Fahad A Bashiri - College of Medicine, King Saud University - Associate Professor

Fahad A Bashiri

College of Medicine, King Saud University

Associate Professor

Riyadh | Saudi Arabia

Main Specialties: Child Neurology, Neurology, Pediatrics

ORCID logohttps://orcid.org/0000-0003-1436-6727

Fahad A Bashiri - College of Medicine, King Saud University - Associate Professor

Fahad A Bashiri

Introduction

Primary Affiliation: College of Medicine, King Saud University - Riyadh , Saudi Arabia

Specialties:

Publications

27Publications

1011Reads

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Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature review.

Eur J Med Genet 2020 May 14;63(5):103844. Epub 2020 Jan 14.

King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.ejmg.2020.103844DOI Listing
May 2020
1.486 Impact Factor

JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.

N Engl J Med 2020 01;382(3):256-265

From the Department of Pediatrics (F.A., M.-H.T., M. Alabdulhafid, M. Alghamdi, N. Alotaibi, A.A., A.A.-E., G.M.H., F.A.B., S.A.-M., N. Alkhamis, Z.A., A.A.A.) and the Immunology Research Laboratory, Department of Pediatrics (R.H., S.A.-M.), College of Medicine, King Saud University, the Department of Pediatrics, College of Medicine, Imam Mohammed bin Saud University (A.A.), and the Department of Radiology and Medical Imaging, King Saud University Medical City (H.H.H.) - all in Riyadh, Saudi Arabia; the Departments of Microbiology and Pediatrics and the Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai (M.M.-F., X.Q., S.B., C.G., D.B.), St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, the Rockefeller University (E.J., J.-L.C., J.B.), and Howard Hughes Medical Institute (J.-L.C.) - all in New York; Paris Descartes University, Imagine Institute, and the Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM Unité 1163 (T.L.V., E.J., J.-L.C., J.B.), and the Pediatric Hematology and Immunology Unit (J.-L.C.) and the Center for the Study of Primary Immunodeficiencies (J.B.), Assistance Publique-Hôpitaux de Paris, Necker Hospital for Sick Children - all in Paris; the Department of Pediatrics, Assiut Faculty of Medicine, Assiut University, Assiut, Egypt (G.M.H.); and Sharjah Institute for Medical Research, Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates (R.H.).

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http://dx.doi.org/10.1056/NEJMoa1905633DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155173PMC
January 2020
55.873 Impact Factor

Pediatric intracranial hypertension. Experience from 2 Tertiary Centers.

Neurosciences (Riyadh) 2019 Oct;24(4):257-263

Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2019.4.20190052DOI Listing
October 2019
0.391 Impact Factor

Hypokalemic periodic paralysis due to CACNA1S gene mutation.

Neurosciences (Riyadh) 2019 Jul;24(3):225-230

Division of Pediatric Nephrology, Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2018.3.20180005DOI Listing
July 2019
3 Reads
0.391 Impact Factor

Satisfaction and perceived usefulness with newly-implemented Electronic Health Records System among pediatricians at a university hospital.

Comput Methods Programs Biomed 2019 Feb 26;169:51-57. Epub 2018 Dec 26.

Pediatrics Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia; Clinical Practice Guidelines Unit, Quality Management Department, King Saud University Medical City, Riyadh, Saudi Arabia; Research Chair for Evidence-Based Health Care and Knowledge Translation, King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.cmpb.2018.12.026DOI Listing
February 2019
7 Reads
1.897 Impact Factor

Effect of new modalities of treatment on physicians management plan for patients with spinal muscular atrophy.

Neurosciences (Riyadh) 2019 01;24(1):16-21

Division of Neurology, Department of Pediatrics, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2019.1.20180321DOI Listing
January 2019
16 Reads
0.391 Impact Factor

Assessment of physicians knowledge and attitudes in the management of febrile seizures.

Neurosciences (Riyadh) 2018 Oct;23(4):314-319

Division of Neurology, Department of Pediatrics, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2018.4.20180097DOI Listing
October 2018
40 Reads
0.391 Impact Factor

GWAS signals revisited using human knockouts.

Genet Med 2018 01 22;20(1):64-68. Epub 2017 Jun 22.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1038/gim.2017.78DOI Listing
January 2018
62 Reads
7.329 Impact Factor

Respiratory support attitudes among pediatric intensive care staff for spinal muscular atrophy patients in Saudi Arabia.

Neurosciences (Riyadh) 2018 Jan;23(1):62-65

Pediatric Intensive Care Unit, Pediatric Department, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia.

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http://www.neurosciencesjournal.org/PDFFiles/Jan18/11Respira
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http://dx.doi.org/10.17712/nsj.2018.1.20170103DOI Listing
January 2018
24 Reads
0.391 Impact Factor

Auto-immune anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis: three case reports.

Paediatr Int Child Health 2017 Aug 22;37(3):222-226. Epub 2016 Jun 22.

a Division of Pediatric Neurology.

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http://dx.doi.org/10.1080/20469047.2016.1191852DOI Listing
August 2017
63 Reads
0.871 Impact Factor

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.

Authors:
Dorota Monies Mohamed Abouelhoda Moeenaldeen AlSayed Zuhair Alhassnan Maha Alotaibi Husam Kayyali Mohammed Al-Owain Ayaz Shah Zuhair Rahbeeni Mohammad A Al-Muhaizea Hamad I Alzaidan Edward Cupler Saeed Bohlega Eissa Faqeih Maha Faden Banan Alyounes Dyala Jaroudi Ewa Goljan Hadeel Elbardisy Asma Akilan Renad Albar Hesham Aldhalaan Shamshad Gulab Aziza Chedrawi Bandar K Al Saud Wesam Kurdi Nawal Makhseed Tahani Alqasim Heba Y El Khashab Hamoud Al-Mousa Amal Alhashem Imaduddin Kanaan Talal Algoufi Khalid Alsaleem Talal A Basha Fathiya Al-Murshedi Sameena Khan Adila Al-Kindy Maha Alnemer Sami Al-Hajjar Suad Alyamani Hasan Aldhekri Ali Al-Mehaidib Rand Arnaout Omar Dabbagh Mohammad Shagrani Dieter Broering Maha Tulbah Amal Alqassmi Maisoon Almugbel Mohammed AlQuaiz Abdulaziz Alsaman Khalid Al-Thihli Raashda A Sulaiman Wajeeh Al-Dekhail Abeer Alsaegh Fahad A Bashiri Alya Qari Suzan Alhomadi Hisham Alkuraya Mohammed Alsebayel Muddathir H Hamad Laszlo Szonyi Faisal Abaalkhail Sulaiman M Al-Mayouf Hamad Almojalli Khalid S Alqadi Hussien Elsiesy Taghreed M Shuaib Mohammed Zain Seidahmed Ibraheem Abosoudah Hana Akleh Abdulaziz AlGhonaium Turki M Alkharfy Fuad Al Mutairi Wafa Eyaid Abdullah Alshanbary Farrukh R Sheikh Fahad I Alsohaibani Abdullah Alsonbul Saeed Al Tala Soher Balkhy Randa Bassiouni Ahmed S Alenizi Maged H Hussein Saeed Hassan Mohamed Khalil Brahim Tabarki Saad Alshahwan Amira Oshi Yasser Sabr Saad Alsaadoun Mustafa A Salih Sarar Mohamed Habiba Sultana Abdullah Tamim Moayad El-Haj Saif Alshahrani Dalal K Bubshait Majid Alfadhel Tariq Faquih Mohamed El-Kalioby Shazia Subhani Zeeshan Shah Nabil Moghrabi Brian F Meyer Fowzan S Alkuraya

Hum Genet 2017 08 9;136(8):921-939. Epub 2017 Jun 9.

Deparment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1007/s00439-017-1821-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502059PMC
August 2017
158 Reads
4.824 Impact Factor

Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination.

Am J Hum Genet 2017 Jun;100(6):969-977

Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.

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http://dx.doi.org/10.1016/j.ajhg.2017.05.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473715PMC
June 2017
64 Reads
10.931 Impact Factor

Childhood epilepsies: What should a pediatrician know?

Authors:
Fahad A Bashiri

Neurosciences (Riyadh) 2017 01;22(1):14-19

Department of Pediatrics, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726831PMC
http://dx.doi.org/10.17712/nsj.2017.1.20160244DOI Listing
January 2017
10 Reads
0.391 Impact Factor

Sturge-Weber syndrome: Continued vigilance is needed.

Sudan J Paediatr 2015 ;15(2):63-70

(1) Division of Pediatric Neurology, College of Medicine and King Saud University Medical City, King Saud University , Riyadh , Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958665PMC
August 2016
25 Reads

Mycoplasma pneumoniae Infection: Risk Factor for Childhood Stroke.

Authors:
Fahad A Bashiri

Glob Pediatr Health 2015 23;2:2333794X15592764. Epub 2015 Jun 23.

Division of Neurology,Department of Pediatrics,College of Medicine & King Khalid University Hospital,King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1177/2333794X15592764DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784591PMC
June 2016

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Sudan J Paediatr 2016 ;16(2):67-76

Division of Neurology, Departments of Pediatrics, King Khalid University Hospital, College of Medicine, King Saud University , Riyadh , Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237838PMC
January 2016
35 Reads

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.

Genet Med 2015 Sep 11;17(9):719-25. Epub 2014 Dec 11.

Department of Genetics, Research Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1038/gim.2014.184DOI Listing
September 2015
65 Reads
7.329 Impact Factor

ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.

Hum Genet 2015 Aug 10;134(8):815-22. Epub 2015 May 10.

Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh, 11211, Saudi Arabia.

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http://link.springer.com/content/pdf/10.1007/s00439-015-1561
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http://link.springer.com/10.1007/s00439-015-1561-6
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http://dx.doi.org/10.1007/s00439-015-1561-6DOI Listing
August 2015
29 Reads
4.824 Impact Factor

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Cell Rep 2015 Jan 31;10(2):148-61. Epub 2014 Dec 31.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2014.12.015DOI Listing
January 2015
123 Reads
7.207 Impact Factor

Top co-authors

Mustafa A Salih
Mustafa A Salih

King Saud University

10
Fowzan S Alkuraya
Fowzan S Alkuraya

King Faisal Specialist Hospital and Research Center

7
Muddathir H Hamad
Muddathir H Hamad

College of Medicine

6
Amal Y Kentab
Amal Y Kentab

King Khalid University Hospital and College of Medicine

5
Ranad Shaheen
Ranad Shaheen

King Faisal Specialist Hospital and Research Center

4
Nisha Patel
Nisha Patel

King Faisal Specialist Hospital and Research Center

4
Ali H Alwadei
Ali H Alwadei

National Neuroscience Institute

4