Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients

by Adi, Ahmad, Bin Abbas, Bassam, Al Hamed, Mohamed, Al Tassan, Nada, Bakheet, Dana
Published in Genes (Basel) (2015)

Molecular classification of blood and bleeding disorder genes

by Baz, Batoul, Abouelhoda, Mohamed, Owaidah, Tarek, Dasouki, Majed, Monies, Dorota, Al Tassan, Nada
Published in NPJ Genom Med (2021)

Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3)

by Khan, Arif O., Shinwari, Jameela, Abu Dhaim, Nada, Khalil, Dania, Al Sharif, Latifa, Al Tassan, Nada
Published 2011

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome

by Khan, Arif O., Shinwari, Jameela, Al Sharif, Latifa, Khalil, Dania, Al-Gehedan, Saeed, Al Tassan, Nada A.
Published 2011

Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia

by Bohlega, Saeed A, Shinwari, Jameela M, Al Sharif, Latifa J, Khalil, Dania S, Alkhairallah, Thamer S, Al Tassan, Nada A
Published 2011

Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families

by Khan, Arif O., Shinwari, Jameela, Omar, Aisha, Al-Sharif, Latifa, Khalil, Dania S., Alanazi, Mohammed, Al-Amri, Abdullah, Al Tassan, Nada
Published 2011

Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder

by Shinwari, Jameela M.A., Khan, Arif, Awad, Salma, Shinwari, Zakia, Alaiya, Ayodele, Alanazi, Mohamad, Tahir, Asma, Poizat, Coralie, Al Tassan, Nada
Published in Am J Hum Genet (2015)

Synergistic divergence: a distinct ocular motility dysinnervation pattern

by Oystreck, Darren T., Khan, Arif O., Vila-Coro, Antonio Aguirre, Oworu, Olugbemisola, Al-Tassan, Nada, Chan, Wai-Man, Engle, Elizabeth C, Bosley, Thomas M.
Published 2009

TP53 genetic alterations in Arab breast cancer patients: Novel mutations, pattern and distribution

by AL-QASEM, ABEER J., TOULIMAT, MOHAMED, ELDALI, ABDELMONEIM M., TULBAH, ASMA, AL-YOUSEF, NUJOUD, AL-DAIHAN, SOOAD K., AL-TASSAN, NADA, AL-TWEIGERI, TAHER, ABOUSSEKHRA, ABDELILAH
Published 2011

A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders

by Muiya, Nzioka P, Wakil, Salma M, Tahir, Asma I, Hagos, Samya, Najai, Mohammed, Gueco, Daisy, Al-Tassan, Nada, Andres, Editha, Mazher, Nejat, Meyer, Brian F, Dzimiri, Nduna
Published 2013

Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder

by Shinwari, Jameela M.A., Al Yemni, Eman A.A., Alnaemi, Faten M., Abebe, Dejene, Al-Abdulaziz, Basma S., Al Mubarak, Bashayer R., Ghaziuddin, Mohammad, Al Tassan, Nada A.
Published in Psychiatr Genet (2017)

Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

by Morales, Jose, Al-Sharif, Latifa, Khalil, Dania S., Shinwari, Jameela M.A., Bavi, Prashant, Al-Mahrouqi, Rahima A., Al-Rajhi, Ali, Alkuraya, Fowzan S., Meyer, Brian F., Al Tassan, Nada
Published 2009

A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24

by Wakil, Salma M., Muiya, Nzioka P., Tahir, Asma I., Al-Najai, Mohammed, Baz, Batoul, Andres, Editha, Mazhar, Nejat, Al Tassan, Nada, Alshahid, Maie, Meyer, Brian F., Dzimiri, Nduna
Published 2014

Estimating transfection efficiency in differentiated and undifferentiated neural cells

by Alabdullah, Abeer A., Al-Abdulaziz, Basma, Alsalem, Hanan, Magrashi, Amna, Pulicat, Subramanian M., Almzroua, Amer A., Almohanna, Falah, Assiri, Abdullah Mohamed, Al Tassan, Nada A., Al-Mubarak, Bashayer R.
Published in BMC Res Notes (2019)

New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses

by AlSahlawi, Aysha, Aljelaify, Rasha, Magrashi, Amna, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatimah, Alturkistani, Abdulellah, AlObaid, Abdullah, Abouelhoda, Mohamed, AlMubarak, Latifa, AlTassan, Nada, Abedalthagafi, Malak
Published in Oncotarget (2019)

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission

by Al-Mubarak, Bashayer R., Omar, Aisha, Baz, Batoul, Al-Abdulaziz, Basma, Magrashi, Amna I., Al-Yemni, Eman, Jabaan, Amjad, Monies, Dorota, Abouelhoda, Mohamed, Abebe, Dejene, Ghaziuddin, Mohammad, Al-Tassan, Nada A.
Published in Eur J Hum Genet (2020)

Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer

by Watts, Katie, Wills, Christopher, Madi, Ayman, Palles, Claire, Maughan, Timothy S., Kaplan, Richard, Al-Tassan, Nada A., Kerr, Rachel, Kerr, David, Gray, Victoria, West, Hannah, Houlston, Richard S., Escott-Price, Valentina, Cheadle, Jeremy P.
Published in Int J Cancer (2021)

IMMU-01. DURABLE RESPONSE TO NIVOLUMAB IN A PEDIATRIC PATIENT WITH REFRACTORY GLIOBLASTOMA AND CONSTITUTIONAL BIALLELIC MISMATCH REPAIR DEFICIENCY

by AlHarbi, Musa, Mobark, Nahla Ali, Al-Mubarak, Latifa, Alaljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatmah, Hussain, Emarat, AlSubaie, Lamia, AlShieban, Saeed, alTassan, Nada, Ramkissoon, Shakti H, Abedalthagafi, Malak
Published in Neuro Oncol (2018)

Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family

by AlHarbi, Musa, Mubarak, Nahla, AlMubarak, Latifa, Aljelaify, Rasha, AlSaeed, Mariam, Almutairi, Amal, AlJabarat, Weal, Alqubaishi, Fatimah, Al-Subaie, Lamia, AlTassan, Nada, Neben, Cynthia L., Zhou, Alicia Y., Abedalthagafi, Malak
Published in NPJ Genom Med (2018)

Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients

by Owaidah, Tarek, Saleh, Mahasen, Baz, Batoul, Abdulaziz, Basma, Alzahrani, Hazza, Tarawah, Ahmed, Almusa, Abdulrahman, AlNounou, Randa, AbaAlkhail, Hala, Al-Numair, Nouf, Altahan, Rahaf, Abouelhoda, Mohammed, Alamoudi, Thamer, Monies, Dorota, Jabaan, Amjad, Al Tassan, Nada
Published in NPJ Genom Med (2019)