Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

Cited by (409)

Items 201–300 of 409

1. Microtubule-dependent formation of the stigmoid body as a cytoplasmic inclusion distinct from pathological aggresomes
   Ryutaro Fujinaga, Yukio Takeshita, Kanako Uozumi, Akie Yanai, Kazuhiro Yoshioka, Keiji Kokubu, Koh Shinoda · 2009 · Histochemistry and Cell Biology
2. Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome
   Filippo Arrigoni, Romina Romaniello, Denis Peruzzo, Alberto De Luca, Cecilia Parazzini, Enza Maria Valente, Renato Borgatti, Fabio Maria Triulzi · 2017 · American Journal of Neuroradiology
3. The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis
   Filippo Arrigoni, Romina Romaniello, Denis Peruzzo, Andrea Poretti, Maria Teresa Bassi, Carlo M. Pierpaoli, Enza Maria Valente, Sara Nuovo, Eugen Boltshauser, Thierry A. G. M. Huisman et al. · 2018 · European Radiology
4. Lateralization of motor control in the human nervous system: genetics of mirror movements
   Jimmy Peng, Frédéric Charron · 2012 · Current Opinion in Neurobiology
5. Functional Interactions between BM88/Cend1, Ran-Binding Protein M and Dyrk1B Kinase Affect Cyclin D1 Levels and Cell Cycle Progression/Exit in Mouse Neuroblastoma Cells
   Konstantinos Tsioras, Florentia Papastefanaki, Panagiotis K. Politis, Rebecca Matsas, Maria Gaitanou · 2013 · PLoS ONE
6. Tyrosine hydroxylase down-regulation after loss of Abelson helper integration site 1 (AHI1) promotes depression via the circadian clock pathway in mice
   Dongkai Guo, Shun Zhang, Hongyang Sun, Xingyun Xu, Zongbing Hao, Chenchen Mu, Xingshun Xu, Guanghui Wang, Haigang Ren · 2018 · Journal of Biological Chemistry
7. Genetic complexity in Joubert syndrome and related disorders
   Peter C. Harris · 2007 · Kidney International
8. The Cerebello-Hypothalamic and Hypothalamo-Cerebellar Pathways via Superior and Middle Cerebellar Peduncle in the Rat
   Safiye Çavdar, Merve Özgür, Yasemin Kuvvet, Hüsniye Hacıoğlu Bay · 2018 · The Cerebellum
9. The mitochondrial Ahi1/GR participates the regulation on mtDNA copy numbers and brain ATP levels and modulates depressive behaviors in mice
   Bin Wang, Haixia Shi, Bo Yang, Zhigang Miao, Miao Sun, Hao Yang, Xingshun Xu · 2023 · Cell Communication and Signaling
10. Impact of the AHI1 Gene on the Vulnerability to Schizophrenia: A Case-Control Association Study
    Olga Rivero, Andreas Reif, Julio Sanjuán, María Dolores Moltó, Sarah Kittel‐Schneider, Carmén Nájera, Theresia Töpner, Klaus‐Peter Lesch · 2010 · PLoS ONE
11. NMR Studies of HAR1 RNA Secondary Structures Reveal Conformational Dynamics in the Human RNA
    Melanie Ziegeler, Mirko Cevec, Christian Paolo Richter, Harald Schwalbe · 2012 · ChemBioChem
12. Brain Evolution and Uniqueness in the Human Genome
    Jordan P. Amadio, Christopher A. Walsh · 2006 · Cell
13. Prenatal diagnosis of Joubert syndrome
    Zhu Lingling, Limei Xie · 2017 · Medicine
14. Cephalocele: Report of 55 Cases over 8 Years
    Nazanin Baradaran, Farideh Nejat, Nima Baradaran, Mostafa El Khashab · 2009 · Pediatric Neurosurgery
15. Meckel syndrome in the Hutterite population is actually a Joubert‐related cerebello‐oculo‐renal syndrome
    Kym M. Boycott, Jillian S. Parboosingh, James N. Scott, D. Ross McLeod, Cheryl R. Greenberg, Takuya Fujiwara, Jean K. Mah, Julian Midgley, Andrew Wade, François P. Bernier et al. · 2007 · American Journal of Medical Genetics Part A
16. Novel Approaches to Studying the Genetic Basis of Cerebellar Development
    Samin A. Sajan, Kathryn E. Waimey, Kathleen J. Millen · 2010 · The Cerebellum
17. Syndromes, Disorders and Maternal Risk Factors Associated with Neural Tube Defects (III)
    Chih‐Ping Chen · 2008 · Taiwanese Journal of Obstetrics and Gynecology
18. Neuronal Migration Defect of the Developing Cerebellar Vermis in Substrains of C57BL/6 Mice: Cytoarchitecture and Prevalence of Molecular Layer Heterotopia
    Zareema Mangaru, Elsaid Salem, Matthew Sherman, Sarah E. Van Dine, Ankur Bhambri, Joshua C. Brumberg, Eric K. Richfield, Lisa A. Gabel, Raddy L. Ramos · 2013 · Developmental Neuroscience
19. Genetics of Cerebellar and Neocortical Expansion in Anthropoid Primates: A Comparative Approach
    Peter W. Harrison, Stephen H. Montgomery · 2017 · Brain Behavior and Evolution
20. AHI-1: a novel signaling protein and potential therapeutic target in human leukemia and brain disorders
    Sharmin Esmailzadeh, Xiaoyan Jiang · 2011 · Oncotarget
21. Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms
    C. Joy Shepard, Sara Guenthner Cline, David Hinds, Seyedehameneh Jahanbakhsh, Jeremy W. Prokop · 2019 · Physiological Genomics
22. Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217, in schizophrenia and bipolar disorder
    Alexandra Slonimsky, Itzchak Levy, Yoav Kohn, Amihai Rigbi, Edna Ben‐Asher, Doron Lancet, Galila Agam, Bernard Lerer · 2010 · Schizophrenia Research
23. Effect of chronic unpredictable stress on mice with developmental under-expression of the Ahi1 gene: behavioral manifestations and neurobiological correlates
    Gilly Wolf, Tzuri Lifschytz, Hagar Ben-Ari, Pavel Tatarskyy, Tirzah Kreisel, Amit Lotan, Bernard Lerer · 2018 · Translational Psychiatry
24. Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration
    Jesús Muñoz‐Estrada, Russell J. Ferland · 2019 · Journal of Cell Science
25. Spectrum of malformations of the hindbrain (cerebellum, pons, and medulla) in a cohort of children with high rate of parental consanguinity
    László Sztriha, Johan G. Johansen · 2005 · American Journal of Medical Genetics Part A
26. Investigating Embryonic Expression Patterns and Evolution of AHI1 and CEP290 Genes, Implicated in Joubert Syndrome
    Cheng, Yu-Zhu, Eley, Lorraine, Hynes, Ann-Marie, Overman, Lynne M., Simms, Roslyn J., Barker, Amy, Dawe, Helen R., Lindsay, Susan, Sayer, John A. · 2012 · PLoS ONE
27. Expression of AHI1 Rescues Amyloidogenic Pathology in Alzheimer’s Disease Model Cells
    Lai‐Lei Ting, Hsien‐Tsung Lu, Shu-Fen Yen, Thi Huong Ngo, Fang-Yu Tu, I-Shih Tsai, Yi‐Hua Tsai, Fu‐Yen Chang, Xiao‐Jiang Li, Shihua Li et al. · 2019 · Molecular Neurobiology
28. Intracellular colocalization of HAP1/STBs with steroid hormone receptors and its enhancement by a proteasome inhibitor
    Ryutaro Fujinaga, Yukio Takeshita, Kazuhiro Yoshioka, Hiroyuki Nakamura, Shuhei Shinoda, Md Nabiul Islam, Mir Rubayet Jahan, Akie Yanai, Keiji Kokubu, Koh Shinoda · 2011 · Experimental Cell Research
29. The role of cilia during organogenesis in zebrafish
    Junjun Liu, Haibo Xie, Mengfan Wu, Yidan Hu, Yunsi Kang · 2023 · Open Biology
30. Brain anatomical substrates of mirror movements in Kallmann syndrome
    Renzo Manara, Alessandro Salvalaggio, Valentina Citton, V. Palumbo, Arianna D'Errico, Andrea Elefante, Chiara Briani, Elena Cantone, Giancarlo Ottaviano, Maria Teresa Pellecchia et al. · 2014 · NeuroImage
31. Why Decussate? Topological Constraints on 3D Wiring
    Troy Shinbrot, Wise Young · 2008 · The Anatomical Record
32. Cortical, subcortical and brain stem connections of the cerebellum via the superior and middle cerebellar peduncle in the rat
    Safiye Çavdar, Merve Özgür, Yasemin Kuvvet, Hüsniye Hacıoğlu Bay, Evren Aydoğmuş · 2018 · Journal of Integrative Neuroscience
33. Congenital Mirror Movements Associated With Brain Malformations
    Andreea Nissenkorn, Keren Yosovich, Zvi Leibovitz, Tamar Gur-Hartman, Itay Zelcer, Mohammad Hugirat, Dorit Lev, Tally Lerman‐Sagie, Lubov Blumkin · 2021 · Journal of Child Neurology
34. The Transition Zone Protein AHI1 Regulates Neuronal Ciliary Trafficking of MCHR1 and Its Downstream Signaling Pathway
    Yi-Chun Hsiao, Jesús Muñoz‐Estrada, Karina Tuz, Russell J. Ferland · 2021 · Journal of Neuroscience
35. Zebrafish models of inherited retinal dystrophies
    Brian D. Perkins · 2022 · Journal of Translational Genetics and Genomics
36. Signatures of adaptive evolution in platyrrhine primate genomes
    Hazel Byrne, Timothy H. Webster, Sarah Frances Brosnan, Patrícia Izar, Jessica Ward Lynch · 2022 · Proceedings of the National Academy of Sciences
37. Alterations in the expression of a neurodevelopmental gene exert long-lasting effects on cognitive-emotional phenotypes and functional brain networks: translational evidence from the stress-resilient Ahi1 knockout mouse
    Amit Lotan, Tzuri Lifschytz, Ben Mernick, O Lory, Ehud Levi, E. Ben-Shimol, Gadi Goelman, Bernard Lerer · 2016 · Molecular Psychiatry
38. Nephronophthisis and Medullary Cystic Kidney Disease
    Heymut Omran, Beate Ermisch-Omran · 2008 · Elsevier eBooks
39. The Major Ciliary Isoforms of RPGR Build Different Interaction Complexes with INPP5E and RPGRIP1L
    Christine Vössing, Paul Atigbire, Jannis Eilers, Fenja Markus, Knut Stieger, Fei Song, John Neidhardt · 2021 · International Journal of Molecular Sciences
40. Development and Developmental Disorders of the Human Cerebellum
    Hans J. ten Donkelaar, Wilfred F.A. den Dunnen, Martin M. Y. Lammens, Pieter Wesseling, Michèl A.A.P. Willemsen, Akira Hori · 2023 · Springer eBooks
41. Hypothalamic Ahi1 Mediates Feeding Behavior through Interaction with 5-HT2C Receptor
    Hao Wang, Zhenbo Huang, Liansha Huang, Shaona Niu, Xiurong Rao, Jing Xu, Hui Kong, Jianzhong Yang, Chuan He Yang, Donghai Wu et al. · 2011 · Journal of Biological Chemistry
42. Cilia in cell signaling and human disorders
    Duldulao, Neil A., Li, Jade, Sun, Zhaoxia · 2010 · Protein & Cell
43. Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression
    Laura L. Baxter, Dawn E. Watkins‐Chow, Nicholas L. Johnson, Nicole Yanjanin Farhat, Frances M. Platt, Ryan Dale, Forbes D. Porter, William J. Pavan, Jorge L. Rodriguez‐Gil · 2022 · Scientific Reports
44. The Influence of AHI1 Variants on the Diagnosis and Treatment Outcome in Schizophrenia
    Stefano Porcelli, Chi‐Un Pae, Changsu Han, Soo-Jung Lee, Ashwin A. Patkar, Prakash S. Masand, Beatrice Balzarro, Siegfried Alberti, Diana De Ronchi, Alessandro Serretti · 2015 · International Journal of Molecular Sciences
45. Something to Sink Your Teeth Into
    Steven M. Couch, Scott E. Brodie, Jacqueline A. Leavitt, Michael C. Brodsky · 2011 · Survey of Ophthalmology
46. Schizotypy and altered hemispheric asymmetries: The role of cilia genes
    Judith Schmitz, Christoph Fraenz, Caroline Schlüter, Patrick Friedrich, Robert Kumsta, Dirk Moser, Onur Güntürkün, Erhan Genç, Sebastian Ocklenburg · 2019 · Psychiatry Research Neuroimaging
47. Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population
    Liansha Huang, Teng Dacai, Hao Wang, Guoqing Sheng, Tonghua Liu · 2012 · European Journal of Endocrinology
48. Le cil primaire, orchestrateur de la morphogenèse cérébrale
    Christine Laclef · 2014 · médecine/sciences
49. Evolución y genómica del cerebro humano
    Mónica Alejandra Rosales Reynoso, Clara Ibet Juárez-Vázquez, Patricio Barros‐Núñez · 2015 · Neurología
50. Evolutionary genomics of human intellectual disability
    Bernard J. Crespi, Kyle Summers, Steve Dorus · 2009 · Evolutionary Applications
51. Physiotherapy and Rehabilitation in a Child with Joubert Syndrome
    Özge İpek Dongaz, Özge Akyolcu, Banu Bayar · 2017 · Case Reports in Pediatrics
52. Spectral signatures of mirror movements in the sensori‐motor connectivity in kallmann syndrome
    Renzo Manara, Federica Di Nardo, Alessandro Salvalaggio, Antonio Agostino Sinisi, Guglielmo Bonanni, Vincenzo Palumbo, Elena Cantone, Arturo Brunetti, Francesco Di Salle, Arianna D'Errico et al. · 2017 · Human Brain Mapping
53. Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome
    Yue Shen, Hao Wang, Zhimin Liu, Minna Luo, Siyu Ma, Chao Lu, Zongfu Cao, Yufei Yu, Ruikun Cai, Cuixia Chen et al. · 2020 · BMC Medical Genetics
54. Novel biomarkers of ciliary extracellular vesicles interact with ciliopathy and Alzheimer's associated proteins
    Mohieldin, Ashraf M., Alachkar, Amal, Yates, John, Nauli, Surya M. · 2021 · Communicative & Integrative Biology
55. Primary Cilia Reconsidered in the Context of Ciliopathies: Extraciliary and Ciliary Functions of Cilia Proteins Converge on a Polarity theme?
    Kiet Hua, Russell J. Ferland · 2018 · BioEssays
56. Exposure to retinoic acid at the onset of hindbrain segmentation induces episodic breathing in mice
    Laura Guimarães, Eduardo Domı́nguez del Toro, Fabrice Chatonnet, Ludovic Jean Wrobel, Cristina Pujades, Luís Silva Monteiro, Jean Champagnat · 2007 · European Journal of Neuroscience
57. Neuroanatomy of autism: what is the role of the cerebellum?
    Joan Susan Baizer · 2024 · Cerebral Cortex
58. Genetics behind Cerebral Disease with Ocular Comorbidity: Finding Parallels between the Brain and Eye Molecular Pathology
    Kao-Jung Chang, Hsin-Yu Wu, Aliaksandr A. Yarmishyn, Cheng-Yi Li, Yu‐Jer Hsiao, Yi‐Chun Chi, Tzu-Chen Lo, He-Jhen Dai, Yi‐Chiang Yang, Ding-Hao Liu et al. · 2022 · International Journal of Molecular Sciences
59. Spontaneous malformations of the cerebellar vermis: Prevalence, inheritance, and relationship to lobule/fissure organization in the C57BL/6 lineage
    Sarah E. Van Dine, Nga Yan Siu, Alyssa R. Toia, Joshua A. Cuoco, Adrienne J. Betz, Valerie J. Bolivar, German Torres, Raddy L. Ramos · 2015 · Neuroscience
60. Axonal anatomy of molecular layer heterotopia of the cerebellar vermis
    Sarah E. Van Dine, Elsaid Salem, Dhruv B. Patel, Elizabeth George, Raddy L. Ramos · 2012 · Journal of Chemical Neuroanatomy
61. The characterization of Abelson helper integration site–1 in skeletal muscle and its links to the metabolic syndrome
    Matthew J. Prior, Victoria C. Foletta, Jeremy B. M. Jowett, David H. Segal, Melanie A. Carless, Joanne E. Curran, Tom Dyer, Eric Keith Moses, Andrew J. McAinch, Nicky Konstantopoulos et al. · 2010 · Metabolism
62. Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT
    Caterina Toma, Giulio Ruberto, Federico Marzi, Giulio Vandelli, Sabrina Giovanna Signorini, Enza Maria Valente, Mauro Antonini, Chiara Bertone, Paolo Emilio Bianchi · 2018 · Documenta Ophthalmologica
63. Reduction of AHI1 in the serum of Taiwanese with probable Alzheimer’s disease
    Jau‐Jiuan Sheu, Li‐Yu Yang, Monika Renuka Sanotra, Sen‐Te Wang, Hsien‐Tsung Lu, Rachel Sook Yee Kam, I-Uen Yvonne Hsu, Shu‐Huei Kao, Ching‐Kuo Lee, Jonathan Chang-Cheng Shieh et al. · 2019 · Clinical Biochemistry
64. Clinical variability in ciliary disorders
    Kirk Mykytyn · 2007 · Nature Genetics
65. Postoperative respiratory complications in Joubert syndrome
    Cari Maria Platis, Ludmyla Kachko, Evelyna Trabikin, Eliahu Simhi, Meshulam Bahar, Jacob Katz · 2006 · Pediatric Anesthesia
66. Uncrossed corticospinal tract in health and genetic disorders: Review, case report, and clinical implications
    Filipp Maximilian Filippopulos, Christian Brem, Klaus Seelos, Thomas Köglsperger, Stefan Sonnenfeld, Lars Kellert, Christian Vollmar · 2021 · European Journal of Neurology
67. Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement
    Justin R. Bourgeois, Russell J. Ferland · 2019 · Developmental Biology
68. Mutant Ahi1 Affects Retinal Axon Projection in Zebrafish via Toxic Gain of Function
    Louyin Zhu, Laiqiang Chen, Ling-Ya Yan, Brian D. Perkins, Shihua Li, Bao‐Ming Li, Hong A. Xu, Xiao-Jiang Li · 2019 · Frontiers in Cellular Neuroscience
69. Cerebral, cerebellar, and colobomatous anomalies in three related males: Sex‐linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndrome
    Hester Y. Kroes, Rutger-Jan Nievelstein, Peter G. Barth, Peter G. J. Nikkels, Carsten Bergmann, Rob H. J. M. Gooskens, Gepke Visser, Hans‐Kristian Ploos van Amstel, Frits A. Beemer · 2005 · American Journal of Medical Genetics Part A
70. Joubert Syndrome Associated with Leber's Congenital Amaurosis
    Hee Kyung Yang, Young Suk Yu, Jeong‐Min Hwang · 2008 · Journal of the Korean Ophthalmological Society
71. Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies
    Olivier Devuyst, V. J. Arnould · 2008 · Nephrology Dialysis Transplantation
72. Expression changes of hypothalamic Ahi1 in mice brain: implication in sensing insulin signaling
    Shaona Niu, Hao Wang, Zhenbo Huang, Xiurong Rao, Xiangsheng Cai, Tao Liang, Jing Xu, Xingshun Xu, Guoqing Sheng · 2012 · Molecular Biology Reports
73. Identification of 2 Potentially Relevant Gene Mutations Involved in Strabismus Using Whole-Exome Sequencing
    Xiangrong Min, Haiying Fan, Guiqiu Zhao, Guixiang Liu · 2017 · Medical Science Monitor
74. Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum
    Arezou Karamzade, Meisam Babaei, Mohammad Saberi, Neda Golchin, Aysun Khalil Nejad Sani Banaei, Yeganeh Eshaghkhani, Zahra Golchehre, Mohammad Keramatipour · 2021 · Molecular Biology Reports
75. The Neanderthal brain: Biological and cognitive evolution
    Fabio M. Macciardi, Fabio Martini · 2022 · Elsevier eBooks
76. The Apparently Blind Infant
    Michael C. Brodsky · 2009 · Springer eBooks
77. Joubert syndrome: large clinical variability and a unique neuroimaging aspect
    Emília Katiane Embiruçu de Araújo Leão, Marcilia Lima Martyn, Otacílio de Oliveira Maia Júnior, Juliana Parizotto, Fernando Kok · 2010 · Arquivos de Neuro-Psiquiatria
78. Regulation of AHI1 expression in adult rat brain: Implication in hypothalamic feeding control
    Seung Baek Han, Byung-il Choi, Dongmin Lee, Sun‐Ho Kee, Hyeon Soo Kim, Woong Sun, Hyun Kim · 2009 · Biochemical and Biophysical Research Communications
79. Congenital Mirror Movements in Gorlin Syndrome: A Case Report With DTI and Functional MRI Features
    Erdal Sağ, Rahşan Göçmen, Fatma Gokcem Yildiz, Zeynelabidin Öztürk, Çağrı Mesut Temuçin, Özlem Tekşam, Eda Ütine · 2016 · PEDIATRICS
80. Complex Ocular Motor Disorders in Children
    Michael C. Brodsky · 2009 · Springer eBooks
81. Molecular Cloning of a Novel Gene ZAhi-1 and its Expression Analysis during Zebrafish Gametogenesis
    Wei Zhou, Ping Song · 2006 · Molecular Biology Reports
82. Erratum: Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome
    Russell J. Ferland, Wafaa Eyaid, Randall V. Collura, Laura D Tully, R. Sean Hill, Doha Al-Nouri, Ahmed R. Al-Rumayyan, Meral Topçu, Generoso G. Gascon, Adria Bodell et al. · 2004 · Nature Genetics
83. GR/Ahi1 regulates WDR68-DYRK1A binding and mediates cognitive impairment in prenatally stressed offspring
    Bin Wei, Haixia Shi, Yu Xi, Yajun Shi, Hongtao Zeng, Yan Zhao, Zejun Zhao, Yueyang Song, Miao Sun, Bin Wang · 2024 · Cellular and Molecular Life Sciences
84. Ciliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish
    Percival P. D’Gama, Inyoung Jeong, Andreas Moe Nygård, Anh‐Tuan Trinh, Emre Yaksi, Nathalie Jurisch‐Yaksi · 2024 · iScience
85. Joubert syndrome with variable features: presentation of two cases.
    Mohammad Barzegar, Majid Malaki, Elyar Sadeghi‐Hokmabadi · 2013 · Iranian journal of child neurology.
86. GWAS Identified IL4R and the Major Histocompatibility Complex Region as the Associated Loci of Total Serum IgE Levels in 9,260 Japanese Individuals
    Kosuke Shido, Kaname Kojima, Matsuyuki Shirota, Kenshi Yamasaki, Ikuko N. Motoike, Atsushi Hozawa, Soichi Ogishima, Naoko Minegishi, Kozo Tanno, Fumiki Katsuoka et al. · 2021 · Journal of Investigative Dermatology
87. Human brain evolution
    Hilliary Creely, Philipp Khaitovich · 2006 · Progress in brain research
88. The mandate for innovation in pediatric surgery; creating the environment for success, parity, and excellence
    Patricia K. Donahoe · 2008 · Journal of Pediatric Surgery
89. Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation
    Michal Gafner, Cathérine Garel, Zvi Leibovitz, Stéphanie Valence, Karina Krajden Haratz, Renske Oegema, Grazia M. S. Mancini, Delphine Héron, Eva Bueltmann, Lydie Bürglen et al. · 2023 · American Journal of Neuroradiology
90. Abnormalities of the Central Nervous System Across the Ciliopathy Spectrum
    Kate Baker, Philip L. Beales · 2012 · Springer eBooks
91. Cellular and Axonal Diversity in Molecular Layer Heterotopia of the Rat Cerebellar Vermis
    Sarah E. Van Dine, Elsaid Salem, Elizabeth George, Nga Yan Siu, Timothy P. Dotzler, Raddy L. Ramos · 2013 · BioMed Research International
92. Cellular signatures in the primary visual cortex of phylogeny and placentation
    Éric Lewitus, Chet C. Sherwood, Patrick R. Hof · 2011 · Brain Structure and Function
93. A cis -eQTL in AHI1 confers risk to schizophrenia in European populations
    Zixiao Ren, A Zhiwei Qiu, Ai-Qi Zhang, Lijun Huang, Shuquan Rao · 2016 · Neuroscience Letters
94. AHI1: linking depression and impaired antiviral immune response
    Weili Yang, Shihua Li, Xiao‐Jiang Li · 2022 · Cell Research
95. Evolution and genomics of the human brain
    Mónica Alejandra Rosales Reynoso, Clara Ibet Juárez-Vázquez, Patricio Barros‐Núñez · 2018 · Neurología (English Edition)
96. Genetic Disorders in Saudi Arabia
    Zuhair N. Al‐Hassnan, Nadia Sakati · 2010 · Springer eBooks
97. Disconnections in Infantile-Onset Saccade Initiation Delay: A Hypothesis
    Michael S. Salman, Kristin M. Ikeda · 2010 · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
98. Gender effects on autism spectrum disorder: a multi-site resting-state functional magnetic resonance imaging study of transcriptome-neuroimaging
    Yanling Li, Rui Li, Ning Wang, Jiahe Gu, Jingjing Gao · 2023 · Frontiers in Neuroscience
99. A Role for Genetic Modifiers in Tubulointerstitial Kidney Diseases
    Gary Leggatt, Eleanor G. Seaby, Kristin V. Veighey, Christine Gast, Rodney D. Gilbert, Sarah Ennis · 2023 · Genes
100. Novel variants identified in five Chinese families with Joubert Syndrome: a case report
     Liwei Fang, Lulu Wang, Yang Li, Xiaoyan Xu, Shanai Pei, De Wu · 2023 · BMC Medical Genomics