Author
Baylor College of MedicineORCID 0000-0002-7631-3703Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
4 papers
Recent·Most cited
Craig Waldence McFarland, Amanda R. Merner, Page M. Trotter, Abigail C. Martinez, Lauren A. Ginn, Jonathan Frumovitz, Daphne M. Ayton, Takahiro Soda, Eric A. Storch, Stacey Pereira, Gabriel Lázaro‐Muñoz
This study explores adult perspectives on psychiatric polygenic risk scores through interviews, highlighting both potential benefits and concerns about their use.
medRxiv · Sep 27, 2026 · PreprintGenetic & Genomic Medicine
Reem El Jammal, Hideo Suzuki, Layth S. Mattar, Thomas A. Hamre, Sarah S. Soubra, Melissa A. Ryan, Raissa K. Mathura, Sanjay J. Mathew, Anusha B. Allawala, Eric A. Storch, Nora Vanegas Arroyave, Garrett P. Banks, Nader Pouratian, Rémi Patriat, Wayne K. Goodman, , Sarah R. Heilbronner
The paper examines the preservation of anterior limb of the internal capsule (ALIC) topography in treatment-resistant psychiatric patients, finding it consistent with healthy and preclinical patterns.
bioRxiv · May 15, 2026 · PreprintNeuroscience
Iasha J Williams, Dalia Yesenia Palafox Márquez., Kara Lopez-Lengowski, Malini Bommiasamy, Ogechi “Cynthia” Onyeka, Slayton J. Underwood, Juliana E. Avery, Jacob Gluckman, Thariana Pichardo, Rhea Chandler, Yulu Brown, Katie H. Mangen, Emma Grace Choplin, Black Abalone Recovery Team Monitoring and Emergency Response Sub Team (BART-MER), Sonyia C. Richardson, , Dorothy E. Grice
BELONG collects DNA and clinical data from 1,250 African ancestry OCD cases to improve genetic research representation and identify OCD risk genes.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics · Jan 12, 2026Peer-reviewedGenetic & Genomic Medicine
Kristy L. Jay, Nikhita Gogate, Kimberly M. Ezell, Jonathan C. Andrews, Sharayu V. Jangam, Paige I. Hall, Hongling Pan, Kelvin Pham, Ryan J. German, Vanessa Gomez, Emily R. Jellinek, Eric A. Storch, Undiagnosed Diseases Network, Shinya Yamamoto, Oguz Kanca, , Michael F. Wangler
The paper identifies a hypomorphic SLC6A1 variant causing variable expressivity in neurodevelopmental disorders using clinical phenotyping and Drosophila models.
medRxiv · Sep 27, 2024 · PreprintGenetic & Genomic Medicine