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

Year Number of Results
1978 2
1980 1
1984 1
1988 1
1989 1
1991 2
1992 1
1993 5
1994 3
1995 2
1996 3
1997 5
1998 1
1999 4
2000 1
2001 2
2002 3
2003 5
2004 9
2005 4
2006 2
2007 3
2008 4
2009 4
2010 7
2011 5
2012 7
2013 8
2014 11
2015 6
2016 3
2017 1
2018 1
2019 2
2020 1
2022 2
2023 1
2024 0

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116 results

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Page 1
Genetics of the patella.
Samuels ME, Campeau PM. Samuels ME, et al. Eur J Hum Genet. 2019 May;27(5):671-680. doi: 10.1038/s41431-018-0329-6. Epub 2019 Jan 21. Eur J Hum Genet. 2019. PMID: 30664715 Free PMC article. Review.
Genetic mosaics and the germ line lineage.
Samuels ME, Friedman JM. Samuels ME, et al. Genes (Basel). 2015 Apr 17;6(2):216-37. doi: 10.3390/genes6020216. Genes (Basel). 2015. PMID: 25898403 Free PMC article. Review.
Single-use syringes.
Samuels ME, Koop CE, Hartsock PI. Samuels ME, et al. N Engl J Med. 1991 Apr 4;324(14):996-7. doi: 10.1056/NEJM199104043241415. N Engl J Med. 1991. PMID: 2002826 No abstract available.
A generalizable pre-clinical research approach for orphan disease therapy.
Beaulieu CL, Samuels ME, Ekins S, McMaster CR, Edwards AM, Krainer AR, Hicks GG, Frey BJ, Boycott KM, Mackenzie AE. Beaulieu CL, et al. Among authors: samuels me. Orphanet J Rare Dis. 2012 Jun 15;7:39. doi: 10.1186/1750-1172-7-39. Orphanet J Rare Dis. 2012. PMID: 22704758 Free PMC article. Review.
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.
Sawyer SL, Hartley T, Dyment DA, Beaulieu CL, Schwartzentruber J, Smith A, Bedford HM, Bernard G, Bernier FP, Brais B, Bulman DE, Warman Chardon J, Chitayat D, Deladoëy J, Fernandez BA, Frosk P, Geraghty MT, Gerull B, Gibson W, Gow RM, Graham GE, Green JS, Heon E, Horvath G, Innes AM, Jabado N, Kim RH, Koenekoop RK, Khan A, Lehmann OJ, Mendoza-Londono R, Michaud JL, Nikkel SM, Penney LS, Polychronakos C, Richer J, Rouleau GA, Samuels ME, Siu VM, Suchowersky O, Tarnopolsky MA, Yoon G, Zahir FR; FORGE Canada Consortium; Care4Rare Canada Consortium; Majewski J, Boycott KM. Sawyer SL, et al. Among authors: samuels me. Clin Genet. 2016 Mar;89(3):275-84. doi: 10.1111/cge.12654. Epub 2015 Sep 22. Clin Genet. 2016. PMID: 26283276 Free PMC article. Review.
Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
Larrivée-Vanier S, Jean-Louis M, Magne F, Bui H, Rouleau GA, Spiegelman D, Samuels ME, Kibar Z, Van Vliet G, Deladoëy J. Larrivée-Vanier S, et al. Among authors: samuels me. Thyroid. 2022 May;32(5):486-495. doi: 10.1089/thy.2021.0597. Epub 2022 Apr 25. Thyroid. 2022. PMID: 35272499 Free PMC article.
The case for locus-specific databases.
Samuels ME, Rouleau GA. Samuels ME, et al. Nat Rev Genet. 2011 Jun;12(6):378-9. doi: 10.1038/nrg3011. Epub 2011 May 4. Nat Rev Genet. 2011. PMID: 21540879
Genetics of cholesterol and lipoprotein metabolism.
Samuels ME. Samuels ME. Recent Pat Cardiovasc Drug Discov. 2007 Nov;2(3):195-204. doi: 10.2174/157489007782418937. Recent Pat Cardiovasc Drug Discov. 2007. PMID: 18221119 Review.
116 results