Ferhaan Ahmad

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Book Reviews

Aaas News, E. Lu, Min-Min Zhou, 1893, Buffalo Medical and Surgical Journal.

Increased &agr;2 Subunit–Associated AMPK Activity and PRKAG2 Cardiomyopathy

Ferhaan Ahmad, J. Seidman, C. Seidman, 2005, Circulation.

A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemia.

Ferhaan Ahmad, S. Saba, R. Tian, 2007, Biochemical and biophysical research communications.

Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban

Ulrike Mende, Christine E Seidman, Ferhaan Ahmad, 2003, Science.

Heart Failure in the Era of Precision Medicine: A Scientific Statement From the American Heart Association.

Carolyn M. Reilly, Ferhaan Ahmad, L. de las Fuentes, 2019, Circulation. Genomic and precision medicine.

SGLT 1 , a Novel Cardiac Glucose Transporter , Mediates Increased Glucose Uptake in PRKAG 2 Cardiomyopathy

Ferhaan Ahmad, K. Hallows, R. Alzamora, 2010 .

SGLT1, a novel cardiac glucose transporter, mediates increased glucose uptake in PRKAG2 cardiomyopathy.

Ferhaan Ahmad, K. Hallows, N. Pastor-Soler, 2010, Journal of molecular and cellular cardiology.

Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.

Matthew W. Martinez, Ferhaan Ahmad, L. Salberg, 2019, Circulation. Genomic and precision medicine.

Activation of cardiac hypertrophic signaling pathways in a transgenic mouse with the human PRKAG2 Thr400Asn mutation.

Ferhaan Ahmad, S. Banerjee, Xueyin N. Huang, 2010, Biochimica et biophysica acta.

Functional role of AMP‐activated protein kinase in the heart during exercise

Ferhaan Ahmad, J. Seidman, N. Fujii, 2005, FEBS letters.

Cardiac Sodium-Glucose Co-Transporter 1 (SGLT1) is a Novel Mediator of Ischemia/Reperfusion Injury.

Ferhaan Ahmad, V. Agrawal, Zhao Li, 2019, Cardiovascular research.

SGLT1 and Sweet Genetic Insights Into Cardiometabolic Risk.

Ferhaan Ahmad, Z. Li, K. Shibbani, 2018, Journal of the American College of Cardiology.

Pathogenic troponin T mutants with opposing effects on myofilament Ca2+ sensitivity attenuate cardiomyopathy phenotypes in mice.

Ferhaan Ahmad, S. Huke, B. Knollmann, 2019, Archives of biochemistry and biophysics.

Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathy

Ferhaan Ahmad, C. Seidman, B. McDonough, 2012, BMC Medical Genetics.

Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathy

Ferhaan Ahmad, C. Seidman, B. McDonough, 2012, BMC Medical Genetics.

Genetic determinants of risk and survival in pulmonary arterial hypertension

Lisa J. Martin, Ferhaan Ahmad, W. Ouwehand, 2018, bioRxiv.

Cellular, Pharmacological, and Biophysical Evaluation of Explanted Lungs from a Patient with Sickle Cell Disease and Severe Pulmonary Arterial Hypertension

Ferhaan Ahmad, M. Gladwin, J. Milošević, 2013, Pulmonary circulation.

High Mobility Group Box 1 Contributes to the Pathogenesis of Experimental Pulmonary Hypertension via Activation of Toll-like Receptor 4

Ferhaan Ahmad, S. Erzurum, S. Comhair, 2012, Molecular medicine.

Genetic determinants of risk and survival in pulmonary arterial hypertension

Lisa J. Martin, Ferhaan Ahmad, W. Ouwehand, 2018, bioRxiv.

Patient with a PRKAG2 mutation who developed Immunoglobulin A nephropathy: a case report

Ferhaan Ahmad, D. Holanda, M. Giudici, 2019, European heart journal. Case reports.

Alterations of Phospholamban Function Can Exhibit Cardiotoxic Effects Independent of Excessive Sarcoplasmic Reticulum Ca2+-ATPase Inhibition

Ferhaan Ahmad, J. Schmitt, J. Seidman, 2009, Circulation.

Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium Desensitization

Stephen H. Smith, Ferhaan Ahmad, G. Salama, 2016, PloS one.

SGLT1 is a novel cardiac glucose transporter that is perturbed in disease states.

Ferhaan Ahmad, N. Pastor-Soler, S. Banerjee, 2009, Cardiovascular research.

Activation of Cardiac Hypertrophic Signaling Pathways in a Transgenic Mouse with the Human Thr400Asn Mutation

Ferhaan Ahmad, S. Banerjee, Xueyin N. Huang, 2020 .

Transgenic Knockdown of Cardiac Sodium/Glucose Cotransporter 1 (SGLT1) Attenuates PRKAG2 Cardiomyopathy, Whereas Transgenic Overexpression of Cardiac SGLT1 Causes Pathologic Hypertrophy and Dysfunction in Mice

Ferhaan Ahmad, So Jung Lee, Ravi K. Sharma, 2014, Journal of the American Heart Association.

IL-12 is required for differentiation of pathogenic CD8+ T cell effectors that cause myocarditis.

Ferhaan Ahmad, J. Seidman, C. Seidman, 2003, The Journal of clinical investigation.

Female Sex Is Associated with Worse Prognosis in Patients with Hypertrophic Cardiomyopathy in China

Ferhaan Ahmad, R. Hui, K. Sun, 2014, PloS one.

The genomic complexity underlying pulmonary arterial hypertension: from mendel to networks.

Ferhaan Ahmad, Revathi Rajkumar, 2014, American journal of respiratory and critical care medicine.

The Role of Cardiac Troponin T Quantity and Function in Cardiac Development and Dilated Cardiomyopathy

Stephen H. Smith, Ferhaan Ahmad, J. Seidman, 2008, PloS one.

Somatic mutations in pulmonary arterial hypertension: primary or secondary events?

Ferhaan Ahmad, R. Hamid, E. Austin, 2010, American journal of respiratory and critical care medicine.

Family Relationships Associated With Communication and Testing for Inherited Cardiac Conditions

Anne L. Ersig, Ferhaan Ahmad, Janet K. Williams, 2018, Western journal of nursing research.

S100A12 as a marker of worse cardiac output and mortality in pulmonary hypertension

Ferhaan Ahmad, N. Kaminski, K. Gibson, 2018, Respirology.

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

Ferhaan Ahmad, T. Wong, B. Keavney, 2021, Cell reports. Medicine.

Consequences of Pressure Overload on Sarcomere Protein Mutation-Induced Hypertrophic Cardiomyopathy

Richard T. Lee, Ferhaan Ahmad, J. Schmitt, 2003, Circulation.

Cardiac sodium-dependent glucose cotransporter 1 is a novel mediator of ischaemia/reperfusion injury

Ferhaan Ahmad, V. Agrawal, W. Kutschke, 2019 .

Diversity, Equity, and Inclusiveness in Medicine and Cardiology: Next Steps for JAHA

Ferhaan Ahmad, K. Rice, H. Jneid, 2020, Journal of the American Heart Association.

Genomewide RNA expression profiling in lung identifies distinct signatures in idiopathic pulmonary arterial hypertension and secondary pulmonary hypertension.

Ferhaan Ahmad, N. Kaminski, Kazuhisa Konishi, 2010, American journal of physiology. Heart and circulatory physiology.

CFTR Heterozygotes Are at Increased Risk of Respiratory Infections: A Population-Based Study

Grant D. Brown, Ferhaan Ahmad, P. Polgreen, 2018, Open forum infectious diseases.

Cerebral Vein Thrombosis due to Hereditary Antithrombin III Deficiency

Ferhaan Ahmad, P. Tuite, R. Ethier, 1993, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Anencephalic infants as organ donors: A nencephalic inans as org an, dnors: Beware the slippery slope

Ferhaan Ahmad, 2006 .

COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine

Ferhaan Ahmad, A. Owens, N. Pereira, 2020, Mayo Clinic Proceedings.

Vanadate Augments Insulin-Stimulated Insulin Receptor Kinase Activity and Prolongs Insulin Action In Rat Adipocytes: Evidence for Transduction of Amplitude of Signaling into Duration of Response

Ferhaan Ahmad, I. G. Fantus, G. Deragon, 1994, Diabetes.

Transcriptional coactivator PGC-1 alpha controls the energy state and contractile function of cardiac muscle.

Jiandie D. Lin, Ferhaan Ahmad, B. Spiegelman, 2005, Cell metabolism.

The genetic basis for cardiac remodeling.

Christine E Seidman, Ferhaan Ahmad, J. Seidman, 2005, Annual review of genomics and human genetics.

Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension

Lisa J. Martin, Ferhaan Ahmad, W. Chung, 2019, Genome Medicine.

Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

Lisa J. Martin, Keith A. Marsolo, Ferhaan Ahmad, 2018, bioRxiv.

Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension

Lisa J. Martin, Ferhaan Ahmad, W. Chung, 2019, Genome Medicine.

Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy

Ferhaan Ahmad, R. Hui, K. Sun, 2014, European journal of heart failure.

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.

Ferhaan Ahmad, J. Seidman, G. Fishman, 2008, Journal of molecular and cellular cardiology.

Characterization of an acquired IgG inhibitor of coagulation factor XIII in a patient with systemic lupus erythematosus

Ferhaan Ahmad, S. Solymoss, M. Poon, 1996, British journal of haematology.

Rare Variants in Genes Encoding MuRF1 and MuRF2 Are Modifiers of Hypertrophic Cardiomyopathy

Ferhaan Ahmad, R. Hui, Y. Zou, 2014, International journal of molecular sciences.

Transgenic Mice Overexpressing Mutant PRKAG2 Define the Cause of Wolff-Parkinson-White Syndrome in Glycogen Storage Cardiomyopathy

Ferhaan Ahmad, J. Schmitt, J. Seidman, 2003, Circulation.

Early Treatment with Fumagillin, an Inhibitor of Methionine Aminopeptidase-2, Prevents Pulmonary Hypertension in Monocrotaline-Injured Rats

Ferhaan Ahmad, A. Saqi, D. Kass, 2012, PloS one.

Reversibility of PRKAG2 Glycogen-Storage Cardiomyopathy and Electrophysiological Manifestations

Ferhaan Ahmad, J. Seidman, C. Seidman, 2008, Circulation.

Autosomal Recessive Transmission of MYBPC3 Mutation Results in Malignant Phenotype of Hypertrophic Cardiomyopathy

Ferhaan Ahmad, R. Hui, Y. Zou, 2013, PloS one.

Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function

Ferhaan Ahmad, J. Schmitt, J. Seidman, 2006, Proceedings of the National Academy of Sciences.

E2F3 plays an essential role in cardiac development and function

Ferhaan Ahmad, J. Seidman, J. Lees, 2008, Cell cycle.

The molecular genetics of arrhythmogenic right ventricular dysplasia-cardiomyopathy.

Ferhaan Ahmad, 2003, Clinical and investigative medicine. Medecine clinique et experimentale.

Midterm Outcomes of Off‐Pump and On‐Pump Coronary Artery Revascularization in Renal Transplant Recipients

Ferhaan Ahmad, Y. Toyoda, C. Bermudez, 2011, Journal of cardiac surgery.

Vanadate augments insulin binding and prolongs insulin action in rat adipocytes.

Ferhaan Ahmad, I. G. Fantus, G. Deragon, 1990, Endocrinology.

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

Ferhaan Ahmad, T. Wong, B. Keavney, 2022, Cell reports. Medicine.

The Mouseion at the JAXlibrary The Mouseion at the JAXlibrary

Ferhaan Ahmad, M. Rynkiewicz, A. Bais, 2022 .