Specialty Grand Challenge - Genetic Disorders

by Jumana Y Al-Aama
Published 2013-11-01

Training Autoencoder using Three Different Reversed Color Models for Anomaly Detection

by Obada Al aama, Hakaru Tamukoh
Published 2020-05-01

Employing Behavioral Analysis to Predict User Attitude towards Unwanted Content in Online Social Network Services: The Case of Makkah Region in Saudi Arabia

by Mashael M. Alsulami, Arwa Yousef Al-Aama
Published 2020-04-01

A Bio Polymeric Adhesive Produced by Photo Cross-Linkable Technique

by Soliman Abdalla, Nabil Al-Aama, Maryam A. Al-Ghamdi
Published 2016-08-01

Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia

by M. Z. A. eBhuiyan, Safar eAl-Shahrani, Jumana eAl-Aama, Jumana eAl-Aama, Arthur eWilde, Tarek S Momenah
Published 2013-11-01

A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family

by Nagwa E. A. Gaboon, Asia Parveen, Asia Parveen, Ahmed El Beheiry, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Mosab S. Alsaedi, Naveed Wasif, Naveed Wasif, Naveed Wasif
Published 2019-06-01

A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients

by Nagwa E. A. Gaboon, Asia Parveen, Asia Parveen, Khaled A. Ahmad, Taghreed Shuaib, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Lereen Abdelwehab, Amina Arif, Naveed Wasif, Naveed Wasif, Naveed Wasif
Published 2020-07-01

Effect of Ramadan fasting in Saudi Arabia on serum bone profile and immunoglobulins

by Suhard M. Bahijri, Ghada M. Ajabnoor, Anwar Borai, Jumana Y. Al-Aama, George P. Chrousos
Published 2015-10-01

Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation

by Sami Raja Alallasi, Amal A. Kokandi, Babajan Banagnapali, Babajan Banagnapali, Noor Ahmad Shaik, Noor Ahmad Shaik, Bandar Ali Al-Shehri, Nuha Mohammad Alrayes, Jumana Yousuf Al-Aama, Jumana Yousuf Al-Aama, Musharraf Jelani, Musharraf Jelani
Published 2019-02-01

Health impact of fasting in Saudi Arabia during Ramadan: association with disturbed circadian rhythm and metabolic and sleeping patterns.

by Ghada M Ajabnoor, Suhad Bahijri, Anwar Borai, Altaf A Abdulkhaliq, Jumana Y Al-Aama, George P Chrousos
Published 2014-01-01

Ramadan fasting in Saudi Arabia is associated with altered expression of CLOCK, DUSP and IL-1alpha genes, as well as changes in cardiometabolic risk factors.

by Ghada M A Ajabnoor, Suhad Bahijri, Noor Ahmad Shaik, Anwar Borai, Aliaa A Alamoudi, Jumana Y Al-Aama, George P Chrousos
Published 2017-01-01

Detection of Secondary Metabolites as Biomarkers for the Early Diagnosis and Prevention of Type 2 Diabetes

by Al-Aama JY, Al Mahdi HB, Salama MA, Bakur KH, Alhozali A, Mosli HH, Bahijri SM, Bahieldin A, Willmitzer L, Edris S
Published 2019-12-01

Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen

by Zuhier Ahmed Awan, Zuhier Ahmed Awan, Omran M. Rashidi, Omran M. Rashidi, Omran M. Rashidi, Bandar Ali Al-Shehri, Bandar Ali Al-Shehri, Kaiser Jamil, Ramu Elango, Ramu Elango, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Robert A. Hegele, Babajan Banaganapalli, Babajan Banaganapalli, Noor A. Shaik, Noor A. Shaik
Published 2021-06-01

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features

by Hussein Sheikh Mohamoud, Saleem Ahmed, Musharraf Jelani, Nuha Alrayes, Kay Childs, Nirmal Vadgama, Mona Mohammad Almramhi, Jumana Yousuf Al-Aama, Steve Goodbourn, Jamal Nasir
Published 2018-02-01

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

by Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli, Naglaa M. Kamal, Naglaa M. Kamal, Ahmed N. Sahly, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Ramu Elango, Ramu Elango
Published 2021-04-01

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients

by Naglaa M. Kamal, Ahmed N. Sahly, Babajan Banaganapalli, Omran M. Rashidi, Preetha J. Shetty, Jumana Y. Al-Aama, Noor A. Shaik, Ramu Elango, Omar I. Saadah
Published 2020-01-01

Modulation of doxorubicin-induced expression of the multidrug resistance gene in breast cancer cells by diltiazem and protection against cardiotoxicity in experimental animals

by Hamdan S. Al-malky, Abdel-Moneim M. Osman, Zoheir A. Damanhouri, Huda M. Alkreathy, Jumana Y. Al Aama, Wafaa S. Ramadan, Ali A. Al Qahtani, Hadiah B. Al Mahdi
Published 2019-07-01

Rapid detection of type II diabetes mellitus in Saudi patients via simultaneous screening of multiple SNPs

by Jumana Al-Aama, Hadiah B. Al Mahdi, Mohammed A. Salama, Khadija Bakur, Amani Alhozali, Hala Mosli, Suhad M. Bahijri, Ahmed Bahieldin, Ramu Elango, Lothar Willmitzer, Sherif Edris
Published 2019-01-01

Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family

by Yaser Mohammad Alkhiary, Musharraf Jelani, Mona Mohammad Almramhi, Hussein Sheikh Ali Mohamoud, Rayan Al-Rehaili, Hams Saeed Al-Zahrani, Rehab Serafi, Huanming Yang, Jumana Yousuf Al-Aama
Published 2016-09-01