Targeted Next generation sequencing as a tool for population screening; blood disorders as an example. 1st Genomics Medicine and Research Symposium: New Horizon in Genomics Applications (10-12 February, 2019)
Genomics is a Big Data Problem. 1st Genomics Medicine and Research Symposium: New Horizon in Genomics Applications (10-12 February, 2019)
IT Resources for Saudi Human Genome Program. 1st Genomics Medicine and Research Symposium: New Horizon in Genomics Applications (10-12 February, 2019)
Genomics Medicine and Research Symposium titled: New Horizon in Genomics Applications Riyadh, Saudi Arabia, February 2019. Investigating the genetic basis of complex disorders 27-Feb-19
"1st National Autism and ADHD research summit. Riyadh, Saudi Arabia 8-9 Jan 2019
Pan Arab Conference for Bleeding Disorders at Alfaisal University, Riyadh, Kingdom of Saudi Arabia. Molecular characterization of FV deficiency 31 January – 1 February 2019
The “7th International Genetic Disorders Conference. November 9-10, 2018. Dubai, UAE 5. Speaker at MIT Hacking Medicine. Riyadh, Kingdom of Saudi Arabia Rare bleeding disorder. December 1st 2018
The Arab Variome: Unlocking the Mysteries of the Human Genome. Pan Arab Human Genetics Conference 2018, Dubai, UAE
Reducing the Burden of Disability Through Genomics. 5th International Conference on Disability 2018, Riyadh, Saudi Arabia
Mendelian Genomics: The Sparrow in The Hand! Precision Medicine Conference 2018, KFSHRC, Riyadh, Saudi Arabia
A New Era of Prenatal Genomics. Prenatal Genetics Conference 2018, Toronto, Canada
International Association of Pathology IAP, 2018
KFSH&RC 20th Annual Research Celebration Day Molecular Genetic Defects of Hereditary Angioedema in Saudi Arabia. 1-May-18
Cases gave me headache”, Dead sea, Jordan, 2018
Precision medicine enters the playing field, Oxford, UK, 2018
Science in Arab world, 2018
MIT SciTech conference Speaker, Cambridge, MA, 2018
Cancer Genomic: Empowering Precision Treatment. 2018
Saudi Medical Genetics Society, Riyadh, Saudi Arabia, 2018
Challenges for women in science, 2018
Somatic Mutation Screening, the Saudi Human Genome Program Experience. (2nd Combined Gulf Cancer Conference Riyadh 27-29 March 2018).
16th Annual Meeting of Saudi Society of Hematology, 7th Pan Arab Hematology Association Congress Advances and Challenges in Hematology, Jeddah, Kingdom of Saudi Arabia. Molecular in glanzmann February 24-25, 2018
Pediatricians at The Front line of the Genomic Revolution. 5th Saudi Pediatric Association Congress 2017, Riyadh, Saudi Arabia
“Gene Mutation Causes the Earliest Known Embryonic Lethality.” The Second International Saudi Society of Medical Genetics Symposium; KACST, Riyadh, 27 April 2017
Homozygosity and The Human Variome. 28th Annual Meeting of the German Society of Human Genetics, Bochum, Germany 2017
The Wrong Question: Exomes or Clinicians? 2nd Annual Australian Clinical Genomics Conference 2017, Melbourne, Australia
Autozygome Reveals Novel Mutation Mechanisms in Human Diseases. Saudi Society of Medical Genetics Workshop, Sakaka, Saudi Arabia 2017
Princess Noura University Riyadh, Saudi Arabia, 2017
Update about Saudi Human Genome Project, 2017
Scientific Research week, King Saud University Riyadh, Saudi Arabia, 2017
Genomic in Cancer: The Era of Precision Medicine in the Gulf Region, 2017
The 2nd Combined Conference on “Cancer Screening and Early Detection in the Gulf Region” (Keynote and scientific chair of molecular track) King Faisal Specialist Hospital and Research Center Riyadh, Saudi Arabia
Saudi women in STEM, 2017
The United Nation, Geneva, Switzerland, 2017
Saudi Human Genome Project: Toward application of precision medicine in the clinic, 2017
IonWorld Conference, Riyadh, Saudi Arabia, 2017
Science Creates Career Avenues, 2017
Women Leaders in Science, Technology and Engineering (WLSTE+10) Kuwait City, Kuwait, 2017
Genomic Landscape of high grade meningioma, 2017
American Association of Neuropathologists meeting Orange County, California
Medulloblastoma genomic subgroup-specific outcomes in irradiated children above 3 years treated at King Fahad medical city (KFMC), 2017
American Association of Neuropathologists meeting Orange County, California, 2017
Bap1 in Rhabdoid meningioma, 2017
United States and Canadian Academy of Pathology San Antonio, TX, 2017
The Saudi Human Genome Project, 2017
British embassy Riyadh, Saudi Arabia, 2017
International conference of medical education, 2017
Saudi commission for health specialties Riyadh, Saudi Arabia,2017
Meningioma genomic, 2017
Embryonic lethal Mendelian phenotypes: A large cohort from a consanguineous population. David W Smith Workshop on Malformations and Morphogenesis, Stoweflake Resort and Conference Center 2017
4TH SAUDI / 2ND GULF BLEEDING DISORDERS & THROMBOSIS SYMPOSIUM as part, of 13TH MADINAH HEMATOLOGY CONFERENCE. Bleeding disorder in Saudi Arabia 5th and 6th of May 2017
13TH MADINAH HEMATOLOGY CONFERENCE BLEEDING DISORDERS & THROMBOSIS SYMPOSIUM, Almadina , Kingdom of Saudi Arabia Bleeding Molecular Screening Project April 29 – May 6, 2017
4TH SAUDI / 2ND GULF BLEEDING DISORDERS SYMPOSIUM. Almadina , Kingdom of Saudi Arabia Bleeding Molecular Screening Project Numbers and statsitcs. May 5-6, 2017
Saudi Human Genome Program; Foundation for Personalized Medicine. (December 5-7 2016, Kuwait 6th international medical genetics conference)
Application of Next Generation Sequencing and Tumor Profiling in Clinical Oncology. (November 5-6 2016, 2nd Saudi Epidemiology conference)
The Role of Positional Mapping in Variant Interpretation. American College of Medical Genetics and Genomics Conference, Tampa, FL, USA 2016
Ion World Tour Riyadh. The application of Next Generation Sequencing in the mutational screening of complex disorders 25-Oct-16
(FENS, 2016, 2-6th July). Mutations in Parkinson’s Disease Common Genes are Rare in a Population of Saudi Patients as Revealed by Whole-exome sequencing. 3-Jul-16
FENS, 2016, 2-6th July. Genetic Heterogeneity in ADHD: Lessons from Highly Consanguineous Saudi Arabian Families 3-Jul-16
the 10th FENS Meeting, Copenhagen, Denmark Exome-based Study of Saudi Parkinson’s disease patients reveals novel candidate genes Jul-16
The Unique Contribution of the Saudi Genome Initiative to Variant Annotation. GA4GH Global Engagement Workshop at ICHG 2016, Kyoto, Japan 2016
Exome Analysis of Autosomal Recessive Disorders. International Congress of Human Genetics, Kyoto, Japan 2016
It’s Your Variant, It’s Your Problem, not and Mine. The Inaugural AGBT Precision Medicine Conference 2016, Phoenix, AZ, USA 2016
Counting Variants and Variants that Count. Annual Meeting of the German Association for Gene Diagnostics 2016, Potsdam, Germany
Saudi Genome Project: What have we learned? Functional Genomics and Beyond Conference (co-hosted by Nature Genetics and Sidra) 2016, Doha, Qatar
Riyadh pathology group monthly meeting Riyadh, Saudi Arabia, 2016
Genomic landscape of Brain tumors, 2016
6th National Genetic Diseases Conference, Dubai, UAE, 2016
Molecular genetics pathology of pituitary adenoma, 2016
American Association of Neuropathologists meeting, Baltimore, MD, 2016
New Trends in Hematology, Histolytic Disorders and Transfusion Medicine Symposium. Riyadh, Kingdom of Saudi Arabia Characterization of molecular basis of bleeding disorder 1 - 3, November, 2016.
Functional Genomics Through Medical Annotation of the Human Genome. Functional Genomics Conference, Doha, Kata 2015.
Unbiased Targeted Next Generation Sequencing Molecular Approach in the Diagnosis of Primary Immunodeficiency Diseases, at the 2nd International Primary Immuno deficiencies Congress, 5-6 November 2015, Budapest, Hungary.
Ion AmpliSeq-based gene research panels—the Saudi Mendeliome Group experience. Thermo Fisher Scientific lunch seminar. ASHG annual meeting. October 7, 2015. Baltimore, MD, USA.
Annual Meeting of the American Society of Human Genetics, Baltimore, 6-10th Oct, 2015: “Exome sequencing identifies SPG3A and OTOF gene mutations in patients with Pure Hereditary Spastic Paraplegia.”
Targeted-Next Generation Sequencing for Primary Immunodeficiency Diseases, at the 4th ASID Congress, African Society for Immunodeficiency, 29-31 May 2015, Algeria.
ESHG2015, 6-9th June. Molecular analysis of Saudi patients with Parkinson’s disease. 5-Jun-15
The Clinical Utility of a Proton Ion Ampliseq Based Inborn Errors of Metabolism Gene Panel. PERSONALIZEDMEDICINECONFERENCE 2015: From the Genome to Precision Medicine, KFSH&RC Vision 20/20. 5–6 May 2015. KFSHRC. Riyadh, Saudi Arabia.
Annual Research Report, 15-16 April, 2015: “Molecular and Genetic Characterization of an Autosomal Recessive Syndromic Familial Dystonia with Myoclonus and Tremor”.
Annual Research Report, 15-16 April, 2015: “Clinical and Pathological Heterogeneity of a Congenital Disorder of Glycosylation Manifesting as a Myasthenic/Myopathic Syndrome”.
Annual Research Report, 15-16 April, 2015: “Mutation in LACC1associated with a monogenic form of systemic Juvenile Idiopathic Arthritis”.
The Saudi Mendeliome Experience. The 15th International Conference of Jordan Pediatric Society and the 20th Congress Union & Arab Pediatric Societies. 29 April - 2 May, 2015. Amman, Jordan.
What is Massively Parallel/Next Generation Sequencing & What is Its Value for the Pediatrician? The 10th Annual Pediatric Review Conference (10th APRC). Amman, Jordan, February 26 -27, 2015.
Arab Health Scientific Seminar, Dubai, January 27, 2015: “Genetic Analysis of LGMD using SHGP Neuro Gene Panel”.
Development and application of a gene panel for investigation of Dysmorphia/ Dysplasia. ThermoFisher Scientific Workshop, Arab Health, 27th January 2015. Dubai, UAE.
Your DNA, Your Health, Let’s Get Personal. Personalized Medicine Symposium, Riyadh, Saudi Arabia 2015.
Towards Medical Annotation of the Human Genome. Genomic Medicine in Practice Symposium, Ankara, Turkey 2015.
Clinical Genomics for Pediatricians. Holistic View to The Future II – Together We Can Do, Kuwait City, Kuwait 2015.
Genetic Research and Neurosurgery. PanArab Pediatric Neurosurgery Meeting, Riyadh, Saudi Arabia 2015.
Human Genomics Workshop, 28-29 May 2014, Jeddah.
Human Genome Project” 1st Saudi Neuromuscular Conference & Electro-Diagnostics Workshop, 9-11 December 2014, Khobar, KSA. “Application of Neuro Gene Panel to the Diagnosis of LGMD”.
Exome and Targeted Sequencing using Ion Torrent Technology, The SHGP experience. (Ion world Tour, 28-29th Oct 2014 Dubai UAE).
Autism as Complex as it Gets. (The “1st International Conference for Saudi Society of Medical Genetics, Riyadh 29-30 April 2014).
Consanguinity Genetics: Moving Beyond the Usual Suspect. Human Genome Meeting 2014, Geneva, Switzerland
Democratizing the Making of a Genetic Diagnosis. Kuwait 5th International Medical Genetics Conference, Kuwait, 2014 Kuwait
How to Be Successful in Gene Identification. European Society of Human Genetics, Milan, Italy 2014
Next Generation Clinical Genetics in a Consanguineous Population: Limitless Opportunities. 16TH Manchester Dysmorphology Meeting, Manchester, UK 2014
Genome Research in MENA Region: Past Lessons and Future Opportunities. Keynote Lecture at the “Children of Turkey Genome Project Initiative Meeting”, Izmir, Turkey 2014
Newborn Genomics. Excellence in Pediatrics (EiP) Conference, Dubai, UAE 2014
Next-Generation Sequencing for Pediatric Neurological Disorders: The Saudi Experience. The 4th Saudi International Conference on Pediatric Neurology, Riyadh, Saudi Arabia 2014
Ion world Tour, 28-29th Oct 2014 Dubai UAE Exome and Targeted Sequencing using Ion Torrent Technology, The SHGP experience. 28-Oct-14
The Saudi Mendeliome Project. The 7th Saudi Society of Medical Genetics Workshop in Genetics, Khamis Mushait, Saudi Arabia 2014