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Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update.
Published in:
Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.580484
By:
- Maddirevula, Sateesh;
- Shamseldin, Hanan E.;
- Sirr, Amy;
- AlAbdi, Lama;
- Lo, Russell S.;
- Ewida, Nour;
- Al-Qahtani, Mashael;
- Hashem, Mais;
- Abdulwahab, Firdous;
- Aboyousef, Omar;
- Kaya, Namik;
- Monies, Dorota;
- Salem, May H.;
- Al Harbi, Naffaa;
- Aldhalaan, Hesham M.;
- Alzaidan, Hamad;
- Almanea, Hadeel M.;
- Alsalamah, Abrar K.;
- Al Mutairi, Fuad;
- Ismail, Samira
Publication type:
Article
Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.
Published in:
Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 705, doi. 10.2147/PGPM.S366826
By:
- Alhazmi, Safiah;
- Alzahrani, Maryam;
- Farsi, Reem;
- Alharbi, Mona;
- Algothmi, Khloud;
- Alburae, Najla;
- Ganash, Magdah;
- Azhari, Sheren;
- Basingab, Fatemah;
- Almuhammadi, Asma;
- Alqosaibi, Amany;
- Alkhatabi, Heba;
- Elaimi, Aisha;
- Jan, Mohammed;
- Aldhalaan, Hesham M;
- Alrafiah, Aziza;
- Alrofaidi, Aisha
Publication type:
Article
Further delineation of Temtamy syndrome of corpus callosum and ocular abnormalities.
Published in:
American Journal of Medical Genetics. Part A, 2018, v. 176, n. 3, p. 715, doi. 10.1002/ajmg.a.38615
By:
- Alrakaf, Laila;
- Al‐Owain, Mohammed A.;
- Busehail, Maryam;
- Alotaibi, Maha A.;
- Monies, Dorota;
- Aldhalaan, Hesham M.;
- Alhashem, Amal;
- Al‐Hassnan, Zuhair N.;
- Rahbeeni, Zuhair A.;
- Murshedi, Fathiya Al;
- Ani, Nadia Al;
- Al‐Maawali, Almundher;
- Ibrahim, Niema A.;
- Abdulwahab, Firdous M.;
- Alsagob, Maysoon;
- Hashem, Mais O.;
- Ramadan, Wafaa;
- Abouelhoda, Mohamed;
- Meyer, Brian F.;
- Kaya, Namik
Publication type:
Article
The Role of Nicotinic Receptors in the Attenuation of Autism‐Related Behaviors in a Murine BTBR T + tf/J Autistic Model.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2020, v. 13, n. 8, p. 1311, doi. 10.1002/aur.2342
By:
- Mahmood, Hafiz M.;
- Aldhalaan, Hesham M.;
- Alshammari, Tahani K.;
- Alqasem, Mashael A.;
- Alshammari, Musaad A.;
- Albekairi, Norah A.;
- AlSharari, Shakir D.
Publication type:
Article
KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases.
Published in:
Epilepsia (Series 4), 2020, v. 61, n. 4, p. 679, doi. 10.1111/epi.16480
By:
- Borlot, Felippe;
- Abushama, Ahmed;
- Morrison‐Levy, Nadine;
- Jain, Puneet;
- Puthenveettil Vinayan, Kollencheri;
- Abukhalid, Musaad;
- Aldhalaan, Hesham M.;
- Almuzaini, Hanin S.;
- Gulati, Sheffali;
- Hershkovitz, Tova;
- Konanki, Ramesh;
- Lingappa, Lokesh;
- Luat, Aimee F.;
- Shafi, Shatha;
- Tabarki, Brahim;
- Thomas, Maya;
- Yoganathan, Sangeetha;
- Alfadhel, Majid;
- Arya, Ravindra;
- Donner, Elizabeth J.
Publication type:
Article
Sociodemographic, clinical characteristics, and service utilization of young children diagnosed with autism spectrum disorder at a research center in Saudi Arabia: The road to autism spectrum disorder diagnosis.
Published in:
Saudi Medical Journal, 2021, v. 42, n. 8, p. 878, doi. 10.15537/smj.2021.42.8.20210297
By:
- Alotaibi, Abdullah M.;
- Craig, Katelyn A.;
- Alshareef, Taghreed M.;
- AlQathmi, Elham S.;
- Aman, Sarah M.;
- Aldhalaan, Hesham M.;
- Oandasan, Cheryl L.
Publication type:
Article
Factors associated with age of diagnosis of autism spectrum disorder among children in Saudi Arabia: new insights from a cross-sectional study.
Published in:
BMC Research Notes, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13104-022-06035-x
By:
- Alnemary, Fahad M.;
- Alnemary, Faisal M.;
- Simon-Cereijido, Gabriela;
- Aldhalaan, Hesham M.;
- Hernandez, Anthony;
- Alyahya, Ahmed;
- Alenezi, Shuliweeh
Publication type:
Article
Services for children with autism in the Kingdom of Saudi Arabia.
Published in:
Autism: The International Journal of Research & Practice, 2017, v. 21, n. 5, p. 592, doi. 10.1177/1362361316664868
By:
- Alnemary, Fahad M.;
- Aldhalaan, Hesham M.;
- Simon-Cereijido, Gabriela;
- Alnemary, Faisal M.
Publication type:
Article
Expanding the Allelic spectrum in ATP1A3-related disorders with 3 novel mutations and clinic features.
Published in:
Neurosciences, 2023, v. 28, n. 3, p. 195, doi. 10.17712/nsj.2023.3.20220131
By:
- Alyamani, Suad A.;
- Aldhalaan, Hesham M.;
- Almuhaizea, Mohammed A.;
- Abukhalid, Musaad F.
Publication type:
Article

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