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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome
Anne S. Bassett, Chelsea Lowther, Daniele Merico, et al.
American Journal of Psychiatry (2017) Vol. 174, Iss. 11, pp. 1054-1063
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome
Erik Boot, Sólveig Óskarsdóttir, Joanne C. Y. Loo, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 3, pp. 100344-100344
Open Access | Times Cited: 51
The contribution of copy number variants to psychiatric symptoms and cognitive ability
Josephine Mollon, Laura Almasy, Sébastien Jacquemont, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 4, pp. 1480-1493
Open Access | Times Cited: 46
Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia
Sarah E. Bergen, Alexander Ploner, Daniel P. Howrigan, et al.
American Journal of Psychiatry (2018) Vol. 176, Iss. 1, pp. 29-35
Open Access | Times Cited: 145
Molecular genetics of 22q11.2 deletion syndrome
Bernice E. Morrow, Donna M. McDonald‐McGinn, Beverly S. Emanuel, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 10, pp. 2070-2081
Open Access | Times Cited: 123
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P. Schaaf, Catalina Betancur, Ryan K. C. Yuen, et al.
Nature Reviews Genetics (2020) Vol. 21, Iss. 6, pp. 367-376
Open Access | Times Cited: 121
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 8, pp. 4496-4510
Open Access | Times Cited: 115
Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study
Samuel J. R. A. Chawner, Michael J. Owen, Peter Holmans, et al.
The Lancet Psychiatry (2019) Vol. 6, Iss. 6, pp. 493-505
Open Access | Times Cited: 110
Neurobiological perspective of 22q11.2 deletion syndrome
Janneke Zinkstok, Erik Boot, Anne S. Bassett, et al.
The Lancet Psychiatry (2019) Vol. 6, Iss. 11, pp. 951-960
Open Access | Times Cited: 97
A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium
Raquel E. Gur, Anne S. Bassett, Donna M. McDonald‐McGinn, et al.
Molecular Psychiatry (2017) Vol. 22, Iss. 12, pp. 1664-1672
Open Access | Times Cited: 80
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Ania Fiksinski, Gil D. Hoftman, Jacob Vorstman, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 1, pp. 341-353
Open Access | Times Cited: 33
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 31
Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome
Blaine Crowley, Melanie A. Ruffner, Donna M. McDonald‐McGinn, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 10, pp. 2082-2086
Open Access | Times Cited: 55
Rediscovering the value of families for psychiatric genetics research
David C. Glahn, Vishwajit L. Nimgaonkar, Henriette Raventós, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 4, pp. 523-535
Open Access | Times Cited: 55
Treatment‐resistant schizophrenia with 22q11.2 deletion and additional genetic defects
Sawako Furukawa, Shusei Arafuka, Hidekazu Kato, et al.
Neuropsychopharmacology Reports (2024) Vol. 44, Iss. 4, pp. 847-851
Open Access | Times Cited: 4
Integrating rare variant genetics and brain transcriptome data implicates novel schizophrenia putative risk genes
Shengtong Han, M Gilmartin, Wenhui Sheng, et al.
Schizophrenia Research (2025) Vol. 276, pp. 205-213
Closed Access
Longitudinal perspectives on the psychosis spectrum in 22q11.2 deletion syndrome
Sunny X. Tang, Raquel E. Gur
American Journal of Medical Genetics Part A (2017) Vol. 176, Iss. 10, pp. 2192-2202
Closed Access | Times Cited: 45
Genomic Disorders in Psychiatry—What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle Baribeau, et al.
Current Psychiatry Reports (2017) Vol. 19, Iss. 11
Closed Access | Times Cited: 42
Inferring the Nature of Missing Heritability in Human Traits Using Data from the GWAS Catalog
Eugenio López‐Cortegano, Armando Caballero
Genetics (2019) Vol. 212, Iss. 3, pp. 891-904
Open Access | Times Cited: 42
Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine N. Jørgensen, Line Olsen, et al.
Biological Psychiatry (2018) Vol. 85, Iss. 1, pp. 13-24
Closed Access | Times Cited: 39
Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imaging
Mandy Johnstone, Navneet A. Vasistha, Miruna C. Barbu, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 2, pp. 294-311
Open Access | Times Cited: 38
Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome
Ania Fiksinski, Maude Schneider, Janneke Zinkstok, et al.
Current Psychiatry Reports (2021) Vol. 23, Iss. 3
Open Access | Times Cited: 29
Contribution of induced pluripotent stem cell technologies to the understanding of cellular phenotypes in schizophrenia
Shabeesh Balan, Manabu Toyoshima, Takeo Yoshikawa
Neurobiology of Disease (2018) Vol. 131, pp. 104162-104162
Open Access | Times Cited: 30
Prevalence and incidence of psychotic disorders in 22q11.2 deletion syndrome: a meta-analysis
Umberto Provenzani, Stefano Damiani, Ilaria Bersano, et al.
International Review of Psychiatry (2022) Vol. 34, Iss. 7-8, pp. 676-688
Open Access | Times Cited: 15
Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients
Mo Li, Lu Shen, Luan Chen, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 22
What a finding of gene copy number variation can add to the diagnosis of developmental neuropsychiatric disorders
Jacob Vorstman, Stephen W. Scherer
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 18-25
Closed Access | Times Cited: 18
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