Pregnancy reduces severity and frequency of attacks in hyperkalemic periodic paralysis due to the mutation c.2111C>T in the SCN4A gene

Por Finsterer, Josef, Wakil, Salma Majid, Laccone, Franco
Publicado no Ann Indian Acad Neurol (2017)

Involvement of ATP-binding cassette, subfamily A polymorphism with susceptibility to coronary artery disease

Por ZARGAR, SEEMA, WAKIL, SALMA, MOBEIREK, ABDUELAH F., AL-JAFARI, ABDULAZIZ A.
Publicado em 2013

Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib

Por Alkhezayem, Sara, Wani, Tanveer A., Wakil, Salma, Aljuraysi, Ashwaq, Zargar, Seema
Publicado no Saudi Pharm J (2020)

Interleukin-8 Dedifferentiates Primary Human Luminal Cells to Multipotent Stem Cells

Por Al-Khalaf, Huda H., Ghebeh, Hazem, Wakil, Salma M., Al-Mohanna, Falah, Aboussekhra, Abdelilah
Publicado no Mol Cell Biol (2020)

Replication of Type 2 diabetes-associated variants in a Saudi Arabian population

Por Li-Gao, Ruifang, Wakil, Salma M., Meyer, Brian F., Dzimiri, Nduna, Mook-Kanamori, Dennis O.
Publicado no Physiol Genomics (2018)

A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients

Por Afzal, Sibtain, Ramzan, Khushnooda, Ullah, Sajjad, Wakil, Salma M., Jamal, Arshad, Basit, Sulman, Waqar, Ahmed Bilal
Publicado no BMC Med Genet (2020)

A novel KIT mutation in a family with expanded syndrome of piebaldism

Por Hamadah, Issam, Chisti, Muzamil, Haider, Mansoor, Al Dosssari, Haya, Alhumaidan, Rawan, Meyer, Brian F., Wakil, Salma M.
Publicado no JAAD Case Rep (2019)

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

Por Alsmadi, Osama, Meyer, Brian F, Alkuraya, Fowzan, Wakil, Salma, Alkayal, Fadi, Al-Saud, Haya, Ramzan, Khushnooda, Al-Sayed, MoeenAldeen
Publicado em 2009

Combining CDKN1A gene expression and genome-wide SNPs in a twin cohort to gain insight into the heritability of individual radiosensitivity

Por Zyla, Joanna, Kabacik, Sylwia, O’Brien, Grainne, Wakil, Salma, Al-Harbi, Najla, Kaprio, Jaakko, Badie, Christophe, Polanska, Joanna, Alsbeih, Ghazi
Publicado no Funct Integr Genomics (2019)

Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

Por Wakil, Salma M., Alhissi, Safa, Al Dossari, Haya, Alqahtani, Ayesha, Shibin, Sherin, Melaiki, Brahim T., Finsterer, Josef, Al-Hashem, Amal, Bohlega, Saeed, Alazami, Anas M.
Publicado no BMC Med Genet (2019)

The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs

Por Wakil, Salma M., Nguyen, Cao, Muiya, Nzioka P., Andres, Editha, Lykowska-Tarnowska, Agnieszka, Baz, Batoul, Tahir, Asma I., Meyer, Brian F., Morahan, Grant, Dzimiri, Nduna
Publicado no Dis Markers (2015)

New or vanishing frontiers: LACC1-associated juvenile arthritis

Por Al-Mayouf, Sulaiman M., Yateem, Mada, Al-Dusery, Haya, Monies, Dorota, Wakil, Salma, AlShiakh, Manal, AlEnazi, Abdullatif, Aladaileh, Boshra, Alzyoud, Raed, Meyer, Brian
Publicado no Int J Pediatr Adolesc Med (2021)

New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3

Por Alshahid, Maie, Wakil, Salma M, Al-Najai, Mohammed, Muiya, Nzioka P, Elhawari, Samar, Gueco, Daisy, Andres, Editha, Hagos, Samia, Mazhar, Nejat, Meyer, Brian F, Dzimiri, Nduna
Publicado em 2013

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

Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs

Por Wakil, Salma M., Ram, Ramesh, Muiya, Nzioka P., Mehta, Munish, Andres, Editha, Mazhar, Nejat, Baz, Batoul, Hagos, Samya, Alshahid, Maie, Meyer, Brian F., Morahan, Grant, Dzimiri, Nduna
Publicado no Data Brief (2016)

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

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

Por 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
Publicado no BMC Med Genet (2016)

Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene

Por Wakil, Salma M., Monies, Dorota, Hagos, Samya, Al-Ajlan, Fahad, Finsterer, Josef, Al Qahtani, Aisha, Ramzan, Khushnooda, Al Humaidy, Rawan, Al-Muhaizea, Mohamed A., Meyer, Brian, Bohlega, Saeed A.
Publicado no Case Rep Genet (2018)

Identification of a novel genetic locus underlying tremor and dystonia

Por Monies, Dorota, Al-Shaar, Hussam Abou, Goljan, Ewa A., Al-Younes, Banan, Al-Breacan, Muna Monther Abdullah, Al-Saif, Maher Mohammed, Wakil, Salma M., Meyer, Brian F., Khabar, Khalid S. A., Bohlega, Saeed
Publicado no Hum Genomics (2017)

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

Por Alsagob, Maysoon, Salih, Mustafa A., Hamad, Muddathir H. A., Al-Yafee, Yusra, Al-Zahrani, Jawaher, Al-Bakheet, Albandary, Nester, Michael, Sakati, Nadia, Wakil, Salma M., AlOdaib, Ali, Colak, Dilek, Kaya, Namik
Publicado no Mol Cytogenet (2019)