CFC1 Mutations in Patients with Transposition of the Great Arteries and Double-Outlet Right Ventricle

Por Goldmuntz, Elizabeth, Bamford, Richard, Karkera, Jayaprakash D., dela Cruz, June, Roessler, Erich, Muenke, Maximilian
Publicado em 2002

Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

Por Roessler, Erich, Ouspenskaia, Maia V., Karkera, Jayaprakash D., Vélez, Jorge I., Kantipong, Amy, Lacbawan, Felicitas, Bowers, Peter, Belmont, John W., Towbin, Jeffrey A., Goldmuntz, Elizabeth, Feldman, Benjamin, Muenke, Maximilian
Publicado em 2008

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

Por Roessler, Erich, Pei, Wuhong, Ouspenskaia, Maia V., Karkera, Jayaprakash D., Veléz, Jorge Ivan, Banerjee-Basu, Sharmilla, Gibney, Gretchen, Lupo, Philip J., Mitchell, Laura E., Towbin, Jeffrey A., Bowers, Peter, Belmont, John W., Goldmuntz, Elizabeth, Baxevanis, Andreas D., Feldman, Benjamin, Muenke, Maximilian
Publicado em 2009

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2

Por Detera-Wadleigh, Sevilla D., Badner, Judith A., Berrettini, Wade H., Yoshikawa, Takeo, Goldin, Lynn R., Turner, Gordon, Rollins, Denise Y., Moses, Tracy, Sanders, Alan R., Karkera, Jayaprakash D., Esterling, Lisa E., Zeng, Jin, Ferraro, Thomas N., Guroff, Juliet J., Kazuba, Diane, Maxwell, Mary E., Nurnberger, John I., Gershon, Elliot S.
Publicado em 1999