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Farida Jennane

Affiliation : Centre Hospitalier Universitaire Ibn Rochd · University of Hassan II Casablanca

• 10Publications (affiliation in Morocco)
• 32Total publications
• 425Citations
• 9h-index

OpenAlex

Research profile

Farida Jennane has 10 indexed publications (2010–2026). Their work appears mainly in “Archives de Pédiatrie”, “Egyptian Journal of Medical Human Genetics” and “Cureus”. Their most cited article, “A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyro” (2014), has been cited 56 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.

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Research areas

• Sexual Differentiation and Disorders
• Diabetes and associated disorders
• Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
• Adrenal Hormones and Disorders
• Genomics and Rare Diseases

Publications (10)

• PTPN22 C1858T polymorphism confers risk for familial type 1 diabetes in Moroccan children and adolescents
  2026 · Egyptian Journal of Medical Human Genetics
• The Clinical and Biological Characterization of Triple A Syndrome (Allgrove Syndrome) in 12 Pediatric Patients
  2026 · Cureus
• Prevalence of celiac disease in Moroccan children with type 1 diabetes mellitus: A 16-year cross-sectional study
  2023 · Qatar medical journal · cited 2 times
• Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village…
  2021 · BMJ Global Health · cited 9 times
• Research of anti-GAD and anti-IA2 autoantibodies by ELISA test in a series of Moroccan pediatric patients with diabetes type 1
  2020 · African Health Sciences · cited 17 times
• Puberté précoce centrale : les aspects clinique, diagnostique et thérapeutique à travers une cohorte de 16 cas
  2016 · Annales d Endocrinologie
• A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyroidism and 33 newly identified mutations in the GNAS gene
  2014 · Molecular Genetics & Genomic Medicine · cited 56 times
• Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome
  2010 · Pediatric Diabetes · cited 23 times
• P149 - Kyste bronchogénique du nourrisson révélé par une dyspnée sifflante récidivante (À propos de deux cas)
  2010 · Archives de Pédiatrie · cited 2 times
• CL010 - Goitre thyroïdien de l’enfant : à propos de 31 cas
  2010 · Archives de Pédiatrie

Publication venues

• Archives de Pédiatrie × 2
• Egyptian Journal of Medical Human Genetics × 1
• Cureus × 1
• Qatar medical journal × 1
• BMJ Global Health × 1
• African Health Sciences × 1

Publications per year

• 20262
• 20231
• 20211
• 20201
• 20161
• 20141
• 20103

Collaborations

Partner institutions : Laboratoire National de Référence · Université Mohammed VI des Sciences et de la Santé

Co-authors

• Ouijdane Belhiba
• Fatima Dehbi
• Ahmed Aziz Bousfiha
• B. Slaoui
• M. Lahbabi
• M. Farès
• Fatimazahra Yakine
• Ilham Bouarab
• H. Sadiki
• Zahra Aadam
• Abderrahmane Errami
• S. Ouchen

Bibliographic data from OpenAlex (open database).