHU Hassan-II de Fès
2022 · BOURAMTANE Abdelhamid · Toubkal
Works count: 24
Citation count: 12
H-index: 2
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