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:
FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 16
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 16
Showing 16 citing articles:
Exploring the relationship between melanopsin gene variants, sleep, and markers of brain health
Ayeisha Milligan Armstrong, Eleanor K. O’Brien, Tenielle Porter, et al.
Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring (2025) Vol. 17, Iss. 1
Open Access
Ayeisha Milligan Armstrong, Eleanor K. O’Brien, Tenielle Porter, et al.
Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring (2025) Vol. 17, Iss. 1
Open Access
Genome-Wide Association Studies: A Powerful Approach for Identifying Genomic Variants for Livestock Breeding and Disease Management
Min‐Jae Jang, Seung-Hoon Lee, Jun‐Mo Kim
(2025), pp. 87-117
Closed Access
Min‐Jae Jang, Seung-Hoon Lee, Jun‐Mo Kim
(2025), pp. 87-117
Closed Access
Genome‐Wide Association Analyses of HPV16 and HPV18 Seropositivity Identify Susceptibility Loci for Cervical Cancer
Theresa Beckhaus, Linda Kachuri, Taishi Nakase, et al.
Journal of Medical Virology (2025) Vol. 97, Iss. 2
Open Access
Theresa Beckhaus, Linda Kachuri, Taishi Nakase, et al.
Journal of Medical Virology (2025) Vol. 97, Iss. 2
Open Access
Mapping the landscape of childhood obesity: genomic insights and socioeconomic status in Indian school‐going children
Janaki M. Nair, Ganesh Chauhan, Gauri Prasad, et al.
Obesity (2025)
Closed Access
Janaki M. Nair, Ganesh Chauhan, Gauri Prasad, et al.
Obesity (2025)
Closed Access
TBC1D30 regulates proinsulin and insulin secretion and is the target of a genomic association signal for proinsulin
Victoria A. Parsons, Swarooparani Vadlamudi, Kayleigh M. Voos, et al.
Diabetologia (2025)
Closed Access
Victoria A. Parsons, Swarooparani Vadlamudi, Kayleigh M. Voos, et al.
Diabetologia (2025)
Closed Access
Novel ABCD1 and MTHFSD Variants in Taiwanese Bipolar Disorder: A Genetic Association Study
Yiguang Wang, Chih-Chung Huang, Ta‐Chuan Yeh, et al.
Medicina (2025) Vol. 61, Iss. 3, pp. 486-486
Open Access
Yiguang Wang, Chih-Chung Huang, Ta‐Chuan Yeh, et al.
Medicina (2025) Vol. 61, Iss. 3, pp. 486-486
Open Access
Novel genetic associations with childhood adipocytokines in Indian adolescents
Janaki M. Nair, Ganesh Chauhan, Gauri Prasad, et al.
Cytokine (2025) Vol. 190, pp. 156935-156935
Closed Access
Janaki M. Nair, Ganesh Chauhan, Gauri Prasad, et al.
Cytokine (2025) Vol. 190, pp. 156935-156935
Closed Access
PPDPF is not a key regulator of human pancreas development
Markus Breunig, Meike Hohwieler, Jasmin Haderspeck, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011657-e1011657
Open Access
Markus Breunig, Meike Hohwieler, Jasmin Haderspeck, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011657-e1011657
Open Access
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Long or short? Telomere length and pancreatic cancer and its precursor lesions, a narrative review
Daniele Campa, Alessio Felici, Chiara Corradi, et al.
Mutagenesis (2023)
Closed Access | Times Cited: 6
Daniele Campa, Alessio Felici, Chiara Corradi, et al.
Mutagenesis (2023)
Closed Access | Times Cited: 6
Genetic variants associated with response to anti-CGRP monoclonal antibody therapy in a chronic migraine Han Chinese population
Yu-Chin An, Kuo‐Sheng Hung, Chih‐Sung Liang, et al.
The Journal of Headache and Pain (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Yu-Chin An, Kuo‐Sheng Hung, Chih‐Sung Liang, et al.
The Journal of Headache and Pain (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Association between CACNA1D polymorphisms and hypospadias in a southern Chinese population
Ye He, Binyao Li, Xinying Zhao, et al.
Journal of Pediatric Urology (2024) Vol. 20, Iss. 3, pp. 438.e1-438.e11
Closed Access | Times Cited: 1
Ye He, Binyao Li, Xinying Zhao, et al.
Journal of Pediatric Urology (2024) Vol. 20, Iss. 3, pp. 438.e1-438.e11
Closed Access | Times Cited: 1
Associations between the New DNA-Methylation-Based Telomere Length Estimator, the Mediterranean Diet and Genetics in a Spanish Population at High Cardiovascular Risk
Óscar Coltell, Eva M. Asensio, José V. Sorlí, et al.
Antioxidants (2023) Vol. 12, Iss. 11, pp. 2004-2004
Open Access | Times Cited: 3
Óscar Coltell, Eva M. Asensio, José V. Sorlí, et al.
Antioxidants (2023) Vol. 12, Iss. 11, pp. 2004-2004
Open Access | Times Cited: 3
The relationship between genetic variation in Aquaporin-4, sleep quality measures and Alzheimer’s disease-related phenotypes.
Simon M. Laws, Tenielle Porter, Ayeisha Milligan Armstrong, et al.
Research Square (Research Square) (2024)
Closed Access
Simon M. Laws, Tenielle Porter, Ayeisha Milligan Armstrong, et al.
Research Square (Research Square) (2024)
Closed Access
CXADR polymorphism rs6517774 modifies islet autoimmunity characteristics and exhibits sex disparity
Lucas Nygård, Milla Valta, Antti‐Pekka Laine, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access
Lucas Nygård, Milla Valta, Antti‐Pekka Laine, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access
