Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Scalable co-sequencing of RNA and DNA from individual nuclei
Timothy R. Olsen, Pranay Talla, Julia Furnari, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 20

Showing 20 citing articles:

Sequencing by avidity enables high accuracy with low reagent consumption
Sinan Arslan, Francisco J. Blanco García, Minghao Guo, et al.
Nature Biotechnology (2023) Vol. 42, Iss. 1, pp. 132-138
Open Access | Times Cited: 41
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
Livius Penter, Mehdi Borji, Adi Nagler, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 12
scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Sarah Cooper, Matthew A. Coelho, Magdalena E. Strauß, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 9
Computational Biology Helps Understand How Polyploid Giant Cancer Cells Drive Tumor Success
Matheus Correia Casotti, Débora Dummer Meira, Aléxia Stefani Siqueira Zetum, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 801-801
Open Access | Times Cited: 15
Analyzing the functional effects of DNA variants with gene editing
Sarah Cooper, Sofia Obolenski, Andrew Waters, et al.
Cell Reports Methods (2024) Vol. 4, Iss. 5, pp. 100776-100776
Open Access | Times Cited: 4
Single-cell mapping of regulatory DNA:Protein interactions
Wei-Yu Chi, Sang-Ho Yoon, Levan Mekerishvili, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Innovations in Short-Read Sequencing Technologies and Their Applications to Clinical Genomics
Katarzyna Polonis, Joseph H. Blommel, Andrew Hughes, et al.
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 97-108
Closed Access
Multimodal hierarchical classification of CITE-seq data delineates immune cell states across lineages and tissues
Daniel P. Caron, William L. Specht, David Chen, et al.
Cell Reports Methods (2025), pp. 100938-100938
Open Access
Exploring genome-transcriptome correlations in cancer
Michael Ronemus, Daniel W. Bradford, Zvi Laster, et al.
Biochemical Society Transactions (2025) Vol. 53, Iss. 01
Closed Access
Concepts and new developments in droplet-based single cell multi-omics
Arthur Chow, Caleb A. Lareau
Trends in biotechnology (2024) Vol. 42, Iss. 11, pp. 1379-1395
Closed Access | Times Cited: 3
Multimodal hierarchical classification of CITE-seq data delineates immune cell states across lineages and tissues
Daniel P. Caron, William L. Specht, David Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 8
Defining the function of disease variants with CRISPR editing and multimodal single cell sequencing
Yuriy Baglaenko, Michelle Curtis, Majd Al Suqri, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
CaClust: linking genotype to transcriptional heterogeneity of follicular lymphoma using BCR and exomic variants
Kazimierz Oksza-Orzechowski, Edwin Quinten, Shadi Darvish-Shafighi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Functional phenotyping of genomic variants using multiomic scDNA-scRNA-seq
Dominik Lindenhofer, Julia Bauman, John A. Hawkins, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Targeted mutagenesis of specific genomic DNA sequences in animals for thein vivogeneration of variant libraries
Julia Falo Sanjuan, Yuliana Diaz-Tirado, Meghan A. Turner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Revealing gene function with statistical inference at single-cell resolution
Cole Trapnell
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 623-638
Closed Access
Cell sorting based on single nucleotide variation enables characterization of mutation-dependent transcriptome and chromatin states
Roberto Salatino, Marianna Franco, Arantxa Romero-Toledo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
CaClust: linking genotype to transcriptional heterogeneity of follicular lymphoma using BCR and exomic variants
Kazimierz Oksza-Orzechowski, Edwin Quinten, Shadi Darvish Shafighi, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access
Echidna: A Bayesian framework for quantifying gene dosage effect impacting phenotypic plasticity
Joy Linyue Fan, Mingxuan Zhang, William E. O’Brien, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
HIPSD&R-seq enables scalable genomic copy number and transcriptome profiling
Olga Lazareva, Jan‐Philipp Mallm, Milena Simovic-Lorenz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top