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    Hereditary Diseases

    Hereditary diseases are diseases that can be passed down to offspring. A common example of this is color blindness, which is an X-linked chromosomal disorder.

    Webinars

    • MAR 22, 2016 | 8:15 AM
      The Top Ten Laboratory Tests
      The Top Ten Laboratory Tests
      Genetic testing has been an important component of medical care for decades but the breadth and impact of testing has been steadily increasing as medical knowledge increases, appreciation of ...
      Speaker: Katherine Rauen, MD, MS, PhD , Robert Nussbaum, MD
      Presented at: GENETICS IN YOUR CLINIC: WHAT YOU CAN AND SHOULD DO NOW
      2
      MAR 16, 2016 | 12:00 PM
      Featured Speaker - Striatal Synaptic Dysfunction in Parkinson's disease
      Featured Speaker - Striatal Synaptic Dysfunction in Parkinson's...
      Traditional models of basal ganglia disorders are grounded in the assumption that network dysfunction is driven by alterations in intrinsic excitability of striatal neurons. Recent work has c...
      Speaker: D James Surmeier, PhD
      Presented at: Neuroscience Virtual Event Series 2016
      0
      MAY 14, 2015 | 1:30 PM
      Germline Cancer Genetics in 2015
      Germline Cancer Genetics in 2015
      Germline cancer genetics became a reality with the cloning of the tumor suppressor gene RB1 for hereditary retinoblastoma in 1986 by Friend and Weinberg. The existence of cancer susceptibili...
      Speaker: Judy E Garber, MD, MPH
      Presented at: Genetics and Genomics Virtual Event Series 2015
      4
      AUG 21, 2014 | 7:30 AM
      Keynote: Clinical Validity and Utility in Whole Exome/Genome Sequencing
      Keynote: Clinical Validity and Utility in Whole Exome/Genome Sequencing
      ...
      Speaker: Robert Nussbaum, MD
      Presented at: Genetics and Genomics Virtual Event Series 2014
      48
      AUG 22, 2013 | 12:00 PM
      C.E. CREDITS
      Exome Sequencing as a Diagnostic Tool
      Exome Sequencing as a Diagnostic Tool
      It is widely accepted that approximately 85% of known disease-causing DNA variants affect the exons and splice junctions, which is about 1% of the whole genome. As a result, Clinical Exome Se...
      Speaker: Pinar Bayrak-Toydemir, MD, PhD
      Presented at: Genetics and Genomics Virtual Event Series 2013
      66
    MAR 22, 2016 | 8:15 AM
    The Top Ten Laboratory Tests
    The Top Ten Laboratory Tests
    Genetic testing has been an important component of medical care for decades but the breadth and impact of testing has been steadily increasing as medical knowledge increases, appreciation of ...
    Speaker: Katherine Rauen, MD, MS, PhD , Robert Nussbaum, MD
    Presented at: GENETICS IN YOUR CLINIC: WHAT YOU CAN AND SHOULD DO NOW
    2
    MAR 16, 2016 | 12:00 PM
    Featured Speaker - Striatal Synaptic Dysfunction in Parkinson's disease
    Featured Speaker - Striatal Synaptic Dysfunction in Parkinson's...
    Traditional models of basal ganglia disorders are grounded in the assumption that network dysfunction is driven by alterations in intrinsic excitability of striatal neurons. Recent work has c...
    Speaker: D James Surmeier, PhD
    Presented at: Neuroscience Virtual Event Series 2016
    0
    MAY 14, 2015 | 1:30 PM
    Germline Cancer Genetics in 2015
    Germline Cancer Genetics in 2015
    Germline cancer genetics became a reality with the cloning of the tumor suppressor gene RB1 for hereditary retinoblastoma in 1986 by Friend and Weinberg. The existence of cancer susceptibili...
    Speaker: Judy E Garber, MD, MPH
    Presented at: Genetics and Genomics Virtual Event Series 2015
    4
    AUG 21, 2014 | 7:30 AM
    Keynote: Clinical Validity and Utility in Whole Exome/Genome Sequencing
    Keynote: Clinical Validity and Utility in Whole Exome/Genome Sequencing
    ...
    Speaker: Robert Nussbaum, MD
    Presented at: Genetics and Genomics Virtual Event Series 2014
    48
    AUG 22, 2013 | 12:00 PM
    C.E. CREDITS
    Exome Sequencing as a Diagnostic Tool
    Exome Sequencing as a Diagnostic Tool
    It is widely accepted that approximately 85% of known disease-causing DNA variants affect the exons and splice junctions, which is about 1% of the whole genome. As a result, Clinical Exome Se...
    Speaker: Pinar Bayrak-Toydemir, MD, PhD
    Presented at: Genetics and Genomics Virtual Event Series 2013
    66
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