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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:

A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder
Kevin A. Strauss, Sander Markx, Benjamin Georgi, et al.
Human Molecular Genetics (2014) Vol. 23, Iss. 23, pp. 6395-6406
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

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
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
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
Ether‐à‐go‐go K+ channels: effective modulators of neuronal excitability
Christiane K. Bauer, Jürgen R. Schwarz
The Journal of Physiology (2018) Vol. 596, Iss. 5, pp. 769-783
Open Access | Times Cited: 74
Whole genome/exome sequencing in mood and psychotic disorders
Tadafumi Kato
Psychiatry and Clinical Neurosciences (2014) Vol. 69, Iss. 2, pp. 65-76
Closed Access | Times Cited: 72
De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism
Takuya Hiraide, Mitsuko Nakashima, Kaori Yamoto, et al.
Human Genetics (2018) Vol. 137, Iss. 1, pp. 95-104
Closed Access | Times Cited: 71
Toward a Deeper Understanding of the Genetics of Bipolar Disorder
Berit Kerner
Frontiers in Psychiatry (2015) Vol. 6
Open Access | Times Cited: 63
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
Anthony J. Griswold, Nicole Dueker, Derek Van Booven, et al.
Molecular Autism (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 62
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
An examination of multiple classes of rare variants in extended families with bipolar disorder
Claudio Toma, Alex D. Shaw, Richard J. N. Allcock, et al.
Translational Psychiatry (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 38
A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice
Bradley R. Miller, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 16
Open Access
Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families
Andreas J. Forstner, Sascha B. Fischer, Lorena M. Schenk, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 30
Finding Rare, Disease-Associated Variants in Isolated Groups: Potential Advantages of Mennonite Populations
Fabiana L. Lopes, Liping Hou, Angelica Beate Winter Boldt, et al.
Human Biology (2016) Vol. 88, Iss. 2, pp. 109-109
Open Access | Times Cited: 26
Potassium channel gene associations with joint processing speed and white matter impairments in schizophrenia
Heather Bruce, Peter Kochunov, Sara A. Paciga, et al.
Genes Brain & Behavior (2017) Vol. 16, Iss. 5, pp. 515-521
Open Access | Times Cited: 25
Arthropod toxins acting on neuronal potassium channels
Juana María Jiménez-Vargas, Lourival D. Possani, Karen Luna-Ramírez
Neuropharmacology (2017) Vol. 127, pp. 139-160
Closed Access | Times Cited: 25
Neurocardiac pathologies associated with potassium channelopathies
Veronica Singh, David S. Auerbach
Epilepsia (2024) Vol. 65, Iss. 9, pp. 2537-2552
Closed Access | Times Cited: 2
Family studies to find rare high risk variants in migraine
Rikke Dyhr Hansen, Anne Francke Christensen, Jes Olesen
The Journal of Headache and Pain (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 23
Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree
Rachel L. Kember, Liping Hou, Xiao Ji, et al.
Translational Psychiatry (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 22
Voltage-gated potassium channels (K<sub>v</sub>) in GtoPdb v.2023.1
Bernard Attali, K. George Chandy, M. Hunter Giese, et al.
IUPHAR/BPS Guide to Pharmacology CITE (2023) Vol. 2023, Iss. 1
Open Access | Times Cited: 6
Effects of Temperature on Heteromeric Kv11.1a/1b and Kv11.3 Channels
Maike Mauerhöfer, Christiane K. Bauer
Biophysical Journal (2016) Vol. 111, Iss. 3, pp. 504-523
Open Access | Times Cited: 18
Exome sequencing in large, multiplex bipolar disorder families from Cuba
Anna Maaser, Andreas J. Forstner, Jana Strohmaier, et al.
PLoS ONE (2018) Vol. 13, Iss. 10, pp. e0205895-e0205895
Open Access | Times Cited: 18
Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points toEFNA5,BAHD1andPPP2R5Eas novel candidates for genes causing human Mendelian disorders
Victor Murcia Pienkowski, Marzena Kucharczyk, Marlena Młynek, et al.
Journal of Medical Genetics (2018) Vol. 56, Iss. 2, pp. 104-112
Open Access | Times Cited: 17
Genetische Grundlagen der bipolaren Störung
Monika Budde, Andreas J. Forstner, Kristina Adorjan, et al.
Der Nervenarzt (2017) Vol. 88, Iss. 7, pp. 755-759
Closed Access | Times Cited: 16
Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability
Valentina Peycheva, Kunka Kamenarova, Neviana Ivanova, et al.
Gene (2018) Vol. 667, pp. 45-55
Closed Access | Times Cited: 15
Kv2.1 voltage‐gated potassium channels in developmental perspective
Justyna Jędrychowska, Vladimir Korzh
Developmental Dynamics (2019) Vol. 248, Iss. 12, pp. 1180-1194
Open Access | Times Cited: 15
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