Genetic Factors Underlying Sudden Infant Death Syndrome

por Keywan, Christine, Poduri, Annapurna H, Goldstein, Richard D, Holm, Ingrid A
Publicado 2021

The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths

por Wojcik, Monica H., Poduri, Annapurna H., Holm, Ingrid A., MacRae, Calum A., Goldstein, Richard D.
Publicado 2023

Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression

por Rochtus, Anne M., Trowbridge, Sara, Goldstein, Richard D., Sheidley, Beth Rosen, Prabhu, Sanjay P., Haynes, Robin, Kinney, Hannah C., Poduri, Annapurna H.
Publicado 2019

The role of sodium channels in sudden unexpected death in pediatrics

por Rochtus, Anne M., Goldstein, Richard D., Holm, Ingrid A., Brownstein, Catherine A., Pérez‐Palma, Eduardo, Haynes, Robin, Lal, Dennis, Poduri, Annapurna H.
Publicado 2020

Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

por Brownstein, Catherine A., Douard, Elise, Haynes, Robin L., Koh, Hyun Yong, Haghighi, Alireza, Keywan, Christine, Martin, Bree, Alexandrescu, Sanda, Haas, Elisabeth A., Vargas, Sara O., Wojcik, Monica H., Jacquemont, Sébastien, Poduri, Annapurna H., Goldstein, Richard D., Holm, Ingrid A.
Publicado 2022

Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy

por Koh, Hyun Yong, Smith, Lacey, Wiltrout, Kimberly N., Podury, Archana, Chourasia, Nitish, D’Gama, Alissa M., Park, Meredith, Knight, Devon, Sexton, Emma L., Koh, Julia J., Oby, Brandon, Pinsky, Rebecca, Shao, Diane D., French, Courtney E., Shao, Wanqing, Rockowitz, Shira, Sliz, Piotr, Zhang, Bo, Mahida, Sonal, Moufawad El Achkar, Christelle, Yuskaitis, Christopher J., Olson, Heather E., Sheidley, Beth Rosen, Poduri, Annapurna H.
Publicado 2023