Harvard Catalyst Profiles

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

Lauren Walsh

Concepts (104)

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?
Polyhydramnios12018410.630 Why?
Sequence Deletion2201814900.480 Why?
Adaptor Proteins, Signal Transducing3201928950.400 Why?
Epilepsy2202132880.280 Why?
ran GTP-Binding Protein12021530.190 Why?
beta Karyopherins12021460.190 Why?
Abnormalities, Multiple2201914220.190 Why?
Karyopherins120211330.180 Why?
Musculoskeletal Abnormalities120211000.180 Why?
Eye Diseases, Hereditary120211220.170 Why?
Myosin-Light-Chain Phosphatase12019200.170 Why?
Holoprosencephaly12019220.170 Why?
Disorders of Sex Development120191280.160 Why?
cdc42 GTP-Binding Protein120181870.140 Why?
Noonan Syndrome120181200.140 Why?
Demyelinating Diseases120193520.140 Why?
Histone-Lysine N-Methyltransferase120216820.140 Why?
Urogenital Abnormalities120192610.140 Why?
Facies120172220.140 Why?
Nerve Growth Factors120195640.140 Why?
COUP Transcription Factor I12016120.130 Why?
Optic Atrophy12016790.130 Why?
Haploinsufficiency120173360.120 Why?
Craniofacial Abnormalities120183190.120 Why?
Muscular Atrophy120183340.120 Why?
Siblings120188240.120 Why?
Genetic Heterogeneity120187330.120 Why?
Genetic Association Studies2201627340.110 Why?
Cell Adhesion Molecules1201916020.110 Why?
Nerve Tissue Proteins2201944080.110 Why?
Developmental Disabilities1202115090.100 Why?
Drosophila Proteins1202116980.100 Why?
Gait120178110.100 Why?
Mutation, Missense2201825700.090 Why?
Autistic Disorder1202112190.090 Why?
Chromosomes, Human, Pair 14120112860.090 Why?
Rett Syndrome120111630.080 Why?
Seizures2202129540.080 Why?
Carrier Proteins1201949350.070 Why?
Protein Structure, Secondary2201912290.060 Why?
Attention Deficit Disorder with Hyperactivity1202137080.060 Why?
Child, Preschool82019421880.060 Why?
Genetic Variation1201965610.060 Why?
Mutation52021300160.060 Why?
Forkhead Transcription Factors1201116140.060 Why?
Adolescent72019882340.050 Why?
Electroencephalography1201862370.050 Why?
Proteins1201760300.050 Why?
Pregnancy22019298680.040 Why?
Pedigree2201945390.040 Why?
Phenotype42021165710.040 Why?
Ranvier's Nodes12019190.040 Why?
Alleles2202168610.040 Why?
Genetic Predisposition to Disease12019178780.040 Why?
Amino Acid Sequence22021134410.040 Why?
Child72019800790.040 Why?
Nervous System Malformations120192440.040 Why?
Growth and Development12017470.040 Why?
Sequence Homology, Amino Acid1202127470.030 Why?
Sequence Alignment1202121780.030 Why?
Gene Dosage1202112170.030 Why?
Female1020213921480.030 Why?
Peripheral Nerves120194790.030 Why?
Myelin Sheath120196530.030 Why?
RNA Stability120173200.030 Why?
Protein Isoforms1201916970.030 Why?
Organ Size1201922520.030 Why?
Neuroglia120199550.030 Why?
Nerve Fibers, Myelinated120199510.030 Why?
Male1020213603580.030 Why?
Base Sequence22017124210.030 Why?
Infant32021361520.030 Why?
Humans1220217606170.030 Why?
Chromosome Deletion1201713860.030 Why?
Brain12019271010.030 Why?
Gene Frequency1201936010.030 Why?
Drosophila melanogaster1202117120.020 Why?
RNA, Small Interfering1202134190.020 Why?
Axons1201916710.020 Why?
Magnetic Resonance Imaging12018364020.020 Why?
Syndrome1201732680.020 Why?
Gestational Age1201935770.020 Why?
Molecular Typing120111160.020 Why?
Dyskinesias12011790.020 Why?
Gene Expression Regulation, Developmental1202136080.020 Why?
Comparative Genomic Hybridization120114730.020 Why?
Methyl-CpG-Binding Protein 2120111830.020 Why?
Gene Deletion1201626610.020 Why?
Genome, Human1202144210.020 Why?
Models, Molecular1201854330.020 Why?
High-Throughput Nucleotide Sequencing1201936340.020 Why?
Microcephaly120114250.020 Why?
Mice, Transgenic1201995290.020 Why?
Corpus Callosum120117510.020 Why?
Gene Expression1201875680.020 Why?
Adult420212209690.010 Why?
Neurons1202194380.010 Why?
Transcription Factors12021121160.010 Why?
Infant, Newborn12021261800.010 Why?
Severity of Illness Index12018158280.010 Why?
Animals220211682010.010 Why?
Molecular Sequence Data12011176290.010 Why?
Genotype12011129780.010 Why?
Mice12019813680.010 Why?
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Concepts (104)
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Co-Authors (9)
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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.