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

Year Number of Results
2000 1
2003 1
2004 2
2005 2
2006 3
2007 4
2008 4
2009 1
2010 1
2011 1
2014 2
2015 1
2017 3
2018 1
2020 1
2021 2
2022 1
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30 results
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Page 1
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Manickam K, McClain MR, Demmer LA, Biswas S, Kearney HM, Malinowski J, Massingham LJ, Miller D, Yu TW, Hisama FM; ACMG Board of Directors. Manickam K, et al. Among authors: mcclain mr. Genet Med. 2021 Nov;23(11):2029-2037. doi: 10.1038/s41436-021-01242-6. Epub 2021 Jul 1. Genet Med. 2021. PMID: 34211152
Gaucher disease type 1 patients from the ICGG Gaucher Registry sustain initial clinical improvements during twenty years of imiglucerase treatment.
Weinreb NJ, Camelo JS Jr, Charrow J, McClain MR, Mistry P, Belmatoug N; International Collaborative Gaucher Group (ICGG) Gaucher Registry (NCT00358943) investigators. Weinreb NJ, et al. Among authors: mcclain mr. Mol Genet Metab. 2021 Feb;132(2):100-111. doi: 10.1016/j.ymgme.2020.12.295. Epub 2021 Jan 8. Mol Genet Metab. 2021. PMID: 33485799 Free article.
How reliable are BRCA1/2 mutation estimates?
McClain MR, Palomaki GE, Haddow JE. McClain MR, et al. Cancer Res. 2007 May 15;67(10):5057; author reply 5057-8. doi: 10.1158/0008-5472.CAN-06-3365. Cancer Res. 2007. PMID: 17510441 No abstract available.
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.
Rose NC, Barrie ES, Malinowski J, Jenkins GP, McClain MR, LaGrave D, Leung ML; ACMG Professional Practice and Guidelines Committee. Electronic address: Rose NC, et al. Among authors: mcclain mr. Genet Med. 2022 May 10:S1098-3600(22)00714-6. doi: 10.1016/j.gim.2022.03.019. Online ahead of print. Genet Med. 2022. PMID: 35608568 Review.
30 results