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Mariam Tajir

Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma
2014 · Jean- Benoît Courcet, Siham Chafai Elalaoui, et al. · European Journal of Human Genetics · 53
An inherited LMNA gene mutation in atypical Progeria syndrome
2012 · Yassamine Doubaj, Annachiara De Sandre‐Giovannoli, et al. · American Journal of Medical Genetics Part A · 51
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund–Thomson/Baller‐Gerold syndromes
2014 · J. Piard, B. Aral, et al. · Clinical Genetics · 28
Acromelic frontonasal dysostosis andZSWIM6mutation: phenotypic spectrum and mosaicism
2015 · S.R.F. Twigg, L.B. Ousager, et al. · Clinical Genetics · 25
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Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco
2020 · Saida Lhousni, Fatiha Daoudi, et al. · Biopreservation and Biobanking · 21
AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population
2015 · Lamiae Boualla, Mariam Tajir, et al. · Genetic Testing and Molecular Biomarkers · 20
Morocco’s First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges
2020 · Saida Lhousni, Karam Yahya Belmokhtar, et al. · BioMed Research International · 18
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Germline mosaicism in Rubinstein–Taybi syndrome
2013 · Mariam Tajir, Patricia Fergelot, et al. · Gene · 18
Assessment of Knowledge, Attitudes and Support of Health Professionals towards Biobanks in Eastern Morocco
2019 · Saida Lhousni, Redouane Boulouiz, et al. · Open Journal of Epidemiology · 13
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Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients
2012 · Mariam Tajir, Jean Baptiste Arnoux, et al. · European Journal of Medical Genetics · 12
A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review
2011 · SihamChafai Elalaoui, Ratbi Ilham, et al. · Indian journal of human genetics · 11
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Cancer du poumon au Maroc Oriental: où en sommes-nous?
2019 · Karam Yahya Belmokhtar, Mariam Tajir, et al. · Pan African Medical Journal · 9
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Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene
2020 · M Tajir, J Lyahyai, et al. · Balkan Journal of Medical Genetics · 8
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Granulomatous Colitis Due to Hermansky-Pudlak Syndrome
2024 · Hajar Koulali, Samira Azzmouri, et al. · ACG Case Reports Journal · 4
Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome
2021 · Siham Chafai Elalaoui, Wiam Smaili, et al. · African Health Sciences · 4
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Frequency of IL28B rs12979860 Single-Nucleotide Polymorphism Alleles in Newborn Infants and in Patients with Chronic Hepatitis C in Morocco
2012 · Mariam Tajir, Mustapha Elmachad, et al. · Genetic Testing and Molecular Biomarkers · 3
Ellis-Van Creveld Syndrome and Dandy-Walker Malformation: An Uncommon Association.
2018 · Khadija Boujtat, Siham Rouf, et al. · PubMed · 2
Contribution of cytogenetic in the diagnosis of Edwards’s syndrome: about 9 cases
2023 · Fatima Ezzahra Aouni, Khawla Zerrouki, et al. · Annales de biologie clinique · 1
Syndrome de Williams-Beuren: étude rétrospective d’une série de 11 cas du Centre Hospitalier Universitaire Mohammed VI de Marrakech
2023 · Nisrine Aboussair, Fatima Zahrae Bouzid, et al. · Pan African Medical Journal · 1
Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature
2022 · K. Zerrouki, A. Babakhouya, et al. · Balkan Journal of Medical Genetics · 1
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Exploring the Antimicrobial Properties Against Human Pathogens and Mode of Action of Various Extracts from Fredolia aretioides, an Endemic Medicinal Plant of Morocco and Algeria
2019 · Btissam Bouchal, Mounia Elidrissi Errahhali, et al. · The Natural Products Journal · 1
Diagnostic et prise en charge de le syndrome 46,XX male : à propos d’un cas
2014 · Hicham Baïzri, Mariam Tajir, et al. · Research · 1
[Prenatal diagnosis of trisomy 21 by fluorescence in situ hybridization (FISH): about the first tests in Morocco].
2012 · Afaf Lamzouri, Abdelhafid Natiq, et al. · PubMed Central · 1
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[Costello syndrome: report of a case].
2012 · Mariam Tajir, Patricia Fergelot, et al. · PubMed Central · 1
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Noonan Syndrome Type 5 Diagnosed by Next-Generation Sequencing: A Report of a Rare Pediatric Case
2026 · Sanae Kheir, Jihane Ahmidi, et al. · Cureus
Works count: 35
Citation count: 307
H-index: 11
I10-index: 11
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