Multivariate piecewise linear regression model to predict radiosensitivity using the association with the genome-wide copy number variation by Tobiasz, Joanna, Al-Harbi, Najla, Bin Judia, Sara, Majid Wakil, Salma, Polanska, Joanna, Alsbeih, Ghazi

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Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis by Aldughaim, Mohammed S., Al-Anazi, Mashael R., Bohol, Marie Fe F., Colak, Dilek, Alothaid, Hani, Wakil, Salma Majid, Hagos, Samya T., Ali, Daoud, Alarifi, Saud, Rout, Sashmita, Alkahtani, Saad, Al-Ahdal, Mohammed N., Al-Qahtani, Ahmed A.

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Pregnancy reduces severity and frequency of attacks in hyperkalemic periodic paralysis due to the mutation c.2111C>T in the SCN4A gene by Finsterer, Josef, Wakil, Salma, Laccone, Franco

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Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases by Al-Mousa, Hamoud, MD, Abouelhoda, Mohamed, PhD, Monies, Dorota M., PhD, Al-Tassan, Nada, PhD, Al-Ghonaium, Abdulaziz, MD, Al-Saud, Bandar, MD, Al-Dhekri, Hasan, MD, Arnaout, Rand, MD, Al-Muhsen, Saleh, MD, Ades, Nazema, BN, Elshorbagi, Sahar, MD, Al Gazlan, Sulaiman, MD, Sheikh, Farrukh, MD, Dasouki, Majed, MD, El-Baik, Lina, BSc, Elamin, Tanzeil, MS, Jaber, Amal, BSc, Kheir, Omnia, BPharm, El-Kalioby, Mohamed, MS, Subhani, Shazia, MS, Al Idrissi, Eman, MD, Al-Zahrani, Mofareh, MD, Alhelale, Maryam, MD, Alnader, Noukha, BSc, Al-Otaibi, Afaf, BSc, Kattan, Rana, BSc, Al Abdelrahman, Khalid, BSc, Al Breacan, Muna M., BSc, Bin Humaid, Faisal S., BSc, Wakil, Salma Majid, PhD, Alzayer, Fadi, BSc, Al-Dusery, Haya, BSc, Faquih, Tariq, MS, Al-Hissi, Safa, BSc, Meyer, Brian F., PhD, Hawwari, Abbas, PhD

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Stroke-like episodes, peri-episodic seizures, and MELAS mutations by Finsterer, Josef, Wakil, Salma Majid

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Telomerase reverse transcriptase promoter mutations in cancers derived from multiple organ sites among middle eastern population by Siraj, Abdul K., Bu, Rong, Iqbal, Kaleem, Parvathareddy, Sandeep Kumar, Siraj, Nabil, Siraj, Sarah, Diaz, Mark Ranier F., Rala, Dionne Rae, Benito, Allianah D., Sabido, Maria Angelita, Al-Rasheed, Maha, Al-Obaisi, Khadija A.S., Al-Haqawi, Wael, Victoria, Ingrid G., Al Balawy, Wafaa, Abedalthagafi, Malak, Wakil, Salma Majid, Ajarim, Dahish, Mohammed, Shamayel, Alhussain, Turki, Tulbah, Asma, Al-Badawi, Ismail A., Al-Dayel, Fouad, Al-Kuraya, Khawla S.

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Design of Arab Diabetes Gene-Centric Array (ADGCA) in population with an epidemic of Type 2 Diabetes: A population specific SNP evaluation by Al-Rubeaan, Khalid, Musambil, Mohthash, Wakil, Salma Majid, Al-Saud, Haya, Saeb, Amr T.M., Al-Qasim, Sara, Al-Naqeb, Dhekra

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Stroke-like episodes, periepisodic seizures, and MELAS mutations by Finsterer, Josef, Univ.Prof. DDr, Wakil, Salma Majid, PhD

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New Analytical Application of Antibody-Based Biosensor in Estimation of Thyroid-Stimulating Hormone in Serum by Wani, Tanveer A, Zargar, Seema, Wakil, Salma Majid, Darwish, Ibrahim A

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A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy by Al-Hassnan, Zuhair N, Shinwari, Zarghuna Ma, Wakil, Salma M, Tulbah, Sahar, Mohammed, Shamayel, Rahbeeni, Zuhair, Alghamdi, Mohammed, Rababh, Monther, Colak, Dilek, Kaya, Namik, Al-Fayyadh, Majid, Alburaiki, Jehad

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Identification of novel genomic imbalances in Saudi patients with congenital heart disease by Al-Hassnan, Zuhair N, Albawardi, Waad, Almutairi, Faten, AlMass, Rawan, AlBakheet, Albandary, Mustafa, Osama M, AlQuait, Laila, Shinwari, Zarghuna M A, Wakil, Salma, Salih, Mustafa A, Al-Fayyadh, Majid, Hassan, Saeed M, Aljoufan, Mansour, Al-Nakhli, Osima, Levy, Brynn, AlMaarik, Balsam, Al-Hakami, Hana A, Alsagob, Maysoon, Colak, Dilek, Kaya, Namik

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