Harvard Catalyst Profiles

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Ryan Doan, 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?
Mosaicism320244811.310 Why?
Mutation, Missense3202425890.840 Why?
Germ-Line Mutation4202418840.680 Why?
Allelic Imbalance12019770.630 Why?
Attention Deficit Disorder with Hyperactivity2202437190.620 Why?
Aortic Aneurysm, Thoracic120247000.570 Why?
Genetic Predisposition to Disease72024180710.540 Why?
Genes, Recessive120196240.530 Why?
Behavior120185350.490 Why?
Neurogenesis320178660.440 Why?
Biological Evolution2202110720.430 Why?
High-Throughput Nucleotide Sequencing3202436550.420 Why?
Point Mutation1201615900.370 Why?
Horses120122930.370 Why?
Social Behavior1201611460.330 Why?
Nervous System Diseases1201816600.290 Why?
Neural Stem Cells320218980.260 Why?
Genomics2201859290.230 Why?
Spectrin120241740.220 Why?
Creutzfeldt-Jakob Syndrome12024920.220 Why?
Genome1201217530.220 Why?
Siblings220248280.200 Why?
Gene Dosage2201712160.200 Why?
Mutation52024301980.200 Why?
Adipokines120243080.200 Why?
Brain72024271710.190 Why?
Gastrulation12021370.180 Why?
Sequence Analysis, DNA1201247720.180 Why?
Polymorphism, Single Nucleotide52021160470.180 Why?
Cerebral Cortex4201857670.170 Why?
Gene Expression Regulation, Developmental3202136070.170 Why?
Alleles3202168970.160 Why?
Malformations of Cortical Development120211740.160 Why?
Prosencephalon120213050.160 Why?
Cognition1201670490.160 Why?
INDEL Mutation120202680.150 Why?
Single-Cell Analysis3202125350.150 Why?
Phenotype32024167210.140 Why?
Gene Frequency1202436240.140 Why?
Language Development120181830.140 Why?
Genome, Human3202144480.140 Why?
Sodium Channels120183340.130 Why?
Arthrogryposis12017700.130 Why?
Quantitative Trait Loci2201621400.130 Why?
Gene Regulatory Networks2202117480.130 Why?
DNA Mutational Analysis2202141080.130 Why?
Homozygote1202017750.120 Why?
Regulatory Elements, Transcriptional120161840.120 Why?
Cell Adhesion Molecules, Neuronal120172620.120 Why?
Genomic Imprinting120173260.120 Why?
Frameshift Mutation120173930.120 Why?
PTEN Phosphohydrolase1202011190.120 Why?
Case-Control Studies22024222230.110 Why?
Ferrets320211820.110 Why?
Introns120169660.110 Why?
Gene Deletion1202026660.100 Why?
Cell Lineage1202125730.100 Why?
Horse Diseases12012540.100 Why?
Developmental Disabilities1202015190.090 Why?
Polymerase Chain Reaction1202160690.090 Why?
Alternative Splicing1201611070.090 Why?
Humans2220247659680.090 Why?
Child62024805640.090 Why?
Prefrontal Cortex1202122240.090 Why?
Epigenesis, Genetic2202138190.090 Why?
Parents1202435920.080 Why?
Child, Preschool52024425000.080 Why?
Molecular Sequence Annotation120125230.080 Why?
Female1520243961120.080 Why?
DNA Copy Number Variations2202020450.080 Why?
Male1220243636980.070 Why?
Ubiquitin-Protein Ligases1201718920.070 Why?
Nerve Tissue Proteins2202343920.070 Why?
Homeodomain Proteins1201624280.070 Why?
Embryonic Development220217180.060 Why?
Repressor Proteins1201629680.060 Why?
Genetic Variation2202166100.060 Why?
Animals920211687640.060 Why?
Nuclear Proteins2201657830.060 Why?
Evolution, Molecular2202418890.060 Why?
Mice, Transgenic1201695500.060 Why?
Neurons3202195250.050 Why?
Cell Division2202144750.050 Why?
Prion Diseases12024990.050 Why?
Genotype22021130240.050 Why?
Exons2202123910.050 Why?
Reproducibility of Results12021201240.050 Why?
Connexins120233560.050 Why?
Antibody Diversity12021710.050 Why?
Pan troglodytes120212240.050 Why?
Transcription, Genetic1201575990.050 Why?
Gastrula12021830.050 Why?
Germ Layers12021720.040 Why?
Mice62021818190.040 Why?
Macaca120214130.040 Why?
Brain Neoplasms1202190710.040 Why?
Pedigree2201845260.040 Why?
Organogenesis120212130.040 Why?
Gene Expression Profiling1201595250.040 Why?
Middle Aged520242230090.040 Why?
Infant42021363860.040 Why?
Adult520242230440.040 Why?
Enhancer Elements, Genetic1202413650.040 Why?
Clone Cells1202116720.040 Why?
Risk Factors12024748400.030 Why?
Delphi Technique120218930.030 Why?
Polypyrimidine Tract-Binding Protein12016220.030 Why?
Transcription Factors12016121310.030 Why?
RNA, Antisense120171350.030 Why?
Heterogeneous-Nuclear Ribonucleoproteins12016690.030 Why?
Cohort Studies12019416490.030 Why?
Brain Chemistry120209520.030 Why?
Epigenomics120219590.030 Why?
Oncogenes1202112350.030 Why?
Adolescent52021888350.030 Why?
Centrosome120162090.030 Why?
Consanguinity120174600.030 Why?
Observer Variation1202126150.030 Why?
Age of Onset1202133440.030 Why?
Yersinia enterocolitica11993130.030 Why?
Sequence Homology, Nucleic Acid1201510560.030 Why?
Databases, Genetic1202017510.030 Why?
Receptors, Thyrotropin11993460.030 Why?
Protein Isoforms1201617180.020 Why?
Cytoskeletal Proteins1201613250.020 Why?
Sequence Alignment1201521710.020 Why?
Species Specificity1201524060.020 Why?
Neurosurgical Procedures1202120740.020 Why?
HEK293 Cells1201842600.020 Why?
Infant, Newborn22021263460.020 Why?
Chromatin1202129800.020 Why?
Basic Helix-Loop-Helix Transcription Factors1201511400.020 Why?
Signal Transduction12012236010.020 Why?
Seizures1202130000.020 Why?
Aged, 80 and over22024594890.020 Why?
Massachusetts1202088750.020 Why?
Immunohistochemistry12021110220.020 Why?
Sequence Analysis, RNA1201520340.020 Why?
Cell Movement1201851940.020 Why?
Comorbidity12020105630.020 Why?
Software1202044620.020 Why?
Electroencephalography1202062730.010 Why?
Autoantibodies1199321130.010 Why?
Age Factors12021183800.010 Why?
Young Adult22021598890.010 Why?
Magnetic Resonance Imaging22021365320.010 Why?
Cells, Cultured12018189730.010 Why?
Molecular Sequence Data12015175940.010 Why?
Aged220241711170.010 Why?
Gene Expression Regulation12017118880.010 Why?
Pregnancy12021302600.010 Why?
Retrospective Studies12023815140.010 Why?
Cross Reactions119938240.010 Why?
Immunization1199312190.000 Why?
Antibodies, Bacterial1199314760.000 Why?
Rabbits1199347340.000 Why?
Mice, Inbred C57BL11993223320.000 Why?
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Concepts (157)
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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.