Author

Reham Khalaf‐Nazzal

Observed names: Khalaf-Nazzal Reham, R. Khalaf-Nazzal, Reham Khalaf, Reham Khalaf-Nazzal

Institutions: University of Exeter, Arab American University

Observed institutions: Inserm, An-Najah National University, University of Exeter, Sorbonne Université, Institut du Fer à Moulin, Université Pierre-et-Marie-Curie, Arab American University

ORCID: 0000-0003-4814-9958

Observed ORCID: 0000-0003-4814-9958

OpenAlex ID: A5041557373

New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum

2013 · Nadia Bahi-Buisson, Isabelle Souville, et al. · Brain · 136

Hippocampal development – Old and new findings

2013 · R. Khalaf-Nazzal, F. Francis · Neuroscience · 114

Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2

2016 · Paula Giménez-Mascarell, Iker Oyenarte, et al. · Journal of Biological Chemistry · 67

SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission

2023 · James Fasham, Antje K Huebner, et al. · Brain · 20

Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency

2021 · Siying Lin, James Fasham, et al. · European Journal of Human Genetics · 14

Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder

2022 · Reham Khalaf-Nazzal, James Fasham, et al. · The American Journal of Human Genetics · 13

Early born neurons are abnormally positioned in the doublecortin knockout hippocampus

2016 · Reham Khalaf-Nazzal, Melissa A. Stouffer, et al. · Human Molecular Genetics · 13

Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse

2014 · Sophie Hamelin, Benoit Pouyatos, et al. · Neurobiology of Disease · 13

Organelle and Cellular Abnormalities Associated with Hippocampal Heterotopia in Neonatal Doublecortin Knockout Mice

2013 · Reham Khalaf-Nazzal, Elodie Bruel-Jungerman, et al. · PLoS ONE · 12

TECPR2 ‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine

2024 · Reham Khalaf‐Nazzal, Imad Dweikat, et al. · American Journal of Medical Genetics Part A · 7

Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells

2022 · M.A. Stouffer, R. Khalaf-Nazzal, et al. · Neurobiology of Disease · 7

Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia

2021 · Reham Khalaf-Nazzal, James Fasham, et al. · Brain Sciences · 7

Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene

2022 · Imad Dweikat, Reham Khalaf-Nazzal · Frontiers in Genetics · 6

Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families

2022 · Reham Khalaf-Nazzal, Imad Dweikat, et al. · Brain and Development · 3

Whole exome sequencing reveals complex inheritance patterns and identifies two gene mutations implicated in the development of Autism and Intellectual Disability in a consanguineous Palestinian family

2016 · Khalaf-Nazzal Reham, Dweikat Imad, et al. · Frontiers in Neuroscience · 2

A distinct phenotype of childhood leukodystrophy presenting as absence seizure

2014 · ImadMohammad Dweikat, Nadera Damsah, et al. · Journal of Pediatric Neurosciences · 2

Biallelic variants in the ERAD pathway gene JKAMP cause a neurodevelopmental disorder with urogenital manifestations

2026 · Reham Khalaf-Nazzal, Fida' Al-Hijawi, et al. · Genetics in Medicine

Clinical Profiles, Genetic Variants, and Neurodevelopmental Outcomes Following Liver Transplantation in Maple Syrup Urine Disease: A Study From Palestine

2026 · Reham Khalaf‐Nazzal, Huthaifa Haj‐Ahmad, et al. · JIMD Reports

Phenotypic and Molecular Heterogeneity Linked to the Magnesium Transporter CNNM2

2019 · Reham Khalaf‐Nazzal, Imad Dweikat, et al. · World Academy of Science, Engineering and Technology, International Journal of Bioengineering and Life Sciences

Structure of PRL-1 in complex with the Bateman domain of CNNM2

2016 · P. GIMENEZ-Mascarell, I. Oyenarte, et al. · Worldwide Protein Data Bank

Caractérisation ultrastructurale, morphologique, et moléculaire des cellules hétérotopiques dans un modèle d'épilepsie hippocampique, chez les souris inactivées pour le gène Dcx

2012 · Reham Khalaf‐Nazzal · HAL

Works count: 21

Citation count: 436

H-index: 9

I10-index: 9