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Xihong Lin
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Year
Rare-variant association testing for sequencing data with the sequence kernel association test
MC Wu, S Lee, T Cai, Y Li, M Boehnke, X Lin
The American Journal of Human Genetics 89 (1), 82-93, 2011
26242011
Quality of life and satisfaction with outcome among prostate-cancer survivors
MG Sanda, RL Dunn, J Michalski, HM Sandler, L Northouse, L Hembroff, ...
New England Journal of Medicine 358 (12), 1250-1261, 2008
25562008
Risk of COVID-19 among front-line health-care workers and the general community: a prospective cohort study
LH Nguyen, DA Drew, MS Graham, AD Joshi, CG Guo, W Ma, RS Mehta, ...
The Lancet Public Health 5 (9), e475-e483, 2020
24382020
Association of public health interventions with the epidemiology of the COVID-19 outbreak in Wuhan, China
A Pan, L Liu, C Wang, H Guo, X Hao, Q Wang, J Huang, N He, H Yu, X Lin, ...
Jama 323 (19), 1915-1923, 2020
18222020
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
12812021
LKB1 modulates lung cancer differentiation and metastasis
H Ji, MR Ramsey, DN Hayes, C Fan, K McNamara, P Kozlowski, C Torrice, ...
Nature 448 (7155), 807-810, 2007
11552007
Rare-variant association analysis: study designs and statistical tests
S Lee, GR Abecasis, M Boehnke, X Lin
The American Journal of Human Genetics 95 (1), 5-23, 2014
11052014
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
S Lee, MJ Emond, MJ Bamshad, KC Barnes, MJ Rieder, DA Nickerson, ...
The American Journal of Human Genetics 91 (2), 224-237, 2012
10572012
Inference in generalized additive mixed models by using smoothing splines
X Lin, D Zhang
Journal of the Royal Statistical Society Series B: Statistical Methodology …, 1999
7651999
Optimal tests for rare variant effects in sequencing association studies
S Lee, MC Wu, X Lin
Biostatistics 13 (4), 762-775, 2012
7532012
Powerful SNP-set analysis for case-control genome-wide association studies
MC Wu, P Kraft, MP Epstein, DM Taylor, SJ Chanock, DJ Hunter, X Lin
The American Journal of Human Genetics 86 (6), 929-942, 2010
6922010
Bias correction in generalised linear mixed models with a single component of dispersion
NE Breslow, X Lin
Biometrika 82 (1), 81-91, 1995
6321995
A century of trends in adult human height
NCD Risk Factor Collaboration (NCD-RisC)
elife 5, e13410, 2016
6092016
Bias correction in generalized linear mixed models with multiple components of dispersion
X Lin, NE Breslow
Journal of the American Statistical Association 91 (435), 1007-1016, 1996
5451996
Sequence kernel association tests for the combined effect of rare and common variants
I Ionita-Laza, S Lee, V Makarov, JD Buxbaum, X Lin
The American Journal of Human Genetics 92 (6), 841-853, 2013
4822013
Reconstruction of the full transmission dynamics of COVID-19 in Wuhan
X Hao, S Cheng, D Wu, T Wu, X Lin, C Wang
Nature 584 (7821), 420-424, 2020
4442020
Nonparametric function estimation for clustered data when the predictor is measured without/with error
X Lin, RJ Carroll
Journal of the American statistical Association 95 (450), 520-534, 2000
4212000
Variance component testing in generalised linear models with random effects
X Lin
Biometrika 84 (2), 309-326, 1997
4201997
Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models
D Liu, X Lin, D Ghosh
Biometrics 63 (4), 1079-1088, 2007
4122007
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
A Mahajan, J Wessel, SM Willems, W Zhao, NR Robertson, AY Chu, ...
Nature genetics 50 (4), 559-571, 2018
4102018
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