Large recurrent microdeletions associated with schizophrenia.

Cited by (1,002)

Items 101–200 of 1,002

1. De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
   S E McCarthy, Jesse Gillis, Melissa Kramer, Jayon Lihm, Seungtai Chris Yoon, Yael Berstein, Meeta Mistry, Paul Pavlidis, R Solomon, Elena Ghiban et al. · 2014 · Molecular Psychiatry
2. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
   Vacic, Vladimir, McCarthy, Shane, Malhotra, Dheeraj, Murray, Fiona, Chou, Hsun-Hua, Peoples, Aine, Makarov, Vladimir, Yoon, Seungtai, Bhandari, Abhishek, Corominas, Roser et al. · 2011 · Nature
3. Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
   Santhosh Girirajan, Zoran Brkanac, Bradley P. Coe, Carl A. Baker, Laura Vives, Tiffany H. Vu, Neil Shafer, Raphael Bernier, Giovanni Battista Ferrero, Margherita Silengo et al. · 2011 · PLoS Genetics
4. Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism
   Horev, Guy, Ellegood, Jacob, Lerch, Jason P., Son, Young-Eun E., Muthuswamy, Lakshmi, Vogel, Hannes, Krieger, Abba M., Buja, Andreas, Henkelman, R. Mark, Wigler, Michael et al. · 2011 · Proceedings of the National Academy of Sciences
5. Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence
   Moreno-De-Luca, Andres, Myers, Scott M, Challman, Thomas D, Moreno-De-Luca, Daniel, Evans, David W, Ledbetter, David H · 2013 · The Lancet Neurology
6. Genomics, Intellectual Disability, and Autism
   Mefford, Heather C., Batshaw, Mark L., Hoffman, Eric P. · 2012 · New England Journal of Medicine
7. De novo rates and selection of large copy number variation
   Itsara, Andy, Wu, Hao, Smith, Joshua D., Nickerson, Deborah A., Romieu, Isabelle, London, Stephanie J., Eichler, Evan E. · 2010 · Genome Research
8. Genetic overlap between autism, schizophrenia and bipolar disorder
   Carroll, Liam S, Owen, Michael J · 2009 · Genome Medicine
9. High frequencies of de novo CNVs in bipolar disorder and schizophrenia
   Malhotra, Dheeraj, McCarthy, Shane, Michaelson, Jacob J., Vacic, Vladimir, Burdick, Katherine E., Yoon, Seungtai, Cichon, Sven, Corvin, Aiden, Gary, Sydney, Gershon, Elliot S. et al. · 2011 · Neuron
10. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn et al. · 2010 · The American Journal of Human Genetics
11. Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
    Soemedi, Rachel, Wilson, Ian J., Bentham, Jamie, Darlay, Rebecca, Töpf, Ana, Zelenika, Diana, Cosgrove, Catherine, Setchfield, Kerry, Thornborough, Chris, Granados-Riveron, Javier et al. · 2012 · The American Journal of Human Genetics
12. The Role of Genetics in the Etiology of Schizophrenia
    Pablo V. Gejman, Alan R. Sanders, Jubao Duan · 2010 · Psychiatric Clinics of North America
13. The genetic basis of non-syndromic intellectual disability: a review
    Liana Kaufman, Muhammad Ayub, John B. Vincent · 2010 · Journal of Neurodevelopmental Disorders
14. The Genetic Basis of Addictive Disorders
    Ducci, Francesca, Goldman, David · 2012 · Psychiatric Clinics of North America
15. MicroRNA expression profiling in the prefrontal cortex of individuals affected with schizophrenia and bipolar disorders
    Kim, Albert H., Reimers, Mark, Maher, Brion, Williamson, Vernell, McMichael, Omari, McClay, Joseph L., van den Oord, Edwin J.C.G., Riley, Brien P., Kendler, Kenneth S., Vladimirov, Vladimir I. · 2010 · Schizophrenia Research
16. Genetic Relationships Between Schizophrenia, Bipolar Disorder, and Schizoaffective Disorder
    Alastair G. Cardno, Michael John Owen · 2014 · Schizophrenia Bulletin
17. Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
    Williams, Nigel M., Franke, Barbara, Mick, Eric, Anney, Richard J.L., Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael C., Owen, Michael J., Holmans, Peter et al. · 2012 · American Journal of Psychiatry
18. Genetic Risk for Schizophrenia: Convergence on Synaptic Pathways Involved in Plasticity
    Hall, Jeremy, Trent, Simon, Thomas, Kerrie L., O’Donovan, Michael C., Owen, Michael J. · 2015 · Biological Psychiatry
19. The Danish 22q11 research initiative
    Henriette Schmock, Anders Vangkilde, Kit Melissa Larsen, Elvira Fischer, Michelle Rosgaard Birknow, Jens Richardt Møllegaard Jepsen, Charlotte Olesen, Flemming Skovby, Kerstin Jessica Plessen, Morten Mørup et al. · 2015 · BMC Psychiatry
20. Decanalization and the origin of complex disease
    Gibson, Greg · 2009 · Nature Reviews Genetics
21. Meta-analysis of 32 genome-wide linkage studies of schizophrenia
    Mandy Ng, Douglas F. Levinson, Stephen V. Faraone, Brian K. Suarez, Lynn E. DeLisi, Tadao Arinami, Brien P. Riley, Tiina Paunio, Ann E. Pulver, Irmansyah et al. · 2008 · Molecular Psychiatry
22. Phenotypic variability and genetic susceptibility to genomic disorders
    Santhosh Girirajan, Evan E. Eichler · 2010 · Human Molecular Genetics
23. Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
    Terry Vrijenhoek, Jacobine E. Buizer‐Voskamp, Inge van der Stelt, Eric Strengman, Chiara Sabatti, Ad Geurts van Kessel, Han G. Brunner, Roel A. Ophoff, Joris A. Veltman · 2008 · The American Journal of Human Genetics
24. Complex human chromosomal and genomic rearrangements
    Feng Zhang, Claudia M.B. Carvalho, James R. Lupski · 2009 · Trends in Genetics
25. Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits
    Erin L. Heinzen, Dongliang Ge, Kenneth D. Cronin, Jessica M. Maia, Kevin V. Shianna, Willow N. Gabriel, Kathleen Anne Welsh-Bohmer, Christine Marie Hulette, Thomas N. Denny, David B. Goldstein · 2008 · PLoS Biology
26. Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
    Glessner, Joseph T., Bick, Alexander G., Ito, Kaoru, Homsy, Jason G., Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy et al. · 2014 · Circulation Research
27. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
    Leanne M. Dibbens, Saul Alator Mullen, Katherine L. Helbig, Heather C. Mefford, Marta A. Bayly, Susannah T. Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig et al. · 2009 · Human Molecular Genetics
28. Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts
    Pierandrea Muglia, Federica Tozzi, Nicholas W. Galwey, Clyde Francks, Ruchi Upmanyu, Xiangyang Kong, Athos Antoniades, Enrico Domenici, J Perry, Stéphane Rothen et al. · 2008 · Molecular Psychiatry
29. Whole-genome resequencing of 292 pigeonpea accessions identifies genomic regions associated with domestication and agronomic traits
    Rajeev Kumar Varshney, Rachit Kumar Saxena, Hari Deo Upadhyaya, Aamir Waseem Khan, Yue Yu, Changhoon Kim, Abhishek Rathore, Dongseon Kim, Jihun Kim, Shaun An et al. · 2017 · Nature Genetics
30. Comparative genomics of autism and schizophrenia
    Crespi, Bernard, Stead, Philip, Elliot, Michael · 2010 · Proceedings of the National Academy of Sciences
31. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
    Ben-Shachar, S, Lanpher, B, German, J R, Qasaymeh, M, Potocki, L, Nagamani, S C Sreenath, Franco, L M, Malphrus, A, Bottenfield, G W, Spence, J E et al. · 2009 · Journal of Medical Genetics
32. Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
    Sebat, Jonathan, Levy, Deborah L., McCarthy, Shane E. · 2009 · Trends in Genetics
33. Down syndrome--recent progress and future prospects
    Frances K. Wiseman, Kate A. Alford, Victor L. J. Tybulewicz, Elizabeth Fisher · 2009 · Human Molecular Genetics
34. Copy number variations of chromosome 16p13.1 region associated with schizophrenia
    Ingason, A, Rujescu, D, Cichon, S, Sigurdsson, E, Sigmundsson, T, Pietiläinen, O P H, Buizer-Voskamp, J E, Strengman, E, Francks, C, Muglia, P et al. · 2011 · Molecular Psychiatry
35. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay
    Burnside, Rachel D., Pasion, Romela, Mikhail, Fady M., Carroll, Andrew J., Robin, Nathaniel H., Youngs, Erin L., Gadi, Inder K., Keitges, Elizabeth, Jaswaney, Vikram L., Papenhausen, Peter R. et al. · 2011 · Human Genetics
36. Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
    Erin L. Heinzen, Rodney A. Radtke, Thomas Jacob Urban, Gianpiero L. Cavalleri, Chantal Depondt, Anna C. Need, Nicole M. Walley, Paola Nicoletti, Dongliang Ge, Claudia B. Catarino et al. · 2010 · The American Journal of Human Genetics
37. Type 2 diabetes: new genes, new understanding
    Prokopenko, Inga, McCarthy, Mark I., Lindgren, Cecilia M. · 2008 · Trends in Genetics
38. NMDA hypofunction as a convergence point for progression and symptoms of schizophrenia
    Melissa A. Snyder, Wen‐Jun Gao · 2013 · Frontiers in Cellular Neuroscience
39. Executive Function, Neural Circuitry, and Genetic Mechanisms in Schizophrenia
    Daniel Paul Eisenberg, Karen Faith Berman · 2009 · Neuropsychopharmacology
40. Rare copy number variants are an important cause of epileptic encephalopathies
    Mefford, Heather C., Yendle, Simone C., Hsu, Cynthia, Cook, Joseph, Geraghty, Eileen, McMahon, Jacinta M., Eeg‐Olofsson, Orvar, Sadleir, Lynette G., Gill, Deepak, Ben‐Zeev, Bruria et al. · 2011 · Annals of Neurology
41. RNA-Seq of Human Neurons Derived from iPS Cells Reveals Candidate Long Non-Coding RNAs Involved in Neurogenesis and Neuropsychiatric Disorders
    Mingyan Lin, Erika Pedrosa, Abhishek Shah, Anastasia Hrabovsky, Shahina Bano Maqbool, Deyou Zheng, Herbert M. Lachman · 2011 · PLoS ONE
42. The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review
    Cox, Devin, Butler, Merlin · 2015 · International Journal of Molecular Sciences
43. Neurodevelopment, GABA System Dysfunction, and Schizophrenia
    Martin J Schmidt, Károly Mirnics · 2014 · Neuropsychopharmacology
44. Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
    Philip Awadalla, Julie Gauthier, Rachel A. Myers, Ferrán Casals, Fadi F. Hamdan, Alexander R. Griffing, Mélanie Côté, Édouard Henrion, Dan Spiegelman, Julien Tarabeux et al. · 2010 · The American Journal of Human Genetics
45. Muscarinic and Nicotinic Acetylcholine Receptor Agonists and Allosteric Modulators for the Treatment of Schizophrenia
    Carrie K. Jones, Nellie E. Byun, Michael Bubser · 2011 · Neuropsychopharmacology
46. Modeling a Genetic Risk for Schizophrenia in iPSCs and Mice Reveals Neural Stem Cell Deficits Associated with Adherens Junctions and Polarity
    Yoon, Ki-Jun, Nguyen, Ha Nam, Ursini, Gianluca, Zhang, Fengyu, Kim, Nam-Shik, Wen, Zhexing, Makri, Georgia, Nauen, David, Shin, Joo Heon, Park, Youngbin et al. · 2014 · Cell Stem Cell
47. Copy-Number Disorders Are a Common Cause of Congenital Kidney Malformations
    Simone Sanna‐Cherchi, Krzysztof Kiryluk, Katelyn E. Burgess, Monica Bodria, Matthew Gordon Sampson, Dexter Hadley, Shannon N. Nees, Miguel Verbitsky, Brittany J. Perry, Roel Sterken et al. · 2012 · The American Journal of Human Genetics
48. Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
    Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne V Hing, Stephanie E Wallace, Patricia I. Bader, Aline I. Hamati, Pamela J. Reitnauer, Rosemarie Smith et al. · 2010 · Genetics in Medicine
49. Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells
    Erin J. Gardiner, Natalie Jane Beveridge, Jing Qin Wu, Vaughan J. Carr, Rodney J. Scott, Paul A. Tooney, Murray J. Cairns · 2011 · Molecular Psychiatry
50. At risk or not at risk? A meta‐analysis of the prognostic accuracy of psychometric interviews for psychosis prediction
    Fusar‐Poli, Paolo, Cappucciati, Marco, Rutigliano, Grazia, Schultze‐Lutter, Frauke, Bonoldi, Ilaria, Borgwardt, Stefan, Riecher‐Rössler, Anita, Addington, Jean, Perkins, Diana, Woods, Scott W. et al. · 2015 · World Psychiatry
51. Schizophrenia, “Just the Facts” 6. Moving ahead with the schizophrenia concept: From the elephant to the mouse
    Matcheri S. Keshavan, Henry A. Nasrallah, Rajiv Tandon · 2011 · Schizophrenia Research
52. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility
    O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, The International Schizophrenia Consortium, Corvin, A · 2011 · Molecular Psychiatry
53. Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice
    Doherty, Joanne L, Owen, Michael J · 2014 · Genome Medicine
54. Increased LIS1 expression affects human and mouse brain development
    Weimin Bi, Tamar Sapir, Oleg A. Shchelochkov, Feng Zhang, Marjorie A. Withers, Jill V. Hunter, Talia Levy, Vera Shinder, Daniel A. Peiffer, Kevin L. Gunderson et al. · 2009 · Nature Genetics
55. Strong synaptic transmission impact by copy number variations in schizophrenia
    Joseph Glessner, Muredach P. Reilly, Cecilia Kim, Nagahide Takahashi, Anthony Albano, Cuiping Hou, Jonathan P. Bradfield, Haitao Zhang, Patrick M. Abou‐Sleiman, James H. Flory et al. · 2010 · Proceedings of the National Academy of Sciences
56. An Evaluation of Copy Number Variation Detection Tools from Whole-Exome Sequencing Data
    Renjie Tan, Yadong Wang, Sarah E. Kleinstein, Yongzhuang Liu, Xiaolin Zhu, Hongzhe Guo, Qinghua Jiang, Andrew S. Allen, Mingfu Zhu · 2014 · Human Mutation
57. Microdeletions of 3q29 confer high risk for schizophrenia
    Mulle, Jennifer Gladys, Dodd, Anne F., McGrath, John A., Wolyniec, Paula S., Mitchell, Adele A., Shetty, Amol C., Sobreira, Nara L., Valle, David, Rudd, M. Katharine, Satten, Glen et al. · 2010 · The American Journal of Human Genetics
58. Genomic disorders ten years on
    James R. Lupski · 2009 · Genome Medicine
59. The copy number variation landscape of congenital anomalies of the kidney and urinary tract
    Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A. Fasel, Ekatherina Batourina, Matthew Gordon Sampson et al. · 2018 · Nature Genetics
60. Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion
    Ruibin Xi, Angela G. Hadjipanayis, Lovelace J. Luquette, Tae‐Min Kim, Eunjung Lee, Jianhua Zhang, Mark D. Johnson, Donna Marie Muzny, David A. Wheeler, Richard A. Gibbs et al. · 2011 · Proceedings of the National Academy of Sciences
61. Copy number variations in neurodevelopmental disorders
    Hannah M. Grayton, Cathy Fernandes, Dan Rujescu, David Andrew Collier · 2012 · Progress in Neurobiology
62. Psychosis Genetics: Modeling the Relationship Between Schizophrenia, Bipolar Disorder, and Mixed (or "Schizoaffective") Psychoses
    Craddock, N., O'Donovan, M. C., Owen, M. J. · 2009 · Schizophrenia Bulletin
63. Genetics of psychosis; insights from views across the genome
    Michael C. O’Donovan, Nick J. Craddock, Michael John Owen · 2009 · Human Genetics
64. Behavior genetics and postgenomics
    Evan Charney · 2012 · Behavioral and Brain Sciences
65. The genetic basis of major depression
    Kendall, K. M., Van Assche, E., Andlauer, T. F. M., Choi, K. W., Luykx, J. J., Schulte, E. C., Lu, Y. · 2021 · Psychological Medicine
66. Synaptic dysfunction in neurodegenerative and neurodevelopmental diseases: an overview of induced pluripotent stem-cell-based disease models
    Era Taoufik, Georgia Kouroupi, Ourania Zygogianni, Rebecca Matsas · 2018 · Open Biology
67. The genetics of Tourette syndrome: A review
    O'Rourke, Julia A., Scharf, Jeremiah M., Yu, Dongmei, Pauls, David L. · 2009 · Journal of Psychosomatic Research
68. A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa
    Wang, K, Zhang, H, Bloss, C S, Duvvuri, V, Kaye, W, Schork, N J, Berrettini, W, Hakonarson, H, the Price Foundation Collaborative Group · 2011 · Molecular Psychiatry
69. A framework for interpreting genome-wide association studies of psychiatric disorders
    The Psychiatric GWAS Consortium Steering Committee · 2008 · Molecular Psychiatry
70. Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap
    Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, Virpi Leppä, Gokul Ramaswami, Christopher Hartl, Andrew Joseph Schork, Vivek Appadurai, Alfonso Buil, Thomas Mears Werge et al. · 2019 · FOCUS The Journal of Lifelong Learning in Psychiatry
71. Advanced Paternal Age Is Associated with Impaired Neurocognitive Outcomes during Infancy and Childhood
    Sukanta Saha, Adrian Gerard Barnett, Claire J. Foldi, Thomas H.J. Burne, Darryl Walter Eyles, Stephen L. Buka, John Joseph McGrath · 2009 · PLoS Medicine
72. The polygenic architecture of schizophrenia — rethinking pathogenesis and nosology
    Olav Bjerkehagen Smeland, Oleksandr Frei, Anders Martin Dale, Ole A. Andreassen · 2020 · Nature Reviews Neurology
73. Copy number polymorphism in plant genomes
    Agnieszka Żmieńko, Anna Samelak-Czajka, Piotr Kozłowski, Marek Figlerowicz · 2013 · Theoretical and Applied Genetics
74. Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism
    Thomas V. Fernandez, Stephan Sanders, Ilana R. Yurkiewicz, A. Gulhan Ercan‐Sencicek, Young-Shin Kim, Daniel O. Fishman, Melanie J. Raubeson, Youeun Song, Katsuhito Yasuno, Winson S. Ho et al. · 2011 · Biological Psychiatry
75. Duplication hotspots, rare genomic disorders, and common disease
    Heather C. Mefford, Evan E. Eichler · 2009 · Current Opinion in Genetics & Development
76. MicroRNAs: Key Regulators in the Central Nervous System and Their Implication in Neurological Diseases
    Dandan Cao, Lu Li, Wai‐Yee Chan · 2016 · International Journal of Molecular Sciences
77. Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease
    Anne S. Bassett, Stephen W. Scherer, Linda M. Brzustowicz · 2010 · American Journal of Psychiatry
78. Genetics of Congenital Heart Disease
    Ashleigh A. Richards, Vidu Garg · 2010 · Current Cardiology Reviews
79. Diverse types of genetic variation converge on functional gene networks involved in schizophrenia
    Gilman, Sarah R, Chang, Jonathan, Xu, Bin, Bawa, Tejdeep S, Gogos, Joseph A, Karayiorgou, Maria, Vitkup, Dennis · 2012 · Nature Neuroscience
80. Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
    Elaine M. Kenny, Paul Cormican, S Furlong, Elizabeth A. Heron, G Kenny, Ciara Fahey, Eric Kelleher, Sean Ennis, Daniela Tropea, Richard Anney et al. · 2013 · Molecular Psychiatry
81. Copy Number and SNP Arrays in Clinical Diagnostics
    Christian Patrick Schaaf, Joanna Wiszniewska, Arthur L. Beaudet · 2011 · Annual Review of Genomics and Human Genetics
82. Implications of gene copy-number variation in health and diseases
    Suhani H. Almal, Harish Padh · 2011 · Journal of Human Genetics
83. Extending genome-wide association studies to copy-number variation
    Steven A. McCarroll · 2008 · Human Molecular Genetics
84. Genomic copy number variation, human health, and disease
    Wain, Louise V, Armour, John AL, Tobin, Martin D · 2009 · The Lancet
85. Overview of the Genetics of Alcohol Use Disorder
    Elisabeth A. Tawa, Samuel D. Hall, Falk W. Lohoff · 2016 · Alcohol and Alcoholism
86. Human adaptation and evolution by segmental duplication
    Megan Y. Dennis, Evan E. Eichler · 2016 · Current Opinion in Genetics & Development
87. Dosage sensitivity is a major determinant of human copy number variant pathogenicity
    Alan M. Rice, Aoife McLysaght · 2017 · Nature Communications
88. Rare Copy Number Variants<subtitle>A Point of Rarity in Genetic Risk for Bipolar Disorder and Schizophrenia</subtitle><alt-title>Rare Copy Number Variants</alt-title>
    Grozeva, Detelina · 2010 · Archives of General Psychiatry
89. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
    Marwan S. Shinawi, Christian Patrick Schaaf, Samarth Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan C. Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel et al. · 2009 · Nature Genetics
90. The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function
    Melissa L. Sinkus, Sharon Louise Graw, Robert Freedman, Randal G. Ross, Henry A. Lester, Sherry S. Leonard · 2015 · Neuropharmacology
91. Autism spectrum disorder in the genetics clinic: a review
    MT Carter, Stephen W. Scherer · 2013 · Clinical Genetics
92. The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines
    Pathania, M, Davenport, E C, Muir, J, Sheehan, D F, López-Doménech, G, Kittler, J T · 2014 · Translational Psychiatry
93. The Genetics of Microdeletion and Microduplication Syndromes: An Update
    Corey T. Watson, Tomàs Marquès‐Bonet, Andrew J. Sharp, Heather C. Mefford · 2014 · Annual Review of Genomics and Human Genetics
94. Copy number variants are frequent in genetic generalized epilepsy with intellectual disability
    Mullen, Saul A., Carvill, Gemma L., Bellows, Susannah, Bayly, Marta A., Berkovic, Samuel F., Dibbens, Leanne M., Scheffer, Ingrid E., Mefford, Heather C. · 2013 · Neurology
95. The clinical context of copy number variation in the human genome
    Charles Lee, Stephen W. Scherer · 2010 · Expert Reviews in Molecular Medicine
96. Altered Social Behaviours in Neurexin 1α Knockout Mice Resemble Core Symptoms in Neurodevelopmental Disorders
    Hannah M. Grayton, Markus Missler, David Andrew Collier, Cathy Fernandes · 2013 · PLoS ONE
97. Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci
    GROUP investigators, Børglum, A D, Demontis, D, Grove, J, Pallesen, J, Hollegaard, M V, Pedersen, C B, Hedemand, A, Mattheisen, M, Uitterlinden, A et al. · 2014 · Molecular Psychiatry
98. Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
    D.N. Cooper, Jian‐Min Chen, Edward V. Ball, Katy Howells, Matthew E. Mort, Andrew D. Phillips, Nadia A Chuzhanova, Michael Krawczak, Hildegard Kehrer‐Sawatzki, Peter D. Stenson · 2010 · Human Mutation
99. Neuromodulation by acetylcholine: examples from schizophrenia and depression
    Higley, Michael J, Picciotto, Marina R · 2014 · Current Opinion in Neurobiology
100. Using XHMM Software to Detect Copy Number Variation in Whole‐Exome Sequencing Data
     Menachem Fromer, Shaun Purcell · 2014 · Current Protocols in Human Genetics