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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:

The impact of paternal age on new mutations and disease in the next generation
K Wood, Anne Goriely
Fertility and Sterility (2022) Vol. 118, Iss. 6, pp. 1001-1012
Open Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature (2024) Vol. 632, Iss. 8026, pp. 832-840
Open Access | Times Cited: 28
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
Adult Human, but Not Rodent, Spermatogonial Stem Cells Retain States with a Foetal-like Signature
Stephen J. Bush, Rafail Nikola, Seungmin Han, et al.
Cells (2024) Vol. 13, Iss. 9, pp. 742-742
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
Prenatal gene editing for neurodevelopmental diseases: Ethical considerations
Rami Major, Eric T. Juengst
The American Journal of Human Genetics (2025)
Open Access
The Executive Functioning of the Chief Executive
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 75-81
Closed Access
Arousal, Attention, and Executive Functioning
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 3-10
Closed Access
Global Decline in General Intelligence
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 43-55
Closed Access
Toward a Consolidated Understanding of Intelligence
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 29-42
Closed Access
The Demands of Office
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 67-73
Closed Access
Senescent Slowing
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 19-25
Closed Access
Myriad Forms of Memory
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 11-17
Closed Access
Aging Brains and Bodies: Evidence and Evolutionary Context
Steven C. Hertler, Aurelio José Figueredo, Mateo Peñaherrera‐Aguirre
(2025), pp. 57-63
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
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
Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies
Ziye Zeng, Lan Zhang, Yuqin Zhou, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Pregnancy Loss: From Cytogenetics to Genomics
Christina G. Tise, Kajal Verma, Ruth B. Lathi
Early pregnancy (2025), pp. 299-316
Closed Access
Identification of intragenic variants in pediatric patients with intellectual disability in Peru
Hugo Hernán Abarca-Barriga, Flor Vásquez Sotomayor, Renzo Punil-Luciano, et al.
BMC Medical Genomics (2025) Vol. 18, Iss. 1
Open Access
Evolutionary medicine and bioastronautics: an innovative approach in addressing adverse mental health effects to astronauts during long term space missions
Arthur Saniotis, Maciej Henneberg, Kazhaleh Mohammadi
Frontiers in Physiology (2025) Vol. 16
Open Access
KEAP1–NRF2 system regulates age‐related spermatogenesis dysfunction
Sohei Kuribayashi, Shinichiro Fukuhara, Hiroaki Kitakaze, et al.
Reproductive Medicine and Biology (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 3
Paternal age, risk of congenital anomalies, and birth outcomes: a population-based cohort study
Xinghe Bu, Wenjing Ye, Jianguo Zhou
European Journal of Pediatrics (2023) Vol. 182, Iss. 8, pp. 3519-3526
Open Access | Times Cited: 8
Exploring the Micro-Mosaic Landscape of FGFR3 Mutations in the Ageing Male Germline and Its Implications in Meiotic Differentiation
Yasmin Striedner, Barbara Arbeithuber, Sofia Moura, et al.
(2024)
Open Access | Times Cited: 2
Exploring the Micro-Mosaic Landscape of FGFR3 Mutations in the Ageing Male Germline and Their Potential Implications in Meiotic Differentiation
Yasmin Striedner, Barbara Arbeithuber, Sofia Moura, et al.
Genes (2024) Vol. 15, Iss. 2, pp. 191-191
Open Access | Times Cited: 2
Sperm sequencing reveals extensive positive selection in the male germline
Matthew D. C. Neville, Andrew Lawson, Rashesh Sanghvi, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Sperm chromatin structure assay (SCSA®) and flow cytometry-assisted TUNEL assay provide a concordant assessment of sperm DNA fragmentation as a function of age in a large cohort of approximately 10,000 patients
Paria Behdarvandian, Ali Nasr-Esfahani, Marziyeh Tavalaee, et al.
Basic and Clinical Andrology (2023) Vol. 33, Iss. 1
Open Access | Times Cited: 6
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