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 2024
Benchmarking Signal Quality and Spatiotemporal Distribution of Interictal Spikes In Prolonged Human Ieeg Recordings Using Cortec Wireless Brain Interchange, Amir Hossein Ayyoubi, Behrang Fazli Besheli, Michael M Quach, et al.
Modeling Antisense Oligonucleotide Therapy in MECP2 Duplication Syndrome Human iPSC-Derived Neurons Reveals Gene Expression Programs Responsive to MeCP2 Levels, Sameer S Bajikar, Yehezkel Sztainberg, Alexander J Trostle, et al.
Signaling Mechanisms Underlying Activity-Dependent Integration of Adult-Born Neurons in the Mouse Olfactory Bulb, Suyang Bao, Juan M Romero, Benjamin D W Belfort, et al.
Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State, Thomas F Barrett, Bhuvic Patel, Saad M Khan, et al.
Author Correction: The Cerebellum Contributes to Generalized Seizures by Altering Activity in the Ventral Posteromedial Nucleus, Jaclyn Beckinghausen, Joshua Ortiz-Guzman, Tao Lin, et al.
Leveraging the T2T Assembly to Resolve Rare and Pathogenic Inversions in Reference Genome Gaps, Kristine Bilgrav Saether, Jesper Eisfeldt, Jesse D Bengtsson, et al.
Targeted Accurate RNA Consensus Sequencing (tARC-Seq) Reveals Mechanisms of Replication Error Affecting SARS-CoV-2 Divergence, Catherine C Bradley, Chen Wang, Alasdair J E Gordon, et al.
Parkinson's Disease and Other Alzheimer's Disease and Related Dementia Pathologies and the Progression of Parkinsonism in Older Adults, Aron S Buchman, Lei Yu, Shahram Oveisgharan, et al.
A Single-Cell Transcriptomic Map of the Developing Atoh1 Lineage Identifies Neural Fate Decisions and Neuronal Diversity in the Hindbrain, Jessica C Butts, Sih-Rong Wu, Mark A Durham, et al.
Lethal Phenotypes in Mendelian Disorders, Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, et al.
An Excitatory Projection from the Basal Forebrain to the Ventral Tegmental Area That Underlies Anorexia-Like Phenotypes, Jing Cai, Yanyan Jiang, Yuanzhong Xu, et al.
TFEB Controls Syncytiotrophoblast Formation and Hormone Production in Placenta, Marcella Cesana, Gennaro Tufano, Francesco Panariello, et al.
A GREB1-Steroid Receptor Feedforward Mechanism Governs Differential GREB1 Action in Endometrial Function and Endometriosis, Sangappa B Chadchan, Pooja Popli, Zian Liao, et al.
The Impact of the Turkish Population Variome on the Genomic Architecture of Rare Disease Traits, Zeynep Coban-Akdemir, Xiaofei Song, Francisco C Ceballos, et al.
Development and Evaluation of a Training Curriculum to Engage Researchers on Accessing and Analyzing the All of Us Data, Julie R Coleman, Jasmine N Baker, Shamika Ketkar, et al.
Exome Sequencing Implicates Ancestry-Related Mendelian Variation at SYNE1 in Childhood-Onset Essential Hypertension, Ian Copeland, Edmond Wonkam-Tingang, Monesha Gupta-Malhotra, et al.
Integrated Electrophysiological and Genomic Profiles of Single Cells Reveal Spiking Tumor Cells in Human Glioma, Rachel N Curry, Qianqian Ma, Malcolm F McDonald, et al.
Strategic Stabilization of Arousal Boosts Sustained Attention, Jan Willem de Gee, Zakir Mridha, Marisa Hudson, et al.
Pushing the Boundaries of Rare Disease Diagnostics With the Help of the First Undiagnosed Hackathon, Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan, et al.
Loss of the Endoplasmic Reticulum Protein Tmem208 Affects Cell Polarity, Development, and Viability, Debdeep Dutta, Oguz Kanca, Rishi V Shridharan, et al.
Mapping SCA1 Regional Vulnerabilities Reveals Neural and Skeletal Muscle Contributions to Disease, Lisa Duvick, W Michael Southern, Kellie A Benzow, et al.
TMEM106B Coding Variant Is Protective and Deletion Detrimental in a Mouse Model of Tauopathy, George A Edwards, Caleb A Wood, Yang He, et al.
Using High-Frequency Oscillations From Brief Intraoperative Neural Recordings To Predict the Seizure Onset Zone, Behrang Fazli Besheli, Zhiyi Sha, Jay R Gavvala, et al.
Novel Hemizygous Single-Nucleotide Duplication in RPGR in a Patient With Retinal Dystrophy and Sensorineural Hearing Loss, Ryan J German, Blake Vuocolo, Liesbeth Vossaert, et al.
Circuit-Specific Deep Brain Stimulation Provides Insights into Movement Control., Aryn H Gittis and Roy V Sillitoe