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, Human7202144160.660 Why?
Sequence Analysis, DNA4201947170.500 Why?
Genetic Testing8202235300.350 Why?
Genetic Counseling120146250.350 Why?
Genetic Variation5202165400.330 Why?
Data Interpretation, Statistical1201926960.330 Why?
Computational Biology2201935040.300 Why?
Genomics7202157900.290 Why?
Cardiomyopathies1201919450.290 Why?
Disease220216710.240 Why?
Pituitary Diseases120051350.230 Why?
Homeodomain Proteins2200524140.230 Why?
Genetic Predisposition to Disease42020177660.200 Why?
Pharmacogenetics320226800.200 Why?
Dwarfism120011370.180 Why?
Lactobacillus120012040.170 Why?
Alternative Splicing2200110910.160 Why?
Biotinidase12018170.160 Why?
Biological Specimen Banks120217760.130 Why?
Colorectal Neoplasms, Hereditary Nonpolyposis120203800.130 Why?
Health120193950.130 Why?
Hyperlipoproteinemia Type II120203960.120 Why?
Transcription Factors22005121000.110 Why?
Incidental Findings220186980.110 Why?
Receptors, Somatotropin22006580.110 Why?
Medical History Taking120177730.110 Why?
Germ-Line Mutation1200118430.110 Why?
Genetic Diseases, Inborn120176010.100 Why?
Polymerase Chain Reaction1200160670.100 Why?
Multifactorial Inheritance1201913510.090 Why?
Primary Health Care2201846490.090 Why?
Base Sequence42017124470.090 Why?
Genes, Dominant320158630.080 Why?
Cardiomyopathy, Hypertrophic1201713000.080 Why?
Family1201931890.080 Why?
Molecular Sequence Data52006176280.080 Why?
DNA-Binding Proteins1200595900.070 Why?
High-Throughput Nucleotide Sequencing2201736180.070 Why?
Information Dissemination1201411320.070 Why?
Transcription Factor Pit-112005160.070 Why?
Pedigree3202045770.060 Why?
Contractile Proteins120062400.060 Why?
Cost-Benefit Analysis1201855070.060 Why?
Randomized Controlled Trials as Topic22019103400.060 Why?
Choristoma120062070.060 Why?
Growth120063650.060 Why?
Intracellular Space120051970.060 Why?
Attitude of Health Personnel2201838700.060 Why?
Disclosure220217380.060 Why?
Protein Isoforms2200616970.060 Why?
Cerebral Ventricles120065430.060 Why?
Cricetulus120058150.050 Why?
Health Knowledge, Attitudes, Practice1201839670.050 Why?
Mutation22021299500.050 Why?
Heterozygote2202027970.050 Why?
CHO Cells1200513890.050 Why?
Duty to Recontact12021190.050 Why?
Exons3200623910.050 Why?
Cricetinae1200524270.050 Why?
Rhombencephalon12001810.050 Why?
Regulatory Sequences, Nucleic Acid120057890.050 Why?
Ribotyping12001350.050 Why?
Physical Chromosome Mapping120011820.050 Why?
Case-Control Studies12019220410.050 Why?
Human Growth Hormone120066380.050 Why?
Point Mutation1200615940.050 Why?
Microfilament Proteins1200611340.050 Why?
Genetic Research120211720.050 Why?
Humans2120227602610.040 Why?
RNA Splice Sites120012110.040 Why?
DNA, Ribosomal120012850.040 Why?
Species Specificity2200124130.040 Why?
Penetrance120013880.040 Why?
Molecular Mimicry120002000.040 Why?
Chromosomes, Human, Pair 1120016350.040 Why?
Transcriptional Activation1200517550.040 Why?
Retroelements120001630.040 Why?
Cloning, Molecular2200141720.040 Why?
Research Design1201461810.040 Why?
Female1320213910110.040 Why?
Introns120019780.040 Why?
Pituitary Gland120016370.040 Why?
Male1220213594130.040 Why?
Primates120005230.040 Why?
Reference Standards1200110040.040 Why?
Sequence Alignment1200121780.040 Why?
Brain Diseases1200615400.040 Why?
Skull120018150.030 Why?
RNA, Ribosomal, 16S1200110060.030 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11120172250.030 Why?
DNA Primers1200128190.030 Why?
Gene Duplication120173140.030 Why?
DNA, Bacterial1200114550.030 Why?
Informed Consent1202110070.030 Why?
Pilot Projects2201885530.030 Why?
Asymptomatic Diseases120175820.030 Why?
Amino Acid Sequence22006134560.030 Why?
Neonatal Screening120185950.030 Why?
Infant, Newborn32019261680.030 Why?
RNA Splicing120189140.030 Why?
Specialization120187790.030 Why?
DNA Mutational Analysis1200141090.030 Why?
Age of Onset1201933020.020 Why?
Evolution, Molecular1200018840.020 Why?
Phenotype22022165430.020 Why?
Databases, Genetic1201717390.020 Why?
Chromosome Mapping1201746250.020 Why?
Cohort Studies22021413170.020 Why?
Gene Frequency1201536050.020 Why?
DNA1202172360.020 Why?
Genotype12022129590.020 Why?
Cardiology1201817230.020 Why?
RNA, Messenger12001127620.020 Why?
Education, Medical1201817280.020 Why?
Twins, Dizygotic120062360.020 Why?
Health Behavior1201726210.020 Why?
Databases, Factual1202180180.020 Why?
Genetic Association Studies1201527160.020 Why?
Proportional Hazards Models12020125320.020 Why?
Middle Aged420212201750.020 Why?
Carrier Proteins1201749380.010 Why?
Referral and Consultation1201735980.010 Why?
Health Personnel1201833100.010 Why?
Health Care Costs1201732570.010 Why?
Reproducibility of Results12021200480.010 Why?
Patient Acceptance of Health Care1201731590.010 Why?
Animals320051679400.010 Why?
Genetic Diseases, X-Linked120063780.010 Why?
Sequence Homology, Amino Acid1200627550.010 Why?
Aged320201689950.010 Why?
Fatal Outcome1200618330.010 Why?
Family Health1200612580.010 Why?
Software1201444200.010 Why?
Hormone Replacement Therapy120067560.010 Why?
Physicians1201845900.010 Why?
Adult320212198470.010 Why?
Insulin-Like Growth Factor I1200619200.010 Why?
Retroviridae120008500.010 Why?
Algorithms12017139670.010 Why?
Lung Diseases1200619150.010 Why?
Risk Assessment12017240860.010 Why?
Polymorphism, Single Nucleotide12015157660.010 Why?
Phylogeny1200027750.010 Why?
Infant12006360300.000 Why?
Child, Preschool12006420340.000 Why?
Child12006797580.000 Why?
Retrospective Studies12006803010.000 Why?
Mice12000812160.000 Why?
Machini's Networks
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Concepts (148)
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Co-Authors (39)
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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.