Morris CA - Search Results

1

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.

Liu D, Billington CJ Jr, Raja N, Wong ZC, Levin MD, Resch W, Alba C, Hupalo DN, Biamino E, Bedeschi MF, Digilio MC, Squeo GM, Villa R, Parrish PCR, Knutsen RH, Osgood S, Freeman JA, Dalgard CL, Merla G, Pober BR, Mervis CB, Roberts AE, Morris CA, Osborne LR, Kozel BA. Liu D, et al. Among authors: morris ca. J Am Heart Assoc. 2024 Feb 6;13(3):e031377. doi: 10.1161/JAHA.123.031377. Epub 2024 Jan 31. J Am Heart Assoc. 2024. PMID: 38293922 Free PMC article.

2

Williams syndrome and related disorders.

Morris CA, Mervis CB. Morris CA, et al. Annu Rev Genomics Hum Genet. 2000;1:461-84. doi: 10.1146/annurev.genom.1.1.461. Annu Rev Genomics Hum Genet. 2000. PMID: 11701637 Review.

3

Diagnosis and management of medical problems in adults with Williams-Beuren syndrome.

Pober BR, Morris CA. Pober BR, et al. Among authors: morris ca. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):280-90. doi: 10.1002/ajmg.c.30139. Am J Med Genet C Semin Med Genet. 2007. PMID: 17639596 Review.

4

The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms.

Tam E, Young EJ, Morris CA, Marshall CR, Loo W, Scherer SW, Mervis CB, Osborne LR. Tam E, et al. Among authors: morris ca. Am J Med Genet A. 2008 Jul 15;146A(14):1797-806. doi: 10.1002/ajmg.a.32360. Am J Med Genet A. 2008. PMID: 18553513 Free PMC article.

5

Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and Europe.

Morris CA, Mervis CB, Osborne LR. Morris CA, et al. Mol Cytogenet. 2011 Feb 28;4:7. doi: 10.1186/1755-8166-4-7. Mol Cytogenet. 2011. PMID: 21356100 Free PMC article.

6

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.

Qaiser F, Yin Y, Mervis CB, Morris CA, Klein-Tasman BP, Tam E, Osborne LR, Yuen RKC. Qaiser F, et al. Among authors: morris ca. Orphanet J Rare Dis. 2021 Jan 6;16(1):6. doi: 10.1186/s13023-020-01648-6. Orphanet J Rare Dis. 2021. PMID: 33407644 Free PMC article.

7

DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number.

Strong E, Mervis CB, Tam E, Morris CA, Klein-Tasman BP, Velleman SL, Osborne LR. Strong E, et al. Among authors: morris ca. NPJ Genom Med. 2023 Sep 14;8(1):25. doi: 10.1038/s41525-023-00368-7. NPJ Genom Med. 2023. PMID: 37709781 Free PMC article.

8

Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome.

Morris CA, Pani AM, Mervis CB, Rios CM, Kistler DJ, Gregg RG. Morris CA, et al. Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):299-306. doi: 10.1002/ajmg.c.30265. Am J Med Genet C Semin Med Genet. 2010. PMID: 20425789 Free PMC article.

9

Longitudinal assessment of intellectual abilities of children with Williams syndrome: multilevel modeling of performance on the Kaufman Brief Intelligence Test-Second Edition.

Mervis CB, Kistler DJ, John AE, Morris CA. Mervis CB, et al. Among authors: morris ca. Am J Intellect Dev Disabil. 2012 Mar;117(2):134-55. doi: 10.1352/1944-7558-117.2.134. Am J Intellect Dev Disabil. 2012. PMID: 22515828 Free PMC article.

10

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.

Strong E, Butcher DT, Singhania R, Mervis CB, Morris CA, De Carvalho D, Weksberg R, Osborne LR. Strong E, et al. Among authors: morris ca. Am J Hum Genet. 2015 Aug 6;97(2):216-27. doi: 10.1016/j.ajhg.2015.05.019. Epub 2015 Jul 9. Am J Hum Genet. 2015. PMID: 26166478 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

360 results

Search Page