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Ahm M. Huq

Observed names: A.H.M. Huq, AHM M Huq, AHM Mahbubul Huq, AHMM Huq, Ahm Huq, Ahm M Huq
ORCID: 0009-0006-5736-0834
Observed ORCID: 0009-0006-5736-0834
OpenAlex ID: A5110055030
Tourette syndrome is associated with recurrent exonic copy number variants
2010 · Senthil K. Sundaram, Ahm M. Huq, et al. · Neurology · 125
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O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling
2018 · Nithya Selvan, Stephan George, et al. · Journal of Biological Chemistry · 69
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Exome sequencing of a pedigree with tourette syndrome or chronic tic disorder
2011 · Senthil K. Sundaram, Ahm M. Huq, et al. · Annals of Neurology · 50
Homozygous Mutation in Synaptic Vesicle Glycoprotein 2A Gene Results in Intractable Epilepsy, Involuntary Movements, Microcephaly, and Developmental and Growth Retardation
2015 · Fatema J. Serajee, Ahm M. Huq · Pediatric Neurology · 49
Expanding the neurodevelopmental phenotype ofPURAsyndrome
2017 · Bo Hoon Lee, Margot R. F. Reijnders, et al. · American Journal of Medical Genetics Part A · 48
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Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation
2018 · Keisuke Ueda, Fatema Serajee, et al. · PEDIATRICS · 22
Longitudinal myelitis, aseptic meningitis, and conus medullaris infarction as presenting manifestations of pediatric sysemic lupus erythematosus
2008 · AM Katramados, R Rabah, et al. · Lupus · 18
Posterior reversible encephalopathy syndrome and autoimmunity
2022 · Yang Li, Junmin Song, et al. · Autoimmunity Reviews · 17
No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21‐q22 and autism
2003 · Rafiqun Nabi, Hailang Zhong, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 15
Exome sequencing and diffusion tensor imaging in developmental disabilities
2013 · Senthil Sundaram, A.H.M. Huq, et al. · Pediatric Research · 9
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Prevalence of Common Mitochondrial Point Mutations in Autism
2006 · FJ Serajee, H Zhong, et al. · Neuropediatrics · 9
Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss
2018 · Kallol K. Set, Amanda R.B. Weber, et al. · Neurology · 6
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A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions
2017 · Keisuke Ueda, Fatema Serajee, et al. · Journal of Clinical Neurology · 4
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Exome Sequencing Identifying Dual Mutations in Calcium Signaling Genes GNAO1 and ATP2B3 in a Patient with Early Infantile Epileptic Encephalopathy
2016 · Fatema Serajee, Ahm Huq, et al. · Journal of Pediatric Neurology · 2
Primary angiitis of the central nervous system
2025 · Sushmitha Meghashyam, Fatema J Serajee, et al. · Current Opinion in Immunology · 1
Atypical presentation of asymmetric limb dystonia in a patient with CHAT gene mutation (P7-13.008)
2022 · Wan Yee Kong, Fatema Serajee, et al. · Neurology · 1
Exome Sequencing Identifies Dual Mutations in Calcium Signaling Genes GNAO1 and ATP2B3 in a Patient with Early Infantile Epileptic Encephalopathy (EIEE) (P5.146)
2016 · Keisuke Ueda, Fatema Serajee, et al. · Neurology · 1
Sibling response to initial antiepileptic medication predicts treatment success
2017 · Keisuke Ueda, Fatema Serajee, et al. · Epilepsy Research
Co-occurrence of pathogenic mutations in mutiple genes in 2 siblings with Brown-Vialetto-Van Laere Syndrome Type 2 phenotype. (P4.177)
2017 · Kallol Set, Ahm Huq · Neurology
Case Report: Novel Histiocytosis with Primary Nerve and Muscle Autoimmunity (P6.141)
2016 · Richa Tripathi, Ahm Huq, et al. · Neurology
Exome Sequencing identifies Carbamazepine responsive Episodic Dystonia and Hallucination due to Pyruvate Dehydrogenase E2 mutation (P2.228)
2015 · Salman Rashid, Meghan Harper-Shankie, et al. · Neurology
Non-syndromic patients with infantile spasms and malformations of cortical development: absence of seizures in siblings
2015 · Vijay N Tiwari, Harry T Chugani, et al. · Journal of the International Child Neurology Association
Immunogenetic Studies in Autism
2006 · FJ Serajee, R Nabi, et al. · Neuropediatrics
Works count: 23
Citation count: 446
H-index: 9
I10-index: 9
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