Standout Papers

Inference of Population Structure Using Multilocus Genotype Data 2000 2026 2008 2017 26.8k
  1. Inference of Population Structure Using Multilocus Genotype Data (2000)
    Jonathan K. Pritchard, Matthew Stephens et al. Genetics
  2. Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies (2003)
    Daniel Falush, Matthew Stephens et al. Genetics
  3. A New Statistical Method for Haplotype Reconstruction from Population Data (2001)
    Matthew Stephens, Nicholas Smith et al. The American Journal of Human Genetics
  4. A Comparison of Bayesian Methods for Haplotype Reconstruction from Population Genotype Data (2003)
    Matthew Stephens, Peter Donnelly The American Journal of Human Genetics
  5. Inference of population structure using multilocus genotype data: dominant markers and null alleles (2007)
    Daniel Falush, Matthew Stephens et al. Molecular Ecology Notes
  6. Inferring weak population structure with the assistance of sample group information (2009)
    Melissa J. Hubisz, Daniel Falush et al. Molecular Ecology Resources
  7. Genome-wide efficient mixed-model analysis for association studies (2012)
    Xiang Zhou, Matthew Stephens Nature Genetics
  8. RNA-seq: An assessment of technical reproducibility and comparison with gene expression arrays (2008)
    John C. Marioni, Christopher E. Mason et al. Genome Research
  9. Association Mapping in Structured Populations (2000)
    Jonathan K. Pritchard, Matthew Stephens et al. The American Journal of Human Genetics
  10. A Fast and Flexible Statistical Model for Large-Scale Population Genotype Data: Applications to Inferring Missing Genotypes and Haplotypic Phase (2006)
    Paul Scheet, Matthew Stephens The American Journal of Human Genetics
  11. Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-Data Imputation (2005)
    Matthew Stephens, Paul Scheet The American Journal of Human Genetics
  12. fastSTRUCTURE: Variational Inference of Population Structure in Large SNP Data Sets (2014)
    Anil Raj, Matthew Stephens et al. Genetics
  13. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing (2012)
    Bryan Howie, Christian Fuchsberger et al. Nature Genetics
  14. Understanding mechanisms underlying human gene expression variation with RNA sequencing (2010)
    Joseph K. Pickrell, John C. Marioni et al. Nature
  15. Genes mirror geography within Europe (2008)
    John Novembre, Toby Johnson et al. Nature
  16. Traces of Human Migrations in Helicobacter pylori Populations (2003)
    Daniel Falush, Thierry Wirth et al. Science
  17. Modeling Linkage Disequilibrium and Identifying Recombination Hotspots Using Single-Nucleotide Polymorphism Data (2003)
    Na Li, Matthew Stephens Genetics
  18. Dealing With Label Switching in Mixture Models (2000)
    Matthew Stephens Journal of the Royal Statistical Society Series B (Statistical Methodology)
  19. Genotype Imputation with Thousands of Genomes (2011)
    Bryan Howie, Jonathan Marchini et al. G3 Genes Genomes Genetics
  20. Efficient multivariate linear mixed model algorithms for genome-wide association studies (2014)
    Xiang Zhou, Matthew Stephens Nature Methods
  21. Polygenic Modeling with Bayesian Sparse Linear Mixed Models (2013)
    Xiang Zhou, Peter Carbonetto et al. PLoS Genetics
  22. False discovery rates: a new deal (2016)
    Matthew Stephens Biostatistics
  23. Visualizing spatial population structure with estimated effective migration surfaces (2015)
    Desislava Petkova, John Novembre et al. Nature Genetics
  24. A Simple New Approach to Variable Selection in Regression, with Application to Genetic Fine Mapping (2020)
    Gao Wang, Abhishek Sarkar et al. Journal of the Royal Statistical Society Series B (Statistical Methodology)
  25. Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics (2020)
    Jean Morrison, Nicholas Knoblauch et al. Nature Genetics
  26. A Multivariate Genome-Wide Association Analysis of 10 LDL Subfractions, and Their Response to Statin Treatment, in 1868 Caucasians (2015)
    Heejung Shim, Daniel I. Chasman et al. PLoS ONE
  27. Fine-mapping from summary data with the “Sum of Single Effects” model (2022)
    Yuxin Zou, Peter Carbonetto et al. PLoS Genetics

Immediate Impact

6 by Nobel laureates 49 from Science/Nature 124 standout
Sub-graph 1 of 14

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29 intermediate papers

Works of Matthew Stephens being referenced

False discovery rates: a new deal
2016 Standout
Interpreting principal component analyses of spatial population genetic variation
2008
and 4 more

Author Peers

Author Last Decade Papers Cites
Matthew Stephens 42899 21381 2692 15372 129 73.3k
Jonathan K. Pritchard 46668 24339 2713 15362 179 75.6k
Peter Donnelly 34463 17192 1573 10976 202 59.7k
Masatoshi Nei 41412 25126 917 20991 194 79.6k
Laurent Excoffier 44692 17578 563 10431 184 69.2k
Makoto Kimura 27330 27009 797 10962 345 62.6k
David Posada 18070 18451 686 12106 157 55.0k
Joseph Felsenstein 25769 43951 973 21487 94 94.5k
Alexei J. Drummond 22980 21357 546 10252 104 68.6k
Arndt von Haeseler 13405 27207 856 12479 177 58.4k
Andrew Rambaut 19707 18839 400 8747 220 70.3k

All Works

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