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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 26-50 of 89 citing articles:

How does genetic variation modify ND-CNV phenotypes?
Thomas J. Dinneen, Fiana Ní Ghrálaigh, Ruth Walsh, et al.
Trends in Genetics (2021) Vol. 38, Iss. 2, pp. 140-151
Closed Access | Times Cited: 18
Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations
Noboru Hiroi, Takahira Yamauchi
The International Journal of Neuropsychopharmacology (2019) Vol. 22, Iss. 8, pp. 488-500
Open Access | Times Cited: 22
Surprising conservation of schizophrenia risk genes in lower organisms reflects their essential function and the evolution of genetic liability
Merve Kasap, Vivek Rajani, Jackie Rajani, et al.
Schizophrenia Research (2018) Vol. 202, pp. 120-128
Closed Access | Times Cited: 21
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome
Maris Alver, Valentina Mancini, Kristi Läll, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 10, pp. 4191-4200
Open Access | Times Cited: 12
Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome
Shengjie Ying, Tracy Heung, Zhaolei Zhang, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11
The 22q11 low copy repeats are characterized by unprecedented size and structure variability
Wolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 18
Polygenic risk for triglyceride levels in the presence of a high impact rare variant
Shengjie Ying, Tracy Heung, Bhooma Thiruvahindrapuram, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 5
A comprehensive screening of copy number variability in dementia with Lewy bodies
Célia Kun‐Rodrigues, Tatiana Orme, Susana Carmona, et al.
Neurobiology of Aging (2018) Vol. 75, pp. 223.e1-223.e10
Open Access | Times Cited: 16
A polymorphism in the glutamate metabotropic receptor 7 is associated with cognitive deficits in the early phases of psychosis
Boris Chaumette, Sarojini M. Sengupta, Martín Lepage, et al.
Schizophrenia Research (2020) Vol. 249, pp. 56-62
Open Access | Times Cited: 14
Schizophrenia and gut-flora related epigenetic factors
Chuanjun Zhuo, Yudong Yao, Yong Xu, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2018) Vol. 90, pp. 49-54
Closed Access | Times Cited: 14
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
Elena Michaelovsky, Miri Carmel, Amos Frisch, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 13
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model
Ania Fiksinski, Tracy Heung, Maria Corral, et al.
Psychological Medicine (2021) Vol. 52, Iss. 14, pp. 3184-3192
Open Access | Times Cited: 11
Bayesian Rare Variant Analysis Identifies Novel Schizophrenia Putative Risk Genes
Shengtong Han
Journal of Personalized Medicine (2024) Vol. 14, Iss. 8, pp. 822-822
Open Access | Times Cited: 1
Mapping the Schizophrenia Genes by Neuroimaging: The Opportunities and the Challenges
Ayla Arslan
International Journal of Molecular Sciences (2018) Vol. 19, Iss. 1, pp. 219-219
Open Access | Times Cited: 12
Precision Child Health: an Emerging Paradigm for Paediatric Quality and Safety
Gregory Costain, Ronald D. Cohn, David Malkin
Current Treatment Options in Pediatrics (2020) Vol. 6, Iss. 4, pp. 317-324
Open Access | Times Cited: 11
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Gregory Costain, Susan Walker, Bob Argiropoulos, et al.
Journal of Neurodevelopmental Disorders (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 9
Prenatal diagnosis of rearrangements in the fetal 22q11.2 region
Suping Li, Yuxia Jin, Jing Yang, et al.
Molecular Cytogenetics (2020) Vol. 13, Iss. 1
Open Access | Times Cited: 8
CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations
Hojka Gregorič Kumperščak, Danijela Krgović, Maja Drobnič Radobuljac, et al.
Frontiers in Psychiatry (2021) Vol. 11
Open Access | Times Cited: 8
Pathways to understanding psychosis through rare – 22q11.2DS - and common variants
Raquel E. Gur, David R. Roalf, Aaron Alexander‐Bloch, et al.
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 35-40
Open Access | Times Cited: 8
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia
Jhih-Rong Lin, Yingjie Zhao, M. Reza Jabalameli, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 5, pp. 2071-2080
Closed Access | Times Cited: 3
Recent developments in understanding the relationship between 22q11.2 deletion syndrome and psychosis
Linda O’Rourke, Kieran C. Murphy
Current Opinion in Psychiatry (2018) Vol. 32, Iss. 2, pp. 67-72
Open Access | Times Cited: 8
Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress
Akane Yoshikawa, Itaru Kushima, Mitsuhiro Miyashita, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Modern understanding of psychosis: from brain disease to stress disorder. And some other important aspects of psychosis…
Jan Olav Johannessen, Inge Joa
Psychosis (2021) Vol. 13, Iss. 4, pp. 289-301
Open Access | Times Cited: 7
Environmental Influences on the Relation between the 22q11.2 Deletion Syndrome and Mental Health: A Literature Review
Yelyzaveta Snihirova, David E.J. Linden, Thérèse van Amelsvoort, et al.
Genes (2022) Vol. 13, Iss. 11, pp. 2003-2003
Open Access | Times Cited: 5
A binational study assessing risk and resilience factors in 22q11.2 deletion syndrome
Raquel E. Gur, Lauren K. White, Shachar Shani, et al.
Journal of Psychiatric Research (2021) Vol. 138, pp. 319-325
Closed Access | Times Cited: 7

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