Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Wellcome Trust Case Control Consortium, Ferreira, Manuel A R, O'Donovan, Michael C, Meng, Yan A, Jones, Ian R, Ruderfer, Douglas M, Jones, Lisa, Fan, Jinbo +55 more·2008·Nature Genetics
DOI 10.1038/ng.209

Cited by (1,000)

Items 201–300 of 1,000

  1. The Effects of CACNA1C Gene Polymorphism on Spatial Working Memory in Both Healthy Controls and Patients with Schizophrenia or Bipolar Disorder
    Qiumei Zhang, Qiuge Shen, Zhansheng Xu, Min Chen, Lina Cheng, Jinguo Zhai, Huang Gu, Xin Bao, Xiongying Chen, Keqin Wang et al. · 2011 · Neuropsychopharmacology
  2. Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia
    Roussos, Panos · 2012 · Archives of General Psychiatry
  3. Axon initial segment dysfunction in epilepsy
    Verena C. Wimmer, Christopher A. Reid, Eva So, Samuel Frank Berkovic, Steven Petrou · 2010 · The Journal of Physiology
  4. Control of neuronal voltage-gated calcium ion channels from RNA to protein
    Diane Lipscombe, Summer E. Allen, Cecilia Phillips Toro · 2013 · Trends in Neurosciences
  5. Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease
    Jonathan Flint, Nicholas John Timpson, Marcus Robert Munafo · 2014 · Trends in Neurosciences
  6. Evidence for Association of an ACCN1 Gene Variant with Response to Lithium Treatment in Sardinian Patients with Bipolar Disorder
    Alessio Squassina, Mirko Manchia, Joseph Borg, Donatella Congiu, Marta Freitas Costa, Marianthi Georgitsi, Caterina Chillotti, Raffaella Ardau, Konstantinos A. Mitropoulos, Giovanni Severino et al. · 2011 · Pharmacogenomics
  7. Kv2.1 mediates spatial and functional coupling of L-type calcium channels and ryanodine receptors in mammalian neurons
    Nicholas C. Vierra, Michael Kirmiz, Deborah A. van der List, Luis Fernando Santana, James S. Trimmer · 2019 · eLife
  8. Association at SYNE1 in both bipolar disorder and recurrent major depression
    Elaine Green, Detelina Grozeva, Liz Forty, Katherine Gordon‐Smith, Elen Russell, ANNE E. FARMER, Marian L. Hamshere, Ian Richard Jones, Lisa Anne Jones, Peter McGuffin et al. · 2012 · Molecular Psychiatry
  9. Genetics of obsessive-compulsive disorder and related disorders
    Browne, Heidi A., Gair, Shannon L., Scharf, Jeremiah M., Grice, Dorothy E. · 2014 · Psychiatric Clinics of North America
  10. Support for calcium channel gene defects in autism spectrum disorders
    Ake Tzu-Hui Lu, Xiaoxian Dai, Julián A. Martínez-Agosto, Rita M. Cantor · 2012 · Molecular Autism
  11. P2RX7 gene is associated consistently with mood disorders and predicts clinical outcome in three clinical cohorts
    Pia Soronen, Outi Mantere, Tarja K. Melartin, Kirsi H. Suominen, Maria S. Vuorilehto, Heikki J. Rytsälä, Petri Arvilommi, Irina A. K. Holma, Mikael Holma, Pekka J. Jylhä et al. · 2011 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  12. Giant ankyrin-G stabilizes somatodendritic GABAergic synapses through opposing endocytosis of GABA <sub>A</sub> receptors
    Tseng, Wei Chou, Jenkins, Paul M., Tanaka, Masashi, Mooney, Richard, Bennett, Vann · 2015 · Proceedings of the National Academy of Sciences
  13. Experimental validation of candidate schizophrenia gene ZNF804A as target for hsa-miR-137
    Albert H. Kim, Erin K. Parker, Vernell S. Williamson, Gowon O. McMichael, Ayman H. Fanous, Vladimir I. Vladimirov · 2012 · Schizophrenia Research
  14. Independent Modulation of Engagement and Connectivity of the Facial Network During Affect Processing byCACNA1CandANK3Risk Genes for Bipolar Disorder
    Danai Dima, Jigar Jogia, David Andrew Collier, Evangelos Vassos, Katherine E. Burdick, Sophia Frangou · 2013 · JAMA Psychiatry
  15. Rescue of impaired sociability and anxiety-like behavior in adult cacna1c-deficient mice by pharmacologically targeting eIF2α
    Zeeba D. Kabir, Alicia Che, Delaney K. Fischer, Richard C. Rice, Bryant K. Rizzo, M Byrne, Michael J. Glass, Natalia V. De Marco García, Anjali M. Rajadhyaksha · 2017 · Molecular Psychiatry
  16. Genome-Wide Association Study of Temperament in Bipolar Disorder Reveals Significant Associations with Three Novel Loci
    Tiffany A. Greenwood, Hagop Souren Akiskal, Kareen K. Akiskal, John R. Kelsoe · 2012 · Biological Psychiatry
  17. CACNA1C Risk Variant and Amygdala Activity in Bipolar Disorder, Schizophrenia and Healthy Controls
    Martin Tesli, Kristina C. Skåtun, Olga Therese Ousdal, Andrew Anand Brown, Christian Thoresen, Ingrid Agartz, Ingrid S. Melle, Srdjan Djurovic, Jimmy Jensen, Ole A. Andreassen · 2013 · PLoS ONE
  18. The Genetics of Major Depression: Moving Beyond the Monoamine Hypothesis
    Stanley I. Shyn, Steven P. Hamilton · 2010 · Psychiatric Clinics of North America
  19. Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability
    Sarah Vergult, Annelies Dheedene, Alfred Meurs, Fran Faes, Bertrand Isidor, Sandra Janssens, Agnès Gautier, Cédric Le Caignec, Björn Menten · 2014 · European Journal of Human Genetics
  20. Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology
    Steven A. McCarroll, Steven E. Hyman · 2013 · Neuron
  21. Identification of shared risk loci and pathways for bipolar disorder and schizophrenia
    Andreas J. Forstner, Julian Hecker, Andrea Hofmann, Anna Maaser, Céline S. Reinbold, Thomas W. Mühleisen, Markus Leber, Jana Strohmaier, Franziska Degenhardt, Jens Treutlein et al. · 2017 · PLoS ONE
  22. Sex and Estrous Cycle Effects on Anxiety- and Depression-Related Phenotypes in a Two-Hit Developmental Stress Model
    Ivana Jarić, Devin Rocks, Heining Cham, Alice Herchek, Marija Kundaković · 2019 · Frontiers in Molecular Neuroscience
  23. Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder
    Lucia Pagani, Patricia A. St. Clair, Terri M. Teshiba, Susan K. Service, Scott C. Fears, Carmen Araya, Xinia Araya, Julio Bejarano, Margarita Ramirez, Gabriel Castrillón et al. · 2015 · Proceedings of the National Academy of Sciences
  24. The CACNA1C risk variant for bipolar disorder influences limbic activity
    Michèle Wessa, Julia Olivia Linke, Stephanie H. Witt, Vanessa Nieratschker, Christine Esslinger, Peter Kirsch, O Grimm, Michael G. Hennerici, Achim Gass, Andrea Victoria King et al. · 2010 · Molecular Psychiatry
  25. Polygenic risk scores in imaging genetics: Usefulness and applications
    Danai Dima, Gerome D. Breen · 2015 · Journal of Psychopharmacology
  26. Genome‐wide association study in German patients with attention deficit/hyperactivity disorder
    A. Hinney, A. Scherag, I. Jarick, Özgür Albayrak, C. Pütter, S. Pechlivanis, M. Dauvermann, S. Beck, H. Weber, S. Scherag et al. · 2011 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
  27. De novo CNVs in bipolar affective disorder and schizophrenia
    Lyudmila Georgieva, Elliott Rees, Jennifer L. Moran, Kimberly D. Chambert, Vihra Krumova Milanova, Nick J. Craddock, Shaun Purcell, Pamela B. Sklar, Steven A. McCarroll, Peter Holmans et al. · 2014 · Human Molecular Genetics
  28. Protein Misfolding and Aggregation in the Brain: Common Pathogenetic Pathways in Neurodegenerative and Mental Disorders
    Aleksandra Ochneva, Yana Zorkina, Olga V. Abramova, Olga Pavlova, Valeriya M. Ushakova, Anna Y. Morozova, Eugene A. Zubkov, Pavlov Ka, Olga Ivanovna Gurina, Vladimir Pavlovich Chekhonin · 2022 · International Journal of Molecular Sciences
  29. Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder
    Erroll H. Rueckert, Douglas Barker, Douglas M. Ruderfer, Sarah E. Bergen, Colm T. O’Dushlaine, Catherine J. Luce, Steven D. Sheridan, Kraig M. Theriault, Kimberly Chambert, Jennifer L. Moran et al. · 2012 · Molecular Psychiatry
  30. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53
    J-C Wang, Tatiana Foroud, Anthony L. Hinrichs, Nhung Le, Sarah E. Bertelsen, John Budde, Ofir Harari, Daniel L. Koller, Leah Flury Wetherill, Arpana Agrawal A et al. · 2012 · Molecular Psychiatry
  31. DNA variations in human and medical genetics: 25 years of my experience
    Yusuke Nakamura · 2009 · Journal of Human Genetics
  32. MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD
    Vanessa Nieratschker, Renaud Massart, Maria Gilles, Alessia Luoni, Matthew J Suderman, B. Krumm, S Meier, Stephanie H. Witt, Markus Maria Nöthen, Stephen J. Suomi et al. · 2014 · Translational Psychiatry
  33. Impact of major depression on cardiovascular outcomes for individuals with hypertension: prospective survival analysis in UK Biobank
    Nicholas Graham, Joey Ward, Daniel Mackay, Jill P. Pell, Jonathan Cavanagh, Sandosh Padmanabhan, Daniel J. Smıth · 2019 · BMJ Open
  34. Structural basis of diverse membrane target recognitions by ankyrins
    Chao Wang, Zhiyi Wei, Keyu Chen, Fei Ye, Cong Yu, Vann Bennett, Mingjie Zhang · 2014 · eLife
  35. Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
    David Curtis, Anna E. Vine, Andrew McQuillin, Nicholas James Bass, A C Pereira, Radhika Kandaswamy, Jacob Lawrence, Adebayo Anjorin, Khalid Choudhury, Susmita R. Datta et al. · 2010 · Psychiatric Genetics
  36. Genome‐wide association studies of bipolar disorder: A systematic review of recent findings and their clinical implications
    Masashi Ikeda, Takeo Saito, Kenji Kondo, Nakao Iwata · 2017 · Psychiatry and Clinical Neurosciences
  37. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans
    Lauren A. Weiss · 2009 · Expert Review of Molecular Diagnostics
  38. Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto‐hippocampal connectivity
    Frieder M. Paulus, Johannes Bedenbender, Sören Krach, Martin Pyka, Axel Krug, Jens Bak Sommer, Miriam Mette, Markus Maria Nöthen, Stephanie H. Witt, Marcella Rietschel et al. · 2013 · Human Brain Mapping
  39. Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac voltage-dependent L-type calcium channel
    Carlo Napolitano, C. Antzelevitch · 2011 · Circulation Research
  40. The association of genetic variation in CACNA1C with structure and function of a frontotemporal system
    Fei Wang, Andrew Mark McIntosh, Yong He A, Joel E. Gelernter, Hilary P. Blumberg · 2011 · Bipolar Disorders
  41. Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
    Mühleisen, Thomas W., Mattheisen, Manuel, Strohmaier, Jana, Degenhardt, Franziska, Priebe, Lutz, Schultz, C. Christoph, Breuer, René, Meier, Sandra, Hoffmann, Per, Rivandeneira, Fernando et al. · 2012 · Schizophrenia Research
  42. Regulation of the Mutually Exclusive Exons 8a and 8 in the CaV1.2 Calcium Channel Transcript by Polypyrimidine Tract-binding Protein
    Zhen Zhi Tang, Shalini Sharma, Sika Zheng, Geetanjali Chawla, Julia M. Nikolic, Douglas L. Black · 2011 · Journal of Biological Chemistry
  43. Genetic Research into Bipolar Disorder: The Need for a Research Framework that Integrates Sophisticated Molecular Biology and Clinically Informed Phenotype Characterization
    Thomas G. Schulze · 2010 · Psychiatric Clinics of North America
  44. The neurobiology of bipolar disorder: identifying targets for specific agents and synergies for combination treatment
    Ana C. Andreazza, Lionel Trevor Young · 2013 · The International Journal of Neuropsychopharmacology
  45. Whole-genome sequencing in an autism multiplex family
    Lingling Shi, Xu Zhang, Ryan Golhar, F. George Otieno, Mingze He, Cuiping Hou, Cecilia Kim, Brendan J. Keating, Gholson J. Lyon, Kai Wang et al. · 2013 · Molecular Autism
  46. Pharmacogenetics of Lithium Response in Bipolar Disorder
    Michael J. McCarthy, Susan G. Leckband, John R. Kelsoe · 2010 · Pharmacogenomics
  47. The microRNA network is altered in anterior cingulate cortex of patients with unipolar and bipolar depression
    Joshua A. Azevedo, Bradley S. Carter, Fan Meng, David L. Turner, Manhong Dai, Alan F. Schatzberg, Jack D. Barchas, Edward G. Jones, William E. Bunney, R Myers et al. · 2016 · Journal of Psychiatric Research
  48. Voltage-gated sodium channel β subunits: The power outside the pore in brain development and disease
    Jacob M. Hull, Lori L. Isom · 2017 · Neuropharmacology
  49. ADHDgene: a genetic database for attention deficit hyperactivity disorder
    Zhang, L., Chang, S., Li, Z., Zhang, K., Du, Y., Ott, J., Wang, J. · 2012 · Nucleic Acids Research
  50. The Role of Kv7.2 in Neurodevelopment: Insights and Gaps in Our Understanding
    Nina Dirkx, Francesco Miceli, Maurizio Taglialatela, Sarah Weckhuysen · 2020 · Frontiers in Physiology
  51. Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies
    Hyung‐Goo Kim, Hyun-Taek Kim, Natalia Tszine Leach, Fei Lan, Reinhard Ullmann, Asli Silahtaroglu, Ingo Kurth, Anja Nowka, Ihn Sik Seong, Yiping Shen et al. · 2012 · The American Journal of Human Genetics
  52. Genomic View of Bipolar Disorder Revealed by Whole Genome Sequencing in a Genetic Isolate
    Benjamin Georgi, David Wesley Craig, Rachel L. Kember, Wen‐Cheng Liu, Ingrid E. Lindquist, Sara Nasser, Christopher D. Brown, Janice A. Egeland, Steven M. Paul, Maja Bućan · 2014 · PLoS Genetics
  53. The Canadian Biomarker Integration Network in Depression (CAN-BIND): Advances in Response Prediction
    Sidney H. Kennedy, Jonathan H. Downar, Kenneth Evans, Harriet E. Feilotter, Raymond Wing Moon Lam, GLENDA M. MacQUEEN, Roumen V. Milev, Sagar V. Parikh, Susan Rotzinger, Cláudio N. Soares · 2012 · Current Pharmaceutical Design
  54. Mitochondrial modulators for bipolar disorder: A pathophysiologically informed paradigm for new drug development
    Andrew Alan Nierenberg, Christine Kansky, Brian P. Brennan, Richard Charles Shelton, Roy H. Perlis, Dan Vlad Iosifescu · 2012 · Australian & New Zealand Journal of Psychiatry
  55. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders
    The Swedish Bipolar Study Group, Hong Chang, Naosuke Hoshina, Changqing Zhang, Yina Ma, Han Cao, Y. Wang, D-d Wu, Sarah E. Bergen, Mikael Landén et al. · 2017 · Molecular Psychiatry
  56. New findings in the genetics of major psychoses
    Markus Maria Nöthen, Vanessa Nieratschker, Sven Cichon, Marcella Rietschel · 2010 · Dialogues in Clinical Neuroscience
  57. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder
    Andreas J. Forstner, A Hofmann, Anna Maaser, Simon Sumer, Sharof Khudayberdiev, Thomas W. Mühleisen, Markus Leber, Thomas G. Schulze, Jana Strohmaier, Franziska Degenhardt et al. · 2015 · Translational Psychiatry
  58. L‐type Ca2+ channels in mood, cognition and addiction: integrating human and rodent studies with a focus on behavioural endophenotypes
    Zeeba D. Kabir, A. S. Lee, Anjali M. Rajadhyaksha · 2016 · The Journal of Physiology
  59. Coming to grips with complex disorders: Genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics
    Sagar D. Patel, Helen Le-Niculescu, Daniel L. Koller, Steven Daniel Green, Debomoy K. Lahiri, Francis J. McMahon, John I. Nürnberger, Alexander B. Niculescu · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  60. Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
    Amelia M. Lindgren, Tatiana Hoyos, Michael E. Talkowski, Carrie Hanscom, Ian Blumenthal, Colby Chiang, Carl Ernst, Shahrin Pereira, Zehra Ordulu, Carol L. Clericuzio et al. · 2013 · Human Genetics
  61. BDNF Val66Met polymorphism and bipolar disorder in European populations: A risk association in case-control, family-based and GWAS studies
    Ming Li, Hong Chang, Xiao Xiao · 2016 · Neuroscience & Biobehavioral Reviews
  62. Functional Characterization of Schizophrenia-Associated Variation in CACNA1C
    Nicole Eckart, Qifeng Song, Rebecca J. Yang, Ruihua Wang, Heng Zhu, Andrew S. McCallion, Dimitrios Avramopoulos · 2016 · PLoS ONE
  63. Genome-wide association studies in schizophrenia: Recent advances, challenges and future perspective
    Charlotte A. Dennison, Sophie E. Legge, Antonio F. Pardiñas, James Walters · 2019 · Schizophrenia Research
  64. Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability
    Ferguson, Amy, Lyall, Laura M., Ward, Joey, Strawbridge, Rona J., Cullen, Breda, Graham, Nicholas, Niedzwiedz, Claire L., Johnston, Keira J.A., MacKay, Daniel, Biello, Stephany M. et al. · 2018 · EBioMedicine
  65. White matter alterations in bipolar disorder: potential for drug discovery and development
    Emeline Marlinge, Frank Bellivier, Josselin Houenou · 2013 · Bipolar Disorders
  66. Aims and Results of the NIMH Systematic Treatment Enhancement Program for Bipolar Disorder (STEP‐BD)
    Charles L. Bowden, Roy H. Perlis, Michael E. Thase, Terence A. Ketter, Michael Joshua Ostacher, Joseph R. Calabrese, Noreen A. Reilly-Harrington, Jodi M. Gonzalez, Vivek Kumar Singh, Andrew Alan Nierenberg et al. · 2011 · CNS Neuroscience & Therapeutics
  67. Development of a bipolar disorder biobank: differential phenotyping for subsequent biomarker analyses
    Mark A. Frye, Susan L. McElroy, Manuel Enrique Fuentes, Bruce Sutor, Kathryn M. Schak, Christine W. Galardy, Brian A. Palmer, Miguel L. Prieto, Simon Kung, Christopher L. Sola et al. · 2015 · International Journal of Bipolar Disorders
  68. CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population
    Kuanjun He, Zhiguo An, Qingzhong Wang, Tao Li, Zhiqiang Li, Jianhua Chen, Wenjin Li, Ti Wang, Jue Ji, Guoyin Feng et al. · 2013 · The British Journal of Psychiatry
  69. Dissecting the phenotype in genome-wide association studies of psychiatric illness
    Nick J. Craddock, Kenneth S. Kendler, Michael Churton Neale, John I. Nürnberger, Shaun Purcell, Marcella Rietschel, Roy H. Perlis, Susan L. Santangelo, Thomas G. Schulze, Thomas G. Schulze et al. · 2009 · The British Journal of Psychiatry
  70. Polygenic dissection of the bipolar phenotype
    Marian L. Hamshere, Michael C. O’Donovan, Ian Richard Jones, Lisa Anne Jones, George Kirov, Elaine Green, Valentina Moskvina, Detelina Grozeva, Nicholas James Bass, Andrew McQuillin et al. · 2011 · The British Journal of Psychiatry
  71. An Ankyrin-G N-terminal Gate and Protein Kinase CK2 Dually Regulate Binding of Voltage-gated Sodium and KCNQ2/3 Potassium Channels
    Mingxuan Xu, Edward C. Cooper · 2015 · Journal of Biological Chemistry
  72. The future of fMRI and genetics research
    Andreas Meyer‐Lindenberg · 2011 · NeuroImage
  73. Diagnostic and therapeutic potential of microRNAs in neuropsychiatric disorders: Past, present, and future
    Begüm Alural, Şermin Genç, Stephen J. Haggarty · 2016 · Progress in Neuro-Psychopharmacology and Biological Psychiatry
  74. Genetic disruption of ankyrin-G in adult mouse forebrain causes cortical synapse alteration and behavior reminiscent of bipolar disorder
    Shanshan Zhu, Zachary A. Cordner, Jiali Xiong, Chi-Tso Chiu, Arabiye Artola, Yanning Zuo, Andrew D. Nelson, Tae-Yeon Kim, Natalya Zaika, Brian M. Woolums et al. · 2017 · Proceedings of the National Academy of Sciences
  75. A composite peripheral blood gene expression measure as a potential diagnostic biomarker in bipolar disorder
    Klaus Munkholm, Lone Peijs, Maj Vinberg, Lars Vedel Kessing · 2015 · Translational Psychiatry
  76. Studies in Humans and Mice Implicate Neurocan in the Etiology of Mania
    Xavier Miró, Sandra Melanie Meier, Marie-Luise Dreisow, Josef Frank, Jana Strohmaier, René Breuer, Christine Schmäl, Önder Albayram, María Teresa Pardo-Olmedilla, Thomas W. Mühleisen et al. · 2012 · American Journal of Psychiatry
  77. Reverse translational strategies for developing animal models of bipolar disorder
    Malkesman, Oz, Austin, Daniel R., Chen, Guang, Manji, Husseini K. · 2009 · Disease Models &amp; Mechanisms
  78. Whole genome/exome sequencing in mood and psychotic disorders
    Tadafumi Kato · 2014 · Psychiatry and Clinical Neurosciences
  79. Schizophrenia genetics: new insights from new approaches
    Hywel J. Williams, M J Owen, Michael C. O’Donovan · 2009 · British Medical Bulletin
  80. Conditional deletion of L1CAM in human neurons impairs both axonal and dendritic arborization and action potential generation
    Christopher Patzke, Claudio Acuna, Louise R. Giam, Marius Wernig, Thomas Christian Südhof · 2016 · The Journal of Experimental Medicine
  81. Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism
    Jun Li, Linnan Zhao, Yang You, Tianlan Lu, Meixiang Jia, Hao Yu, Yanyan Ruan, Weihua Yue, Jing Liu, Lin Lu et al. · 2015 · PLoS ONE
  82. Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration
    Anne Senabouth, Maciej Daniszewski, Grace E. Lidgerwood, Helena Hai Liang, Damián Hernández, Mehdi Mirzaei, Stacey N. Keenan, Ran Zhang, Xikun Han, Drew R. Neavin et al. · 2022 · Nature Communications
  83. Glycogen synthase kinase 3 substrates in mood disorders and schizophrenia
    Adam R. Cole · 2013 · FEBS Journal
  84. Node of Ranvier Disruption as a Cause of Neurological Diseases
    Keiichiro Susuki · 2013 · ASN NEURO
  85. Selective Alterations in Postsynaptic Markers of Chandelier Cell Inputs to Cortical Pyramidal Neurons in Subjects with Schizophrenia
    Dianne A. Cruz, Cassandra L. Weaver, Emily Lovallo, Darlene S. Melchitzky, David A. Lewis · 2009 · Neuropsychopharmacology
  86. Emerging phenotyping strategies will advance our understanding of psychiatric genetics
    Sandra Sanchez‐Roige, Abraham A. Palmer · 2020 · Nature Neuroscience
  87. Homer1 promotes dendritic spine growth through ankyrin-G and its loss reshapes the synaptic proteome
    Sehyoun Yoon, Nicolas H. Piguel, Natalia Khalatyan, Leonardo E. Dionisio, Jeffrey N. Savas, Peter Penzes · 2021 · Molecular Psychiatry
  88. The Prevention of Schizophrenia--What Can We Learn From Eco-Epidemiology?
    James Bowes Kirkbride, Peter Brian Jones · 2010 · Schizophrenia Bulletin
  89. Replication of Genome‐Wide association studies ( GWAS ) loci for sleep in the British G1219 cohort
    Michael J. Parsons, Kathryn J. Lester, Nicola L. Barclay, Patrick M. Nolan, Thalia Catherine Eley, Alice M. Gregory · 2013 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  90. Transcription factor 4 (TCF4) and schizophrenia: integrating the animal and the human perspective
    Boris B. Quednow, Magdalena M. Brzózka, Moritz J. Rossner · 2014 · Cellular and Molecular Life Sciences
  91. Ankyrin-G regulates neurogenesis and Wnt signaling by altering the subcellular localization of β-catenin
    Omer Durak, Froylán Calderón de Anda, Karun Kar Singh, Melanie P. Leussis, Tracey L. Petryshen, Pamela B. Sklar, L-H Tsai · 2014 · Molecular Psychiatry
  92. Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes
    Erin N. Smith, Daniel L. Koller, Corrie B. Panganiban, Szabolcs Szelinger, Peng Zhang, Judith Ann Badner, Thomas B. Barrett, Wade H. Berrettini, Cinnamon S. Bloss, William Byerley et al. · 2011 · PLoS Genetics
  93. A New Role for Endophenotypes in the GWAS Era: Functional Characterization of Risk Variants
    Hall, Mei-Hua · 2010 · Harvard Review of Psychiatry
  94. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility
    Ming Li, X-j Luo, M. Rietschel, Cathryn M. Lewis, Manuel Mattheisen, Bertram Müller-Myhsok, Stéphane Jamain, Marion Leboyer, Mikael Landén, Paul M. Thompson et al. · 2013 · Molecular Psychiatry
  95. Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogation
    Benjamin M. Neale, Pamela B. Sklar · 2014 · Current Opinion in Neurobiology
  96. Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia
    Alessia Fiorentino, Sally Isabel Sharp, Andrew McQuillin · 2014 · European Journal of Human Genetics
  97. Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder
    Gregory John Lydall, Nicholas James Bass, Andrew McQuillin, Jacob Lawrence, Adebayo Anjorin, Radhika Kandaswamy, A C Pereira, Irene Guerrini, David Curtis, Anna E. Vine et al. · 2011 · Psychiatric Genetics
  98. Toward a Deeper Understanding of the Genetics of Bipolar Disorder
    Berit Kerner · 2015 · Frontiers in Psychiatry
  99. The impact of the CACNA1C risk allele on limbic structures and facial emotions recognition in bipolar disorder subjects and healthy controls
    Márcio Gerhardt Soeiro‐de‐Souza, Maria Concepción García Otaduy, Carolina Zadres Dias, Danielle Soares Bio, Rodrigo Machado‐Vieira, Ricardo Alberto Moreno · 2012 · Journal of Affective Disorders
  100. Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome
    Georgia Panagiotakos, Christos S. Haveles, Arpana Arjun, Ralitsa Petrova, Anshul Rana, Thomas Portmann, Sergiu P. Pașca, Theo D. Palmer, Ricardo E. Dolmetsch · 2019 · eLife