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

Bacteria help discover human cancer-causing proteinsJan 10, 2019
A team led by researchers at Baylor College of Medicine and the University of Texas at Austin has applied an unconventional approach that used bacteria to discover human proteins that can lead to DNA damage and promote cancer.
Evenings with Genetics focuses on cystic fibrosisJan 8, 2019
On Tuesday, Jan. 15, Evenings with Genetics will highlight cystic fibrosis is a genetic condition that causes persistent lung infections.
Researchers analyze impact of newborn genomic screeningJan 3, 2019
As genomic sequencing becomes increasingly popular and accessible, an effort called the BabySeq Project aims to explore the medical, behavioral, economic and ethical impacts of adding genomic sequencing to the roster of screenings for newborns.
Dr. Kjersti Aagaard awarded mentor award from NatureDec 19, 2018
Dr. Kjersti Aagaard has been honored with a 2018 Nature Award for Mentoring in Science.
Mecanismos de infección de los virus del dengue y Zika y conexión con microcefaliaDec 13, 2018
Investigadores de la Universidad de California, San Francisco y Baylor College of Medicine, Houston revelan cómo los virus del dengue y Zika causan infección y como el virus del Zika puede causar microcefalia.
New insights into Zika's microcephaly link, dengue infectionDec 13, 2018
New insights into how dengue and Zika viruses cause disease reveal shared and virus-specific mechanisms, and led to an understanding of Zika's like to microcephaly.
Baylor faculty elected National Academy of Inventors fellows Dec 12, 2018
Drs. Mary K. Estes, Bert O’Malley and Huda Zoghbi of Baylor College of Medicine were three of the 148 renowned academic inventors named fellows of the National Academy of Inventors this week.
Without Dna2, genes can jump into DNA breaksDec 5, 2018
A study reveals that when Dna2 is absent, small DNA fragments jump from all over the genome into chromosome breaks. This novel mechanism may explain similar events commonly seen in cancer or during antibody diversification.
Understanding formation of neurons in adult brainsDec 5, 2018
A team of researchers at Baylor College of Medicine, the Texas Heart Institute and Texas Children’s Hospital has developed a powerful new approach to understand the formation of new neurons in the mammalian adult brain.
FDA recognizes database of clinically relevant genetic variantsDec 5, 2018
The database created by the Clinical Genome Resource program (ClinGen) has been recognized by the U.S. Food and Drug Administration.
Parents, researchers work to find cause of neonatal epilepsyNov 19, 2018
A shared goal to raise awareness and develop better treatments for neonatal-onset epilepsy has brought Baylor College of Medicine researchers together with three U.S. families.
Evenings with Genetics offers update on rare Angelman SyndromeNov 6, 2018
The next installment of Evenings with Genetics on Tuesday, Nov. 13, will focus on Angelman Syndrome, with expert speakers providing an update on treatment and research efforts for the disease.
Researchers solve mystery surrounding form of Batten diseaseNov 5, 2018
A team led by researchers at Baylor College of Medicine has uncovered an unexpected mechanism that can explain a form of Batten disease called neuronal ceroid lipofuscinosis 8.
Protein connection shown to be major player in cancer growthOct 19, 2018
A team of researchers at Baylor College of Medicine and Texas Children’s Hospital has revealed a connection between mTORC1 and Src, two proteins known to be hyperactive in cancer.
Special issue of journal highlights ClinGen programOct 12, 2018
A special issue of the journal Human Mutation contains 25 papers related to the activities of the National Human Genome Research Institute-funded Clinical Genome Resource program (ClinGen) and ClinVar.
Undiagnosed Diseases Network finds 31 new syndromesOct 10, 2018
The Undiagnosed Diseases Network, a consortium of researchers including Baylor College of Medicine, Texas Children’s Hospital, Stanford University and other institutions, has found 31 new syndromes within two years of the group’s inception.
Grant funds somatic cell genome editing mouse models studyOct 9, 2018
As part of a larger effort of the National Institutes of Health’s Somatic Cell Genome Editing program, researchers received a U42 grant to create mouse model resources for testing the therapeutic potential of novel genome editing approaches.
Dynamin-binding protein linked to congenital cataractsOct 4, 2018
A new study has now found compelling evidence that links dynamin-binding protein (DNMBP) to congenital bilateral cataracts and severe vision loss. 
Researchers find missplicing Scn5a alters cardiac functionSep 28, 2018
A new study shows that reproducing in mice the missplicing of gene Scn5a observed in patients with myotonic dystrophy type 1(DM1) recapitulates defects in cardiac function present in the patients.
Baylor’s HGSC named an NIH All of Us research centerSep 26, 2018
The All of Us Research Program, part of the National Institutes of Health, has named a consortia led by Baylor's Human Genome Sequencing Center as one of three centers responsible for generating clinical grade genomic data for the program.