الرئيسية › دليل الباحثين › Wafa Slimani

Wafa Slimani

الانتماء : Hôpital Farhat Hached · University of Sousse

• 15منشورات (انتماء تونسي)
• 15مجموع المنشورات
• 66الاستشهادات
• 6مؤشر h

ORCIDOpenAlex

مجالات البحث

• Genomic variations and chromosomal abnormalities
• Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
• Genetics and Neurodevelopmental Disorders
• Sexual Differentiation and Disorders
• Fetal and Pediatric Neurological Disorders

المنشورات (15)

• Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights
  2026 · Molecular Cytogenetics
• Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
  2026 · Frontiers in Genetics
• Toward autism spectrum disorders and Williams-Beuren syndrome co-occurrence condition in Tunisian patients: Genetic insights
  2024 · AIMS molecular science · استُشهد به 1 مرة
• Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development
  2023 · Reproductive Biology and Endocrinology · استُشهد به 13 مرة
• Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis
  2022 · Journal of Clinical Research in Pediatric Endocrinology · استُشهد به 6 مرة
• Genotype-phenotype correlations for the type 1 lissencephaly of eight Tunisian children
  2022 · Journal of Clinical Images and Medical Case Reports
• Autism in patients with Williams-Beuren syndrome: A re-evaluation of 31 Tunisian patients’ phenotype
  2022 · Research Square
• Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene
  2021 · Molecular Cytogenetics · استُشهد به 11 مرة
• Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives
  2020 · Journal of Assisted Reproduction and Genetics · استُشهد به 9 مرة
• Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
  2020 · BMC Medical Genetics · استُشهد به 3 مرة
• Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization
  2019 · Molecular Cytogenetics · استُشهد به 10 مرة
• Sperm fluorescent in situ hybridisation study of interchromosomal effect in six Tunisian carriers of reciprocal and Robertsonian translocations
  2018 · Andrologia · استُشهد به 10 مرة
• Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.
  2018 · Europe PMC (PubMed Central) · استُشهد به 2 مرة
• CLINICAL AND MOLECULAR FINDINGS IN NINE NEW CASES OF TETRASOMY 18p SYNDROME: CO-OCCURRENCE OF ISOCHROMOSOME 18p AND COPY NUMBER VARIATION
  2018
• Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature
  2017 · Journal of Pediatric Genetics · استُشهد به 1 مرة

مجلات النشر

• Molecular Cytogenetics × 3
• Frontiers in Genetics × 1
• AIMS molecular science × 1
• Reproductive Biology and Endocrinology × 1
• Journal of Clinical Research in Pediatric Endocrinology × 1
• Journal of Clinical Images and Medical Case Reports × 1

المنشورات حسب السنة

• 20262
• 20241
• 20231
• 20223
• 20211
• 20202
• 20191
• 20183
• 20171

التعاون العلمي

المؤسسات الشريكة : University of Monastir · Hôpital Sahloul · Hospital Fatuma Bourguiba Monastir · University of Kairouan · National Institute of Neurology Mongi-Ben Hamida

بلدان المؤلفين المشاركين : فرنسا

المؤلفون المشاركون

• Soumaya Mougou-Zerelli
• Ali Saâd
• Molka Kammoun
• Afef Jelloul
• Khouloud Rjiba
• S. Dimassi
• Hela Ben Khelifa
• Hanene Hannachi
• Hamza Hadj Abdallah
• Mohamed Bibi
• Amira Sallem
• Houda Ajmi

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).