Alexej Abyzov

Boston Children's Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

58h-index65.6kcitations180works19.62yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(50), Cancer Genomics and Diagnostics(42), Genomics and Rare Diseases(41), Single-cell and spatial transcriptomics(25), Genomics and Chromatin Dynamics(24)

Publications162 total

Karyotypic Profiling of Induced Pluripotent Stem Cells Derived from a Xeroderma Pigmentosum Group C Patient
Cells·2025Open Access
A comprehensive view of somatic mosaicism by single-cell DNA analysis
2025· 3 citedOpen Access
PATH-36. DNA copy number clustering reveals alterations that influence survival in primary IDH-mutant astrocytoma patients
Neuro-Oncology·2025Open Access
Single cell whole genome and transcriptome sequencing links somatic mutations to cell identity and ancestry
2025· 2 cited
Allele-specific correction of ATAD3A pathogenic variants via template-free CRISPR-Cas9 editing and gene conversion
2025Open Access
Comprehensive benchmarking of somatic mutation detection by the SMaHT Network
2025· 3 citedOpen Access
The Somatic Mosaicism across Human Tissues Network
Nature·2025· 28 citedOpen Access
Specification of human brain regions with orthogonal gradients of WNT and SHH in organoids reveals patterning variations across cell lines
Cell stem cell·2025· 21 cited
Author Correction: Transgenerational transmission of post-zygotic mutations suggests symmetric contribution of first two blastomeres to human germline
Nature Communications·2025Open Access
Interneuron Loss and Microglia Activation by Transcriptome Analyses in the Basal Ganglia of Tourette Disorder
Biological Psychiatry·2025· 5 citedOpen Access
Accurate Detection of Sub-1% Frequency Somatic Mutations by Whole Genome Sequencing
SSRN Electronic Journal·2025Open Access
Transgenerational transmission of post-zygotic mutations suggests symmetric contribution of first two blastomeres to human germline
Nature Communications·2024Open Access
Somatic mosaicism in schizophrenia brains reveals prenatal mutational processes
Science·2024· 16 citedOpen Access
Resolving the 22q11.2 deletion using CTLR-Seq reveals chromosomal rearrangement mechanisms and individual variance in breakpoints
Proceedings of the National Academy of Sciences·2024· 3 citedOpen Access
Genome-wide analysis and visualization of copy number with CNVpytor in igv.js
Bioinformatics·2024· 1 citedOpen Access
Transgenerational transmission of post-zygotic mutations suggests symmetric contribution of first two blastomeres to human germline
2024Open Access
Massively parallel characterization of regulatory elements in the developing human cortex
Science·2024· 55 citedOpen Access
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Science·2024· 40 citedOpen Access
Single-cell multi-cohort dissection of the schizophrenia transcriptome
Science·2024· 108 citedOpen Access
A data-driven single-cell and spatial transcriptomic map of the human prefrontal cortex
Science·2024· 61 citedOpen Access
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Frequent Co-authors

Mark Gerstein(26), Alexander E. Urban(15), Flora M. Vaccarino(15), Taejeong Bae(13), Schahram Akbarian(11), Bo Zhou(9), Andrew Chess(9), Reenal Pattni(8), Christopher A. Walsh(8), Yifan Wang(8), M Snyder(7), Declan Clarke(7), Jessica Mariani(7), Gianfilippo Coppola(7), Livia Tomasini(7), Daniel R. Weinberger(7), Thomas M. Hyde(7), Daniel H. Geschwind(7), Nenad Šestan(7), Andrew E. Jaffe(7)