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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:

The impact of rare and low-frequency genetic variants in common disease
Lorenzo Bomba, Klaudia Walter, Nicole Soranzo
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 334

Showing 1-25 of 334 citing articles:

Genome-wide association studies
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1135
Accurate proteome-wide missense variant effect prediction with AlphaMissense
Jun Cheng, Guido Novati, Joshua Pan, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 882
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations
Roseann E. Peterson, Karoline Kuchenbaecker, Raymond K. Walters, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 589-603
Open Access | Times Cited: 635
Genetics of Parkinson's disease: An introspection of its journey towards precision medicine
Sara Bandrés‐Ciga, Mónica Díez-Fairén, Jonggeol Jeff Kim, et al.
Neurobiology of Disease (2020) Vol. 137, pp. 104782-104782
Open Access | Times Cited: 313
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Nature Genetics (2020) Vol. 52, Iss. 9, pp. 969-983
Open Access | Times Cited: 216
Advancing Personalized Medicine Through the Application of Whole Exome Sequencing and Big Data Analytics
Pawel Suwinski, ChuangKee Ong, Maurice HT Ling, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 188
Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power
Elizabeth G. Atkinson, Adam X. Maihofer, Masahiro Kanai, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 195-204
Open Access | Times Cited: 186
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts
Guiyan Ni, Jian Zeng, Joana Revez, et al.
Biological Psychiatry (2021) Vol. 90, Iss. 9, pp. 611-620
Open Access | Times Cited: 171
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
Olivia M. de Goede, Daniel Nachun, Nicole M. Ferraro, et al.
Cell (2021) Vol. 184, Iss. 10, pp. 2633-2648.e19
Open Access | Times Cited: 133
The human genetic epidemiology of COVID-19
Mari Niemi, Mark J. Daly, Andrea Ganna
Nature Reviews Genetics (2022) Vol. 23, Iss. 9, pp. 533-546
Open Access | Times Cited: 119
The contribution of copy number variants to psychiatric symptoms and cognitive ability
Josephine Mollon, Laura Almasy, Sébastien Jacquemont, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 4, pp. 1480-1493
Open Access | Times Cited: 49
Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance
Juan Camilo Chacón-Duque, Kaustubh Adhikari, Macarena Fuentes‐Guajardo, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 153
Transcriptomic signatures across human tissues identify functional rare genetic variation
Nicole M. Ferraro, Benjamin J. Strober, Jonah Einson, et al.
Science (2020) Vol. 369, Iss. 6509
Open Access | Times Cited: 135
Spontaneous preterm birth: advances toward the discovery of genetic predisposition
Jerome F. Strauss, Roberto Romero, Nardhy Gomez‐Lopez, et al.
American Journal of Obstetrics and Gynecology (2017) Vol. 218, Iss. 3, pp. 294-314.e2
Open Access | Times Cited: 131
Unique roles of rare variants in the genetics of complex diseases in humans
Yukihide Momozawa, Keijiro Mizukami
Journal of Human Genetics (2020) Vol. 66, Iss. 1, pp. 11-23
Open Access | Times Cited: 130
A Multiplexed Assay for Exon Recognition Reveals that an Unappreciated Fraction of Rare Genetic Variants Cause Large-Effect Splicing Disruptions
Rockie Chong, Kimberly D. Insigne, David Yao, et al.
Molecular Cell (2018) Vol. 73, Iss. 1, pp. 183-194.e8
Open Access | Times Cited: 113
Beyond large-effect loci: large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmon
Marion Sinclair‐Waters, Jørgen Ødegård, Sven Arild Korsvoll, et al.
Genetics Selection Evolution (2020) Vol. 52, Iss. 1
Open Access | Times Cited: 103
Genetic architecture of Alzheimer's disease
Sarah M. Neuner, Julia TCW, Alison Goate
Neurobiology of Disease (2020) Vol. 143, pp. 104976-104976
Open Access | Times Cited: 99
SPINK1 , PRSS1 , CTRC , and CFTR Genotypes Influence Disease Onset and Clinical Outcomes in Chronic Pancreatitis
Wen‐Bin Zou, Xin‐Ying Tang, Daizhan Zhou, et al.
Clinical and Translational Gastroenterology (2018) Vol. 9, Iss. 11, pp. e204-e204
Open Access | Times Cited: 94
NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population
Peng Zhang, Huaxia Luo, Yanyan Li, et al.
Cell Reports (2021) Vol. 37, Iss. 7, pp. 110017-110017
Open Access | Times Cited: 76
The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy
Ray E. Hershberger, Jason Cowan, Elizabeth Jordan, et al.
Circulation Research (2021) Vol. 128, Iss. 10, pp. 1514-1532
Open Access | Times Cited: 74
Variable number tandem repeats mediate the expression of proximal genes
Mehrdad Bakhtiari, Jonghun Park, Yuan-Chun Ding, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 72
Polygenic risk scores: An overview from bench to bedside for personalised medicine
Benjamin Cross, Richard Turner, Munir Pirmohamed
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 47
The Bovine Pangenome Consortium: democratizing production and accessibility of genome assemblies for global cattle breeds and other bovine species
Timothy P. L. Smith, Derek M. Bickhart, Didier Boichard, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 24
Massively parallel screen uncovers many rare 3′ UTR variants regulating mRNA abundance of cancer driver genes
Ting Fu, Kofi Amoah, Tracey W. Chan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
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