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Journal of Central Nervous System Disease, 2020, Vol.12, p.117957352096223-1179573520962230
2020
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Genetics in medicine, 2018-11, Vol.20 (11), p.1328-1333
2018
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American journal of medical genetics. Part A, 2017-10, Vol.173 (10), p.2614-2621
2017
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Annals of Saudi medicine, 2022-01, Vol.42 (1), p.29-35
2022
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Human genetics, 2016-11, Vol.135 (11), p.1263-1268
2016
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Journal of dermatology, 2020-09, Vol.47 (9), p.e335-e336
2020
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Therapeutics and clinical risk management, 2016-01, Vol.12 (Issue 1), p.479-487
2016
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Journal of central nervous system disease, 2018, Vol.10, p.1179573518759682-1179573518759682
2018
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Proceedings of the National Academy of Sciences - PNAS, 2021-04, Vol.118 (15), p.1
- Le Voyer, Tom
- Neehus, Anna-Lena
- Yang, Rui
- Ogishi, Masato
- Rosain, Jérémie
- Alroqi, Fayhan
- Alshalan, Maha
- Blumental, Sophie
- Al Ali, Fatima
- Khan, Taushif
- Ata, Manar
- Rozen, Laurence
- Demulder, Anne
- Bastard, Paul
- Gruber, Conor
- Roynard, Manon
- Seeleuthener, Yoann
- Rapaport, Franck
- Bigio, Benedetta
- Chrabieh, Maya
- Sng, Danielle
- Berteloot, Laureline
- Boddaert, Nathalie
- Rozenberg, Flore
- Al-Muhsen, Saleh
- Bertoli-Avella, Aida
- Abel, Laurent
- Bogunovic, Dusan
- Marr, Nico
- Mansouri, Davood
- Al Mutairi, Fuad
- Béziat, Vivien
- Weil, Dominique
- Mahdaviani, Seyed Alireza
- Ferster, Alina
- Zhang, Shen-Ying
- Reversade, Bruno
- Boisson-Dupuis, Stéphanie
- Casanova, Jean-Laurent
- Bustamante, Jacinta
2021
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American journal of medical genetics. Part A, 2022-01, Vol.188 (1), p.83-88
2022
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Brain (London, England : 1878), 2017-08, Vol.140 (8), p.e49-e49
2017
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Experimental biology and medicine (Maywood, N.J.), 2015-03, Vol.240 (3), p.400-402
2015
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Genetics in medicine, 2021-08, Vol.23 (8), p.1551-1568
- Bertoli-Avella, Aida M.
- Kandaswamy, Krishna K.
- Khan, Suliman
- Ordonez-Herrera, Natalia
- Tripolszki, Kornelia
- Beetz, Christian
- Rocha, Maria Eugenia
- Urzi, Alize
- Hotakainen, Ronja
- Leubauer, Anika
- Al-Ali, Ruslan
- Karageorgou, Vasiliki
- Moldovan, Oana
- Dias, Patrícia
- Alhashem, Amal
- Tabarki, Brahim
- Albalwi, Mohammed A.
- Alswaid, Abdulrahman Faiz
- Al-Hassnan, Zuhair N.
- Alghamdi, Malak Ali
- Hadipour, Zahra
- Hadipour, Fatemeh
- Al Hashmi, Nadia
- Al-Gazali, Lihadh
- Cheema, Huma
- Zaki, Maha S.
- Hüning, Irina
- Alfares, Ahmed
- Eyaid, Wafaa
- Al Mutairi, Fuad
- Alfadhel, Majid
- Alkuraya, Fowzan S.
- Al-Sannaa, Nouriya Abbas
- AlShamsi, Aisha M.
- Ameziane, Najim
- Rolfs, Arndt
- Bauer, Peter
2021
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Annals of neurology, 2018-02, Vol.83 (2), p.433-436
2018
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Orphanet journal of rare diseases, 2016-09, Vol.11 (1), p.126-126, Article 126
2016
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Movement disorders, 2021-04, Vol.36 (4), p.1029-1031
2021
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Journal of paediatrics and child health, 2017-06, Vol.53 (6), p.585-591
- Alfadhel, Majid
- Al Othaim, Ali
- Al Saif, Saif
- Al Mutairi, Fuad
- Alsayed, Moeenaldeen
- Rahbeeni, Zuhair
- Alzaidan, Hamad
- Alowain, Mohammed
- Al‐Hassnan, Zuhair
- Saeedi, Mohamad
- Aljohery, Saeed
- Alasmari, Ali
- Faqeih, Eissa
- Alwakeel, Mansour
- AlMashary, Maher
- Almohameed, Sulaiman
- Alzahrani, Mohammed
- Migdad, Abeer
- Al‐Dirbashi, Osama Y
- Rashed, Mohamed
- Alamoudi, Mohamed
- Jacob, Minnie
- Alahaidib, Lujane
- El‐Badaoui, Fahd
- Saadallah, Amal
- Alsulaiman, Ayman
- Eyaid, Wafaa
- Al‐Odaib, Ali
2017
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Computers in biology and medicine, 2022-06, Vol.145, p.105492-105492, Article 105492
2022
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The Journal of experimental medicine, 2018-09, Vol.215 (9), p.2339-2353
2018
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Frontiers in neurology, 2023-04, Vol.14, p.1131490
2023
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Annals of human genetics, 2020-09, Vol.84 (5), p.370-379
2020
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Molecular genetics and metabolism, 2017-06, Vol.121 (2), p.91-95
- Alfares, Ahmed
- Alfadhel, Majid
- Wani, Tariq
- Alsahli, Saud
- Alluhaydan, Iram
- Al Mutairi, Fuad
- Alothaim, Ali
- Albalwi, Mohammed
- Al subaie, Lamia
- Alturki, Saeed
- Al-Twaijri, Waleed
- Alrifai, Muhammad
- Al-Rumayya, Ahmed
- Alameer, Seham
- Faqeeh, Eissa
- Alasmari, Ali
- Alsamman, Abdulaziz
- Tashkandia, Soha
- Alghamdi, Abdulaziz
- Alhashem, Amal
- Tabarki, Brahim
- AlShahwan, Saad
- Hundallah, Khalid
- Wali, Sami
- Al-Hebbi, Homoud
- Babiker, Amir
- Mohamed, Sarar
- Eyaid, Wafaa
- Zada, Abdul Ali Peer
2017
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Orphanet journal of rare diseases, 2021-10, Vol.16 (1), p.1-422, Article 422
- Alfadhel, Majid
- Nashabat, Marwan
- Saleh, Mohammed
- Elamin, Mohammed
- Alfares, Ahmed
- Al Othaim, Ali
- Umair, Muhammad
- Ahmed, Hind
- Ababneh, Faroug
- Al Mutairi, Fuad
- Eyaid, Wafaa
- Alswaid, Abdulrahman
- Alohali, Lina
- Faqeih, Eissa
- Almannai, Mohammed
- Aljeraisy, Majed
- Albdah, Bayan
- Hussein, Mohamed A.
- Rahbeeni, Zuhair
- Alasmari, Ali
2021
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Annals of human genetics, 2020-11, Vol.84 (6), p.431-436
2020
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Clinical genetics, 2024-06, Vol.105 (6), p.620-629
- Almannai, Mohammed
- Marafi, Dana
- Zaki, Maha S.
- Maroofian, Reza
- Efthymiou, Stephanie
- Saadi, Nebal Waill
- Filimban, Bilal
- Dafsari, Hormos Salimi
- Rahman, Fatima
- Maqbool, Shazia
- Faqeih, Eissa
- Al Mutairi, Fuad
- Alsharhan, Hind
- Abdelaty, Omar
- Bin‐Hasan, Saadoun
- Duan, Ruizhi
- Noureldeen, Mahmoud M.
- Alqattan, Alaa
- Houlden, Henry
- Hunter, Jill V.
- Posey, Jennifer E.
- Lupski, James R.
- El‐Hattab, Ayman W.
2024
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