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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:

Bioinformatics Strategies, Challenges, and Opportunities for Next Generation Sequencing-Based HLA Genotyping
Steffen Klasberg, Vineeth Surendranath, Vinzenz Lange, et al.
Transfusion Medicine and Hemotherapy (2019) Vol. 46, Iss. 5, pp. 312-325
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

Next-generation sequencing technologies: An overview
Taishan Hu, Nilesh Chitnis, Dimitri Monos, et al.
Human Immunology (2021) Vol. 82, Iss. 11, pp. 801-811
Closed Access | Times Cited: 587
NovAT tool—Reliable novel HLA alleles identification from next‐generation sequencing data
Tamara Simakova, Arina Suvorova, Kristina Krivonosova, et al.
HLA (2021) Vol. 99, Iss. 1, pp. 3-11
Closed Access | Times Cited: 72
The polymorphism of HLA‐A, ‐C, ‐B, ‐DRB3/4/5, ‐DRB1, ‐DQB1 loci in Zhejiang Han population, China using NGS technology
Fang Wang, Lina Dong, Wei Wang, et al.
International Journal of Immunogenetics (2021) Vol. 48, Iss. 6, pp. 485-489
Open Access | Times Cited: 70
Human Leukocyte Antigen (HLA) System: Genetics and Association with Bacterial and Viral Infections
Sadeep Medhasi, Narisara Chantratita
Journal of Immunology Research (2022) Vol. 2022, pp. 1-15
Open Access | Times Cited: 59
Applying Next-Generation Sequencing Platforms for Pharmacogenomic Testing in Clinical Practice
Alireza Tafazoli, Henk‐Jan Guchelaar, Wojciech Miltyk, et al.
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 44
Benchmark of tools for in silico prediction of MHC class I and class II genotypes from NGS data
A. Claeys, Peter Merseburger, Jasper Staut, et al.
BMC Genomics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 17
Germline immunoglobulin genes: Disease susceptibility genes hidden in plain sight?
Andrew M. Collins, Gur Yaari, Adrian J. Shepherd, et al.
Current Opinion in Systems Biology (2020) Vol. 24, pp. 100-108
Open Access | Times Cited: 41
High-resolution HLA typing by long reads from the R10.3 Oxford nanopore flow cells
Chang Liu, Xiao Yang, Brian Duffy, et al.
Human Immunology (2021) Vol. 82, Iss. 4, pp. 288-295
Closed Access | Times Cited: 39
New challenges, new opportunities: Next generation sequencing and its place in the advancement of HLA typing
Valia Bravo-Egaña, Holly Sanders, Nilesh Chitnis
Human Immunology (2021) Vol. 82, Iss. 7, pp. 478-487
Closed Access | Times Cited: 35
Artificial intelligence and neoantigens: paving the path for precision cancer immunotherapy
Alla Bulashevska, Zsófia Nacsa, Franziska Lang, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 5
A long road/read to rapid high-resolution HLA typing: The nanopore perspective
Chang Liu
Human Immunology (2020) Vol. 82, Iss. 7, pp. 488-495
Open Access | Times Cited: 38
Perspective Chapter: Decoding the Complexity of HLA Genes – The Heart of Modern Immunogenetics
Andreea Mirela Caragea, Laurențiu Camil Bohîlțea, Alexandra Elena Constantinescu, et al.
IntechOpen eBooks (2025)
Closed Access
Reference Grade Characterization of Polymorphisms in Full-Length HLA Class I and II Genes With Short-Read Sequencing on the ION PGM System and Long-Reads Generated by Single Molecule, Real-Time Sequencing on the PacBio Platform
Shingo Suzuki, Swati Ranade, Ken Osaki, et al.
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 33
Major histocompatibility complex (MHC) associations with diseases in ethnic groups of the Arabian Peninsula
Halima Al Naqbi, Aurélie Mawart, Jawaher Alshamsi, et al.
Immunogenetics (2021) Vol. 73, Iss. 2, pp. 131-152
Open Access | Times Cited: 24
Approaching Genetics Through the MHC Lens: Tools and Methods for HLA Research
Venceslas Douillard, Erick C. Castelli, Steven J. Mack, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 24
Full resolution HLA and KIR genes annotation for human genome assemblies
Ying Zhou, Li Song, Heng Li
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Matchmaker, matchmaker make me a match: Opportunities and challenges in optimizing compatibility of HLA eplets in transplantation
William Lemieux, Hossein Mohammadhassanzadeh, William Klement, et al.
International Journal of Immunogenetics (2021) Vol. 48, Iss. 2, pp. 135-144
Closed Access | Times Cited: 23
Benchmarking freely available HLA typing algorithms across varying genes, coverages and typing resolutions
Nikolas Hallberg Thuesen, Michael Schantz Klausen, Shyam Gopalakrishnan, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 16
Personalized HLA typing leads to the discovery of novel HLA alleles and tumor‐specific HLA variants
Irantzu Anzar, Angelina Sverchkova, Pubudu Samarakoon, et al.
HLA (2022) Vol. 99, Iss. 4, pp. 313-327
Open Access | Times Cited: 12
Advancements and hurdles in the development of a vaccine for triple-negative breast cancer: A comprehensive review of multi-omics and immunomics strategies
T Dhanushkumar, Santhosh Mukundan, Prasanna Kumar Selvam, et al.
Life Sciences (2023) Vol. 337, pp. 122360-122360
Closed Access | Times Cited: 6
NGS and HLA: The long road ahead
Kelly J. Ingram, Elaine F. O’Shields, David F. Kiger, et al.
Human Immunology (2020) Vol. 81, Iss. 6, pp. 280-284
Closed Access | Times Cited: 14
Automated Pharmacogenomic Reports for Clinical Genome Sequencing
Barbara J. Klanderman, Christopher Koch, Kalotina Machini, et al.
Journal of Molecular Diagnostics (2022) Vol. 24, Iss. 3, pp. 205-218
Open Access | Times Cited: 8
Risk-conferringHLAvariants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice
Angeliki Vakrinou, Ravishankara Bellampalli, Medine I. Gulcebi, et al.
Journal of Neurology Neurosurgery & Psychiatry (2023) Vol. 94, Iss. 11, pp. 887-892
Open Access | Times Cited: 4
Can long-read sequencing tackle the barriers, which the next-generation could not? A review
Nikolett Szakállas, Barbara Kinga Barták, Gábor Valcz, et al.
Pathology & Oncology Research (2024) Vol. 30
Open Access | Times Cited: 1
PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and Interpretation
Jittima Piriyapongsa, Chanathip Sukritha, Pavita Kaewprommal, et al.
Journal of Personalized Medicine (2021) Vol. 11, Iss. 11, pp. 1230-1230
Open Access | Times Cited: 10
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