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

Dr. Brendan Lee honored with American Society of Human Genetics Curt Stern AwardJun 22, 2016
Dr. Brendan Lee, the Robert and Janice McNair Endowed Chair in Molecular and Human Genetics and professor and chair of the department of molecular and human genetics at Baylor College of Medicine, has been awarded the ASHG 2016 Curt Stern Award.
Baylor recognizes excellence among cliniciansJun 16, 2016
A select group of Baylor College of Medicine faculty members were recognized for excellence in patient care at the Master Clinician and Rising Star Clinician Awards ceremony.
Baylor, The Chinese University of Hong Kong join to advance genetic research, trainingJun 15, 2016
Baylor College of Medicine and The Chinese University of Hong Kong will establish The Chinese University of Hong Kong-Baylor College of Medicine Joint Center for Medical Genetics in Hong Kong.
Zoghbi to receive the Shaw Prize in Life Science and Medicine for 2016Jun 10, 2016
Dr. Huda Y. Zoghbi was awarded the 2016 Shaw Prize in Life Science and Medicine for her groundbreaking discovery of the genes and the encoded proteins associated with Rett syndrome.
Targeting B-cell malignancies with κ-specific T cells can lead to complete clinical responsesJun 6, 2016
Treating B cell malignancies with the patients’ own T cells modified so as to target specific B cell markers has shown clinical success.
Gene TMEM230 suggests novel mechanism for Parkinson’s diseaseJun 6, 2016
The discovery of a new gene, TMEM230, illuminates a possible mechanism to explain Parkinson’s disease.
Evening With Genetics heads to McAllen, focuses on developmental disabilitiesJun 2, 2016
Answers to questions about the cause of children’s disabilities, new testing, specific treatment and resources will be the focus of a public seminar in both English and Spanish.
Genetic series provides updates on neurofibromatosis type 1May 31, 2016
Neurofibromatosis type 1, a disorder characterized by the growth of noncancerous tumors, will be the focus of discussion in the June 7 Evenings with Genetics
Mutations in RERE gene result in features that coincide with those associated with 1p36 deletion syndromeApr 14, 2016
RERE mutations alone can cause developmental problems typical of 1p36 deletions.
Monthly genetic series focuses on new perspectives on reducing stress in parents of children with developmental disabilities Mar 31, 2016
Coping with stress while parenting individuals with intellectual and developmental disabilities is the topic of the next Evenings with Genetics on April 11, 2016.
Born to run? Study suggests love of exercise starts in the wombMar 31, 2016
Baylor College of Medicine researchers have discovered that female mice that voluntarily exercise during pregnancy have offspring that are more physically active as adults.
Evolution meets biochemistry to better understand how dopamine receptors workMar 16, 2016
Baylor-led team develops new mathematical tool that, together with biochemical analyses, allows them to pinpoint specific structural changes in the dopamine 2 receptor.
Largest genomic study on kidney cancer brings hope for more effective treatments Mar 4, 2016
Baylor's Dr. Chad Creighton led a study that distinguished nine major subtypes of kidney cancer.
Evenings With Genetics focuses on neurofibromatosis type 1Mar 3, 2016
Neurofibromatosis type 1, a disorder characterized by the growth of noncancerous tumors, will be the focus of the next Evenings with Genetics on March 8.
Whole genome sequencing advances pancreatic tumor classificationFeb 26, 2016
Researchers from the Human Genome Sequencing Center and the Elkins Pancreas Center at Baylor College of Medicine have collaborated with researchers in a breakthrough reclassification of pancreatic cancer.
Alliance to discover transformational therapies for people with neurodegenerative diseaseFeb 9, 2016
Dr. Huda Zoghbi will lead a team with UCB, a global biopharmaceutical company, to find therapies for people with neurodegenerative diseases. 
Blood sucking fated in bed bug’s genomeFeb 2, 2016
International consortium sequence the genome of the common bed bug, findings could lead to pesticide resistance.
Zoghbi to receive the prestigious Jessie Stevenson Kovalenko MedalFeb 1, 2016
 The National Academy of Science announced Dr. Huda Zoghbi will be the recipient of this year’s prestigious Jessie Stevenson Kovalenko Medal.
Identification of a new hearing impairment gene implicates the involvement of the S1PR gene family in human diseaseJan 21, 2016
An international group of researchers led by those at Baylor College of Medicine find gene mutation associated with hearing loss.
Exome sequencing helps identify cataract gene in members of religious sectJan 14, 2016
Link between a type of cataract and sudden cardiac death may have been found thanks to exome sequencing.