Bradley W. Popovich - Concepedia

Author

Bradley W. Popovich

Also Known As

B Popovich, B W Popovich, B. POPOVICH, B. Popovich, B. W. Popovich, B.W. Popovich, Bradley Popovich, Bradley W Popovich, Bradley W. Popovich

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Oregon Health & Science University Kaiser Permanente Xenon Pharmaceuticals (Canada)Icahn School of Medicine at Mount Sinai University of North Carolina at Chapel Hill

About

Bradley W. Popovich is an author at Oregon Health & Science University specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1.8K
2	Public Health	3	3	196
3	Engineering	1	1	128
4	Health Sciences	1	1	42
5	Natural Sciences	1	1	13

Bradley W. Popovich

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Length of uninterrupted CGG repeats determines instability in the FMR1 gene Evan E. Eichler, Jeanette J. A. Holden, Bradley W. Popovich, Nature Genetics ChromatinGenome InstabilityFmr1 GeneGenetic DisorderGenetics	1994	479
Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel Michael S. Watson, Garry R. Cutting, Robert J. Desnick, Genetics in Medicine Genetic TestingGenetic DisorderMedicineGeneticsAmerican College	2004	450
Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics Anne Maddalena, Carolyn Sue Richards, Matthew J. McGinniss, Genetics in Medicine Genetic TestingClinical Genetics LaboratoriesFragile XTechnical StandardsGenetic Disorder	2001	230
Standards and Guidelines for CFTR Mutation Testing Carolyn Sue Richards, Linda Bradley, Jean Amos, Genetics in Medicine Cftr Mutation TestingGenetic TestingEngineeringMutation-based TestingMedicine	2002	128
Toward clinical genomics in everyday medicine: perspectives and recommendations Susan Delaney, Michael Hultner, Howard J. Jacob, Expert Review of Molecular Diagnostics SequencingHealth InformaticsTranslational BioinformaticsExome SequencingClinical Genome	2016	104
Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy. F Quan, Jadwiga Janas, S Toth-Fejel, PubMed	1997	99
GeneTests-GeneClinics: Genetic testing information for a growing audience Roberta A Pagon, Peter Tarczy‐Hornoch, Patricia K. Baskin, Human Mutation	2002	83
An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene. F Quan, J. Zonana, Kristine A. Gunter, PubMed	1995	69
Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism Franklin Quan, Markus Grompe, Petra Jakobs, Human Molecular Genetics Genetic TestingGeneticsPathologyMolecular BiologyMolecular Genetics	1995	69
Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy. Lisa Schwartz, Jack Tarleton, Bradley W. Popovich, PubMed	1992	61

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