Harvard Catalyst Profiles

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

Alissa Maria D'Gama, M.D., 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?
Malformations of Cortical Development420212001.730 Why?
Mosaicism420234411.390 Why?
Intensive Care Units, Neonatal320247801.290 Why?
Epilepsy5202333101.200 Why?
Seizures, Febrile120231110.840 Why?
Mutation152023297860.770 Why?
Neonatology120231220.760 Why?
Optic Atrophy12020790.720 Why?
TOR Serine-Threonine Kinases3202121090.690 Why?
Thiolester Hydrolases12020860.690 Why?
Epilepsies, Partial120234360.670 Why?
Amino Acid Metabolism, Inborn Errors120202550.600 Why?
Telencephalon120171420.590 Why?
Abnormalities, Multiple2202014160.520 Why?
Mitochondrial Proteins120209960.480 Why?
Developmental Disabilities1202014560.410 Why?
Histone-Lysine N-Methyltransferase120156700.390 Why?
Infant, Newborn82024256250.340 Why?
Carrier Proteins1202050210.290 Why?
Stem Cells1201735670.240 Why?
High-Throughput Nucleotide Sequencing4202135970.240 Why?
Repressor Proteins1201530230.230 Why?
Transcription Factors32022122080.230 Why?
Signal Transduction22017234030.220 Why?
Ontario120233830.210 Why?
Vigabatrin12021920.190 Why?
Critical Illness2202426700.190 Why?
Brain42023263850.170 Why?
Genomics3202457200.170 Why?
Infant62024351360.170 Why?
Transcription Factor AP-212019820.170 Why?
Congenital Hypothyroidism12018390.170 Why?
Autistic Disorder2202211850.170 Why?
Mutation, Missense2201925640.170 Why?
Metal Metabolism, Inborn Errors12018150.160 Why?
Diabetes Insipidus120191510.160 Why?
Ataxia120203040.160 Why?
Hypoventilation12018380.160 Why?
DNA-Binding Proteins1201596480.160 Why?
Mutagenesis1202212660.160 Why?
Myopathies, Structural, Congenital120181020.160 Why?
Stereotypic Movement Disorder12017290.150 Why?
Ductus Arteriosus, Patent120192090.150 Why?
Sleep Apnea, Central12018840.150 Why?
Pedigree3202046440.150 Why?
Humans2920247443430.140 Why?
Germ-Line Mutation2202117880.140 Why?
Chromosomes, Human120184570.140 Why?
Minority Groups1202412230.140 Why?
Fingers120195130.140 Why?
Neoplasms, Germ Cell and Embryonal120215010.130 Why?
Rett Syndrome120171650.130 Why?
Cation Transport Proteins120183270.130 Why?
Manganese120184080.130 Why?
Parkinsonian Disorders120182750.130 Why?
Structure-Activity Relationship1202031290.120 Why?
Loss of Heterozygosity120176840.120 Why?
Child92024777090.120 Why?
Dystonic Disorders120183290.120 Why?
Class I Phosphatidylinositol 3-Kinases120178900.110 Why?
Feasibility Studies1202350780.110 Why?
Muscle Proteins1201811590.110 Why?
Face120199940.110 Why?
Protein Conformation1202040110.110 Why?
Genetic Predisposition to Disease42021174460.100 Why?
Hand120178840.100 Why?
Anticonvulsants1202119160.100 Why?
Cell Lineage2201725040.100 Why?
GTPase-Activating Proteins120154980.100 Why?
Pilot Projects1202383240.090 Why?
Prefrontal Cortex1202121470.090 Why?
Databases, Genetic1201717830.090 Why?
Molecular Targeted Therapy1202127270.090 Why?
Cohort Studies42023405610.090 Why?
Oligonucleotide Array Sequence Analysis1201839200.090 Why?
Phenotype42020163650.090 Why?
Child, Preschool72021410060.090 Why?
DNA Mutational Analysis2201541860.080 Why?
Neurons3201793380.080 Why?
Cerebral Cortex2201557080.080 Why?
Homeodomain Proteins1201824210.080 Why?
Mass Screening1202352550.080 Why?
Female1420233801940.080 Why?
Genetic Testing1202034440.080 Why?
Sequence Analysis, DNA2201548030.070 Why?
Proto-Oncogene Proteins c-akt1201525030.070 Why?
Gene Expression Regulation, Developmental1201736170.070 Why?
Phosphatidylinositol 3-Kinases1201529380.060 Why?
Male1020233501180.060 Why?
Aging1202286640.060 Why?
Hospitalization12023102620.060 Why?
Polymorphism, Single Nucleotide32021155190.060 Why?
Genetic Variation1201765440.050 Why?
Transcription, Genetic1201577220.050 Why?
Germinoma120211330.050 Why?
Brain Neoplasms1202188630.040 Why?
Animals320211687570.040 Why?
Young Adult32021564300.040 Why?
Chromosomes, Human, Pair 10120192870.040 Why?
Adolescent52021857810.040 Why?
Sequence Analysis120182560.040 Why?
Colorectal Neoplasms1201767730.040 Why?
Zygote120171160.040 Why?
Consanguinity120184540.040 Why?
Chromosomes, Human, Pair 1120196580.040 Why?
Chelating Agents120183800.040 Why?
Embryonic Development120217110.030 Why?
Enhancer Elements, Genetic1202213410.030 Why?
Muscle Weakness120184130.030 Why?
Magnetic Resonance Imaging22020354210.030 Why?
Classical Lissencephalies and Subcortical Band Heterotopias12014130.030 Why?
Growth Substances120177840.030 Why?
Exons1202124370.030 Why?
Lissencephaly12014380.030 Why?
Testicular Neoplasms120218040.030 Why?
Periventricular Nodular Heterotopia12014570.030 Why?
Genome-Wide Association Study12013122610.030 Why?
Cell Division1202145680.030 Why?
Chromosome Aberrations1201918130.030 Why?
Gene Regulatory Networks1202117080.030 Why?
Video Recording120179490.030 Why?
Mice12017811830.020 Why?
Seizures1202328590.020 Why?
Mitosis1201512080.020 Why?
Protein Binding1202293860.020 Why?
Central Nervous System1201713570.020 Why?
Insulin-Like Growth Factor I1201720150.020 Why?
Genetic Association Studies1201827030.020 Why?
Chromatin1202129340.020 Why?
DNA Replication1201513990.020 Why?
Epigenesis, Genetic1202136470.020 Why?
Genome, Human1202144200.020 Why?
Receptors, Cell Surface1201728660.020 Why?
Recombinant Proteins1201766220.020 Why?
Biopsy1201867560.020 Why?
Genetic Loci1201525750.020 Why?
Adult120202140550.020 Why?
Single-Cell Analysis1201521830.020 Why?
Genotype12019129510.020 Why?
Gene Expression Regulation12022120720.010 Why?
Muscle, Skeletal1201849310.010 Why?
Middle Aged120152133830.010 Why?
Pregnancy12021291440.010 Why?
Prognosis12018290630.010 Why?
Cells, Cultured12013192290.010 Why?
Prospective Studies12021532880.010 Why?
Rats12013242600.010 Why?
Retrospective Studies12021774490.010 Why?
D'Gama's Networks
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Concepts (148)
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Co-Authors (63)
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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.