Articoli con mandati relativi all'accesso pubblico - Saharon RossetUlteriori informazioni
Disponibili pubblicamente: 26
Surprises in high-dimensional ridgeless least squares interpolation
T Hastie, A Montanari, S Rosset, RJ Tibshirani
Annals of statistics 50 (2), 949, 2022
Mandati: US National Science Foundation, US Department of Defense, US National …
Measuring missing heritability: inferring the contribution of common variants
D Golan, ES Lander, S Rosset
Proceedings of the National Academy of Sciences 111 (49), E5272-E5281, 2014
Mandati: US National Institutes of Health
Random lasso
S Wang, B Nan, S Rosset, J Zhu
The annals of applied statistics 5 (1), 468, 2011
Mandati: US National Institutes of Health
Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology
E Rahmani, R Schweiger, B Rhead, LA Criswell, LF Barcellos, E Eskin, ...
Nature communications 10 (1), 3417, 2019
Mandati: US National Science Foundation, US National Institutes of Health
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris
O Sarig, S Bercovici, L Zoller, I Goldberg, M Indelman, S Nahum, S Israeli, ...
Journal of investigative dermatology 132 (7), 1798-1805, 2012
Mandati: German Research Foundation
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
DM Behar, S Rosset, S Tzur, S Selig, G Yudkovsky, S Bercovici, JB Kopp, ...
Human molecular genetics 19 (9), 1816-1827, 2010
Mandati: US National Institutes of Health
Estimating SNP-based heritability and genetic correlation in case-control studies directly and with summary statistics
O Weissbrod, J Flint, S Rosset
The American Journal of Human Genetics 103 (1), 89-99, 2018
Mandati: US National Institutes of Health, Wellcome Trust
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi Levites
S Rootsi, DM Behar, M Järve, AA Lin, NM Myres, B Passarelli, GD Poznik, ...
Nature communications 4 (1), 2928, 2013
Mandati: European Commission
Effective genetic-risk prediction using mixed models
D Golan, S Rosset
The American Journal of Human Genetics 95 (4), 383-393, 2014
Mandati: Wellcome Trust
Multikernel linear mixed models for complex phenotype prediction
O Weissbrod, D Geiger, S Rosset
Genome research 26 (7), 969-979, 2016
Mandati: Wellcome Trust
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy
KL Skorecki, JH Lee, CD Langefeld, S Rosset, S Tzur, WG Wasser, ...
Nephrology Dialysis Transplantation 33 (2), 323-330, 2018
Mandati: US National Institutes of Health, Doris Duke Charitable Foundation
Fast and accurate construction of confidence intervals for heritability
R Schweiger, S Kaufman, R Laaksonen, ME Kleber, W März, E Eskin, ...
The American Journal of Human Genetics 98 (6), 1181-1192, 2016
Mandati: US National Science Foundation, US National Institutes of Health
RL-SKAT: an exact and efficient score test for heritability and set tests
R Schweiger, O Weissbrod, E Rahmani, M Müller-Nurasyid, S Kunze, ...
Genetics 207 (4), 1275-1283, 2017
Mandati: US National Science Foundation, Helmholtz Association, Wellcome Trust …
Weighted pooling—practical and cost-effective techniques for pooled high-throughput sequencing
D Golan, Y Erlich, S Rosset
Bioinformatics 28 (12), i197-i206, 2012
Mandati: US National Institutes of Health
Using stochastic approximation techniques to efficiently construct confidence intervals for heritability
R Schweiger, E Fisher, E Rahmani, L Shenhav, S Rosset, E Halperin
Journal of Computational Biology 25 (7), 794-808, 2018
Mandati: Wellcome Trust
Association testing of bisulfite-sequencing methylation data via a Laplace approximation
O Weissbrod, E Rahmani, R Schweiger, S Rosset, E Halperin
Bioinformatics 33 (14), i325-i332, 2017
Mandati: US National Science Foundation
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests
R Schweiger, E Fisher, O Weissbrod, E Rahmani, M Müller-Nurasyid, ...
Nature communications 9 (1), 4919, 2018
Mandati: US National Science Foundation, Helmholtz Association, Federal Ministry of …
The everlasting database: Statistical validity at a fair price
BE Woodworth, V Feldman, S Rosset, N Srebro
Advances in neural information processing systems 31, 2018
Mandati: US National Science Foundation
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
H Levi, S Carmi, S Rosset, R Yerushalmi, A Zick, T Yablonski-Peretz, ...
Journal of medical genetics 60 (12), 1186-1197, 2023
Mandati: National Health and Medical Research Council, Australia, Genome Canada …
Maximum Likelihood for Gaussian Process Classification and Generalized Linear Mixed Models under Case-Control Sampling
O Weissbrod, S Kaufman, D Golan, S Rosset
Journal of Machine Learning Research 20 (108), 1-30, 2019
Mandati: Wellcome Trust
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