C. Sue Richards - Concepedia

Author

C. Sue Richards

Also Known As

Amendola, Laura M., C RICHARDS, C Richards, C S Richards, C Sue Richards, C. S. Richards, C. SUE RICHARDS, C. Sue Richards, C.S. Richards, Charles S. Richards

Publications

6.4K

Citations

H-Index

Concepts

All Affiliations

Oregon Health & Science University Baylor College of Medicine University of North Carolina at Chapel Hill University of Washington Medical Center Boston Children's Hospital

About

C. Sue Richards is an author at Oregon Health & Science University specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	25	5.6K
2	Public Health	7	7	586
3	Engineering	3	3	887
4	Natural Sciences	2	2	93
5	Management	1	1	17

C. Sue Richards

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics Sarah S. Kalia, Kathy Adelman, Sherri J. Bale, Genetics in Medicine Secondary FindingsMedicineAmerican CollegeNext-generation SequencingPathology	2016	1.7K
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 C. Sue Richards, Sherri J. Bale, Daniel B. Bellissimo, Genetics in Medicine EngineeringMedicineReporting StandardSoftware TestingAcmg Recommendations	2008	814
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG) David T. Miller, Kristy Lee, Wendy K. Chung, Genetics in Medicine Secondary FindingsAcmg SfNext-generation SequencingGeneticsGenetic Epidemiology	2021	541
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
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) David T. Miller, Kristy Lee, Noura S. Abul‐Husn, Genetics in Medicine Secondary FindingsSequencingAcmg SfNext-generation SequencingGenetics	2023	364
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
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG) David T. Miller, Kristy Lee, Laura M. Amendola, Genetics in Medicine American CollegeClinical ExomeDiagnosisPathologyGynecology	2021	244
Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent. L.-j. Wong, Tetsuo Ashizawa, Darren G. Monckton, PubMed	1995	208
A Homozygous Mutation in <i>MSH6</i> Causes Turcot Syndrome Madhuri Hegde, Belinda Chong, Maria E. Blazo, Clinical Cancer Research	2005	84

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