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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:

Genomic analyses implicate noncoding de novo variants in congenital heart disease
Felix Richter, Sarah U. Morton, Seong Won Kim, et al.
Nature Genetics (2020) Vol. 52, Iss. 8, pp. 769-777
Open Access | Times Cited: 136

Showing 1-25 of 136 citing articles:

Heart Disease and Stroke Statistics—2022 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2022) Vol. 145, Iss. 8
Open Access | Times Cited: 4330
Heart Disease and Stroke Statistics—2023 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2023) Vol. 147, Iss. 8
Open Access | Times Cited: 4309
2024 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association
Seth S. Martin, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2024) Vol. 149, Iss. 8
Open Access | Times Cited: 979
Effective gene expression prediction from sequence by integrating long-range interactions
Žiga Avsec, Vikram Agarwal, Daniel Visentin, et al.
Nature Methods (2021) Vol. 18, Iss. 10, pp. 1196-1203
Open Access | Times Cited: 721
Enhancer redundancy in development and disease
Evgeny Z. Kvon, Rachel Waymack, Mario Gad, et al.
Nature Reviews Genetics (2021) Vol. 22, Iss. 5, pp. 324-336
Open Access | Times Cited: 202
Genomic frontiers in congenital heart disease
Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, et al.
Nature Reviews Cardiology (2021) Vol. 19, Iss. 1, pp. 26-42
Open Access | Times Cited: 160
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 81
Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease
Feng Xiao, Xiaoran Zhang, Sarah U. Morton, et al.
Nature Genetics (2024) Vol. 56, Iss. 3, pp. 420-430
Open Access | Times Cited: 21
Molecular Genetics and Complex Inheritance of Congenital Heart Disease
Nicholas S. Diab, Syndi Barish, Weilai Dong, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 1020-1020
Open Access | Times Cited: 84
Lifespan Perspective on Congenital Heart Disease Research
Gerhard‐Paul Diller, Alexandra Arvanitaki, Alexander R. Opotowsky, et al.
Journal of the American College of Cardiology (2021) Vol. 77, Iss. 17, pp. 2219-2235
Open Access | Times Cited: 79
Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association
Andrew P. Landstrom, Jeffrey J. Kim, Bruce D. Gelb, et al.
Circulation Genomic and Precision Medicine (2021) Vol. 14, Iss. 5
Open Access | Times Cited: 76
Decoding disease: from genomes to networks to phenotypes
Aaron K. Wong, Rachel Sealfon, Chandra L. Theesfeld, et al.
Nature Reviews Genetics (2021) Vol. 22, Iss. 12, pp. 774-790
Open Access | Times Cited: 71
Effective gene expression prediction from sequence by integrating long-range interactions
Žiga Avsec, Vikram Agarwal, Daniel Visentin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 63
Transcription factor protein interactomes reveal genetic determinants in heart disease
Bárbara González‐Terán, Maureen Pittman, Franco Felix, et al.
Cell (2022) Vol. 185, Iss. 5, pp. 794-814.e30
Open Access | Times Cited: 62
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease
Mohamed Ameen, Laksshman Sundaram, Mengcheng Shen, et al.
Cell (2022) Vol. 185, Iss. 26, pp. 4937-4953.e23
Open Access | Times Cited: 60
Genetics of congenital heart disease: a narrative review of recent advances and clinical implications
Jun Yasuhara, Vidu Garg
Translational Pediatrics (2021) Vol. 10, Iss. 9, pp. 2366-2386
Open Access | Times Cited: 58
Fetal Brain Development in Congenital Heart Disease
Shabnam Peyvandi, Caitlin K. Rollins
Canadian Journal of Cardiology (2022) Vol. 39, Iss. 2, pp. 115-122
Open Access | Times Cited: 47
Analyses of rare predisposing variants of lung cancer in 6,004 whole genomes in Chinese
Cheng Wang, Juncheng Dai, Na Qin, et al.
Cancer Cell (2022) Vol. 40, Iss. 10, pp. 1223-1239.e6
Open Access | Times Cited: 43
Recessive genetic contribution to congenital heart disease in 5,424 probands
Weilai Dong, Sheng Chih Jin, Michael C. Sierant, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 10
Open Access | Times Cited: 1
Integrating convolution and self-attention improves language model of human genome for interpreting non-coding regions at base-resolution
Meng Yang, Lichao Huang, Haiping Huang, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 14, pp. e81-e81
Open Access | Times Cited: 35
Genomics enters the deep learning era
Etienne Routhier, Julien Mozziconacci
PeerJ (2022) Vol. 10, pp. e13613-e13613
Open Access | Times Cited: 29
Single-nucleotide variants within heart enhancers increase binding affinity and disrupt heart development
Granton A. Jindal, Alexis Bantle, Joe J. Solvason, et al.
Developmental Cell (2023) Vol. 58, Iss. 21, pp. 2206-2216.e5
Open Access | Times Cited: 23
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi, Leticia S. Matsuoka, Michael March, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 10, pp. 1117-1124
Closed Access | Times Cited: 17
Genetic Etiology of Left‐Sided Obstructive Heart Lesions: A Story in Development
Lauren E. Parker, Andrew P. Landstrom
Journal of the American Heart Association (2021) Vol. 10, Iss. 2
Open Access | Times Cited: 38
Association of assisted reproductive technology, germline de novo mutations and congenital heart defects in a prospective birth cohort study
Cheng Wang, Hong Lv, Xiufeng Ling, et al.
Cell Research (2021) Vol. 31, Iss. 8, pp. 919-928
Open Access | Times Cited: 38
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