Publications by authors named "Lilia Romdhane"

25Publications

The morbid cutaneous anatomy of the human genome revealed by a bioinformatic approach.

Genomics 2020 Jul 7. Epub 2020 Jul 7.

Molecular and Cellular Screening Process Laboratory, Centre of Biotechnology of Sfax, Sfax, Tunisia.

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http://dx.doi.org/10.1016/j.ygeno.2020.07.009DOI Listing
July 2020

Genetic diversity and functional effect of common polymorphisms in genes involved in the first heterodimeric complex of the Nucleotide Excision Repair pathway.

DNA Repair (Amst) 2020 02 12;86:102770. Epub 2019 Dec 12.

Laboratory of Biomedical Genomics and Oncogenetics, LR16IPT05, Institut Pasteur de Tunis, University of Tunis El Manar, Tunis, Tunisia.

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http://dx.doi.org/10.1016/j.dnarep.2019.102770DOI Listing
February 2020

Consanguinity and Inbreeding in Health and Disease in North African Populations.

Annu Rev Genomics Hum Genet 2019 08 30;20:155-179. Epub 2019 Apr 30.

Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, 1002 Tunis Belvédère, Tunisia; email:

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http://dx.doi.org/10.1146/annurev-genom-083118-014954DOI Listing
August 2019

A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci.

BMC Cancer 2018 Dec 29;18(1):1295. Epub 2018 Dec 29.

Laboratory of biomedical genomics and oncogenetics, Institut Pasteur de Tunis, Université Tunis El Manar, 13, Place Pasteur BP 74, 1002, Tunis, Belvédère, Tunisie.

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http://dx.doi.org/10.1186/s12885-018-5133-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310952PMC
December 2018

Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population.

Neurol Sci 2016 Mar 14;37(3):403-9. Epub 2015 Nov 14.

Laboratoire de Génomique Biomédicale et Oncogénétique, Institut Pasteur de Tunis, BP 74, 13 Place Pasteur, 1002, Tunis, Belvédère, Tunisia.

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http://dx.doi.org/10.1007/s10072-015-2417-5DOI Listing
March 2016

Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity.

Ann Hum Genet 2015 Nov 29;79(6):402-17. Epub 2015 Sep 29.

Laboratory of Biomedical Genomics and Oncogenetics, Pasteur Institute of Tunis, Tunis, Le Belvédère, Tunisia.

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http://dx.doi.org/10.1111/ahg.12131DOI Listing
November 2015

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Hum Mutat 2015 Nov 30;36(11):E2441-53. Epub 2015 Jul 30.

Laboratoire de Génétique Moléculaire Humaine, Institut Pasteur du Maroc, 1 Place Louis Pasteur, 20360, Casablanca, Morocco.

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http://dx.doi.org/10.1002/humu.22835DOI Listing
November 2015

A Tunisian patient with two rare syndromes: triple a syndrome and congenital hypogonadotropic hypogonadism.

Horm Res Paediatr 2014 18;82(5):338-43. Epub 2014 Sep 18.

LR11IPT05, Laboratoire de Génomique Biomédicale et Oncogénétique, Institut Pasteur de Tunis, Université de Tunis El Manar, Tunis, Tunisia.

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http://dx.doi.org/10.1159/000365888DOI Listing
July 2015

Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region.

Mitochondrial DNA A DNA Mapp Seq Anal 2016 4;27(2):1558-63. Epub 2015 Sep 4.

a Biomedical Genomics and Oncogenetics laboratory (LR 11 IPT 05), Institut Pasteur de Tunis, Université El Manar de Tunis , Tunis , Tunisia .

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http://dx.doi.org/10.3109/19401736.2014.953136DOI Listing
October 2016

Specific aspects of consanguinity: some examples from the Tunisian population.

Hum Hered 2014 29;77(1-4):167-74. Epub 2014 Jul 29.

Biomedical Genomics and Oncogenetics Laboratory LR11IPT05, Institut Pasteur de Tunis, Université Tunis El Manar, Tunis, Tunisia.

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http://dx.doi.org/10.1159/000362167DOI Listing
March 2015

Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations.

Mitochondrial DNA 2015 Aug 3;26(4):593-604. Epub 2014 Feb 3.

Biomedical Genomics and Oncogenetics Laboratory (LR 11 IPT 05), Institut Pasteur de Tunis, Université El Manar de Tunis , Tunis , Tunisia and.

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http://www.tandfonline.com/doi/full/10.3109/19401736.2013.87
Publisher Site
http://dx.doi.org/10.3109/19401736.2013.879649DOI Listing
August 2015

Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.

Gene 2013 Oct 13;529(1):45-9. Epub 2013 Aug 13.

Université Tunis El Manar, Institut Pasteur de Tunis, LR11IPT05, Génomique Biomédicale et Oncogénétique, 1002 Tunis,Tunisia; Université de Monastire, Institut Supérieur de Biotechnologie, Monastir 5000, Tunisia.

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http://dx.doi.org/10.1016/j.gene.2013.07.066DOI Listing
October 2013

Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.

Int J Pediatr Otorhinolaryngol 2013 Sep 12;77(9):1481-4. Epub 2013 Jul 12.

Laboratoire de Génomique Biomédicale et Oncogénétique, Institut Pasteur de Tunis, BP 74, 13 Place Pasteur, Tunis 1002, Tunisia.

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http://linkinghub.elsevier.com/retrieve/pii/S016558761300295
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http://dx.doi.org/10.1016/j.ijporl.2013.06.013DOI Listing
September 2013

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.

Gene 2013 Aug 13;525(1):1-4. Epub 2013 May 13.

Laboratoire de Génomique Biomédicale et Oncogénétique, Institut Pasteur de Tunis, BP 74, 13 Place Pasteur, Tunis 1002, Tunisia.

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http://dx.doi.org/10.1016/j.gene.2013.04.078DOI Listing
August 2013

Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.

Orphanet J Rare Dis 2012 Aug 21;7:52. Epub 2012 Aug 21.

Laboratory of Biomedical Genomics and Oncogenetics, Institut Pasteur de Tunis, BP 74, 13 Place Pasteur, Tunis 1002, Tunisia.

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http://dx.doi.org/10.1186/1750-1172-7-52DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495028PMC
August 2012

Genetic diseases in the Tunisian population.

Am J Med Genet A 2011 Jan;155A(1):238-67

Institut Pasteur de Tunis, Tunisia.

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http://dx.doi.org/10.1002/ajmg.a.33771DOI Listing
January 2011