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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 intronic branch point sequence is under strong evolutionary constraint in the bovine and human genome
Naveen Kumar Kadri, Xena Marie Mapel, Hubert Pausch
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 24

Showing 24 citing articles:

Graph construction method impacts variation representation and analyses in a bovine super-pangenome
Alexander S. Leonard, Danang Crysnanto, Xena Marie Mapel, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 28
Genome-wide detection of human variants that disrupt intronic branchpoints
Peng Zhang, Quentin Philippot, Weicheng Ren, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 44
Open Access | Times Cited: 36
A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project
Alexander J. M. Blakes, Htoo A. Wai, Ian Davies, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 32
Practical Recommendations for the Selection of Patients for Individualized Splice-Switching ASO-Based Treatments
Bianca Zardetto, Marlen C. Lauffer, Willeke M. C. van Roon‐Mom, et al.
Human Mutation (2024) Vol. 2024, pp. 1-13
Open Access | Times Cited: 3
The nature and pathological impact of the c.1748A > G variant of the neurofibromin 1 gene
Ji‐Young Lee, Eun Sook Kim, Su Yeon Kim, et al.
Gene (2025), pp. 149381-149381
Closed Access
Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression in human B cells
Y. Nagura, Mihoko Shimada, Ryoji Kuribayashi, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
A 1-bp deletion in bovine QRICH2 causes low sperm count and immotile sperm with multiple morphological abnormalities
Maya Hiltpold, Fredi Janett, Xena Marie Mapel, et al.
Genetics Selection Evolution (2022) Vol. 54, Iss. 1
Open Access | Times Cited: 11
Review: Genetic mutations affecting bull fertility
Hubert Pausch, Xena Marie Mapel
animal (2023) Vol. 17, pp. 100742-100742
Open Access | Times Cited: 6
Structural variants and short tandem repeats impact gene expression and splicing in bovine testis tissue
Meenu Bhati, Xena Marie Mapel, Audald Lloret-Villas, et al.
Genetics (2023) Vol. 225, Iss. 3
Open Access | Times Cited: 5
From the comparative study of a circRNA originating from an mammalian ATXN2L intron to understanding the genesis of intron lariat-derived circRNAs
Annie Robic, Chloé Cerutti, Julie Demars, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2022) Vol. 1865, Iss. 4, pp. 194815-194815
Open Access | Times Cited: 8
On a kneading theory for gene-splicing
Ethan Speakman, Gemunu H. Gunaratne
Chaos An Interdisciplinary Journal of Nonlinear Science (2024) Vol. 34, Iss. 4
Open Access | Times Cited: 1
Introns with branchpoint-distant 3′ splice sites: Splicing mechanism and regulatory roles
Anupa T Anil, Rakesh Pandian, Shravan Kumar Mishra
Biophysical Chemistry (2024) Vol. 314, pp. 107307-107307
Closed Access | Times Cited: 1
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1
Pilar Álvarez Jerez, Peter Wild Crea, Daniel M. Ramos, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Splicing of branchpoint-distant exons is promoted by Cactin, Tls1 and the ubiquitin-fold-activated Sde2
Anupa T Anil, Karan Choudhary, Rakesh Pandian, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 17, pp. 10000-10014
Open Access | Times Cited: 6
Graph construction method impacts variation representation and analyses in a bovine super-pangenome
Alexander S. Leonard, Danang Crysnanto, Xena Marie Mapel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 6
Characterization of intronic SNP located in candidate genes influencing cattle temperament
Gilberto Ruiz-De-La-Cruz, Ana María Sifuentes‐Rincón, Francisco Alejandro Paredes-Sánchez, et al.
Revista Brasileira de Zootecnia (2023) Vol. 52
Open Access | Times Cited: 3
Exploiting public databases of genomic variation to quantify evolutionary constraint on the branch point sequence in 30 plant and animal species
Adéla Nosková, Chao Li, Xiaolong Wang, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 22, pp. 12069-12075
Open Access | Times Cited: 2
A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project
Alexander J. M. Blakes, Htoo A. Wai, Ian Davies, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Mechanisms of RNA alternative splicing dysregulation in triple-negative breast cancer.
Zi-Yu Cao, Yingrui Li
PubMed (2024) Vol. 49, Iss. 7, pp. 1143-1154
Closed Access
Structural variants and short tandem repeats impact gene expression and splicing in bovine testis tissue
Meenu Bhati, Xena Marie Mapel, Audald Lloret-Villas, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Harnessing ADAR-Mediated Site-Specific RNA Editing in Immune-Related Disease: Prediction and Therapeutic Implications
Shenghui Weng, Xinyi Yang, Nan-Nan Yu, et al.
International Journal of Molecular Sciences (2023) Vol. 25, Iss. 1, pp. 351-351
Open Access | Times Cited: 1
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1
Pilar Álvarez Jerez, Peter Wild Crea, Daniel M. Ramos, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 12, pp. 1955-1963
Open Access
Genome-wide detection of human variants that disrupt intronic branchpoints
Peng Zhang, Quentin Philippot, Weicheng Ren, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
533. Conserved non-coding elements of the bovine genome
Naveen Kumar Kadri, Hubert Pausch
(2022), pp. 2212-2215
Open Access
548. eQTL mapping in Brown Swiss bulls to identify variants associated with male fertility
Xena Marie Mapel, Maya Hiltpold, Audald Lloret-Villas, et al.
(2022), pp. 2273-2276
Open Access
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