Harvard Catalyst Profiles

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Amy Kritzer, M.D.

Concepts (84)

Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Amino Acid Metabolism, Inborn Errors220222730.800 Why?
Brain Diseases, Metabolic12022420.800 Why?
Metabolism, Inborn Errors220212800.770 Why?
Osteogenesis Imperfecta12022820.770 Why?
Child Abuse1202210440.430 Why?
Quality Improvement1202036660.240 Why?
Failure to Thrive220221350.230 Why?
Lipid Metabolism, Inborn Errors120241190.220 Why?
Glutaryl-CoA Dehydrogenase12022190.210 Why?
Delivery of Health Care1202051760.200 Why?
Urea Cycle Disorders, Inborn12021300.200 Why?
Spectrin120211710.190 Why?
Muscle Hypotonia120221610.180 Why?
Chloride Channels120212210.180 Why?
Thiolester Hydrolases12020840.170 Why?
Biotinidase12018170.160 Why?
Hydroxocobalamin12018270.160 Why?
Anemia, Megaloblastic12018240.160 Why?
Genes, Dominant120218590.160 Why?
Maple Syrup Urine Disease12018400.160 Why?
Rare Diseases120226060.140 Why?
Thrombotic Microangiopathies120181250.140 Why?
Ion Channels1202110280.140 Why?
Triglycerides1202423580.140 Why?
Genetic Variation2202164120.130 Why?
Fatty Acids1202417560.130 Why?
Guidelines as Topic1202213630.130 Why?
Abnormalities, Multiple1202013900.100 Why?
Referral and Consultation2202234750.100 Why?
Phenotype42021160660.100 Why?
Pancreatitis1201810880.090 Why?
Nerve Tissue Proteins1202143780.080 Why?
Diagnosis, Differential12022128400.070 Why?
Mutation22021294060.070 Why?
Child62024773440.060 Why?
Transcription Factors22022119490.060 Why?
Heterozygote2202127380.060 Why?
Rhabdomyolysis120241450.050 Why?
NF-E2-Related Factor 112022210.050 Why?
Disease Models, Animal12021177000.050 Why?
Genetic Association Studies2202126530.050 Why?
Disease Progression12018131170.050 Why?
Genitalia120221120.050 Why?
Language Development Disorders120211870.040 Why?
Genetic Predisposition to Disease12021172010.040 Why?
Infant42024349480.040 Why?
Humans1320247354580.040 Why?
Child, Preschool42024408120.040 Why?
Oxidation-Reduction1202421700.040 Why?
Laboratories120214600.040 Why?
Health Resources120248850.040 Why?
Vitamin B 12 Deficiency120181150.040 Why?
Hematologic Tests120182330.040 Why?
Injections, Intramuscular120185430.040 Why?
Hypoglycemia120248240.040 Why?
Homozygote1202117350.030 Why?
Blood Chemical Analysis120184280.030 Why?
Infant, Newborn32021254030.030 Why?
Neonatal Screening120185870.030 Why?
RNA Splicing120188890.030 Why?
Early Diagnosis1201811540.030 Why?
Cardiomyopathies1202418330.030 Why?
Blood Transfusion1201812910.020 Why?
Young Adult32024561510.020 Why?
Adolescent32024851250.020 Why?
Odds Ratio1202195420.020 Why?
Male620243461690.020 Why?
Healthcare Disparities1202231140.020 Why?
Mice, Knockout12021141470.020 Why?
Epilepsy1202132930.020 Why?
Female520243767080.020 Why?
Mice22021795480.010 Why?
Gene Expression Regulation12022117810.010 Why?
Adult320242123710.010 Why?
Emergency Service, Hospital1202176520.010 Why?
Severity of Illness Index12018153060.010 Why?
Obesity12021125020.010 Why?
Animals220211654790.010 Why?
Prognosis12018285480.010 Why?
Risk Assessment12018229010.010 Why?
United States12024690050.010 Why?
Retrospective Studies12022768870.010 Why?
Treatment Outcome12018624300.010 Why?
Middle Aged120242113050.010 Why?
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Concepts (84)
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Co-Authors (38)
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.