Submissions from 2026
A Three Generation Family with VACTERL Association is Found to have a Rare Form of Diamond-blackfan Anaemia., Iryna Leshchynska, Debjani Das, Victoria O'Reilly, Alena Sipka, Kavitha Iyer, Dimuthu Alankarage, Emma Rath, Akshita Kumar, Beth A. Kurt, and Maria E. Voydanoff
Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity., Jeremy W. Prokop, Sanjana Arora, Austin Goodyke, Katie L Buelow, Mason Westgate, Elizabeth A. VanSickle, Caleb P. Bupp, Amanda Holsworth, Nicholas L. Hartog, Jena M. Krueger, Marcos Cordoba, Matthew Sims, Maximiliano A. Tamae Kakazu, Angela M. Peraino, Stewart Graham, Elora Hussain, Mara L. Leimanis-Laurens, and Surender Rajasekaran
Submissions from 2025
Pathogenic UNC13A Variants Cause a Neurodevelopmental Syndrome by Impairing Synaptic Function, Reza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, Jasmine Shahanoor Hinzen, Mareike Lohse, Boris Bouazza-Arostegui, Siqi Sun, Tillmann Utesch, Caleb Bupp, and Bethany Grysko
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models., Clara Houdayer, A Marie Phillips, Marie Chabbert, Jennifer Bourreau, Reza Maroofian, Henry Houlden, Kay Richards, Nebal Waill Saadi, Eliška Dad'ová, and Laurie H. Seaver
The molecular architecture of severe pediatric traumatic brain injury: integrated omics reveal therapeutic pathways., Elora Hussain, Jeremy W. Prokop, Emily Nonnemacher, Nadia Ashrafi, Ali Yilmaz, Romana Ashrafi Mimi, Abdullah Khalid, Karolis Krinickis, Vilija Lomeikaite, Lena Sanfilippo, Kylie Maxton, Jacob Charron, Charitha Subrahmanya, Austin Goodyke, Annie Needs, Daniel R Woldring, Caleb P. Bupp, Nicholas Hartog, Stewart F. Graham, and Surender Rajasekaran
A Zebrafish Model of Nicotinamide Adenine Dinucleotide (NAD(+)) Deficiency-Derived Congenital Disorders., Visakuo Tsurho, Carla Gilliland, Jessica Ensing, Elizabeth A. VanSickle, Nathan J Lanning, Paul R. Mark, and Stephanie Grainger