Peggy D. Robertson - Concepedia

Author

Peggy D. Robertson

Also Known As

Bryan Paeper, Frederic Reinier, Martha Horike-Pyne, Murray, Mitzi L., P D Robertson, P Robertson, P. D. Robertson, P. Robertson, P.D. Robertson, Pamela Ajuyah Robertson

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

University of Washington Seattle Children's Hospital University of Washington Medical Center HudsonAlpha Institute for Biotechnology Baylor College of Medicine

About

Peggy D. Robertson is an author at University of Washington specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	3.1K
2	Public Health	5	5	686
3	Biostatistics	2	2	377
4	Natural Sciences	1	1	53
5	Biochemistry	1	1	21

Peggy D. Robertson

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Targeted capture and massively parallel sequencing of 12 human exomes Sarah Ng, Emily H. Turner, Peggy D. Robertson, Nature BioinformaticsLong-read SequencingDna SequencingParallel SequencingNext-generation Sequencing	2009	2K
Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes Michael O. Dorschner, Laura M. Amendola, Emily H. Turner, The American Journal of Human Genetics Pathogenic Incidental FindingsGenetic EpidemiologyMendelian DisorderPathology	2013	381
Actionable exomic incidental findings in 6503 participants: challenges of variant classification Laura M. Amendola, Michael O. Dorschner, Peggy D. Robertson, Genome Research Genome-wide Association StudyEpidemiologySequencingExome SequencingGenetics	2015	356
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, The American Journal of Human Genetics EpidemiologySequencingMedicineNext-generation SequencingGenomics	2016	161
Automating sequence-based detection and genotyping of SNPs from diploid samples Matthew Stephens, James S. Sloan, Peggy D. Robertson, Nature Genetics Genetic AnalysisHaplotype DeterminationNext-generation SequencingGeneticsComputational Genomics	2006	145
Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era Nadine Norton, Peggy D. Robertson, Mark J. Rieder, Circulation Cardiovascular Genetics	2012	119
Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy Nadine Norton, Duanxiang Li, Evadnie Rampersaud, Circulation Cardiovascular Genetics Dcm CauseExome SequencingGeneticsGenetic EpidemiologyMolecular Biology	2013	110
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder Gali Heimer, Juha M. Kerätär, Lisa G. Riley, The American Journal of Human Genetics Mitochondrial MyopathyNeurodegenerative DiseasesMendelian DisorderMitochondrial FunctionGenetic Disorder	2016	101
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3 Jessica X. Chong, Lindsay C. Burrage, Anita E. Beck, The American Journal of Human Genetics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsPathology	2015	65
Exome Sequencing Reveals Novel Rare Variants in the Ryanodine Receptor and Calcium Channel Genes in Malignant Hyperthermia Families Jerry H. Kim, Gail P. Jarvik, Brian L. Browning, Anesthesiology	2013	61

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