Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families von Al-Mubarak, Bashayer, Abouelhoda, Mohamed, Omar, Aisha, AlDhalaan, Hesham, Aldosari, Mohammed, Nester, Michael, Alshamrani, Hussain. A., El-Kalioby, Mohamed, Goljan, Ewa, Albar, Renad, Subhani, Shazia, Tahir, Asma, Asfahani, Sultana, Eskandrani, Alaa, Almusaiab, Ahmed, Magrashi, Amna, Shinwari, Jameela, Monies, Dorota, Al Tassan, Nada

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Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development von Engle, Elizabeth C, Tischfield, Max A, Bosley, Thomas M, Salih, Mustafa A M, Alorainy, Ibrahim A, Sener, Emin C, Nester, Michael J, Oystreck, Darren T, Chan, Wai-Man, Andrews, Caroline, Erickson, Robert P

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Mercury (Hg) exposure and its effects on Saudi breastfed infant's neurodevelopment von Al-Saleh, Iman, Nester, Michael, Abduljabbar, Mai, Al-Rouqi, Reem, Eltabache, Chafica, Al-Rajudi, Tahreer, Elkhatib, Rola

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Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative von Bashiri, Fahad A., Albatti, Turki H., Hamad, Muddathir H., Al-Joudi, Haya F., Daghash, Hadeel F., Al-Salehi, Saleh M., Varnham, Jeremy L., Alhaidar, Fatimah, Almodayfer, Omar, Alhossein, Abdulkarim, Aldhalaan, Hesham, Ad-Dab'bagh, Yasser A., Al Backer, Nouf, Altwaijri, Waleed, Alburikan, Khalid, Buraik, Maysaa W., Ghaziuddin, Mohammad, Nester, Michael J., Wahabi, Hayfaa A., Alhabib, Samia, Jamal, Amr A., Amer, Yasser S.

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A novel X-linked disorder with developmental delay and autistic features von Kaya, Namik, Colak, Dilek, Albakheet, Albandary, Al-Owain, Mohammad, Abu-Dheim, Nada, Al-Younes, Banan, Al-Zahrani, Jawaher, Mukaddes, Nahit M., Dervent, Aysin, Al-Dosari, Naji, Al-Odaib, Ali, Kayaalp, Inci V., Al-Sayed, Moeenaladin, Al-Hassnan, Zuhair, Nester, Michael J., Al-Dosari, Mohammad, Al-Dhalaan, Hesham, Chedrawi, Aziza, Gunoz, Hulya, Karakas, Bedri, Sakati, Nadia, Alkuraya, Fowzan S., Gascon, Generaso G., Ozand, Pinar T.

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First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient von Alsagob, Maysoon, Salih, Mustafa A, Hamad, Muddathir H A, Al-Yafee, Yusra, Al-Zahrani, Jawaher, Al-Bakheet, Albandary, Nester, Michael, Sakati, Nadia, Wakil, Salma M, AlOdaib, Ali, Colak, Dilek, Kaya, Namik

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

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Standardization of an Arabic-Language Neuropsychological Battery for Epilepsy Surgical Evaluations von Al-Joudi, Haya F., Mincari, Lina, Baz, Salah, Nester, Michael, Al-Marzouki, Najla, Abalkhail, Tariq, Aljehani, Noha, Al-Ibrahim, Camellia, Brandt, Jason

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Alterations in biochemical markers due to mercury (Hg) exposure and its influence on infant's neurodevelopment von Al-Saleh, Iman, Elkhatib, Rola, Al-Rouqi, Reem, Abduljabbar, Mai, Eltabache, Chafica, Al-Rajudi, Tahreer, Nester, Michael

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The extent of mercury (Hg) exposure among Saudi mothers and their respective infants von Al-Saleh, Iman, Abduljabbar, Mai, Al-Rouqi, Reem, Eltabache, Chafica, Al-Rajudi, Tahreer, Elkhatib, Rola, Nester, Michael

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Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature von Khalifa, Ola, Al-Sahlawi, Zahra, Imtiaz, Faiqa, Ramzan, Khushnooda, Allam, Rabab, Al-Mostafa, Abeer, Abdel-Fattah, Maaly, Abuharb, Gheid, Nester, Michael, Verloes, Alain, Al-Zaidan, Hamad

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Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII von Kaya, Namik, Aldhalaan, Hesham, Al-Younes, Banan, Colak, Dilek, Shuaib, Taghreed, Al-Mohaileb, Fahad, Al-Sugair, Abdulaziz, Nester, Michael, Al-Yamani, Suad, Al-Bakheet, Albandary, Al-Hashmi, Nadia, Al-Sayed, Moeen, Meyer, Brian, Jungbluth, Heinz, Al-Owain, Mohammed

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Use of a Brief Assessment Examination in a Study of Subacute Sclerosing Panencephalitis von Nester, Michael J.

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Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways von Colak, Dilek, Al-Dhalaan, Hesham, Nester, Michael, AlBakheet, AlBandary, Al-Younes, Banan, Al-Hassnan, Zohair, Al-Dosari, Mohammad, Chedrawi, Aziza, Al-Owain, Muhammad, AbuDheim, Nada, Al-Alwan, Laila, Al-Odaib, Ali, Ozand, Pinar, Inan, Mehmet Sait, Kaya, Namik

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Homozygosity analysis in subjects with autistic spectrum disorder von ADI, AHMAD, TAWIL, BASMA, ALDOSARI, MOHAMMED, SHINWARI, JAMEELA, NESTER, MICHAEL, ALDHALAAN, HISHAM, ALSHAMRANI, HUSSAIN, GHANNAM, MANAR, MEYER, BRIAN, TASSAN, NADA AL

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Longitudinal Study of Prenatal and Postnatal Lead Exposure and Early Cognitive Development in Al-Kharj, Saudi Arabia: A Preliminary Results of Cord Blood Lead Levels von Al-Saleh, Iman, Shinwari, Neptune, Nester, Michael, Mashhour, Abdullah, Moncari, Lina, El Din Mohamed, Gamal, Rabah, Abdullah

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Mental Assessment in Subacute Sclerosing Panencephalitis: Hacettepe Cognitive Short Assessment Scale von Öktem, Ferhunde, Nester, Michael J., Anlar, Banu, Griesemer, David A.

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Phenotypical Spectrum of Cerebellar Ataxic Associated With a Novel Mutation the CA8 Gene, Encoding Carbonic Anhydrase (CA) VIII von KAYA, Namik, ALDHALAAN, Hesham, AL-HASHMI, Nadia, AL-SAYED, Moeen, MEYER, Brian, JUNGBLUTH, Heinz, AL-OWAIN, Mohammed, AL-YOUNES, Banan, COLAK, Dilek, SHUAIB, Taghreed, AL-MOHAILEB, Fahad, AL-SUGAIR, Abdulaziz, NESTER, Michael, AL-YAMANI, Suad, AL-BAKHEET, Albandary

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Relationships between blood lead concentrations, intelligence, and academic achievement of Saudi Arabian schoolgirls von Al-Saleh, Iman, Nester, Michael, DeVol, Edward, Shinwari, Neptune, Munchari, Lina, Al-Shahria, Sulieman

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Combined oral isoprinosine-intraventricular α-interferon therapy for subacute sclerosing panencephalitis von Gascon, Generoso, Yamani, Soad, Crowell, Janice, Stigsby, Bent, Nester, Michael, Kanaan, Imaduddin, Jallu, Ashraf

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