Zarrei M - Search Results

1

Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma.

Hoffman M, Gillmor AH, Kunz DJ, Johnston MJ, Nikolic A, Narta K, Zarrei M, King J, Ellestad K, Dang NH, Cavalli FMG, Kushida MM, Coutinho FJ, Zhu Y, Luu B, Ma Y, Mungall AJ, Moore R, Marra MA, Taylor MD, Pugh TJ, Dirks PB, Strother D, Lafay-Cousin L, Resnick AC, Scherer S, Senger DL, Simons BD, Chan JA, Morrissy AS, Gallo M. Hoffman M, et al. Among authors: zarrei m. Cancer Res. 2019 May 1;79(9):2111-2123. doi: 10.1158/0008-5472.CAN-18-3441. Epub 2019 Mar 15. Cancer Res. 2019. PMID: 30877103 Free PMC article.

2

A copy number variation map of the human genome.

Zarrei M, MacDonald JR, Merico D, Scherer SW. Zarrei M, et al. Nat Rev Genet. 2015 Mar;16(3):172-83. doi: 10.1038/nrg3871. Epub 2015 Feb 3. Nat Rev Genet. 2015. PMID: 25645873 Review.

3

Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing.

Naseer MI, Sogaty S, Rasool M, Chaudhary AG, Abutalib YA, Walker S, Marshall CR, Merico D, Carter MT, Scherer SW, Al-Qahtani MH, Zarrei M. Naseer MI, et al. Among authors: zarrei m. Am J Med Genet A. 2016 Nov;170(11):3018-3022. doi: 10.1002/ajmg.a.37845. Epub 2016 Aug 17. Am J Med Genet A. 2016. PMID: 27531570

4

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.

Butcher NJ, Merico D, Zarrei M, Ogura L, Marshall CR, Chow EWC, Lang AE, Scherer SW, Bassett AS. Butcher NJ, et al. Among authors: zarrei m. PLoS One. 2017 Apr 21;12(4):e0173944. doi: 10.1371/journal.pone.0173944. eCollection 2017. PLoS One. 2017. PMID: 28430790 Free PMC article.

5

Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes.

Woodbury-Smith M, Nicolson R, Zarrei M, Yuen RKC, Walker S, Howe J, Uddin M, Hoang N, Buchanan JA, Chrysler C, Thompson A, Szatmari P, Scherer SW. Woodbury-Smith M, et al. Among authors: zarrei m. NPJ Genom Med. 2017 May 3;2:17. doi: 10.1038/s41525-017-0020-9. NPJ Genom Med. 2017. PMID: 28649445 Free PMC article.

6

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.

Woodbury-Smith M, Deneault E, Yuen RKC, Walker S, Zarrei M, Pellecchia G, Howe JL, Hoang N, Uddin M, Marshall CR, Chrysler C, Thompson A, Szatmari P, Scherer SW. Woodbury-Smith M, et al. Among authors: zarrei m. Mol Autism. 2017 Nov 9;8:59. doi: 10.1186/s13229-017-0175-3. eCollection 2017. Mol Autism. 2017. PMID: 29152164 Free PMC article.

7

Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.

Zhang Y, Liu Y, Zarrei M, Tong W, Dong R, Wang Y, Zhang H, Yang X, MacDonald JR, Uddin M, Scherer SW, Gai Z. Zhang Y, et al. Among authors: zarrei m. Am J Med Genet B Neuropsychiatr Genet. 2018 Jan;177(1):93-100. doi: 10.1002/ajmg.b.32608. Epub 2017 Nov 20. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29152845

8

Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.

da Silva Montenegro EM, Costa CS, Campos G, Scliar M, de Almeida TF, Zachi EC, Silva IMW, Chan AJS, Zarrei M, Lourenço NCV, Yamamoto GL, Scherer S, Passos-Bueno MR. da Silva Montenegro EM, et al. Among authors: zarrei m. Autism Res. 2020 Feb;13(2):199-206. doi: 10.1002/aur.2238. Epub 2019 Nov 6. Autism Res. 2020. PMID: 31696658

9

Refining critical regions in 15q24 microdeletion syndrome pertaining to autism.

Liu Y, Zhang Y, Zarrei M, Dong R, Yang X, Zhao D, Scherer SW, Gai Z. Liu Y, et al. Among authors: zarrei m. Am J Med Genet B Neuropsychiatr Genet. 2020 Jun;183(4):217-226. doi: 10.1002/ajmg.b.32778. Epub 2020 Jan 18. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 31953991

10

Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer.

Bobyn A, Zarrei M, Zhu Y, Hoffman M, Brenner D, Resnick AC, Scherer SW, Gallo M. Bobyn A, et al. Among authors: zarrei m. BMC Med Genet. 2020 May 6;21(1):92. doi: 10.1186/s12881-020-01033-x. BMC Med Genet. 2020. PMID: 32375678 Free PMC article.

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