S L Naylor

Author PubWeight™ 355.10‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Initial sequencing and analysis of the human genome. Nature 2001 212.86
2 A polymorphic DNA marker genetically linked to Huntington's disease. Nature 1984 16.71
3 Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 2001 7.34
4 Structure and variability of human chromosome ends. Mol Cell Biol 1990 6.18
5 Human lymphotoxin and tumor necrosis factor genes: structure, homology and chromosomal localization. Nucleic Acids Res 1985 5.22
6 Mapping the human genome, cloned genes, DNA polymorphisms, and inherited disease. Adv Hum Genet 1982 3.04
7 Human apolipoprotein B-100: cloning, analysis of liver mRNA, and assignment of the gene to chromosome 2. Proc Natl Acad Sci U S A 1985 2.53
8 Structure of the human and murine R-ras genes, novel genes closely related to ras proto-oncogenes. Cell 1987 2.36
9 Chromosome localization in normal human cells and neuroblastomas of a gene related to c-myc. Nature 1984 2.32
10 High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization. Proc Natl Acad Sci U S A 1983 1.87
11 Human transferrin: cDNA characterization and chromosomal localization. Proc Natl Acad Sci U S A 1984 1.85
12 Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes. Adv Cancer Res 1997 1.81
13 Human immune interferon gene is located on chromosome 12. J Exp Med 1983 1.64
14 PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids. Genomics 1991 1.58
15 Molecular cloning of cDNAs encoding the human bombesin-like peptide neuromedin B. Chromosomal localization and comparison to cDNAs encoding its amphibian homolog ranatensin. J Biol Chem 1988 1.58
16 Human group-specific component (Gc) is a member of the albumin family. Proc Natl Acad Sci U S A 1985 1.44
17 Loss of heterozygosity in breast cancer: cause or effect? J Natl Cancer Inst 1989 1.38
18 Localization of the human prealbumin gene to chromosome 18. Biochem Biophys Res Commun 1985 1.32
19 Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography. Proc Natl Acad Sci U S A 1978 1.28
20 Clustering of leukocyte and fibroblast interferon genes of human chromosome 9. Science 1982 1.27
21 Mapping of aminoacylase-1 and beta-galactosidase-A to homologous regions of human chromosome 3 and mouse chromosome 9 suggests location of additional genes. Am J Hum Genet 1982 1.27
22 Definition of a tumor suppressor locus within human chromosome 3p21-p22. Proc Natl Acad Sci U S A 1992 1.24
23 Chromosome assignments of four mouse cellular homologs of sarcoma and leukemia virus oncogenes. Proc Natl Acad Sci U S A 1984 1.23
24 DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. Proc Natl Acad Sci U S A 1984 1.22
25 Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancer. Genomics 1996 1.21
26 Localization of human U1 small nuclear RNA genes to band p36.3 of chromosome 1 by in situ hybridization. Somat Cell Mol Genet 1984 1.19
27 Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5. Proc Natl Acad Sci U S A 1991 1.17
28 A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity. Oncogene 1993 1.16
29 Human parathyroid hormone gene (PTH) is on short arm of chromosome 11. Somatic Cell Genet 1983 1.16
30 PHC3, a component of the hPRC-H complex, associates with E2F6 during G0 and is lost in osteosarcoma tumors. Oncogene 2006 1.14
31 Detection of a length polymorphism for human GIP gene by polymerase chain reaction. Nucleic Acids Res 1991 1.14
32 Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer. Cancer Res 1990 1.11
33 Human c-Ki-ras2 proto-oncogene on chromosome 12. Science 1983 1.11
34 Two nonallelic tRNAiMet genes are located in the p23 leads to q12 region of human chromosome 6. Proc Natl Acad Sci U S A 1983 1.07
35 A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A. Pain 1998 1.07
36 Human apolipoprotein A-I and C-III genes reside in the p11----q13 region of chromosome 11. Biochem Biophys Res Commun 1984 1.06
37 Characterization, mapping, and expression of the human ceruloplasmin gene. Proc Natl Acad Sci U S A 1986 1.06
38 Polymorphic human somatostatin gene is located on chromosome 3. Proc Natl Acad Sci U S A 1983 1.02
39 Two novel human serine/threonine kinases with homologies to the cell cycle regulating Xenopus MO15, and NIMA kinases: cloning and characterization of their expression pattern. Oncogene 1994 1.01
40 Bioautographic visualization of aminoacylase-1: assignment of the structural gene ACY-1 to chromosome 3 in man. Somatic Cell Genet 1979 1.01
41 Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse. Somatic Cell Genet 1983 0.99
42 Isolation, characterization, and mapping of a human acid beta-galactosidase cDNA. DNA Cell Biol 1990 0.98
43 The human apolipoprotein A-II gene is located on chromosome 1. Biochem Biophys Res Commun 1984 0.97
44 Promise and challenge: Markers of prostate cancer detection, diagnosis and prognosis. Dis Markers 2004 0.96
45 Physical and functional mapping of a tumor suppressor locus for renal cell carcinoma within chromosome 3p12. Cancer Res 1998 0.96
46 Human renin gene is on chromosome 1. Somat Cell Mol Genet 1984 0.96
47 A single Cys706 to Phe substitution in the retinoblastoma protein causes the loss of binding to SV40 T antigen. Cell Growth Differ 1990 0.96
48 Retention of chromosome 3 in extrapulmonary small cell cancer shown by molecular and cytogenetic studies. J Natl Cancer Inst 1989 0.95
49 Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man. Proc Natl Acad Sci U S A 1984 0.94
50 Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2. Genomics 1999 0.93
51 Human ferritin H and L sequences lie on ten different chromosomes. Hum Genet 1987 0.93
52 Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesis. Cancer Res 1997 0.93
53 Specific expression of the annexin VIII gene in acute promyelocytic leukemia. Blood 1992 0.92
54 Human and mouse cellular myc protooncogenes reside on chromosomes involved in numerical and structural aberrations in cancer. Somatic Cell Genet 1983 0.92
55 Use of the single strand conformation polymorphism technique and PCR to detect p53 gene mutations in small cell lung cancer. Oncogene 1991 0.92
56 Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region. Genes Chromosomes Cancer 1997 0.92
57 Cell attachment to collagen. Isolation of a cell attachment mutant. Exp Cell Res 1977 0.91
58 A sequence homologous to Rous sarcoma virus v-src Is on human chromosome 20. Prog Nucleic Acid Res Mol Biol 1983 0.91
59 Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3. Am J Hum Genet 2000 0.90
60 Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumors. J Clin Invest 1988 0.90
61 Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme. Genomics 1989 0.90
62 Report of the committee on the genetic constitution of chromosome 3. Cytogenet Cell Genet 1989 0.90
63 The localization of the gene for apolipoprotein C-II to chromosome 19. Biochem Biophys Res Commun 1984 0.90
64 In situ hybridization of metaphase and prometaphase chromosomes. Methods Enzymol 1987 0.90
65 An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivo. Oncogene 1996 0.90
66 Organization of rDNA spacer fragment variants among human acrocentric chromosomes in somatic cell hybrids. J Mol Appl Genet 1983 0.90
67 Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR. Genomics 1993 0.90
68 Characterization of the mouse loricrin gene: linkage with profilaggrin and the flaky tail and soft coat mutant loci on chromosome 3. Genomics 1994 0.89
69 Dinucleotide repeat polymorphism in the human surfactant-associated protein 3 gene (SFTP3). Nucleic Acids Res 1991 0.89
70 Report and abstracts of the fifth international workshop on human chromosome 3 mapping 1994. Ann Arbor, Michigan, May 8-9, 1994. Cytogenet Cell Genet 1995 0.88
71 Human ApoB-100 gene resides in the p23----pter region of chromosome 2. Biochem Biophys Res Commun 1985 0.88
72 Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9. Somat Cell Mol Genet 1987 0.88
73 A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3. Eur J Hum Genet 1999 0.87
74 Report of the committee on the genetic constitution of chromosomes 5 and 6. Cytogenet Cell Genet 1987 0.86
75 Chromosomal assignments of genes for trypsin, chymotrypsin B, and elastase in mouse. Somat Cell Mol Genet 1984 0.85
76 Biochemical selection systems for mammalian cells: the essential amino acids. Somatic Cell Genet 1976 0.84
77 Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms. Biochem Biophys Res Commun 1986 0.84
78 Mapping of the DNA locus D4S10 and the linked Huntington's disease gene to 4p16----p15. Cytogenet Cell Genet 1986 0.84
79 Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse. Somat Cell Mol Genet 1987 0.84
80 Regional assignment of human protooncogene c-myb to 6q21----qter. Somat Cell Mol Genet 1984 0.84
81 Bioautography of cell attachment proteins. Exp Cell Res 1978 0.84
82 Assignment of the gene for carboxypeptidase A to human chromosome 7q22----qter and to mouse chromosome 6. Hum Genet 1986 0.83
83 Human insulin-related DNA sequences map to chromosomes 2 and 11. Somat Cell Mol Genet 1986 0.83
84 The human apoB-100 gene: apoB-100 is encoded by a single copy gene in the human genome. Biochem Biophys Res Commun 1987 0.83
85 Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map. Genomics 1993 0.83
86 Report of the committee on the genetic constitution of chromosome 3. Cytogenet Cell Genet 1990 0.82
87 Assignment of SAFB encoding Hsp27 ERE-TATA binding protein (HET)/scaffold attachment factor B (SAF-B) to human chromosome 19 band p13. Cytogenet Cell Genet 1997 0.82
88 An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers. Genomics 1999 0.82
89 cDNA sequence, interspecies comparison, and gene mapping analysis of argininosuccinate lyase. Genomics 1989 0.81
90 cDNAs encoding members of a family of proteins related to human sterol carrier protein 2 and assignment of the gene to human chromosome 1 p21----pter. DNA Cell Biol 1991 0.81
91 Report of the Third International Workshop on Human Chromosome 8 Mapping. San Antonio, Texas, October 25-27, 1996. Cytogenet Cell Genet 1996 0.81
92 Report of the committee on the genetic constitution of chromosome 3. Cytogenet Cell Genet 1988 0.80
93 Mouse immune interferon (IFN-gamma) gene is on chromosome 10. Somat Cell Mol Genet 1984 0.80
94 Sigje, a member of the small inducible gene family that includes platelet factor 4 and melanoma growth stimulatory activity, is on mouse chromosome 11. Cytogenet Cell Genet 1989 0.80
95 Regional localization of two human cellular Kirsten ras genes on chromosomes 6 and 12. Mol Cell Biol 1984 0.80
96 Chromosomal assignments of human genes for serine proteases trypsin, chymotrypsin B, and elastase. Somat Cell Mol Genet 1984 0.80
97 Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients. Am J Med Genet 1998 0.80
98 Genetic structure and chromosomal mapping of MyD88. Genomics 1997 0.80
99 Mouse UDP-GlcNAc: dolichyl-phosphate N-acetylglucosaminephosphotransferase. Molecular cloning of the cDNA, generation of anti-peptide antibodies and chromosomal localization. Biochem J 1992 0.80
100 Assignment of xeroderma pigmentosum group C (XPC) gene to chromosome 3p25. Genomics 1994 0.80
101 Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1. Biochem Biophys Res Commun 1985 0.79
102 Characterization of naturally occurring auxotrophic mammalian cells. Somatic Cell Genet 1979 0.79
103 Linkage of cystic fibrosis locus and polymorphic DNA markers in 14 families. Am J Hum Genet 1986 0.79
104 Assignment of the gene for human tetranectin (TNA) to chromosome 3p22-->p21.3 by somatic cell hybrid mapping. Cytogenet Cell Genet 1997 0.79
105 Localization of mouse melanoma growth stimulatory activity gene (Mgsa) between Afp and Gus on chromosome 5 using interspecific backcross mice. Cytogenet Cell Genet 1990 0.78
106 Bioautography: a general method for the visualization of isozymes. Biochem Genet 1977 0.78
107 Chromosomal assignments of human 27-kDa heat shock protein gene family. Somat Cell Mol Genet 1989 0.78
108 Structural characterization and fine chromosomal mapping of the human P2Y1 purinergic receptor gene (P2RY1). Somat Cell Mol Genet 1996 0.78
109 Human gastrin-releasing peptide gene is located on chromosome 18. Somat Cell Mol Genet 1987 0.78
110 Structure and chromosomal localization of the human lymphotoxin gene. J Cell Biochem 1985 0.77
111 Mapping thyrotropin beta subunit gene in man and mouse. Somat Cell Mol Genet 1986 0.77
112 Mouse melanoma growth stimulatory activity gene (Mgsa) is polymorphic and syntenic with the W, patch, rumpwhite, and recessive spotting loci on chromosome 5. Genomics 1989 0.77
113 Mapping of the gene encoding the regulatory subunit RII alpha of cAMP-dependent protein kinase (locus PRKAR2A) to human chromosome region 3p21.3-p21.2. Genomics 1998 0.76
114 Assignment of retinoblastoma susceptibility gene to mouse chromosome 14. Somat Cell Mol Genet 1989 0.76
115 Dinucleotide repeat polymorphism in the human tubulin alpha 1 (testis specific) gene (TUBA1). Nucleic Acids Res 1991 0.75
116 Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectively. Somat Cell Mol Genet 1988 0.75
117 Dinucleotide repeat polymorphism in the human interleukin 1, alpha gene (IL1A). Nucleic Acids Res 1991 0.75
118 Regional mapping of unique DNA sequences from human chromosome 3 derived from a flow-sorted chromosome library. Cytogenet Cell Genet 1988 0.75
119 A human c-src gene resides on the proximal long arm of chromosome 20 (cen----q131). Cancer Genet Cytogenet 1985 0.75
120 Branched-chain aminotransferase deficiency in Chinese hamster cells complemented by two independent genes on human chromosomes 12 and 19. Somatic Cell Genet 1980 0.75
121 Dinucleotide repeat polymorphism (D3S1776) on human chromosome 3p. Hum Mol Genet 1994 0.75
122 Bioautographic visualization of enzymes. Isozymes Curr Top Biol Med Res 1980 0.75
123 Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization. Biochem Biophys Res Commun 1997 0.75
124 Bioautographic visualization of dihydrofolate reductase in enzyme overproducing BHK mutants. Biochem Genet 1980 0.75
125 Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22. Cancer Genet Cytogenet 1996 0.75
126 New chromosomal mapping assignments for argininosuccinate synthetase pseudogene 1, interferon-beta 3 gene, and the diazepam binding inhibitor gene. Somat Cell Mol Genet 1992 0.75
127 Workshop on mapping by somatic cell hybridization. Prog Clin Biol Res 1982 0.75
128 Dinucleotide repeat polymorphisms at the D2S108 and D2S109 loci. Hum Mol Genet 1993 0.75
129 Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene. Hum Mol Genet 1997 0.75
130 Report of the First International Workshop on Human Chromosome 2 mapping 1991. Cytogenet Cell Genet 1992 0.75