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 and common variants: twenty arguments
Greg Gibson
Nature Reviews Genetics (2012) Vol. 13, Iss. 2, pp. 135-145
Open Access | Times Cited: 1249

Showing 1-25 of 1249 citing articles:

Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
Matthew T. Maurano, Richard Humbert, Eric Rynes, et al.
Science (2012) Vol. 337, Iss. 6099, pp. 1190-1195
Open Access | Times Cited: 3548
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
Amit V. Khera, Mark Chaffin, Krishna G. Aragam, et al.
Nature Genetics (2018) Vol. 50, Iss. 9, pp. 1219-1224
Open Access | Times Cited: 2505
Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
Jacob A. Tennessen, Abigail W. Bigham, Timothy D. O’Connor, et al.
Science (2012) Vol. 337, Iss. 6090, pp. 64-69
Open Access | Times Cited: 1672
The advantages and limitations of trait analysis with GWAS: a review
Arthur Korte, Ashley Farlow
Plant Methods (2013) Vol. 9, Iss. 1, pp. 29-29
Open Access | Times Cited: 1477
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, et al.
Nature Genetics (2015) Vol. 48, Iss. 2, pp. 134-143
Open Access | Times Cited: 1407
Rare-Variant Association Analysis: Study Designs and Statistical Tests
Seunggeung Lee, Gonçalo R. Abecasis, Michael Boehnke, et al.
The American Journal of Human Genetics (2014) Vol. 95, Iss. 1, pp. 5-23
Open Access | Times Cited: 991
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
Wenqing Fu, Timothy D. O’Connor, Goo Jun, et al.
Nature (2012) Vol. 493, Iss. 7431, pp. 216-220
Open Access | Times Cited: 972
The Next-Generation Sequencing Revolution and Its Impact on Genomics
Daniel C. Koboldt, Karyn Meltz Steinberg, David E. Larson, et al.
Cell (2013) Vol. 155, Iss. 1, pp. 27-38
Open Access | Times Cited: 966
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Angli Xue, Yang Wu, Zhihong Zhu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 758
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C. Francioli, Androniki Menelaou, Sara L. Pulit, et al.
Nature Genetics (2014) Vol. 46, Iss. 8, pp. 818-825
Open Access | Times Cited: 691
A tutorial on conducting genome‐wide association studies: Quality control and statistical analysis
Andries T. Marees, Hilde de Kluiver, Sven Stringer, et al.
International Journal of Methods in Psychiatric Research (2018) Vol. 27, Iss. 2
Open Access | Times Cited: 666
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Alexander Gusev, Sang Lee, Gosia Trynka, et al.
The American Journal of Human Genetics (2014) Vol. 95, Iss. 5, pp. 535-552
Open Access | Times Cited: 625
Mendelian randomization in cardiometabolic disease: challenges in evaluating causality
Michael V. Holmes, Mika Ala‐Korpela, George Davey Smith
Nature Reviews Cardiology (2017) Vol. 14, Iss. 10, pp. 577-590
Open Access | Times Cited: 582
Genetics of coronary artery disease: discovery, biology and clinical translation
Amit V. Khera, Sekar Kathiresan
Nature Reviews Genetics (2017) Vol. 18, Iss. 6, pp. 331-344
Open Access | Times Cited: 572
Comprehensive genotyping of the USA national maize inbred seed bank
M. Cinta Romay, Mark J. Millard, Jeffrey C. Glaubitz, et al.
Genome biology (2013) Vol. 14, Iss. 6
Open Access | Times Cited: 538
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
Po−Ru Loh, Gaurav Bhatia, Alexander Gusev, et al.
Nature Genetics (2015) Vol. 47, Iss. 12, pp. 1385-1392
Open Access | Times Cited: 503
Interpreting noncoding genetic variation in complex traits and human disease
Lucas D. Ward, Manolis Kellis
Nature Biotechnology (2012) Vol. 30, Iss. 11, pp. 1095-1106
Open Access | Times Cited: 497
Redefining the role of Broca’s area in speech
Adeen Flinker, Anna Korzeniewska, Avgusta Y. Shestyuk, et al.
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 9, pp. 2871-2875
Open Access | Times Cited: 454
Dissecting the genetics of complex traits using summary association statistics
Bogdan Paşaniuc, Alkes L. Price
Nature Reviews Genetics (2016) Vol. 18, Iss. 2, pp. 117-127
Open Access | Times Cited: 451
Induced Pluripotent Stem Cells Meet Genome Editing
Dirk Hockemeyer, Rudolf Jaenisch
Cell stem cell (2016) Vol. 18, Iss. 5, pp. 573-586
Open Access | Times Cited: 441
Exploiting genetic diversity from landraces in wheat breeding for adaptation to climate change
Marta S. Lopes, Ibrahim S. Elbasyoni, P. Stephen Baenziger, et al.
Journal of Experimental Botany (2015) Vol. 66, Iss. 12, pp. 3477-3486
Open Access | Times Cited: 438
Concepts, estimation and interpretation of SNP-based heritability
Jian Yang, Jian Zeng, Michael E. Goddard, et al.
Nature Genetics (2017) Vol. 49, Iss. 9, pp. 1304-1310
Closed Access | Times Cited: 416
Using Extended Genealogy to Estimate Components of Heritability for 23 Quantitative and Dichotomous Traits
Noah Zaitlen, Peter Kraft, Hon‐Cheong So, et al.
PLoS Genetics (2013) Vol. 9, Iss. 5, pp. e1003520-e1003520
Open Access | Times Cited: 394
Genome-wide Association Studies in Maize: Praise and Stargaze
Yingjie Xiao, Haijun Liu, Liuji Wu, et al.
Molecular Plant (2016) Vol. 10, Iss. 3, pp. 359-374
Open Access | Times Cited: 370
A population genetic interpretation of GWAS findings for human quantitative traits
Yuval B. Simons, Kevin Bullaughey, Richard R. Hudson, et al.
PLoS Biology (2018) Vol. 16, Iss. 3, pp. e2002985-e2002985
Open Access | Times Cited: 357
Page 1 - Next Page

Scroll to top