Harvard Catalyst Profiles

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Lauren Walsh

Concepts (104)

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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?
Polyhydramnios12018410.650 Why?
Sequence Deletion2201815220.490 Why?
Adaptor Proteins, Signal Transducing3201929270.400 Why?
Epilepsy2202133190.280 Why?
ran GTP-Binding Protein12021510.200 Why?
beta Karyopherins12021470.200 Why?
Abnormalities, Multiple2201914150.190 Why?
Karyopherins120211360.190 Why?
Musculoskeletal Abnormalities12021970.180 Why?
Eye Diseases, Hereditary120211170.180 Why?
Myosin-Light-Chain Phosphatase12019200.180 Why?
Holoprosencephaly12019220.180 Why?
Disorders of Sex Development120191220.170 Why?
Noonan Syndrome120181220.150 Why?
cdc42 GTP-Binding Protein120181900.150 Why?
Histone-Lysine N-Methyltransferase120216750.140 Why?
Demyelinating Diseases120193550.140 Why?
Facies120171960.140 Why?
Urogenital Abnormalities120192620.140 Why?
COUP Transcription Factor I12016120.140 Why?
Nerve Growth Factors120195730.140 Why?
Optic Atrophy12016800.130 Why?
Haploinsufficiency120173320.130 Why?
Craniofacial Abnormalities120183160.130 Why?
Muscular Atrophy120183490.120 Why?
Genetic Heterogeneity120187330.120 Why?
Genetic Association Studies2201627110.120 Why?
Siblings120188500.120 Why?
Cell Adhesion Molecules1201916140.110 Why?
Nerve Tissue Proteins2201944550.110 Why?
Developmental Disabilities1202114840.110 Why?
Drosophila Proteins1202117170.100 Why?
Gait120178000.100 Why?
Autistic Disorder1202111740.100 Why?
Mutation, Missense2201825590.100 Why?
Chromosomes, Human, Pair 14120112870.090 Why?
Rett Syndrome120111660.080 Why?
Seizures2202128870.080 Why?
Carrier Proteins1201950060.070 Why?
Attention Deficit Disorder with Hyperactivity1202136610.060 Why?
Protein Structure, Secondary2201912490.060 Why?
Child, Preschool82019413900.060 Why?
Mutation52021299810.060 Why?
Genetic Variation1201965670.060 Why?
Adolescent72019867130.060 Why?
Forkhead Transcription Factors1201116210.060 Why?
Electroencephalography1201861170.060 Why?
Proteins1201760930.050 Why?
Phenotype42021164840.050 Why?
Pregnancy22019296300.040 Why?
Ranvier's Nodes12019200.040 Why?
Pedigree2201946370.040 Why?
Alleles2202169540.040 Why?
Genetic Predisposition to Disease12019176350.040 Why?
Child72019785940.040 Why?
Nervous System Malformations120192510.040 Why?
Growth and Development12017510.040 Why?
Amino Acid Sequence22021137780.040 Why?
Sequence Homology, Amino Acid1202128200.040 Why?
Sequence Alignment1202122500.040 Why?
Gene Dosage1202112550.040 Why?
Female1020213850900.030 Why?
Peripheral Nerves120194720.030 Why?
Myelin Sheath120196530.030 Why?
RNA Stability120173210.030 Why?
Protein Isoforms1201917310.030 Why?
Organ Size1201922650.030 Why?
Neuroglia120199440.030 Why?
Male1020213543110.030 Why?
Nerve Fibers, Myelinated120199560.030 Why?
Infant32021354470.030 Why?
Humans1220217527410.030 Why?
Base Sequence22017127690.030 Why?
Brain12019265980.030 Why?
Gene Frequency1201935910.030 Why?
Chromosome Deletion1201714000.030 Why?
Drosophila melanogaster1202117300.030 Why?
RNA, Small Interfering1202134940.030 Why?
Axons1201916800.020 Why?
Magnetic Resonance Imaging12018357980.020 Why?
Syndrome1201732610.020 Why?
Gestational Age1201935550.020 Why?
Molecular Typing120111060.020 Why?
Dyskinesias12011800.020 Why?
Gene Expression Regulation, Developmental1202136260.020 Why?
Comparative Genomic Hybridization120114910.020 Why?
Methyl-CpG-Binding Protein 2120111890.020 Why?
Gene Deletion1201627460.020 Why?
Genome, Human1202144460.020 Why?
Models, Molecular1201854600.020 Why?
High-Throughput Nucleotide Sequencing1201936050.020 Why?
Mice, Transgenic1201997430.020 Why?
Microcephaly120114380.020 Why?
Corpus Callosum120117360.020 Why?
Gene Expression1201877710.020 Why?
Adult420212166580.010 Why?
Neurons1202194390.010 Why?
Transcription Factors12021121650.010 Why?
Infant, Newborn12021259030.010 Why?
Severity of Illness Index12018156570.010 Why?
Animals220211696000.010 Why?
Molecular Sequence Data12011180500.010 Why?
Genotype12011129700.010 Why?
Mice12019817660.010 Why?
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Concepts (104)
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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.