Kathryn Roeder - Dissemin

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All papers authored by Kathryn Roeder

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2024 Jin-Hong Du

ORCID

, Pratik Patil, Kathryn Roeder

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, Arun Kumar Kuchibhotla

Extrapolated Cross-Validation for Randomized Ensembles

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2023 Zhanrui Cai

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, Jing Lei, Kathryn Roeder

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Asymptotic Distribution-Free Independence Test for High-Dimension Data

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John A. Morris

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, Christina Caragine

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, Zharko Daniloski

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, Júlia Domingo, Timothy Barry, Lu Lu

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, Kyrie Davis, Marcello Ziosi, Dafni A. Glinos

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, Stephanie Hao, Eleni P. Mimitou

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, Peter Smibert

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, Kathryn Roeder

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, Eugene Katsevich

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, Tuuli Lappalainen

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and 1 other authors

Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens

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2022 Jin-Hong Du

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, Zhanrui Cai, Kathryn Roeder

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Robust probabilistic modeling for single-cell multimodal mosaic integration and imputation via scVAEIT

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Zhanrui Cai, Jing Lei

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, Kathryn Roeder

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Model-free prediction test with application to genomics data

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2021 Xuran Wang, David Choi, Kathryn Roeder

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Constructing local cell-specific networks from single-cell data

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Behrang Mahjani

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, Silvia De Rubeis

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, Christina Gustavsson Mahjani, Maureen Mulhern, Xinyi Xu, Lambertus Klei

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, F. Kyle Satterstrom

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, Jack Fu, Michael E. Talkowski

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, Abraham Reichenberg, Sven Sandin

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, Christina M. Hultman

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, Dorothy E. Grice

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, Kathryn Roeder

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, Bernie Devlin

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and 1 other authors

Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

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Ronald Yurko, Kathryn Roeder

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, Bernie Devlin, Max G’Sell

An approach to gene-based testing accounting for dependence of tests among nearby genes

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John A. Morris, Zharko Daniloski, Júlia Domingo, Timothy Barry, Marcello Ziosi, Dafni A. Glinos, Stephanie Hao, Eleni P. Mimitou, Peter Smibert, Kathryn Roeder

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, Eugene Katsevich, Tuuli Lappalainen, Neville E. Sanjana

Discovery of target genes and pathways of blood trait loci using pooled CRISPR screens and single cell RNA sequencing

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Minshi Peng, Yue Li, Brie Wamsley, Yuting Wei, Kathryn Roeder

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Integration and transfer learning of single-cell transcriptomes via cFIT

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Behrang Mahjani, Lambertus Klei, Manuel Mattheisen, Matthew W. Halvorsen, Abraham Reichenberg, Kathryn Roeder

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, Nancy L. Pedersen, Julia Boberg, Elles de Schipper, Cynthia M. Bulik, Mikael Landén, Bengt Fundín, David Mataix-Cols, Sven Sandin, Christina M. Hultman and 5 other authors

The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

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2020 Ronald Yurko, Kathryn Roeder

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, Bernie Devlin, Max G'Sell

H‐MAGMA, inheriting a shaky statistical foundation, yields excess false positives

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Siwei Chen

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ORCID

, Ercument Cicek

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, Kathryn Roeder

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ORCID

, Bernie Devlin

ORCID

De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types

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Ronald Yurko

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, Max G’Sell, Kathryn Roeder

ORCID

, Bernie Devlin

ORCID

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

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2017 Pauline Chaste, Kathryn Roeder

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, Bernie Devlin

The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability

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Jack A. Kosmicki, Kaitlin E. Samocha

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, Daniel P. Howrigan, Stephan J. Sanders

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, Kamil Slowikowski, Monkol Lek, Konrad J. Karczewski, David J. Cutler, Bernie Devlin, Kathryn Roeder

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, Joseph D. Buxbaum, Benjamin M. Neale

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, Daniel G. MacArthur, Dennis P. Wall, Elise B. Robinson and 1 other authors

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

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R. J. L. Anney, S. Ripke, J. Grove, P. Holmans, H. Huang, L. Klei, P. H. Lee, S. E. Medland, B. Neale, E. Robinson, L. A. Weiss, L. Zwaigenbaum, T. W. Yu, K. Wittemeyer, A. J. Willsey and 149 other authors

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

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2016 Herman van Engeland, Emilie M. Wigdor, Lonnie Zwaigenbaum, Timothy W. Yu, Kerstin Wittemeyer, A. Jeremy Willsey, Ellen M. Wijsman, Daniel J. Weiner, Raymond K. Walters, Kaitlin E. Samocha

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, Jacob Taylor, David Skuse, Stephan J. Sanders, George Davey Smith, Christine Stevens and 187 other authors

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

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Menachem Fromer

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, Panos Roussos, Solveig K. Sieberts, Jessica S. Johnson, David H. Kavanagh, Thanneer M. Perumal

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, Douglas M. Ruderfer, Edwin C. Oh, Aaron Topol, Hardik R. Shah, Lambertus L. Klei, Robin Kramer, Dalila Pinto

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, Zeynep H. Gümüş, Zeynep H. Gumus and 48 other authors

Gene expression elucidates functional impact of polygenic risk for schizophrenia

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Corneliu A. Bodea, Stephan Ripke, Benjamin M. Neale, Bernie Devlin, Murray Barclay, Kathryn Roeder

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, Laurent Peyrin-Biroulet, Mathias Chamaillard, Jean-Frederick Colombel, Mario Cottone, Anthony Croft, Renata D’Incà, Jonas Halfvarson, Katherine Hanigan, Paul Henderson and 335 other authors

A method to exploit the structure of genetic ancestry space to enhance case-control studies

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