Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes
Suhas Ganesh, Husayn Ahmed Pallikonda, Ravi Kumar Nadella, et al.
Psychiatry and Clinical Neurosciences (2018) Vol. 73, Iss. 1, pp. 11-19
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

Lithium response in bipolar disorder correlates with improved cell viability of patient derived cell lines
Pradip Paul, Shruti Iyer, Ravi Kumar Nadella, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 37
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson’s disease in mainland China
Yi‐Min Sun, Xinyue Zhou, Xiaoniu Liang, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 12
Neuropeptides and oligopeptidases in schizophrenia
Benjamín Rodríguez, João V. Nani, Priscila G.C. Almeida, et al.
Neuroscience & Biobehavioral Reviews (2019) Vol. 108, pp. 679-693
Closed Access | Times Cited: 32
Genomic and neuroimaging approaches to bipolar disorder
Mojtaba Oraki Kohshour, Sergi Papiol, Christopher R. K. Ching, et al.
BJPsych Open (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 18
Exon-variant interplay and multi-modal evidence identify endocrine dysregulation in severe psychiatric disorders impacting excitatory neurons
Karolina Worf, Natalie Matosin, Nathalie Gerstner, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
Altered Sphingolipid Hydrolase Activities and Alpha-Synuclein Level in Late-Onset Schizophrenia
Tatiana Usenko, Anastasia Bezrukova, Katerina Basharova, et al.
Metabolites (2023) Vol. 14, Iss. 1, pp. 30-30
Open Access | Times Cited: 8
Recent Updates on Corticosteroid-Induced Neuropsychiatric Disorders and Theranostic Advancements through Gene Editing Tools
Manisha Singh, Vinayak Agarwal, Divya Jindal, et al.
Diagnostics (2023) Vol. 13, Iss. 3, pp. 337-337
Open Access | Times Cited: 7
Clinical and biochemical footprints of inherited metabolic diseases. III. Psychiatric presentations
Gabriella Horváth, Robert Stowe, Carlos R. Ferreira, et al.
Molecular Genetics and Metabolism (2020) Vol. 130, Iss. 1, pp. 1-6
Closed Access | Times Cited: 19
Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability
Maria Protasova, Т. В. Андреева, S. A. Klyushnikov, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1551-1551
Open Access | Times Cited: 6
Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder
Chia‐Hsiang Chen, Yu‐Shu Huang, Ting-Hsuan Fang
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13189-13189
Open Access | Times Cited: 13
Psychiatric symptoms and syndromes transcending diagnostic boundaries in Indian multiplex families: The cohort of ADBS study
Vanteemar S. Sreeraj, Bharath Holla, Dhruva Ithal, et al.
Psychiatry Research (2020) Vol. 296, pp. 113647-113647
Open Access | Times Cited: 12
RGS3andIL1RAPL1missense variants implicate defective neurotransmission in early-onset inherited schizophrenias
Ambreen Kanwal, José V. Pardo, Sadaf Naz
Journal of Psychiatry and Neuroscience (2022) Vol. 47, Iss. 6, pp. E379-E390
Open Access | Times Cited: 7
Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation
Hiromi Umehara, Masayuki Nakamura, Mio Nagai, et al.
Journal of Human Genetics (2020) Vol. 66, Iss. 3, pp. 243-249
Closed Access | Times Cited: 10
Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance
Ravi Kumar Nadella, Anirudh Chellappa, Anand G. Subramaniam, et al.
Human Genomics (2019) Vol. 13, Iss. 1
Open Access | Times Cited: 9
New approach to mental disorders systematics: starting point or point of view?
Н. Г. Незнанов, Г. В. Рукавишников, E. D. Kaysanov, et al.
V M BEKHTEREV REVIEW OF PSYCHIATRY AND MEDICAL PSYCHOLOGY (2020), Iss. 3, pp. 3-10
Open Access | Times Cited: 8
Abnormalities in the migration of neural precursor cells in familial bipolar disorder
Salil K. Sukumaran, Pradip Paul, Vishwesha Guttal, et al.
Disease Models & Mechanisms (2022) Vol. 15, Iss. 10
Open Access | Times Cited: 5
Genetics of Bipolar Spectrum Disorders: Focus on Family Studies Using Whole Exome Sequencing
E. D. Kasyanov, Т. В. Меркулова, А.О. Кибитов, et al.
Russian Journal of Genetics (2020) Vol. 56, Iss. 7, pp. 786-801
Closed Access | Times Cited: 7
The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Exome hits demystified: The next frontier
Dhruva Ithal, Salil K. Sukumaran, Debanjan Bhattacharjee, et al.
Asian Journal of Psychiatry (2021) Vol. 59, pp. 102640-102640
Closed Access | Times Cited: 6
Transdiagnostic neurocognitive endophenotypes in major psychiatric illness
Bharath Holla, Pavithra Dayal, Aswathy Das, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 5
Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes
Suhas Ganesh, Alekhya Vemula, Samsiddhi Bhattacharjee, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 3
Altered neuroepithelial morphogenesis and migration defects in iPSC-derived cerebral organoids and 2D neural stem cells in familial bipolar disorder
Kruttika Phalnikar, M Srividya, Starlin Vijay Mythri, et al.
Oxford Open Neuroscience (2024) Vol. 3
Open Access
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes
Jayant Mahadevan, Ajai Kumar Pathak, Alekhya Vemula, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 3
Variant-risk-exon interplay impacts circadian rhythm and dopamine signaling pathway in severe psychiatric disorders
Karolina Worf, Natalie Matosin, Nathalie Gerstner, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
Inherited Metabolic Diseases as a Multisystem Model of Mental Disorders Research
Г. В. Рукавишников, E. D. Kasyanov, T. V. Zhilyaeva, et al.
Journal of Inborn Errors of Metabolism and Screening (2021) Vol. 9
Open Access | Times Cited: 2
Page 1 - Next Page

Scroll to top