Cecilia de Bustos - Concepedia

Author

Cecilia de Bustos

Uppsala University

Also Known As

C De Bustos, Cecilia De Bustos, Cecilia de Bustos

Publications

365

Citations

H-Index

Concepts

All Affiliations

Uppsala University Howard Hughes Medical Institute Addenbrooke's Hospital Uppsala University Hospital Fred Hutch Cancer Center

About

Cecilia de Bustos is an author at Uppsala University specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	63
2	Pathology	2	2	47
3	Engineering	1	1	22
4	Public Health	1	1	16
5	Biostatistics	1	1	16

Cecilia de Bustos

Publications

344

Citations

H-Index

Page 1

	Year	Citations
Chromatin and siRNA pathways cooperate to maintain DNA methylation of small transposable elements in Arabidopsis Robert K. Tran, Daniel Zilberman, Cecilia de Bustos, Genome biology	2005	122
Tissue-specific variation in DNA methylation levels along human chromosome 1 Cecilia de Bustos, Edward Ramos, Janet M. Young, Epigenetics & Chromatin	2009	67
Chromosome 22 tiling‐path array–CGH analysis identifies germ‐line‐ and tumor‐specific aberrations in patients with glioblastoma multiforme Teresita Díaz de Ståhl, Christian Hartmann, Cecilia de Bustos, Genes Chromosomes and Cancer	2005	34
A <i>PDGFRA</i> promoter polymorphism, which disrupts the binding of ZNF148, is associated with primitive neuroectodermal tumours and ependymomas Cecilia de Bustos Journal of Medical Genetics	2005	30
Localization of a putative low‐penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling‐path genomic microarray Anneke C. J. Ammerlaan, Cecilia de Bustos, Abdelhay Ararou, Genes Chromosomes and Cancer	2005	28
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas Teresita Díaz de Ståhl, Caisa M. Hansson, Cecilia de Bustos, Human Genetics Neuro-oncologyTumor BiologySomatic VariantTumor HeterogeneityMedicine	2005	25
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH. Kiran K. Mantripragada, Patrick G. Buckley, Magdalena Benetkiewicz, PubMed Neuro-oncologyEngineeringMedicineSchwannoma DevelopmentContinuous Deletion	2003	22
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH Cecilia de Bustos, Teresita Díaz de Ståhl, Arkadiusz Piotrowski, Genomics Complex Segmental DuplicationsMedicineGeneticsCopy Number VariationNormal Human Population	2006	16

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