Rhinolith Misdiagnosed as Fungal Mucin

por Alrayes, Nuha, Alhumaizi, Abdulrahman, Alomair, Alanoud, Simsim, Rehab
Publicado 2023

The value of repeating fine-needle aspiration for thyroid nodules

por Doubi, Aseel, Alrayes, Nuha S., Alqubaisi, Abdulaziz K., Al-Dhahri, Saleh F.
Publicado 2021

Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer

por Banaganapalli, Babajan, Mallah, Bayan, Alghamdi, Kawthar Saad, Albaqami, Walaa F., Alshaer, Dalal Sameer, Alrayes, Nuha, Elango, Ramu, Shaik, Noor A.
Publicado 2022

Truncating mutation in intracellular phospholipase A(1) gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)

por Alrayes, Nuha, Mohamoud, Hussein Sheikh Ali, Jelani, Musharraf, Ahmad, Saleem, Vadgama, Nirmal, Bakur, Khadijah, Simpson, Michael, Al-Aama, Jumana Yousuf, Nasir, Jamal
Publicado 2015

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

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

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

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

Identifying significant genes and functionally enriched pathways in familial hypercholesterolemia using integrated gene co-expression network analysis

por Awan, Zuhier, Alrayes, Nuha, Khan, Zeenath, Almansouri, Majid, Ibrahim Hussain Bima, Abdulhadi, Almukadi, Haifa, Ibrahim Kutbi, Hussam, Jayasheela Shetty, Preetha, Ahmad Shaik, Noor, Banaganapalli, Babajan
Publicado 2022

Association of a single nucleotide polymorphism in SOD2 with susceptibility for the development of diabetic nephropathy in patients with type 2 diabetes: A Saudi population study

por Sultan, Samar, Alharbi, Meshari, Alrayes, Nuha, Makki, Nehad, Faruqui, Hanan, Basuni, Lama, Alhozali, Amani, Abdulnoor, Reham, Borai, Anwar, Almalki, Abdullah, Alzahrani, Abdullah, Alamoudi, Reem, Almaghrabi, Mazin
Publicado 2023

The Association of Sociodemographic Factors, Postictal Symptoms, and Medical History With Seizure Type in Patients With Epilepsy: A Cross-Sectional Study

por Alyoubi, Reem, Kobeisy, Summayah A, Basheikh, Mazen, Al-Sharief, Rayan A, Al-Hayani, Majed M, Rayes, Yousof O, Alharthi, Atheer, Alyazidi, Anas S, Alrayes, Nuha, Tayeb, Haythum O
Publicado 2023

Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients

por Al-Numan, Huda Husain, Jan, Rana Mohammed, Al-Saud, Najla bint Saud, Rashidi, Omran M., Alrayes, Nuha Mohammad, Alsufyani, Hadeel A., Mujalli, Abdulrahman, Shaik, Noor Ahmad, Mosli, Mahmoud Hisham, Elango, Ramu, Saadah, Omar I., Banaganapalli, Babajan
Publicado 2022

Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis

por Jan, Rana Mohammed, Al-Numan, Huda Husain, Al-Twaty, Nada Hassan, Alrayes, Nuha, Alsufyani, Hadeel A., Alaifan, Meshari A., Alhussaini, Bakr H., Shaik, Noor Ahmad, Awan, Zuhier, Qari, Yousef, Saadah, Omar I., Banaganapalli, Babajan, Mosli, Mahmoud Hisham, Elango, Ramu
Publicado 2023

Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease

por Bokhari, Hifaa A., Shaik, Noor Ahmad, Banaganapalli, Babajan, Nasser, Khalidah Khalid, Ageel, Hossain Ibrahim, Al Shamrani, Ali Saad, Rashidi, Omran M., Al Ghubayshi, Omar Yaseen, Shaik, Jilani, Ahmad, Aftab, Alrayes, Nuha Mohammad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar Ibrahim
Publicado 2020