(top 60%)
Impact Factor
(top 60%)
extended IF
56(top 7%)
H-Index
182
authors
934
papers
18.1K
citations
2K
citing journals
6K
citing authors

Most Cited Articles of Somatic Cell and Molecular Genetics

TitleYearCitations
Isolation and genetic characterization of human KB cell lines resistant to multiple drugs1985413
Sonoporation: mechanical DNA delivery by ultrasonic cavitation2002274
Molecular analysis and chromosomal mapping of amplified genes isolated from a transformed mouse 3T3 cell line1987258
Fractionation of large mammalian DNA restriction fragments using vertical pulsed-field gradient gel electrophoresis1986236
Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy1990226
Histochemical staining of clonal mammalian cell lines expressing E. coli beta galactosidase indicates heterogeneous expression of the bacterial gene1987211
Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat1994210
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins1998207
Effect of gamma rays at the dihydrofolate reductase locus: deletions and inversions1986193
Transforming growth factor beta gene maps to human chromosome 19 long arm and to mouse chromosome 71986170
Factors involved in production of helper virus-free retrovirus vectors1986153
Expression of the receptor for epidermal growth factor correlates with increased dosage of chromosome 7 in malignant melanoma1985150
Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations1986138
HIV-1 replication2001135
Cell cycle-dependent repair of double-strand DNA breaks in a gamma-ray-sensitive Chinese hamster cell1985135
High-frequency transfection of CHO cells using polybrene1986131
Interleukin 2 (IL2) is assigned to human chromosome 41984129
Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations1990124
Identification of two complementation groups in Fanconi anemia1985122
Selection of highly transfectable variant from mouse mastocytoma P8151985118
A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids1989116
Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules1993106
Sequence specificity of mutations induced by benzo[a]pyrene-7,8-diol-9,10-epoxide at endogenous aprt gene in CHO cells1988104
Organization of the HPRT gene and related sequences in the human genome198497
Gene targeting using a mouse HPRT minigene/HPRT-deficient embryonic stem cell system: inactivation of the mouse ERCC-1 gene199295