Publications by authors named "Hesham Aldhalaan"

24Publications

Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.

Authors:
Sateesh Maddirevula Hanan E Shamseldin Amy Sirr Lama AlAbdi Russell S Lo Nour Ewida Mashael Al-Qahtani Mais Hashem Firdous Abdulwahab Omar Aboyousef Namik Kaya Dorota Monies May H Salem Naffaa Al Harbi Hesham M Aldhalaan Hamad Alzaidan Hadeel M Almanea Abrar K Alsalamah Fuad Al Mutairi Samira Ismail Ghada M H Abdel-Salam Amal Alhashem Ali Asery Eissa Faqeih Amal AlQassmi Waleed Al-Hamoudi Talal Algoufi Mohammad Shagrani Aimée M Dudley Fowzan S Alkuraya

Front Genet 2020 31;11:580484. Epub 2020 Dec 31.

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

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December 2020

Stigmatization among parents of autism spectrum disorder children in Riyadh, Saudi Arabia.

Authors:
Kahlid Alshaigi Reema Albraheem Khalid Alsaleem Moneer Zakaria Aman Jobeir Hesham Aldhalaan

Int J Pediatr Adolesc Med 2020 Sep 17;7(3):140-146. Epub 2019 Jun 17.

King Faisal Specialist Hospital & Research Centre (KFSH & RC), Saudi Arabia.

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September 2020

Effects of early and recent mercury and lead exposure on the neurodevelopment of children with elevated mercury and/or developmental delays during lactation: A follow-up study.

Authors:
Iman Al-Saleh Lina Moncari Ahmed Jomaa Rola Elkhatib Reem Al-Rouqi Chafica Eltabache Tahreer Al-Rajudi Hissah Alnuwaysir Michael Nester Hesham Aldhalaan

Int J Hyg Environ Health 2020 Sep 18;230:113629. Epub 2020 Sep 18.

Center for Autism Research, King Faisal Specialist Hospital and Research Centre, P.O. Box: 3354, Riyadh, 11211, Saudi Arabia.

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September 2020

The Role of Nicotinic Receptors in the Attenuation of Autism-Related Behaviors in a Murine BTBR T + tf/J Autistic Model.

Authors:
Hafiz M Mahmood Hesham M Aldhalaan Tahani K Alshammari Mashael A Alqasem Musaad A Alshammari Norah A Albekairi Shakir D AlSharari

Autism Res 2020 08 21;13(8):1311-1334. Epub 2020 Jul 21.

Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

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August 2020

KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases.

Authors:
Felippe Borlot Ahmed Abushama Nadine Morrison-Levy Puneet Jain Kollencheri Puthenveettil Vinayan Musaad Abukhalid Hesham M Aldhalaan Hanin S Almuzaini Sheffali Gulati Tova Hershkovitz Ramesh Konanki Lokesh Lingappa Aimee F Luat Shatha Shafi Brahim Tabarki Maya Thomas Sangeetha Yoganathan Majid Alfadhel Ravindra Arya Elizabeth J Donner Salleh N Ehaideb Vykuntaraju K Gowda Vivek Jain Priyanka Madaan Kenneth A Myers Hiroshi Otsubo Prateek Panda Jitendra K Sahu Letícia P B Sampaio Suvasini Sharma Elisabeth Simard-Tremblay Maria Zak Robyn Whitney

Epilepsia 2020 04 13;61(4):679-692. Epub 2020 Mar 13.

Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.

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April 2020

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.

Authors:
Holger Hengel Célia Bosso-Lefèvre George Grady Emmanuelle Szenker-Ravi Hankun Li Sarah Pierce Élise Lebigot Thong-Teck Tan Michelle Y Eio Gunaseelan Narayanan Kagistia Hana Utami Monica Yau Nader Handal Werner Deigendesch Reinhard Keimer Hiyam M Marzouqa Meral Gunay-Aygun Michael J Muriello Helene Verhelst Sarah Weckhuysen Sonal Mahida Sakkubai Naidu Terrence G Thomas Jiin Ying Lim Ee Shien Tan Damien Haye Michèl A A P Willemsen Renske Oegema Wendy G Mitchell Tyler Mark Pierson Marisa V Andrews Marcia C Willing Lance H Rodan Tahsin Stefan Barakat Marjon van Slegtenhorst Ralitza H Gavrilova Diego Martinelli Tal Gilboa Abdullah M Tamim Mais O Hashem Moeenaldeen D AlSayed Maha M Abdulrahim Mohammed Al-Owain Ali Awaji Adel A H Mahmoud Eissa A Faqeih Ali Al Asmari Sulwan M Algain Lamyaa A Jad Hesham M Aldhalaan Ingo Helbig David A Koolen Angelika Riess Ingeborg Kraegeloh-Mann Peter Bauer Suleyman Gulsuner Hannah Stamberger Alvin Yu Jin Ng Sha Tang Sumanty Tohari Boris Keren Laura E Schultz-Rogers Eric W Klee Sabina Barresi Marco Tartaglia Hagar Mor-Shaked Sateesh Maddirevula Amber Begtrup Aida Telegrafi Rolph Pfundt Rebecca Schüle Brian Ciruna Carine Bonnard Mahmoud A Pouladi James C Stewart Adam Claridge-Chang Dirk J Lefeber Fowzan S Alkuraya Ajay S Mathuru Byrappa Venkatesh Joseph J Barycki Melanie A Simpson Saumya S Jamuar Ludger Schöls Bruno Reversade

Nat Commun 2020 01 30;11(1):595. Epub 2020 Jan 30.

Institute of Medical Biology, A*STAR, Biopolis, Singapore, 138648, Singapore.

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January 2020

Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.

Authors:
Muhammad Ansar Hyung-Lok Chung Ali Al-Otaibi Mohammad Nael Elagabani Thomas A Ravenscroft Sohail A Paracha Ralf Scholz Tayseer Abdel Magid Muhammad T Sarwar Sayyed Fahim Shah Azhar Ali Qaisar Periklis Makrythanasis Paul C Marcogliese Erik-Jan Kamsteeg Emilie Falconnet Emmanuelle Ranza Federico A Santoni Hesham Aldhalaan Ali Al-Asmari Eissa Ali Faqeih Jawad Ahmed Hans-Christian Kornau Hugo J Bellen Stylianos E Antonarakis

Am J Hum Genet 2019 11 10;105(5):907-920. Epub 2019 Oct 10.

Department of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland; Service of Genetic Medicine, University Hospitals of Geneva, 1205 Geneva, Switzerland; iGE3 Institute of Genetics and Genomics of Geneva, 1211 Geneva, Switzerland. Electronic address:

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November 2019

Telehealth Services for Children With Autism Spectrum Disorders in Rural Areas of the Kingdom of Saudi Arabia: Overview and Recommendations.

Authors:
Shahad Alkhalifah Hesham Aldhalaan

JMIR Pediatr Parent 2018 Nov 15;1(2):e11402. Epub 2018 Nov 15.

Centre for Autism Research, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

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November 2018

Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases.

Authors:
Yoshiko Murakami Thi Tuyet Mai Nguyen Nissan Baratang Praveen K Raju Alexej Knaus Sian Ellard Gabriela Jones Baiba Lace Justine Rousseau Norbert Fonya Ajeawung Atsushi Kamei Gaku Minase Manami Akasaka Nami Araya Eriko Koshimizu Jenneke van den Ende Florian Erger Janine Altmüller Zita Krumina Jurgis Strautmanis Inna Inashkina Janis Stavusis Areeg El-Gharbawy Jessica Sebastian Ratna Dua Puri Samarth Kulshrestha Ishwar C Verma Esther M Maier Tobias B Haack Anil Israni Julia Baptista Adam Gunning Jill A Rosenfeld Pengfei Liu Marieke Joosten María Eugenia Rocha Mais O Hashem Hesham M Aldhalaan Fowzan S Alkuraya Satoko Miyatake Naomichi Matsumoto Peter M Krawitz Elsa Rossignol Taroh Kinoshita Philippe M Campeau

Am J Hum Genet 2019 08 27;105(2):384-394. Epub 2019 Jun 27.

Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada; Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine and University of Montreal, Montreal, QC H3T 1C5, Canada. Electronic address:

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August 2019

Validation of the Arabic version of the Social Communication Questionnaire.

Authors:
Mohammed Aldosari Eric Fombonne Hesham Aldhalaan Mohammed Ouda Saba Elhag Hawraa Alshammari Iman Ghazal Asma Alsaleh Tala Alqadoumi Richard Thomson Mohanad Al Khasawneh Mohamed Tolefat Fouad Alshaban

Autism 2019 10 3;23(7):1655-1662. Epub 2019 Jan 3.

5 Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar.

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October 2019

Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study.

Authors:
Sulaiman Almobarak Mohammad Almuhaizea Musaad Abukhaled Suad Alyamani Omar Dabbagh Aziza Chedrawi Sameena Khan Hesham Aldhalaan

Transl Neurosci 2018 12;9:154-160. Epub 2018 Nov 12.

Department of Neuroscience, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.

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November 2018

Further delineation of Temtamy syndrome of corpus callosum and ocular abnormalities.

Authors:
Laila Alrakaf Mohammed A Al-Owain Maryam Busehail Maha A Alotaibi Dorota Monies Hesham M Aldhalaan Amal Alhashem Zuhair N Al-Hassnan Zuhair A Rahbeeni Fathiya Al Murshedi Nadia Al Ani Almundher Al-Maawali Niema A Ibrahim Firdous M Abdulwahab Maysoon Alsagob Mais O Hashem Wafaa Ramadan Mohamed Abouelhoda Brian F Meyer Namik Kaya Sateesh Maddirevula Fowzan S Alkuraya

Am J Med Genet A 2018 03 31;176(3):715-721. Epub 2018 Jan 31.

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

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March 2018

Correction to: Expanding the genetic heterogeneity of intellectual disability.

Authors:
Shams Anazi Sateesh Maddirevula Vincenzo Salpietro Yasmine T Asi Saud Alsahli Amal Alhashem Hanan E Shamseldin Fatema AlZahrani Nisha Patel Niema Ibrahim Firdous M Abdulwahab Mais Hashem Nadia Alhashmi Fathiya Al Murshedi Adila Al Kindy Ahmad Alshaer Ahmed Rumayyan Saeed Al Tala Wesam Kurdi Abdulaziz Alsaman Ali Alasmari Selina Banu Tipu Sultan Mohammed M Saleh Hisham Alkuraya Mustafa A Salih Hesham Aldhalaan Tawfeg Ben-Omran Fatima Al Musafri Rehab Ali Jehan Suleiman Brahim Tabarki Ayman W El-Hattab Caleb Bupp Majid Alfadhel Nada Al Tassan Dorota Monies Stefan T Arold Mohamed Abouelhoda Tammaryn Lashley Henry Houlden Eissa Faqeih Fowzan S Alkuraya

Hum Genet 2018 01;137(1):105-109

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

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January 2018

Training Parents in Saudi Arabia to Implement Discrete Trial Teaching with their Children with Autism Spectrum Disorder.

Authors:
Ahmad M Eid Sarah M Aljaser Anoud N AlSaud Sultana M Asfahani Ohoud A Alhaqbani Rafat S Mohtasib Hesham M Aldhalaan Mitch Fryling

Behav Anal Pract 2017 Dec 10;10(4):402-406. Epub 2017 Jan 10.

California State University, Los Angeles, USA.

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December 2017

Intraoperative direct cortical stimulation motor evoked potentials: Stimulus parameter recommendations based on rheobase and chronaxie.

Authors:
Tariq M Abalkhail David B MacDonald Ibrahim AlThubaiti Faisal A AlOtaibi Bent Stigsby Amal A Mokeem Iftetah A AlHamoud Maher I Hassounah Salah M Baz Abdulaziz AlSemari Hesham M AlDhalaan Sameena Khan

Clin Neurophysiol 2017 11 28;128(11):2300-2308. Epub 2017 Sep 28.

Section of Pediatric Neurology, Department of Neurosciences, KFSH, Saudi Arabia.

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November 2017

Expanding the genetic heterogeneity of intellectual disability.

Authors:
Shams Anazi Sateesh Maddirevula Vincenzo Salpietro Yasmine T Asi Saud Alsahli Amal Alhashem Hanan E Shamseldin Fatema AlZahrani Nisha Patel Niema Ibrahim Firdous M Abdulwahab Mais Hashem Nadia Alhashmi Fathiya Al Murshedi Adila Al Kindy Ahmad Alshaer Ahmed Rumayyan Saeed Al Tala Wesam Kurdi Abdulaziz Alsaman Ali Alasmari Selina Banu Tipu Sultan Mohammed M Saleh Hisham Alkuraya Mustafa A Salih Hesham Aldhalaan Tawfeg Ben-Omran Fatima Al Musafri Rehab Ali Jehan Suleiman Brahim Tabarki Ayman W El-Hattab Caleb Bupp Majid Alfadhel Nada Al Tassan Dorota Monies Stefan T Arold Mohamed Abouelhoda Tammaryn Lashley Henry Houlden Eissa Faqeih Fowzan S Alkuraya

Hum Genet 2017 11 22;136(11-12):1419-1429. Epub 2017 Sep 22.

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

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November 2017

Congenital disorders of glycosylation: The Saudi experience.

Authors:
Sarah Alsubhi Amal Alhashem Eissa Faqeih Majid Alfadhel Abdullah Alfaifi Waleed Altuwaijri Saud Alsahli Hesham Aldhalaan Fowzan S Alkuraya Khalid Hundallah Adel Mahmoud Ali Alasmari Fuad Al Mutairi Hanem Abduraouf Layan AlRasheed Saad Alshahwan Brahim Tabarki

Am J Med Genet A 2017 Oct 25;173(10):2614-2621. Epub 2017 Jul 25.

Division of Pediatric Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

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October 2017

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.

Authors:
Bashayer Al-Mubarak Mohamed Abouelhoda Aisha Omar Hesham AlDhalaan Mohammed Aldosari Michael Nester Hussain A Alshamrani Mohamed El-Kalioby Ewa Goljan Renad Albar Shazia Subhani Asma Tahir Sultana Asfahani Alaa Eskandrani Ahmed Almusaiab Amna Magrashi Jameela Shinwari Dorota Monies Nada Al Tassan

Sci Rep 2017 07 18;7(1):5679. Epub 2017 Jul 18.

Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital & Research Center, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.

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July 2017

Services for children with autism in the Kingdom of Saudi Arabia.

Authors:
Fahad M Alnemary Hesham M Aldhalaan Gabriela Simon-Cereijido Faisal M Alnemary

Autism 2017 07 20;21(5):592-602. Epub 2016 Oct 20.

1 University of California, Los Angeles, USA.

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July 2017

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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August 2017