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:

Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation
Thomas A. Sasani, Brent S. Pedersen, Ziyue Gao, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 166

Showing 26-50 of 166 citing articles:

Post-transcriptional regulation in spermatogenesis: all RNA pathways lead to healthy sperm
Marcos Morgan, Lokesh Kumar, Yin Li, et al.
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 24, pp. 8049-8071
Open Access | Times Cited: 49
Developmental and temporal characteristics of clonal sperm mosaicism
Xiaoxu Yang, Martin W. Breuss, Xin Xu, et al.
Cell (2021) Vol. 184, Iss. 18, pp. 4772-4783.e15
Open Access | Times Cited: 46
Role of sperm DNA damage in creating de-novo mutations in human offspring: the ‘post-meiotic oocyte collusion’ hypothesis
R. John Aitken
Reproductive BioMedicine Online (2022) Vol. 45, Iss. 1, pp. 109-124
Open Access | Times Cited: 35
Fertility in the aging male: a systematic review
Masaya Jimbo, Jason Kunisaki, Mohammadali Ghaed, et al.
Fertility and Sterility (2022) Vol. 118, Iss. 6, pp. 1022-1034
Closed Access | Times Cited: 33
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
The mutational dynamics of short tandem repeats in large, multigenerational families
Cody J. Steely, W. Scott Watkins, Lisa Baird, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 24
Revisiting mutagenesis at non-B DNA motifs in the human genome
Ryan J. McGinty, Shamil Sunyaev
Nature Structural & Molecular Biology (2023) Vol. 30, Iss. 4, pp. 417-424
Open Access | Times Cited: 15
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair
Kitty Sherwood, Joseph C. Ward, Ignacio Soriano, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Causes and Consequences of Varying Transposable Element Activity: An Evolutionary Perspective
Andrea J. Betancourt, Kevin H.-C. Wei, Yuheng Huang, et al.
Annual Review of Genomics and Human Genetics (2024) Vol. 25, Iss. 1, pp. 1-25
Closed Access | Times Cited: 5
The Evolutionary Interplay of Somatic and Germline Mutation Rates
Annabel C. Beichman, Luke Zhu, Kelley Harris
Annual Review of Biomedical Data Science (2024) Vol. 7, Iss. 1, pp. 83-105
Closed Access | Times Cited: 5
High and Highly Variable Spontaneous Mutation Rates in Daphnia
Eddie K. H. Ho, Fenner Macrae, Leigh C. Latta, et al.
Molecular Biology and Evolution (2020) Vol. 37, Iss. 11, pp. 3258-3266
Open Access | Times Cited: 39
Transgenerational effects of paternal exposures: the role of germline de novo mutations
Hojat Dehghanbanadaki, Masaya Jimbo, Kiarad Fendereski, et al.
Andrology (2024)
Open Access | Times Cited: 4
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline
K Wood, R. Spencer Tong, Marialetizia Motta, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 9, pp. 1953-1969
Open Access | Times Cited: 4
The importance of family-based sampling for biobanks
Neil M Davies, Gibran Hemani, Jenae M. Neiderhiser, et al.
Nature (2024) Vol. 634, Iss. 8035, pp. 795-803
Closed Access | Times Cited: 4
Inherent instability of simple DNA repeats shapes an evolutionarily stable distribution of repeat lengths
Ryan J. McGinty, Daniel J. Balick, Sergei M. Mirkin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Unprecedented female mutation bias in the aye-aye, a highly unusual lemur from Madagascar
Richard J. Wang, Yadira Peña-García, Muthuswamy Raveendran, et al.
PLoS Biology (2025) Vol. 23, Iss. 2, pp. e3003015-e3003015
Open Access
Identification ofde novovariants from parent-proband duos via long-read sequencing
Leandros Boukas, Emmanuèle C. Délot, Georgia Pitsava, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Paternal age, de novo mutation, and age at onset among co-affected schizophrenia sib-pairs: whole-genome sequencing in multiplex families
Yen‐Chen Anne Feng, Wei J. Chen, Mei‐Chen Lin, et al.
Molecular Psychiatry (2025)
Closed Access
Quantifying the effects of computational filter criteria on the accurate identification of de novo mutations at varying levels of sequencing coverage
Mark Milhaven, Aman Garg, Cyril J. Versoza, et al.
Heredity (2025)
Closed Access
Direct measurement of the male germline mutation rate in individuals using sequential sperm samples
Jonathan E. Shoag, Amoolya Srinivasa, Caitlin A. Loh, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Efficient identification of de novo mutations in family trios: a consensus-based informatic approach
Mariya Shadrina, Özem Kalay, Sinem Demirkaya-Budak, et al.
Life Science Alliance (2025) Vol. 8, Iss. 6, pp. e202403039-e202403039
Open Access
Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counselling
François Lecoquierre, Nathalie Drouot, Sophie Coutant, et al.
PLoS Genetics (2025) Vol. 21, Iss. 3, pp. e1011651-e1011651
Open Access
Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells
Zhao Yan, Olga Tšuiko, Tatjana Jatsenko, et al.
Nucleic Acids Research (2025) Vol. 53, Iss. 6
Open Access
Human de novo mutation rates from a four-generation pedigree reference
David Porubský, Harriet Dashnow, Thomas A. Sasani, et al.
Nature (2025)
Open Access
Inferring evolutionary dynamics of mutation rates through the lens of mutation spectrum variation
Jedidiah Carlson, William S. DeWitt, Kelley Harris
Current Opinion in Genetics & Development (2020) Vol. 62, pp. 50-57
Open Access | Times Cited: 29

Scroll to top