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:

The Role of Noncoding Variants in Heritable Disease
Juliet D. French, Stacey L. Edwards
Trends in Genetics (2020) Vol. 36, Iss. 11, pp. 880-891
Closed Access | Times Cited: 88

Showing 1-25 of 88 citing articles:

Gene–environment interactions and their impact on human health
Samuel J. Virolainen, Andrew VonHandorf, Kenyatta C. M. F. Viel, et al.
Genes and Immunity (2022) Vol. 24, Iss. 1, pp. 1-11
Open Access | Times Cited: 146
The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models
Joel Rozowsky, Jiahao Gao, Beatrice Borsari, et al.
Cell (2023) Vol. 186, Iss. 7, pp. 1493-1511.e40
Open Access | Times Cited: 54
Impact of Lineage Plasticity to and from a Neuroendocrine Phenotype on Progression and Response in Prostate and Lung Cancers
Mark A. Rubin, Robert G. Bristow, Phillip Thienger, et al.
Molecular Cell (2020) Vol. 80, Iss. 4, pp. 562-577
Open Access | Times Cited: 103
The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 55
Genome interpretation using in silico predictors of variant impact
Panagiotis Katsonis, Kevin Wilhelm, Amanda M. Williams, et al.
Human Genetics (2022) Vol. 141, Iss. 10, pp. 1549-1577
Open Access | Times Cited: 54
High-throughput PRIME-editing screens identify functional DNA variants in the human genome
Xingjie Ren, Han Yang, Jovia L. Nierenberg, et al.
Molecular Cell (2023) Vol. 83, Iss. 24, pp. 4633-4645.e9
Open Access | Times Cited: 32
Functional genomics and small molecules in mitochondrial neurodevelopmental disorders
Daniel G. Calame, Lisa Emrick
Neurotherapeutics (2024) Vol. 21, Iss. 1, pp. e00316-e00316
Open Access | Times Cited: 7
Mapping the functional impact of non-coding regulatory elements in primary T cells through single-cell CRISPR screens
Celia Alda-Catalinas, Ximena Ibarra-Soria, Christina Flouri, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Genetic and epigenetic studies in non‐syndromic oral clefts
Azeez Alade, Waheed Awotoye, Azeez Butali
Oral Diseases (2022) Vol. 28, Iss. 5, pp. 1339-1350
Closed Access | Times Cited: 27
GREEN-DB: a framework for the annotation and prioritization of non-coding regulatory variants from whole-genome sequencing data
Edoardo Giacopuzzi, Niko Popitsch, Jenny C. Taylor
Nucleic Acids Research (2022) Vol. 50, Iss. 5, pp. 2522-2535
Open Access | Times Cited: 25
Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma risk
Pelin Gürkan Ünal, Ye Lu, Bas Bueno‐de‐Mesquita, et al.
Human Genomics (2024) Vol. 18, 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
Modeling regulatory network topology improves genome-wide analyses of complex human traits
Xiang Zhu, Zhana Duren, Wing Hung Wong
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 28
A unified model of human hemoglobin switching through single-cell genome editing
Yong Shen, Jeffrey M. Verboon, Yuannyu Zhang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 28
Toward a comprehensive catalog of regulatory elements
Kaili Fan, Edith L. Pfister, Zhiping Weng
Human Genetics (2023) Vol. 142, Iss. 8, pp. 1091-1111
Closed Access | Times Cited: 12
Unravelling the genetic architecture of human complex traits through whole genome sequencing
Ozvan Bocher, Cristen J. Willer, Eleftheria Zeggini
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 12
A conserved NR5A1-responsive enhancer regulates SRY in testis-determination
Denis Houzelstein, Caroline Eozénou, Carlos F. Lagos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease
Estela M. Bruxel, Danielle Bruno, Amanda M. do Canto, et al.
Seizure (2021) Vol. 90, pp. 34-50
Open Access | Times Cited: 27
Joint disease-specificity at the regulatory base-pair level
Pushpanathan Muthuirulan, Dewei Zhao, Mariel Young, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 27
Epigenetic Transgenerational Inheritance of the Effects of Obesogen Exposure
Nicole Mohajer, Erika M. Joloya, Jeongbin Seo, et al.
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 27
An alternative splicing hypothesis for neuropathology of schizophrenia: evidence from studies on historical candidate genes and multi-omics data
Chuyi Zhang, Xiao Xiao, Zhuohua Zhang, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 95-112
Closed Access | Times Cited: 24
Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-Coding Variants
Zheng Wang, Guihu Zhao, Bin Li, et al.
Genomics Proteomics & Bioinformatics (2022) Vol. 21, Iss. 3, pp. 649-661
Open Access | Times Cited: 19
Genetic Modulation of BET1L Confers Colorectal Cancer Susceptibility by Reducing miRNA Binding and m6A Modification
Shuwei Li, Mulong Du, Kaili Xu, et al.
Cancer Research (2023) Vol. 83, Iss. 13, pp. 2142-2154
Open Access | Times Cited: 11
POSTRE: a tool to predict the pathological effects of human structural variants
Víctor Sánchez-Gaya, Álvaro Rada-Iglesias
Nucleic Acids Research (2023) Vol. 51, Iss. 9, pp. e54-e54
Open Access | Times Cited: 10
Oligogenic risk score for Gilles de la Tourette syndrome reveals a genetic continuum of tic disorders
Małgorzata Borczyk, Jakub Fichna, Marcin Piechota, et al.
Journal of Applied Genetics (2025)
Closed Access
Page 1 - Next Page

Scroll to top