Harvard Catalyst Profiles

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Ryan Doan, Ph.D.

Concepts (155)

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?
Mosaicism320244751.340 Why?
Germ-Line Mutation4202418580.700 Why?
Allelic Imbalance12019770.650 Why?
Aortic Aneurysm, Thoracic120246960.590 Why?
Genes, Recessive120196280.540 Why?
Genetic Predisposition to Disease62024178720.500 Why?
Behavior120185400.500 Why?
Neurogenesis320178620.450 Why?
Biological Evolution2202110730.440 Why?
High-Throughput Nucleotide Sequencing3202436380.430 Why?
Horses120123000.370 Why?
Point Mutation1201615950.370 Why?
Mutation, Missense2202325700.370 Why?
Social Behavior1201611340.340 Why?
Attention Deficit Disorder with Hyperactivity1202437040.310 Why?
Nervous System Diseases1201816650.290 Why?
Neural Stem Cells320218880.260 Why?
Genomics2201858170.230 Why?
Creutzfeldt-Jakob Syndrome12024930.220 Why?
Genome1201217400.220 Why?
Siblings220248250.210 Why?
Gene Dosage2201712180.200 Why?
Mutation52024300440.200 Why?
Adipokines120243100.200 Why?
Brain72024271030.200 Why?
Gastrulation12021360.190 Why?
Sequence Analysis, DNA1201247400.180 Why?
Polymorphism, Single Nucleotide52021158790.180 Why?
Cerebral Cortex4201857760.180 Why?
Gene Expression Regulation, Developmental3202136120.170 Why?
Alleles3202169090.160 Why?
Malformations of Cortical Development120211760.160 Why?
Prosencephalon120213050.160 Why?
Cognition1201669870.160 Why?
INDEL Mutation120202670.160 Why?
Single-Cell Analysis3202124480.150 Why?
Language Development120181830.140 Why?
Genome, Human3202144230.140 Why?
Sodium Channels120183390.140 Why?
Arthrogryposis12017680.130 Why?
Quantitative Trait Loci2201621050.130 Why?
Gene Regulatory Networks2202117410.130 Why?
DNA Mutational Analysis2202141080.130 Why?
Homozygote1202017960.130 Why?
Regulatory Elements, Transcriptional120161830.130 Why?
Cell Adhesion Molecules, Neuronal120172630.120 Why?
Genomic Imprinting120173300.120 Why?
Frameshift Mutation120173920.120 Why?
PTEN Phosphohydrolase1202011140.120 Why?
Case-Control Studies22024221240.110 Why?
Ferrets320211770.110 Why?
Introns120169810.110 Why?
Gene Deletion1202026670.100 Why?
Cell Lineage1202125560.100 Why?
Horse Diseases12012550.100 Why?
Developmental Disabilities1202015080.100 Why?
Polymerase Chain Reaction1202160860.100 Why?
Alternative Splicing1201610930.090 Why?
Prefrontal Cortex1202122190.090 Why?
Epigenesis, Genetic2202137930.090 Why?
Parents1202435640.080 Why?
Molecular Sequence Annotation120125230.080 Why?
Humans2120247613260.080 Why?
Phenotype22024166030.080 Why?
DNA Copy Number Variations2202020200.080 Why?
Ubiquitin-Protein Ligases1201718910.070 Why?
Nerve Tissue Proteins2202344140.070 Why?
Homeodomain Proteins1201624130.070 Why?
Female1420243924850.070 Why?
Embryonic Development220217200.060 Why?
Repressor Proteins1201629850.060 Why?
Genetic Variation2202165710.060 Why?
Animals920211683880.060 Why?
Nuclear Proteins2201657940.060 Why?
Evolution, Molecular2202418880.060 Why?
Male1120243606210.060 Why?
Mice, Transgenic1201695340.060 Why?
Child52024801560.060 Why?
Neurons3202194580.060 Why?
Cell Division2202144660.050 Why?
Prion Diseases120241000.050 Why?
Genotype22021129820.050 Why?
Exons2202123920.050 Why?
Reproducibility of Results12021200920.050 Why?
Connexins120233520.050 Why?
Antibody Diversity12021720.050 Why?
Pan troglodytes120212250.050 Why?
Gastrula12021820.050 Why?
Transcription, Genetic1201575970.050 Why?
Germ Layers12021720.050 Why?
Mice62021814740.040 Why?
Macaca120214110.040 Why?
Brain Neoplasms1202190300.040 Why?
Pedigree2201845890.040 Why?
Organogenesis120212150.040 Why?
Gene Expression Profiling1201594140.040 Why?
Middle Aged520242207740.040 Why?
Infant42021362020.040 Why?
Adult520242211220.040 Why?
Enhancer Elements, Genetic1202413630.040 Why?
Child, Preschool42021422510.040 Why?
Clone Cells1202116610.040 Why?
Delphi Technique120218460.040 Why?
Risk Factors12024741520.040 Why?
Polypyrimidine Tract-Binding Protein12016220.030 Why?
RNA, Antisense120171360.030 Why?
Transcription Factors12016121220.030 Why?
Heterogeneous-Nuclear Ribonucleoproteins12016690.030 Why?
Cohort Studies12019414400.030 Why?
Brain Chemistry120209590.030 Why?
Epigenomics120219410.030 Why?
Oncogenes1202112230.030 Why?
Adolescent52021883050.030 Why?
Centrosome120162090.030 Why?
Consanguinity120174560.030 Why?
Observer Variation1202126050.030 Why?
Age of Onset1202133030.030 Why?
Yersinia enterocolitica11993130.030 Why?
Sequence Homology, Nucleic Acid1201510580.030 Why?
Receptors, Thyrotropin11993450.030 Why?
Databases, Genetic1202017380.030 Why?
Protein Isoforms1201616980.020 Why?
Cytoskeletal Proteins1201613420.020 Why?
Species Specificity1201524190.020 Why?
Sequence Alignment1201521800.020 Why?
Neurosurgical Procedures1202120710.020 Why?
Infant, Newborn22021262110.020 Why?
HEK293 Cells1201842800.020 Why?
Chromatin1202129600.020 Why?
Basic Helix-Loop-Helix Transcription Factors1201511350.020 Why?
Signal Transduction12012234270.020 Why?
Seizures1202129560.020 Why?
Aged, 80 and over22024589460.020 Why?
Massachusetts1202088370.020 Why?
Immunohistochemistry12021110700.020 Why?
Sequence Analysis, RNA1201520190.020 Why?
Cell Movement1201852020.020 Why?
Comorbidity12020104980.020 Why?
Software1202044390.020 Why?
Electroencephalography1202062240.020 Why?
Autoantibodies1199321230.010 Why?
Young Adult22021591960.010 Why?
Age Factors12021184010.010 Why?
Magnetic Resonance Imaging22021364300.010 Why?
Cells, Cultured12018189620.010 Why?
Molecular Sequence Data12015176400.010 Why?
Aged220241691790.010 Why?
Gene Expression Regulation12017119000.010 Why?
Pregnancy12021298580.010 Why?
Retrospective Studies12023805750.010 Why?
Cross Reactions119938180.010 Why?
Immunization1199312260.000 Why?
Antibodies, Bacterial1199314690.000 Why?
Rabbits1199347790.000 Why?
Mice, Inbred C57BL11993221540.000 Why?
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Concepts (155)
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Co-Authors (73)
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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.