Analysis of copy number variations at 15 schizophrenia-associated loci

Cited by (442)

Items 401–442 of 442

1. Faculty Opinions recommendation of Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
   John I. Nürnberger · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
2. Index
   Denis R. Alexander · 2020 · Cambridge University Press eBooks
3. From the Editor's desk
   Kamaldeep Singh Bhui · 2014 · The British Journal of Psychiatry
4. Faculty Opinions recommendation of Psychiatric disorders in children with 16p11.2 deletion and duplication.
   Santhosh Girirajan · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
5. Faculty Opinions recommendation of Copy number variation in bipolar disorder.
   JANUSZ K. RYBAKOWSKI · 2017 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
6. Notes
   Denis R. Alexander · 2020 · Cambridge University Press eBooks
7. Animal and Cellular Models of Psychotic Disorders
   Mikhail V. Pletnikov, Guo‐li Ming, Christopher A. Ross · 2017
8. Functional ultrasound imaging reveals an aberrant developmental trajectory of functional connectivity in a mouse model of the 15q13.3 copy number variant microdeletion
   Gillian Grohs, Bastian Hengerer, Hugo Cruces-Solís · 2022 · bioRxiv (Cold Spring Harbor Laboratory)
9. Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability
   Nicholas A Donnelly, Adam C. Cunningham, Matthew Bracher‐Smith, Samuel J. R. A. Chawner, Jan Štochl, Tamsin Jane Ford, Frances Lucy Raymond, Valentina Escott‐Price, Marianne B. M. van den Bree · 2022 · medRxiv
10. Changes in social behaviour with alterations of MAPK3 and KCTD13/CUL3 pathways in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders
    Sandra Martín Lorenzo, Maria del Mar Muñiz Moreno, Helin Atas-Özcan, Marion Pellen, Valérie Nalesso, Wolfgang Raffelsberger, Géraldine Prevost, Loïc Lindner, Marie‐Christine Birling, Séverine Ménoret et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
11. Genetics of psychotic disorders with focus on early-onset psychosis
    Katrine Verena Wirgenes, Olav Bjerkehagen Smeland, Ole A. Andreassen · 2023 · Elsevier eBooks
12. Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia
    Livia Jurisova, Roman Šolc · 2023 · Journal of Genetics
13. Genome-scale copy number variant analysis in schizophrenia patients and controls from South India
    Minali Singh, Dibyabhabha Pradhan, Poornima Kkani, Gundugurti Prasad Rao, Naveen Kumar Dhagudu, Lov Kumar, Chellamuthu Ramasubramanian, Srinivasan Ganesh Kumar, Surekha Sonttineni, Kommu Naga Mohan · 2023 · Frontiers in Molecular Neuroscience
14. The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis
    Natalie Wellard, Nicholas E. Clifton, Elliott Rees, Kerrie L. Thomas, Jérémy Hall · 2024 · International Journal of Molecular Sciences
15. Conditional deletion of neurexin-2 impaired behavioral flexibility to alterations in action–outcome contingency
    Sheraz Khoja, Lulu Y. Chen · 2024 · Scientific Reports
16. Childhood onset violence and early onset schizophrenia. A molecular diagnosis of 15q13.2-13.3 duplication syndrome and the effects on insight and engagement
    Edward Silva · 2024 · Journal of Forensic Psychiatry and Psychology
17. Duplication 15q Syndrome
    Dana Q. Tran · 2024 · Springer eBooks
18. Medical Multimorbidity in Patients with Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 Patients
    Tyler E Dietterich, Rose Mary Xavier, Maya L. Lichtenstein, Matthew K. Harner, Lisa Bruno, Robert Stowe, Martilias S. Farrell, Rita A. Shaughnessy, Jonathan S. Berg, Patrick F. Sullivan et al. · 2025 · medRxiv
19. 16p11.2 duplication shows early male-biased impacts on reward learning, but NMDA receptor antagonism reduces optimal choice selection in both wildtypes and 16p11.2 duplication
    Dana Mueller, Evan Knep, Angelica Velosa, Erin Giglio, Cathy S. Chen, Sarah R. Heilbronner, R. Becket Ebitz, Patrick E. Rothwell, Nicola M. Grissom · 2025 · bioRxiv (Cold Spring Harbor Laboratory)
20. Copy Number Variation in Adult‐Onset Neuropsychiatric Disease
    Gergely Büki, Judit Bene · 2025 · Encyclopedia of Life Sciences
21. Current Trends
    Dawn N. Albertson, Derek Kenneth Tracy, Dan W. Joyce, Sukhwinder Singh Shergill · 2025 · Cambridge University Press eBooks
22. Exploring hippocampal dysfunction in schizophrenia with pluripotent stem cell models
    Deepak A. Kaji · 2025 · Schizophrenia Research
23. Additional file 1 of Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review
    Mezinska, S., Louise Gallagher, Verbrugge, M., Eline Maria Bunnik · 2021 · Figshare
24. Additional file 4 of Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review
    Mezinska, S., Louise Gallagher, Verbrugge, M., Eline Maria Bunnik · 2021 · Figshare
25. Additional file 3 of Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review
    Mezinska, S., Louise Gallagher, Verbrugge, M., Eline Maria Bunnik · 2021 · Figshare
26. Additional file 2 of Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review
    Mezinska, S., Louise Gallagher, Verbrugge, M., Eline Maria Bunnik · 2021 · Figshare
27. Additional file 1 of Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach
    Nicholas A Donnelly, Cunningham, Adam, Salas, Sergio Marco, Matthew Bracher‐Smith, Samuel J. R. A. Chawner, Jan Štochl, Tamsin Jane Ford, Frances Lucy Raymond, Valentina Escott‐Price, van den Bree, Marianne B. M. · 2024 · Figshare
28. Additional file 1 of Schizophrenia risk ZNF804A interacts with its associated proteins to modulate dendritic morphology and synaptic development
    Fengping Dong, Joseph Mao, Miranda K. Chen, Joy Yoon, Yingwei Mao · 2021 · Figshare
29. Additional file 1 of Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
    Kanako Ishizuka, Tomoyuki Yoshida, Kawabata, Takeshi, Ayako Imai, Hisashi Mori, Kimura, Hiroki, Inada, Toshiya, Okahisa, Yuko, Egawa, Jun, Usami, Masahide et al. · 2020 · Figshare
30. The impact of CNV burden on age at onset of schizophrenia
    Gerard Muntané, A. Valle, Pol Ramon-Cañellas, Lourdes Martorell, Elisabet Vilella · 2026 · Schizophrenia Research
31. Convergent and Divergent Cerebellar Alterations in 22q11.2 Copy Number Variants
    Hoki Fung, Kathleen O’Hora, Rune Bøen, Haley R. Wang, Carolyn Amir, Charles H. Schleifer, Leila Kushan, Blake A. Miranda, Elizabeth Bondy, Paul J. Mathews et al. · 2026 · Biological Psychiatry Global Open Science
32. Recurrent and Non-Recurrent Copy Number Variants in Native Americans and a Cosmopolitan Sample in Relation to Alcohol Use Disorder and Other Psychiatric Diseases
    Salma Majid Wakil, Keita Morisaki, Pei‐Hong Shen, Dylan G. Sucich, Melanie L. Schwandt, James Fielding Hejtmancik, Cheryl A. Marietta, Qiaoping Yuan, Nancy Diazgranados, Colin A. Hodgkinson et al. · 2026 · Molecular Neurobiology
33. Approches génétiques et thérapeutiques visant à comprendre et atténuer les conséquences de la délétion et duplication de la région 16p11.2 dans des modèles précliniques
    Sandra Martín Lorenzo · 2019 · theses.fr (ABES)
34. Approche neuropsychologique des patients souffrant de Troubles Complexes du Développement (TCD) à l’âge adulte
    Charlotte Danset-Alexandre · 2019 · theses.fr (ABES)
35. De l'imagerie cérébrale au recueil de données en vie quotidienne : vers une compréhension intégrée des liens entre fonctionnement cognitif, expériences émotionnelles, perception du temps et symptômes de la schizophrénie
    Maud Dupuy · 2018 · theses.fr (ABES)
36. Rare protein-disrupting variants in NPY5R, DLGAP1 and MAPK8IP3 segregate with OCD in two multiplex pedigrees
    Cathal Ormond, Mathieu Cap, Yi-Chieh Chang, Niamh Ryan, Denise April Chavira, Kyle Williams, Jon Edgar Grant, Carol A. Mathews, Elizabeth A. Heron, Aiden Peter Corvin · 2026 · medRxiv
37. 16p11.2 duplication and NMDA receptor antagonism have distinct impacts on reward learning and decision making
    Dana Mueller, Evan Knep, Angelica Velosa, Erin Giglio, Cathy S. Chen, Sarah R. Heilbronner, R. Becket Ebitz, Patrick E. Rothwell, Nicola M. Grissom · 2026 · Psychopharmacology
38. Synaptic and Circuit Mechanisms Shaping Neurodevelopmental and Psychiatric Outcomes Associated with 16p11.2 Copy Number Variation
    Alžbeta Námešná, Jasmine Pickford, Jérémy Hall, Marianne B. M. van den Bree, Luke Tait, Lawrence S. Wilkinson, Matthew W. Jones · 2026 · Genes
39. The Molecular Machinery of Synaptic Plasticity and Its Potential Role in the Aetiology of Schizophrenia
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40. Transsynaptic Bridges: Molecular Architects of Synaptic Identity, Plasticity and Disease
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41. The association of schizophrenia polygenic scores with continuously-hospitalized, treatment-resistant schizophrenia
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42. Contribution of copy number variants to schizophrenia in East Asian populations
    Yu Chen, Qidi Feng, Max Lam, Mingrui Yu, Yaoyao Sun, Cong Huai, Bimal Jana, Jack M. Fu, Calwing Liao, Robert Ye et al. · 2026 · Nature Genetics