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 Transducing3201929140.410 Why?
Epilepsy2202132760.280 Why?
ran GTP-Binding Protein12021510.200 Why?
beta Karyopherins12021470.200 Why?
Abnormalities, Multiple2201914140.200 Why?
Karyopherins120211350.190 Why?
Musculoskeletal Abnormalities12021960.180 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-Methyltransferase120216710.150 Why?
Demyelinating Diseases120193510.140 Why?
Urogenital Abnormalities120192610.140 Why?
Facies120171950.140 Why?
COUP Transcription Factor I12016120.140 Why?
Nerve Growth Factors120195730.140 Why?
Optic Atrophy12016790.130 Why?
Haploinsufficiency120173290.130 Why?
Craniofacial Abnormalities120183140.130 Why?
Muscular Atrophy120183480.120 Why?
Genetic Heterogeneity120187300.120 Why?
Genetic Association Studies2201627000.120 Why?
Siblings120188440.120 Why?
Cell Adhesion Molecules1201916010.110 Why?
Nerve Tissue Proteins2201944540.110 Why?
Developmental Disabilities1202114610.110 Why?
Drosophila Proteins1202117110.100 Why?
Gait120177940.100 Why?
Autistic Disorder1202111610.100 Why?
Mutation, Missense2201825470.100 Why?
Chromosomes, Human, Pair 14120112980.090 Why?
Rett Syndrome120111640.080 Why?
Seizures2202128420.080 Why?
Carrier Proteins1201950090.070 Why?
Attention Deficit Disorder with Hyperactivity1202136420.070 Why?
Protein Structure, Secondary2201912450.060 Why?
Child, Preschool82019409110.060 Why?
Mutation52021297010.060 Why?
Genetic Variation1201965200.060 Why?
Adolescent72019857570.060 Why?
Forkhead Transcription Factors1201116140.060 Why?
Electroencephalography1201860610.060 Why?
Proteins1201760950.050 Why?
Phenotype42021163380.050 Why?
Pregnancy22019292090.050 Why?
Ranvier's Nodes12019190.040 Why?
Pedigree2201946240.040 Why?
Alleles2202169300.040 Why?
Genetic Predisposition to Disease12019174320.040 Why?
Child72019775770.040 Why?
Nervous System Malformations120192470.040 Why?
Growth and Development12017510.040 Why?
Amino Acid Sequence22021137980.040 Why?
Sequence Homology, Amino Acid1202128400.040 Why?
Sequence Alignment1202122520.040 Why?
Gene Dosage1202112520.040 Why?
Female1020213798750.040 Why?
Peripheral Nerves120194630.030 Why?
Myelin Sheath120196490.030 Why?
RNA Stability120173190.030 Why?
Protein Isoforms1201917190.030 Why?
Organ Size1201922440.030 Why?
Neuroglia120199300.030 Why?
Male1020213497710.030 Why?
Infant32021350590.030 Why?
Nerve Fibers, Myelinated120199560.030 Why?
Humans1220217435210.030 Why?
Base Sequence22017127910.030 Why?
Brain12019263030.030 Why?
Chromosome Deletion1201713940.030 Why?
Gene Frequency1201935850.030 Why?
Drosophila melanogaster1202117150.030 Why?
RNA, Small Interfering1202134970.030 Why?
Magnetic Resonance Imaging12018353000.020 Why?
Axons1201916710.020 Why?
Gestational Age1201934930.020 Why?
Syndrome1201732560.020 Why?
Molecular Typing120111060.020 Why?
Dyskinesias12011800.020 Why?
Gene Expression Regulation, Developmental1202136180.020 Why?
Comparative Genomic Hybridization120114920.020 Why?
Methyl-CpG-Binding Protein 2120111890.020 Why?
Genome, Human1202144130.020 Why?
Gene Deletion1201627480.020 Why?
Models, Molecular1201854440.020 Why?
High-Throughput Nucleotide Sequencing1201935810.020 Why?
Mice, Transgenic1201996970.020 Why?
Microcephaly120114340.020 Why?
Corpus Callosum120117350.020 Why?
Gene Expression1201877790.020 Why?
Adult420212138700.020 Why?
Neurons1202193400.010 Why?
Infant, Newborn12021255590.010 Why?
Transcription Factors12021121430.010 Why?
Severity of Illness Index12018155270.010 Why?
Animals220211684340.010 Why?
Molecular Sequence Data12011180900.010 Why?
Genotype12011129190.010 Why?
Mice12019809990.010 Why?
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Concepts (104)
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.