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

Year Number of Results
2002 2
2003 1
2004 3
2006 1
2007 1
2008 2
2009 3
2010 5
2011 5
2012 5
2013 8
2014 11
2015 5
2016 2
2017 1
2018 1
2019 2
2020 1
2022 2
2023 1
2024 0

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56 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.
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.
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.
Bioinactive ACTH causing glucocorticoid deficiency.
Samuels ME, Gallo-Payet N, Pinard S, Hasselmann C, Magne F, Patry L, Chouinard L, Schwartzentruber J, René P, Sawyer N, Bouvier M, Djemli A, Delvin E, Huot C, Eugene D, Deal CL, Van Vliet G, Majewski J, Deladoëy J; FORGE Canada Consortium. Samuels ME, et al. J Clin Endocrinol Metab. 2013 Feb;98(2):736-42. doi: 10.1210/jc.2012-3199. Epub 2013 Jan 4. J Clin Endocrinol Metab. 2013. PMID: 23293326
Human monogenic disorders - a source of novel drug targets.
Brinkman RR, Dubé MP, Rouleau GA, Orr AC, Samuels ME. Brinkman RR, et al. Among authors: samuels me. Nat Rev Genet. 2006 Apr;7(4):249-60. doi: 10.1038/nrg1828. Nat Rev Genet. 2006. PMID: 16534513 Review.
56 results