Molecular and Human Genetics News
Dr. Malcolm Brenner receives prestigious lifetime achievement honor from Human Gene Therapy journal Aug 5, 2014 Renowned cell and gene therapy clinician-scientist Dr. Malcolm Brenner has received the prestigious Pioneer Award from the journal Human Gene Therapy.
Mosaicism: study clarifies parents as source of new disease mutations Jul 31, 2014 Baylor-led study sheds new light on the frequency of mosaicism in genomic disorders and its influence on recurrence risk.
Marmoset sequence sheds light on primate biology, evolution Jul 20, 2014 Sequencing genome the common marmoset – the first sequence of a New World Monkey – sheds new light on primate biology and evolution.
Baylor announces 2014 Michael E. DeBakey, M.D., Excellence in Research Awards Jul 2, 2014 The award, named in honor of the college’s first president and pioneering heart surgeon, was presented to the six recipients July 2.
Baylor, Texas Children’s join national collaboration to solve most difficult, rare medical cases Jul 1, 2014 New national network of clinicians and scientists are joining forces to address prolonged undiagnosed medical conditions.
Dr. Richard Gibbs awarded prestigious Companion of the Order of Australia Jun 9, 2014 Renowned genomics researcher Dr. Richard Gibbs awarded prestigious honor of the Companion of the Order of Australia – an accolade issued by the Australian government that recognizes eminent achievement, merit of the highest degree in service to Australia.
Zoghbi receives honorary degree from Yale University May 20, 2014 Baylor's Dr. Huda Zoghbi was the recipient of an honorary Doctor of Medical Sciences degree at Yale University’s 2014 commencement ceremony.
Study unveils new approach to treating brittle bone disease May 5, 2014 Researchers at Baylor College of Medicine have identified a new approach to treating brittle bone disease, a congenital disorder that results in fragile bones that break easily.
New tool analyzes sequence data to identify disease-causing genes May 1, 2014 Baylor researchers outline best practices for computer program used to discover underlying genetic causes of complex traits and diseases.
New syndrome caused by mutations in AHDC1 May 1, 2014 Study identifies gene underlying newly recognized syndrome that has symptoms of sleep apnea, delayed speech and hypotonia, or generalized upper body weakness.