Author

Ramzi H. Nasir

Observed names: Nasir, Ramzi, R Nasir, Ramzi Nasir, Ramzi H. Nasir

Institution: Imperial College Healthcare NHS Trust

Observed institutions: Boston Children's Hospital, Howard Hughes Medical Institute, Harvard University, Imperial College Healthcare NHS Trust, Royal Free London NHS Foundation Trust, University of California, San Francisco, New York Medical College, United Arab Emirates University, Keio University, Hokkaido University, Massachusetts General Hospital, The Portland Hospital, Autism Consortium, Jordan University Hospital

OpenAlex ID: A5111298940

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

2013 · Timothy W. Yu, Maria H. Chahrour, et al. · Neuron · 463

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

2008 · D T Miller, Y Shen, et al. · Journal of Medical Genetics · 436

Clinical Genetic Testing for Patients With Autism Spectrum Disorders

2010 · Yiping Shen, Kira A. Dies, et al. · PEDIATRICS · 403

Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders

2010 · Michael S.L. Ching, Yiping Shen, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 304

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Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome

2010 · Ellen Hanson, Ramzi H. Nasir, et al. · Journal of Developmental & Behavioral Pediatrics · 128

Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans

2013 · L. Benjamin Hills, Amira Masri, et al. · Neurology · 105

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Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination

2015 · Tojo Nakayama, Almundher Al-Maawali, et al. · The American Journal of Human Genetics · 83

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Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features

2016 · Qing Ouyang, Tojo Nakayama, et al. · Proceedings of the National Academy of Sciences · 66

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PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features

2018 · Raida Khalil, Connor Kenny, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 42

Developmental and degenerative features in a complicated spastic paraplegia

2009 · M. Chiara Manzini, Anna Rajab, et al. · Annals of Neurology · 37

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Diagnostic delay of autism in Jordan: review of 84 cases

2013 · Amira T. Masri, Najati Al Suluh, et al. · Libyan Journal of Medicine · 30

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Neurodevelopmental Disorders: Autism Spectrum Disorder

2023 · Robyn P. Thom, Nora D. B. Friedman, et al. · Springer eBooks · 8

Neurodevelopmental Disorders: Autism Spectrum Disorder

2024 · Robyn P. Thom, Nora D. B. Friedman, et al. · Springer eBooks · 6

Children and Adolescents with Developmental Disabilities in Humanitarian Settings

2020 · Vanessa Cavallera, Ramzi Nasir, et al. · Springer eBooks · 4

Child Development and Developmental Concerns

2021 · Ramzi Nasir · Springer eBooks · 3

Letter to Editor: Diagnostic delay of autism in Jordan: review of 84 cases

2013 · AT Masri, NA Suluh, et al. · Libyan Journal of Medicine · 1

When Visa Policy Becomes Health Policy: Children With Developmental Disabilities, War and Humanitarian Access

2026 · Sarah Dababnah, Ramzi Nasir · Child Care Health and Development

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1216 Implementing a telehealth autism diagnostic service in barnet in response to COVID-19 restrictions

2021 · Ramzi Nasir, Pam Czerniewska, et al. · Abstracts

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Table 1. [Genomic Testing Used for the 16p11.2 Recurrent Microdeletion].

2015 · David T. Miller, Wendy K. Chung, et al.

Urinary Function and Enuresis

2009 · Ramzi Nasir, Alison Schonwald · Elsevier eBooks

Works count: 23

Citation count: 2,119

H-index: 11

I10-index: 11