Rosalyn Slater - Concepedia

Author

Rosalyn Slater

Also Known As

R M Slater, R Slater, R. M. SLATER, R. M. Slater, R. Slater, R.M. SLATER, R.M. Slater, Rosalyn M Slater, Rosalyn M. Slater, Rosalyn Slater

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University of Amsterdam Emma Kinderziekenhuis Amsterdam UMC Location University of Amsterdam Erasmus University Rotterdam The Netherlands Cancer Institute

About

Rosalyn Slater is an author at University of Amsterdam specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	30	1.6K
2	Cell Biology	8	8	554
3	Health Sciences	7	7	355
4	Natural Sciences	2	2	39
5	Biology	1	1	33

Rosalyn Slater

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma Huib N. Caron, Peter van Sluis, Jan de Kraker, New England Journal of Medicine	1996	427
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours Marcel M. A. M. Mannens, Rosalyn Slater, Christa Heyting, Human Genetics Genetic ChangesSomatic VariantCytogeneticsGenetic DisorderGenetics	1988	188
Overall and event-free survival are not improved by the use of myeloablative therapy following intensified chemotherapy in previously untreated patients with multiple myeloma: a prospective randomized phase 3 study Christine M. Segeren, Pieter Sonneveld, Bronno van der Holt, Blood	2003	163
Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification Huib N. Caron, Martine Peter, Peter van Sluis, Human Molecular Genetics	1995	143
Maintenance of Vascular Endothelial Cell-Specific Properties after Immortalization with an Amphotrophic Replication-Deficient Retrovirus Containing Human Papilloma Virus 16 E6/E7 DNA Ruud D. Fontijn, Caroline Hop, Herm‐Jan Brinkman, Experimental Cell Research Viral ReplicationE6/e7 DnaImmunologyDna ReplicationVirology	1995	109
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma Mario Hermsen, Hans Joenje, Fré Arwert, Genes Chromosomes and Cancer Genetic ImbalanceCytogeneticsPathologyCytogenetic AbnormalitiesTumor Biology	1996	108
Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia Marcel M. A. M. Mannens, J.M.N. Hoovers, E. Redeker, European Journal of Human Genetics Beckwith-wiedemann SyndromeGenetic DisorderGeneticsPathologyMolecular Genetics	1994	108
Molecular cytogenetic and clinical findings inETV6/ABL1-positive leukemia Heidi Van Limbergen, H. Berna Beverloo, Ellen van Drunen, Genes Chromosomes and Cancer Hematological MalignancyChromatinChronic Myeloid LeukemiaMedicineMixed-phenotype Acute Leukemia	2001	105
In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype N. L. Ramakers-Van Woerden, H. Berna Beverloo, A. Veerman, Leukemia Hematological MalignancyHealth SciencesMedicineMalignant Blood DisorderMixed-phenotype Acute Leukemia	2004	89
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Marcel M. A. M. Mannens, Peter Devilee, Jet Bliek, PubMed Dna MarkersSomatic VariantCancer PathologyCytogeneticsGenetic Disorder	1990	82

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