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Articles in Scholarly Journals [Incomplete List]

1. Cancer genome sequencing: The challenges ahead
   BioEssays, vol. 29, no. 8, pp. 783–794, 2007
2. Dynamic stromal-epithelial interactions during progression of MCF10DCIS.com xenografts
   International Journal of Cancer, vol. 120, no. 10, pp. 2127–2134, 2007
3. Elimination of altered karyotypes by sexual reproduction preserves species identity
   Genome, vol. 50, no. 5, pp. 517–524, 2007
4. Mitotic Cell Death by Chromosome Fragmentation
   Cancer Research, vol. 67, no. 16, pp. 7686–7694, 2007
5. Clonal and non-clonal chromosome aberrations and genome variation and aberration
   Genome, vol. 49, no. 3, pp. 195–204, 2006
6. Combined multicolor-FISH and immunostaining
   Cytogenetic and Genome Research, vol. 114, no. 3-4, pp. 227–234, 2006
7. Stochastic cancer progression driven by non-clonal chromosome aberrations
   Journal of Cellular Physiology, vol. 208, no. 2, pp. 461–472, 2006
8. Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination
   The American Journal of Human Genetics, vol. 77, no. 6, pp. 966–987, 2005
9. ATM and p21 Cooperate to Suppress Aneuploidy and Subsequent Tumor Development
   Cancer Research, vol. 65, no. 19, pp. 8747–8753, 2005
10. Overexpression of Cyclin D1 Promotes Tumor Cell Growth and Confers Resistance to Cisplatin-Mediated Apoptosis in an Elastase-myc Transgene-Expressing Pancreatic Tumor Cell Line
    Clinical Cancer Research, vol. 11, no. 16, pp. 6075–6086, 2005
11. Sequential Molecular and Cellular Events during Neoplastic Progression: A Mouse Syngeneic Ovarian Cancer Model
    Neoplasia, vol. 7, no. 10, pp. 944–956, 2005
12. Imaging genome abnormalities in cancer research
    Cell & Chromosome, vol. 3, no. 1, p. 1, 2004
13. Chromatin loops are selectively anchored using scaffold/matrix-attachment regions
    Journal of Cell Science, vol. 117, no. 7, pp. 999–1008, 2004
14. Complexity of CNC Transcription Factors As Revealed by Gene Targeting of the Nrf3 Locus
    Molecular and Cellular Biology, vol. 24, no. 8, pp. 3286–3294, 2004
15. Male mouse meiotic chromosome cores deficient in structural proteins SYCP3 and SYCP2 align by homology but fail to synapse and have possible impaired specificity of chromatin loop attachment
    Cytogenetic and Genome Research, vol. 105, no. 2-4, pp. 182–188, 2004
16. SV40 T antigen interacts with Nbs1 to disrupt DNA replication control
    Genes & Development, vol. 18, no. 11, pp. 1305–1316, 2004
17. Corrigendum to “The hyaluronidase gene HYAL1 maps to chromosome 3p21.2–p21.3 in human and 9F1–F2 in mouse, a conserved candidate tumor suppressor locus” [Genomics 48 (1998) 63–70]
    Genomics, vol. 84, no. 1, p. 227, 2004
18. From DNA structure to gene expression: mediators of nuclear compartmentalization and dynamics
    Chromosome Research, vol. 11, no. 5, pp. 435–445, 2003
19. Analysis of marker or complex chromosomal rearrangements present in pre- and post-natal karyotypes utilizing a combination of G-banding, spectral karyotyping and fluorescence in situ hybridization
    Clinical Genetics, vol. 63, no. 5, pp. 358–367, 2003
20. Human Chromosome 7: DNA Sequence and Biology
    Science, vol. 300, no. 5620, pp. 767–772, 2003
21. Alternative promoters and polyadenylation regulate tissue-specific expression ofHemogen isoforms during hematopoiesis and spermatogenesis
    Developmental Dynamics, vol. 228, no. 4, pp. 606–616, 2003
22. Circling, Deafness, and Yellow Coat Displayed by Yellow Submarine (Ysb) and Light Coat and Circling (Lcc) Mice with Mutations on Chromosome 3
    Genomics, vol. 79, no. 6, pp. 777–784, 2002
23. Sperm nuclear matrix association of the PRM1->PRM2->TNP2 domain is independent of Alu methylation
    Molecular Human Reproduction, vol. 7, no. 10, pp. 903–911, 2001
24. Association of deletions and translocation of the reduced folate carrier gene with profound loss of gene expression in methotrexate-resistant K562 human erythroleukemia cells
    Biochemical Pharmacology, vol. 61, no. 6, pp. 665–675, 2001
25. Spectral karyotyping (SKY) of mouse meiotic chromosomes
    Genome, vol. 44, no. 2, pp. 293–298, 2001
26. Re-defining the chromatin loop domain
    Cytogenetic and Genome Research, vol. 93, no. 3-4, pp. 155–161, 2001
27. The combination of SKY and specific loci detection with FISH or immunostaining
    Cytogenetic and Genome Research, vol. 93, no. 3-4, pp. 195–202, 2001
28. Spectral karyotyping of mouse cell line WMP2
    Cytogenetic and Genome Research, vol. 90, no. 3-4, pp. 271–274, 2000
29. Cloning and characterization of additional members of the G protein-coupled receptor family
    Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1490, no. 3, pp. 311–323, 2000
30. Identification of the mouse β`-COP golgi component as a spermatocyte autoantigen in scleroderma and mapping of its gene Copb2 to mouse Chromosome 9
    Cytogenetic and Genome Research, vol. 87, no. 3-4, pp. 201–204, 1999
31. Identification of a Human Histone Acetyltransferase Related to Monocytic Leukemia Zinc Finger Protein
    Journal of Biological Chemistry, vol. 274, no. 40, pp. 28528–28536, 1999
32. Identification and cloning of three novel human G protein-coupled receptor genes GPR52, ?GPR53 and GPR55: GPR55 is extensively expressed in human brain
    Molecular Brain Research, vol. 64, no. 2, pp. 193–198, 1999
33. Nontargeted Stable Integration of Recombinant Adeno-Associated Virus into Human Leukemia and Lymphoma Cell Lines as Evaluated by Fluorescence in Situ Hybridization
    Human Gene Therapy, vol. 10, no. 4, pp. 537–543, 1999
34. Discovery of Three Novel Orphan G-Protein-Coupled Receptors
    Genomics, vol. 56, no. 1, pp. 12–21, 1999
35. Cloning and Expression Analysis of a Novel WD Repeat Gene, WDR3, Mapping to 1p12–p13
    Genomics, vol. 59, no. 1, pp. 85–89, 1999
36. The Hyaluronidase Gene HYAL1 Maps to Chromosome 3p21.2–p21.3 in Human and 9F1–F2 in Mouse, a Conserved Candidate Tumor Suppressor Locus,
    Genomics, vol. 48, no. 1, pp. 63–70, 1998
37. Discovery of Three Novel G-Protein-Coupled Receptor Genes
    Genomics, vol. 47, no. 2, pp. 310–313, 1998
38. Mapping of the HumanHPRP3andHPRP4Genes Encoding U4/U6-Associated Splicing Factors to Chromosomes 1q21.1 and 9q31–q33,
    Genomics, vol. 48, no. 2, pp. 273–275, 1998
39. Cloning Genes Encoding Receptors Related to Chemoattractant Receptors
    Genomics, vol. 50, no. 2, pp. 281–286, 1998
40. Aquarius, a novel gene isolated by gene trapping with an RNA-dependent RNA polymerase motif
    Developmental Dynamics, vol. 212, no. 2, pp. 304–317, 1998
41. Chromosomal mapping and expression of the human B120 gene
    Gene, vol. 213, no. 1-2, pp. 189–193, 1998
42. Assignment of the Gene Encoding the Limbic System-Associated Membrane Protein (LAMP) to Mouse Chromosome 16B5 and Human Chromosome 3q13.2–q21?
    Genomics, vol. 49, no. 3, pp. 472–474, 1998
43. Structure and mapping of the human ß-defensin HBD-2 gene and its expression at sites of inflammation
    Gene, vol. 222, no. 2, pp. 237–244, 1998
44. Assignment of Mouse Fibroblast Growth Factor 10 (Fgf10) Gene to the Telomeric Region of Chromosome 13
    Genomics, vol. 53, no. 2, pp. 247–248, 1998
45. Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria
    Proceedings of the National Academy of Sciences, vol. 95, no. 6, pp. 3059–3064, 1998
46. High resolution free chromatin/DNA fiber fluorescent in situ hybridization
    Journal of Chromatography A, vol. 806, no. 1, pp. 219–229, 1998
47. Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis
    Mechanisms of Development, vol. 78, no. 1-2, pp. 81–84, 1998
48. Rad51 immunocytology in rat and mouse spermatocytes and oocytes
    Chromosoma, vol. 106, no. 4, pp. 207–215, 1997
49. Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14
    Mammalian Genome, vol. 8, no. 2, pp. 159–160, 1997
50. Fish technology in chromosome and genome research
    BioEssays, vol. 19, no. 1, pp. 75–84, 1997
51. The Human ß-Defensin-1 and a-Defensins Are Encoded by Adjacent Genes: Two Peptide Families with Differing Disulfide Topology Share a Common Ancestry,
    Genomics, vol. 43, no. 3, pp. 316–320, 1997
52. Assignment of the Human dUTPase Gene (DUT) to Chromosome 15q15–q21.1 by Fluorescencein SituHybridization
    Genomics, vol. 40, no. 1, pp. 213–215, 1997
53. Expression Analysis and Chromosomal Assignment of the HumanSFRS5/SRp40Gene
    Genomics, vol. 43, no. 2, pp. 165–170, 1997
54. Cloning and chromosomal mapping of four putative novel human G-protein-coupled receptor genes
    Gene, vol. 187, no. 1, pp. 75–81, 1997
55. Genomic Organization and Functional Analysis of the Murine Protein Phosphatase 1c ? (Ppp1cc) Gene
    Genomics, vol. 45, no. 1, pp. 211–215, 1997
56. Discovery of a Novel Human G Protein-Coupled Receptor Gene (GPR25) Located on Chromosome 1
    Biochemical and Biophysical Research Communications, vol. 230, no. 1, pp. 69–72, 1997
57. PMS2-Related Genes Flank the Rearrangement Breakpoints Associated with Williams Syndrome and Other Diseases on Human Chromosome 7
    Genomics, vol. 45, no. 2, pp. 402–406, 1997
58. Amplification of CFTR Exon 9 Sequences to Multiple Locations in the Human Genome
    Genomics, vol. 45, no. 3, pp. 554–561, 1997
59. Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome
    Human Molecular Genetics, vol. 6, no. 12, pp. 2117–2126, 1997
60. Regulation of meiotic chromatin loop size by chromosomal position
    Proceedings of the National Academy of Sciences, vol. 93, no. 7, pp. 2795–2800, 1996
61. Localization of a novel zinc finger gene to the human chromosome 7p11.2-p12 by fluorescencein situ hybridization
    Somatic Cell and Molecular Genetics, vol. 22, no. 3, pp. 237–239, 1996
62. Localization of a novel zinc finger gene to human chromosome 7q22 region by fluorescencein situ hybridization
    Somatic Cell and Molecular Genetics, vol. 22, no. 3, pp. 233–235, 1996
63. Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniques
    American Journal of Medical Genetics, vol. 67, no. 1, pp. 85–91, 1996
64. The Genes for the a and ß Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23
    Genomics, vol. 37, no. 1, pp. 141–143, 1996
65. Localization of three novel zinc finger genes to the centromeric region of human chromosome 10 by fluorescencein situ hybridization
    Somatic Cell and Molecular Genetics, vol. 22, no. 3, pp. 241–244, 1996
66. Localization of Two Metabotropic Glutamate Receptor Genes,GRM3andGRM8, to Human Chromosome 7q
    Genomics, vol. 31, no. 2, pp. 230–233, 1996
67. Tissue Distribution, Genomic Structure, and Chromosome Mapping of Mouse and Human Eukaryotic Initiation Factor 4E-Binding Proteins 1 and 2
    Genomics, vol. 38, no. 3, pp. 353–363, 1996
68. Physical Mapping of Receptor Type Protein Tyrosine Phosphatase Sigma (PTPRS) to Human Chromosome 19p13.3
    Genomics, vol. 38, no. 1, pp. 76–78, 1996
69. Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients
    Genomics, vol. 36, no. 2, pp. 328–336, 1996
70. A Novel Human Gene Encoding a G-Protein-Coupled Receptor (GPR15) Is Located on Chromosome 3
    Genomics, vol. 32, no. 3, pp. 462–465, 1996
71. Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
    Nature Genetics, vol. 14, no. 3, Article ID ng1196-353, 3 pages, 1996
72. Identification of a locus of zinc finger genes in human chromosome 19q13.1-q13.3 region by fluorescencein situ hybridization
    Somatic Cell and Molecular Genetics, vol. 22, no. 3, pp. 245–248, 1996
73. A novel family of repeat sequences in the mouse genome responsive to retinoic acid
    Mammalian Genome, vol. 7, no. 10, pp. 741–748, 1996
74. Chromosomal mapping of the second human CD8B gene locus
    Immunogenetics, vol. 43, no. 4, pp. 220–226, 1996
75. A novel gene codes for a putative G protein-coupled receptor with an abundant expression in brain
    FEBS Letters, vol. 394, no. 3, pp. 325–329, 1996
76. Characterization of a human gene related to genes encoding somatostatin receptors
    FEBS Letters, vol. 398, no. 2-3, pp. 253–258, 1996
77. Genomic Organization and FISH Mapping of Human Pmel 17, the Putative Silver Locus
    Pigment Cell Research, vol. 9, no. 1, pp. 42–48, 1996
78. Sequence Analysis and Chromosomal Localization of Human Cap Z
    Journal of Biological Chemistry, vol. 270, no. 37, pp. 21472–21479, 1995
79. Cloning, Expression, and Chromosomal Localization of the Human Uridine Nucleotide Receptor Gene
    Journal of Biological Chemistry, vol. 270, no. 52, pp. 30845–30848, 1995
80. Assignment of the Human GABA Transporter Gene (GABATHG) Locus to Chromosome 3p24-p25
    Genomics, vol. 29, no. 1, pp. 302–304, 1995
81. Cloning and Chromosomal Mapping of Three Novel Genes, GPR9, GPR10, and GPR14, Encoding Receptors Related to Interleukin 8, Neuropeptide Y, and Somatostatin Receptors
    Genomics, vol. 29, no. 2, pp. 335–344, 1995
82. Mapping of a Human LIM Protein (CLP) to Human Chromosome 11p15.1 by Fluorescence in Situ Hybridization
    Genomics, vol. 28, no. 3, pp. 602–603, 1995
83. Structure of the Murine MPTP-PEST Gene: Genomic Organization and Chromosomal Mapping
    Genomics, vol. 28, no. 3, pp. 501–507, 1995
84. The Cloning and Chromosomal Mapping of Two Novel Human Opioid-Somatostatin-like Receptor Genes, GPR7 and GPR8, Expressed in Discrete Areas of the Brain
    Genomics, vol. 28, no. 1, pp. 84–91, 1995
85. Assignment of the human homolog of mouse Dlx3 to Chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization
    Mammalian Genome, vol. 6, no. 4, pp. 310–311, 1995
86. Regional Localization of 725 Human Chromosome 7-Specific Yeast Artificial Chromosome Clones
    Genomics, vol. 22, no. 2, pp. 439–448, 1994
87. Cloning of Human Genes Encoding Novel G Protein-Coupled Receptors
    Genomics, vol. 23, no. 3, pp. 609–618, 1994
88. Localization of the Human Gene for Inducible Nitric Oxide Synthase (NOS2) to Chromosome 17q11.2-q12
    Genomics, vol. 19, no. 1, pp. 183–185, 1994
89. Organization of heterologous DNA inserts on the mouse meiotic chromosome core
    Chromosoma, vol. 103, no. 6, pp. 401–407, 1994
90. The murine Xe169 gene escapes X–inactivation like its human homologue
    Nature Genetics, vol. 7, no. 4, Article ID ng0894-491, 5 pages, 1994
91. Isolation of P1 bacteriophage clones containing large contiguous segments of the human and mouse loci for the T-cell coreceptor molecule CD8
    Genetic Analysis: Biomolecular Engineering, vol. 11, no. 5-6, pp. 129–139, 1994
92. A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11
    Gene, vol. 136, no. 1-2, pp. 355–360, 1993
93. Modes of DAPI banding and simultaneous in situ hybridization
    Chromosoma, vol. 102, no. 5, pp. 325–332, 1993
94. Chromosomal Localization of the Human Gene Encoding the 51-kDa Subunit of Mitochondrial Complex I (NDUFV1) to 11q13
    Genomics, vol. 18, no. 2, pp. 435–439, 1993
95. Refined Mapping of the GM2 Activator Protein (GM2A) Locus to 5q31.3-q33.1, Distal to the Spinal Muscular Atrophy Locus
    Genomics, vol. 18, no. 2, pp. 429–431, 1993
96. High-Resolution Mapping of Mammalian Genes by In situ Hybridization to Free Chromatin
    Proceedings of the National Academy of Sciences, vol. 89, no. 20, pp. 9509–9513, 1992