PubRank

N A Doggett

Author PubWeight™ 75.29‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature 2001 10.96
2 Comparison of human genetic and sequence-based physical maps. Nature 2001 4.97
3 Physical mapping of human chromosomes by repetitive sequence fingerprinting. Proc Natl Acad Sci U S A 1990 2.57
4 The relationship between chromosome structure and function at a human telomeric region. Nat Genet 1997 2.48
5 A case for evolutionary genomics and the comprehensive examination of sequence biodiversity. Mol Biol Evol 2000 2.07
6 MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3). Proc Natl Acad Sci U S A 1997 2.01
7 Efficient pooling designs for library screening. Genomics 1995 1.97
8 Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution. Hum Mol Genet 1996 1.93
9 A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers. Genes Chromosomes Cancer 1998 1.79
10 All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders. Blood 1997 1.71
11 Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Hum Mol Genet 1997 1.70
12 Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat. Cell 1997 1.55
13 Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science 1994 1.51
14 Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16. Hum Mol Genet 2001 1.32
15 Construction of a BAC contig map of chromosome 16q by two-dimensional overgo hybridization. Genome Res 2000 1.32
16 A PCR-based genetic linkage map of human chromosome 16. Genomics 1994 1.22
17 Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci. Genomics 1993 1.16
18 Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3. Genomics 1997 1.15
19 A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2. Genome Res 1999 1.14
20 Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12. Genomics 1995 1.07
21 The genomic organization of the Fanconi anemia group A (FAA) gene. Genomics 1997 1.05
22 Chromosomal localization of the human and mouse hyaluronan synthase genes. Genomics 1997 1.02
23 High-resolution cytogenetic-based physical map of human chromosome 16. Genomics 1992 1.01
24 Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene. Genomics 1998 1.00
25 Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions. Genomics 1998 1.00
26 Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3. Genomics 1997 0.98
27 Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28. Genomics 1996 0.98
28 Identification of Alu-mediated deletions in the Fanconi anemia gene FAA. Hum Mutat 1998 0.97
29 Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer. Genomics 1998 0.95
30 A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groups. Genomics 1997 0.93
31 Cytological and molecular characterization of centromeres in Mus domesticus and Mus spretus. Mamm Genome 1992 0.93
32 Construction of human chromosome 16- and 5-specific circular YAC/BAC libraries by in vivo recombination in yeast (TAR cloning). Genomics 1998 0.93
33 The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer. Genomics 1999 0.90
34 Mouse MutS homolog 4 is predominantly expressed in testis and interacts with MutS homolog 5. Mamm Genome 2001 0.90
35 Construction of a cosmid library of DNA replicated early in the S phase of normal human fibroblasts. J Cell Biochem 2000 0.88
36 Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene. Hum Mol Genet 1998 0.88
37 Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer. Genomics 1998 0.88
38 Chromosome 16-specific repetitive DNA sequences that map to chromosomal regions known to undergo breakage/rearrangement in leukemia cells. Genomics 1992 0.87
39 Evaluation of a cosmid contig physical map of human chromosome 16. Genomics 1992 0.87
40 Identification and characterization of the mouse MutS homolog 5: Msh5. Mamm Genome 1999 0.86
41 Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3. Cytogenet Cell Genet 1995 0.85
42 Refined physical mapping of chromosome 16-specific low-abundance repetitive DNA sequences. Cytogenet Cell Genet 1993 0.83
43 Dinucleotide repeat polymorphisms at the D16S525, D16S359, D16S531 and D16S522 loci. Hum Mol Genet 1994 0.82
44 A matrix associated region localizes the human SOCS-1 gene to chromosome 16p13.13. Somat Cell Mol Genet 1998 0.81
45 Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein. Neuropediatrics 1997 0.81
46 Extended analysis of the region encompassing the PRM1-->PRM2-->TNP2 domain: genomic organization, evolution and gene identification. J Exp Zool 1998 0.80
47 Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3. Genome Res 1998 0.80
48 Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3. Genomics 1997 0.80
49 Genomic organization and DNA sequence of the human catecholamine-sulfating phenol sulfotransferase gene (STM). Biochem Biophys Res Commun 1994 0.78
50 Physical map of the region containing the gene for Batten disease (CLN3). Am J Med Genet 1995 0.78
51 Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten disease. Biochem Biophys Res Commun 1994 0.78
52 Four dinucleotide repeat polymorphisms on human chromosome 16. Hum Mol Genet 1993 0.78
53 Genomic organization and the 5' flanking region of the gamma subunit of the human amiloride-sensitive epithelial sodium channel. J Biol Chem 1996 0.78
54 ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors. Genomics 1998 0.77
55 The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Res 1996 0.76
56 Five dinucleotide repeat polymorphisms on human chromosome 16q24.2-q24.3. Hum Mol Genet 1993 0.75
57 Three dinucleotide repeat polymorphisms on human chromosome 16p13.11-p13.3. Hum Mol Genet 1993 0.75
58 Vector for high-throughput sequencing: construction and preparation with cyclic cut-ligation. Biotechniques 2001 0.75
59 Phenol sulfotransferases: candidate genes for Batten disease. Am J Med Genet 1995 0.75
60 An analysis of the distribution and dose response of chromosome aberrations in human lymphocytes after in vitro exposure to 137Cesium gamma radiation. Radiat Environ Biophys 1983 0.75
61 Microsatellite repeat polymorphism at the D16S366 locus. Hum Mol Genet 1994 0.75
62 Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1. Hum Mol Genet 1993 0.75
63 Isolation of genes from the Batten candidate region using exon amplification. Batten Disease Consortium. Am J Med Genet 1995 0.75
64 In situ hybridization mapping of human chromosome 16: evidence for a high frequency of repetitive DNA sequences. Cytogenet Cell Genet 1994 0.75