Somatic Mosaicism and Autism Spectrum Disorder

por D’Gama, Alissa M.
Publicado 2021

Role of genomic medicine and implementing equitable access for critically ill infants in neonatal intensive care units

por D’Gama, Alissa M., Agrawal, Pankaj B.
Publicado 2023

Integrating rapid exome sequencing into NICU clinical care after a pilot research study

por D’Gama, Alissa M., Del Rosario, Maya C., Bresnahan, Mairead A., Yu, Timothy W., Wojcik, Monica H., Agrawal, Pankaj B.
Publicado 2022

GCT-37. PREVALENCE OF AUTISM SPECTRUM DISORDER AND OTHER NEURODEVELOPMENTAL DISORDERS IN PEDIATRIC PATIENTS WITH INTRACRANIAL GERM CELL TUMORS

por Liu, Kevin X, Sethi, Roshan V, Pulsifer, Margaret B, D’Gama, Alissa M, Lavally, Beverly, Tarbell, Nancy J, Yock, Torunn I, MacDonald, Shannon M
Publicado 2020

Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency

por Fan, Xin, Xie, Bobo, Zou, Jun, Luo, Jingsi, Qin, Zailong, D'Gama, Alissa M., Shi, Jiahai, Yi, Shang, Yang, Qi, Wang, Jin, Luo, Shiyu, Chen, Shaoke, Agrawal, Pankaj B., Li, Qifei, Shen, Yiping
Publicado 2018

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

por Rodin, Rachel E., Dou, Yanmei, Kwon, Minseok, Sherman, Maxwell A., D’Gama, Alissa M., Doan, Ryan N., Rento, Lariza M., Girskis, Kelly M., Bohrson, Craig L., Kim, Sonia N., Nadig, Ajay, Luquette, Lovelace J., Gulhan, Doga C., Park, Peter J., Walsh, Christopher A.
Publicado 2021

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

Biallelic Mutations In Human DCC Cause Developmental Split Brain Syndrome

por Jamuar, Saumya S., Schmitz-Abe, Klaus, D’Gama, Alissa M., Drottar, Marie, Chan, Wai-Man, Peeva, Maya, Servattalab, Sarah, Lam, Anh-Thu N., Delgado, Mauricio R., Clegg, Nancy J., Al Zayed, Zayed, Dogar, Mohammad Asif, Alorainy, Ibrahim A., Jamea, Abdullah Abu, Abu-Amero, Khaled, Griebel, May, Ward, Wendy, Lein, Ed S., Markianos, Kyriacos, Barkovich, A. James, Robson, Caroline D., Grant, P. Ellen, Bosley, Thomas M., Engle, Elizabeth C., Walsh, Christopher A., Yu, Timothy W.
Publicado 2017