D. A. McDermott

发表

the Functional Genomics and Translational Biology Interdisciplinary Working Association Council on Epidemiology and Prevention, the Stroke Council, and Cardiovascular Disease: A Scientific Statement From the American Heart Relevance of Genetics and Genomics for Prevention and Treatment of

Yuling Hong, D. Arnett, S. Ganesh, 2007 .

Preimplantation genetic diagnosis of human congenital heart malformation and Holt–Oram syndrome

C. Basson, D. McDermott, F. Gilbert, 2004, American journal of medical genetics. Part A.

Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease: A Scientific Statement From the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group

David M Herrington, Eric Boerwinkle, Donna K Arnett, 2007, Circulation.

Corrigendum: Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

G. Breithardt, P. Ellinor, E. Schulze-Bahr, 2005, Nature Genetics.

Holt-Oram Syndrome

C. Basson, J. Fong, D. McDermott, 2015, Hypertext 2015.

Using the TBX5 transcription factor to grow and sculpt the heart

C. Hatcher, D. A. McDermott, D. A. Mcdermott, 2006, American journal of medical genetics. Part A.

TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome

M. Brueckner, C. Basson, S. Aftimos, 2005, Pediatric Research.

Atrial Fibrillation and Other Clinical Manifestations of Altered TBX5 Dosage in Typical Holt-Oram Syndrome.

C. Basson, D. McDermott, C. Hatcher, 2008, Circulation research.

Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management

E. Zackai, C. Morris, A. Rope, 2008, Genetics in Medicine.

Clinical phenotypes and molecular genetic mechanisms of Carney complex.

C. Basson, D. Wilkes, D. McDermott, 2005, The Lancet. Oncology.

The carney complex: unusual skin findings and recurrent cardiac myxoma.

K. R. Bennett, L. Creswell, C. Basson, 2005, Archives of dermatology.

Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice.

Kimberly Burton, Tsuneo Imai, Yan Song, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association.

David M Herrington, Donna K Arnett, Themistocles L Assimes, 2013, Circulation.

Cardiac Septation Defects and Their PreImplantation Diagnosis

C. Basson, D. McDermott, C. Hatcher, 2017 .

Genetics of cardiac septation defects and their pre-implantation diagnosis.

C. Basson, D. McDermott, C. Hatcher, 2006, Methods in molecular medicine.

Transcription factor cascades in congenital heart malformation.

C. Basson, D. McDermott, C. Hatcher, 2003, Trends in molecular medicine.

Haploinsufficiency at the protein kinase A RI alpha gene locus leads to fertility defects in male mice and men.

M. Goldstein, C. Basson, G. McKnight, 2006, Molecular endocrinology.

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

Walter Birchmeier, Günter Breithardt, Rainer Dietz, 2004, Nature Genetics.

Mutation of perinatal myosin heavy chain associated with a Carney complex variant.

Mark Veugelers, Cynthia C Morton, S. Weremowicz, 2004, The New England journal of medicine.

Molecular Genetic Analysis of PRKAG2 in Sporadic Wolff‐Parkinson‐White Syndrome

B. Lerman, C. Basson, D. McDermott, 2003, Journal of cardiovascular electrophysiology.

Update: PGD and Holt‐Oram syndrome

C. Basson, I. Kligman, D. A. McDermott, 2005, American journal of medical genetics. Part A.