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

Concepts (134)

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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?
Cockayne Syndrome42018200.700 Why?
Ornithine Carbamoyltransferase Deficiency Disease12017230.590 Why?
Hyperammonemia12017760.540 Why?
Werner Syndrome12009120.330 Why?
DNA Repair Enzymes320183460.320 Why?
Carbidopa12008300.320 Why?
Lamin Type A120091890.300 Why?
Lipodystrophy120091480.300 Why?
Levodopa120082210.290 Why?
Meningocele12006460.260 Why?
Chromosome Inversion120061200.260 Why?
DNA Helicases320188510.250 Why?
Anterior Chamber120061940.250 Why?
Chromosomes, Human, Pair 4120063750.250 Why?
Movement Disorders120084590.230 Why?
alpha-Glucosidases12024450.230 Why?
Glycogen Storage Disease Type II12024430.230 Why?
Eye Abnormalities120062420.220 Why?
Abnormalities, Multiple1200614240.160 Why?
Rare Diseases120246210.150 Why?
RNA Splice Sites120182110.140 Why?
Mutagenesis, Insertional119996560.130 Why?
Wolman Disease1201530.130 Why?
Sterol Esterase12015390.130 Why?
Maple Syrup Urine Disease12014400.120 Why?
Genetic Vectors2202433930.110 Why?
Phospholipase C beta12012490.100 Why?
Lactation120143970.100 Why?
Chromosome Disorders120144990.090 Why?
Germ-Line Mutation1199918580.090 Why?
Protein Stability120125780.090 Why?
Aging1200987040.080 Why?
Epilepsies, Partial120124310.080 Why?
Primary Ovarian Insufficiency120091070.080 Why?
Osteitis Deformans12008540.080 Why?
Registries1202482230.080 Why?
Energy Metabolism1201828790.070 Why?
Ultraviolet Rays1201210790.070 Why?
Ear120061720.060 Why?
DNA Copy Number Variations1201420200.060 Why?
Gene Deletion1201226670.060 Why?
Infant42018362020.060 Why?
Enzyme Replacement Therapy12024800.060 Why?
Otitis Media120062870.060 Why?
Adenosine Triphosphatases120088330.060 Why?
Muscular Diseases120085530.050 Why?
DNA Damage2201224420.050 Why?
Cardiomyopathy, Dilated120098290.050 Why?
DNA Repair1201220440.050 Why?
Syndrome1200932680.050 Why?
Gene Expression Profiling2201494140.050 Why?
Vital Capacity120249700.050 Why?
Mutation22018300440.050 Why?
Cleft Lip120065060.050 Why?
Gene Expression Regulation22014119000.040 Why?
Cleft Palate120065890.040 Why?
Pregnancy Complications1201429470.040 Why?
Mutation, Missense1200925700.040 Why?
Moloney murine leukemia virus119991090.040 Why?
Carrier Proteins1201249360.040 Why?
Gene Transfer Techniques1202412050.040 Why?
Dependovirus120247150.040 Why?
Epilepsy1201432900.040 Why?
Drug Therapy, Combination1200863090.040 Why?
Transcription, Genetic1201275970.040 Why?
Male1020243606210.040 Why?
Gene Products, env119992500.040 Why?
beta-Galactosidase119995740.040 Why?
Family1200831970.030 Why?
Cell Cycle Proteins1200834480.030 Why?
Mice, Inbred Strains1199917590.030 Why?
Oligonucleotide Array Sequence Analysis2201437770.030 Why?
Humans1420247613260.030 Why?
Mice, Mutant Strains1199917510.030 Why?
RNA Splicing119999170.030 Why?
Cell Transdifferentiation120141850.030 Why?
Dementia1200826860.030 Why?
Cloning, Molecular1199941750.030 Why?
Child, Preschool32024422510.030 Why?
Alanine Transaminase120156050.030 Why?
Models, Biological1200994680.030 Why?
Nutritional Requirements120142750.030 Why?
Pedigree2201245890.030 Why?
Female820243924850.020 Why?
Amino Acids, Branched-Chain120142690.020 Why?
Adolescent32024883050.020 Why?
Phenotype22018166030.020 Why?
DNA Mutational Analysis1201841080.020 Why?
Heart Defects, Congenital1200646960.020 Why?
Parenteral Nutrition120146590.020 Why?
Cholesterol, HDL1201518140.020 Why?
Metabolomics1201816560.020 Why?
International Classification of Diseases120149090.020 Why?
Dyslipidemias120158680.020 Why?
RNA Polymerase II120125390.020 Why?
Cells, Cultured22014189620.020 Why?
Homozygote1201217960.020 Why?
Reverse Transcriptase Polymerase Chain Reaction1201445670.020 Why?
Microscopy, Fluorescence1201426480.020 Why?
Blotting, Western1201450340.020 Why?
Inclusion Bodies120082810.020 Why?
Energy Intake1201421340.020 Why?
Mice, Transgenic1199995340.020 Why?
Cholesterol, LDL1201523810.020 Why?
Molecular Sequence Data11999176400.020 Why?
RNA Interference1201428320.020 Why?
Gene Regulatory Networks1201417410.020 Why?
Magnetic Resonance Imaging22018364300.020 Why?
HEK293 Cells1201442800.020 Why?
Fibroblasts1201441390.010 Why?
Young Adult22024591960.010 Why?
Biopsy1201567680.010 Why?
Follow-Up Studies12024391080.010 Why?
Child22024801560.010 Why?
Adult420242211220.010 Why?
Double-Blind Method12015123290.010 Why?
Cell Line12014155990.010 Why?
Liver1201575310.010 Why?
Mice22014814740.010 Why?
Middle Aged320242207740.010 Why?
Electroencephalography1201462240.010 Why?
Cell Line, Tumor12014169660.010 Why?
Kidney1201270490.010 Why?
Genetic Predisposition to Disease12018178720.010 Why?
Neurons1201494580.010 Why?
Tomography, X-Ray Computed12018205550.010 Why?
Animals220141683880.010 Why?
Muscle, Skeletal1200849270.010 Why?
Retrospective Studies22014805750.010 Why?
Transcription Factors12012121220.010 Why?
Pregnancy12014298580.010 Why?
Treatment Outcome12014646450.000 Why?
Cross-Sectional Studies12008261080.000 Why?
Aged120151691790.000 Why?
Neilan's Networks
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Concepts (134)
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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.