Samuels ME - Search Results

1

Association of Circulating YKL-40 Levels and CHI3L1 Variants with the Risk of Spinal Deformity Progression in Adolescent Idiopathic Scoliosis.

Nada D, Julien C, Rompré PH, Akoume MY, Gorman KF, Samuels ME, Levy E, Kost J, Li D, Moreau A. Nada D, et al. Among authors: samuels me. Sci Rep. 2019 Apr 5;9(1):5712. doi: 10.1038/s41598-019-41191-4. Sci Rep. 2019. PMID: 30952886 Free PMC article.

2

Identification of FAT3 as a new candidate gene for adolescent idiopathic scoliosis.

Nada D, Julien C, Papillon-Cavanagh S, Majewski J, Elbakry M, Elremaly W, Samuels ME, Moreau A. Nada D, et al. Among authors: samuels me. Sci Rep. 2022 Jul 19;12(1):12298. doi: 10.1038/s41598-022-16620-6. Sci Rep. 2022. PMID: 35853984 Free PMC article.

3

A Replication Study for Association of LBX1 Locus With Adolescent Idiopathic Scoliosis in French-Canadian Population.

Nada D, Julien C, Samuels ME, Moreau A. Nada D, et al. Among authors: samuels me. Spine (Phila Pa 1976). 2018 Feb 1;43(3):172-178. doi: 10.1097/BRS.0000000000002280. Spine (Phila Pa 1976). 2018. PMID: 28604496

4

Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.

Magne F, Ge B, Larrivée-Vanier S, Van Vliet G, Samuels ME, Pastinen T, Deladoëy J. Magne F, et al. Among authors: samuels me. Thyroid. 2016 Jun;26(6):852-9. doi: 10.1089/thy.2016.0009. Epub 2016 May 18. Thyroid. 2016. PMID: 27125219

5

Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.

Srour M, Schwartzentruber J, Hamdan FF, Ospina LH, Patry L, Labuda D, Massicotte C, Dobrzeniecka S, Capo-Chichi JM, Papillon-Cavanagh S, Samuels ME, Boycott KM, Shevell MI, Laframboise R, Désilets V; FORGE Canada Consortium; Maranda B, Rouleau GA, Majewski J, Michaud JL. Srour M, et al. Among authors: samuels me. Am J Hum Genet. 2012 Apr 6;90(4):693-700. doi: 10.1016/j.ajhg.2012.02.011. Epub 2012 Mar 15. Am J Hum Genet. 2012. PMID: 22425360 Free PMC article.

6

Germline mutations in MAP3K6 are associated with familial gastric cancer.

Gaston D, Hansford S, Oliveira C, Nightingale M, Pinheiro H, Macgillivray C, Kaurah P, Rideout AL, Steele P, Soares G, Huang WY, Whitehouse S, Blowers S, LeBlanc MA, Jiang H, Greer W, Samuels ME, Orr A, Fernandez CV, Majewski J, Ludman M, Dyack S, Penney LS, McMaster CR, Huntsman D, Bedard K. Gaston D, et al. Among authors: samuels me. PLoS Genet. 2014 Oct 23;10(10):e1004669. doi: 10.1371/journal.pgen.1004669. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25340522 Free PMC article.

7

Functional zebrafish studies based on human genotyping point to netrin-1 as a link between aberrant cardiovascular development and thyroid dysgenesis.

Opitz R, Hitz MP, Vandernoot I, Trubiroha A, Abu-Khudir R, Samuels M, Désilets V, Costagliola S, Andelfinger G, Deladoëy J. Opitz R, et al. Endocrinology. 2015 Jan;156(1):377-88. doi: 10.1210/en.2014-1628. Endocrinology. 2015. PMID: 25353184 Free PMC article.

8

Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria.

Capo-Chichi JM, Boissel S, Brustein E, Pickles S, Fallet-Bianco C, Nassif C, Patry L, Dobrzeniecka S, Liao M, Labuda D, Samuels ME, Hamdan FF, Vande Velde C, Rouleau GA, Drapeau P, Michaud JL. Capo-Chichi JM, et al. Among authors: samuels me. J Med Genet. 2015 May;52(5):303-11. doi: 10.1136/jmedgenet-2014-102952. Epub 2015 Feb 3. J Med Genet. 2015. PMID: 25650066

9

Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of UBIAD1 gene expression.

Morales CR, Grigoryeva LS, Pan X, Bruno L, Hickson G, Ngo MH, McMaster CR, Samuels ME, Pshezhetsky AV. Morales CR, et al. Among authors: samuels me. Mol Genet Metab Rep. 2014 Sep 19;1:407-411. doi: 10.1016/j.ymgmr.2014.09.001. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896114 Free PMC article.

10

Identification and biochemical characterization of a novel mutation in DDX11 causing Warsaw breakage syndrome.

Capo-Chichi JM, Bharti SK, Sommers JA, Yammine T, Chouery E, Patry L, Rouleau GA, Samuels ME, Hamdan FF, Michaud JL, Brosh RM Jr, Mégarbane A, Kibar Z. Capo-Chichi JM, et al. Among authors: samuels me. Hum Mutat. 2013 Jan;34(1):103-7. doi: 10.1002/humu.22226. Epub 2012 Oct 17. Hum Mutat. 2013. PMID: 23033317 Free PMC article.

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