Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Kalotina Machini, Ph.D.

Concepts (148)

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?
Genome, Human7202144200.680 Why?
Sequence Analysis, DNA4201948010.510 Why?
Genetic Testing8202234390.370 Why?
Genetic Counseling120146000.370 Why?
Genetic Variation5202165400.340 Why?
Data Interpretation, Statistical1201927140.340 Why?
Computational Biology2201935180.300 Why?
Genomics7202156920.300 Why?
Cardiomyopathies1201919120.300 Why?
Disease220216810.250 Why?
Pituitary Diseases120051410.240 Why?
Homeodomain Proteins2200524170.240 Why?
Genetic Predisposition to Disease42020174000.210 Why?
Pharmacogenetics320226760.210 Why?
Dwarfism120011450.180 Why?
Lactobacillus120011890.180 Why?
Alternative Splicing2200111180.170 Why?
Biotinidase12018190.170 Why?
Biological Specimen Banks120217070.140 Why?
Colorectal Neoplasms, Hereditary Nonpolyposis120203790.130 Why?
Health120193900.130 Why?
Hyperlipoproteinemia Type II120203730.130 Why?
Incidental Findings220186880.120 Why?
Transcription Factors22005121640.120 Why?
Receptors, Somatotropin22006760.110 Why?
Germ-Line Mutation1200117860.110 Why?
Medical History Taking120177830.110 Why?
Genetic Diseases, Inborn120175870.100 Why?
Multifactorial Inheritance1201911900.100 Why?
Polymerase Chain Reaction1200161710.100 Why?
Primary Health Care2201845510.100 Why?
Base Sequence42017127970.090 Why?
Cardiomyopathy, Hypertrophic1201712630.080 Why?
Genes, Dominant320158800.080 Why?
Family1201931440.080 Why?
DNA-Binding Proteins1200596390.080 Why?
Molecular Sequence Data52006181120.080 Why?
High-Throughput Nucleotide Sequencing2201735850.070 Why?
Information Dissemination1201411000.070 Why?
Transcription Factor Pit-112005160.070 Why?
Pedigree3202046460.060 Why?
Cost-Benefit Analysis1201853850.060 Why?
Contractile Proteins120062460.060 Why?
Randomized Controlled Trials as Topic2201999410.060 Why?
Choristoma120062130.060 Why?
Growth120063760.060 Why?
Intracellular Space120052120.060 Why?
Attitude of Health Personnel2201838390.060 Why?
Disclosure220217360.060 Why?
Protein Isoforms2200617270.060 Why?
Cerebral Ventricles120065440.060 Why?
Cricetulus120058170.060 Why?
Mutation22021297170.060 Why?
Health Knowledge, Attitudes, Practice1201839150.060 Why?
Heterozygote2202027900.050 Why?
CHO Cells1200514070.050 Why?
Duty to Recontact12021200.050 Why?
Exons3200624310.050 Why?
Rhombencephalon12001850.050 Why?
Ribotyping12001350.050 Why?
Regulatory Sequences, Nucleic Acid120057940.050 Why?
Cricetinae1200524710.050 Why?
Physical Chromosome Mapping120011830.050 Why?
Case-Control Studies12019217190.050 Why?
Human Growth Hormone120066830.050 Why?
Genetic Research120211740.050 Why?
Humans2120227420880.050 Why?
Point Mutation1200616240.050 Why?
Microfilament Proteins1200611520.050 Why?
RNA Splice Sites120012090.050 Why?
DNA, Ribosomal120012890.040 Why?
Penetrance120013800.040 Why?
Species Specificity2200124790.040 Why?
Molecular Mimicry120002010.040 Why?
Retroelements120001640.040 Why?
Chromosomes, Human, Pair 1120016570.040 Why?
Female1320213795920.040 Why?
Transcriptional Activation1200517820.040 Why?
Male1220213495380.040 Why?
Research Design1201459790.040 Why?
Introns120019910.040 Why?
Cloning, Molecular2200143220.040 Why?
Pituitary Gland120016650.040 Why?
Primates120005430.040 Why?
RNA, Ribosomal, 16S120019470.040 Why?
Reference Standards1200110200.040 Why?
Skull120018100.040 Why?
Sequence Alignment1200122570.040 Why?
Brain Diseases1200615540.040 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11120172340.040 Why?
DNA Primers1200128920.030 Why?
Gene Duplication120173300.030 Why?
DNA, Bacterial1200114650.030 Why?
Informed Consent120219910.030 Why?
Pilot Projects2201882970.030 Why?
Asymptomatic Diseases120175520.030 Why?
Neonatal Screening120185910.030 Why?
Infant, Newborn32019255750.030 Why?
Amino Acid Sequence22006138140.030 Why?
RNA Splicing120189070.030 Why?
Specialization120187770.030 Why?
DNA Mutational Analysis1200141870.030 Why?
Age of Onset1201932660.030 Why?
Evolution, Molecular1200019370.020 Why?
Phenotype22022163310.020 Why?
Databases, Genetic1201717800.020 Why?
Chromosome Mapping1201747420.020 Why?
Cohort Studies22021404500.020 Why?
Gene Frequency1201535870.020 Why?
DNA1202172890.020 Why?
Genotype12022129460.020 Why?
Cardiology1201816580.020 Why?
RNA, Messenger12001130290.020 Why?
Databases, Factual1202177160.020 Why?
Education, Medical1201817170.020 Why?
Twins, Dizygotic120062360.020 Why?
Health Behavior1201726300.020 Why?
Proportional Hazards Models12020123440.020 Why?
Genetic Association Studies1201526990.020 Why?
Middle Aged420212131270.020 Why?
Health Personnel1201832100.020 Why?
Referral and Consultation1201735270.020 Why?
Carrier Proteins1201750190.010 Why?
Health Care Costs1201732030.010 Why?
Patient Acceptance of Health Care1201730140.010 Why?
Reproducibility of Results12021198620.010 Why?
Animals320051685610.010 Why?
Genetic Diseases, X-Linked120063700.010 Why?
Aged320201629440.010 Why?
Sequence Homology, Amino Acid1200628370.010 Why?
Fatal Outcome1200618490.010 Why?
Family Health1200612820.010 Why?
Hormone Replacement Therapy120067440.010 Why?
Software1201444340.010 Why?
Adult320212137120.010 Why?
Physicians1201845540.010 Why?
Insulin-Like Growth Factor I1200620140.010 Why?
Retroviridae120009140.010 Why?
Algorithms12017138530.010 Why?
Lung Diseases1200618840.010 Why?
Risk Assessment12017233200.010 Why?
Polymorphism, Single Nucleotide12015154940.010 Why?
Phylogeny1200027970.010 Why?
Infant12006350700.000 Why?
Child, Preschool12006409550.000 Why?
Child12006774780.000 Why?
Retrospective Studies12006770980.000 Why?
Mice12000810450.000 Why?
Machini's Networks
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Concepts (148)
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Co-Authors (43)
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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.