EGL Genetics Blog

Divide, Recombine, Repeat With Dr. Sherman

Posted by Danyella Davis on Mar 22, 2017 11:00:00 AM

This week, EGL Genetics is featuring published work by Dr. Stephanie L. Sherman, Professor in the Department of Human Genetics and Co-Director of the Down Syndrome Center at Emory University.

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Dr. Sherman's more recent research identifies gene-environment interactions associated with the causes and consequences of trisomy 21 and meiotic recombination. 

Esteemed as a genetic epidemiologist, Dr. Sherman has published 175 articles and nearly 9,500 citations relating to clinical research and therapeutic interventions for genetic disorders. Her specialization areas include:

  • Genetic causes of intellectual and developmental disorders
  • 
Nondisjunction of human chromosomes
  • Primary ovarian insufficiency

  • Genetic mapping of complex traits
  • 
Fragile X syndrome
  • Down syndrome


She recently published a compelling article, titled: "Genome-Wide Association Study of Meiotic Recombination Phenotypes."

Amidst Trisomy Awareness Month, Dr. Sherman is teaming up with EGL Genetics and the Trisomy 18 Foundation for an exciting live broadcast. Please see below for additional details.

 

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                                                                                   Register Today

Topics: Down syndrome, Meiotic recombination

 

 

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