Masalha R, Afawi Z,Mahajnah M, Mashal A, Hallak M , Alsaied I, Bolotin A, Ifergan G, Wirguin I, Impact of dietary vitamin B12 deficiency on school performance. J Pediat Neurol 6;2008
Afawi Z, Abu-Hammad T, Shorar Z, Grotto I Mahajnah M. Prevalence of epilepsy in Bedouin children: A cross-sectional study in southern Israel. J Pediat Neurol 6;2008
Shimony A, Afawi Z, Asher T, Mahajnah M, Shorer Z. Epidemiological characteristics of febrile seizures--comparing between Bedouin and Jews in the southern part of Israel. Seizure. 18:26-29;2009
Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA. A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. Am J Hum Genet. 85:897-902;2009
Masalha R, Kordysh E, Alpert G, Hallak M, Morad M, Mahajnah M, Farkas P, Herishanu Y. The prevalence of Parkinson's disease in an Arab population, Wadi Ara, Israel. IMAJ 12:32-35;2010
Sharkia R, Azem A, Kaiyal Q, Zelnik N, Mahajnah M, Mental retardation and consanguinity in a selected region of the Israeli Arab community. Cent Eur J Med 5:91-96;2010
Spiegel R, Pines O, Ta-Shma A, Burak E, Shaag A, Halvardson J, Edvardson S, Mahajna M, Zenvirt S, Saada A, Shalev S, Feuk L, Elpeleg O. Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2. Am J Hum Genet. 90:518-523;2012
Yang YJ, Baltus AE, Mathew RS, Murphy EA, Evrony GD, Gonzalez DM, Wang EP, Marshall-Walker CA, Barry BJ, Murn J, Tatarakis A, Mahajan MA, Samuels HH, Shi Y, Golden JA, Mahajnah M, Shenhav R, Walsh CA. Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation. Cell. 151:1097-1112;2012
Mahajnah M, Zelnik N. Phenotypic heterogeneity in consanguineous patients with a common CLN8 mutation. Pediatr Neurol. 47:303-305;2012
Abu Rashid M, Mahajnah M, Jaber L, Kornreich L, Bar On E, Basel-Vanagaite L, Soffer D, Koenin M, Straussberg R. A Novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab – Israeli family. Eur J Paediatr Neurol. 17:259-264;2013
Sharkia R, Mahajnah M, Zalan A, Athamna M, Azem A, Badarneh K, Faris F.Comparative screening of FMF mutations in various communities of the Israeli society.Eur J Med Genet. 56:351-355;2013
Mallaret M1, Synofzik M, Lee J, Sagum CA, Mahajnah M, Sharkia R, Drouot N, Renaud M, Klein FA, Anheim M, Tranchant C, Mignot C, Mandel JL, Bedford M, Bauer P, Salih MA, Schüle R, Schöls L, Aldaz CM, Koenig M. The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain. 137:411-419;2014
Watemberg N, Matar M, Har-Gil M, Mahajnah M. The influence of excessive chewing gum use on headache frequency and severity among adolescents. Pediatr Neurol. 50:69-72;2014
Sharkia R, Mahajnah M, Zalan A, Sourlis C, Bauer P, Schöls L. Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report. J Med Case Rep. 8:78;2014
Mahajnah M, Sharkia R, Shalabe H, Terkel-Dawer R, Akawi A, Zelnik N. Clinical Characteristics of Autism Spectrum Disorder in Israel - Impact of Ethnic and Social Diversities. Accepted for publication. Biomed Research Internat 2014
Mahajnah M, Abu-Rashid M, Lerman-Sagie T, Goikhman I, Nathanel Zelnik N. Alexander Disease in Israel – Megalencephaly and Leukoencephalopathy and its Differential Diagnosis. Accepted for publication. J Pediat Neurology 2014
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