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

Mechanism of environment-microbe-host interactions revealedApr 24, 2017
Researchers have uncovered a mechanism showing how microbes can alter the physiology of the organisms in which they live.
Medical mystery solved in record timeApr 17, 2017
In a study published today, a team of researchers reports solving a medical mystery of the genetic cause of intellectual disability in four male patient in a day’s work.
Landmark autism genetic study seeking participantsMar 28, 2017
Families affected by autism are invited to a special on-site registration and data collection event for the nation’s largest-ever autism research study. 
New genetic risk factors identify two distinct glioma subtypesMar 27, 2017
Researchers led by Dr. Melissa Bondy have conducted the largest study to date of malignant brain tumors looking for genetic markers of glioma, a highly aggressive form of brain cancer.
OTUD6B gene mutations cause intellectual, physical disabilityMar 23, 2017
An international team of researchers from institutions around the world has discovered that mutations of the OTUD6B gene result in a spectrum of physical and intellectual deficits.
OTUD6B gene mutations cause intellectual, physical disabilityMar 23, 2017
An international team of researchers from institutions around the world has discovered that mutations of the OTUD6B gene result in a spectrum of physical and intellectual deficits.
Gene mutation may be linked to unexplained female infertilityMar 21, 2017
Researchers have uncovered a gene mutation that may provide answers to unexplained female infertility.
Gene mutation may be linked to unexplained female infertilityMar 21, 2017
Researchers have uncovered a gene mutation that may provide answers to unexplained female infertility.
New SMA treatment topic of March Evenings with GeneticsMar 21, 2017
On Tuesday, March 28, Evenings with Genetics will highlight a new drug that has been approved by the FDA to treat Spinal Muscular Atrophy.
Mouse study helps find causes of human behavioral disordersMar 13, 2017
Research of a mouse model led to the discovery of the genetic cause of the human neurological condition of five patients who, until now, had not received a genetic diagnosis.
Mouse study helps find causes of human behavioral disordersMar 13, 2017
Research of a mouse model led to the discovery of the genetic cause of the human neurological condition of five patients who, until now, had not received a genetic diagnosis.
Gene ABL1 implicated in cancer, developmental disorderMar 13, 2017
Researchers link ABL1, a human gene well-known for its association with cancer, to a developmental disorder. 
Gene ABL1 implicated in cancer, developmental disorderMar 13, 2017
Researchers link ABL1, a human gene well-known for its association with cancer, to a developmental disorder. 
Mutations in CWC27 result in spectrum of conditionsMar 9, 2017
Researchers has discovered that mutations in the human gene CWC27 result in a spectrum of clinical conditions that include retinal degeneration and problems with craniofacial and skeletal development.
Genetic driver behind rare skeletal dysplasia condition foundMar 6, 2017
Researchers have identified a previously unimplicated gene behind a particular form of chondrodysplasia, a skeletal dysplasia that affects cartilage formation and causes disproportionate short stature and premature osteoarthritis.
Genetic driver behind rare skeletal dysplasia condition foundMar 6, 2017
Researchers have identified a previously unimplicated gene behind a particular form of chondrodysplasia, a skeletal dysplasia that affects cartilage formation and causes disproportionate short stature and premature osteoarthritis.
Baylor’s Human Genome Sequencing Center looks to bring adult whole genome sequencing to clinical space with unprecedented NHLBI grantMar 1, 2017
The Human Genome Sequencing Center has been named a participant in a half-billion dollar program to bring whole genome sequencing to the forefront of clinical research.
Many genetic changes can occur early in human developmentFeb 23, 2017
When multiple genetic changes occur before or early after conception, they may inform scientists about fundamental knowledge underlying many diseases.
Many genetic changes can occur early in human developmentFeb 23, 2017
When multiple genetic changes occur before or early after conception, they may inform scientists about fundamental knowledge underlying many diseases.
Research finds strategy that may treat juvenile Batten diseaseFeb 6, 2017
Researchers have discovered a treatment that improves the neurological symptoms in a mouse model of juvenile Batten disease.