Tawfeg Ben-Omran

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 8

Top Topics

Attention Deficit Hyperactivity Disorder

Duchenne Muscular Dystrophy

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Neurology. Clinical practice

This page only lists publications with an associated author ORCID identifier.

Publications

Victor D Armengol, Basil T Darras, Ahmad Abdulaziz Abulaban, Ali Alshehri, Nina Barisic, Tawfeg Ben-Omran, Guenther Bernert, Claudia Castiglioni, Yin-Hsiu Chien, Michelle Anne Farrar, Gwendoline Q Kandawasvika, Satish V Khadilkar, Jean K Mah, Chiara Marini-Bettolo, Damjan Osredkar, Gerald Pfeffer, Flavia B Piazzon, Inmaculada Pitarch Castellano, Susana Quijano-Roy, Kayoko Saito, Jin-Hong Shin, Juan Francisco Vázquez Costa, Maggie C Walter, Jithangi Wanigasinghe, Hui Xiong, Robert C Griggs, Bhaskar Roy
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and Availability. Neurology. Clinical practice 14 (1) (2023)
Victor D Armengol, Basil T Darras, Ahmad Abdulaziz Abulaban, Ali Alshehri, Nina Barisic, Tawfeg Ben-Omran, Guenther Bernert, Claudia Castiglioni, Yin-Hsiu Chien, Michelle Anne Farrar, Gwendoline Q Kandawasvika, Satish V Khadilkar, Jean K Mah, Chiara Marini-Bettolo, Damjan Osredkar, Gerald Pfeffer, Flavia B Piazzon, Inmaculada Pitarch Castellano, Susana Quijano-Roy, Kayoko Saito, Jin-Hong Shin, Juan Francisco Vázquez Costa, Maggie C Walter, Jithangi Wanigasinghe, Hui Xiong, Robert C Griggs, Bhaskar Roy
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and Availability. Neurology. Clinical practice 14 (1) (2023)
Victor D Armengol, Basil T Darras, Ahmad Abdulaziz Abulaban, Ali Alshehri, Nina Barisic, Tawfeg Ben-Omran, Guenther Bernert, Claudia Castiglioni, Yin-Hsiu Chien, Michelle Anne Farrar, Gwendoline Q Kandawasvika, Satish V Khadilkar, Jean K Mah, Chiara Marini-Bettolo, Damjan Osredkar, Gerald Pfeffer, Flavia B Piazzon, Inmaculada Pitarch Castellano, Susana Quijano-Roy, Kayoko Saito, Jin-Hong Shin, Juan Francisco Vázquez Costa, Maggie C Walter, Jithangi Wanigasinghe, Hui Xiong, Robert C Griggs, Bhaskar Roy
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and Availability. Neurology. Clinical practice 14 (1) (2023)
Thomas O Crawford, Kathryn J Swoboda, Darryl C De Vivo, Enrico Silvio Bertini, Paul Wuh-Liang Hwu, Richard S Finkel, Janbernd Kirschner, Nancy L Kuntz, Aledie Navas Nazario, Julie A Parsons, Astrid Pechmann, Monique M Ryan, Russell J Butterfield, Haluk A Topaloglu, Tawfeg Ben-Omran, Valeria Ada Sansone, Yuh-Jyh Jong, Francy Shu, Cong Zhu, Stephanie Raynaud, Tiffany R Lago, Angela D Paradis, Richard Foster, Russell Chin, Zdenek Berger, null null
Continued benefit of nusinersen initiated in the presymptomatic stage of spinal muscular atrophy: 5-year update of the NURTURE study. Muscle & nerve (2023)
Rehab Ali, Nader Al Dewik, Shayma Mohammed, Mahmud Elfituri, Sahar Agouba, Sara Musa, Laila Mahmoud, Mariam Almulla, Karen El-Akouri, Howaida Mohd, Reem Bux, Hajer Almulla, Amna Othman, Fatma Al-Mesaifri, Noora Shahbeck, Mariam Al-Muriekhi, Amal Khalifa, Reem Al-Sulaiman, Tawfeg Ben-Omran
Expanding on the phenotypic spectrum of Woodhouse-Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review. American journal of medical genetics. Part A (2021)
Hossamaldein Gaber Ali, Khalid Ibrahim, Mahmoud Fawzi Elsaid, Reem Babiker Mohamed, Mahmoud I A Abeidah, Azhar Othman Al Rawwas, Khaled Elshafey, Hajer Almulla, Karen El-Akouri, Mariam Almulla, Amna Othman, Sara Musa, Fatma Al-Mesaifri, Rehab Ali, Noora Shahbeck, Mariam Al-Mureikhi, Reem Alsulaiman, Saad Alkaabi, Tawfeg Ben-Omran
Gene therapy for spinal muscular atrophy: the Qatari experience. Gene therapy 28 (10-11) (2021)
Caroline Dias, Rolph Pfundt, Tjitske Kleefstra, Janneke Shuurs-Hoeijmakers, Elles M J Boon, Johanna M van Hagen, Petra Zwijnenburg, Marjan M Weiss, Boris Keren, Cyril Mignot, Arnaud Isapof, Karin Weiss, Tova Hershkovitz, Maria Iascone, Silvia Maitz, René G Feichtinger, Dieter Kotzot, Johannes A Mayr, Tawfeg Ben-Omran, Laila Mahmoud, Lynn S Pais, Christopher A Walsh, Vandana Shashi, Jennifer A Sullivan, Nicholas Stong, Francois Lecoquierre, Anne-Marie Guerrot, Aude Charollais, Lance H Rodan
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. American journal of medical genetics. Part A 185 (8) (2021)
Reem Al-Sulaiman, Amna Othman, Karen El-Akouri, Shehab Fareed, Hajer AlMulla, Aseel Sukik, Mariam Al-Mureikhi, Noora Shahbeck, Rehab Ali, Fatma Al-Mesaifri, Sara Musa, Mariam Al-Mulla, Khalid Ibrahim, Khalid Mohamed, Maryam A Y Al-Nesf, Mohammad Ehlayel, Tawfeg Ben-Omran
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. American journal of medical genetics. Part A 182 (11) (2020)