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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:

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Max Schubach, Thorben Maaß, Lusiné Nazaretyan, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. D1, pp. D1143-D1154
Open Access | Times Cited: 92

Showing 26-50 of 92 citing articles:

MATR3’s Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases
Jhune Rizsan Santos, Jeehye Park
Cells (2024) Vol. 13, Iss. 11, pp. 980-980
Open Access | Times Cited: 1
Exploring Stroke Risk through Mendelian Randomization: A Comprehensive Study Integrating Genetics and Metabolic Traits in the Korean Population
Hyo-Jeong Ban, Si-Woo Lee, Hee-Jeong Jin
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1311-1311
Open Access | Times Cited: 1
Benchmarking computational variant effect predictors by their ability to infer human traits
Daniel Tabet, Da Kuang, Megan Lancaster, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Case report: two novel PPARG pathogenic variants associated with type 3 familial partial lipodystrophy in Brazil
Monique Alvares da Silva, Reivla Marques Vasconcelos Soares, Antônio Fernandes de Oliveira Filho, et al.
Diabetology & Metabolic Syndrome (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder
Marla Mendes, D. Chen, Worrawat Engchuan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution
Fırat Özçelik, Mehmet Sait Dündar, Abdulbaki Yildirim, et al.
Functional & Integrative Genomics (2024) Vol. 24, Iss. 4
Closed Access | Times Cited: 1
Genetic Variants in Canonical Wnt Signaling Pathway Associated with Pediatric Immune Thrombocytopenia
Taylor Olmsted Kim, Jennifer M. Geris, Jonathan M. Flanagan, et al.
Blood Advances (2024) Vol. 8, Iss. 21, pp. 5529-5538
Open Access | Times Cited: 1
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum
Daniel G. Calame, Jovi Huixin Wong, Puravi Panda, et al.
Genetics in Medicine (2024) Vol. 27, Iss. 1, pp. 101273-101273
Closed Access | Times Cited: 1
Utility of exome sequencing in primary spermatogenic disorders: From research to diagnostics
Antoni Riera‐Escamilla, Liina Nagirnaja
Andrology (2024)
Closed Access | Times Cited: 1
Genetic Analysis of Heterotaxy in a Consanguineous Cohort
Maarab Alkorashy, Hadeel Binomar, Abeer Al‐Mostafa, et al.
Clinical Genetics (2024)
Closed Access | Times Cited: 1
Spectrum and Prevalence of Rare APOE Variants and Their Association with Familial Dysbetalipoproteinemia
А. В. Блохина, А. И. Ершова, А. В. Киселева, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 12651-12651
Open Access | Times Cited: 1
Exploring Aerobic Energy Metabolism in Breast Cancer: A Mutational Profile of Glycolysis and Oxidative Phosphorylation
Ricardo Cunha de Oliveira, Giovanna C. Cavalcante, Giordano B. Soares‐Souza
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 12585-12585
Open Access | Times Cited: 1
Alzheimer's Disease Sequencing Project Release 4 Whole Genome Sequencing Dataset
Yuk Yee Leung, Wan‐Ping Lee, Amanda B. Kuzma, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Chromosome X-wide common variant association study in autism spectrum disorder
Marla Mendes, D. Chen, Worrawat Engchuan, et al.
The American Journal of Human Genetics (2024)
Closed Access | Times Cited: 1
PSAP-genomic-regions: a method leveraging population data to prioritize coding and non-coding variants in whole genome sequencing for rare disease diagnosis
Marie‐Sophie C. Ogloblinsky, Ozvan Bocher, Chaker Aloui, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
From Sequence to Structure to Function: De Novo Protein Design, the Role of AI and Structure Prediction Neural Networks
Marcelo A. Kauffman
(2024)
Open Access
A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient
He Xiaohong, Peirun Tian, Lijuan Zhong, et al.
Hemoglobin (2024) Vol. 48, Iss. 3, pp. 203-208
Closed Access
Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits
Paola Nicoletti, Samreen Zafer, Lital Matok, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101851-101851
Open Access
A 37-Year-Old Man With Intellectual Disability Discovered to Have Aspartylglucosaminuria
Mutsuo Kouhashi, K Yukawa, Naoko Yano, et al.
Neurology Genetics (2024) Vol. 10, Iss. 3
Open Access
Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literature
Abolfazl Rad, Oliver Bartsch, Somayeh Bakhtiari, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 413-426
Open Access
Glucose transporter type 1 deficiency syndrome and paroxysmal exercise-induced dyskinesia
Rawan Matar, Danielle Tang, Samuel McCall, et al.
Practical Neurology (2024), pp. pn-004118
Closed Access
Familial Episodic Pain Syndrome: A Japanese Family Harboring the Novel Variant c.2431C>T (p.Leu811Phe) in SCN11A
Chioko Nagao, Hiroko Okuda, Gert‐Jan Bekker, et al.
Biochemical Genetics (2024)
Closed Access
Machine learning-based proteogenomic data modeling identifies circulating plasma biomarkers for early detection of lung cancer
Marcela A. Johnson, Liping Hou, Bevan E. Huang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Recessive loss‐of‐function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine–Lubinsky syndrome
Emily Waskow, Lisa Emrick, Jill A. Rosenfeld, et al.
American Journal of Medical Genetics Part A (2024) Vol. 197, Iss. 1
Closed Access
Abordagens alternativas para caracterização da arquitetura genética do transtorno do espectro autista
Claudia Ismania Samogy Costa
(2024)
Open Access

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