Duncan NRI Faculty and Staff Publications
The Jan and Dan Duncan Neurological Institute is home to 37 Principal Investigators, more than 400+ scientists and 10 Core labs.
Dan and Duncan Neurological Institute also house the Gordon and Mary Cain Pediatric Neurology Research Foundation Laboratories which are focused on epilepsy research and Baylor College's of Medicine's Center for Drug Discovery which is aimed at quick identification and advancement of small molecules to clinical trials.
Since inception, more than 1700 scientific studies have been published, and more than 85 disease-causing genetic mutations have been discovered or co-discovered by our scientists. There are currently 6 active clinical trials and studies.
Submissions from 2022
The microRNA Processor DROSHA Is a Candidate Gene for a Severe Progressive Neurological Disorder, Scott Barish, Mumine Senturk, Kelly Schoch, et al.
Multiple Approaches Converge on Three Biological Subtypes of Meningioma and Extract New Insights From Published Studies, James C Bayley, Caroline C Hadley, Arif O Harmanci, et al.
A Sparse Representation Strategy To Eliminate Pseudo-HFO Events From Intracranial EEG for Seizure Onset Zone Localization, Behrang Fazli Besheli, Zhiyi Sha, Jay R Gavvala, et al.
Two Neuronal Peptides Encoded From a Single Transcript Regulate Mitochondrial Complex III in Drosophila, Justin A Bosch, Berrak Ugur, Israel Pichardo-Casas, et al.
De Novo Variants in EMC1 Lead to Neurodevelopmental Delay and Cerebellar Degeneration and Affect Glial Function in Drosophila, Hyung-Lok Chung, Patrick Rump, Di Lu, et al.
Development of Myelinating Glia: An Overview, Carlo D Cristobal and Hyun Kyoung Lee
Daam2 Regulates Myelin Structure and the Oligodendrocyte Actin Cytoskeleton through Rac1 and Gelsolin, Carlo D Cristobal, Chih-Yen Wang, Zhongyuan Zuo, et al.
BERENICE Final Analysis: Cardiac Safety Study of Neoadjuvant Pertuzumab, Trastuzumab, and Chemotherapy Followed by Adjuvant Pertuzumab and Trastuzumab in HER2-Positive Early Breast Cancer, Chau Dang, Michael S Ewer, Suzette Delaloge, et al.
Gene-Based Therapeutics for Rare Genetic Neurodevelopmental Psychiatric Disorders, Beverly L Davidson, Guangping Gao, Elizabeth Berry-Kravis, et al.
Regulation of Drosophila Oviduct Muscle Contractility by Octopamine, Sonali A Deshpande, Ethan W Rohrbach, James D Asuncion, et al.
Emerging Roles of Alternative Cleavage and Polyadenylation (APA) in Human Disease, Prakash Dharmalingam, Rajasekaran Mahalingam, Hari Krishna Yalamanchili, et al.
A Minimal Role for Synonymous Variation in Human Disease, Ryan S Dhindsa, Quanli Wang, Dimitrios Vitsios, et al.
A Multidisciplinary Approach and Consensus Statement To Establish Standards of Care for Angelman Syndrome, Jessica Duis, Mark Nespeca, Jane Summers, et al.
Cardiovascular Adverse Events in Oncology Trials: Understanding and Appreciating the Differences Between Clinical Trial Data and Real-World Reports, Michael S Ewer and Jay Herson
Disrupting the MYC-TFEB Circuit Impairs Amino Acid Homeostasis and Provokes Metabolic Anergy, Mario R Fernandez, Franz X Schaub, Chunying Yang, et al.
Evidence for an Association Between Coffin-Siris Syndrome and Congenital Diaphragmatic Hernia, Yoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
Recent Insights Into the Role of Glia and Oxidative Stress in Alzheimer’s Disease Gained From Drosophila, Lindsey D Goodman and Hugo J Bellen
Kalium Channelrhodopsins Are Natural Light-Gated Potassium Channels That Mediate Optogenetic Inhibition, Elena G Govorunova, Yueyang Gou, Oleg A Sineshchekov, et al.
Dynamics of Huntingtin Protein Interactions in the Striatum Identifies Candidate Modifiers of Huntington Disease, Todd M Greco, Christopher Secker, Eduardo Silva Ramos, et al.
Improved SARS-CoV-2 Sequencing Surveillance Allows the Identification of New Variants and Signatures in Infected Patients, Antonio Grimaldi, Francesco Panariello, Patrizia Annunziata, et al.
Identifying Phenotypic Expansions for Congenital Diaphragmatic Hernia Plus (Cdh+) Using Decipher Data, Amy Hardcastle, Aliska M Berry, Ian M Campbell, et al.
XCVATR: Detection and Characterization of Variant Impact on the Embeddings of Single -Cell and Bulk RNA-Sequencing Samples, Arif Harmanci, Akdes Serin Harmanci, Tiemo J Klisch, et al.
ModelMatcher: A Scientist-Centric Online Platform To Facilitate Collaborations Between Stakeholders of Rare and Undiagnosed Disease Research, J Michael Harnish, Lucian Li, Sanja Rogic, et al.
A Weakened Recurrent Circuit in the Hippocampus of Rett Syndrome Mice Disrupts Long-Term Memory Representations, Lingjie He, Matthew S Caudill, Junzhan Jing, et al.
Genome Sequencing in the Parkinson Disease Clinic, Emily J Hill, Laurie A Robak, Rami Al-Ouran, et al.