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:

Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke M. Evans, Allison Fialkowski, et al.
Nature Human Behaviour (2022) Vol. 6, Iss. 11, pp. 1577-1586
Open Access | Times Cited: 22

Showing 22 citing articles:

Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 111
Pharmacogenomics: Driving Personalized Medicine
Wolfgang Sadée, Daqing Wang, Katherine E. Hartmann, et al.
Pharmacological Reviews (2023) Vol. 75, Iss. 4, pp. 789-814
Open Access | Times Cited: 87
The schizophrenia syndrome, circa 2024: What we know and how that informs its nature
Rajiv Tandon, Henry A. Nasrallah, Schahram Akbarian, et al.
Schizophrenia Research (2023) Vol. 264, pp. 1-28
Open Access | Times Cited: 60
Genomic findings in schizophrenia and their implications
Michael J. Owen, Sophie E. Legge, Elliott Rees, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 9, pp. 3638-3647
Open Access | Times Cited: 58
Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes
Sylvanus Toikumo, Mariela Jennings, Benjamin K. Pham, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 6, pp. 1177-1193
Open Access | Times Cited: 18
The complete and fully-phased diploid genome of a male Han Chinese
Chentao Yang, Yang Zhou, Yanni Song, et al.
Cell Research (2023) Vol. 33, Iss. 10, pp. 745-761
Open Access | Times Cited: 37
A method to estimate the contribution of rare coding variants to complex trait heritability
Nazia Pathan, Wei Q. Deng, Matteo Di Scipio, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 7
The Genetically Informed Neurobiology of Addiction (GINA) model
Ryan Bogdan, Alexander S. Hatoum, Emma C. Johnson, et al.
Nature reviews. Neuroscience (2022) Vol. 24, Iss. 1, pp. 40-57
Closed Access | Times Cited: 28
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M. Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1138-1148
Open Access | Times Cited: 12
Genetic liability to sedentary behaviour and cardiovascular disease incidence in the FinnGen and HUNT cohorts
Laura Joensuu, Kaisa Koivunen, Niko Paavo Tynkkynen, et al.
British Journal of Sports Medicine (2025), pp. bjsports-109491
Closed Access
Trajectories of genetic risk across dimensions of alcohol use behaviors
Jeanne E. Savage, Fazil Alıev, Peter B. Barr, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Animal board invited review: Practical applications of genomic information in livestock
D.P. Berry, Matthew L Spangler
animal (2023) Vol. 17, Iss. 11, pp. 100996-100996
Open Access | Times Cited: 8
Using polygenic risk scores to investigate the evolution of smoking and mental health outcomes in UK biobank participants
Lloyd Balbuena, Evyn M. Peters, Doug Speed
Acta Psychiatrica Scandinavica (2023) Vol. 148, Iss. 5, pp. 447-456
Open Access | Times Cited: 7
Multi-ancestry Whole-exome Sequencing Study of Alcohol Use Disorder in Two Cohorts
Lu Wang, Henry R. Kranzler, Joel Gelernter, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Rare variations within the serine/arginine‐rich splicing factor PtoRSZ21 modulate stomatal size to determine drought tolerance in Populus
Rui Huang, Zhuoying Jin, Donghai Zhang, et al.
New Phytologist (2024) Vol. 243, Iss. 5, pp. 1776-1794
Closed Access | Times Cited: 2
Whole-exome sequencing study of opioid dependence offers novel insights into the contributions of exome variants
Lu Wang, Yaira Z. Nuñez, Henry R. Kranzler, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 2
Multi-ancestry meta-analysis of tobacco use disorder prioritizes novel candidate risk genes and reveals associations with numerous health outcomes
Sylvanus Toikumo, Mariela Jennings, Benjamin K. Pham, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L. Clarke, Gaëlle Auguste, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Rare coding variants inCHRNB2reduce the likelihood of smoking
Veera M. Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 3
Genetic liability to sedentary behavior increases the risk of cardiovascular disease incidence: Evidence from the FinnGen cohort with 293,250 individuals
Laura Joensuu, Kaisa Koivunen, Niko Paavo Tynkkynen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Contribution of rare coding variants to complex trait heritability
Nazia Pathan, Wei Q. Deng, Mohammad Daud Khan, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 1
Characterizing the genetic architecture of chronic kidney disease
Kim Ngan Tran
(2023)
Open Access
Page 1

Scroll to top