Harvard Catalyst Profiles

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Edward George Neilan, M.D.,Ph.D.

Concepts (134)

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?
Cockayne Syndrome42018200.700 Why?
Ornithine Carbamoyltransferase Deficiency Disease12017230.590 Why?
Hyperammonemia12017770.540 Why?
Werner Syndrome12009120.330 Why?
DNA Repair Enzymes320183450.330 Why?
Carbidopa12008300.320 Why?
Lamin Type A120091870.300 Why?
Lipodystrophy120091480.300 Why?
Levodopa120082170.290 Why?
Meningocele12006460.270 Why?
Chromosome Inversion120061200.260 Why?
Anterior Chamber120061940.260 Why?
DNA Helicases320188540.250 Why?
Chromosomes, Human, Pair 4120063770.250 Why?
Movement Disorders120084590.240 Why?
alpha-Glucosidases12024450.230 Why?
Glycogen Storage Disease Type II12024430.230 Why?
Eye Abnormalities120062410.230 Why?
Abnormalities, Multiple1200614150.160 Why?
Rare Diseases120246190.160 Why?
RNA Splice Sites120182110.140 Why?
Mutagenesis, Insertional119996520.130 Why?
Wolman Disease1201530.130 Why?
Sterol Esterase12015400.130 Why?
Maple Syrup Urine Disease12014400.120 Why?
Genetic Vectors2202433800.110 Why?
Phospholipase C beta12012490.100 Why?
Lactation120143970.100 Why?
Chromosome Disorders120144990.100 Why?
Germ-Line Mutation1199918420.090 Why?
Protein Stability120125660.090 Why?
Aging1200986520.090 Why?
Primary Ovarian Insufficiency120091050.080 Why?
Epilepsies, Partial120124300.080 Why?
Osteitis Deformans12008540.080 Why?
Registries1202484580.070 Why?
Energy Metabolism1201828690.070 Why?
Ultraviolet Rays1201210780.070 Why?
Ear120061720.060 Why?
DNA Copy Number Variations1201420130.060 Why?
Gene Deletion1201226680.060 Why?
Infant42018360530.060 Why?
Enzyme Replacement Therapy12024790.060 Why?
Otitis Media120062850.060 Why?
Adenosine Triphosphatases120088330.060 Why?
Muscular Diseases120085510.060 Why?
Cardiomyopathy, Dilated120098190.050 Why?
DNA Damage2201224420.050 Why?
DNA Repair1201220380.050 Why?
Syndrome1200932800.050 Why?
Gene Expression Profiling2201494060.050 Why?
Vital Capacity120249650.050 Why?
Mutation22018299570.050 Why?
Cleft Lip120065040.050 Why?
Gene Expression Regulation22014119020.040 Why?
Cleft Palate120065870.040 Why?
Pregnancy Complications1201429420.040 Why?
Mutation, Missense1200925670.040 Why?
Moloney murine leukemia virus119991090.040 Why?
Dependovirus120247090.040 Why?
Carrier Proteins1201249380.040 Why?
Gene Transfer Techniques1202412040.040 Why?
Epilepsy1201432670.040 Why?
Transcription, Genetic1201275930.040 Why?
Drug Therapy, Combination1200864980.040 Why?
Male1020243597180.040 Why?
Gene Products, env119992500.040 Why?
beta-Galactosidase119995750.040 Why?
Family1200831890.040 Why?
Cell Cycle Proteins1200834480.030 Why?
Mice, Inbred Strains1199917630.030 Why?
Oligonucleotide Array Sequence Analysis2201437740.030 Why?
Humans1420247606130.030 Why?
Mice, Mutant Strains1199917540.030 Why?
RNA Splicing119999150.030 Why?
Cell Transdifferentiation120141850.030 Why?
Dementia1200826500.030 Why?
Cloning, Molecular1199941690.030 Why?
Alanine Transaminase120156070.030 Why?
Child, Preschool32024420560.030 Why?
Models, Biological1200994680.030 Why?
Nutritional Requirements120142750.030 Why?
Pedigree2201245780.030 Why?
Female820243912460.020 Why?
Amino Acids, Branched-Chain120142630.020 Why?
Adolescent32024878090.020 Why?
Phenotype22018165480.020 Why?
DNA Mutational Analysis1201841080.020 Why?
Heart Defects, Congenital1200646730.020 Why?
Parenteral Nutrition120146560.020 Why?
Metabolomics1201816280.020 Why?
Cholesterol, HDL1201518170.020 Why?
International Classification of Diseases120148940.020 Why?
RNA Polymerase II120125370.020 Why?
Dyslipidemias120158950.020 Why?
Cells, Cultured22014189550.020 Why?
Homozygote1201217880.020 Why?
Reverse Transcriptase Polymerase Chain Reaction1201445710.020 Why?
Microscopy, Fluorescence1201426510.020 Why?
Blotting, Western1201450390.020 Why?
Inclusion Bodies120082810.020 Why?
Energy Intake1201421290.020 Why?
Mice, Transgenic1199995300.020 Why?
Molecular Sequence Data11999176240.020 Why?
Cholesterol, LDL1201524200.020 Why?
RNA Interference1201428460.020 Why?
Gene Regulatory Networks1201417410.020 Why?
Magnetic Resonance Imaging22018362860.020 Why?
HEK293 Cells1201442630.020 Why?
Fibroblasts1201440890.010 Why?
Young Adult22024587480.010 Why?
Biopsy1201567710.010 Why?
Follow-Up Studies12024392620.010 Why?
Child22024797990.010 Why?
Adult420242200070.010 Why?
Double-Blind Method12015124270.010 Why?
Cell Line12014156200.010 Why?
Liver1201575100.010 Why?
Mice22014812090.010 Why?
Middle Aged320242203590.010 Why?
Electroencephalography1201461890.010 Why?
Cell Line, Tumor12014169320.010 Why?
Kidney1201270640.010 Why?
Genetic Predisposition to Disease12018177900.010 Why?
Neurons1201494240.010 Why?
Tomography, X-Ray Computed12018205090.010 Why?
Animals220141679600.010 Why?
Muscle, Skeletal1200849240.010 Why?
Retrospective Studies22014803450.010 Why?
Transcription Factors12012121020.010 Why?
Pregnancy12014297460.010 Why?
Treatment Outcome12014649810.000 Why?
Cross-Sectional Studies12008259410.000 Why?
Aged120151691430.000 Why?
Neilan's Networks
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Concepts (134)
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Co-Authors (32)
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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.