Ellen K. Brundage - Concepedia

Author

Ellen K. Brundage

Baylor College of Medicine

Also Known As

E Brundage, E K Brundage, E. Brundage, Ellen Brundage, Ellen K Brundage, Ellen K. Brundage

Publications

592

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine Texas Children's Hospital Baylor Genetics

About

Ellen K. Brundage is an author at Baylor College of Medicine specializing in molecular biology, genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	182
2	Molecular Biology	6	6	177
3	Molecular Genetics	5	5	163
4	Natural Sciences	3	3	101
5	Pathology	3	3	89

Ellen K. Brundage

Publications

538

Citations

H-Index

Page 1

	Year	Citations
20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits Seema R. Lalani, Joseph V. Thakuria, Gerald F. Cox, Journal of Medical Genetics	2008	109
Utility of Oligonucleotide Array–Based Comparative Genomic Hybridization for Detection of Target Gene Deletions Lee‐Jun C. Wong, David Dimmock, Michael T. Geraghty, Clinical Chemistry	2008	79
Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome Svetlana A. Yatsenko, Ellen K. Brundage, Erin K. Roney, Human Molecular Genetics	2009	75
Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes Bekim Sadiković, Jing Wang, Ayman W. El‐Hattab, PLoS ONE GeneticsMolecular BiologyPathologyMolecular GeneticsDisease Gene Identification	2010	56
Application of dual-genome oligonucleotidearray-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes A. Craig Chinault, Chad A. Shaw, Ellen K. Brundage, Genetics in Medicine Genetic AnalysisMolecular DiagnosisGenetic TestingGenetic DisorderMedicine	2009	48
HERV‐mediated genomic rearrangement of <i>EYA1</i> in an individual with branchio‐oto‐renal syndrome Amarilis Sanchez‐Valle, Xueqing Wang, Lorraine Potocki, American Journal of Medical Genetics Part A	2010	45
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies Daniel R. Jensen, Donna M. Martin, Stephen S. Gebarski, American Journal of Medical Genetics Part A	2009	34
Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion Shulin Zhang, Fang-Yuan Li, Harold N. Bass, Molecular Genetics and Metabolism ChromatinDna SequencingMtdna DepletionNatural SciencesGenetics	2009	24
Fine Mapping of MEP1A, the Gene Encoding the α Subunit of the Metalloendopeptidase Meprin, to Human Chromosome 6p21 W. Jiang, G. Dewald, Ellen K. Brundage, Biochemical and Biophysical Research Communications Natural SciencesGeneticsMetalloproteinProtein GeneticsMolecular Biology	1995	21
Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL Magdalena Ratajska, Jolanta Wierzba, Davut Pehli̇van, European Journal of Medical Genetics Mendelian DisorderGenetic DisorderLange Syndrome CaseGeneticsDna Replication	2010	19

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