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

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. 
Grant supports identifying leukemia, Down syndrome linkSep 18, 2018
To better understand a predisposition for acute lymphoblastic leukemia in children with Down syndrome, a team of researchers will sequence the genomes of more than 2,000 individuals with Down syndrome.
Breakthrough reveals mutation driving acute myeloid leukemiaSep 10, 2018
Researchers have discovered that the growth of leukemic cells depends on mutant NPM1 gene and its abnormal transport out of the nucleus into the cytoplasm of the cell.
INSiGHT identifies unique retinal regulatory genesAug 29, 2018
Researches at Baylor College of Medicine, Texas Children’s Hospital and the Hospital for Sick Children have developed a new platform called INSiGHT that enables them to uncover new regulators of retina neurons.
Research reveals gene regulation can be digital or stochasticAug 23, 2018
A team of researchers from the National Institutes of Health Roadmap Epigenomics Project has discovered that DNA methylation involved in gene regulation is largely digital and stochastic.
Scientists turn unexpected results into research toolAug 10, 2018
Puzzled by their experimental results, a team of scientists investigated why a research tool that was expected to suppress neuronal activity actually was stimulating it.
Dr. Lupski recognized for leadership in geneticsAug 9, 2018
The American Society of Human Genetics (ASHG) has honored Dr. James Lupski with the 2018 Victor A. McKusick Leadership Award.
Dr. Cheryl Lyn Walker receives Outstanding Investigator AwardAug 6, 2018
Dr. Cheryl Lyn Walker has been awarded an Outstanding Investigator Award (R35) from the National Cancer Institute (NCI).