University of Pittsburgh Department of Human Genetics
Primary Faculty



Secondary Faculty

Ferhaan Ahmad
Position: Assistant Professor
Office:Scaife Hall, Suite S-558
Phone:412-647-5840
Email:
Education:M.D., Medical Degree, McGill University, 1991
Residency, Internal Medicine,, McGill University, 1994
Fellowship, Cardiology, McGill University, 1996
Ph.D., Cardiovascular Sciences, Baylor College of Medicine, 2001
Fellowship, , Genetics, Harvard Medical School and Howard, 2005
 


Research Interests:
My laboratory uses a wide range of techniques in human and mouse genetics to elucidate the pathogenesis of hereditary cardiovascular diseases, such as hypertrophic and dilated cardiomyopathy. Mutations are mapped and identified in human families and individual patients with cardiovascular disorders. In addition, we use gene targeting and transgenic technology to generate novel murine models carrying mutations previously identified in humans with cardiovascular diseases. These models are studied to elucidate the pathways linking genotype to phenotype. Our research is dependent on crosstalk between clinical studies, human molecular genetic studies, animal modeling, and basic cellular and molecular studies. We welcome collaborations with other scientists, clinicians, and patients. Trainees in my laboratory are exposed to a breadth of techniques in statistical genetics, molecular genetics, molecular and cell biology, biochemistry, and physiology. They have the opportunity to pursue projects with clinical or basic orientations, within a multidisciplinary "bedside to bench to bedside" environment.
 
Recent Publications:

SGLT1 is a novel cardiac glucose transporter that is perturbed in disease states.
Sanjay K Banerjee, Kenneth R McGaffin, NĂºria M Pastor-Soler, Ferhaan Ahmad
Cardiovasc. Res. 2009 Oct;84:111-8
PMC2741348    

Alterations of phospholamban function can exhibit cardiotoxic effects independent of excessive sarcoplasmic reticulum Ca2+-ATPase inhibition.
Joachim P Schmitt, Ferhaan Ahmad, Kristina Lorenz, Lutz Hein, Stefan Schulz, Michio Asahi, David H Maclennan, Christine E Seidman, J G Seidman, Martin J Lohse
Circulation 2009 Jan;119:436-44

E2F3 plays an essential role in cardiac development and function.
Jennifer C King, Ivan P G Moskowitz, Patrick G Burgon, Ferhaan Ahmad, James R Stone, Jonathan G Seidman, Jacqueline A Lees
Cell Cycle 2008 Dec;7:3775-80
PMC2723769    

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
Ferhaan Ahmad, Sanjay K Banerjee, Michele L Lage, Xueyin N Huang, Stephen H Smith, Samir Saba, Jennifer Rager, David A Conner, Andrzej M Janczewski, Kimimasa Tobita, Joseph P Tinney, Ivan P Moskowitz, Antonio R Perez-Atayde, Bradley B Keller, Michael A Mathier, Sanjeev G Shroff, Christine E Seidman, J G Seidman
PLoS ONE 2008 ;3:e2642
PMC2441440    

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
Cordula M Wolf, Libin Wang, Ronny Alcalai, Anne Pizard, Patrick G Burgon, Ferhaan Ahmad, Megan Sherwood, Dorothy M Branco, Hiroko Wakimoto, Glenn I Fishman, Vincent See, Colin L Stewart, David A Conner, Charles I Berul, Christine E Seidman, J G Seidman
J. Mol. Cell. Cardiol. 2008 Feb;44:293-303

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