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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:

Common variants at 12q14 and 12q24 are associated with hippocampal volume
Joshua C. Bis, Charles DeCarli, Albert V. Smith, et al.
Nature Genetics (2012) Vol. 44, Iss. 5, pp. 545-551
Open Access | Times Cited: 239

Showing 1-25 of 239 citing articles:

Religious Orders Study and Rush Memory and Aging Project
David A. Bennett, Aron S. Buchman, Patricia A. Boyle, et al.
Journal of Alzheimer s Disease (2018) Vol. 64, Iss. s1, pp. S161-S189
Open Access | Times Cited: 1007
Common genetic variants influence human subcortical brain structures
Derrek P. Hibar, Jason L. Stein, Miguel E. Rentería, et al.
Nature (2015) Vol. 520, Iss. 7546, pp. 224-229
Open Access | Times Cited: 866
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Paul M. Thompson, Jason L. Stein, Sarah E. Medland, et al.
Brain Imaging and Behavior (2014) Vol. 8, Iss. 2, pp. 153-182
Open Access | Times Cited: 803
Identification of common variants associated with human hippocampal and intracranial volumes
Jason L. Stein, Sarah E. Medland, Alejandro Arias Väsquez, et al.
Nature Genetics (2012) Vol. 44, Iss. 5, pp. 552-561
Open Access | Times Cited: 640
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Gail Davies, Max Lam, Sarah E. Harris, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 613
Neuroimaging of the Philadelphia Neurodevelopmental Cohort
Theodore D. Satterthwaite, Mark A. Elliott, Kosha Ruparel, et al.
NeuroImage (2013) Vol. 86, pp. 544-553
Open Access | Times Cited: 546
The effects of aging in the hippocampus and cognitive decline
Luis E.B. Bettio, Luckshi Rajendran, Joana Gil‐Mohapel
Neuroscience & Biobehavioral Reviews (2017) Vol. 79, pp. 66-86
Closed Access | Times Cited: 514
Review: Hippocampal sclerosis in epilepsy: a neuropathology review
Maria Thom
Neuropathology and Applied Neurobiology (2014) Vol. 40, Iss. 5, pp. 520-543
Open Access | Times Cited: 499
Moderate alcohol consumption as risk factor for adverse brain outcomes and cognitive decline: longitudinal cohort study
Anya Topiwala, Charlotte L. Allan, Vyara Valkanova, et al.
BMJ (2017), pp. j2353-j2353
Open Access | Times Cited: 400
Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group
Neda Jahanshad, Peter Kochunov, Emma Sprooten, et al.
NeuroImage (2013) Vol. 81, pp. 455-469
Open Access | Times Cited: 395
The Rotterdam Study: 2016 objectives and design update
Albert Hofman, Guy Brusselle, Sarwa Darwish Murad, et al.
European Journal of Epidemiology (2015) Vol. 30, Iss. 8, pp. 661-708
Open Access | Times Cited: 369
The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth
Theodore D. Satterthwaite, John J. Connolly, Kosha Ruparel, et al.
NeuroImage (2015) Vol. 124, pp. 1115-1119
Open Access | Times Cited: 343
The Rotterdam Study: 2014 objectives and design update
Albert Hofman, Sarwa Darwish Murad, Cornelia M. van Duijn, et al.
European Journal of Epidemiology (2013) Vol. 28, Iss. 11, pp. 889-926
Open Access | Times Cited: 322
Novel genetic loci associated with hippocampal volume
Derrek P. Hibar, Hieab H.H. Adams, Neda Jahanshad, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 300
Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits
Bingxin Zhao, Tianyou Luo, Tengfei Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 11, pp. 1637-1644
Open Access | Times Cited: 254
Impact of the Alzheimer's Disease Neuroimaging Initiative, 2004 to 2014
Michael W. Weiner, Dallas P. Veitch, Paul Aisen, et al.
Alzheimer s & Dementia (2015) Vol. 11, Iss. 7, pp. 865-884
Open Access | Times Cited: 220
Genetics of Alzheimer’s Disease
Vincent Chouraki, Sudha Seshadri
Advances in genetics (2014), pp. 245-294
Closed Access | Times Cited: 196
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide
Paul M. Thompson, Ole A. Andreassen, Alejandro Arias Väsquez, et al.
NeuroImage (2015) Vol. 145, pp. 389-408
Open Access | Times Cited: 185
Genomic variants, genes, and pathways of Alzheimer's disease: An overview
Adam C. Naj, Gerard D. Schellenberg
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2016) Vol. 174, Iss. 1, pp. 5-26
Open Access | Times Cited: 171
Prior-Guided Adversarial Learning With Hypergraph for Predicting Abnormal Connections in Alzheimer’s Disease
Qiankun Zuo, Huisi Wu, C. L. Philip Chen, et al.
IEEE Transactions on Cybernetics (2024) Vol. 54, Iss. 6, pp. 3652-3665
Closed Access | Times Cited: 36
The paradox of syndromic diversity in Alzheimer disease
Jason D. Warren, Phillip D. Fletcher, Hannah L. Golden
Nature Reviews Neurology (2012) Vol. 8, Iss. 8, pp. 451-464
Closed Access | Times Cited: 194
Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease
Peter T. Nelson, Charles D. Smith, Erin L. Abner, et al.
Acta Neuropathologica (2013) Vol. 126, Iss. 2, pp. 161-177
Open Access | Times Cited: 187
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers
Li Shen, Paul M. Thompson, Steven G. Potkin, et al.
Brain Imaging and Behavior (2013) Vol. 8, Iss. 2, pp. 183-207
Open Access | Times Cited: 168
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, et al.
Human Molecular Genetics (2013) Vol. 23, Iss. 10, pp. 2752-2768
Open Access | Times Cited: 163
Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential
Ryan Bogdan, Betty Jo Salmeron, Caitlin E. Carey, et al.
Biological Psychiatry (2017) Vol. 82, Iss. 3, pp. 165-175
Open Access | Times Cited: 158
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