Articles in Scholarly Journals [Incomplete List]

1. hORFeome v3.1: A resource of human open reading frames representing over 10,000 human genes
   Genomics, vol. 89, no. 3, pp. 307–315, 2007
2. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
   Nature, vol. 447, no. 7146, Article ID nature05874, 17 pages, 2007
3. Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes
   Genome Research, vol. 17, no. 6, pp. 708–719, 2007
4. The landscape of histone modifications across 1% of the human genome in five human cell lines
   Genome Research, vol. 17, no. 6, pp. 691–707, 2007
5. The portability of tagSNPs across populations: A worldwide survey
   Genome Research, vol. 16, no. 3, pp. 323–330, 2006
6. Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites
   Genome Research, vol. 16, no. 10, pp. 1310–1319, 2006
7. Evidence for Widespread Reticulate Evolution within Human Duplicons
   The American Journal of Human Genetics, vol. 77, no. 5, pp. 824–840, 2005
8. Investigating chromosome organization with genomic microarrays
   Chromosome Research, vol. 13, no. 3, pp. 249–257, 2005
9. Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays
   Human Molecular Genetics, vol. 14, no. 22, pp. 3435–3447, 2005
10. The DNA sequence and analysis of human chromosome 13
    Nature, vol. 428, no. 6982, Article ID nature02379, 6 pages, 2004
11. Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer ( TOC ) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene
    Human Genetics, vol. 114, no. 6, pp. 534–540, 2004
12. Replication timing of the human genome
    Human Molecular Genetics, vol. 13, no. 5, pp. 575–575, 2004
13. Complete MHC Haplotype Sequencing for Common Disease Gene Mapping
    Genome Research, vol. 14, no. 6, pp. 1176–1187, 2004
14. The ENCODE (ENCyclopedia Of DNA Elements) Project
    Science, vol. 306, no. 5696, pp. 636–640, 2004
15. Replication timing of the human genome
    Human Molecular Genetics, vol. 13, no. 2, pp. 191–202, 2003
16. Reevaluating Human Gene Annotation: A Second-Generation Analysis of Chromosome 22
    Genome Research, vol. 13, no. 1, pp. 27–36, 2003
17. The characteristics of human genes: analysis of human chromosome 22
    Comparative and Functional Genomics, vol. 4, no. 6, pp. 635–646, 2003
18. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications
    Human Molecular Genetics, vol. 11, no. 25, pp. 3221–3229, 2002
19. Human genome sequences: enigmatic variations
    Mutagenesis, vol. 17, no. 6, pp. 457–461, 2002
20. A first-generation linkage disequilibrium map of human chromosome 22
    Nature, vol. 418, no. 6897, Article ID nature00864, 4 pages, 2002
21. An Anthropoid-Specific Locus of Orphan C to U RNA-Editing Enzymes on Chromosome 22
    Genomics, vol. 79, no. 3, pp. 285–296, 2002
22. BMC Genetics, vol. 3, no. 1, p. 20, 2002
23. A SNP Resource for Human Chromosome 22: Extracting Dense Clusters of SNPs From the Genomic Sequence
    Genome Research, vol. 11, no. 1, pp. 170–178, 2001
24. A Sequence-Based Integrated Map of Chromosome 22
    Genome Research, vol. 11, no. 7, pp. 1290–1295, 2001
25. Initial sequencing and analysis of the human genome
    Nature, vol. 409, no. 6822, Article ID 35057062, 61 pages, 2001
26. The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X
    Nature, vol. 409, no. 6822, Article ID 35057165, 1 pages, 2001
27. An Integrated Map of Human 6q22.3–q24 Including a 3-Mb High-Resolution BAC/PAC Contig Encompassing a QTL for Fetal Hemoglobin
    Genomics, vol. 64, no. 3, pp. 264–276, 2000
28. Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22
    European Journal of Human Genetics, vol. 8, no. 3, Article ID 5200434, 5 pages, 2000
29. Nature, vol. 407, no. 6803, pp. 516–520, 2000
30. The Extent of Linkage Disequilibrium in Four Populations with Distinct Demographic Histories
    The American Journal of Human Genetics, vol. 67, no. 6, pp. 1544–1554, 2000
31. The gene guessing game
    Yeast, vol. 17, no. 3, pp. 218–224, 2000
32. Genomics – the new rock and roll?
    Trends in Genetics, vol. 16, no. 10, pp. 456–461, 2000
33. Report of the fourth international chromosome 6 workshop 1999
    Cytogenetic and Genome Research, vol. 88, no. 3-4, pp. 173–196, 2000
34. Psoriasis Upregulated Phorbolin-1 Shares Structural but not Functional Similarity to the mRNA-Editing Protein Apobec-1
    Journal of Investigative Dermatology, vol. 113, no. 2, pp. 162–169, 1999
35. Mapping and complex expression pattern of the human NPAP60L nucleoporin gene
    Cytogenetic and Genome Research, vol. 85, no. 3-4, pp. 221–226, 1999
36. Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human
    Mammalian Genome, vol. 10, no. 7, pp. 744–749, 1999
37. The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family
    Proceedings of the National Academy of Sciences, vol. 96, no. 2, pp. 598–603, 1999
38. Nature, vol. 402, no. 6761, pp. 489–495, 1999
39. Chromosome Research, vol. 7, no. 7, pp. 571–573, 1999
40. Nature Genetics, vol. 20, no. 2, pp. 171–174, 1998
41. Characterization of the human synaptogyrin gene family
    Human Genetics, vol. 103, no. 2, pp. 131–141, 1998
42. Fine-Mapping, Genomic Organization, and Transcript Analysis of the Human Ubiquitin-Conjugating Enzyme Gene UBE2L3
    Genomics, vol. 51, no. 1, pp. 124–127, 1998
43. Data disclosure in the Human Genome Project
    Molecular Medicine Today, vol. 4, no. 8, p. 335, 1998
44. A bacterial artificial chromosome-based framework contig map of human chromosome 22q
    Proceedings of the National Academy of Sciences, vol. 93, no. 13, pp. 6297–6301, 1996
45. A Gene Map of the Human Genome
    Science, vol. 274, no. 5287, pp. 540–546, 1996
46. Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11
    Human Molecular Genetics, vol. 5, no. 5, pp. 625–631, 1996
47. Identification and characterization of NF1 -related loci on human chromosomes 22, 14 and 2
    Human Genetics, vol. 98, no. 1, pp. 7–11, 1996
48. Assignment of the ßB1 Crystallin Gene (CRYBB1) to Human Chromosome 22 and Mouse Chromosome 5
    Genomics, vol. 29, no. 3, pp. 712–718, 1995
49. Mapping human chromosomes
    Current Opinion in Genetics & Development, vol. 5, no. 3, pp. 328–334, 1995
50. A YAC Contig Spanning the Ataxia-Telangiectasia Locus (Groups A and C) at 11q22-q23
    Genomics, vol. 24, no. 2, pp. 234–242, 1994
51. The development and application of automated gridding for efficient screening of yeast and bacterial ordered libraries
    Genomics, vol. 12, no. 3, pp. 534–541, 1992
52. Possible role for COMT in psychosis associated with velo-cardio-facial syndrome
    The Lancet, vol. 340, no. 8831, pp. 1361–1362, 1992
53. Rapid generation of chromosome-specific alphoid DNA probes using the polymerase chain reaction
    Human Genetics, vol. 88, no. 4, pp. 457–462, 1992
54. Characterization of the class III region in different MHC haplotypes by pulsed-field gel electrophoresis
    Immunogenetics, vol. 32, no. 3, pp. 175–182, 1990
55. Human Major Histocompatibility Complex Contains Genes for the Major Heat Shock Protein HSP70
    Proceedings of the National Academy of Sciences, vol. 86, no. 6, pp. 1968–1972, 1989
56. Direct observation of the gene organization of the complement C4 and 21- hydroxylase loci by pulsed field gel electrophoresis
    Journal of Experimental Medicine, vol. 169, no. 5, pp. 1803–1818, 1989
57. Molecular Mapping of the Human Major Histocompatibility Complex by Pulsed-Field Gel Electrophoresis
    Proceedings of the National Academy of Sciences, vol. 84, no. 20, pp. 7237–7241, 1987