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:

Rare variants in neuronal excitability genes influence risk for bipolar disorder
Seth A. Ament, Szabolcs Szelinger, Gustavo Glusman, et al.
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 11, pp. 3576-3581
Open Access | Times Cited: 171

Showing 1-25 of 171 citing articles:

The Inositol Trisphosphate/Calcium Signaling Pathway in Health and Disease
Michael J. Berridge
Physiological Reviews (2016) Vol. 96, Iss. 4, pp. 1261-1296
Open Access | Times Cited: 620
Targeting voltage-gated calcium channels in neurological and psychiatric diseases
Gerald W. Zamponi
Nature Reviews Drug Discovery (2015) Vol. 15, Iss. 1, pp. 19-34
Open Access | Times Cited: 350
The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies
Azmeraw T. Amare, Klaus Oliver Schubert, Manuela Klingler‐Hoffmann, et al.
Translational Psychiatry (2017) Vol. 7, Iss. 1, pp. e1007-e1007
Open Access | Times Cited: 299
GABAA receptors: structure, function, pharmacology, and related disorders
Amr Ghit, Dina Assal, Ahmed S. Al‐Shami, et al.
Journal of Genetic Engineering and Biotechnology (2021) Vol. 19, Iss. 1, pp. 123-123
Open Access | Times Cited: 248
The genetics of bipolar disorder
Francis James A. Gordovez, Francis J. McMahon
Molecular Psychiatry (2020) Vol. 25, Iss. 3, pp. 544-559
Closed Access | Times Cited: 214
The Emerging Neurobiology of Bipolar Disorder
Paul J. Harrison, John Geddes, Elizabeth M. Tunbridge
Trends in Neurosciences (2017) Vol. 41, Iss. 1, pp. 18-30
Open Access | Times Cited: 185
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Sébastien Küry, Geeske M. van Woerden, Thomas Besnard, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 768-788
Open Access | Times Cited: 165
GABA A Receptors and the Diversity in their Structure and Pharmacology
Han Chow Chua, Mary Chebib
Advances in pharmacology (2017), pp. 1-34
Closed Access | Times Cited: 138
Neurobiological basis of bipolar disorder: Mitochondrial dysfunction hypothesis and beyond
Tadafumi Kato
Schizophrenia Research (2016) Vol. 187, pp. 62-66
Open Access | Times Cited: 109
Exome Sequencing of Familial Bipolar Disorder
Fernando S. Goes, Mehdi Pirooznia, Jennifer Parla, et al.
JAMA Psychiatry (2016) Vol. 73, Iss. 6, pp. 590-590
Open Access | Times Cited: 108
From Gene to Behavior: L-Type Calcium Channel Mechanisms Underlying Neuropsychiatric Symptoms
Zeeba D. Kabir, Arlene Martínez-Rivera, Anjali M. Rajadhyaksha
Neurotherapeutics (2017) Vol. 14, Iss. 3, pp. 588-613
Open Access | Times Cited: 107
Innovative approaches to bipolar disorder and its treatment
Paul J. Harrison, Andrea Cipriani, Catherine J. Harmer, et al.
Annals of the New York Academy of Sciences (2016) Vol. 1366, Iss. 1, pp. 76-89
Open Access | Times Cited: 104
Current understanding of bipolar disorder: Toward integration of biological basis and treatment strategies
Tadafumi Kato
Psychiatry and Clinical Neurosciences (2019) Vol. 73, Iss. 9, pp. 526-540
Open Access | Times Cited: 102
A systematic review of calcium channel antagonists in bipolar disorder and some considerations for their future development
Andrea Cipriani, Kate Saunders, Mary-Jane Attenburrow, et al.
Molecular Psychiatry (2016) Vol. 21, Iss. 10, pp. 1324-1332
Open Access | Times Cited: 100
Characterization of a Human-Specific Tandem Repeat Associated with Bipolar Disorder and Schizophrenia
Janet Song, Craig B. Lowe, David M. Kingsley
The American Journal of Human Genetics (2018) Vol. 103, Iss. 3, pp. 421-430
Open Access | Times Cited: 98
Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations
Mayumi Kataoka, Nana Matoba, Tomoyo Sawada, et al.
Molecular Psychiatry (2016) Vol. 21, Iss. 7, pp. 885-893
Open Access | Times Cited: 96
Trio-based exome sequencing arrests de novo mutations in early-onset high myopia
Zi‐Bing Jin, Jinyu Wu, Xiu‐Feng Huang, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 16, pp. 4219-4224
Open Access | Times Cited: 96
Neurodevelopmental origins of bipolar disorder: iPSC models
K. Sue O’Shea, Melvin G. McInnis
Molecular and Cellular Neuroscience (2015) Vol. 73, pp. 63-83
Closed Access | Times Cited: 95
Genetic Associations between Voltage-Gated Calcium Channels and Psychiatric Disorders
Arturo Andrade, Ashton Brennecke, Shayna Mallat, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 14, pp. 3537-3537
Open Access | Times Cited: 95
Neurobiological and behavioral mechanisms of circadian rhythm disruption in bipolar disorder: A critical multi‐disciplinary literature review and agenda for future research from the ISBD task force on chronobiology
Michael J. McCarthy, John F. Gottlieb, Robert Gonzalez, et al.
Bipolar Disorders (2021) Vol. 24, Iss. 3, pp. 232-263
Open Access | Times Cited: 72
Missense variants in GABAA receptor beta2 subunit disrupt receptor biogenesis and cause loss of function
Xi Chen, Yajuan Wang, Ting‐Wei Mu
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Genetics of Bipolar Disorder
Fernando S. Goes
Psychiatric Clinics of North America (2016) Vol. 39, Iss. 1, pp. 139-155
Open Access | Times Cited: 84
Addiction pharmacogenetics
Michelle A. Patriquin, Isabelle E. Bauer, Jair C. Soares, et al.
Psychiatric Genetics (2015) Vol. 25, Iss. 5, pp. 181-193
Open Access | Times Cited: 83
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene
Kerstin U. Ludwig, Syeda Ahmed, Anne C. Böhmer, et al.
PLoS Genetics (2016) Vol. 12, Iss. 3, pp. e1005914-e1005914
Open Access | Times Cited: 80
Research Domain Criteria: Strengths, Weaknesses, and Potential Alternatives for Future Psychiatric Research
Christopher A. Ross, Russell L. Margolis
Complex Psychiatry (2019) Vol. 5, Iss. 4, pp. 218-236
Open Access | Times Cited: 72
Page 1 - Next Page

Scroll to top