Pesquisa | BVS Educação Profissional em Saúde

1.

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.

Van Driest, Sara L; Wells, Quinn S; Stallings, Sarah; Bush, William S; Gordon, Adam; Nickerson, Deborah A; Kim, Jerry H; Crosslin, David R; Jarvik, Gail P; Carrell, David S; Ralston, James D; Larson, Eric B; Bielinski, Suzette J; Olson, Janet E; Ye, Zi; Kullo, Iftikhar J; Abul-Husn, Noura S; Scott, Stuart A; Bottinger, Erwin; Almoguera, Berta; Connolly, John; Chiavacci, Rosetta; Hakonarson, Hakon; Rasmussen-Torvik, Laura J; Pan, Vivian; Persell, Stephen D; Smith, Maureen; Chisholm, Rex L; Kitchner, Terrie E; He, Max M; Brilliant, Murray H; Wallace, John R; Doheny, Kimberly F; Shoemaker, M Benjamin; Li, Rongling; Manolio, Teri A; Callis, Thomas E; Macaya, Daniela; Williams, Marc S; Carey, David; Kapplinger, Jamie D; Ackerman, Michael J; Ritchie, Marylyn D; Denny, Joshua C; Roden, Dan M.

JAMA ; 315(1): 47-57, 2016 Jan 05.

Artigo em Inglês | MEDLINE | ID: mdl-26746457

2.

The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation.

Chen, Jian-Fu; Mandel, Elizabeth M; Thomson, J Michael; Wu, Qiulian; Callis, Thomas E; Hammond, Scott M; Conlon, Frank L; Wang, Da-Zhi.

Nat Genet ; 38(2): 228-33, 2006 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-16380711

3.

The BMP pathway acts to directly regulate Tbx20 in the developing heart.

Mandel, Elizabeth M; Kaltenbrun, Erin; Callis, Thomas E; Zeng, Xin-Xin I; Marques, Sara R; Yelon, Deborah; Wang, Da-Zhi; Conlon, Frank L.

Development ; 137(11): 1919-29, 2010 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-20460370

4.

miR-155 inhibits expression of the MEF2A protein to repress skeletal muscle differentiation.

Seok, Hee Young; Tatsuguchi, Mariko; Callis, Thomas E; He, Aibin; Pu, William T; Wang, Da-Zhi.

J Biol Chem ; 286(41): 35339-35346, 2011 Oct 14.

Artigo em Inglês | MEDLINE | ID: mdl-21868385

5.

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing.

Dellefave-Castillo, Lisa M; Cirino, Allison L; Callis, Thomas E; Esplin, Edward D; Garcia, John; Hatchell, Kathryn E; Johnson, Britt; Morales, Ana; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Nussbaum, Robert L; McNally, Elizabeth M.

JAMA Cardiol ; 7(9): 966-974, 2022 09 01.

Artigo em Inglês | MEDLINE | ID: mdl-35947370

6.

Myocardin inhibits cellular proliferation by inhibiting NF-kappaB(p65)-dependent cell cycle progression.

Tang, Ru-Hang; Zheng, Xi-Long; Callis, Thomas E; Stansfield, William E; He, Jiayin; Baldwin, Albert S; Wang, Da-Zhi; Selzman, Craig H.

Proc Natl Acad Sci U S A ; 105(9): 3362-7, 2008 Mar 04.

Artigo em Inglês | MEDLINE | ID: mdl-18296632

7.

Targeted deletion of Dicer in the heart leads to dilated cardiomyopathy and heart failure.

Chen, Jian-Fu; Murchison, Elizabeth P; Tang, Ruhang; Callis, Thomas E; Tatsuguchi, Mariko; Deng, Zhongliang; Rojas, Mauricio; Hammond, Scott M; Schneider, Michael D; Selzman, Craig H; Meissner, Gerhard; Patterson, Cam; Hannon, Gregory J; Wang, Da-Zhi.

Proc Natl Acad Sci U S A ; 105(6): 2111-6, 2008 Feb 12.

Artigo em Inglês | MEDLINE | ID: mdl-18256189

8.

Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis.

Sturm, Amy C; Truty, Rebecca; Callis, Thomas E; Aguilar, Sienna; Esplin, Edward D; Garcia, Sarah; Haverfield, Eden V; Morales, Ana; Nussbaum, Robert L; Rojahn, Susan; Vatta, Matteo; Rader, Daniel J.

JAMA Cardiol ; 6(8): 902-909, 2021 08 01.

Artigo em Inglês | MEDLINE | ID: mdl-34037665

9.

ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.

Moya-Mendez, Mary E; Ogbonna, Chiagoziem; Ezekian, Jordan E; Rosamilia, Michael B; Prange, Lyndsey; de la Uz, Caridad; Kim, Jeffrey J; Howard, Taylor; Garcia, John; Nussbaum, Robert; Truty, Rebecca; Callis, Thomas E; Funk, Emily; Heyes, Matthew; Dear, Guy de Lisle; Carboni, Michael P; Idriss, Salim F; Mikati, Mohamad A; Landstrom, Andrew P.

J Am Heart Assoc ; 10(17): e019887, 2021 09 07.

Artigo em Inglês | MEDLINE | ID: mdl-34459253

10.

Taking microRNAs to heart.

Callis, Thomas E; Wang, Da-Zhi.

Trends Mol Med ; 14(6): 254-60, 2008 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-18457996

11.

Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy.

Morales, Ana; Moretz, Chad; Ren, Sheng; Smith, Elizabeth; Callis, Thomas E; Hall, Taryn; Hatchell, Kathryn E; Nussbaum, Robert L; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Esplin, Edward D; Murillo, Jaime.

Circ Genom Precis Med ; 17(1): e004028, 2024 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-38088168

12.

Muscling through the microRNA world.

Callis, Thomas E; Deng, Zhongliang; Chen, Jian-Fu; Wang, Da-Zhi.

Exp Biol Med (Maywood) ; 233(2): 131-8, 2008 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-18222968

13.

Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation.

Kapplinger, Jamie D; Pundi, Krishna N; Larson, Nicholas B; Callis, Thomas E; Tester, David J; Bikker, Hennie; Wilde, Arthur A M; Ackerman, Michael J.

Circ Genom Precis Med ; 11(2): e001424, 2018 02.

Artigo em Inglês | MEDLINE | ID: mdl-29453246

14.

MicroRNAs in skeletal and cardiac muscle development.

Callis, Thomas E; Chen, Jian-Fu; Wang, Da-Zhi.

DNA Cell Biol ; 26(4): 219-25, 2007 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-17465888

15.

Bone morphogenetic protein signaling modulates myocardin transactivation of cardiac genes.

Callis, Thomas E; Cao, Dongsun; Wang, Da-Zhi.

Circ Res ; 97(10): 992-1000, 2005 Nov 11.

Artigo em Inglês | MEDLINE | ID: mdl-16224060

16.

Common Variants in KCNE1, KCNH2, and SCN5A May Impact Cardiac Arrhythmia Risk.

Vatta, Matteo; Truty, Rebecca; Garcia, John; Callis, Thomas E; Hatchell, Kathryn; Rojahn, Susan; Morales, Ana; Aradhya, Swaroop; Nussbaum, Robert.

Circ Genom Precis Med ; 14(1): e003206, 2021 02.

Artigo em Inglês | MEDLINE | ID: mdl-33517668

17.

Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel.

Kapplinger, Jamie D; Giudicessi, John R; Ye, Dan; Tester, David J; Callis, Thomas E; Valdivia, Carmen R; Makielski, Jonathan C; Wilde, Arthur A; Ackerman, Michael J.

Circ Cardiovasc Genet ; 8(4): 582-95, 2015 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-25904541

18.

Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel.

Kapplinger, Jamie D; Tseng, Andrew S; Salisbury, Benjamin A; Tester, David J; Callis, Thomas E; Alders, Marielle; Wilde, Arthur A M; Ackerman, Michael J.

J Cardiovasc Transl Res ; 8(3): 187-97, 2015 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-25854863

19.

Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise.

Kapplinger, Jamie D; Landstrom, Andrew P; Bos, J Martijn; Salisbury, Benjamin A; Callis, Thomas E; Ackerman, Michael J.

J Cardiovasc Transl Res ; 7(3): 347-61, 2014 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-24510615

20.

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

Kapplinger, Jamie D; Landstrom, Andrew P; Salisbury, Benjamin A; Callis, Thomas E; Pollevick, Guido D; Tester, David J; Cox, Moniek G P J; Bhuiyan, Zahir; Bikker, Hennie; Wiesfeld, Ans C P; Hauer, Richard N W; van Tintelen, J Peter; Jongbloed, Jan D H; Calkins, Hugh; Judge, Daniel P; Wilde, Arthur A M; Ackerman, Michael J.

J Am Coll Cardiol ; 57(23): 2317-27, 2011 Jun 07.

Artigo em Inglês | MEDLINE | ID: mdl-21636032

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