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:
Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases Database
Charlotte Nachtegael, Barbara Gravel, Arnau Dillen, et al.
Database (2022) Vol. 2022
Open Access | Times Cited: 27
Charlotte Nachtegael, Barbara Gravel, Arnau Dillen, et al.
Database (2022) Vol. 2022
Open Access | Times Cited: 27
Showing 1-25 of 27 citing articles:
Implications of combined NOD2 and other gene mutations in autoinflammatory diseases
Hafsa Nomani, Zuoming Deng, Brianne Navetta-Modrov, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 15
Hafsa Nomani, Zuoming Deng, Brianne Navetta-Modrov, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 15
A knowledge graph approach to predict and interpret disease-causing gene interactions
Alexandre Renaux, Chloé Terwagne, Michael Cochez, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 13
Alexandre Renaux, Chloé Terwagne, Michael Cochez, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 13
Oligogenic basis of premature ovarian insufficiency: an observational study
Panpan Long, Le Wang, Hang-Jing Tan, et al.
Journal of Ovarian Research (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 5
Panpan Long, Le Wang, Hang-Jing Tan, et al.
Journal of Ovarian Research (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 5
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards
Jevin Parmar, Nigel G. Laing, Marina Kennerson, et al.
Journal of Neurology Neurosurgery & Psychiatry (2024) Vol. 95, Iss. 11, pp. 992-1001
Open Access | Times Cited: 5
Jevin Parmar, Nigel G. Laing, Marina Kennerson, et al.
Journal of Neurology Neurosurgery & Psychiatry (2024) Vol. 95, Iss. 11, pp. 992-1001
Open Access | Times Cited: 5
Development of multiplexed orthogonal base editor (MOBE) systems
Quinn T. Cowan, Sifeng Gu, Wanjun Gu, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 5
Quinn T. Cowan, Sifeng Gu, Wanjun Gu, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 5
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Faster and more accurate pathogenic combination predictions with VarCoPP2.0
Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 11
Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 11
Early-Onset Ovarian Cancer <30 Years: What Do We Know about Its Genetic Predisposition?
Klara Horáčková, Markéta Janatová, Petra Kleiblová, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17020-17020
Open Access | Times Cited: 11
Klara Horáčková, Markéta Janatová, Petra Kleiblová, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17020-17020
Open Access | Times Cited: 11
Genetic variations in NLRP3 and NLRP12 genes in adult-onset patients with autoinflammatory diseases: a comparative study
Mark Yun, Zuoming Deng, Brianne Navetta-Modrov, et al.
Frontiers in Immunology (2024) Vol. 14
Open Access | Times Cited: 4
Mark Yun, Zuoming Deng, Brianne Navetta-Modrov, et al.
Frontiers in Immunology (2024) Vol. 14
Open Access | Times Cited: 4
Digenic variant interpretation with hypothesis-driven explainable AI
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
NAR Genomics and Bioinformatics (2025) Vol. 7, Iss. 2
Open Access
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
NAR Genomics and Bioinformatics (2025) Vol. 7, Iss. 2
Open Access
Benchmark of computational methods to detect digenism in sequencing data
Marie‐Sophie C. Ogloblinsky, Donald F. Conrad, Anaı̈s Baudot, et al.
European Journal of Human Genetics (2025)
Closed Access
Marie‐Sophie C. Ogloblinsky, Donald F. Conrad, Anaı̈s Baudot, et al.
European Journal of Human Genetics (2025)
Closed Access
Prioritization of oligogenic variant combinations in whole exomes
Barbara Gravel, Alexandre Renaux, Sofia Papadimitriou, et al.
Bioinformatics (2024) Vol. 40, Iss. 4
Open Access | Times Cited: 3
Barbara Gravel, Alexandre Renaux, Sofia Papadimitriou, et al.
Bioinformatics (2024) Vol. 40, Iss. 4
Open Access | Times Cited: 3
Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases
Sofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, et al.
Human Genetics and Genomics Advances (2022) Vol. 4, Iss. 1, pp. 100165-100165
Open Access | Times Cited: 13
Sofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, et al.
Human Genetics and Genomics Advances (2022) Vol. 4, Iss. 1, pp. 100165-100165
Open Access | Times Cited: 13
Digenic Inheritance in Rare Disorders and Mitochondrial Disease—Crossing the Frontier to a More Comprehensive Understanding of Etiology
Christiane Neuhofer, Holger Prokisch
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4602-4602
Open Access | Times Cited: 2
Christiane Neuhofer, Holger Prokisch
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4602-4602
Open Access | Times Cited: 2
DUVEL: an active-learning annotated biomedical corpus for the recognition of oligogenic combinations
Charlotte Nachtegael, Jacopo De Stefani, Anthony Cnudde, et al.
Database (2024) Vol. 2024
Open Access | Times Cited: 2
Charlotte Nachtegael, Jacopo De Stefani, Anthony Cnudde, et al.
Database (2024) Vol. 2024
Open Access | Times Cited: 2
Digenic variant interpretation with hypothesis-driven explainable AI
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
VUStruct: a compute pipeline for high throughput and personalized structural biology
Christopher W. Moth, Jonathan H. Sheehan, Abdullah Al Mamun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Christopher W. Moth, Jonathan H. Sheehan, Abdullah Al Mamun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Toward Accessible Reproductive Genetic Carrier Screening
Erin Tutty, Alison D. Archibald, Tiffany Boughtwood, et al.
Advances in Molecular Pathology (2024) Vol. 7, Iss. 1, pp. 1-14
Closed Access | Times Cited: 1
Erin Tutty, Alison D. Archibald, Tiffany Boughtwood, et al.
Advances in Molecular Pathology (2024) Vol. 7, Iss. 1, pp. 1-14
Closed Access | Times Cited: 1
Detection of Major Mutations in CFTR, SERPINA1, HFE Genes in Benign Unconjugated Hyperbilirubinemia Phenotype
А. А. Иванова, N. E. Apartseva, А. П. Каширина, et al.
Sovremennye tehnologii v medicine (2024) Vol. 16, Iss. 4, pp. 38-38
Open Access | Times Cited: 1
А. А. Иванова, N. E. Apartseva, А. П. Каширина, et al.
Sovremennye tehnologii v medicine (2024) Vol. 16, Iss. 4, pp. 38-38
Open Access | Times Cited: 1
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype
Ellen Knierim, Johannes Vogt, Michael Kintscher, et al.
Cerebral Cortex (2023) Vol. 33, Iss. 12, pp. 7454-7467
Closed Access | Times Cited: 2
Ellen Knierim, Johannes Vogt, Michael Kintscher, et al.
Cerebral Cortex (2023) Vol. 33, Iss. 12, pp. 7454-7467
Closed Access | Times Cited: 2
Molecular genetic mechanisms of neurodevelopmental and neurodegenerative disease
Daniel G. Calame, Dana Marafi, James R. Lupski
Elsevier eBooks (2024), pp. 17-37
Closed Access
Daniel G. Calame, Dana Marafi, James R. Lupski
Elsevier eBooks (2024), pp. 17-37
Closed Access
Complex Disease Prediction Using Systems Biology Approach
H. R. Meghashree, Saravanan Yuvaraj, Sunitha C. Mesta, et al.
(2024), pp. 415-435
Closed Access
H. R. Meghashree, Saravanan Yuvaraj, Sunitha C. Mesta, et al.
(2024), pp. 415-435
Closed Access
Variant Impact Predictor database (VIPdb), version 2: Trends from 25 years of genetic variant impact predictors
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Modern approaches to the assessment of individual risk of CHD development: status, problems, prospects
В. Н. Максимов, S. V. Minnikh, А. А. Иванова
Ateroscleroz (2024) Vol. 20, Iss. 2, pp. 154-161
Open Access
В. Н. Максимов, S. V. Minnikh, А. А. Иванова
Ateroscleroz (2024) Vol. 20, Iss. 2, pp. 154-161
Open Access
Exploring the Genotype–Phenotype Correlations in a Child with Inherited Seizure and Thrombocytopenia by Digenic Network Analysis
Shuanglong Lu, Zhixiao Niu, Xiaohong Qiao
Genes (2024) Vol. 15, Iss. 8, pp. 1004-1004
Open Access
Shuanglong Lu, Zhixiao Niu, Xiaohong Qiao
Genes (2024) Vol. 15, Iss. 8, pp. 1004-1004
Open Access
