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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:

From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health
Jesse D. Riordan, Joseph H. Nadeau
The American Journal of Human Genetics (2017) Vol. 101, Iss. 2, pp. 177-191
Open Access | Times Cited: 134

Showing 51-75 of 134 citing articles:

Developmental processes regulate craniofacial variation in disease and evolution
Fjodor Merkuri, Jennifer L. Fish
genesis (2018) Vol. 57, Iss. 1
Open Access | Times Cited: 16
Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype
Drenushe Zhuri̇, Hakan Gürkan, Damla Eker, et al.
Global Medical Genetics (2022) Vol. 09, Iss. 03, pp. 226-236
Open Access | Times Cited: 9
A genome-wide CRISPR screen identifies DPM1 as a modifier of DPAGT1 deficiency and ER stress
Hans M. Dalton, Raghuvir Viswanatha, Roderick Brathwaite, et al.
PLoS Genetics (2022) Vol. 18, Iss. 9, pp. e1010430-e1010430
Open Access | Times Cited: 9
Lnc-EPB41-Protein Interactions Associated with Congenital Pouch Colon
Sonal Gupta, Nidhi Gupta, Pradeep Tiwari, et al.
Biomolecules (2018) Vol. 8, Iss. 3, pp. 95-95
Open Access | Times Cited: 14
DNA repair in trinucleotide repeat ataxias
Wai Yan Yau, Emer O’Connor, Roisin Sullivan, et al.
FEBS Journal (2018) Vol. 285, Iss. 19, pp. 3669-3682
Open Access | Times Cited: 13
Validation and Classification of Atypical Splicing Variants Associated With Osteogenesis Imperfecta
Lulu Li, Yixuan Cao, Feiyue Zhao, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 13
Cryptic genetic variation of expression quantitative trait locus architecture revealed by genetic perturbation in Caenorhabditis elegans
Marijke H. van Wijk, Joost A. G. Riksen, Mark Elvin, et al.
G3 Genes Genomes Genetics (2023) Vol. 13, Iss. 5
Open Access | Times Cited: 4
Genetic Modifiers at the Crossroads of Personalised Medicine for Haemoglobinopathies
Coralea Stephanou, Stella Tamana, Anna Minaidou, et al.
Journal of Clinical Medicine (2019) Vol. 8, Iss. 11, pp. 1927-1927
Open Access | Times Cited: 12
Disease-linked mutations in Munc18-1 deplete synaptic Doc2
Noah Guy Lewis Guiberson, Luca S Black, Jillian E. Haller, et al.
Brain (2024) Vol. 147, Iss. 6, pp. 2185-2202
Open Access | Times Cited: 1
Bmpr1aa modulates the severity of the skeletal phenotype in an fkbp10-deficient Bruck syndrome zebrafish model
Tamara Jarayseh, Sophie Debaenst, Hanna De Saffel, et al.
Journal of Bone and Mineral Research (2024) Vol. 40, Iss. 1, pp. 154-166
Closed Access | Times Cited: 1
DominantRDH12-retinitis pigmentosa impairs photoreceptor development and cone function in retinal organoids
Cécile Méjécase, Ya Zhou, Nicholas Owen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Full genetic analysis for genome-wide association study of Fangji: a powerful approach for effectively dissecting the molecular architecture of personalized traditional Chinese medicine
Gang Chen, Wenda Xue, Jun Zhu
Acta Pharmacologica Sinica (2018) Vol. 39, Iss. 6, pp. 906-911
Open Access | Times Cited: 10
An Imperative Need for Further Genetic Studies of Alopecia Areata
Lynn Petukhova
Journal of Investigative Dermatology Symposium Proceedings (2020) Vol. 20, Iss. 1, pp. S22-S27
Open Access | Times Cited: 10
The complex role of genetic background in shaping the effects of spontaneous and induced mutations
Ilan Goldstein, Ian M. Ehrenreich
Yeast (2020) Vol. 38, Iss. 3, pp. 187-196
Open Access | Times Cited: 10
Pairwise effects between lipid GWAS genes modulate lipid plasma levels and cellular uptake
M. Zimoń, Yunfeng Huang, Anthi Trasta, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 9
The Fbn1 gene variant governs passive ascending aortic mechanics in the mgΔlpn mouse model of Marfan syndrome when superimposed to perlecan haploinsufficiency
Samar A. Tarraf, Rodrigo Barbosa de Souza, Ashley Herrick, et al.
Frontiers in Cardiovascular Medicine (2024) Vol. 11
Open Access | Times Cited: 1
An in vitro neurogenetics platform for precision disease modeling in the mouse
Daniel Cortés, Mélanie Escudero, Austin C. Korgan, et al.
Science Advances (2024) Vol. 10, Iss. 14
Open Access | Times Cited: 1
Design principles of multi-map variation in biological systems
Juan F. Poyatos
Physical Biology (2024) Vol. 21, Iss. 4, pp. 043001-043001
Open Access | Times Cited: 1
Lesch-Nyhan disease: I. Construction of expression vectors for hypoxanthine-guanine phosphoribosyltransferase (HGprt) enzyme and amyloid precursor protein (APP)
Khue Vu Nguyen, Robert K. Naviaux, William L. Nyhan
Nucleosides Nucleotides & Nucleic Acids (2020) Vol. 39, Iss. 6, pp. 905-922
Closed Access | Times Cited: 9
Genetic modifiers and phenotypic variability in neuromuscular disorders
Magdalena Mroczek, Maria Gabriela Sanchez
Journal of Applied Genetics (2020) Vol. 61, Iss. 4, pp. 547-558
Closed Access | Times Cited: 9
Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies
Ionut-Florin Iancu, Irene Perea‐Romero, Gonzalo Núñez‐Moreno, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8431-8431
Open Access | Times Cited: 6
Turning strains into strengths for understanding psychiatric disorders
Shannon J. Moore, Geoffrey G. Murphy, Victor A. Cazares
Molecular Psychiatry (2020) Vol. 25, Iss. 12, pp. 3164-3177
Open Access | Times Cited: 8
Candidate Genetic Modifiers for RPGR Retinal Degeneration
Tatyana Appelbaum, Leonardo Murgiano, Doreen Becker, et al.
Investigative Ophthalmology & Visual Science (2020) Vol. 61, Iss. 14, pp. 20-20
Open Access | Times Cited: 8
Influence of allelic differences in Down syndrome
Randall J. Roper, Laura E. Hawley, Charles R. Goodlett
Progress in brain research (2020), pp. 29-54
Open Access | Times Cited: 7
Moderating Role of Stress, Anxiety, and Depression in the Relationship Between Tinnitus and Hearing Loss Among Patients
Ammar Ahmed, Muhammad Aqeel, Tanvir Akhtar, et al.
Pakistan Journal of Psychological Research (2020) Vol. 34, Iss. 4, pp. 753-772
Closed Access | Times Cited: 7

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