Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel

av Sharkia, Rajech, Sheikh-Muhammad, Ahmad, Mahajnah, Muhammad, Khatib, Mohammad, Zalan, Abdelnaser
I publikationen Ann Glob Health (2019)

Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report

av Sharkia, Rajech, Mahajnah, Muhammad, Zalan, Abdelnaser, Sourlis, Chrysovalantis, Bauer, Peter, Schöls, Ludger
Publicerad 2014

Parental mosaicism in another case of Dravet syndrome caused by a novel SCN1A deletion: a case report

av Sharkia, Rajech, Hengel, Holger, Schöls, Ludger, Athamna, Muhammad, Bauer, Peter, Mahajnah, Muhammad
I publikationen J Med Case Rep (2016)

Novel homozygous large deletion including the 5′ part of the SPATA7 gene in a consanguineous Israeli Muslim Arab family

av Mayer, Anja-Kathrin, Mahajnah, Muhammad, Zobor, Ditta, Bonin, Michael, Sharkia, Rajech, Wissinger, Bernd
I publikationen Mol Vis (2015)

Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities

av Mahajnah, Muhammad, Sharkia, Rajech, Shalabe, Haitham, Terkel-Dawer, Ruth, Akawi, Ashraf, Zelnik, Nathanel
I publikationen Biomed Res Int (2015)

Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR Mutation

av Borovok, Natalia, Weiss, Celeste, Sharkia, Rajech, Reichenstein, Michal, Wissinger, Bernd, Azem, Abdussalam, Mahajnah, Muhammad
I publikationen Front Genet (2020)

Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian Authority

av Mayer, Anja K., Balousha, Ghassan, Sharkia, Rajech, Mahajnah, Muhammad, Ayesh, Suhail, Schulze, Martin, Buchert, Rebecca, Zobor, Ditta, Azem, Abdussalam, Schöls, Ludger, Bauer, Peter, Wissinger, Bernd
I publikationen Eur J Hum Genet (2020)

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

av Hengel, Holger, Magee, Alex, Mahanjah, Muhammad, Vallat, Jean-Michel, Ouvrier, Robert, Abu-Rashid, Mohammad, Mahamid, Jamal, Schüle, Rebecca, Schulze, Martin, Krägeloh-Mann, Ingeborg, Bauer, Peter, Züchner, Stephan, Sharkia, Rajech, Schöls, Ludger
I publikationen Neurol Genet (2017)

Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus

av Mayer, Anja K., Mahajnah, Muhammad, Thomas, Mervyn G., Cohen, Yuval, Habib, Adib, Schulze, Martin, Maconachie, Gail, AlMoallem, Basamat, De Baere, Elfride, Lorenz, Birgit, Traboulsi, Elias I., Kohl, Susanne, Azem, Abdussalam, Bauer, Peter, Gottlob, Irene, Sharkia, Rajech, Wissinger, Bernd
I publikationen Brain (2019)

First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

av Hengel, Holger, Buchert, Rebecca, Sturm, Marc, Haack, Tobias B., Schelling, Yvonne, Mahajnah, Muhammad, Sharkia, Rajech, Azem, Abdussalam, Balousha, Ghassan, Ghanem, Zaid, Falana, Mohammed, Balousha, Osama, Ayesh, Suhail, Keimer, Reinhard, Deigendesch, Werner, Zaidan, Jimmy, Marzouqa, Hiyam, Bauer, Peter, Schöls, Ludger
I publikationen Eur J Hum Genet (2020)

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

av Mallaret, Martial, Synofzik, Matthis, Lee, Jaeho, Sagum, Cari A., Mahajnah, Muhammad, Sharkia, Rajech, Drouot, Nathalie, Renaud, Mathilde, Klein, Fabrice A. C., Anheim, Mathieu, Tranchant, Christine, Mignot, Cyril, Mandel, Jean-Louis, Bedford, Mark, Bauer, Peter, Salih, Mustafa A., Schüle, Rebecca, Schöls, Ludger, Aldaz, C. Marcelo, Koenig, Michel
Publicerad 2014

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia

av Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S, Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmüller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A, Stirnberg, Rüdiger, Sturm, Marc, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan, Heilmann-Heimbach, Stefanie, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Brüstle, Oliver, Klopstock, Thomas, Mathews, Katherine D, Shy, Michael E, de Jonghe, Peter, Chinnery, Patrick F, Horvath, Rita, Kohlhase, Jürgen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schöls, Ludger, Nürnberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo, Schüle, Rebecca
I publikationen Brain (2017)