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Jehan Suleiman

Expanding the genetic heterogeneity of intellectual disability
2017 · Shams Anazi, Sateesh Maddirevula, et al. · Human Genetics · 162
Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases
2018 · Ayman W. El-Hattab, Jehan Suleiman, et al. · Molecular Genetics and Metabolism · 141
VGKC antibodies in pediatric encephalitis presenting with status epilepticus
2011 · J. Suleiman, T. Brenner, et al. · Neurology · 103
Autoimmune epilepsy in children: Case series and proposed guidelines for identification
2013 · Jehan Suleiman, Fabienne Brilot, et al. · Epilepsia · 98
The recognition and treatment of autoimmune epilepsy in children
2014 · Jehan Suleiman, Russell C Dale · Developmental Medicine & Child Neurology · 89
Autoantibodies to neuronal antigens in children with new‐onset seizures classified according to the revised ILAE organization of seizures and epilepsies
2013 · Jehan Suleiman, Sukhvir Wright, et al. · Epilepsia · 63
Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies
2011 · JEHAN SULEIMAN, TANJA BRENNER, et al. · Developmental Medicine & Child Neurology · 46
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WDR45B ‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome
2017 · J. Suleiman, D. Allingham‐Hawkins, et al. · Clinical Genetics · 43
Severe Encephalopathy With Swine Origin Influenza a H1n1 Infection in Childhood: Case Reports
2010 · R.I. Webster, B. Hazelton, et al. · Neurology · 42
B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker–Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss
2018 · Muna Al Dhaibani, Ayman El-Hattab, et al. · Neuropediatrics · 26
A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract
2016 · Jozef Hertecant, Makanko Komara, et al. · Meta Gene · 26
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West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations
2018 · Qudsia Shaukat, Jozef Hertecant, et al. · Epileptic Disorders · 25
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Pediatric Multiple Sclerosis in the United Arab Emirates: Characteristics From a Multicenter Study and Global Comparison
2018 · Fatima Y. Ismail, Eliza Gordon-Lipkin, et al. · Journal of Child Neurology · 23
Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family
2015 · Makanko Komara, Anne John, et al. · American Journal of Medical Genetics Part A · 22
ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease
2018 · Jehan Suleiman, Nadia Hamwi, et al. · Brain and Development · 19
Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus
2018 · Nesreen K. Al-Jezawi, Aisha M. Al-Shamsi, et al. · BMC Medical Genetics · 17
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PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities
2018 · J. Suleiman, A.M. Al Hashem, et al. · Clinical Genetics · 16
Homozygous loss‐of‐function variants of TASP1 , a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies
2019 · Jehan Suleiman, Korbinian M. Riedhammer, et al. · Human Mutation · 15
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TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies
2018 · J. Suleiman, M. Mundt, et al. · Clinical Genetics · 14
17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report
2017 · Karen Wessel, Jehan Suleiman, et al. · BMC Medical Genetics · 12
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Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency
2022 · Korbinian M Riedhammer, Anna L Burgemeister, et al. · Human Molecular Genetics · 10
Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy
2022 · Shuk Ching Chong, Ye Cao, et al. · American Journal of Medical Genetics Part A · 7
VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features
2019 · Christian Beetz, Najim Ameziane, et al. · Clinical Genetics · 7
Correction to: Expanding the genetic heterogeneity of intellectual disability
2017 · Shams Anazi, Sateesh Maddirevula, et al. · Human Genetics · 4
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Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review
2023 · Musaad Abukhaled, Mohammed Al Muqbil, et al. · European Journal of Pediatrics · 3
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Works count: 36
Citation count: 1,036
H-index: 16
I10-index: 21
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