ИЛ
И. Н. Лебедев

Highly Cited


285
Works
1,432
Citations
19
H-Index
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Author Statistics

И. Н. Лебедев

Also known as: I Lebedev, I N Lebedev, I. Lebedev, I. N Lebedev, I. N. Lebedev

285

Total Works

1,432

Citations

19

H-Index

41

i10-Index

Citation & Works Trend by Year
27 years active
Top Research Topics
Genomic variations and chromosomal abnormalities (137) Prenatal Screening and Diagnostics (73) Epigenetics and DNA Methylation (66) Genetic Syndromes and Imprinting (56) Genomics and Rare Diseases (46)
Recent Publications
15 shown
Year Publication Title Citations Action
2026 Role of CNTN6 in neurodevelopment and neuropathology Frontiers in Neuroscience 1
2026 Novel Biallelic Variants in IQSEC1 in a Patient With Intellectual Developmental Disorder With Short Stature and Behavioral Abnormalities ( IDDSSBA ) and Corpus Callosum Dysgenesis American Journal of Medical Genetics Part A 0
2025 Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X Journal of Assisted Reproduction and Genetics 0
2025 Biop-C enables genome-wide detection of balanced and unbalanced rearrangements in preimplantation human embryos Research Square 0
2025 Genomics of pregnancy loss Journal of Assisted Reproduction and Genetics 1
2025 A novel role for the CNTN6 locus in lumenization and radial glial cell fate determination during early human cortical development revealed in cerebral organoids bioRxiv (Cold Spring Harbor Laboratory) 0
2025 A familial case of interstitial deletion of the short arm of chromosome 6p22.3-p24.3 in twins with severe delay in psychomotor and speech development Vavilov Journal of Genetics and Breeding 0
2025 A family case of a rare Xq28 duplication Vavilov Journal of Genetics and Breeding 1
2025 Embryoid bodies as a model system for exploring early human embryonic development Journal of Assisted Reproduction and Genetics 4
2025 Methylation index of the DLK1 and MKRN3 genes in precocious puberty Vavilov Journal of Genetics and Breeding 0
2025 Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants Genome Medicine 4
2025 Genetic variants of the DLK1, KISS1R, MKRN3 genes in girls with precocious puberty Vavilov Journal of Genetics and Breeding 1
2025 The chromosomal challenge of human embryos: Mechanisms and fundamentals Human Genetics and Genomics Advances 3
2025 A variant of p.Arg1623Gln of the DYNC1H1 gene in a patient with corpus callosum agenesis, polydactyly, mental development disorder, and neuromuscular system disorders S S Korsakov Journal of Neurology and Psychiatry 0
2025 Copy number variations in spontaneous abortions: a meta-analysis Journal of Assisted Reproduction and Genetics 5

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