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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:

Measuring intolerance to mutation in human genetics
Zachary L. Fuller, Jeremy J. Berg, Hakhamanesh Mostafavi, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 772-776
Open Access | Times Cited: 123

Showing 1-25 of 123 citing articles:

The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 434-443
Open Access | Times Cited: 8031
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1305-1319
Open Access | Times Cited: 266
Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 161
Evaluating drug targets through human loss-of-function genetic variation
Eric Vallabh Minikel, Konrad J. Karczewski, Hilary C. Martin, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 459-464
Open Access | Times Cited: 160
Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia
Eric J. Duncavage, Adam Bagg, Robert P. Hasserjian, et al.
Blood (2022) Vol. 140, Iss. 21, pp. 2228-2247
Open Access | Times Cited: 145
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
Mendelian inheritance revisited: dominance and recessiveness in medical genetics
Johannes Zschocke, Peter H. Byers, Andrew O.M. Wilkie
Nature Reviews Genetics (2023) Vol. 24, Iss. 7, pp. 442-463
Closed Access | Times Cited: 54
Bayesian estimation of gene constraint from an evolutionary model with gene features
Tony Zeng, Jeffrey P. Spence, Hakhamanesh Mostafavi, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1632-1643
Open Access | Times Cited: 28
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Sun, Xiaodong Bai, Siying Chen, et al.
Nature (2024) Vol. 631, Iss. 8021, pp. 583-592
Open Access | Times Cited: 25
Causal Genetic Variants in Stillbirth
Kate E. Stanley, Jessica L. Giordano, Vanessa Thorsten, et al.
New England Journal of Medicine (2020) Vol. 383, Iss. 12, pp. 1107-1116
Open Access | Times Cited: 95
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 90
The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel
Xiao Mao, Nadine Bruneau, Quwen Gao, et al.
Frontiers in Cellular Neuroscience (2020) Vol. 14
Open Access | Times Cited: 82
Transcription factor protein interactomes reveal genetic determinants in heart disease
Bárbara González‐Terán, Maureen Pittman, Franco Felix, et al.
Cell (2022) Vol. 185, Iss. 5, pp. 794-814.e30
Open Access | Times Cited: 62
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance
Franck Rapaport, Bertrand Boisson, Anne Gregor, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 3
Open Access | Times Cited: 57
Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies
Alexander S. Leonard, Danang Crysnanto, Zih‐Hua Fang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 45
The impact of rare protein coding genetic variation on adult cognitive function
Chia‐Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 927-938
Open Access | Times Cited: 43
Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs
Ipsita Agarwal, Zachary L. Fuller, Simon Myers, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 36
Causes and effects of haploinsufficiency
Adam F. Johnson, Há Thi Nguyen, Reiner A. Veitia
Biological reviews/Biological reviews of the Cambridge Philosophical Society (2019) Vol. 94, Iss. 5, pp. 1774-1785
Closed Access | Times Cited: 58
The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects
Hila Fridman, Helger G. Yntema, Reedik Mägi, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 608-619
Open Access | Times Cited: 53
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
Takaki Asano, Joëlle Khourieh, Peng Zhang, et al.
The Journal of Experimental Medicine (2021) Vol. 218, Iss. 8
Open Access | Times Cited: 42
Extreme purifying selection against point mutations in the human genome
Noah Dukler, Mehreen R. Mughal, Ritika Ramani, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 33
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort
Aaron Alexander‐Bloch, Guillaume Huguet, Laura M. Schultz, et al.
JAMA Psychiatry (2022) Vol. 79, Iss. 7, pp. 699-699
Open Access | Times Cited: 30
Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants
Kohei Hamanaka, Noriko Miyake, Takeshi Mizuguchi, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 29
Genomic Underpinnings of Population Persistence in Isle Royale Moose
Christopher C. Kyriazis, Annabel C. Beichman, Kristin E. Brzeski, et al.
Molecular Biology and Evolution (2023) Vol. 40, Iss. 2
Open Access | Times Cited: 23
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences
Mamiko Yamada, Yohei Nitta, Tomoko Uehara, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 8, pp. 104804-104804
Open Access | Times Cited: 20
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