Novel and Extremely Sensitive NiAl2O4-NiO Nanostructures on an ITO Sensing Electrode for Enhanced Detection of Ascorbic Acid von Hammami, Asma, Bardaoui, Afrah, Eissa, Shimaa, Elgaher, Walid A M, Chtourou, Radhouane, Messaoud, Olfa

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About the 2-cohomology of the orthosymplectic superalgebra von Messaoud, Olfa

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Editorial: Monogenic vs. Oligogenic Reclassification von Messaoud, Olfa, Dutta, Atanu Kumar, Cornejo-Olivas, Mario Reynaldo, Bhuiyan, Zahurul A.

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Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases von Hamdi, Yosr, Boujemaa, Maroua, Ben Rekaya, Mariem, Ben Hamda, Cherif, Mighri, Najah, El Benna, Houda, Mejri, Nesrine, Labidi, Soumaya, Daoud, Nouha, Naouali, Chokri, Messaoud, Olfa, Chargui, Mariem, Ghedira, Kais, Boubaker, Mohamed Samir, Mrad, Ridha, Boussen, Hamouda, Abdelhak, Sonia

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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci von Hamdi, Yosr, Ben Rekaya, Mariem, Jingxuan, Shan, Nagara, Majdi, Messaoud, Olfa, Benammar Elgaaied, Amel, Mrad, Ridha, Chouchane, Lotfi, Boubaker, Mohamed Samir, Abdelhak, Sonia, Boussen, Hamouda, Romdhane, Lilia

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment von Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Ben Youssef, Ilhem Turki, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha

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The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes von Dallali, Hamza, Boukhalfa, Wided, Kheriji, Nadia, Fassatoui, Meriem, Jmel, Haifa, Hechmi, Meriem, Gouiza, Ismail, Gharbi, Mariem, Kammoun, Wafa, Mrad, Mehdi, Taoueb, Marouen, Krir, Asma, Trabelsi, Hajer, Bahlous, Afef, Jamoussi, Henda, Messaoud, Olfa, Abid, Abdelmajid, Kefi, Rym

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Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers von Hamdi, Yosr, Mighri, Najah, Boujemaa, Maroua, Mejri, Nesrine, Ben Nasr, Sonia, Ben Rekaya, Mariem, Messaoud, Olfa, Bouaziz, Hanen, Berrazega, Yosra, Rachdi, Haifa, Jaidane, Olfa, Daoud, Nouha, Zribi, Aref, Ayari, Jihene, El Benna, Houda, Labidi, Soumaya, Ben Hassouna, Jamel, Haddaoui, Abderazzek, Rahal, Khaled, Benna, Farouk, Mrad, Ridha, Ben Ahmed, Slim, Boussen, Hamouda, Boubaker, Samir, Abdelhak, Sonia

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Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism von Mkaouar, Rahma, Ben Abdallah, Lamia Cherif, Naouali, Chokri, Lahbib, Saida, Turki, Zinet, Elouej, Sahar, Bouyacoub, Yosra, Somai, Maali, Mcelreavey, Kenneth, Bashamboo, Anu, Abdelhak, Sonia, Messaoud, Olfa

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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa von Romdhane, Lilia, Mezzi, Nessrine, Dallali, Hamza, Messaoud, Olfa, Shan, Jingxuan, Fakhro, Khalid A., Kefi, Rym, Chouchane, Lotfi, Abdelhak, Sonia

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health von Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hajer, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health von Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hager, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype von Nabouli, Imen, Chikhaoui, Asma, Othman, Houcemeddine, Elouej, Sahar, Jones, Meriem, Lagarde, Arnaud, Ben Rekaya, Meriem, Messaoud, Olfa, Zghal, Mohamed, Delague, Valerie, Levy, Nicolas, De Sandre-Giovannoli, Annachiara, Abdelhak, Sonia, Yacoub-Youssef, Houda

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FANCA Gene Mutations in North African Fanconi Anemia Patients von Ben Haj Ali, Abir, Messaoud, Olfa, Elouej, Sahar, Talmoudi, Faten, Ayed, Wiem, Mellouli, Fethi, Ouederni, Monia, Hadiji, Sondes, De Sandre-Giovannoli, Annachiara, Delague, Valerie, Levy, Nicolas, Bogliolo, Massimo, Surralles, Jordi, Abdelhak, Sonia, Amouri, Ahlem

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A broad survey of DNA sequence data simulation tools von Alosaimi, Shatha, Bandiang, Armand, van Biljon, Noelle, Awany, Denis, Thami, Prisca K., Tchamga, Milaine S. S., Kiran, Anmol, Messaoud, Olfa, Hassan, Radia Ismaeel Mohammed, Mugo, Jacquiline, Ahmed, Azza, Bope, Christian D., Allali, Imane, Mazandu, Gaston K., Mulder, Nicola J., Chimusa, Emile R.

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First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP‐C founder mutation von Khalat, Najlaa, Messaoud, Olfa, Ben Rekaya, Mariem, Chargui, Mariem, Zghal, Mohamed, Zendah, Bashir, Saqer, Najat, Mokni, Mourad, Abdelhak, Sonia, Mohamed, Othman A.

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Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype von Chikhaoui, Asma, Elouej, Sahar, Nabouli, Imen, Jones, Meriem, Lagarde, Arnaud, Ben Rekaya, Meriem, Messaoud, Olfa, Hamdi, Yosr, Zghal, Mohamed, Delague, Valerie, Levy, Nicolas, De Sandre-Giovannoli, Annachiara, Abdelhak, Sonia, Yacoub-Youssef, Houda

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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis von Ben Rekaya, Mariem, Naouali, Chokri, Messaoud, Olfa, Jones, Meriem, Bouyacoub, Yosra, Nagara, Majdi, Pippucci, Tommaso, Jmel, Haifa, Chargui, Mariem, Jerbi, Manel, Alibi, Mohamed, Dallali, Hamza, Bashamboo, Anu, McElreavey, Kenneth, Romeo, Giovanni, Barakat, Abdelhamid, Zghal, Mohamed, Yacoub-Youssef, Houda, Abdelhak, Sonia

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H syndrome: Clinical, histological and genetic investigation in Tunisian patients von Jaouadi, Hager, Zaouak, Anissa, Sellami, Khadija, Messaoud, Olfa, Chargui, Mariem, Hammami, Houda, Jones, Meriem, Jouini, Raja, Chadli Debbiche, Achraf, Chraiet, Karima, Fenniche, Sami, Mrad, Ridha, Mokni, Mourad, Turki, Hamida, Benkhalifa, Rym, Abdelhak, Sonia

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CVD Graphene Electrode for Direct Electrochemical Detection of Double-Stranded DNA von Bardaoui, Afrah, Hammami, Asma, Elkarous, Rabiaa, Ali Aloui, Mohamed, Oueslati, Rania, Messaoud, Olfa, Santos, Diogo M. F., Chtourou, Radhouane

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