C. Anwar A. Chahal
C. Anwar A. Chahal publishes mostly in Cardiology and Cardiovascular Medicine, Physiology and Surgery, on topics such as Cardiomyopathy and Myosin Studies, Cardiovascular Effects of Exercise and Cardiac electrophysiology and arrhythmias.
- World rank
- #613,958 of 7,710,434 ranked researchers
- Rank in United States
- #210,197 of 1,627,098
- Works
- 307
- Citations
- 4.7k
- Citations per work
- 15.3
What does C. Anwar A. Chahal research?
C. Anwar A. Chahal's work is mostly in Medicine (63%), Biochemistry, Genetics and Molecular Biology (5%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Health Sciences19463.1%
- Medicine19463.1%
- Everything else9932.2%
- Life Sciences144.7%
- 1Cardiology and Cardiovascular Medicine45% of their works
- 2Physiology5% of their works
- 3Surgery5% of their works
- 4Molecular Biology5% of their works
- 5Radiology, Nuclear Medicine and Imaging4% of their works
- 6Epidemiology4% of their works
Research topics
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Cardiac electrophysiology and arrhythmias
- Cardiac Arrhythmias and Treatments
- Atrial Fibrillation Management and Outcomes
- Cardiovascular Function and Risk Factors
- Cardiac Valve Diseases and Treatments
- Cardiac pacing and defibrillation studies
Which keywords describe C. Anwar A. Chahal's research?
The keywords of their largest research topics: Genetic Mutations, Atrial Fibrillation, Arrhythmias, Sudden Cardiac Death, Catheter Ablation, Echocardiography, Heart Failure and Cardiomyopathies.
- Cardiac Resynchronization Therapy
- Surgical Aortic-Valve Replacement
- Chamber Quantification
- Anticoagulant Therapy
- Radiofrequency Ablation
- Ion Channels
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Cardiomyopathies
- Echocardiography
- Sudden Cardiac Death
- Atrial Fibrillation
- Genetic Mutations
- Arrhythmias
- Catheter Ablation
- Heart Failure
- Myosin
- Sudden Death
- Long-QT Syndrome
- Ventricular Tachycardia
- Stroke Prevention
- Diastolic Function
- Transcatheter Aortic-Valve Replacement
- Implantable Cardioverter-Defibrillator
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.
All 23 words, with their numbers
- Genetic Mutations1022 topics
- Atrial Fibrillation782 topics
- Arrhythmias762 topics
- Sudden Cardiac Death682 topics
- Catheter Ablation662 topics
- Echocardiography572 topics
- Heart Failure572 topics
- Cardiomyopathies561 topic
- Myosin561 topic
- Arrhythmogenic Right Ventricular Cardiomyopathy461 topic
- Sudden Death461 topic
- Ion Channels421 topic
- Long-QT Syndrome421 topic
- Radiofrequency Ablation341 topic
- Ventricular Tachycardia341 topic
- Anticoagulant Therapy321 topic
- Stroke Prevention321 topic
- Chamber Quantification311 topic
- Diastolic Function311 topic
- Surgical Aortic-Valve Replacement271 topic
- Transcatheter Aortic-Valve Replacement271 topic
- Cardiac Resynchronization Therapy261 topic
- Implantable Cardioverter-Defibrillator261 topic
Where does C. Anwar A. Chahal work?
C. Anwar A. Chahal's main affiliation in the publication record is WellSpan Health, United States.
How many publications and citations does C. Anwar A. Chahal have?
OpenAlex counts 307 works and 4,706 citations for C. Anwar A. Chahal, an h-index of 31, ranking #613,958 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised citation excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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