What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Mutation
George W. Padberg mainly focuses on Facioscapulohumeral muscular dystrophy, Genetics, DUX4, Muscular dystrophy and Molecular biology.
His Facioscapulohumeral muscular dystrophy study combines topics in areas such as Facial muscles, Ankle, Humerus, Physical therapy and Scapula.
His Genetics study focuses mostly on Haplotype, Chromosome 4, Subtelomere, Gene and Genetic heterogeneity.
He combines subjects such as Homeobox, Dystrophy, Allele, Locus and Pediatrics with his study of DUX4.
His Muscular dystrophy research incorporates themes from Genotype, Myopathy, Pathology and DNA methylation.
His research in Molecular biology intersects with topics in Gene rearrangement, Gene mapping and EcoRI.
His most cited work include:
- Treatment of single brain metastasis: Radiotherapy alone or combined with neurosurgery (796 citations)
- Localization of the gene for Cowden disease to chromosome 10q22-23 (534 citations)
- Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. (530 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Facioscapulohumeral muscular dystrophy, Genetics, Muscular dystrophy, Locus and Internal medicine.
George W. Padberg is involved in the study of Facioscapulohumeral muscular dystrophy that focuses on DUX4 in particular.
George W. Padberg works mostly in the field of Muscular dystrophy, limiting it down to concerns involving Hearing loss and, occasionally, Early onset and Pediatrics.
George W. Padberg has researched Locus in several fields, including Genetic marker and Candidate gene.
His research investigates the connection between Internal medicine and topics such as Cardiology that intersect with problems in Surgery.
His Molecular biology study integrates concerns from other disciplines, such as Gene rearrangement, Cosmid and EcoRI.
He most often published in these fields:
- Facioscapulohumeral muscular dystrophy (52.60%)
- Genetics (40.62%)
- Muscular dystrophy (21.88%)
What were the highlights of his more recent work (between 2012-2021)?
- Facioscapulohumeral muscular dystrophy (52.60%)
- Physical therapy (11.98%)
- Internal medicine (12.50%)
In recent papers he was focusing on the following fields of study:
George W. Padberg mainly investigates Facioscapulohumeral muscular dystrophy, Physical therapy, Internal medicine, Muscular dystrophy and Dystrophy.
His Facioscapulohumeral muscular dystrophy research incorporates elements of Facial weakness, Physical medicine and rehabilitation and Muscle weakness, Anatomy, Skeletal muscle.
He interconnects University medical, Neurology, Family medicine and Clinical trial in the investigation of issues within Physical therapy.
His Internal medicine research is multidisciplinary, incorporating perspectives in Penetrance and Cardiology.
To a larger extent, George W. Padberg studies Genetics with the aim of understanding Muscular dystrophy.
Many of his studies on Genetics involve topics that are commonly interrelated, such as Otosclerosis.
Between 2012 and 2021, his most popular works were:
- Population-based incidence and prevalence of facioscapulohumeral dystrophy. (161 citations)
- Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2 (97 citations)
- Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltration (91 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Mutation
Facioscapulohumeral muscular dystrophy, Physical therapy, Muscular dystrophy, Genetics and DUX4 are his primary areas of study.
His study in Facioscapulohumeral muscular dystrophy is interdisciplinary in nature, drawing from both Family medicine and Anatomy.
His Physical therapy research is multidisciplinary, incorporating elements of Clinical trial, Dystrophy, Outcome assessment, University medical and Pediatrics.
His Muscular dystrophy research includes elements of Adductor muscles, Hyperintensity and Weakness.
Genetics is a component of his Epigenetics, DNA methylation, DNA damage, Hindbrain and Mutation studies.
His Edema, Adipose tissue and Phosphocreatine study in the realm of Internal medicine interacts with subjects such as Increased intramuscular fat.
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