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Asma Tahir, M.B.,B.S.

Concepts (63)

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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?
Coronary Artery Disease5201465580.140 Why?
Arabs220131900.110 Why?
GATA2 Transcription Factor120141580.110 Why?
GATA4 Transcription Factor120131250.100 Why?
Chromosomes, Human, Pair 12120144320.100 Why?
Angiotensinogen120131610.100 Why?
3' Untranslated Regions120135150.090 Why?
Hypoxia-Inducible Factor 1, alpha Subunit120146270.090 Why?
Dyslipidemias220148720.080 Why?
Saudi Arabia320142110.080 Why?
Atherosclerosis2201434200.070 Why?
Adiponectin1201311210.070 Why?
Hearing Loss, Sensorineural120147830.070 Why?
Haplotypes4201427270.070 Why?
Metabolic Diseases120136860.070 Why?
Genetic Predisposition to Disease52014180750.070 Why?
Hypertension3201486160.060 Why?
Receptors, Cell Surface1201428150.060 Why?
Diabetes Mellitus, Type 242014122450.050 Why?
Polymorphism, Single Nucleotide42014160440.050 Why?
Genetic Linkage2201323420.040 Why?
Obesity32014130900.030 Why?
Gene Frequency2201436240.030 Why?
Case-Control Studies42014222480.030 Why?
DNA Mutational Analysis2201441140.030 Why?
Genetic Association Studies2201427460.030 Why?
Base Sequence22014124150.030 Why?
Chromosomes, Human, Pair 3120143220.030 Why?
Sequence Analysis, DNA2201447800.030 Why?
Myocardial Infarction12013115130.030 Why?
Consanguinity120144600.020 Why?
Chromosomes, Human, Pair 8120134510.020 Why?
Genes, Recessive120146250.020 Why?
Protein Structure, Secondary1201412110.020 Why?
Mutation12014302130.020 Why?
Family Health1201412540.020 Why?
Lipoproteins, HDL120136770.020 Why?
Linkage Disequilibrium1201319960.020 Why?
Logistic Models22013132780.020 Why?
Protein Structure, Tertiary1201437570.020 Why?
Hypercholesterolemia1201411450.020 Why?
Heterozygote1201327950.020 Why?
Chi-Square Distribution1201334320.020 Why?
Pedigree1201445390.020 Why?
Chromosome Mapping1201446190.020 Why?
Phenotype22013167240.020 Why?
Genetic Loci1201426300.010 Why?
Oligonucleotide Array Sequence Analysis1201337960.010 Why?
Models, Molecular1201453860.010 Why?
Middle Aged520142232570.010 Why?
Amino Acid Sequence12014134110.010 Why?
Risk Factors32014748810.010 Why?
Risk1201496020.010 Why?
Male620143641420.010 Why?
Coronary Angiography1201345080.010 Why?
Odds Ratio1201396610.010 Why?
Female620143965200.010 Why?
Genotype12014130360.010 Why?
Genetic Variation1201466120.010 Why?
Humans620147667660.010 Why?
Risk Assessment12013242950.010 Why?
Cardiovascular Diseases12013156570.000 Why?
Child12014806680.000 Why?
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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.