Harvard Catalyst Profiles

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

Concepts (128)

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 Syndrome42018210.720 Why?
Ornithine Carbamoyltransferase Deficiency Disease12017230.620 Why?
Hyperammonemia12017760.570 Why?
Werner Syndrome12009130.340 Why?
DNA Repair Enzymes320183490.340 Why?
Carbidopa12008310.330 Why?
Lamin Type A120091900.310 Why?
Lipodystrophy120091470.310 Why?
Levodopa120082210.300 Why?
Meningocele12006450.270 Why?
Chromosome Inversion120061270.270 Why?
Anterior Chamber120061970.260 Why?
DNA Helicases320188610.260 Why?
Chromosomes, Human, Pair 4120063740.260 Why?
Movement Disorders120084480.250 Why?
Eye Abnormalities120062460.230 Why?
Rare Diseases120245520.170 Why?
Abnormalities, Multiple1200614160.160 Why?
RNA Splice Sites120182090.150 Why?
Wolman Disease1201530.140 Why?
Mutagenesis, Insertional119996540.140 Why?
Sterol Esterase12015370.130 Why?
Maple Syrup Urine Disease12014390.120 Why?
Genetic Vectors2202434210.110 Why?
Phospholipase C beta12012500.110 Why?
Lactation120144110.100 Why?
Chromosome Disorders120145100.100 Why?
Germ-Line Mutation1199917870.090 Why?
Protein Stability120125560.090 Why?
Aging1200986550.090 Why?
Primary Ovarian Insufficiency120091150.080 Why?
Epilepsies, Partial120124350.080 Why?
Osteitis Deformans12008530.080 Why?
Ultraviolet Rays1201210600.070 Why?
Energy Metabolism1201828990.070 Why?
DNA Copy Number Variations1201419370.070 Why?
Ear120061720.070 Why?
Infant42018351220.060 Why?
Gene Deletion1201227490.060 Why?
Otitis Media120062770.060 Why?
Adenosine Triphosphatases120088390.060 Why?
Muscular Diseases120085550.060 Why?
DNA Damage2201224290.050 Why?
DNA Repair1201220450.050 Why?
Cardiomyopathy, Dilated120098510.050 Why?
Syndrome1200932490.050 Why?
Gene Expression Profiling2201494400.050 Why?
Cleft Lip120064780.050 Why?
Mutation22018297770.050 Why?
Cleft Palate120065600.050 Why?
Gene Expression Regulation22014120660.050 Why?
Pregnancy Complications1201428610.040 Why?
Mutation, Missense1200925660.040 Why?
Moloney murine leukemia virus119991390.040 Why?
Dependovirus120247050.040 Why?
Carrier Proteins1201250210.040 Why?
Gene Transfer Techniques1202412240.040 Why?
Epilepsy1201432840.040 Why?
Drug Therapy, Combination1200864870.040 Why?
Transcription, Genetic1201277190.040 Why?
Gene Products, env119992630.040 Why?
beta-Galactosidase119995740.040 Why?
Family1200831440.040 Why?
Male920183497760.040 Why?
Cell Cycle Proteins1200834630.030 Why?
Mice, Inbred Strains1199918260.030 Why?
Oligonucleotide Array Sequence Analysis2201439170.030 Why?
Mice, Mutant Strains1199918620.030 Why?
Humans1320247438110.030 Why?
RNA Splicing119999070.030 Why?
Dementia1200825180.030 Why?
Cell Transdifferentiation120141720.030 Why?
Cloning, Molecular1199943200.030 Why?
Alanine Transaminase120155930.030 Why?
Pedigree2201246430.030 Why?
Nutritional Requirements120142860.030 Why?
Models, Biological1200995820.030 Why?
Amino Acids, Branched-Chain120142510.020 Why?
Phenotype22018163610.020 Why?
Metabolomics1201814870.020 Why?
Heart Defects, Congenital1200645840.020 Why?
DNA Mutational Analysis1201841830.020 Why?
Female720153800200.020 Why?
Parenteral Nutrition120146500.020 Why?
International Classification of Diseases120148660.020 Why?
Cholesterol, HDL1201518130.020 Why?
Dyslipidemias120158510.020 Why?
RNA Polymerase II120125480.020 Why?
Homozygote1201217870.020 Why?
Cells, Cultured22014192320.020 Why?
Microscopy, Fluorescence1201426920.020 Why?
Reverse Transcriptase Polymerase Chain Reaction1201447490.020 Why?
Inclusion Bodies120082790.020 Why?
Blotting, Western1201451790.020 Why?
Mice, Transgenic1199997310.020 Why?
Energy Intake1201421490.020 Why?
Cholesterol, LDL1201523540.020 Why?
Gene Regulatory Networks1201417070.020 Why?
Molecular Sequence Data11999181070.020 Why?
RNA Interference1201428900.020 Why?
Magnetic Resonance Imaging22018354090.020 Why?
HEK293 Cells1201442040.020 Why?
Adolescent22015857290.020 Why?
Child, Preschool22018409640.020 Why?
Fibroblasts1201441620.010 Why?
Biopsy1201567500.010 Why?
Double-Blind Method12015120200.010 Why?
Cell Line12014159930.010 Why?
Liver1201574790.010 Why?
Mice22014811540.010 Why?
Electroencephalography1201460610.010 Why?
Cell Line, Tumor12014166740.010 Why?
Genetic Predisposition to Disease12018174390.010 Why?
Kidney1201271850.010 Why?
Tomography, X-Ray Computed12018201210.010 Why?
Neurons1201493360.010 Why?
Animals220141686600.010 Why?
Adult320152138890.010 Why?
Retrospective Studies22014774100.010 Why?
Muscle, Skeletal1200849250.010 Why?
Transcription Factors12012122090.010 Why?
Pregnancy12014291400.010 Why?
Young Adult12015563920.010 Why?
Middle Aged220152132410.000 Why?
Child12015776370.000 Why?
Treatment Outcome12014630420.000 Why?
Cross-Sectional Studies12008250320.000 Why?
Aged120151631780.000 Why?
Neilan's Networks
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Concepts (128)
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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.