Judge DP - Search Results

1

The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice.

Gan P, Baicu C, Watanabe H, Wang K, Tao G, Judge DP, Zile MR, Makita T, Mukherjee R, Sucov HM. Gan P, et al. Among authors: judge dp. Hum Mol Genet. 2021 Jan 6;29(21):3504-3515. doi: 10.1093/hmg/ddaa234. Hum Mol Genet. 2021. PMID: 33084860 Free PMC article.

2

Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.

Gan P, Patterson M, Velasquez A, Wang K, Tian D, Windle JJ, Tao G, Judge DP, Makita T, Park TJ, Sucov HM. Gan P, et al. Among authors: judge dp. PLoS Genet. 2019 Oct 7;15(10):e1008354. doi: 10.1371/journal.pgen.1008354. eCollection 2019 Oct. PLoS Genet. 2019. PMID: 31589606 Free PMC article.

3

Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family.

Caulfield TR, Richter JE Jr, Brown EE, Mohammad AN, Judge DP, Atwal PS. Caulfield TR, et al. Among authors: judge dp. Mol Genet Genomic Med. 2018 Apr 26;6(4):666-72. doi: 10.1002/mgg3.401. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 29700987 Free PMC article.

4

FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.

Brun F, Gigli M, Graw SL, Judge DP, Merlo M, Murray B, Calkins H, Sinagra G, Taylor MR, Mestroni L, James CA. Brun F, et al. Among authors: judge dp. J Med Genet. 2020 Apr;57(4):254-257. doi: 10.1136/jmedgenet-2019-106394. Epub 2020 Jan 10. J Med Genet. 2020. PMID: 31924696 Free PMC article.

5

Epidemiology of the inherited cardiomyopathies.

McKenna WJ, Judge DP. McKenna WJ, et al. Among authors: judge dp. Nat Rev Cardiol. 2021 Jan;18(1):22-36. doi: 10.1038/s41569-020-0428-2. Epub 2020 Sep 7. Nat Rev Cardiol. 2021. PMID: 32895535 Review.

6

Inheritance Impacts Mitral Valve Insufficiency.

Judge DP, Norris RA. Judge DP, et al. Circ Cardiovasc Genet. 2017 Oct;10(5):e001920. doi: 10.1161/CIRCGENETICS.117.001920. Circ Cardiovasc Genet. 2017. PMID: 28993408 No abstract available.

7

Multivalvular Pulsus Alternans.

Alimohamed M, Usher BW, Judge DP, Houston BA. Alimohamed M, et al. Among authors: judge dp. Circ Heart Fail. 2020 Dec;13(12):e007134. doi: 10.1161/CIRCHEARTFAILURE.120.007134. Epub 2020 Dec 11. Circ Heart Fail. 2020. PMID: 33302708 No abstract available.

8

PLEKHM2 Loss-of-Function Is Associated With Dilated Cardiomyopathy.

Atkins J, Gensemer C, Foil K, Morningstar J, Ramos H, Van Bakel AB, Norris RA, Judge DP. Atkins J, et al. Among authors: judge dp. Circ Genom Precis Med. 2022 Aug;15(4):e003594. doi: 10.1161/CIRCGEN.121.003594. Epub 2022 Jul 6. Circ Genom Precis Med. 2022. PMID: 35862026 Free PMC article. No abstract available.

9

DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, Tucker A, Russell SD, Bluemke DA, Dietz HC, Calkins H, Judge DP. Awad MM, et al. Among authors: judge dp. Am J Hum Genet. 2006 Jul;79(1):136-42. doi: 10.1086/504393. Epub 2006 Apr 28. Am J Hum Genet. 2006. PMID: 16773573 Free PMC article.

10

Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.

Houston BA, Judge DP, Brown E, Halushka M, Barouch LA. Houston BA, et al. Among authors: judge dp. J Card Fail. 2017 Aug;23(8):652-655. doi: 10.1016/j.cardfail.2017.06.001. Epub 2017 Jun 15. J Card Fail. 2017. PMID: 28624653

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