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:
Increasing accuracy of HLA imputation by a population-specific reference panel in a FinnGen biobank cohort
Jarmo Ritari, Kati Hyvärinen, Jonna Clancy, et al.
NAR Genomics and Bioinformatics (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 52
Jarmo Ritari, Kati Hyvärinen, Jonna Clancy, et al.
NAR Genomics and Bioinformatics (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 52
Showing 1-25 of 52 citing articles:
Genetic risk factors have a substantial impact on healthy life years
Sakari Jukarainen, Tuomo Kiiskinen, Sara Kuitunen, et al.
Nature Medicine (2022) Vol. 28, Iss. 9, pp. 1893-1901
Open Access | Times Cited: 40
Sakari Jukarainen, Tuomo Kiiskinen, Sara Kuitunen, et al.
Nature Medicine (2022) Vol. 28, Iss. 9, pp. 1893-1901
Open Access | Times Cited: 40
The Network Zoo: a multilingual package for the inference and analysis of gene regulatory networks
Marouen Ben Guebila, Tian Wang, Camila M. Lopes‐Ramos, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 24
Marouen Ben Guebila, Tian Wang, Camila M. Lopes‐Ramos, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 24
An immunogenetic basis for lung cancer risk
Chirag Krishna, Anniina Tervi, Miriam Saffern, et al.
Science (2024) Vol. 383, Iss. 6685
Closed Access | Times Cited: 15
Chirag Krishna, Anniina Tervi, Miriam Saffern, et al.
Science (2024) Vol. 383, Iss. 6685
Closed Access | Times Cited: 15
Genetic drivers and cellular selection of female mosaic X chromosome loss
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
Nature (2024) Vol. 631, Iss. 8019, pp. 134-141
Closed Access | Times Cited: 11
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
Nature (2024) Vol. 631, Iss. 8019, pp. 134-141
Closed Access | Times Cited: 11
HLA imputation and its application to genetic and molecular fine-mapping of the MHC region in autoimmune diseases
Tatsuhiko Naito, Yukinori Okada
Seminars in Immunopathology (2021) Vol. 44, Iss. 1, pp. 15-28
Open Access | Times Cited: 37
Tatsuhiko Naito, Yukinori Okada
Seminars in Immunopathology (2021) Vol. 44, Iss. 1, pp. 15-28
Open Access | Times Cited: 37
Immune system-wide Mendelian randomization and triangulation analyses support autoimmunity as a modifiable component in dementia-causing diseases
Joni V. Lindbohm, Nina Mars, Pyry N. Sipilä, et al.
Nature Aging (2022) Vol. 2, Iss. 10, pp. 956-972
Open Access | Times Cited: 26
Joni V. Lindbohm, Nina Mars, Pyry N. Sipilä, et al.
Nature Aging (2022) Vol. 2, Iss. 10, pp. 956-972
Open Access | Times Cited: 26
Epstein-Barr Virus in the Cerebrospinal Fluid and Blood Compartments of Patients With Multiple Sclerosis and Controls
Joonas Lehikoinen, Katariina Nurmi, Mari Ainola, et al.
Neurology Neuroimmunology & Neuroinflammation (2024) Vol. 11, Iss. 3
Closed Access | Times Cited: 4
Joonas Lehikoinen, Katariina Nurmi, Mari Ainola, et al.
Neurology Neuroimmunology & Neuroinflammation (2024) Vol. 11, Iss. 3
Closed Access | Times Cited: 4
Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer
Mary Pat Reeve, Mari Vehviläinen, Shuang Luo, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 1047-1060
Open Access | Times Cited: 4
Mary Pat Reeve, Mari Vehviläinen, Shuang Luo, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 1047-1060
Open Access | Times Cited: 4
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: 25
Venceslas Douillard, Erick C. Castelli, Steven J. Mack, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 25
Sequencing whole genomes of the West Javanese population in Indonesia reveals novel variants and improves imputation accuracy
Edwin Ardiansyah, Anca‐Lelia Riza, Sofiati Dian, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Edwin Ardiansyah, Anca‐Lelia Riza, Sofiati Dian, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Laura Mustonen, Janne Nieminen, Satu Koskela, et al.
European Journal of Pain (2025) Vol. 29, Iss. 4
Closed Access
Effects of parental autoimmune diseases on type 1 diabetes in offspring can be partially explained by HLA and non-HLA polymorphisms
Feiyi Wang, Aoxing Liu, Zhiyu Yang, et al.
Cell Genomics (2025), pp. 100854-100854
Open Access
Feiyi Wang, Aoxing Liu, Zhiyu Yang, et al.
Cell Genomics (2025), pp. 100854-100854
Open Access
Female-mediated selective sperm activation may remodel major histocompatibility complex-based mate choice decisions in humans
Annalaura Jokiniemi, Tanja Turunen, Mikko Kohonen, et al.
Heredity (2025)
Open Access
Annalaura Jokiniemi, Tanja Turunen, Mikko Kohonen, et al.
Heredity (2025)
Open Access
HLA-disease association and pleiotropy landscape in over 235,000 Finns
Jarmo Ritari, Satu Koskela, Kati Hyvärinen, et al.
Human Immunology (2022) Vol. 83, Iss. 5, pp. 391-398
Open Access | Times Cited: 16
Jarmo Ritari, Satu Koskela, Kati Hyvärinen, et al.
Human Immunology (2022) Vol. 83, Iss. 5, pp. 391-398
Open Access | Times Cited: 16
Genome Canada precision medicine strategy for structured national implementation of epitope matching in renal transplantation
Karen Sherwood, Jenny Tran, Oliver P. Günther, et al.
Human Immunology (2022) Vol. 83, Iss. 3, pp. 264-269
Open Access | Times Cited: 15
Karen Sherwood, Jenny Tran, Oliver P. Günther, et al.
Human Immunology (2022) Vol. 83, Iss. 3, pp. 264-269
Open Access | Times Cited: 15
Blood donor biobank as a resource in personalised biomedical genetic research
Jonna Clancy, Jarmo Ritari, Eevaleena Vaittinen, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 3
Jonna Clancy, Jarmo Ritari, Eevaleena Vaittinen, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 3
18th International HLA and Immunogenetics Workshop: Report on the SNP‐HLA Reference Consortium (SHLARC ) component
Nayane S. B. Silva, Sonia Bourguiba, Venceslas Douillard, et al.
HLA (2023) Vol. 103, Iss. 1
Open Access | Times Cited: 7
Nayane S. B. Silva, Sonia Bourguiba, Venceslas Douillard, et al.
HLA (2023) Vol. 103, Iss. 1
Open Access | Times Cited: 7
Mismatches in Gene Deletions and Kidney-related Proteins as Candidates for Histocompatibility Factors in Kidney Transplantation
Salla Markkinen, Ilkka Helanterä, Jouni Lauronen, et al.
Kidney International Reports (2022) Vol. 7, Iss. 11, pp. 2484-2494
Open Access | Times Cited: 11
Salla Markkinen, Ilkka Helanterä, Jouni Lauronen, et al.
Kidney International Reports (2022) Vol. 7, Iss. 11, pp. 2484-2494
Open Access | Times Cited: 11
Optimal population‐specific HLA imputation with dimension reduction
Venceslas Douillard, Nayane S. B. Silva, Sonia Bourguiba, et al.
HLA (2023) Vol. 103, Iss. 1
Open Access | Times Cited: 6
Venceslas Douillard, Nayane S. B. Silva, Sonia Bourguiba, et al.
HLA (2023) Vol. 103, Iss. 1
Open Access | Times Cited: 6
A machine-learning method for biobank-scale genetic prediction of blood group antigens
Kati Hyvärinen, Katri Haimila, Camous Moslemi, et al.
PLoS Computational Biology (2024) Vol. 20, Iss. 3, pp. e1011977-e1011977
Open Access | Times Cited: 2
Kati Hyvärinen, Katri Haimila, Camous Moslemi, et al.
PLoS Computational Biology (2024) Vol. 20, Iss. 3, pp. e1011977-e1011977
Open Access | Times Cited: 2
HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study
Mikael Koskela, Julia Nihtilä, Elisa Ylinen, et al.
Pediatric Nephrology (2021)
Open Access | Times Cited: 14
Mikael Koskela, Julia Nihtilä, Elisa Ylinen, et al.
Pediatric Nephrology (2021)
Open Access | Times Cited: 14
Welfare Genome Project: A Participatory Korean Personal Genome Project With Free Health Check-Up and Genetic Report Followed by Counseling
Yeonsu Jeon, Sungwon Jeon, Asta Blažytė, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 12
Yeonsu Jeon, Sungwon Jeon, Asta Blažytė, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 12
Blood donor biobank and HLA imputation as a resource for HLA homozygous cells for therapeutic and research use
Jonna Clancy, Kati Hyvärinen, Jarmo Ritari, et al.
Stem Cell Research & Therapy (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 8
Jonna Clancy, Kati Hyvärinen, Jarmo Ritari, et al.
Stem Cell Research & Therapy (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 8
Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Genetic risk factors have a substantial impact on healthy life years
Sakari Jukarainen, Tuomo Kiiskinen, Aki S. Havulinna, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
Sakari Jukarainen, Tuomo Kiiskinen, Aki S. Havulinna, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
