Chung WK - Search Results

1

Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.

Selamet Tierney ES, Marans Z, Rutkin MB, Chung WK. Selamet Tierney ES, et al. Among authors: chung wk. Cardiol Young. 2007 Jun;17(3):268-74. doi: 10.1017/S1047951107000455. Epub 2007 Apr 20. Cardiol Young. 2007. PMID: 17445335

2

Recipient genotype is a predictor of allograft cytokine expression and outcomes after pediatric cardiac transplantation.

Auerbach SR, Manlhiot C, Reddy S, Kinnear C, Richmond ME, Gruber D, McCrindle BW, Deng L, Chen JM, Addonizio LJ, Chung WK, Mital S. Auerbach SR, et al. Among authors: chung wk. J Am Coll Cardiol. 2009 May 19;53(20):1909-17. doi: 10.1016/j.jacc.2009.02.027. J Am Coll Cardiol. 2009. PMID: 19442892 Free article.

3

Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.

Ma L, Selamet Tierney ES, Lee T, Lanzano P, Chung WK. Ma L, et al. Among authors: chung wk. Cardiol Young. 2012 Apr;22(2):194-201. doi: 10.1017/S1047951111001181. Epub 2011 Aug 25. Cardiol Young. 2012. PMID: 21864452 Free PMC article.

4

Rapidly progressive mitral valve stenosis in patients with acromelic dysplasia.

Rama G, Chung WK, Cunniff CM, Krishnan U. Rama G, et al. Among authors: chung wk. Cardiol Young. 2017 May;27(4):797-800. doi: 10.1017/S1047951116002006. Epub 2017 Jan 12. Cardiol Young. 2017. PMID: 28077185

5

Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease.

Morton SU, Shimamura A, Newburger PE, Opotowsky AR, Quiat D, Pereira AC, Jin SC, Gurvitz M, Brueckner M, Chung WK, Shen Y, Bernstein D, Gelb BD, Giardini A, Goldmuntz E, Kim RW, Lifton RP, Porter GA Jr, Srivastava D, Tristani-Firouzi M, Newburger JW, Seidman JG, Seidman CE. Morton SU, et al. Among authors: chung wk. JAMA Cardiol. 2021 Apr 1;6(4):457-462. doi: 10.1001/jamacardio.2020.4947. JAMA Cardiol. 2021. PMID: 33084842 Free PMC article.

6

Association of K121Q polymorphism in ENPP1 (PC-1) with BMI in Caucasian and African-American adults.

Matsuoka N, Patki A, Tiwari HK, Allison DB, Johnson SB, Gregersen PK, Leibel RL, Chung WK. Matsuoka N, et al. Among authors: chung wk. Int J Obes (Lond). 2006 Feb;30(2):233-7. doi: 10.1038/sj.ijo.0803132. Int J Obes (Lond). 2006. PMID: 16231022

7

RAAS gene polymorphisms influence progression of pediatric hypertrophic cardiomyopathy.

Kaufman BD, Auerbach S, Reddy S, Manlhiot C, Deng L, Prakash A, Printz BF, Gruber D, Papavassiliou DP, Hsu DT, Sehnert AJ, Chung WK, Mital S. Kaufman BD, et al. Among authors: chung wk. Hum Genet. 2007 Dec;122(5):515-23. doi: 10.1007/s00439-007-0429-9. Epub 2007 Sep 13. Hum Genet. 2007. PMID: 17851694

8

Polymorphism in the angiotensin II type 1 receptor (AGTR1) is associated with age at diagnosis in pulmonary arterial hypertension.

Chung WK, Deng L, Carroll JS, Mallory N, Diamond B, Rosenzweig EB, Barst RJ, Morse JH. Chung WK, et al. J Heart Lung Transplant. 2009 Apr;28(4):373-9. doi: 10.1016/j.healun.2009.01.016. J Heart Lung Transplant. 2009. PMID: 19332265 Free PMC article.

9

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

10

De novo copy number variants are associated with congenital diaphragmatic hernia.

Yu L, Wynn J, Ma L, Guha S, Mychaliska GB, Crombleholme TM, Azarow KS, Lim FY, Chung DH, Potoka D, Warner BW, Bucher B, LeDuc CA, Costa K, Stolar C, Aspelund G, Arkovitz MS, Chung WK. Yu L, et al. Among authors: chung dh, chung wk. J Med Genet. 2012 Oct;49(10):650-9. doi: 10.1136/jmedgenet-2012-101135. J Med Genet. 2012. PMID: 23054247 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

1,023 results

Search Page