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Soumaya Mougou-Zerelli

Observed names: Mougou Soumaya, Mougou Zerelli, Soumaya, S Mougou, S. Mougou, S. Mougou-Zerelli, S. Mougou‐Zerelli, S. mougou, Soumaya Mougou, Soumaya Mougou Zerelli, Soumaya Mougou Zerrelli, Soumaya Mougou-Zereli, Soumaya Mougou-Zrelli
Observed institutions: Hôpital Necker-Enfants Malades, Inserm, Institut Necker Enfants Malades, Hôpital Farhat Hached, Assistance Publique – Hôpitaux de Paris, Institut des Maladies Génétiques Imagine, Université Paris Descartes, University of Sousse
ORCID: 0000-0003-3172-1313
Observed ORCID: 0000-0003-3172-1313
OpenAlex ID: A5001557130
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
2010 · Enza Maria Valente, Clare V Logan, et al. · Nature Genetics · 304
Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6
2007 · Christelle Golzio, Jelena Martinovic-Bouriel, et al. · The American Journal of Human Genetics · 203
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Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss
2015 · Ines Zidi-Jrah, Amani Hajlaoui, et al. · Fertility and Sterility · 171
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TCTN3 Mutations Cause Mohr-Majewski Syndrome
2012 · Sophie Thomas, Marine Legendre, et al. · The American Journal of Human Genetics · 140
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New insights into genotype–phenotype correlation for GLI3 mutations
2014 · Florence Démurger, Amale Ichkou, et al. · European Journal of Human Genetics · 130
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Semen Parameters and Sperm DNA Fragmentation as Causes of Recurrent Pregnancy Loss
2011 · Sonia Brahem, Meriem Mehdi, et al. · Urology · 105
NovelTMEM67mutations and genotype-phenotype correlates in meckelin-related ciliopathies
2010 · Miriam Iannicelli, Francesco Brancati, et al. · Human Mutation · 100
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CC2D2Amutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
2009 · Soumaya Mougou-Zerelli, Sophie Thomas, et al. · Human Mutation · 95
Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
2015 · S. Dimassi, A. Labalme, et al. · Clinical Genetics · 84
New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family
2017 · Nouha Bouali, Bruno Francou, et al. · Fertility and Sterility · 71
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Prevalence of chromosomal abnormalities in couples with recurrent miscarriage
2007 · Hatem Elghezal, Samir Hidar, et al. · Fertility and Sterility · 64
Xp22.3 interstitial deletion: A recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation
2013 · Hela Ben Khelifa, Najla Soyah, et al. · Gene · 43
Molecular and Phenotypic Characterization of Ring Chromosome 22 in Two Unrelated Patients
2013 · H. Hannachi, S. Mougou, et al. · Cytogenetic and Genome Research · 41
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia
2012 · Inesse Ben-Abdallah-Bouhjar, Hanene Hannachi, et al. · European Journal of Medical Genetics · 41
A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers
2013 · Sana Bouraoui, Soumaya Mougou, et al. · International Journal of Occupational Medicine and Environmental Health · 38
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Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA
2015 · Sarra Dimassi, Thomas Simonet, et al. · Applied & Translational Genomics · 37
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High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy
2010 · Sophie Thomas, Ferechté Encha-Razavi, et al. · Human Mutation · 34
BBS10 mutations are common in ‘Meckel’-type cystic kidneys
2010 · Audrey Putoux, Soumaya Mougou-Zerelli, et al. · Journal of Medical Genetics · 31
Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci
2007 · Hatem Elghezal, Hanene Hannachi, et al. · European Journal of Medical Genetics · 26
NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency
2016 · N. Bouali, B. Francou, et al. · Clinical Genetics · 25
A Combination of Micronucleus Assay and Fluorescence In Situ Hybridization Analysis to Evaluate the Genotoxicity of Formaldehyde
2012 · Sana Bouraoui, Soumaya Mougou, et al. · Archives of Environmental Contamination and Toxicology · 23
Large duplication 4q25–q34 with mild clinical effect
2004 · Hatem Elghezal, Halima Sennana Sendi, et al. · Annales de Génétique · 23
Array‐CGH study of partial trisomy 9p without mental retardation
2011 · Inesse Ben Abdallah Bouhjar, Hanane Hannachi, et al. · American Journal of Medical Genetics Part A · 17
Genome Tunisia Project: paving the way for precision medicine in North Africa
2024 · Yosr Hamdi, Mediha Trabelsi, et al. · Genome Medicine · 16
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Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development
2023 · Khouloud Rjiba, Soumaya Mougou-Zerelli, et al. · Reproductive Biology and Endocrinology · 15
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Works count: 88
Citation count: 2,076
H-index: 22
I10-index: 35
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