Mohamed Ahakoud

Fes, 30000, Morocco

Last Updated: 09/26/2026

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Found 15 publications

Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation.

Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation.

Journal: Epigenomes
Published: December 08, 2025

Prevalence and spectrum of AZFc copy number variations in infertile Moroccan men.

Prevalence and spectrum of AZFc copy number variations in infertile Moroccan men.

Journal: Clinical and experimental reproductive medicine
Published: September 04, 2025

A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic Correlation.

A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic Correlation.

Journal: Cureus
Published: August 20, 2025

The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatment.

The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatment.

Journal: BMC medical genomics
Published: May 27, 2025

Novel Variant in the NLRP12 Gene: Insights From a Case Report and Systematic Review.

Novel Variant in the NLRP12 Gene: Insights From a Case Report and Systematic Review.

Journal: International journal of immunogenetics
Published: March 04, 2025

A Case Report of a Rare 46,XX/47,XXY Mosaicism With Ovotesticular Disorder of Sex Development and a Literature Review.

A Case Report of a Rare 46,XX/47,XXY Mosaicism With Ovotesticular Disorder of Sex Development and a Literature Review.

Journal: Cureus
Published: July 31, 2024

The first assessment of Angiotensin-Converting Enzyme 1 (ACE1) D/I polymorphism and demographic factors in association with COVID-19 outcomes in the Moroccan Population.

The first assessment of Angiotensin-Converting Enzyme 1 (ACE1) D/I polymorphism and demographic factors in association with COVID-19 outcomes in the Moroccan Population.

Journal: Molecular biology reports
Published: July 28, 2024

In-depth exploration of differences of sex development: 5-year experience in a tertiary center.

In-depth exploration of differences of sex development: 5-year experience in a tertiary center.

Journal: Endocrine connections
Published: May 14, 2024

FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies.

FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies.

Journal: Cureus
Published: September 18, 2023

A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene.

A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene.

Journal: Cureus
Published: August 12, 2023

Novel ABL1 mutation in a Moroccan CML patient with Imatinib resistance.

Novel ABL1 mutation in a Moroccan CML patient with Imatinib resistance.

Journal: Cancer genetics
Published: August 01, 2023

Rare and Atypical Case of Turner Syndrome With Three Cell Lines.

Rare and Atypical Case of Turner Syndrome With Three Cell Lines.

Journal: Cureus
Published: June 27, 2023
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Last Updated: 09/26/2026