Rim LOUATI

Born on 14-06-1979 in Sfax (Tunisia)

Married

CIN 08411276// mobile 21697678089

ORCID ID:// https://orcid.org/0000-0002-8360-295X

Researcher ID :   D-9717-2019

Address

Faculté de Médecine de Sfax, Avenue Majida Boulila, 3029 Sfax, Tunisie

L’Unité de Recherche Génomique des signalopathies UR17ES36, laboratoire d’histologie et embryologie

Tel/Fax: 00216 74 241 888 – 74 246 217

EDUCATION

·         PhD degree in Biological Sciences: Research area: “the signaling pathway RAS MAP Kinase study during of developmental abnormalities and oncogenesis”. Medical university of Sfax (FMS) .Faculty of Science of Sfax (F.S.S), Tunisia (2017)

·         Master Degree in Human Genetics: “Use of molecular and cellular genetic to research the mutations of PTPN11 gene in congenital cardiac defect”. Faculty of medical Science of Sfax, Tunisia, 2009.

·         Master in Sciences of life: Faculty of Science of Sfax (FSS), Tunisia (2006)

·         Graduate of a senior technician in medical biology, Tunisia (2003)

·         Baccalaureate in Experimental Sciences : lycée 20 Mars 1956, Tunisie (2000)

FIELDS OF RESEARCH

·         Have good experience in many molecular biology techniques

Extraction of genomic and tumoral DNA (from a histological section) and RNA, PCR,
MLPA (Multiplexe Ligation Dependent Probe Amplification), HRM (melting curve hybridization), Genotyping and mapping of heterozygous, Automatic sequencing and protein electrophoresis, SNP genotyping…)

·         Familiar with most sequence databases.

EXPERIENCES PEDAGOGIQUE

2010-2011: Contractual assistant teaching TP / TD of histology at the Faculty of Medicine of Sfax.
2007-2009: Student researcher in Histology embryology anatomy laboratory at the Faculty of Medicine of Sfax.
2007: Obtaining a Certificate of Validation of Training in University Pedagogy.

TRAININGS
March-June 2012: internship at the Laboratory of Human Genetics at the University of Magdeburg, Germany.
February 2012: participation in a bioinformatics workshop at the Faculty of Medicine of Sfax.
April-May2009: Internship at the Laboratory of Human Genetics at Erlangen-Nuremberg University, Germany.
January 2008: Workshop on the DHPLC: Transgenomic system and navigator software organized by the transgenomic company and ensured by its representative “Alexander Idiria”. Faculty of Sciences of Tunis from 26 to 29 January.
April 2009: Training the use of bioinformatics in medical research. Faculty of Medicine of Sfax.
November 2009: National workshop on bioinformatics: Bioinformatics method for the study of genetic polymorphisms from at the biotechnology center of Sfax organized by the Tunisian society of immunology.
October 2009: Assistance to the workshop: diagnostic approach to neonatal neurological distress at the 8th day of the school of hereditary diseases organized by ATEMMH in at the Syphax hotel.
June 2006: 1-month internship at the Laboratory of Prokaryote Metabolites and Enzymology at the Biotechnology Center (CBS).
July 2005: 20-day internship at the Laboratory of Prokaryote Metabolites and Enzymology at the Biotechnology Center (CBS).
2001-2004: Hospital internship as part of training of senior medical technician in the laboratories of CHU Habib Bourguiba Hospital of Sfax in fields of biochemistry, microbiology, parasitology, hematology, immunology.

LANGUAGE

English, French, Arabic.

HOBBIES

Sport, music, movies, cooking.

Publications

1.       R. Louati, S. Aloulou, N. Gouia Moalla, H. Denguir, W. Smaoui, S. Kammoun, K. Trigui, M. Ben Aziza, W. Ltaif, O. Kaabi, A. Kaabi, N. Abdellaoui, S. Kammoun, W. Ben Romdhane, J. Jabeur, J. Elleuch, S. Mrabet, H. Ben Ameur, F. Turki, F. Abid, H. Fourati, K. Chaker, W. Kammoun, O. Bedoui, M. N. Mhiri, M. Zenker, N. B. Abdelmoula (2019) Lack of BRAF V600E mutation in a Tunisian colorectal adenocarcinoma cohort. European Society of Human Genetics Conference 2017 May; 25. Abstracts Collection Published: 01 October 2018 Abstracts from the 50th European Society of Human Genetics Conference. European Journal of Human Genetics (2019) 26:963. https://doi.org/10.1038/s41431-018-0248-6

Impact Factor 4.287

2.       F. Turki, S. Aloulou, O. Trabelsi, S. Charfi, A. Chakroun, I. Achour, N. Abdellaoui,R. Louati, Y. Kaabi, W. Smaoui, H. Fourati, K. Chaker, K. Trigui, M. Ben Aziza, W. Ltaif,H. Denguir, H. Ben Ameur, S. Mallek, W. Aloulou, J. Jabeur, J. Dammak, S. Mrabet, S.Kammoun, F. Mzid, W. Kammoun, O. Bedoui, A. Kaabi, N. Mhiri, N. Maalla, A.Ghorbel, T. Boudawara1, N. Abdelmoula Bouayed (2019) BRAF V600E mutational analysis of metastatic lymph nodes from two Tunisian females with papillary thyroid carcinoma. European Society of Human Genetics Conference 2017 May; 25. Abstracts Collection Published: 01 October 2018 Abstracts from the 50th European Society of Human Genetics Conference. European Journal of Human Genetics (2019) 26:594. https://doi.org/10.1038/s41431-018-0247-7

Impact Factor 4.287

3.       F. Turki, S. Aloulou, O. Trabelsi, S. Charfi, A. Chakroun, I. Achour, N. Abdellaoui,R. Louati, Y. Kaabi, W. Smaoui, H. Fourati, K. Chaker, K. Trigui, M. Ben Aziza, W. Ltaif,H. Denguir, H. Ben Ameur, S. Mallek, W. Aloulou, J. Jabeur, J. Dammak, S. Mrabet, S.Kammoun, F. Mzid, W. Kammoun, O. Bedoui, A. Kaabi, N. Mhiri, N. Maalla, A.Ghorbel, T. Boudawara1, N. Abdelmoula Bouayed (2019) BRAF V600E mutational analysis of metastatic lymph nodes from two Tunisian females with papillary thyroid carcinoma. European Society of Human Genetics Conference 2017 May; 25. Abstracts Collection Published: 01 October 2018 Abstracts from the 50th European Society of Human Genetics Conference. European Journal of Human Genetics (2019) 26:594. https://doi.org/10.1038/s41431-018-0247-7

Impact Factor 4.287

4.       N. B. Abdelmoula, S. Aloulou, N. Gouia Moalla, R. Louati, F. Turki, W. Ben Romdhane, J. Jabeur, J. Elleuch, S. Mrabet, H. Ben Ameur, M. Ben Aziza, W. Smaoui, M. Mhiri, M.Ben Dhaou, T. Rebai, R. Mhiri, M. Jallouli, M. Buisine. (2019) A rare familial APC deletion in a Tunisian family revealed in a 18-monthold boy with paravertabral Gardner fibroma. European Society of Human Genetics Conference 2017 May; 25. Abstracts Collection Published: 01 October 2018 Abstracts from the 50th European Society of Human Genetics Conference. European Journal of Human Genetics (2019) 26:516. https://doi.org/10.1038/s41431-018-0247-7

Impact Factor 4.287

5.       Abdelmoula Bouayed Nouha , Smaoui Walid , Louati Rim , Kaabi Oldez , Trigui Khaled, Ltaif Wided, Sbaii Akram, ben ayed Hedi moez , Ben Aziza Mustapha, Abdellaoui Nawel , Abdelmoula Balkiss , Kammoun Sonda , Gouiaa Naourez , Mhiri Med Nabil , Aloulou Samir (2019) Monomorphic Teratozoospermia: Genetics and Fertility Prognosis. World Journal Urology. 2019 Oct; 37(Suppl 1):1-344. doi: 10.1007/s00345-019-02955-9. Abstracts from the 39th Congress of the Société Internationale d’Urologie, Athens, Greece, October 17-20, 2019. PMID: 31620861 DOI: 10.1007/s00345-019-02955-9

Impact Factor 4.743

6.       Balkiss Abdelmoula, Walid Smaoui, Kays Chaker, Fatma Abid, Wided Ltaif, Nawel Abdellaoui, Rim Louati, Asma Yaich, Khaled Trigui, Sourour Ben Ali, Hadil Chaari, Sourour Fellah, Samir M’rabet, Akram Sbai, Haytham Fourati, Oldez Kaabi, Hamdi Yahia, Asma Kaabi, Hédi Ben Ameur, Moez Hédi Ben Ayed, Samir Aloulou, Med Nabil Mhiri, Naourez Gouiaa, Wafa Kammoun, Sonda Kammoun, Souad Mallek, Mustapha Ben Aziza, Nouha Bouayed Abdelmoula (2019) The Influence of Multiple Occupational Exposure on Male Reproductive Function: A Cross Study Among Infertile Men in Tunisia. World Journal Urology. 2019 Oct; 37(Suppl 1):1-344. doi: 10.1007/s00345-019-02955-9. Abstracts from the 39th Congress of the Société Internationale d’Urologie, Athens, Greece, October 17-20, 2019. PMID: 31620861 DOI: 10.1007/s00345-019-02955-9

Impact Factor 4.743

7.       Nouha Bouayed Abdelmoula, Balkiss Abdelmoula, Kays Chaker, Fatma Abid, Wided Ltaif, Nawel Abdellaoui, Rim Louati, Asma Yaich, Walid Smaoui, Khaled .Ben Ali, Hadil Chaari, Sourour Fellah, Samir M’rabet, Akram Sbai, Haytham Fourati, Oldez Kaabi, Hamdi Yahia, Asma Kaabi, Hédi Ben Ameur, Moez Hédi Ben Ayed, Samir Aloulou, Amir Karra, Takwa Sammouda, Wafa Kammoun, Souad Mallek, Mustapha Ben Aziza, Sonda Kammoun, Med Nabil Mhiri (2019) Genital Phenotypic Heterogeneity in Bardet-Biedl Syndrome. World Journal Urology. 2019 Oct; 37(Suppl 1):1-344. doi: 10.1007/s00345-019-02955-9. Abstracts from the 39th Congress of the Société Internationale d’Urologie, Athens, Greece, October 17-20, 2019. PMID: 31620861 DOI: 10.1007/s00345-019-02955-9

Impact Factor 4.743

8.       A. Samet, W. Smaoui, K. Trigui, B. Abdelmoula, F. Abid, N. Abdeleoui, K. Chaker, H. Fourati, O. Kaabi, R. Louati, S. Mayouf, A. Rekhis, M. Fourati, S. Kammoun, M. Mhiri, S. Aloulou, N. Abdelmoula bouayed, N. Rebai (2019) Le syndrome de Klinefelter : quel est le pronostic de fertilité ? Progrès en Urologie Volume 29, Issue 13, November 2019, Page 722. 113ème congrès français d’urologie 20-23 Novembre 2019 PARIS, France (CO-130) https://doi.org/10.1016/j.purol.2019.08.177.

CO-130 www.cfu-congres.com https://www.urofrance.org/sites/default/files/cfu_19-programme-v7.pdf

Impact Factor 0.586

9.       Abdellaoui Nawel, Abdelmoula Balkiss, Smaoui Walid, Ltaif Wided, Trigui Khaled, Mzid Abid Fatma, Kammoun Sonda, Ben Aziza Mustapha, Kammoun Mallek Souad, M’rabet Samir, Ben Ameur Hédi, Hamdi Yahia, Chaker Kays, Yaich Asma, Rim louati, Oldez Kaabi, Kaabi Asma, Ben Ali Sourour, Chaari Hadil, Sourour Falleh, Mhiri Mohamed Nabil, Moalla Gouiaa Naourez, Aloulou Samir, Abdelmoula Bouayed Nouha (2019) Un marqueur RFLP pour le variant UGT1A1*60 ? Revue Tunisienne de Biologie Clinique Supplément Avril 2019.

10.   Abdelmoula Bouayed Nouha, Rim louati, Oldez Kaabi, Abdellaoui Nawel, Mzid Abid Fatma, abdelmoula Balkiss, Smaoui Walid, Ltaif Wided, Trigui Khaled, Kammoun Sonda, Ben Aziza Mustapha, Kammoun Mallek Souad, M’rabet Samir, Ben Ameur Hédi, Hamdi Yahia, Chaker Kays, Yaich Asma, Kaabi Asma, Ben Ali Sourour, Chaari Hadil, Sourour Falleh, Mhiri Mohamed Nabil, Moalla Gouiaa Naourez, Aloulou Samir (2019) Marqueurs RFLP de la pathologie thrombophilique. Revue Tunisienne de Biologie Clinique Supplément Avril 2019.

11.   Abdelmoula Bouayed Nouha, Mzid Abid Fatma, Abdelmoula Balkiss, Smaoui Walid, Ltaif Wided, Trigui Khaled, Abdellaoui Nawel, Kammoun Sonda, Ben Aziza Mustapha, Kammoun Mallek Souad, M’rabet Samir, Ben Ameur Hédi, Hamdi Yahia, Chaker Kays, Yaich Asma, Rim louati, Oldez Kaabi, Kaabi Asma, Ben Ali Sourour, Chaari Hadil, Sourour Falleh, Mhiri Mohamed Nabil, Moalla Gouiaa Naourez, Aloulou Samir (2019) Marqueurs RFLP du chromosome 22. Revue Tunisienne de Biologie Clinique Supplément Avril 2019.

12.   N. Abdelmoula, W. Smaoui, K.H. Trigui, F. Abid, S. Kammoun, S. Aloulou, M.H. Ben Ayed, A. Sbai, H. Yahia, K. Chaker, H. Fourati, S. Fellah, S. Ben Ali, A. Yaich, A. Kaabi, H. Chaari, W. Kammoun, S. Kammoun, O. Kaabi, R. Louati, N. Abdellaoui, W. Ltaif, M. Ben Aziza, J. Jabr, J. Dammak, S. M’rabet, H. Ben Ameur, B. Abdelmoula, M.N. Mhiri, N. Gouiaa. (2019) Preconception TGM1 carrier screening for autosomal recessive congenital ichthyosis: A new variant. 2019 ASHG Annual Meeting (Annual Meeting of the American Society of Human Genetics), the George R. Brown Convention Center in Houston, Texas, October 15-19, 2019 (3065F) https://www.ashg.org/2019meeting/pdf/ASHG-2019-poster-abstracts.pdf (PgmNr 3065 page3073)

13.   B. Abdelmoula, R. Louati, W. Smaoui, K.H. Trigui, F. Abid, S. Kammoun, O. Kaabi, N. Abdellaoui, K. Chaker, H. Fourati, S. Aloulou, H. Yahia, M.H. Ben Ayed, A. Sbai, S. Fellah, S. Ben Ali, H. Chaari, A. Yaich, A. Kaabi, S. Mrabet, M. Ben Aziza, J. Jabr, S. Mallek, W. Kammoun, W. Ltaif, J. Dammak, H. Ben Ameur, N. Gouiaa, M.N. Mhiri, N. Bouayed Abdelmoula. (2019) A possible crosstalk disorder between BMP15 and TGF-β family ligands and receptors in Mayer-Rokitansky-Küster-Hauser syndrome. 2019 ASHG Annual Meeting (Annual Meeting of the American Society of Human Genetics), the George R. Brown Convention Center in Houston, Texas, October 15-19, 2019 (3120W) https://www.ashg.org/2019meeting/pdf/ASHG-2019-poster-abstracts.pdf (PgmNr 3120 page 3136)

14.   Nouha Bouayed Abdelmoula Balkiss Abdelmoula,  Sonda Kammoun,  Rim Louati,  Nawel Abdellaoui,  Oldez Kaabi,  Fatma Abid,  Khaled Trigui, Wided Ltaif,  Samir Aloulou (2019) De novo proximal Xq duplication and functional Xq disomy in mosaic Turner syndrome: Gonadal dysgenesis without short stature. 13 Congress of the European Society of Gynecology Wien (AT) October 16 2019 to October 19 2019 ID#8918 https://esg2019.esgynecology.org/program/

15.   Abdelmoula Bouayed Nouha, Rim louati, Oldez Kaabi, Abdellaoui Nawel, Mzid Abid Fatma, Abdelmoula Balkiss, Smaoui Walid, Ltaif Wided, Trigui Khaled, Kammoun Sonda, Ben Aziza Mustapha, M’rabet Samir, Ben Ameur Hédi, Hamdi Yahia, Chaker Kays, Yaich Asma, Kaabi Asma, Ben Ali Sourour, Chaari Hadil, Sourour Falleh, Aloulou Samir, Mhiri Mohamed Nabil, Moalla Gouiaa Naourez, Kammoun  Mallek Souad (2019) Les 16èmes Journées Afro Européennes de Cardiologie Pratique 27, 28, 29 et 30 Juin 2019, El Mouradi Congress Center Hammam Sousse. https://www.cardiologie-pratique.com/services/agenda/journees-afro-europeennes-cardiologie-pratique

16.   Bouayed Abdelmoula N, Abdelmoula B, Smaoui W, Trabelsi I, Louati R, Aloulou S,Aloulou W, Abid F, Kammoun S, Trigui K, Bedoui O, Denguir H, Mallek S, Ben Aziza M, Dammak J, Kaabi O, Abdellaoui N, Turki F, Kaabi A, Kamoun W, Jabeur J, Ltaif W, Chaker K, Fourati H, M’rabet S, Ben Ameur H, Gouia N, Mhiri MN, Rebai T.Left-sided congenital heart lesions in mosaic Turner syndrome. Mol GenetGenomics. 2018 Apr;293(2):495-501.
17.   Louati R, Abdelmoula NB , Sanga Mitra Boppudi, Tarek rebai: Short fragment approach for genotyping KRAS and BRAF genes in Tunisian patients with colorectal cancer. March 2017

18.      Louati R, Abdelmoula NB, Trabelsi I, Abid D, Lissewski C, Kharrat N, Kamoun S,Zenker M,Rebai T. Clinical and Molecular Findings of Tunisian Patients with RASopathies. Mol Syndromol. 2014 Aug;5(5):212-7.
19.                         Badraoui R, Ben Nasr H, Louati R, Ellouze F, Rebai T. Nephrotoxic effect of tetradifon in rats: a biochemical and histomorphometric study. Exp ToxicolPathol. 2012 Sep;64(6)