ArticleFrontiers in genetics2023
Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders.
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Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.
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12citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% of its field
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Who cites it
12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.
- Diagnostic and clinical utility of exome sequencing and chromosomal microarray in children with GDD/iD: a meta-analysis.Annals of medicine · 2026Pooled it
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- Genetic risk factor identification for common epilepsies guided by integrative omics data analysis.Epilepsia · 2026Article
- Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis.Human genetics · 2026Article
- Mapping human brain cell type origin and diseases through single-cell transcriptomics.Translational psychiatry · 2025Review
- Genetic Landscape of Dystonia in Asian Indians.Movement disorders clinical practice · 2025Article
- The Current Situation of Neurological Health in Bangladesh: A Perspective.Health science reports · 2025Article
- Genomic insights into Rett syndrome-like features in Bangladeshi participants.Genetics in medicine open · 2025Article
- Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.Brain and behavior · 2024Article
- Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers.Molecular biology reports · 2024Article
- Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.Scientific reports · 2023Article
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Authors and funding
34 authors at 13 institutions in 5 countries.
Hosneara AkterGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Muhammad Mizanur RahmanDepartment of Paediatric Neurology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Shaoli SarkerDepartment of Child Neurology, NeuroGen Healthcare, Dhaka, Bangladesh.
Mohammed BasiruzzamanDepartment of Child Neurology, NeuroGen Healthcare, Dhaka, Bangladesh.
Md Mazharul IslamDepartment of Child Neurology, NeuroGen Healthcare, Dhaka, Bangladesh.
Md Atikur RahamanGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Md Ashiquir RahamanCentre for Precision Therapeutics, NeuroGen Healthcare, Dhaka, Bangladesh.
Tamannyat Binte EshaqueGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Nushrat Jahan DityGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Shouvik SarkerInstitute of Plant Genetics, Department of Plant Biotechnology, Leibniz University Hannover, Hanover, Germany.
Md Robed AminDepartment of Medicine, Dhaka Medical College, Dhaka, Bangladesh.
Mohammad Monir HossainDepartment of Paediatric Neurology, National Institute of Neuroscience and Hospital, Dhaka, Bangladesh.
Maksuda LopaCentre for Precision Therapeutics, NeuroGen Healthcare, Dhaka, Bangladesh.
Nargis JahanCentre for Precision Therapeutics, NeuroGen Healthcare, Dhaka, Bangladesh.
Shafaat HossainDepartment of Biology and Biochemistry, University of Houston, Houston, TX, United States.
Amirul IslamGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Ashaduzzaman MondolCentre for Precision Therapeutics, NeuroGen Healthcare, Dhaka, Bangladesh.
Md Omar FarukCentre for Precision Therapeutics, NeuroGen Healthcare, Dhaka, Bangladesh.
Narayan SahaDepartment of Paediatric Neurology, National Institute of Neuroscience and Hospital, Dhaka, Bangladesh.
Gopen Kumar KunduDepartment of Child Neurology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Shayla Imam KantaDepartment of Paediatric Neuroscience, Dhaka Shishu Hospital, Dhaka, Bangladesh.
Rezaul Karim KazalDepartment of Obstetrics and Gynaecology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Kanij FatemaDepartment of Paediatric Neurology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Md Ashrafur RahmanDepartment of Pharmaceutical Sciences, Wilkes University, Pennsylvania, PA, United States.
Maruf HasanDepartment of Biomedical Engineering, Military Institute of Science and Technology, Dhaka, Bangladesh.
Md Abid Hossain MollahDepartment of Paediatrics, BIRDEM General Hospital, Dhaka, Bangladesh.
Md Ismail HosenDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
Noushad KaruvantevidaCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Ghausia BegumCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Binte ZehraCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Nasna NassirCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
A H M Nurun NabiDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
K M Furkan UddinGenetics and Genomic Medicine Centre, NeuroGen Healthcare, Dhaka, Bangladesh.
Mohammed UddinCollege of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Precision Therapeutics (United States) · USBangabandhu Sheikh Mujib Medical University · BDMohammed Bin Rashid University of Medicine and Health Sciences · AEDhaka Shishu Hospital · BDNational Institute of Neurosciences & Hospital · BDUniversity of Dhaka · BDGenome Canada · CABangladesh Institute of Research and Rehabilitation for Diabetes Endocrine and Metabolic Disorders · BDChild Health Research Foundation · BDDhaka Medical College and Hospital · BDHoly Family Red Crescent Medical CollegeUniversity of Houston · USWilkes University · US
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Autism Diagnostic Observation Schedule-Second Edition (ADOS-2)autism spectrum disorder (ASD)chromosomal microarray analysis (CMA)copy number variation (CNV)critical exon gene (CEG)neurodevelopmental disorders (NDDs)variant of uncertain significance (VOUS)
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What OpenQuestion holds
Textfull text, public
LicenceCC BY
reference markers read5
measurements read41
Read underepoch 390
Registered trials
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.