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Baylor College of Medicine News

Genetics News

Master molecule SRC-2 sets stage for embryo implantationOct 24, 2013
Baylor researchers find understanding how SRC-2 reprograms the endometrium to be receptive to implantation is a critical to developing methods to help women at high risk for early pregnancy loss.
Doubling Shank3 corresponds with mania seen in bipolar patientsOct 23, 2013
A team led by scientists at Baylor and the Jan and Dan Duncan Neurological Research Institute at Texas Children’s Hospital have found that too little or too much of the Shank3 influences brain function.
Prepare for unexpected when making genetic diagnosis in sequencing eraOct 15, 2013
Baylor part of research group that finds whole genome or exome sequencing can provide new answers to physicians and families seeking the source of what are obviously genetic diseases, but for whom the clinical picture is not always same for each patient.
Gene that affects epigenetics of rare molar pregnancies gives clues about genetic imprintingOct 8, 2013
Baylor researchers unraveled the first clues as to how loss or mutation of a gene called NLRP7 in women can cause their pregnancies to develop as hydatidiform moles.
1000 Genomes Project provides functional insights on genetic variationOct 3, 2013
Baylor College of Medicine researchers part of international project that provide insights on genetic variation.
Whole exome sequencing takes new technology into the clinicOct 2, 2013
Baylor researchers find new genetic test helped provide a diagnosis to 25 percent of the first 250 such patients referred to the Baylor Whole Genome Laboratory, demonstrating the value of such technology to individual patients.
Healthy volunteers benefit from whole exome sequencingSep 30, 2013
Baylor researchers find whole exome sequencing serves as a new screening risk detection approach toward the objective of improved health.
Baylor, Smith-Magenis Syndrome Research Foundation team up to advance research of complex syndromeSep 30, 2013
With new funding support from the Smith-Magenis Syndrome Research Foundation, Baylor College of Medicine will establish a new center focused on expanding research into this complex genomic disorder.
Sequencing studies help pinpoint gene in Prader-Willi syndromeSep 29, 2013
Baylor part of collaboration with UTHealth, Complete Genomics to study genome sequencing to help pinpoint gene in Prader-Willi syndrome.
Baylor, Stanford medical schools seek to improve clinical understanding of gene changesSep 25, 2013
Baylor and Standford medical schools partner for $8.4 million grant to develop genetic database to help share data, expertise.