Impact of SLCO1B1*5 on Flucloxacillin and Co-Amoxiclav–Related Liver Injury

por Alshabeeb, Mohammad, Alomar, Fadhel A., Khan, Amjad
Publicado 2022

Prevalence of exposure to pharmacogenetic drugs by the Saudis treated at the health care centers of the Ministry of National Guard

por Alshabeeb, Mohammad A., Alyabsi, Mesnad, Paras, Bien
Publicado 2022

Pharmacogenes that demonstrate high association evidence according to CPIC, DPWG, and PharmGKB

por Alshabeeb, Mohammad A., Alyabsi, Mesnad, Aziz, Mohammad A., Abohelaika, Salah
Publicado 2022

Use of Pharmacogenetic Drugs by the Dutch Population

por Alshabeeb, Mohammad A., Deneer, Vera H. M., Khan, Amjad, Asselbergs, Folkert W.
Publicado 2019

Impact of telemedicine on glycemic control in type 2 diabetes mellitus during the COVID-19 lockdown period

por Al-Mutairi, Abrar M., Alshabeeb, Mohammad A., Abohelaika, Salah, Alomar, Fadhel A., Bidasee, Keshore R.
Publicado 2023

A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family

por Khan, Amjad, Wang, Rongrong, Han, Shirui, Umair, Muhammad, Alshabeeb, Mohammad A., Ansar, Muhammad, Ahmad, Wasim, Alaamery, Manal, Zhang, Xue
Publicado 2020

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

por Khan, Amjad, Wang, Rongrong, Han, Shirui, Umair, Muhammad, Abbas, Safdar, Khan, Muhammad Ismail, Alshabeeb, Mohammad A., Alfadhel, Majid, Zhang, Xue
Publicado 2019

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

por Khan, Amjad, Wang, Rongrong, Han, Shirui, Umair, Muhammad, Abbas, Safdar, Khan, Muhammad Ismail, Alshabeeb, Mohammad A., Alfadheland, Majid, Zhang, Xue
Publicado 2019

Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants

por Khan, Amjad, Miao, Zhichao, Umair, Muhammad, Ullah, Amir, Alshabeeb, Mohammad A., Bilal, Muhammad, Ahmad, Farooq, Rappold, Gudrun A., Ansar, Muhammad, Carapito, Raphael
Publicado 2020

Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease

por Alshabeeb, Mohammad A., Alwadaani, Deemah, Al Qahtani, Farjah H., Abohelaika, Salah, Alzahrani, Mohsen, Al Zayed, Abdullah, Al Saeed, Hussain H., Al Ajmi, Hala, Alsomaie, Barrak, Rashid, Mamoon, Daly, Ann K.
Publicado 2023