Veatch OJ - Search Results

1

Next-generation sequencing and analysis of consecutive patients referred for connective tissue disorders.

Steinle J, Hossain WA, Veatch OJ, Strom SP, Butler MG. Steinle J, et al. Among authors: veatch oj. Am J Med Genet A. 2022 Oct;188(10):3016-3023. doi: 10.1002/ajmg.a.62905. Epub 2022 Jul 29. Am J Med Genet A. 2022. PMID: 35903967 Free PMC article.

2

Brief report: non-random X chromosome inactivation in females with autism.

Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG. Talebizadeh Z, et al. Among authors: veatch oj. J Autism Dev Disord. 2005 Oct;35(5):675-81. doi: 10.1007/s10803-005-0011-z. J Autism Dev Disord. 2005. PMID: 16167093 Free PMC article.

3

An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder.

Veatch OJ, Butler MG, Elsea SH, Malow BA, Sutcliffe JS, Moore JH. Veatch OJ, et al. Int J Mol Sci. 2020 Nov 27;21(23):9029. doi: 10.3390/ijms21239029. Int J Mol Sci. 2020. PMID: 33261099 Free PMC article.

4

ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders.

Steinle J, Hossain WA, Lovell S, Veatch OJ, Butler MG. Steinle J, et al. Among authors: veatch oj. Am J Med Genet A. 2021 Mar;185(3):743-752. doi: 10.1002/ajmg.a.62030. Epub 2020 Dec 27. Am J Med Genet A. 2021. PMID: 33369194 Free PMC article.

5

Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families.

Baldwin I, Shafer RL, Hossain WA, Gunewardena S, Veatch OJ, Mosconi MW, Butler MG. Baldwin I, et al. Among authors: veatch oj. Int J Mol Sci. 2021 Feb 7;22(4):1660. doi: 10.3390/ijms22041660. Int J Mol Sci. 2021. PMID: 33562221 Free PMC article.

6

Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.

Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Veatch OJ, et al. Pediatr Neurol. 2021 Oct;123:30-37. doi: 10.1016/j.pediatrneurol.2021.07.009. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34388423 Free PMC article.

7

PHIP gene variants with protein modeling, interactions, and clinical phenotypes.

Dietrich J, Lovell S, Veatch OJ, Butler MG. Dietrich J, et al. Among authors: veatch oj. Am J Med Genet A. 2022 Feb;188(2):579-589. doi: 10.1002/ajmg.a.62557. Epub 2021 Nov 13. Am J Med Genet A. 2022. PMID: 34773373

8

Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study.

Veatch OJ, Steinle J, Hossain WA, Butler MG. Veatch OJ, et al. BMC Med Genomics. 2022 Aug 2;15(1):169. doi: 10.1186/s12920-022-01321-w. BMC Med Genomics. 2022. PMID: 35918752 Free PMC article.

9

Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and Review.

Butler MG, Hossain WA, Steinle J, Gao H, Cox E, Niu Y, Quach M, Veatch OJ. Butler MG, et al. Among authors: veatch oj. Int J Mol Sci. 2022 Aug 13;23(16):9090. doi: 10.3390/ijms23169090. Int J Mol Sci. 2022. PMID: 36012355 Free PMC article.

10

Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

Talebizadeh Z, Bittel DC, Veatch OJ, Butler MG, Takahashi TN, Miles JH. Talebizadeh Z, et al. Among authors: veatch oj. J Autism Dev Disord. 2004 Dec;34(6):735-6. doi: 10.1007/s10803-004-5295-x. J Autism Dev Disord. 2004. PMID: 15679194 Free PMC article. No abstract available.

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