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Light Has Diverse Spatiotemporal Molecular Changes in the Mouse Suprachiasmatic Nucleus.
Published in:
Journal of Biological Rhythms, 2020, v. 35, n. 6, p. 576, doi. 10.1177/0748730420961214
By:
- Duy, Phan Q.;
- Komal, Ruchi;
- Richardson, Melissa E. S.;
- Hahm, Katie S.;
- Fernandez, Diego C.;
- Hattar, Samer
Publication type:
Article
Chronic Circadian Misalignment without Circadian Arrhythmicity or Sleep Deprivation Does Not Impair Adult Hippocampal Neurogenesis.
Published in:
Journal of Biological Rhythms, 2017, v. 32, n. 6, p. 621, doi. 10.1177/0748730417736960
By:
- Duy, Phan Q.;
- Hattar, Samer
Publication type:
Article
Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis.
Published in:
Journal of Neurosurgery: Pediatrics, 2024, v. 33, n. 1, p. 59, doi. 10.3171/2023.8.PEDS23155
By:
- Kiziltug, Emre;
- Duy, Phan Q.;
- Allington, Garrett;
- Timberlake, Andrew T.;
- Kawaguchi, Riki;
- Long, Aaron S.;
- Almeida, Mariana N.;
- DiLuna, Michael L.;
- Alper, Seth L.;
- Alperovich, Michael;
- Geschwind, Daniel H.;
- Kahle, Kristopher T.
Publication type:
Article
Genomic approaches to improve the clinical diagnosis and management of patients with congenital hydrocephalus.
Published in:
Journal of Neurosurgery: Pediatrics, 2022, v. 29, n. 2, p. 168, doi. 10.3171/2021.8.PEDS21368
By:
- Allington, Garrett;
- Duy, Phan Q.;
- Ryou, Jian;
- Singh, Amrita;
- Kiziltug, Emre;
- Robert, Stephanie M.;
- Kundishora, Adam J.;
- King, Spencer;
- Haider, Shozeb;
- Kahle, Kristopher T.;
- Sheng Chih Jin
Publication type:
Article
Biomechanical instability of the brain–CSF interface in hydrocephalus.
Published in:
Brain: A Journal of Neurology, 2024, v. 147, n. 10, p. 3274, doi. 10.1093/brain/awae155
By:
- Duy, Phan Q;
- Mehta, Neel H;
- Kahle, Kristopher T
Publication type:
Article
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.
Published in:
Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1553, doi. 10.1093/brain/awad405
By:
- Singh, Amrita K;
- Allington, Garrett;
- Viviano, Stephen;
- McGee, Stephen;
- Kiziltug, Emre;
- Ma, Shaojie;
- Zhao, Shujuan;
- Mekbib, Kedous Y;
- Shohfi, John P;
- Duy, Phan Q;
- DeSpenza, Tyrone;
- Furey, Charuta G;
- Reeves, Benjamin C;
- Smith, Hannah;
- Sousa, André M M;
- Cherskov, Adriana;
- Allocco, August;
- Nelson-Williams, Carol;
- Haider, Shozeb;
- Rizvi, Syed R A
Publication type:
Article
Inflammatory hydrocephalus.
Published in:
Child's Nervous System, 2021, v. 37, n. 11, p. 3341, doi. 10.1007/s00381-021-05255-z
By:
- Robert, Stephanie M.;
- Reeves, Benjamin C.;
- Marlier, Arnaud;
- Duy, Phan Q.;
- DeSpenza, Tyrone;
- Kundishora, Adam;
- Kiziltug, Emre;
- Singh, Amrita;
- Allington, Garrett;
- Alper, Seth L.;
- Kahle, Kristopher T.
Publication type:
Article
Genomics of human congenital hydrocephalus.
Published in:
Child's Nervous System, 2021, v. 37, n. 11, p. 3325, doi. 10.1007/s00381-021-05230-8
By:
- Kundishora, Adam J.;
- Singh, Amrita K.;
- Allington, Garrett;
- Duy, Phan Q.;
- Ryou, Jian;
- Alper, Seth L.;
- Jin, Sheng Chih;
- Kahle, Kristopher T.
Publication type:
Article
DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease.
Published in:
JAMA Neurology, 2021, v. 78, n. 8, p. 993, doi. 10.1001/jamaneurol.2021.1681
By:
- Kundishora, Adam J.;
- Peters, Samuel T.;
- Pinard, Amélie;
- Duran, Daniel;
- Panchagnula, Shreyas;
- Barak, Tanyeri;
- Miyagishima, Danielle F.;
- Dong, Weilai;
- Smith, Hannah;
- Ocken, Jack;
- Dunbar, Ashley;
- Nelson-Williams, Carol;
- Haider, Shozeb;
- Walker, Rebecca L.;
- Li, Boyang;
- Zhao, Hongyu;
- Thumkeo, Dean;
- Marlier, Arnaud;
- Duy, Phan Q.;
- Diab, Nicholas S.
Publication type:
Article
Exome Sequencing as a Potential Diagnostic Adjunct in Sporadic Congenital Hydrocephalus.
Published in:
JAMA Pediatrics, 2021, v. 175, n. 3, p. 310, doi. 10.1001/jamapediatrics.2020.4878
By:
- Sullivan, William;
- Reeves, Benjamin C.;
- Duy, Phan Q.;
- Nelson-Williams, Carol;
- Dong, Weilai;
- Jin, Sheng Chih;
- Kahle, Kristopher T.
Publication type:
Article
Motoneuron development influences dorsal root ganglia survival and Schwann cell development in a vertebrate model of spinal muscular atrophy.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 2, p. 346, doi. 10.1093/hmg/ddu447
By:
- Hao, Le Thi;
- Duy, Phan Q.;
- Jontes, James D.;
- Beattie, Christine E.
Publication type:
Article
Temporal requirement for SMN in motoneuron development.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 13, p. 2612, doi. 10.1093/hmg/ddt110
By:
- Hao, Le T.;
- Duy, Phan Q.;
- Jontes, James D.;
- Wolman, Marc;
- Granato, Michael;
- Beattie, Christine E.
Publication type:
Article
"Floppy brain" in congenital hydrocephalus.
Published in:
Cerebral Cortex, 2023, v. 33, n. 15, p. 9339, doi. 10.1093/cercor/bhad206
By:
- Duy, Phan Q;
- Kahle, Kristopher T
Publication type:
Article
A neural stem cell paradigm of pediatric hydrocephalus.
Published in:
Cerebral Cortex, 2023, v. 33, n. 8, p. 4262, doi. 10.1093/cercor/bhac341
By:
- Duy, Phan Q;
- Rakic, Pasko;
- Alper, Seth L;
- Robert, Stephanie M;
- Kundishora, Adam J;
- Butler, William E;
- Walsh, Christopher A;
- Sestan, Nenad;
- Geschwind, Daniel H;
- Jin, Sheng Chih;
- Kahle, Kristopher T
Publication type:
Article
A novel signature predicts recurrence risk and therapeutic response in breast cancer patients.
Published in:
International Journal of Cancer, 2021, v. 148, n. 11, p. 2848, doi. 10.1002/ijc.33512
By:
- Tran, Quynh Hoa;
- Than, Van Thai;
- Luu, Phuc Loi;
- Clarke, Declan;
- Lam, Hanh Ngoc;
- Nguyen, Thanh‐Giang Tan;
- Nguyen, Dinh‐Truong;
- Duy, Phan Q.;
- Phung, Dung;
- Nguyen, Minh Nam
Publication type:
Article
The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact.
Published in:
Fluids & Barriers of the CNS, 2024, v. 21, n. 1, p. 1, doi. 10.1186/s12987-024-00513-z
By:
- Hale, Andrew T.;
- Boudreau, Hunter;
- Devulapalli, Rishi;
- Duy, Phan Q.;
- Atchley, Travis J.;
- Dewan, Michael C.;
- Goolam, Mubeen;
- Fieggen, Graham;
- Spader, Heather L.;
- Smith, Anastasia A.;
- Blount, Jeffrey P.;
- Johnston, James M.;
- Rocque, Brandon G.;
- Rozzelle, Curtis J.;
- Chong, Zechen;
- Strahle, Jennifer M.;
- Schiff, Steven J.;
- Kahle, Kristopher T.
Publication type:
Article
HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation.
Published in:
Journal of Neuroscience, 2017, v. 37, n. 48, p. 11559, doi. 10.1523/JNEUROSCI.1528-17.2017
By:
- Thi Hao le;
- Duy, Phan Q.;
- Min An;
- Talbot, Jared;
- Iyer, Chitra C.;
- Wolman, Marc;
- Beattie, Christine E.
Publication type:
Article
Utility of cortical tissue analysis in normal pressure hydrocephalus.
Published in:
Cerebral Cortex, 2024, v. 34, n. 2, p. 1, doi. 10.1093/cercor/bhae001
By:
- Greenberg, Ana B W;
- Mekbib, Kedous Y;
- Mehta, Neel H;
- Kiziltug, Emre;
- Duy, Phan Q;
- Smith, Hannah R;
- Junkkari, Antti;
- Leinonen, Ville;
- Hyman, Bradley T;
- Chan, Diane;
- Jr, William T Curry;
- Arnold, Steven E;
- II, Frederick G Barker;
- Frosch, Matthew P;
- Kahle, Kristopher T
Publication type:
Article
The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology.
Published in:
Cerebral Cortex, 2024, v. 34, n. 1, p. 1, doi. 10.1093/cercor/bhad432
By:
- Duy, Phan Q;
- Mehta, Neel H;
- Kahle, Kristopher T
Publication type:
Article
Cases of familial idiopathic normal pressure hydrocephalus implicate genetic factors in disease pathogenesis.
Published in:
Cerebral Cortex, 2023, v. 33, n. 23, p. 11400, doi. 10.1093/cercor/bhad374
By:
- Greenberg, Ana B W;
- Mehta, Neel H;
- Mekbib, Kedous Y;
- Kiziltug, Emre;
- Smith, Hannah R;
- Hyman, Bradley T;
- Chan, Diane;
- Curry Jr., William T;
- Arnold, Steven E;
- Frosch, Matthew P;
- Duy, Phan Q;
- Kahle, Kristopher T
Publication type:
Article
Identification of KCC2 Mutations in Human Epilepsy Suggests Strategies for Therapeutic Transporter Modulation.
Published in:
Frontiers in Cellular Neuroscience, 2019, v. 13, p. 1, doi. 10.3389/fncel.2019.00515
By:
- Duy, Phan Q.;
- David, Wyatt B.;
- Kahle, Kristopher T.
Publication type:
Article
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.
Published in:
Frontiers in Cellular Neuroscience, 2019, p. 1, doi. 10.3389/fncel.2019.00425
By:
- Allocco, August A.;
- Jin, Sheng Chih;
- Duy, Phan Q.;
- Furey, Charuta G.;
- Zeng, Xue;
- Dong, Weilai;
- Nelson-Williams, Carol;
- Karimy, Jason K.;
- DeSpenza, Tyrone;
- Hao, Le T.;
- Reeves, Benjamin;
- Haider, Shozeb;
- Gunel, Murat;
- Lifton, Richard P.;
- Kahle, Kristopher T.
Publication type:
Article

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