A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY
ANNALS OF APPLIED STATISTICS (2010)
期刊
ANNALS OF APPLIED STATISTICS
卷 4, 期 1, 页码 179-202出版社
INST MATHEMATICAL STATISTICS
关键词
资金
- NIH [MH057881]
- ONR [N0014-08-1-0673]
作者
我是这篇论文的作者
推荐
A closed-form solution for conditional multidimensional scaling
Anh Tuan Bui
PATTERN RECOGNITION LETTERS (2022)
Multidimensional scaling of noisy high dimensional data
Erez Peterfreund, Matan Gavish
APPLIED AND COMPUTATIONAL HARMONIC ANALYSIS (2021)
Statistical Significance of Clustering with Multidimensional Scaling
Hui Shen, Shankar Bhamidi, Yufeng Liu
JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS (2023)
Reduced multidimensional scaling
Emmanuel Paradis
COMPUTATIONAL STATISTICS (2022)
Visualizing Population Structures by Multidimensional Scaling of Smoothed PCA-Transformed Data
Dimitrios Charalampidis
IEEE ACCESS (2023)
Structure-based hyperparameter selection with Bayesian optimization in multidimensional scaling
Thomas Rusch, Patrick Mair, Kurt Hornik
STATISTICS AND COMPUTING (2023)
An analysis of classical multidimensional scaling with applications to clustering
Anna Little, Yuying Xie, Qiang Sun
INFORMATION AND INFERENCE-A JOURNAL OF THE IMA (2023)
Local biplots for multidimensional scaling, with application to the microbiome
Julia Fukuyama
JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS (2022)
Infinite multidimensional scaling for metric measure spaces*
Alexey Kroshnin, Eugene Stepanov, Dario Trevisan
ESAIM-CONTROL OPTIMISATION AND CALCULUS OF VARIATIONS (2022)
Multidimensional scaling and visualization of patterns in global large-scale accidents
Antonio M. Lopes, J. A. Tenreiro Machado
CHAOS SOLITONS & FRACTALS (2022)
Geometric multidimensional scaling: A new approach for data dimensionality reduction
Gintautas Dzemyda, Martynas Sabaliauskas
APPLIED MATHEMATICS AND COMPUTATION (2021)
Toward automated extraction and characterization of scaling regions in dynamical systems
Varad Deshmukh, Elizabeth Bradley, Joshua Garland, James D. Meiss
CHAOS (2021)
Enriching representation learning using 53 million patient notes through human phenotype ontology embedding
Maryam Daniali, Peter D. Galer, David Lewis-Smith, Shridhar Parthasarathy, Edward Kim, Dario D. Salvucci, Jeffrey M. Miller, Scott Haag, Ingo Helbig
ARTIFICIAL INTELLIGENCE IN MEDICINE (2023)
Ensemble dimension reduction based on spectral disturbance for subspace clustering
Xiaoyun Chen, Qiaoping Wang, Shanshan Zhuang
KNOWLEDGE-BASED SYSTEMS (2021)
Robust dimensionality reduction method based on relaxed energy and structure preserving embedding for multiview clustering
Zhongyan Gui, Jing Yang, Zhiqiang Xie
INFORMATION SCIENCES (2023)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
Robert Maier, Gerhard Moser, Guo-Bo Chen, Stephan Ripke, William Coryell, James B. Potash, William A. Scheftner, Jianxin Shi, Myrna M. Weissman, Christina M. Hultman, Mikael Landen, Douglas F. Levinson, Kenneth S. Kendler, Jordan W. Smoller, Naomi R. Wray, S. Hong Lee
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM
Li Liu, Jing Lei, Kathryn Roeder
ANNALS OF APPLIED STATISTICS (2015)
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies
Corneliu A. Bodea, Benjamin M. Neale, Stephan Ripke, Mark J. Daly, Bernie Devlin, Kathryn Roeder
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Gene expression elucidates functional impact of polygenic risk for schizophrenia
Menachem Fromer, Panos Roussos, Solveig K. Sieberts, Jessica S. Johnson, David H. Kavanagh, Thanneer M. Perumal, Douglas M. Ruderfer, Edwin C. Oh, Aaron Topol, Hardik R. Shah, Lambertus L. Klei, Robin Kramer, Dalila Pinto, Zeynep H. Gumus, A. Ercument Cicek, Kristen K. Dang, Andrew Browne, Cong Lu, Lu Xie, Ben Readhead, Eli A. Stahl, Jianqiu Xiao, Mahsa Parvizi, Tymor Hamamsy, John F. Fullard, Ying-Chih Wang, Milind C. Mahajan, Jonathan M. J. Derry, Joel T. Dudley, Scott E. Hemby, Benjamin A. Logsdon, Konrad Talbot, Towfique Raj, David A. Bennett, Philip L. De Jager, Jun Zhu, Bin Zhang, Patrick F. Sullivan, Andrew Chess, Shaun M. Purcell, Leslie A. Shinobu, Lara M. Mangravite, Hiroyoshi Toyoshiba, Raquel E. Gur, Chang-Gyu Hahn, David A. Lewis, Vahram Haroutunian, Mette A. Peters, Barbara K. Lipska, Joseph D. Buxbaum, Eric E. Schadt, Keisuke Hirai, Kathryn Roeder, Kristen J. Brennand, Nicholas Katsanis, Enrico Domenici, Bernie Devlin, Pamela Sklar
NATURE NEUROSCIENCE (2016)
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, Stephan J. Sanders, Kamil Slowikowski, Monkol Lek, Konrad J. Karczewski, David J. Cutler, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum, Benjamin M. Neale, Daniel G. MacArthur, Dennis P. Wall, Elise B. Robinson, Mark J. Daly
NATURE GENETICS (2017)
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Daniel J. Weiner, Emilie M. Wigdor, Stephan Ripke, Raymond K. Walters, Jack A. Kosmicki, Jakob Grove, Kaitlin E. Samocha, Jacqueline I. Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm, Thomas Werge, David M. Hougaard, Jacob Taylor, David Skuse, Bernie Devlin, Richard Anney, Stephan J. Sanders, Somer Bishop, Preben Bo Mortensen, Anders D. Borglum, George Davey Smith, Mark J. Daly, Elise B. Robinson, Marie Baekvad-Hansen, Ashley Dumont, Christine Hansen, Thomas F. Hansen, Daniel Howrigan, Manuel Mattheisen, Jennifer Moran, Ole Mors, Merete Nordentoft, Bent Norgaard-Pedersen, Timothy Poterba, Jesper Poulsen, Christine Stevens, Verneri Anttila, Peter Holmans, Hailiang Huang, Lambertus Klei, Phil H. Lee, Sarah E. Medland, Benjamin Neale, Lauren A. Weiss, Lonnie Zwaigenbaum, Timothy W. Yu, Kerstin Wittemeyer, A. Jeremy Willsey, Ellen M. Wijsman, Thomas H. Wassink, Regina Waltes, Christopher A. Walsh, Simon Wallace, Jacob A. S. Vorstman, Veronica J. Vieland, Astrid M. Vicente, Herman van Engeland, Kathryn Tsang, Ann P. Thompson, Peter Szatmari, Oscar Svantesson, Stacy Steinberg, Kari Stefansson, Hreinn Stefansson, Matthew W. State, Latha Soorya, Teimuraz Silagadze, Stephen W. Scherer, Gerard D. Schellenberg, Sven Sandin, Evald Saemundsen, Guy A. Rouleau, Bernadette Roge, Kathryn Roeder, Wendy Roberts, Jennifer Reichert, Abraham Reichenberg, Karola Rehnstrom, Regina Regan, Fritz Poustka, Christopher S. Poultney, Joseph Piven, Dalila Pinto, Margaret A. Pericak-Vance, Milica Pejovic-Milovancevic, Marianne G. Pedersen, Carsten B. Pedersen, Andrew D. Paterson, Jeremy R. Parr, Alistair T. Pagnamenta, Guiomar Oliveira, John I. Nurnberger, Merete Nordentoft, Michael T. Murtha, Susana Mouga, Ole Mors, Eric M. Morrow, Daniel Moreno De Luca, Anthony P. Monaco, Nancy Minshew, Alison Merikangas, William M. McMahon, Susan G. McGrew, Manuel Mattheisen, Igor Martsenkovsky, Donna M. Martin, Shrikant M. Mane, Pall Magnusson, Tiago Magalhaes, Elena Maestrini, Jennifer K. Lowe, Catherine Lord, Pat Levitt, Christa Lese Martin, David H. Ledbetter, Marion Leboyer, Ann S. Le Couteur, Christine Ladd-Acosta, Alexander Kolevzon, Sabine M. Klauck, Suma Jacob, Bozenna Iliadou, Christina M. Hultman, Irva Hertz-Picciotto, Robert Hendren, Christine S. Hansen, Jonathan L. Haines, Stephen J. Guter, Dorothy E. Grice, Jonathan M. Green, Andrew Green, Arthur P. Goldberg, Christopher Gillberg, John Gilbert, Louise Gallagher, Christine M. Freitag, Eric Fombonne, Susan E. Folstein, Bridget Fernandez, M. Daniele Fallin, A. Gulhan Ercan-Sencicek, Sean Ennis, Frederico Duque, Eftichia Duketis, Richard Delorme, Silvia De Rubeis, Maretha V. De Jonge, Geraldine Dawson, Michael L. Cuccaro, Catarina T. Correia, Judith Conroy, Ines C. Conceicao, Andreas G. Chiocchetti, Patricia B. S. Celestino-Soper, Jillian Casey, Rita M. Cantor, Catia Cafe, Sean Brennan, Thomas Bourgeron, Patrick F. Bolton, Sven Boelte, Nadia Bolshakova, Catalina Betancur, Raphael Bernier, Arthur L. Beaudet, Agatino Battaglia, Vanessa H. Bal, Gillian Baird, Anthony J. Bailey, Marie Baekvad-Hansen, Joel S. Bader, Elena Bacchelli, Evdokia Anagnostou, David Amaral, Joana Almeida, Joseph D. Buxbaum, Aravinda Chakravarti, Edwin H. Cook, Hilary Coon, Daniel H. Geschwind, Michael Gill, Hakon Hakonarson, Joachim Hallmayer, Aarno Palotie, Susan Santangelo, James S. Sutcliffe, Dan E. Arking
NATURE GENETICS (2017)
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
Richard J. L. Anney, Stephan Ripke, Verneri Anttila, Jakob Grove, Peter Holmans, Hailiang Huang, Lambertus Klei, Phil H. Lee, Sarah E. Medland, Benjamin Neale, Elise Robinson, Lauren A. Weiss, Lonnie Zwaigenbaum, Timothy W. Yu, Kerstin Wittemeyer, A. Jeremy Willsey, Ellen M. Wijsman, Thomas Werge, Thomas H. Wassink, Regina Waltes, Christopher A. Walsh, Simon Wallace, Jacob A. S. Vorstman, Veronica J. Vieland, Astrid M. Vicente, Herman vanEngeland, Kathryn Tsang, Ann P. Thompson, Peter Szatmari, Oscar Svantesson, Stacy Steinberg, Kari Stefansson, Hreinn Stefansson, Matthew W. State, Latha Soorya, Teimuraz Silagadze, Stephen W. Scherer, Gerard D. Schellenberg, Sven Sandin, Stephan J. Sanders, Evald Saemundsen, Guy A. Rouleau, Bernadette Roge, Kathryn Roeder, Wendy Roberts, Jennifer Reichert, Abraham Reichenberg, Karola Rehnstrom, Regina Regan, Fritz Poustka, Christopher S. Poultney, Joseph Piven, Dalila Pinto, Margaret A. Pericak-Vance, Milica Pejovic-Milovancevic, Marianne Giortz Pedersen, Carsten Bocker Pedersen, Andrew D. Paterson, Jeremy R. Parr, Alistair T. Pagnamenta, Guiomar Oliveira, John I. Nurnberger, Merete Nordentoft, Michael T. Murtha, Susana Mouga, Preben Bo Mortensen, Ole Mors, Eric M. Morrow, Daniel Moreno-De-Luca, Anthony P. Monaco, Nancy Minshew, Alison Merikangas, William M. McMahon, Susan G. McGrew, Manuel Mattheisen, Igor Martsenkovsky, Donna M. Martin, Shrikant M. Mane, Pall Magnusson, Tiago Magalhaes, Elena Maestrini, Jennifer K. Lowe, Catherine Lord, Pat Levitt, Christa LeseMartin, David H. Ledbetter, Marion Leboyer, Ann S. LeCouteur, Christine Ladd-Acosta, Alexander Kolevzon, Sabine M. Klauck, Suma Jacob, Bozenna Iliadou, Christina M. Hultman, David M. Hougaard, Irva Hertz-Picciotto, Robert Hendren, Christine Soholm Hansen, Jonathan L. Haines, Stephen J. Guter, Dorothy E. Grice, Jonathan M. Green, Andrew Green, Arthur P. Goldberg, Christopher Gillberg, John Gilbert, Louise Gallagher, Christine M. Freitag, Eric Fombonne, Susan E. Folstein, Bridget Fernandez, M. Daniele Fallin, A. Gulhan Ercan-Sencicek, Sean Ennis, Frederico Duque, Eftichia Duketis, Richard Delorme, Silvia DeRubeis, Maretha V. DeJonge, Geraldine Dawson, Michael L. Cuccaro, Catarina T. Correia, Judith Conroy, Ines C. Conceicao, Andreas G. Chiocchetti, Patrcia B. S. Celestino-Soper, Jillian Casey, Rita M. Cantor, Catia Cafe, Jonas Bybjerg-Grauholm, Sean Brennan, Thomas Bourgeron, Patrick F. Bolton, Sven Boelte, Nadia Bolshakova, Catalina Betancur, Raphael Bernier, Arthur L. Beaudet, Agatino Battaglia, Vanessa H. Bal, Gillian Baird, Anthony J. Bailey, Marie Baekvad-Hansen, Joel S. Bader, Elena Bacchelli, Evdokia Anagnostou, David Amaral, Joana Almeida, Anders D. Borglum, Joseph D. Buxbaum, Aravinda Chakravarti, Edwin H. Cook, Hilary Coon, Daniel H. Geschwind, Michael Gill, Hakon Hakonarson, Joachim Hallmayer, Aarno Palotie, Susan Santangelo, James S. Sutcliffe, Dan E. Arking, Bernie Devlin, Mark J. Daly
MOLECULAR AUTISM (2017)
A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk
Ronald Yurko, Max G'Sell, Kathryn Roeder, Bernie Devlin
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types
Siwei Chen, Jiebiao Wang, Ercument Cicek, Kathryn Roeder, Haiyuan Yu, Bernie Devlin
MOLECULAR AUTISM (2020)
H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives
Ronald Yurko, Kathryn Roeder, Bernie Devlin, Max G'Sell
ANNALS OF HUMAN GENETICS (2021)
Integration and transfer learning of single-cell transcriptomes via cFIT
Minshi Peng, Yue Li, Brie Wamsley, Yuting Wei, Kathryn Roeder
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2021)
Model-free prediction test with application to genomics data
Zhanrui Cai, Jing Lei, Kathryn Roeder
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2022)
Robust probabilistic modeling for single-cell multimodal mosaic integration and imputation via scVAEIT
Jin-Hong Du, Zhanrui Cai, Kathryn Roeder
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2022)
Constructing local cell-specific networks from single-cell data
Xuran Wang, David Choi, Kathryn Roeder
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2021)
The Genetic Architecture of Obsessive-Compulsive Disorder: Alleles Across the Frequency Spectrum Contribute Liability to OCD
Behrang Mahjani, Lambertus Klei, Manuel Mattheisen, Matthew Halvorsen, Abraham Reichenberg, Kathryn Roeder, Nancy Pedersen, Julia Boberg, Elles de Schipper, Cynthia Bulik, Mikael Landen, Bengt Fundin, David Mataix-Cols, Sven Sandin, Christina Hultman, James Crowley, Joseph Buxbaum, Christian Ruck, Bernie Devlin, Dorothy Grice
NEUROPSYCHOPHARMACOLOGY (2021)