Kathryn Roeder
Statistics and Probability · 1999–2019
A researcher in the Science corpus: 21 papers; trusts 17 researchers and is trusted by 25 researchers here, as inferred from the citation graph.
Subfields
- Statistics and Probability — 30 citations into it; #2,051 of 12,932 by trust here, #2,751 by citations
- Artificial Intelligence — 23 citations into it
- Evaluation & Benchmarks — 6 citations into it
Whom Kathryn Roeder trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Nicolai Meinshausen
- Robert Tibshirani
- Bradley Efron
- Han Liu
- Ming Yuan
- Jerome H. Friedman
- Peter Buhlmann
- Hirotogu Akaike
- Trevor J. Hastie
- Larry A. Wasserman
Who trusts Kathryn Roeder overall
- David A. Hensher
- Dan Nagin
- Amelia Haviland
- B. Jones
- William H. Greene
- Bradley Efron
- Margit Wiesner
- B. Muthén
- Mathias Drton
- Rina Foygel Barber
Papers from Kathryn Roeder's perspective
Ordered by how strongly the researchers Kathryn Roeder trusts endorse each paper. Same corpus, a different order for every researcher.
- Regression Shrinkage and Selection via the Lasso
- High-dimensional graphs and variable selection with the Lasso
- PATHWISE COORDINATE OPTIMIZATION
- Model selection and estimation in the Gaussian graphical model
- Estimating the Dimension of a Model
- Sure independence screening for ultrahigh dimensional feature space
- Introduction to Graphical Modelling (Technometrics)
- © Institute of Mathematical Statistics, 2009 HIGH-DIMENSIONAL VARIABLE SELECTION BY LARRY WASSERMAN AND KATHRYN ROEDER 1
- Information Theory and an Extension of the Maximum Likelihood Principle
- Operating characteristics and extensions of the false discovery rate procedure
Their papers
- False discovery control with p-value weighting (2006) — 354 citations
- Stability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models (2010) — 526 citations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations
- Testing for an Unusual Distribution of Rare Variants (2011) — 617 citations
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
- Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) — 1,080 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders (2018) — 67 citations
- Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples (2016) — 373 citations
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) — 1,391 citations
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
- Most genetic risk for autism resides with common variation (2014) — 1,198 citations
- Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism (2013) — 905 citations
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) — 2,079 citations
- Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
- The huge Package for High-dimensional Undirected Graph Estimation in R (2012) — 531 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories (2001) — 2,394 citations