Interactions between BRD4S, LOXL2, and MED1 drive cell cycle transcription in triple‐negative breast cancer
Pascual‐Reguant, Laura, Serra‐Camprubí, Queralt, Datta, Debayan, Cianferoni, Damiano, Kourtis, Savvas, Gañez‐Zapater, Antoni, Cannatá, Chiara, Espinar, Lorena, Querol, Jessica, García‐López, Laura, Musa‐Afaneh, Sara, Guirola, Maria, Gkanogiannis, Anestis, Miró Canturri, Andrea, Guzman, Marta, Rodríguez, Olga, Herencia‐Ropero, Andrea, Arribas, Joaquin, Serra, Violeta, Serrano, Luis, Tian, Tian V, Peiró, Sandra, Sdelci, Sara
Published in EMBO molecular medicine (07.12.2023)
Published in EMBO molecular medicine (07.12.2023)
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Journal Article
A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients
Musa, Sara, Eyaid, Wafaa, Kamer, Kimberli, Ali, Rehab, Al-Mureikhi, Mariam, Shahbeck, Noora, Al Mesaifri, Fatma, Makhseed, Nawal, Mohamed, Zakkiriah, AlShehhi, Wafaa Ali, Mootha, Vamsi K., Juusola, Jane, Ben-Omran, Tawfeg
Published in JIMD Reports, Volume 43 (2019)
Published in JIMD Reports, Volume 43 (2019)
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Book Chapter
Journal Article
The impact of armed conflict on nursing students' self-esteem: a cross-sectional comparative study
Mohammead, Mohammead, Alenezi, Atallah, Abdelmalik, Mohammed, Alhowaymel, Fahad, Abdallah, Mohamed, Saeed, Abdalrahman, Musa, Sara, Ebrahim, Elturabi, Salih, Shahenda
Published in Journal of medicine and life (01.07.2024)
Published in Journal of medicine and life (01.07.2024)
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Journal Article
Refractory Hyperammonemic encephalopathy in Fibrolamellar hepatocellular carcinoma, a case report and literature review
Ahmed, Arwa, Ata, Fateen, Gaber, Mohammed, Petkar, Mahir, Mahfouz, Ahmed, Schirmacher, Peter, Musa, Sara, Hashim, Ahmed
Published in Current problems in cancer (01.06.2022)
Published in Current problems in cancer (01.06.2022)
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Journal Article
Gene therapy for spinal muscular atrophy: the Qatari experience
Ali, Hossamaldein Gaber, Ibrahim, Khalid, Elsaid, Mahmoud Fawzi, Mohamed, Reem Babiker, Abeidah, Mahmoud I. A., Al Rawwas, Azhar Othman, Elshafey, Khaled, Almulla, Hajer, El-Akouri, Karen, Almulla, Mariam, Othman, Amna, Musa, Sara, Al-Mesaifri, Fatma, Ali, Rehab, Shahbeck, Noora, Al-Mureikhi, Mariam, Alsulaiman, Reem, Alkaabi, Saad, Ben-Omran, Tawfeg
Published in Gene therapy (01.11.2021)
Published in Gene therapy (01.11.2021)
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Journal Article
WITHDRAWN: Refractory Hyperammonemic encephalopathy in Fibrolamellar hepatocellular carcinoma, a case report and literature review
Ahmed, Arwa, Ata, Fateen, Gaber, Mohammed, Petkar, Mahir, Mahfouz, Ahmed, Schirmacher, Peter, Musa, Sara, Hashim, Ahmed
Published in Current problems in cancer. Case reports (01.01.2022)
Published in Current problems in cancer. Case reports (01.01.2022)
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Journal Article
Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience
Al‐Dewik, Nader, Mohd, Howaida, Al‐Mureikhi, Mariam, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Shahbeck, Noora, El‐Akouri, Karen, Almulla, Mariam, Al Sulaiman, Reem, Musa, Sara, Al‐Marri, Ajayeb Al‐Nabet, Richard, Gabriele, Juusola, Jane, Solomon, Benjamin D., Alkuraya, Fowzan S., Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.06.2019)
Published in American journal of medical genetics. Part A (01.06.2019)
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Journal Article
Natural history, with clinical, biochemical, and molecular characterization of classical homocystinuria in the Qatari population
Al‐Dewik, Nader, Ali, Alaa, Mahmoud, Yassmin, Shahbeck, Noora, Ali, Rehab, Mahmoud, Laila, Al‐Mureikhi, Mariam, Al‐Mesaifri, Fatma, Musa, Sara, El‐Akouri, Karen, Almulla, Mariam, Al Saadi, Reem, Nasrallah, Gheyath K., Samara, Muthanna, Abdoh, Ghassan, Rifai, Hilal Al, Häberle, Johannes, Thöny, Beat, Kruger, Warren, Blom, Henk J., Ben‐Omran, Tawfeg
Published in Journal of inherited metabolic disease (01.09.2019)
Published in Journal of inherited metabolic disease (01.09.2019)
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Journal Article
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
Ali, Rehab, Al‐Dewik, Nader, Mohammed, Shayma, Elfituri, Mahmud, Agouba, Sahar, Musa, Sara, Mahmoud, Laila, Almulla, Mariam, El‐Akouri, Karen, Mohd, Howaida, Bux, Reem, Almulla, Hajer, Othman, Amna, Al‐Mesaifri, Fatma, Shahbeck, Noora, Al‐Muriekhi, Mariam, Khalifa, Amal, Al‐Sulaiman, Reem, Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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Journal Article
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families
Al‐Sulaiman, Reem, Othman, Amna, El‐Akouri, Karen, Fareed, Shehab, AlMulla, Hajer, Sukik, Aseel, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Musa, Sara, Al‐Mulla, Mariam, Ibrahim, Khalid, Mohamed, Khalid, Al‐Nesef, Maryam Ali, Ehlayel, Mohammad, Ben‐Omran, Tawfeg
Published in American journal of medical genetics. Part A (01.11.2020)
Published in American journal of medical genetics. Part A (01.11.2020)
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Journal Article
Qatar’s genetic counseling landscape: Current insights and future prospects
Abiib, Sumaya, Khodjet-El-khil, Houssein, El-Akouri, Karen, Bux, Reem Ibrahim, Rezoug, Zoulikha, Abualainin, Wafa, Alkowari, Moza, Musa, Sara Osman, Al Mulla, Mariam, Al Saleh, Rehab, Shahbeck, Noora, Farag, Maria, Ismail, Said I., Al Sulaiman, Reem, Ben-Omran, Tawfeg, Al-Thani, Asma, Al-Shafai, Mashael
Published in Genetics in Medicine Open (01.07.2024)
Published in Genetics in Medicine Open (01.07.2024)
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Journal Article
Delineating the phenotypic spectrum of hyperphosphatasia with mental retardation syndrome 4 in 14 patients of Middle‐Eastern origin
Balobaid, Ameera, Ben‐Omran, Tawfeg, Ramzan, Khushnooda, Altassan, Ruqaiah, Almureikhi, Mariam, Musa, Sara, Al‐Hashmi, Nadia, Al‐Owain, Mohammed, Al‐Zaidan, Hamad, Al‐Hassnan, Zuhair, Imtiaz, Faiqa, Al‐Sayed, Moeenaldeen
Published in American journal of medical genetics. Part A (01.12.2018)
Published in American journal of medical genetics. Part A (01.12.2018)
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Journal Article
Clinical genetics and genomic medicine in Qatar
Al‐Dewik, Nader, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Othman, Amna, AlMulla, Mariam, Sulaiman, Reem Al, Musa, Sara, Abdoh, Ghassan, El‐Akouri, Karen, Solomon, Benjamin D., Ben‐Omran, Tawfeg
Published in Molecular genetics & genomic medicine (01.09.2018)
Published in Molecular genetics & genomic medicine (01.09.2018)
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Journal Article