D. Pinkel

Hospital Clínico Universitario de Valencia — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index5.2kcitations44works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(12), Chromosomal and Genetic Variations(8), Cancer Genomics and Diagnostics(6), DNA Repair Mechanisms(4), Advanced biosensing and bioanalysis techniques(4)

Publications44 total

Whole genome scanning strongly predicts clinical outcome in differently treated subgroups of patients with lymph-node negative breast cancer
Journal of Clinical Oncology·2005· 1 cited
Braf and Melanocytic diseases.
Pigment Cell Research·2004· 3 cited
BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications
Journal of Medical Genetics·2004· 101 citedOpen Access
Determinants of BRAF Mutations in Primary Melanomas
JNCI Journal of the National Cancer Institute·2003· 655 citedOpen Access
High-resolution array CGH A validation study for the detection of submicroscopic deletions in DiGeorge and velo-cardio-facial syndromes
The American Journal of Human Genetics·2003· 1 cited
Mutations and Copy Number Increase of HRAS in Spitz Nevi with Distinctive Histopathological Features
American Journal Of Pathology·2000· 452 citedOpen Access
Quantitative 3d Analysis Of Intra-Nuclear Organization In The Tissue Context
Microscopy and Microanalysis·1999
Segmentation of confocal microscope images of cell nuclei in thick tissue sections
Journal of Microscopy·1999· 156 citedOpen Access
Chromosomal gains and losses in primary cutaneous melanomas detected by compartive genomic hybridization
Journal of Dermatological Science·1998· 20 cited
Automatic Hough Transform-Based 3D Segmentation of Cell Nuclei in Thick Tissue Sections
Microscopy and Microanalysis·1997· 2 cited
Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells
Cytometry·1995· 24 citedOpen Access
Deficiency of p53 accelerates mammary tumorigenesis in Wnt-1 transgenic mice and promotes chromosomal instability.
Genes & Development·1995· 274 citedOpen Access
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization.
Proceedings of the National Academy of Sciences·1994· 747 cited
Digital imaging microscopy for molecular cytogenetics
Proceedings annual meeting Electron Microscopy Society of America·1994· 1 cited
Comparative genomic hybridization: a rapid new method for detecting and mapping DNA amplification in tumors.
PubMed·1993· 229 cited
Deletion mapping of chr. 16q in breast cancer using dual color FISH with highly efficient cosmid contig probes
OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)·1993
Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization.
PubMed·1992· 108 cited
2 Molecular cytogenetic analysis of chromosome aberrations
Cancer Genetics and Cytogenetics·1992· 1 cited
Rapid Translocation Frequency Analysis in Humans Decades after Exposure to Ionizing Radiation
International Journal of Radiation Biology·1992· 438 cited
MOLECULAR CYTOGENETIC APPROACHES TO BIOLOGICAL DOSIMETRY AND TO CHARACTERIZATION OF SPECIFIC GENETIC CHANGES IN HUMAN TUMORS
Elsevier eBooks·1992
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Frequent Co-authors

Joe W. Gray(19), Anne Kallioniemi(9), Olli Kallioniemi(9), J. N. Lucas(8), Richard Segraves(6), T. Straume(6), Douglas Tkachuk(6), Fred Waldman(6), J. W. Gray(6), Damir Sudar(4), W.-L. Kuo(4), David A. Peters(4), J. E. Trebes(4), Jane Fridlyand(3), Donna G. Albertson(3), A A Awa(3), Carlos Ortíz-de-Solórzano(3), Kouji Matsumura(3), James M. Brase(3), Richard A. London(3)