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Imane Samri
Affiliation : Sidi Mohamed Ben Abdellah University
- 16Publications (affiliation in Morocco)
- 20Total publications
- 156Citations
- 5h-index
Research profile
Imane Samri has 16 indexed publications (2012–2026). Their work appears mainly in “Pan African Medical Journal”, “Egyptian Journal of Medical Human Genetics” and “Revue d Épidémiologie et de Santé Publique”. Their most cited article, “Noonan syndrome-causing genes” (2016), has been cited 80 times. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Cardiac electrophysiology and arrhythmias
- Congenital Heart Disease Studies
- Genomic variations and chromosomal abnormalities
- Congenital heart defects research
Publications (16)
- High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approach
- Male Breast Cancer: About 05 Cases
- Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
- Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects
- Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age
- GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot
- Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
- Noonan syndrome-causing genes
- Syndrome de Lynch: à propos d’un cas et revue de la litterature
- TPMT alleles in the Moroccans
- L’exploration moléculaire du gène NKX2.5 dans deux populations atteintes de communication inter-auriculaire (CIA) et de tétralogie de Fallot (TOF)
- Analyse mutationnelle des mutations germinales des gènes mlh1 et msh2 chez des patients atteints de cancer colorectal montrant une extinction des protéines MLH1 et MSH2
- Marqueurs chromosomiques: à propos d'un cas
- [Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations].
- [The Cri du Chat syndrome: report of an observation].
- Consanguinité et prédisposition aux néphropathies dans la population marocaine (à propos de 265 cas)
Publication venues
- Pan African Medical Journal × 3
- Egyptian Journal of Medical Human Genetics × 2
- Revue d Épidémiologie et de Santé Publique × 2
- PubMed Central × 2
- Neurogenetics × 1
- EAS Journal of Medicine and Surgery × 1
Publications per year
- 20261
- 20231
- 20211
- 20202
- 20181
- 20171
- 20162
- 20153
- 20131
- 20123
Collaborations
Partner institutions : Centre Hospitalier Universitaire Hassan II · Hôpital Militaire Avicenne · Instituts Supérieurs des Professions Infirmières et Techniques de Santé
Co-authors
- Karim Ouldim
- Laila Bouguenouch
- Khadija Belhassan
- Fatima Zohra Moufid
- Samir Atmani
- Ihssane El Bouchikhi
- Mohammed Iraqui Houssaïni
- Hasna Hamdaoui
- Ihsane El Otmani
- Sana Chaouki
- Sanae Bennis
- Moustapha Hida
Bibliographic data from OpenAlex (open database).
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