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

Por Adi, Ahmad, Bin Abbas, Bassam, Al Hamed, Mohamed, Al Tassan, Nada, Bakheet, Dana
Publicado no Genes (Basel) (2015)

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

Por Khan, Arif O., Shinwari, Jameela, Abu Dhaim, Nada, Khalil, Dania, Al Sharif, Latifa, Al Tassan, Nada
Publicado em 2011

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome

Por Khan, Arif O., Shinwari, Jameela, Al Sharif, Latifa, Khalil, Dania, Al-Gehedan, Saeed, Al Tassan, Nada A.
Publicado em 2011

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

Por Bohlega, Saeed A, Shinwari, Jameela M, Al Sharif, Latifa J, Khalil, Dania S, Alkhairallah, Thamer S, Al Tassan, Nada A
Publicado em 2011

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

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

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

Por Shinwari, Jameela M.A., Khan, Arif, Awad, Salma, Shinwari, Zakia, Alaiya, Ayodele, Alanazi, Mohamad, Tahir, Asma, Poizat, Coralie, Al Tassan, Nada
Publicado no Am J Hum Genet (2015)

Synergistic divergence: a distinct ocular motility dysinnervation pattern

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

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

Por 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
Publicado em 2011

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

Por 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
Publicado em 2013

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

Por 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.
Publicado no Psychiatr Genet (2017)

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

Por 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
Publicado em 2009

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

Por 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
Publicado em 2014

Estimating transfection efficiency in differentiated and undifferentiated neural cells

Por 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.
Publicado no BMC Res Notes (2019)

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

Por AlSahlawi, Aysha, Aljelaify, Rasha, Magrashi, Amna, AlSaeed, Mariam, Almutairi, Amal, Alqubaishi, Fatimah, Alturkistani, Abdulellah, AlObaid, Abdullah, Abouelhoda, Mohamed, AlMubarak, Latifa, AlTassan, Nada, Abedalthagafi, Malak
Publicado no Oncotarget (2019)

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

Por 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.
Publicado no 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

Por 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.
Publicado no Int J Cancer (2021)

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

Por 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
Publicado no Neuro Oncol (2018)

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

Por 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
Publicado no NPJ Genom Med (2018)

Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients

Por 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
Publicado no NPJ Genom Med (2019)

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

Por Bohlega, Saeed A., Al-Mubarak, Bashayer R., Alyemni, Eman A., Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E., Khalil, Dania S., Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I., Al Tassan, Nada A.
Publicado no BMC Res Notes (2016)