Most Recent Additions*
Comments on "Asymptomatic tarsal tunnel syndrome in rheumatoid arthritis: an electrophysiological perspective with insights into clinical and laboratory correlates".
Peyman Roomizadeh and Ayushi Chugh
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations
Shujuan Zhao, Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew Prendergast, Jocelyn E. Chau, Hannah Smith, John Shohfi, Jack Ocken, Daniel Duran, Charuta G. Furey, Le Thi Hao, Phan Q. Duy, Benjamin C. Reeves, Junhui Zhang, Carol Nelson-Williams, Di Chen, Boyang Li, Timothy Nottoli, Suxia Bai, Myron Rolle, Xue Zeng, Weilai Dong, Po-Ying Fu, Yung-Chun Wang, Shrikant Mane, Paulina Piwowarczyk, Katie Pricola Fehnel, Alfred Pokmeng See, Bermans J. Iskandar, and Beverly Aagaard-Kienitz
Beyond motor: clinical manifestations of right hemisphere gliomas - a systematic review
Esteban Ramirez-Ferrer, Kyle Noll, Juliana Mayorga-Corvacho, Maria Alejandra Sierra, Charuta Furey, Alejandro Bugarini, Juan P. Zuluaga-Garcia, Priscella Asman, Chibawanye Ene, Sherise D. Ferguson, Jeffrey S. Weinberg, Frederick F. Lang, Hugues Duffau, and Sujit S. Prabhu
A novel SMARCC1 -mutant BAFopathy implicates epigenetic dysregulation of neural progenitors in hydrocephalus
Amrita K. Singh, Stephen Viviano, Garrett Allington, Stephen McGee, Emre Kiziltug, Kedous Y. Mekbib, John P. Shohfi, Phan Q. Duy, Tyrone DeSpenza, Charuta G. Furey, Benjamin C. Reeves, Hannah Smith, Shaojie Ma, André M. Sousa, Adriana Cherskov, August Allocco, Carol Nelson-Williams, Shozeb Haider, Syed R. Rizvi, Seth L. Alper, Nenad Sestan, Hermela Shimelis, Lauren K. Walsh, Richard P. Lifton, Andres Moreno-De-Luca, Sheng Chih Jin, Paul Kruszka, Engin Deniz, and Kristopher T. Kahle
Xp22.2 Chromosomal Duplication in Familial Intracranial Arachnoid Cyst
Charuta G. Furey, Andrew T. Timberlake, Carol Nelson-Williams, Daniel Duran, Peining Li, Eric M. Jackson, and Kristopher T. Kahle
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus
Priya Date, Pascal Ackermann, Charuta Furey, Ina Berenice Fink, Stephan Jonas, Mustafa K. Khokha, Kristopher T. Kahle, and Engin Deniz
Trim71/lin-41 Links an Ancient miRNA Pathway to Human Congenital Hydrocephalus
Phan Q. Duy, Charuta G. Furey, and Kristopher T. Kahle
T-Bar Angular Offset: A Novel Angle for Predicting Postoperative Coronal Balance Using Intraoperative Stitched Radiographs
James J. Zhou, S Harrison Farber, Timothy C. Gooldy, Charuta G. Furey, Steve S. Cho, Jeff Ehresman, Luke K. O'Neill, Juan S. Uribe, U Kumar Kakarla, and Jay D. Turner
SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus
Sheng Chih Jin, Charuta G. Furey, Xue Zeng, August Allocco, Carol Nelson-Williams, Weilai Dong, Jason K. Karimy, Kevin Wang, Shaojie Ma, Eric Delpire, and Kristopher T. Kahle
Picket fence technique for clip reconstruction of complex intracranial aneurysms
Sirin Gandhi, Joelle N. Hartke, Samuel L. Malnik, Charuta G. Furey, Anthony M. Asher, Anna L. Huguenard, and Michael T. Lawton
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3
August A. Allocco, Sheng Chih Jin, Phan Q. Duy, Charuta G. Furey, Xue Zeng, Weilai Dong, Carol Nelson-Williams, Jason K. Karimy, Tyrone DeSpenza, Le T. Hao, Benjamin Reeves, Shozeb Haider, Murat Gunel, Richard P. Lifton, and Kristopher T. Kahle
Mutations in TFAP2B and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis
Andrew T. Timberlake, Sheng Chih Jin, Carol Nelson-Williams, Robin Wu, Charuta G. Furey, Barira Islam, Shozeb Haider, Erin Loring, and Amy Galm
Magnetic Resonance-Guided Laser Interstitial Thermal Therapy for Management of Low-Grade Gliomas and Radiation Necrosis: A Single-Institution Case Series
Lea Scherschinski, Jubran H. Jubran, Kelly A. Shaftel, Charuta G. Furey, Dara S. Farhadi, Dimitri Benner, Benjamin K. Hendricks, and Kris A. Smith
Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
Adam J. Kundishora, Garrett Allington, Stephen McGee, Kedous Y. Mekbib, Vladimir Gainullin, Andrew T. Timberlake, Carol Nelson-Williams, Emre Kiziltug, Hannah Smith, Jack Ocken, John Shohfi, August Allocco, Phan Q. Duy, Aladine A. Elsamadicy, Weilai Dong, Shujuan Zhao, Yung-Chun Wang, Hanya M. Qureshi, Michael L. DiLuna, Shrikant Mane, Irina R. Tikhonova, Po-Ying Fu, Christopher Castaldi, Francesc López-Giráldez, James R. Knight, Charuta G. Furey, Bob S. Carter, Shozeb Haider, Andres Moreno-De-Luca, Seth L. Alper, and Murat Gunel
Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus
Jason K. Karimy, Jinwei Zhang, David B. Kurland, Brianna Carusillo Theriault, Daniel Duran, Jesse A. Stokum, Charuta Gavankar Furey, Xu Zhou, M Shahid Mansuri, Julio Montejo, Alberto Vera, Michael L. DiLuna, Eric Delpire, Seth L. Alper, Murat Gunel, Volodymyr Gerzanich, Ruslan Medzhitov, J Marc Simard, and Kristopher T. Kahle
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus
Phan Q. Duy, Stefan C. Weise, Claudia Marini, Xiao-Jun Li, Dan Liang, Peter J. Dahl, Shaojie Ma, Ana Spajic, Weilai Dong, Jane Juusola, Emre Kiziltug, Adam J. Kundishora, Sunil Koundal, Maysam Z. Pedram, Lucia A. Torres-Fernández, Kristian Händler, Elena De Domenico, Matthias Becker, Thomas Ulas, Stefan A. Juranek, Elisa Cuevas, Le Thi Hao, Bettina Jux, André M. Sousa, Fuchen Liu, Suel-Kee Kim, Mingfeng Li, Yiying Yang, Yutaka Takeo, Alvaro Duque, and Carol Nelson-Williams
Human Genetics and Molecular Mechanisms of Congenital Hydrocephalus
Charuta Gavankar Furey, Xue Zeng, Weilai Dong, Sheng Chih Jin, Jungmin Choi, Andrew T. Timberlake, Ashley M. Dunbar, August A. Allocco, Murat Günel, Richard P. Lifton, and Kristopher T. Kahle
Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations
Shujuan Zhao, Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew Prendergast, Jocelyn E. Chau, Hannah Smith, John Shohfi, Jack Ocken, Daniel Duran, Charuta G. Furey, Hao Thi Le, Phan Q. Duy, Benjamin C. Reeves, Junhui Zhang, Carol Nelson-Williams, Di Chen, Boyang Li, Timothy Nottoli, Suxia Bai, Myron Rolle, Xue Zeng, Weilai Dong, Po-Ying Fu, Yung-Chun Wang, Shrikant Mane, Paulina Piwowarczyk, Katie Pricola Fehnel, Alfred Pokmeng See, Bermans J. Iskandar, and Beverly Aagaard-Kienitz
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia
Weilai Dong, Sheng Chih Jin, August Allocco, Xue Zeng, Amar H. Sheth, Shreyas Panchagnula, Annie Castonguay, Louis-Étienne Lorenzo, Barira Islam, Geneviève Brindle, Karine Bachand, Jamie Hu, Agata Sularz, Jonathan Gaillard, Jungmin Choi, Ashley Dunbar, Carol Nelson-Williams, Emre Kiziltug, Charuta Gavankar Furey, Sierra Conine, Phan Q. Duy, Adam J. Kundishora, Erin Loring, Boyang Li, Qiongshi Lu, Geyu Zhou, Wei Liu, Xinyue Li, Michael C. Sierant, Shrikant Mane, and Christopher Castaldi
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
Sheng Chih Jin, Weilai Dong, Adam J. Kundishora, Shreyas Panchagnula, Andres Moreno-De-Luca, Charuta G. Furey, August A. Allocco, Rebecca L. Walker, Carol Nelson-Williams, Hannah Smith, Ashley Dunbar, Sierra Conine, Qiongshi Lu, Xue Zeng, Michael C. Sierant, James R. Knight, William Sullivan, Phan Q. Duy, Tyrone DeSpenza, Benjamin C. Reeves, Jason K. Karimy, Arnaud Marlier, Christopher Castaldi, Irina R. Tikhonova, Boyang Li, Helena Perez Peña, James R. Broach, Edith M. Kabachelor, Peter Ssenyonga, Christine Hehnly, and Li Ge
*Updated as of 09/16/26.