Hosneara Akter

发表

Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes

M. Uddin, M. Woodbury-Smith, S. Islam, 2019, Molecular genetics & genomic medicine.

Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1

H. Yeger, A. Alaiya, S. Islam, 2019, EBioMedicine.

Detection of Clinically Relevant Copy Number Variations and Genes in a Bangladeshi Cohort of Neurodevelopmental Disorders

M. Uddin, Md. Ismail Hosen, O. Faruk, 2021 .

Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19

Asma R. Bankapur, J. Casanova, W. Kuebler, 2021, iScience.

Analyzing single cell transcriptome data from severe COVID-19 patients

Asma R. Bankapur, A. Alsheikh-Ali, M. Hachim, 2022, STAR Protocols.

Impact of Social Isolation on Mental Health Amid COVID-19 Pandemic: A Nationwide Survey

M. Hasan, M. Woodbury-Smith, O. Faruk, 2021 .

Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development

M. Uddin, B. Berdiev, Hosneara Akter, 2022, Human Genetics.

Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh

S. Scherer, D. Stavropoulos, M. Uddin, 2021, NPJ genomic medicine.

Novel mutations in actionable breast cancer genes by targeted sequencing in an ethnically homogenous cohort

M. Uddin, M. Woodbury-Smith, R. Awwal, 2019, BMC Medical Genetics.

Mutational Landscape of Autism Spectrum Disorder Brain Tissue

S. Scherer, P. Rahman, M. Uddin, 2022, Genes.

Detection of Clinically Relevant Copy Number Variation of SEZ6L2 Gene in a Bangladeshi Autism Spectrum Disorder Cohort

L. Banu, R. Amin, Hosneara Akter, 2019, Bangladesh Journal of Medicine.

Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

Md. Mazharul Islam, Md Mazharul Islam, M. Uddin, 2023, Frontiers in Genetics.

Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort

A. A. Tayoun, M. Uddin, M. Woodbury-Smith, 2022, neurogenetics.

Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome

Asma R. Bankapur, S. Scherer, B. Thiruvahindrapuram, 2021, International journal of molecular sciences.

Precision Therapies in Neurodevelopmental Disorders

A. A. Tayoun, M. Uddin, D. Andrade, 2020 .

An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

S. Scherer, M. Uddin, M. Woodbury-Smith, 2018, Clinical case reports.

Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population

M. Woodbury-Smith, S. I. Kanta, Hosneara Akter, 2023, Scientific reports.

Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region

Noushad Karuvantevida, Hosneara Akter, Md. Atikur Rahaman, 2024, Brain and behavior.

Mutational analyses of mitochondrial ATP6 gene reveal a possible association with abnormal levels of lactic acid and ammonia in Bangladeshi children with autism spectrum disorder: A case-control study

Hosneara Akter, Maisha Adiba, Tahirah Yasmin, 2024, Human Gene.