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Judge Lab Publications

Selected Publications:

  1. Den Haan AD, Tan BY, Zikusoka M, Lladó LI, Jain R, Daly A, Tichnell C, James C, Amat-Alarcon N, Abraham T, Russell SD, Bluemke DA, Calkins H, Dalal D, Judge DP. “Comprehensive Desmosome Mutation Analysis in North Americans with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy” Circulation CV Genetics 2009; in press.

  2. Judge DP, “Phenotypic diversity arising from a single mutation” Heart Rhythm 2009; in press, DOI 10.1016/j.hrthm.2009.08.008

  3. Brooke BS, Habashi JP, Judge DP, Patel N, Loeys B, Dietz HC 3rd. “Angiotensin II Blockade and Aortic-Root Dilation in Marfan Syndrome.” New England Journal of Medicine 2008; 358:2787-95.

  4. Cohn RD, van Erp C, Habashi JP, Soleimani AA, Klein EC, Lisi MT, Gamradt M, ap Rhys CM, Holm TM, Loeys BL, Ramirez F, Judge DP, Ward CW, Dietz HC. “Angiotensin II type 1 receptor blockade attenuates TGF?-induced failure of muscle regeneration in multiple myopathic states.” Nature Medicine 2007; 13:204-210

  5. Awad MM, Dalal D, Tichnell C, Tucker A, James C, Abraham T, Spevak PJ, Calkins H, Judge DP. “Recessive Arrhythmogenic Right Ventricular Dysplasia due to novel cryptic splice mutation in PKP2” Human Mutation 2006; 27:1157

  6. Dalal D*, James C*, Devanagondi R, Tichnell C, Tucker A, Prakasa K, Spevak PJ, Bluemke DA, Abraham T, Russell SD, Calkins H, Judge DP. “Penetrance of mutations in plakophilin-2 among families with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy” JACC 2006; 48:1416-24

  7. 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. “DSG2 mutations contribute to Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.” Am J Hum Genet 2006; 79:136-42

  8. Habashi JP*, Judge DP*(co-first author), Holm TM, Cohn RD, Loeys BL, Cooper TK, Myers L, Klein EC, Liu G, Calvi C, Podowski M, Neptune ER, Halushka MK, Bedja D, Gabrielson K, Rifkin DB, Carta L, Ramirez F, Huso DL, Dietz HC. “Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome” Science 2006; 312:117-21

  9. Loeys BL, Chen J, Neptune ER, Judge DP, Podowski M, Holm R, Meyers J, Leitch C, Katsanis N, Sharifi N, Xu FL, De Backer J, Hellemans J, Chen Y, Davis EC, Webb CL, Spevak PJ, Coucke P, Rifkin DB, De Paepe AM, Dietz HC. “A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.” Nature Genetics 2005, 37:275-81

  10. Ng CM, Cheng A, Myers LA, Martinez-Murillo F, Jie C, Bedja D, Gabrielson K, Hausladen JMW, Mecham RP, Judge DP*, Dietz HC. “TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome” Journal of Clinical Investigation 2004; 114:1586-92

 
 

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