1p36 deletion syndrome: an update

le Jordan, Valerie K, Zaveri, Hitisha P, Scott, Daryl A
Foilsithe in Appl Clin Genet (2015)

Duplication of HEY2 in Cardiac and Neurologic Development

le Jordan, Valerie K., Rosenfeld, Jill A., Lalani, Seema R., Scott, Daryl A.
Foilsithe in Am J Med Genet A (2015)

RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects

le Kim, Bum Jun, Zaveri, Hitisha P., Jordan, Valerie K., Hernandez-Garcia, Andres, Jacob, Daron J., Zamora, Diana L., Yu, Wei, Schwartz, Robert J., Scott, Daryl A.
Foilsithe in Dis Model Mech (2018)

Ryanodine-Receptor Mediated Calcium Leak Drives Progressive Development of an Atrial Fibrillation Substrate in a Transgenic Mouse Model

le Li, Na, Chiang, David Y., Wang, Sufen, Wang, Qiongling, Sun, Liang, Voigt, Niels, Respress, Jonathan L., Ather, Sameer, Skapura, Darlene G., Jordan, Valerie K., Horrigan, Frank T., Schmitz, Wilhelm, Müller, Frank U., Valderrabano, Miguel, Nattel, Stanley, Dobrev, Dobromir, Wehrens, Xander H.T.
Foilsithe 2014

FBN1 Contributing to Familial Congenital Diaphragmatic Hernia

le Beck, Tyler F., Campeau, Philippe M., Jhangiani, Shalini N., Gambin, Tomasz, Li, Alexander H., Abo-Zahrah, Reem, Jordan, Valerie K., Hernandez-Garcia, Andres, Wiszniewski, Wojciech K., Muzny, Donna, Gibbs, Richard A., Boerwinkle, Eric, Lupski, James R., Lee, Brendan, Reardon, Willie, Scott, Daryl A.
Foilsithe in Am J Med Genet A (2015)

The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia

le Jordan, Valerie K, Beck, Tyler F, Hernandez-Garcia, Andres, Kundert, Peter N, Kim, Bum-Jun, Jhangiani, Shalini N, Gambin, Tomasz, Starkovich, Molly, Punetha, Jaya, Paine, Ingrid S, Posey, Jennifer E, Li, Alexander H, Muzny, Donna, Hsu, Chih-Wei, Lashua, Amber J, Sun, Xin, Fernandes, Caraciolo J, Dickinson, Mary E, Lally, Kevin P, Gibbs, Richard A, Boerwinkle, Eric, Lupski, James R, Scott, Daryl A
Foilsithe in Hum Mol Genet (2018)

De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions

le Fregeau, Brieana, Kim, Bum Jun, Hernández-García, Andrés, Jordan, Valerie K., Cho, Megan T., Schnur, Rhonda E., Monaghan, Kristin G., Juusola, Jane, Rosenfeld, Jill A., Bhoj, Elizabeth, Zackai, Elaine H., Sacharow, Stephanie, Barañano, Kristin, Bosch, Daniëlle G.M., de Vries, Bert B.A., Lindstrom, Kristin, Schroeder, Audrey, James, Philip, Kulch, Peggy, Lalani, Seema R., van Haelst, Mieke M., van Gassen, Koen L.I., van Binsbergen, Ellen, Barkovich, A. James, Scott, Daryl A., Sherr, Elliott H.
Foilsithe in Am J Hum Genet (2016)

Genotype–phenotype correlations in individuals with pathogenic RERE variants

le Jordan, Valerie K., Fregeau, Brieana, Ge, Xiaoyan, Giordano, Jessica, Wapner, Ronald J., Balci, Tugce B., Carter, Melissa T., Bernat, John A., Moccia, Amanda N., Srivastava, Anshika, Martin, Donna M., Bielas, Stephanie L., Pappas, John, Svoboda, Melissa D., Rio, Marlène, Boddaert, Nathalie, Cantagrel, Vincent, Lewis, Andrea M., Scaglia, Fernando, Kohler, Jennefer N., Bernstein, Jonathan A., Dries, Annika M., Rosenfeld, Jill A., DeFilippo, Colette, Thorson, Willa, Yang, Yaping, Sherr, Elliott H., Bi, Weimin, Scott, Daryl A.
Foilsithe in Hum Mutat (2018)