Noah Zaitlen

Active 2007–2025

122
Papers
21,781
Citations
57
h-index
102
i10-index

Citations

Citations per year for Noah Zaitlen1998: 1 citations2000: 2 citations2002: 2 citations2003: 1 citations2006: 1 citations2007: 2 citations2008: 10 citations2009: 34 citations2010: 93 citations2011: 127 citations2012: 189 citations2013: 187 citations2014: 208 citations2015: 246 citations2016: 259 citations2017: 322 citations2018: 327 citations2019: 785 citations2020: 840 citations2021: 907 citations2022: 899 citations2023: 787 citations2024: 1,010 citations2025: 551 citations2026: 30 citations1999: no citations, so this year is not shown2001: no citations, so this year is not shown2004–2005: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,054 citing papers, 26.5% of this breakdownUnited Kingdom: 1,318 citing papers, 8.6% of this breakdownChina: 1,168 citing papers, 7.6% of this breakdownGermany: 712 citing papers, 4.7% of this breakdownAustralia: 637 citing papers, 4.2% of this breakdownCanada: 570 citing papers, 3.7% of this breakdownNetherlands: 531 citing papers, 3.5% of this breakdownFrance: 475 citing papers, 3.1% of this breakdownSweden: 367 citing papers, 2.4% of this breakdownItaly: 356 citing papers, 2.3% of this breakdownFinland: 313 citing papers, 2% of this breakdownDenmark: 307 citing papers, 2% of this breakdown
0%26.5%Other 29.4%

Fields

  • Biochemistry, Genetics and Molecular Biology62.1%
  • Medicine20.1%
  • Agricultural and Biological Sciences6%
  • Immunology and Microbiology3.7%
  • Neuroscience2.4%
  • Psychology1.2%
  • Other4.5%

Topics

  • Genetic Associations and Epidemiology10.6%
  • Genetic Mapping and Diversity in Plants and Animals6.9%
  • Genetic and phenotypic traits in livestock5.2%
  • Single-cell and spatial transcriptomics3%
  • Epigenetics and DNA Methylation2.6%
  • Bioinformatics and Genomic Networks2.3%
  • Other69.4%

Coauthors

All papers

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  1. Multiplexed droplet single-cell RNA-sequencing using natural genetic variation

    Authors: , , , , , , , , , , , , , , , - Nature Biotechnology 2017 cited by 1,274

  2. Variance component model to account for sample structure in genome-wide association studies

    Authors: , , , , , , , - Nature Genetics 2010 cited by 3,054

  3. TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pietro Fratta, Gregory A. Cox, Leslie M. Thompson, Steven Finkbeiner, Efthimios Dardiotis, Timothy M. Miller, Siddharthan Chandran, Suvankar Pal, Eran Hornstein, Daniel J. MacGowan, Terry Heiman‐Patterson, Molly Hammell, Nikolaos A. Patsopoulos, Oleg Butovsky, Josh Dubnau, Avindra Nath, Robert Bowser, Matthew B. Harms, Eleonora Aronica, Mary Poss, Jennifer E. Phillips‐Cremins, John F. Crary, Nazem Atassi, Dale J. Lange, Darius J. Adams, Leonidas Stefanis, Marc Gotkine, Robert H. Baloh, Suma Babu, Towfique Raj, Sabrina Paganoni, Ophir Shalem, Colin Smith, Bin Zhang, Brent T. Harris, Iris Broce, Vivian E. Drory, John Ravits, Corey T. McMillan, Vilas Menon, Lani F. Wu, Steven J. Altschuler, Yossef Lerner, Rita Sattler, Kendall Van Keuren‐Jensen, Orit Rozenblatt–Rosen, Kerstin Lindblad‐Toh, Katharine Nicholson, Peter K. Gregersen, Jeong‐Ho Lee, Sulev Kõks, Stephen Muljo, Jia Newcombe, Emil K. Gustavsson, Sahba Seddighi, Joel F. Reyes, Steven L. Coon, Daniel M. Ramos, Giampietro Schiavo, Elizabeth Fisher, Towfique Raj, Maria Secrier, Tammaryn Lashley, Jernej Ule, Emanuele Buratti, Jack Humphrey, Michael E. Ward, Pietro Fratta - Nature 2022 cited by 514

  4. Single-cell RNA-seq reveals cell type–specific molecular and genetic associations to lupus

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2022 cited by 559

  5. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter M. Visscher, Peter Kraft, Nick Patterson, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price and 302 more - The American Journal of Human Genetics 2015 cited by 1,489

  6. Race and Genetic Ancestry in Medicine — A Time for Reckoning with Racism

    Authors: , , , , , , , , , , , , , , , - New England Journal of Medicine 2021 cited by 660

  7. Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eran Hornstein, Daniel J. MacGowan, Terry Heiman‐Patterson, Molly Hammell, Nikolaos A. Patsopoulos, Oleg Butovsky, Josh Dubnau, Avindra Nath, Robert Bowser, Matt Harms, Eleonora Aronica, Mary Poss, Jennifer E. Phillips‐Cremins, John F. Crary, Nazem Atassi, Dale J. Lange, Darius J. Adams, Leonidas Stefanis, Marc Gotkine, Robert W. Baloh, Suma Babu, Towfique Raj, Sabrina Paganoni, Ophir Shalem, Colin Smith, Bin Zhang, Brent T. Harris, Delphine Fagegaltier, Brent T. Harris, Lyle W. Ostrow, Hemali Phatnani, John Ravits, Josh Dubnau, Molly Hammell - Cell Reports 2019 cited by 333

  8. Advantages and pitfalls in the application of mixed-model association methods

    Authors: , , , , - Nature Genetics 2014 cited by 1,105

  9. Transethnic Genetic-Correlation Estimates from Summary Statistics

    Authors: , , , - The American Journal of Human Genetics 2016 cited by 410

  10. New approaches to population stratification in genome-wide association studies

    Authors: , , , - Nature Reviews Genetics 2010 cited by 1,284

  11. Multi-ancestry polygenic mechanisms of type 2 diabetes

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Medicine 2024 cited by 109

  12. Efficient Control of Population Structure in Model Organism Association Mapping

    Authors: , , , , , , - Genetics 2008 cited by 1,964

  13. Ancestry-driven recalibration of tumor mutational burden and disparate clinical outcomes in response to immune checkpoint inhibitors

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jian Carrot‐Zhang, Alexander Gusev - Cancer Cell 2022 cited by 116

  14. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries

    Authors: , , , , , , , , , , , , - Nature Genetics 2023 cited by 52

  15. COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Feroz R. Papa, Donna M. Muzny, Noah Zaitlen, Suzanne M. Leal, Claudia Gonzaga‐Jauregui, Eric Boerwinkle, N. Tony Eissa, Richard A. Gibbs, James R. Lupski, Jordan S. Orange, Anthony K. Shum - Nature Genetics 2015 cited by 399

  16. Toward a fine-scale population health monitoring system

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Cell 2021 cited by 161

  17. Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture

    Authors: , , , , , , , , , , , , , , , , , , - Nature Genetics 2023 cited by 101

  18. Methylation risk scores are associated with a collection of phenotypes within electronic health record systems

    Authors: , , , , , , , , , - npj Genomic Medicine 2022 cited by 57

  19. Differential methylation between ethnic sub-groups reflects the effect of genetic ancestry and environmental exposures

    Authors: , , , , , , , , , , , , , , , , , , , , , - eLife 2017 cited by 246

  20. Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

    Authors: , , , , , , , , , - Bioinformatics, Bioinform. 2014 cited by 231

  21. Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE

    Authors: , , , , , , , , - Nature Communications 2021 cited by 93

  22. Massively parallel analysis of human 3′ UTRs reveals that AU-rich element length and registration predict mRNA destabilization

    Authors: , , , , - G3 Genes Genomes Genetics 2021 cited by 62

  23. Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 57

  24. Dual gene activation and knockout screen reveals directional dependencies in genetic networks

    Authors: , , , , , , , , , , , , - Nature Biotechnology 2018 cited by 163