Lewis MES - Search Results

1

Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder.

Budd MA, Calli K, Samson L, Bowes J, Hsieh AYY, Forbes JC, Bitnun A, Singer J, Kakkar F, Alimenti A, Maan EJ, Lewis MES, Gentile C, Côté HCF, Brophy JC. Budd MA, et al. Among authors: lewis mes. Viruses. 2018 Feb 11;10(2):77. doi: 10.3390/v10020077. Viruses. 2018. PMID: 29439467 Free PMC article.

2

Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.

Callaghan DB, Rogic S, Tan PPC, Calli K, Qiao Y, Baldwin R, Jacobson M, Belmadani M, Holmes N, Yu C, Li Y, Li Y, Kurtzke FE, Kuzeljevic B, Yu AY, Hudson M, Mcaughton AJM, Xu Y, Dionne-Laporte A, Girard S, Liang P, Separovic ER, Liu X, Rouleau G, Pavlidis P, Lewis MES. Callaghan DB, et al. Among authors: lewis mes. Clin Genet. 2019 Sep;96(3):199-206. doi: 10.1111/cge.13556. Epub 2019 May 30. Clin Genet. 2019. PMID: 31038196

3

Genome-wide detection of tandem DNA repeats that are expanded in autism.

Trost B, Engchuan W, Nguyen CM, Thiruvahindrapuram B, Dolzhenko E, Backstrom I, Mirceta M, Mojarad BA, Yin Y, Dov A, Chandrakumar I, Prasolava T, Shum N, Hamdan O, Pellecchia G, Howe JL, Whitney J, Klee EW, Baheti S, Amaral DG, Anagnostou E, Elsabbagh M, Fernandez BA, Hoang N, Lewis MES, Liu X, Sjaarda C, Smith IM, Szatmari P, Zwaigenbaum L, Glazer D, Hartley D, Stewart AK, Eberle MA, Sato N, Pearson CE, Scherer SW, Yuen RKC. Trost B, et al. Among authors: lewis mes. Nature. 2020 Oct;586(7827):80-86. doi: 10.1038/s41586-020-2579-z. Epub 2020 Jul 27. Nature. 2020. PMID: 32717741 Free PMC article.

4

Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous POLR2A Variant.

Evans DR, Qiao Y, Trost B, Calli K, Martell S, Jones SJM, Scherer SW, Lewis MES. Evans DR, et al. Among authors: lewis mes. Genes (Basel). 2022 Mar 7;13(3):470. doi: 10.3390/genes13030470. Genes (Basel). 2022. PMID: 35328024 Free PMC article.

5

Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant.

Yip S, Calli K, Qiao Y, Trost B, Scherer SW, Lewis MES. Yip S, et al. Among authors: lewis mes. Genes (Basel). 2023 Nov 24;14(12):2122. doi: 10.3390/genes14122122. Genes (Basel). 2023. PMID: 38136944 Free PMC article.

6

Correlates of age at diagnosis of autism spectrum disorders in six Canadian regions.

Coo H, Ouellette-Kuntz H, Lam M, Yu CT, Dewey D, Bernier FP, Chudley AE, Hennessey PE, Breitenbach MM, Noonan AL, Lewis ME, Holden JJ. Coo H, et al. Chronic Dis Inj Can. 2012 Mar;32(2):90-100. Chronic Dis Inj Can. 2012. PMID: 22414306 Free article.

7

The changing prevalence of autism in three regions of Canada.

Ouellette-Kuntz H, Coo H, Lam M, Breitenbach MM, Hennessey PE, Jackman PD, Lewis ME, Dewey D, Bernier FP, Chung AM. Ouellette-Kuntz H, et al. J Autism Dev Disord. 2014 Jan;44(1):120-36. doi: 10.1007/s10803-013-1856-1. J Autism Dev Disord. 2014. PMID: 23771514

8

Status report - National Epidemiologic Database for the Study of Autism in Canada (NEDSAC).

Ouellette-Kuntz H, Coo H, Yu CT, Lewis ME, Dewey D, Hennessey PE, Jackman PD, Breitenbach MM, Holden JJ. Ouellette-Kuntz H, et al. Chronic Dis Inj Can. 2012 Mar;32(2):84-9. Chronic Dis Inj Can. 2012. PMID: 22414305 Free article. No abstract available.

9

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.

Liu X, Malenfant P, Reesor C, Lee A, Hudson ML, Harvard C, Qiao Y, Persico AM, Cohen IL, Chudley AE, Forster-Gibson C, Rajcan-Separovic E, Lewis ME, Holden JJ. Liu X, et al. Eur J Hum Genet. 2011 Dec;19(12):1264-70. doi: 10.1038/ejhg.2011.112. Epub 2011 Jul 13. Eur J Hum Genet. 2011. PMID: 21750575 Free PMC article.

10

Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication.

Dastan J, Chijiwa C, Tang F, Martell S, Qiao Y, Rajcan-Separovic E, Lewis MES. Dastan J, et al. Among authors: lewis mes. BMC Med Genet. 2016 Nov 10;17(1):78. doi: 10.1186/s12881-016-0340-0. BMC Med Genet. 2016. PMID: 27832746 Free PMC article.

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