Genetic Medicine
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Two Vanderbilt School of Medicine Ph.D. students, their faculty advisers selected for HHMI Gilliam Fellows Program
Four Vanderbilt graduate students, faculty advisers named to Howard Hughes Medical Institute Gilliam Fellows Program for their leadership in science and commitment to advancing equity and inclusion in science. Read MoreAug 4, 2023
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Three Vanderbilt biomedical researchers named 2022 Pew Scholars
Mariana Byndloss, assistant professor of pathology, microbiology and immunology, and William Wan, assistant professor of biochemistry, have been named 2022 Pew Scholars in the Biomedical Sciences. The Pew Charitable Trusts and the Alexander and Margaret Stewart Trust have selected Alexander Bick, assistant professor of genetic medicine, to join the 2022 class of Pew-Stewart Scholars for Cancer Research. Read MoreJun 14, 2022
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Study finds genetic risk factors for severe COVID-19 illness
A massive worldwide collaboration including researchers from Vanderbilt University Medical Center (VUMC) has identified several genetic factors associated with SARS-CoV-2 infection and severe COVID-19 illness. Read MoreJul 8, 2021
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Genetics of hydrocephalus
Fluid build-up in the brain — hydrocephalus — increases pressure and risk for brain damage; Vanderbilt researchers have now identified genes and signaling pathways associated with the condition. Read MoreJul 8, 2021
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EHRs, biobanks and Mendelian diseases
Electronic health records and biobanks can be effectively combined to detect and study Mendelian diseases such as cystic fibrosis. Read MoreApr 30, 2020
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Vanderbilt-led team discovers new genetic disease and defines underlying mechanism
An international research team has discovered a new genetic syndrome caused by mutation of a single gene and named it CATIFA, an acronym for its core symptoms. Read MoreJan 13, 2020
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Gamazon receives NIH Genomic Innovator Award
VUMC's Eric Gamazon has received a Genomic Innovator Award from the National Human Genome Research Institute, part of the NIH. Read MoreSep 19, 2019
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Shared genetics may shape treatment options for certain brain disorders
Symptoms of schizophrenia and bipolar disorder, including psychosis, depression and manic behavior, have both shared and distinguishing genetic factors, an international consortium led by researchers from Vanderbilt University and Virginia Commonwealth University is reporting. Read MoreJun 14, 2018
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Vanderbilt’s Gamazon named visiting fellow at Cambridge University
Eric Gamazon, PhD, research instructor in the Division of Genetic Medicine at Vanderbilt University School of Medicine, is spending part of the academic year at Cambridge University in England as one of 40 Clare Hall Visiting Fellows. Read MoreFeb 15, 2018
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Genetics Institute director Cox set for next Discovery Lecture
Nancy Cox, Ph.D., founding director of the Vanderbilt Genetics Institute, will deliver the next Flexner Discovery Lecture on Thursday, Dec. 17. Read MoreDec 10, 2015
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New clue to a devastating disease
New findings suggest a previously unrecognized role for the Sox10 transcription factor in Hirschsprung’s disease, and may lead to improved diagnostic and therapeutic approaches for this disease. Read MoreJan 28, 2015
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Study tracks genes involved in heart rhythm disorders
A team led by Vanderbilt University investigators has discovered two new genes — both coding for the signaling protein calmodulin — associated with severe early-onset disorders of heart rhythm. Read MoreFeb 7, 2013
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Gene linked to familial prostate cancer
A rare, inherited mutation confers an eightfold increased risk of prostate cancer, a recent study shows. Read MoreAug 23, 2012
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Vanderbilt identifies genes linked to breast cancer chemo resistance
A study led by Vanderbilt-Ingram Cancer Center investigators has identified a gene expression pattern that may explain why chemotherapy prior to surgery isn’t effective against some tumors and suggests new therapy options for patients with specific subtypes of breast cancer. Read MoreJun 11, 2012
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Digestive disease research bolstered by grant renewal
The Vanderbilt Digestive Disease Research Center celebrates its 10th anniversary this year with a second five-year renewal of its federal research grant. Read MoreJan 20, 2012
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Potassium channel gene modifies epilepsy risk
The discovery of a new gene that can influence a person's risk for developing epilepsy could improve diagnostic tools and open the door for new therapies. Read MoreApr 18, 2011