Events

Evenings with Genetics

Evenings with Genetics is a seminar series about genetics and your family’s health. This series offers the most current information on care and research for many genetic conditions and is open to the public.

Press Releases

Evolution of marine mammals to water life converges in some genesJan 26, 2015
Baylor researchers contribute to study examining genomes of four marine mammals compared to their closest land kin to examine genetic evidence for convergent evolution.
Baylor scientists identify a novel precursor to neurodegenerationJan 15, 2015
Researchers connect the presence of lipid droplet accumulation in the glia of specific mutants as a harbinger of neurodegeneration.
A “null” gene and one that is just a little inactive are the recipe for scoliosisJan 8, 2015
Research led by Baylor finds "null" gene and one that is just a little inactive results in a child born with a curved spine – congenital scoliosis.
Dr. Atul Chopra named Caroline Wiess Law ScholarDec 31, 2014

Dr. Atul Chopra has been named a Caroline Wiess Law Scholar, an award designated to recruit and retain accomplished, young physician-scientists.

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.
New study identifies first gene associated with familial gliomaDec 7, 2014
Baylor-led research identifies for the first time a gene associated with familial glioma, brain tumors that appear in two or more members of the same family.
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?”
International collaboration completes genome sequence of centipede Nov 26, 2014
An international collaboration of scientists including Baylor College of Medicine has completed the first genome sequence of a myriapod, Strigamia maritima.
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.
Largest ever genomic study of liver cancer identifies mutations that distinguish Asian and Western diseaseNov 7, 2014
Baylor part of study that identifies a mutation signature that contributes more to cases of liver tumors in Japanese males than in men of European ancestry.
Baylor, Miraca Holdings agree to joint venture on clinical genetic testingOct 31, 2014
Baylor Miraca Genetics Laboratories will be built on Baylor’s existing Medical Genetics Laboratories, which engages in clinical laboratory genetic testing.
Immune-related gene may predispose to HPV-related cancerOct 23, 2014
Baylor-led research identifies immune related gene that appears to play an important role in determining whether a person develops a cancer related to human papilloma virus.
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.
Developmental transcription factors oversee glioma sub-typesOct 6, 2014
Researchers find transcription factors NFIA, Sox10 play important roles in the development of different subtypes of deadly brain tumors.
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.