Get started
Author

Lilia Romdhane

Observed names: L. Romdhane, Romdhane, Lilia
ORCID: 0000-0001-5310-7272
Observed ORCID: 0000-0001-5310-7272
OpenAlex ID: A5062052623
Consanguinity, endogamy, and genetic disorders in Tunisia
2012 · Nizar Ben Halim, Nissaf Ben Alaya Bouafif, et al. · Journal of Community Genetics · 111
PDF
Consanguinity and Inbreeding in Health and Disease in North African Populations
2019 · Lilia Romdhane, Nessrine Mezzi, et al. · Annual Review of Genomics and Human Genetics · 86
PDF
A Review of Clinical Pharmacogenetics Studies in African Populations
2020 · Fouzia Radouani, Lyndon Zass, et al. · Personalized Medicine · 82
Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East
2012 · Lilia Romdhane, Rym Kefi, et al. · Orphanet Journal of Rare Diseases · 79
PDF
Genetic diseases in the Tunisian population
2010 · Lilia Romdhane, Sonia Abdelhak, et al. · American Journal of Medical Genetics Part A · 64
Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations
2014 · Rym Kefi, Sana Hsouna, et al. · Mitochondrial DNA · 40
Human OMICs and Computational Biology Research in Africa: Current Challenges and Prospects
2021 · Yosr Hamdi, Lyndon Zass, et al. · OMICS A Journal of Integrative Biology · 37
Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss
2013 · Zied Riahi, Hassen Hammami, et al. · Gene · 36
Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome
2016 · Sahar Elouej, Hanen Belfki-Benali, et al. · Metabolic Syndrome and Related Disorders · 30
Specific Aspects of Consanguinity: Some Examples from the Tunisian Population
2014 · Lilia Romdhane, Nizar Ben Halim, et al. · Human Heredity · 27
Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity
2015 · Nizar Ben Halim, Majdi Nagara, et al. · Annals of Human Genetics · 23
A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
2018 · Yosr Hamdi, Mariem Ben Rekaya, et al. · BMC Cancer · 20
PDF
Comorbidity in the Tunisian population
2015 · L. Romdhane, O. Messaoud, et al. · Clinical Genetics · 18
Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population
2015 · Hicham Charoute, Amina Bakhchane, et al. · Human Mutation · 17
PDF
Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
2014 · Majdi Nagara, Konstantinos Voskarides, et al. · Genetic Testing and Molecular Biomarkers · 17
Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome
2013 · Yosra Bouyacoub, Hela Zribi, et al. · Gene · 17
Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved
2021 · Nessrine Mezzi, Olfa Messaoud, et al. · Genes · 15
PDF
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
2018 · Haifa Jmel, Lilia Romdhane, et al. · PLoS ONE · 15
PDF
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
2021 · Maroua Boujemaa, Yosr Hamdi, et al. · PLoS ONE · 14
PDF
Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population
2015 · Nizar Ben Halim, Imen Dorboz, et al. · Neurological Sciences · 13
A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism
2014 · Lamia Cherif Ben Abdallah, Youssef Lakhoua, et al. · Hormone Research in Paediatrics · 13
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome
2013 · Zied Riahi, Rim Zainine, et al. · International Journal of Pediatric Otorhinolaryngology · 13
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
2021 · Lilia Romdhane, Nessrine Mezzi, et al. · npj Genomic Medicine · 9
PDF
Fertilizer effect of composted sewage sludge and cattle manure onPelargoniumgrowth
2020 · Nesrine Dridi, Lilia Romdhane, et al. · Journal of Water Sanitation and Hygiene for Development · 9
PDF
Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
2019 · Abir Ben Haj Ali, Ahlem Amouri, et al. · Molecular Genetics & Genomic Medicine · 8
PDF
Works count: 60
Citation count: 872
H-index: 16
I10-index: 22
Year
Topic
Type