Consanguinity Mapping of Congenital Heart Disease in a South Indian Population

Por McGregor, Tracy L., Misri, Amit, Bartlett, Jackie, Orabona, Guilherme, Friedman, Richard D., Sexton, David, Maheshwari, Sunita, Morgan, Thomas M.
Publicado em 2010

A Single-Nucleotide Polymorphism in the Fetal Catechol-O-methyltransferase Gene is Associated With Spontaneous Preterm Birth in African Americans

Por Thota, Chandrasekhar, Menon, Ramkumar, Wentz, Melissa J., Fortunato, Stephen J., Bartlett, Jackie, Drobek, Cayce O., Nair, Sangeeta, Al-Hendy, Ayman
Publicado em 2012

GENETIC VARIATION IN SOLUBLE EPOXIDE HYDROLASE (EPHX2) IS ASSOCIATED WITH FOREARM VASODILATOR RESPONSES IN HUMANS

Por Lee, Craig R., Pretorius, Mias, Schuck, Robert N., Burch, Lauranell H., Bartlett, Jackie, Williams, Scott M., Zeldin, Darryl C., Brown, Nancy J.
Publicado em 2010

Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10

Por Liang, Xueying, Slifer, Michael, Martin, Eden R., Schnetz-Boutaud, Nathalie, Bartlett, Jackie, Anderson, Brent, Züchner, Stephan, Gwirtsman, Harry, Gilbert, John R., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2009