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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1990 1
1991 1
1994 2
1995 1
1997 3
1998 2
1999 2
2001 1
2002 2
2003 1
2006 2
2008 2
2010 1
2011 4
2013 1
2014 4
2015 4
2016 4
2017 5
2018 2
2019 3
2020 4
2021 3
2022 3
2023 0
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54 results
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Page 1
Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.
Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group; Topper S. Nykamp K, et al. Among authors: topper s. Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Genet Med. 2017. PMID: 28492532 Free PMC article.
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Best RG, Khushf G, Rabin-Havt SS, Clayton EW, Grebe TA, Hagenkord J, Topper S, Fivecoat J, Chen M, Grody WW; ACMG Social, Ethical and Legal Issues Committee. Electronic address: Best RG, et al. Among authors: topper s. Genet Med. 2022 Mar;24(3):509-511. doi: 10.1016/j.gim.2021.11.001. Epub 2021 Dec 16. Genet Med. 2022. PMID: 35253644 No abstract available.
Ulnar styloid impaction syndrome.
Topper SM, Wood MB, Ruby LK. Topper SM, et al. J Hand Surg Am. 1997 Jul;22(4):699-704. doi: 10.1016/S0363-5023(97)80131-1. J Hand Surg Am. 1997. PMID: 9260629
Predominance of antibody-resistant SARS-CoV-2 variants in vaccine breakthrough cases from the San Francisco Bay Area, California.
Servellita V, Morris MK, Sotomayor-Gonzalez A, Gliwa AS, Torres E, Brazer N, Zhou A, Hernandez KT, Sankaran M, Wang B, Wong D, Wang C, Zhang Y, Reyes KR, Glasner D, Deng X, Streithorst J, Miller S, Frias E, Rodgers M, Cloherty G, Hackett J Jr, Hanson C, Wadford D, Philip S, Topper S, Sachdev D, Chiu CY. Servellita V, et al. Among authors: topper s. Nat Microbiol. 2022 Feb;7(2):277-288. doi: 10.1038/s41564-021-01041-4. Epub 2022 Jan 10. Nat Microbiol. 2022. PMID: 35013591
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program.
Venner E, Muzny D, Smith JD, Walker K, Neben CL, Lockwood CM, Empey PE, Metcalf GA, Kachulis C; All of Us Research Program Regulatory Working Group; Mian S, Musick A, Rehm HL, Harrison S, Gabriel S, Gibbs RA, Nickerson D, Zhou AY, Doheny K, Ozenberger B, Topper SE, Lennon NJ. Venner E, et al. Among authors: topper se. Genome Med. 2022 Mar 28;14(1):34. doi: 10.1186/s13073-022-01031-z. Genome Med. 2022. PMID: 35346344 Free PMC article.
54 results