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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:

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

Showing 1-25 of 42 citing articles:

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan, Daniel H. Geschwind
Cell (2019) Vol. 177, Iss. 1, pp. 162-183
Open Access | Times Cited: 398
A large data resource of genomic copy number variation across neurodevelopmental disorders
Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, et al.
npj Genomic Medicine (2019) Vol. 4, Iss. 1
Open Access | Times Cited: 159
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
Ólafur Ó. Guðmundsson, G. Bragi Walters, Andrés Ingason, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 100
Not every sperm is sacred; a perspective on male infertility
R. John Aitken
Molecular Human Reproduction (2018)
Open Access | Times Cited: 65
Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders
Xabier Calle Sánchez, Dorte Helenius, Jonas Bybjerg‐Grauholm, et al.
JAMA Psychiatry (2021) Vol. 79, Iss. 1, pp. 59-59
Open Access | Times Cited: 43
Consensus on potential biomarkers developed for use in clinical tests for schizophrenia
Ping Lin, Junyu Sun, Xiaoyan Lou, et al.
General Psychiatry (2022) Vol. 35, Iss. 1, pp. e100685-e100685
Open Access | Times Cited: 25
Schizophrenia is a later‐onset feature ofPCDH19Girls Clustering Epilepsy
Danique R.M. Vlaskamp, Anne S. Bassett, Joseph Sullivan, et al.
Epilepsia (2019) Vol. 60, Iss. 3, pp. 429-440
Open Access | Times Cited: 34
The genomics of schizophrenia: Shortcomings and solutions
Chuanjun Zhuo, Weihong Hou, Gongying Li, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2019) Vol. 93, pp. 71-76
Closed Access | Times Cited: 29
Enrichment of rare copy number variation in children with developmental language disorder
Nelli Kalnak, Sofia Stamouli, Myriam Peyrard‐Janvid, et al.
Clinical Genetics (2018) Vol. 94, Iss. 3-4, pp. 313-320
Closed Access | Times Cited: 21
Copy Number Variations and Schizophrenia
Kamila Szecówka, Błażej Misiak, Izabela Łaczmańska, et al.
Molecular Neurobiology (2022) Vol. 60, Iss. 4, pp. 1854-1864
Open Access | Times Cited: 12
Blindness, Psychosis, and the Visual Construction of the World
Thomas A. Pollak, Philip R. Corlett
Schizophrenia Bulletin (2019) Vol. 46, Iss. 6, pp. 1418-1425
Open Access | Times Cited: 18
Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders
Danijela Krgović, Nadja Kokalj Vokač, Andreja Zagorac, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 18
Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder
Kristiina Tammimies, Danyang Li, Ielyzaveta Rabkina, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 16
CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders
Madelyn A. Gillentine, Ricardo Lozoya, Jiani Yin, et al.
Journal of Affective Disorders (2018) Vol. 239, pp. 247-252
Open Access | Times Cited: 16
Treatment-resistant psychotic symptoms and the 15q11.2 BP1–BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature
Martilias S. Farrell, Maya Lichtenstein, Matthew K. Harner, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 14
Collaborative Care in the Identification and Management of Psychosis in Adolescents and Young Adults
Liwei L. Hua, Elizabeth M. Alderman, Richard J. Chung, et al.
PEDIATRICS (2021) Vol. 147, Iss. 6
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
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
Deletion at 12q12 increases the risk of developmental delay and intellectual disability
Ying Weng, Xiaoping Luo, Ling Hou
Annals of Human Genetics (2018) Vol. 82, Iss. 6, pp. 482-487
Open Access | Times Cited: 8
Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients
Zuzana Capkova, Pavlína Čapková, Josef Srovnal, et al.
PeerJ (2019) Vol. 7, pp. e7979-e7979
Open Access | Times Cited: 8
Chromosomal Microarray Analysis as First-Tier Genetic Test for Schizophrenia
Chia‐Hsiang Chen, Min-Chih Cheng, Tsung‐Ming Hu, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 7
Client-centred clinical genetic diagnostics
Maarten Otter, Constance T. R. M. Stumpel, Thérèse van Amelsvoort
Advances in Mental Health and Intellectual Disabilities (2017) Vol. 12, Iss. 1, pp. 1-10
Closed Access | Times Cited: 4
Neutrophils to lymphocytes ratio and psychosis in 22q11.2 deletion syndrome – Clinical and scientific implications
Ehud Mekori‐Domachevsky, Michal Taler, Ronnie Weinberger, et al.
Schizophrenia Research (2021) Vol. 231, pp. 164-169
Closed Access | Times Cited: 4
Translational Study of Copy Number Variations in Schizophrenia
Min-Chih Cheng, Wei‐Hsien Chien, Yu‐Shu Huang, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 457-457
Open Access | Times Cited: 4
Perceptions of causal attribution and attitudes to genetic testing among people with schizophrenia and their first-degree relatives
Melissa B. R. Cullen, Bettina Meiser, Kristine Barlow‐Stewart, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 10, pp. 1147-1154
Open Access | Times Cited: 3
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