Harvard Catalyst Profiles

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Alissa Maria D'Gama, M.D., Ph.D.

Concepts (157)

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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?
Intensive Care Units, Neonatal520248621.860 Why?
Malformations of Cortical Development420211761.680 Why?
Mosaicism420234801.280 Why?
Epilepsy5202333271.150 Why?
Seizures, Febrile120231090.800 Why?
Mutation152023302380.730 Why?
Neonatology120231410.720 Why?
Optic Atrophy12020790.680 Why?
TOR Serine-Threonine Kinases3202120620.670 Why?
Thiolester Hydrolases12020910.640 Why?
Epilepsies, Partial120234350.640 Why?
Telencephalon120171430.560 Why?
Amino Acid Metabolism, Inborn Errors120202830.550 Why?
Genetic Testing4202435910.550 Why?
Abnormalities, Multiple2202014240.500 Why?
Mitochondrial Proteins120209790.470 Why?
Genomics4202459260.460 Why?
Infant, Newborn112024264220.400 Why?
Developmental Disabilities1202015180.380 Why?
Histone-Lysine N-Methyltransferase120157010.370 Why?
Carrier Proteins1202049370.280 Why?
Transcription Factors42024121680.280 Why?
Stem Cells1201735370.240 Why?
High-Throughput Nucleotide Sequencing4202136710.220 Why?
Repressor Proteins1201529820.220 Why?
Muscle Hypotonia120241660.210 Why?
Signal Transduction22017236450.210 Why?
Ontario120234030.200 Why?
Homeodomain Proteins2202424290.200 Why?
Mutation, Missense3202425920.190 Why?
Vigabatrin12021880.190 Why?
Critical Illness2202427560.170 Why?
Movement Disorders120244630.170 Why?
Infant72024365350.170 Why?
Brain42023273600.160 Why?
Transcription Factor AP-212019780.160 Why?
Congenital Hypothyroidism12018400.160 Why?
Autistic Disorder2202212400.160 Why?
Diabetes Insipidus120191440.150 Why?
Metal Metabolism, Inborn Errors12018140.150 Why?
Humans3320247681660.150 Why?
DNA-Binding Proteins1201596150.150 Why?
Mutagenesis1202212280.150 Why?
Ataxia120203070.150 Why?
Hypoventilation12018440.150 Why?
Myopathies, Structural, Congenital120181040.150 Why?
Focus Groups1202414600.150 Why?
Stereotypic Movement Disorder12017310.140 Why?
Ductus Arteriosus, Patent120192160.140 Why?
Sleep Apnea, Central12018880.140 Why?
Pedigree3202045390.140 Why?
Chromosomes, Human120184380.140 Why?
Minority Groups1202412160.130 Why?
Germ-Line Mutation2202118850.130 Why?
Fingers120195110.130 Why?
Neoplasms, Germ Cell and Embryonal120214980.130 Why?
Rett Syndrome120171640.130 Why?
Cation Transport Proteins120183260.120 Why?
Manganese120183940.120 Why?
Structure-Activity Relationship1202030550.120 Why?
Parkinsonian Disorders120182850.120 Why?
Child102024809170.120 Why?
Loss of Heterozygosity120176630.120 Why?
Dystonic Disorders120183540.110 Why?
Class I Phosphatidylinositol 3-Kinases120179050.110 Why?
Muscle Proteins1201811650.110 Why?
Face1201910290.100 Why?
Protein Conformation1202039560.100 Why?
Feasibility Studies1202353150.100 Why?
Genetic Predisposition to Disease42021180650.100 Why?
Female1820243971920.100 Why?
GTPase-Activating Proteins120154670.100 Why?
Hand120179130.100 Why?
Anticonvulsants1202119230.090 Why?
Cell Lineage2201725750.090 Why?
Child, Preschool82024426690.090 Why?
Health Personnel1202433850.090 Why?
Databases, Genetic1201717580.090 Why?
Oligonucleotide Array Sequence Analysis1201838000.090 Why?
Prefrontal Cortex1202122380.090 Why?
Molecular Targeted Therapy1202128300.090 Why?
Pilot Projects1202387410.080 Why?
Cohort Studies42023417540.080 Why?
Male1420243647190.080 Why?
DNA Mutational Analysis2201541200.080 Why?
Phenotype42020167260.080 Why?
Neurons3201795140.080 Why?
Cerebral Cortex2201558120.080 Why?
Mass Screening1202354580.070 Why?
Sequence Analysis, DNA2201547860.070 Why?
Heart Defects, Congenital1202447120.070 Why?
Proto-Oncogene Proteins c-akt1201524570.070 Why?
Gene Expression Regulation, Developmental1201736100.060 Why?
Phosphatidylinositol 3-Kinases1201528850.060 Why?
Aging1202287440.050 Why?
Polymorphism, Single Nucleotide32021160450.050 Why?
Hospitalization12023108400.050 Why?
Genetic Variation1201766110.050 Why?
Transcription, Genetic1201576080.050 Why?
Australia1202412650.050 Why?
Germinoma120211320.040 Why?
Brain Neoplasms1202191180.040 Why?
Canada1202421300.040 Why?
Animals320211692460.040 Why?
Chromosomes, Human, Pair 10120192750.040 Why?
Sequence Analysis120182400.040 Why?
Young Adult32021600660.040 Why?
Adolescent52021891690.040 Why?
Colorectal Neoplasms1201769740.030 Why?
Zygote120171170.030 Why?
Chromosomes, Human, Pair 1120196400.030 Why?
Consanguinity120184600.030 Why?
Chelating Agents120183850.030 Why?
Embryonic Development120217240.030 Why?
Muscle Weakness120184120.030 Why?
Enhancer Elements, Genetic1202213670.030 Why?
Magnetic Resonance Imaging22020367430.030 Why?
Growth Substances120177590.030 Why?
Classical Lissencephalies and Subcortical Band Heterotopias12014130.030 Why?
Exons1202123940.030 Why?
Testicular Neoplasms120218060.030 Why?
Lissencephaly12014360.030 Why?
Periventricular Nodular Heterotopia12014570.030 Why?
Genome-Wide Association Study12013127950.030 Why?
Cell Division1202144730.030 Why?
Chromosome Aberrations1201917780.030 Why?
Gene Regulatory Networks1202117520.020 Why?
Video Recording120179760.020 Why?
Mice12017820290.020 Why?
Mitosis1201511780.020 Why?
Seizures1202329980.020 Why?
Protein Binding1202293430.020 Why?
Central Nervous System1201713460.020 Why?
Insulin-Like Growth Factor I1201719420.020 Why?
Genetic Association Studies1201827440.020 Why?
Logistic Models12024132900.020 Why?
Chromatin1202129810.020 Why?
DNA Replication1201514270.020 Why?
Genome, Human1202144460.020 Why?
Receptors, Cell Surface1201728190.020 Why?
Recombinant Proteins1201765140.020 Why?
Epigenesis, Genetic1202138330.020 Why?
Biopsy1201867930.020 Why?
Genetic Loci1201526290.020 Why?
Adult120202236460.020 Why?
Genotype12019130450.010 Why?
Gene Expression Regulation12022119280.010 Why?
Single-Cell Analysis1201525400.010 Why?
Retrospective Studies22024817620.010 Why?
Muscle, Skeletal1201849780.010 Why?
Middle Aged120152234920.010 Why?
Pregnancy12021302560.010 Why?
Prognosis12018300100.010 Why?
Cells, Cultured12013190150.010 Why?
Rats12013237600.010 Why?
United States12024730390.010 Why?
Prospective Studies12021549260.010 Why?
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Concepts (157)
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Co-Authors (91)
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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.