Chung WK - Search Results

1

Cases in Precision Medicine: Genetic Assessment After a Sudden Cardiac Death in the Family.

Laracuente R, Waase MP, Kalia I, Wilde AAM, Chung WK. Laracuente R, et al. Among authors: chung wk. Ann Intern Med. 2019 May 21;170(10):710-716. doi: 10.7326/M18-2359. Epub 2019 May 14. Ann Intern Med. 2019. PMID: 31083726 Free PMC article. Review.

2

Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death.

Chung WK, Kitner C, Maron BJ. Chung WK, et al. Cardiol Young. 2011 Jun;21(3):345-8. doi: 10.1017/S1047951110001927. Epub 2011 Jan 25. Cardiol Young. 2011. PMID: 21262074

3

Clinical and molecular genetic features of hereditary pulmonary arterial hypertension.

Brenner L, Chung WK. Brenner L, et al. Among authors: chung wk. Compr Physiol. 2011 Oct;1(4):1721-8. doi: 10.1002/cphy.c100063. Compr Physiol. 2011. PMID: 23733703 Review.

4

Genetic testing preferences in families containing multiple individuals with epilepsy.

Okeke JO, Tangel VE, Sorge ST, Hesdorffer DC, Winawer MR, Goldsmith J, Phelan JC, Chung WK, Shostak S, Ottman R. Okeke JO, et al. Among authors: chung wk. Epilepsia. 2014 Nov;55(11):1705-13. doi: 10.1111/epi.12810. Epub 2014 Sep 29. Epilepsia. 2014. PMID: 25266816 Free PMC article.

5

Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.

Lopez HU, Haverfield E, Chung WK. Lopez HU, et al. Among authors: chung wk. Pediatr Dev Pathol. 2015 Jul-Aug;18(4):324-6. doi: 10.2350/14-08-1543-CR.1. Epub 2015 Apr 29. Pediatr Dev Pathol. 2015. PMID: 25923035

6

23andMe Paves the Way for Direct-to-Consumer Genetic Health Risk Tests of Limited Clinical Utility.

Wynn J, Chung WK. Wynn J, et al. Among authors: chung wk. Ann Intern Med. 2017 Jul 18;167(2):125-126. doi: 10.7326/M17-1045. Epub 2017 May 30. Ann Intern Med. 2017. PMID: 28554190 No abstract available.

7

Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies.

Wynn J, Holland DT, Duong J, Ahimaz P, Chung WK. Wynn J, et al. Among authors: chung wk. J Genet Couns. 2018 Aug;27(4):927-934. doi: 10.1007/s10897-017-0186-4. Epub 2017 Dec 15. J Genet Couns. 2018. PMID: 29243008

8

The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.

Rasouly HM, Groopman EE, Heyman-Kantor R, Fasel DA, Mitrotti A, Westland R, Bier L, Weng C, Ren Z, Copeland B, Krithivasan P, Chung WK, Sanna-Cherchi S, Goldstein DB, Gharavi AG. Rasouly HM, et al. Among authors: chung wk. Ann Intern Med. 2019 Jan 1;170(1):11-21. doi: 10.7326/M18-1241. Epub 2018 Nov 27. Ann Intern Med. 2019. PMID: 30476936

9

Cases in Precision Medicine: When Patients Present With Direct-to-Consumer Genetic Test Results.

Artin MG, Stiles D, Kiryluk K, Chung WK. Artin MG, et al. Among authors: chung wk. Ann Intern Med. 2019 May 7;170(9):643-650. doi: 10.7326/M18-2356. Epub 2019 Apr 30. Ann Intern Med. 2019. PMID: 31035287 Free PMC article.

10

Precision Medicine in Internal Medicine.

Kiryluk K, Goldstein DB, Rowe JW, Gharavi AG, Wapner R, Chung WK. Kiryluk K, et al. Among authors: chung wk. Ann Intern Med. 2019 May 7;170(9):635-642. doi: 10.7326/M18-0425. Epub 2019 Apr 30. Ann Intern Med. 2019. PMID: 31035290 Free PMC article.

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