Daniela S. Gerhard

Articles in Scholarly Journals [Incomplete List]

  1. Replicating genotype–phenotype associations
    Nature, vol. 447, no. 7145, Article ID 447655a, 5 pages, 2007
  2. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
    Nature Genetics, vol. 39, no. 5, Article ID ng2022, 4 pages, 2007
  3. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
    Nature Genetics, vol. 39, no. 7, Article ID ng2075, 4 pages, 2007
  4. Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling
    Genome Research, vol. 16, no. 6, pp. 796–803, 2006
  5. Small Molecules, Big Players: the National Cancer Institute's Initiative for Chemical Genetics
    Cancer Research, vol. 66, no. 18, pp. 8935–8942, 2006
  6. Transcriptional Maps of 10 Human Chromosomes at 5-Nucleotide Resolution
    Science, vol. 308, no. 5725, pp. 1149–1154, 2005
  7. A mouse atlas of gene expression: Large-scale digital gene-expression profiles from precisely defined developing C57BL/6J mouse tissues and cells
    Proceedings of the National Academy of Sciences, vol. 102, no. 51, pp. 18485–18490, 2005
  8. Fine mapping and evaluation of candidate genes for cervical cancer on 11q23
    Genes, Chromosomes and Cancer, vol. 43, no. 1, pp. 95–103, 2005
  9. Human papillomavirus type and tobacco use as predictors of survival in early stage cervical carcinoma
    Gynecologic Oncology, vol. 98, no. 1, pp. 84–91, 2005
  10. A relationship between methylenetetrahydrofolate reductase variants and the development of invasive cervical cancer
    Gynecologic Oncology, vol. 90, no. 3, pp. 560–565, 2003
  11. Denaturing High-Performance Liquid Chromatography for Detecting and Typing Genital Human Papillomavirus
    Journal of Clinical Microbiology, vol. 41, no. 12, pp. 5563–5571, 2003
  12. Novel mutations ofAPOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia
    Human Mutation, vol. 20, no. 2, pp. 110–116, 2002
  13. Novel mutations of APOB cause apoB truncations undetectable in plasma and familial hypobetalipoproteinemia
    Human Mutation, vol. 20, no. 5, pp. 402–402, 2002
  14. Loss of heterozygosity at 11q23.3 in vasculoinvasive and metastatic squamous cell carcinoma of the cervix
    Human Pathology, vol. 32, no. 5, pp. 475–478, 2001
  15. The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication
    Cytogenetic and Genome Research, vol. 94, no. 3-4, pp. 137–141, 2001
  16. Cervical cancer suppressor gene is within 1 cM on 6p23
    Genes, Chromosomes and Cancer, vol. 27, no. 4, pp. 373–379, 2000
  17. Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998
    Cytogenetic and Genome Research, vol. 86, no. 3-4, pp. 168–186, 1999
  18. Loss of heterozygosity in clinical stage IB cervical carcinoma: Relationship with clinical and histopathologic features*1
    Human Pathology, vol. 29, no. 4, pp. 364–370, 1998
  19. Cervial intraepithelial neoplasia III shows frequent allelic loss in 3p and 6p
    Genes, Chromosomes and Cancer, vol. 22, no. 1, pp. 57–65, 1998
  20. A transcript map of an 800-kb region on human chromosome 11q13, part of the candidate region for SCA5 and BBS1
    Human Genetics, vol. 103, no. 6, pp. 674–680, 1998
  21. A Sequence-Ready High-Resolution Physical Map of the Best Macular Dystrophy Gene Region in 11q12–q13
    Genomics, vol. 41, no. 2, pp. 185–192, 1997
  22. The Human HNP36 Gene Is Localized to Chromosome 11q13 and Produces Alternative Transcripts That Are Not Mutated in Multiple Endocrine Neoplasia, Type 1 (MEN I) Syndrome
    Genomics, vol. 42, no. 2, pp. 325–330, 1997
  23. A high-resolution physical map of human chromosome 11
    Proceedings of the National Academy of Sciences, vol. 93, no. 7, pp. 3149–3154, 1996
  24. Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay
    Human Molecular Genetics, vol. 5, no. 2, pp. 239–247, 1996
  25. Sequence of human FEN-1, a structure-specific endonuclease, and chromosomal localization of the gene (FEN1) in mouse and human
    Genomics, vol. 25, no. 1, pp. 220–225, 1995
  26. Initial report of a genome search for the affective disorder predisposition gene in the old order Amish pedigrees: Chromosomes 1 and 11
    American Journal of Medical Genetics, vol. 54, no. 4, pp. 398–404, 1994
  27. Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13?p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids
    Genomics, vol. 13, no. 4, pp. 1133–1142, 1992
  28. Linkage of bipolar affective disorders to markers on chromosome 11p is excluded in a second lateral extension of Amish Pedigree 110
    Genomics, vol. 11, no. 3, pp. 730–736, 1991
  29. On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes
    Genomics, vol. 9, no. 3, pp. 429–434, 1991
  30. Description of amish study data set
    Genetic Epidemiology, vol. 6, no. 1, pp. 195–199, 1989
  31. Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish
    Nature, vol. 342, no. 6247, Article ID 342238a0, 5 pages, 1989
  32. Evidence against Ha-ras-1 involvement in sporadic and familial melanoma
    Nature, vol. 325, no. 6099, Article ID 325073a0, 2 pages, 1987
  33. Bipolar affective disorders linked to DNA markers on chromosome 11
    Nature, vol. 325, no. 6107, Article ID 325783a0, 4 pages, 1987
  34. Analysis of human chromosome 11 by somatic cell genetics: Reexamination of derivatives of human-hamster cell line J1
    Somatic Cell and Molecular Genetics, vol. 13, no. 4, pp. 293–304, 1987
  35. Search for a gene that predisposes individuals to BPI disorder
    Journal of Psychiatric Research, vol. 21, no. 4, pp. 569–575, 1987
  36. Isolation of the Human Insulin-Like Growth Factor Genes: Insulin-Like Growth Factor II and Insulin Genes are Contiguous
    Proceedings of the National Academy of Sciences, vol. 82, no. 19, pp. 6450–6454, 1985
  37. Assignment of the Gene Coding for the T3-delta Subunit of the T3--T-Cell Receptor Complex to the Long Arm of Human Chromosome 11 and to Mouse Chromosome 9
    Proceedings of the National Academy of Sciences, vol. 82, no. 9, pp. 2920–2924, 1985
  38. Identification of a Recent Recombination Event within the Human   -globin Gene Cluster
    Proceedings of the National Academy of Sciences, vol. 81, no. 24, pp. 7875–7879, 1984
  39. Localization of a Unique Gene by Direct Hybridization in Situ
    Proceedings of the National Academy of Sciences, vol. 78, no. 6, pp. 3755–3759, 1981
  40. Journal of Organic Chemistry, vol. 45, no. 16, pp. 3344–3347, 1980