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:

Genetic architecture: the shape of the genetic contribution to human traits and disease
Nicholas J. Timpson, Celia M.T. Greenwood, Nicole Soranzo, et al.
Nature Reviews Genetics (2017) Vol. 19, Iss. 2, pp. 110-124
Open Access | Times Cited: 416

Showing 1-25 of 416 citing articles:

The personal and clinical utility of polygenic risk scores
Ali Torkamani, Nathan E. Wineinger, Eric J. Topol
Nature Reviews Genetics (2018) Vol. 19, Iss. 9, pp. 581-590
Closed Access | Times Cited: 1380

A global overview of pleiotropy and genetic architecture in complex traits
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, et al.
Nature Genetics (2019) Vol. 51, Iss. 9, pp. 1339-1348
Open Access | Times Cited: 1094

An atlas of genetic influences on osteoporosis in humans and mice
John Morris, John P. Kemp, Scott E. Youlten, et al.
Nature Genetics (2018) Vol. 51, Iss. 2, pp. 258-266
Open Access | Times Cited: 688

The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, Parsa Akbari, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1214-1231.e11
Open Access | Times Cited: 560

Deep learning in biomedicine
Michael Wainberg, Daniele Merico, Andrew Delong, et al.
Nature Biotechnology (2018) Vol. 36, Iss. 9, pp. 829-838
Closed Access | Times Cited: 536

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan, Daniel H. Geschwind
Cell (2019) Vol. 177, Iss. 1, pp. 162-183
Open Access | Times Cited: 400

Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
Nina Mars, Jukka Koskela, Pietari Ripatti, et al.
Nature Medicine (2020) Vol. 26, Iss. 4, pp. 549-557
Closed Access | Times Cited: 386

Update on NAFLD genetics: From new variants to the clinic
Eric Trépo, Luca Valenti
Journal of Hepatology (2020) Vol. 72, Iss. 6, pp. 1196-1209
Open Access | Times Cited: 318

The genetics of human ageing
David Melzer, Luke C. Pilling, Luigi Ferrucci
Nature Reviews Genetics (2019) Vol. 21, Iss. 2, pp. 88-101
Open Access | Times Cited: 293

A road map for understanding molecular and genetic determinants of osteoporosis
Tie‐Lin Yang, Hui Shen, Anqi Liu, et al.
Nature Reviews Endocrinology (2019) Vol. 16, Iss. 2, pp. 91-103
Open Access | Times Cited: 280

Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Dmitry Shungin, Simon Haworth, Kimon Divaris, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 279

Genetic contributions to NAFLD: leveraging shared genetics to uncover systems biology
Mohammed Eslam, Jacob George
Nature Reviews Gastroenterology & Hepatology (2019) Vol. 17, Iss. 1, pp. 40-52
Closed Access | Times Cited: 270

The influence of evolutionary history on human health and disease
Mary Lauren Benton, Abin Abraham, Abigail L. LaBella, et al.
Nature Reviews Genetics (2021) Vol. 22, Iss. 5, pp. 269-283
Open Access | Times Cited: 226

Lactose Intolerance, Dairy Avoidance, and Treatment Options
Andrew Szilagyi, Norma Ishayek
Nutrients (2018) Vol. 10, Iss. 12, pp. 1994-1994
Open Access | Times Cited: 205

Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore
Degang Wu, Jinzhuang Dou, Xiaoran Chai, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 736-749.e15
Open Access | Times Cited: 191

Exome sequencing of Finnish isolates enhances rare-variant association power
Adam E. Locke, Karyn Meltz Steinberg, Charleston W. K. Chiang, et al.
Nature (2019) Vol. 572, Iss. 7769, pp. 323-328
Open Access | Times Cited: 188

Genetic disease risks can be misestimated across global populations
Michelle S. Kim, Kane Patel, Andrew K. Teng, et al.
Genome biology (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 169

Genomics of hypertension: the road to precision medicine
Sandosh Padmanabhan, Anna F. Dominiczak
Nature Reviews Cardiology (2020) Vol. 18, Iss. 4, pp. 235-250
Open Access | Times Cited: 158

DNA methylation-based predictors of health: applications and statistical considerations
Paul Yousefi, Matthew Suderman, Ryan Langdon, et al.
Nature Reviews Genetics (2022) Vol. 23, Iss. 6, pp. 369-383
Closed Access | Times Cited: 146

MetaRNN: differentiating rare pathogenic and rare benign missense SNVs and InDels using deep learning
Chang Li, Degui Zhi, Kai Wang, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 102

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project
Peikuan Cong, Wei-Yang Bai, Jinchen Li, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 81

Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706)
Bingxin Zhao, Jingwen Zhang, Joseph G. Ibrahim, et al.
Molecular Psychiatry (2019) Vol. 26, Iss. 8, pp. 3943-3955
Open Access | Times Cited: 136

Insights into the genetic architecture of the human face
Julie D. White, Karlijne Indencleef, Sahin Naqvi, et al.
Nature Genetics (2020) Vol. 53, Iss. 1, pp. 45-53
Open Access | Times Cited: 131

First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Diana L. Cousminer, Emma Ahlqvist, Rajashree Mishra, et al.
Diabetes Care (2018) Vol. 41, Iss. 11, pp. 2396-2403
Open Access | Times Cited: 118

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