Landis BJ - Search Results

1

Chromosome 4q28.3q32.3 duplication in a patient with lymphatic malformations, craniosynostosis, and dysmorphic features.

Traub ES, Sheppard SE, Dori Y, Burns KD, Zackai EH, Ware SM, Landis BJ, Li D, Weaver DD. Traub ES, et al. Among authors: landis bj. Clin Dysmorphol. 2021 Apr 1;30(2):89-92. doi: 10.1097/MCD.0000000000000347. Clin Dysmorphol. 2021. PMID: 32925199 Free PMC article.

2

Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutation.

Ware SM, Shikany A, Landis BJ, James JF, Hinton RB. Ware SM, et al. Among authors: landis bj. Pediatrics. 2014 Oct;134(4):e1218-23. doi: 10.1542/peds.2013-2503. Epub 2014 Sep 15. Pediatrics. 2014. PMID: 25225139

3

Clinical Stratification of Pediatric Patients with Idiopathic Thoracic Aortic Aneurysm.

Landis BJ, Ware SM, James J, Shikany AR, Martin LJ, Hinton RB. Landis BJ, et al. J Pediatr. 2015 Jul;167(1):131-7.e1-5. doi: 10.1016/j.jpeds.2015.02.042. Epub 2015 Mar 24. J Pediatr. 2015. PMID: 25812776

4

Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing.

Schubert JA, Landis BJ, Shikany AR, Hinton RB, Ware SM. Schubert JA, et al. Among authors: landis bj. Am J Med Genet A. 2016 May;170A(5):1288-94. doi: 10.1002/ajmg.a.37568. Epub 2016 Feb 7. Am J Med Genet A. 2016. PMID: 26854089 Free PMC article.

5

The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges.

Landis BJ, Ware SM. Landis BJ, et al. Front Cardiovasc Med. 2016 Jul 25;3:22. doi: 10.3389/fcvm.2016.00022. eCollection 2016. Front Cardiovasc Med. 2016. PMID: 27504451 Free PMC article. Review.

6

Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling.

Freeze SL, Landis BJ, Ware SM, Helm BM. Freeze SL, et al. Among authors: landis bj. J Genet Couns. 2016 Dec;25(6):1171-1178. doi: 10.1007/s10897-016-0002-6. Epub 2016 Aug 22. J Genet Couns. 2016. PMID: 27550231 Free PMC article. Review.

7

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity.

Landis BJ, Schubert JA, Lai D, Jegga AG, Shikany AR, Foroud T, Ware SM, Hinton RB. Landis BJ, et al. J Cardiovasc Transl Res. 2017 Aug;10(4):423-432. doi: 10.1007/s12265-017-9753-1. Epub 2017 May 26. J Cardiovasc Transl Res. 2017. PMID: 28550590 Free PMC article.

8

Genotype-phenotype correlations in Marfan syndrome.

Landis BJ, Veldtman GR, Ware SM. Landis BJ, et al. Heart. 2017 Nov;103(22):1750-1752. doi: 10.1136/heartjnl-2017-311513. Epub 2017 Jun 8. Heart. 2017. PMID: 28596305 No abstract available.

9

Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling.

Armstrong ME, Weaver DD, Lah MD, Vance GH, Landis BJ, Ware SM, Helm BM. Armstrong ME, et al. Among authors: landis bj. Mol Cytogenet. 2018 Mar 27;11:23. doi: 10.1186/s13039-018-0372-6. eCollection 2018. Mol Cytogenet. 2018. PMID: 29599822 Free PMC article.

10

Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic risk.

Crawford CA, Vujakovich CE, Elmore L, Fleming E, Landis BJ, Spoonamore KG, Ware SM. Crawford CA, et al. Among authors: landis bj. Cardiol Young. 2020 Feb;30(2):219-226. doi: 10.1017/S1047951119002646. Epub 2020 Jan 27. Cardiol Young. 2020. PMID: 31983361 Free PMC article.

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