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  • Genetic Locus

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  • Disorders

    • Alzheimer's Disease

    • Parkinson's Disease

    • Genetic Markers

    • Genetic Association Studies

    • Frontotemporal Lobar Degeneration

    • Gout

    • Amyotrophic Lateral Sclerosis

    • Spastic Paraplegia, Hereditary

  • Chemicals & Drugs

    • Monomeric Clathrin Assembly Proteins

    • tau Proteins

    • Nuclear Receptor Subfamily 1, Group D, Member 1

    • Sodium-Phosphate Cotransporter Proteins, Type IIa

    • NAV1.8 Voltage-Gated Sodium Channel

    • Formate-Tetrahydrofolate Ligase

    • Receptor, EphA1

    • Methylenetetrahydrofolate Dehydrogenase (NADP+)

    • Thyroid Hormone Receptors alpha

    • Presenilin-2

  • Procedures

    • Genome Wide Association Studies

    • Chromosome Mapping

    • Case Control Studies

  • Anatomy

    • Chromosomes, Human, Pair 6

    • Chromosomes, Human, Pair 21

    • Human Chromosomes

    • Chromosomes, Human, Pair 12

    • Chromosomes, Human, Pair 17

    • Neurofibrils

    • Chromosomes, Human, Pair 19

  • Physiology

    • Genetic Predisposition to Disease

    • Genotype

    • DNA Copy Number Variations

    • Phenotype

    • Genetic Heterogeneity

    • Haplotypes

  • Genes & Molecular Sequences

    • Single Nucleotide Polymorphism

    • Quantitative Trait Loci

    • Genome, Human

    • Alleles

  • Living Beings

    • European Continental Ancestry Group

  • Concepts & Ideas

    • Age of Onset

    • Meta-Analysis

    • Lod Score

    • Pedigree

    • Cohort Studies

    • Databases, Genetic

    • Gene Frequency

    • Linkage Disequilibrium

    • Disease Susceptibility

    • Risk Factors

  • Geographic Areas

    • Netherlands