Promoting early autism detection and intervention in underserved communities: study protocol for a pragmatic trial using a stepped-wedge design

por Ibañez, Lisa V., Stoep, Ann Vander, Myers, Kathleen, Zhou, Chuan, Dorsey, Shannon, Steinman, Kyle J., Stone, Wendy L.
Publicado 2019

Longitudinal report of child with de novo 16p11.2 triplication

por Wallace, Arianne S., Hudac, Caitlin M., Steinman, Kyle J., Peterson, Jessica L., DesChamps, Trent D., Duyzend, Michael H., Nuttle, Xander, Eichler, Evan E., Bernier, Raphael A.
Publicado 2017

Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region

por Moufawad El Achkar, Christelle, Rosen, Alyssa, Kessler, Sudha Kilaru, Steinman, Kyle J., Spence, Sarah J., Ramocki, Melissa, Marco, Elysa Jill, Green Snyder, LeeAnne, Spiro, John E., Chung, Wendy K., Annapurna, Poduri, Sherr, Elliott H.
Publicado 2022

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

por Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien
Publicado 2012