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Assessing non-Mendelian inheritance in inherited axonopathies
Inherited Neuropathy Consortium
Neurology
Research output
:
Contribution to journal
›
Article
›
peer-review
23
Scopus citations
Overview
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Dive into the research topics of 'Assessing non-Mendelian inheritance in inherited axonopathies'. Together they form a unique fingerprint.
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Keyphrases
Axon
16%
Axonopathy
100%
Burden Analysis
33%
Causative Gene
16%
Complex Inheritance
16%
Disease Genes
16%
EXOC4
16%
Exome
33%
Genetic Diagnosis
16%
Hereditary Spastic Paraplegia
50%
Heterogeneous Disease
16%
High Penetrance
16%
Inheritance Mechanism
16%
International Collaboration
16%
Large Cohort
16%
Length-dependent
16%
Mendelian Disorders
16%
Multilocus Approach
50%
Mutational Burden
33%
Nervous System
16%
Non-Mendelian Inheritance
100%
Odds Ratio
16%
Oligogenic
16%
Quality Control
16%
Rare Variant Burden
33%
Risk Allele
33%
Medicine and Dentistry
Allele
66%
Axon
16%
DeJerine-Sottas Disease
50%
Disease
16%
Diseases
33%
Exome
33%
Mendelian Inheritance
100%
Nervous System
16%
Neuropathy
100%
Odds Ratio
16%
Penetrance
16%
Biochemistry, Genetics and Molecular Biology
Allele
100%
Axon
25%
Exome
50%
Genetics
25%
Non-Mendelian Inheritance
100%
Penetrance
25%
Quality Control
25%
Rare Variant
50%
Immunology and Microbiology
Allele
100%
Axon
25%
Exome
50%
Neurological System
25%
Penetrance
25%
Neuroscience
Axon
16%
Hereditary Spastic Paraplegia
50%
Nervous System
16%
Neuropathy
100%