PubRank

U Tantravahi

Author PubWeight™ 46.89‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A strategy to reveal high-frequency RFLPs along the human X chromosome. Am J Hum Genet 1984 7.73
2 Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Res 1982 4.67
3 Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions. EMBO J 1990 4.49
4 Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 1986 4.13
5 Homology of lubricin and superficial zone protein (SZP): products of megakaryocyte stimulating factor (MSF) gene expression by human synovial fibroblasts and articular chondrocytes localized to chromosome 1q25. J Orthop Res 2001 1.87
6 A novel alteration in the structure of an activated c-myc gene in a variant t(2;8) Burkitt lymphoma. Cell 1984 1.74
7 A microsatellite genetic linkage map of human chromosome 13. Genomics 1993 1.57
8 A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis. Genomics 1991 1.55
9 Identification and isolation of transcribed human X chromosome DNA sequences. Nucleic Acids Res 1983 1.45
10 Amplified ribosomal RNA genes in a rat hepatoma cell line are enriched in 5-methylcytosine. Proc Natl Acad Sci U S A 1981 1.44
11 Overexpression of the HER-2/neu oncogene in pancreatic adenocarcinoma. Am J Clin Oncol 2001 1.22
12 High resolution analysis of the timing of replication of specific DNA sequences during S phase of mammalian cells. Nucleic Acids Res 1983 1.11
13 Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center. Hum Genet 1983 1.05
14 Isolation and characterization of two repetitive DNA fragments located near the centromere of the mouse X chromosome. Cytogenet Cell Genet 1985 0.99
15 Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis. Cytogenet Cell Genet 1986 0.88
16 Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis. Am J Hum Genet 1989 0.87
17 Parental imprinting of an Igf-2 transgene. Mol Reprod Dev 1993 0.86
18 46,XX gonadal agenesis in a neonate with multiple congenital anomalies: case report and review of the literature. Pediatr Pathol 1995 0.83
19 DNA methylation patterns of human pachytene spermatocytes. Exp Cell Res 1982 0.82
20 Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy. Neurology 1990 0.81
21 Characterization of microsatellite polymorphisms DXS691 and DXS692: genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2. Genomics 1993 0.81
22 5alpha-reductase 1 and 2 expression and activity in human ovarian follicles, stroma and corpus luteum as compared to neonatal foreskin. J Steroid Biochem Mol Biol 1996 0.80
23 Applications of fluorescence spectroscopy to molecular cytogenetics. Biopolymers 1985 0.79
24 Bilateral semilunar valve dysplasia in a patient with inverted duplication 2p25-22. Pediatr Cardiol 2007 0.79
25 Regional localization of 32 NotI-HindIII fragments from a human chromosome 13 library by a somatic cell hybrid panel and in situ hybridization. Genomics 1993 0.78
26 Biological effects of a bifunctional DNA crosslinker. I. Generation of triradial and quadriradial chromosomes. Mutat Res 1999 0.78
27 Evidence for methylation of inactive human rRNA genes in amplified regions. Hum Genet 1981 0.77
28 Inhibins and activins in human fetal abnormalities. Mol Cell Endocrinol 2004 0.76
29 Molecular analysis of inhibin A and activin A subunit gene loci in epithelial ovarian cancer. Int J Gynecol Cancer 2002 0.76
30 Use of Y chromosome specific probes to detect low level sex chromosome mosaicism. Clin Genet 1986 0.75
31 Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1. Somat Cell Mol Genet 1994 0.75
32 Homogeneously staining regions (HSRs) of a rat hepatoma cell line are not early replicating. Exp Cell Res 1985 0.75
33 Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22. Hereditas 1989 0.75
34 The rat XC sarcoma cell line: ribosomal RNA gene amplification and banded karyotype. Cancer Genet Cytogenet 1982 0.75
35 Correspondence between effects of 5-azacytidine on SCE formation, cell cycling and DNA methylation in Chinese hamster cells. Mutat Res 1985 0.75
36 Biological effects of a bifunctional DNA cross-linker. II. Generation of micronuclei and attached micronuclear-like structures. Mutat Res 1999 0.75
37 Molecular genetic approaches to human diseases involving mental retardation. Am J Ment Defic 1984 0.75
38 Immunocytochemical evidence for methylation of the inactive X chromosome in human fetal oogonia. Proc Soc Exp Biol Med 1987 0.75
39 Repeated DNA sequences in the distal long arm of the human X chromosome. Hum Genet 1986 0.75