Baylor College of Medicine News

Molecular and Human Genetics News

Dr. Brendan Lee named chair of genetics at Baylor College of MedicineDec 19, 2014
Lee has been serving as interim chair since June of this year. He succeeds Dr. Arthur Beaudet, who continues as a professor of molecular and human genetics, molecular and cellular biology and pediatrics at the College.
Scientists map human loop-ome, revealing new form of genetic regulationDec 11, 2014
Researchers uncover “folding code” that turns genes and chromosomes on and off.
Dr. Trey Westbrook named TAMEST 2015 Edith and Peter O’Donnell Award winner in medicine Dec 9, 2014
Baylor College of Medicine researcher Dr. Thomas “Trey” Westbrook tapped for prestigious honor given annually to one scientist across the state of Texas for outstanding innovation in medicine.
Baylor researchers join 'Centers Without Walls' to study sudden unexpected death in epilepsyDec 8, 2014
Baylor College of Medicine part of research consortium to receive $5.9 million from the National Institute of Neurological Disorders and Stroke to support understanding of sudden unexpected death in epilepsy.
Taking the 'mute' off silenced gene may be answer to Angelman syndromeDec 1, 2014
Research led by Baylor College of Medicine answers the question “Can we turn on the activity of the paternal gene?”
Baylor researchers recognized with prestigious AAAS honorNov 24, 2014
Baylor College of Medicine scientists Drs. Margaret “Peggy” Goodell, Brendan Lee, David Nelson and Theodore Wensel have been named 2014 Fellows of the American Association for the Advancement of Science.
Whole exome sequencing closer to becoming “new family history”Oct 20, 2014
Baylor researchers find one-fourth of patients whose DNA was submitted for clinical whole exome testing received a diagnosis related to a known genetic disease, often ending a long search for answers for them and their parents.
$6.25M NIH award to lead brittle bone disease clinical research consortiumOct 8, 2014
Baylor College of Medicine has received funding from the National Institutes of Health to lead the Brittle Bone Disorders Consortium of the Rare Disease Clinical Research Network.
Researchers harness power of fly genetics, genomics to speed identification of human neurological disease genesSep 26, 2014
Fly genetics and genomics help with rapid identification of human disease-causing mutations, including rare single gene or Mendelian disorders.
Mathematical analysis reveals mosaicism, parent of origin as drivers of genetic disease recurrence riskSep 18, 2014
Baylor researchers develop a new mathematical framework that sheds additional light on mosaicism.