Shili Lin

发表

Mixture modeling of progression pathways of heterogeneous breast tumors.

Shili Lin, 2007, Journal of theoretical biology.

Characterization of histone modification patterns and prediction of novel promoters using functional principal component analysis

Shili Lin, Mijeong Kim, 2020, PloS one.

Agonist and antagonist switch DNA motifs recognized by human androgen receptor in prostate cancer

Wei Li, Xun Lan, K. Nephew, 2015, The EMBO journal.

Statistical Challenges in Analyzing Methylation and Long-Range Chromosomal Interaction Data

Zhaohui S. Qin, Z. Qin, K. Conneely, 2016, Statistics in Biosciences.

Detecting Rare Haplotype‐Environment Interaction With Logistic Bayesian LASSO

Shili Lin, S. Biswas, Shuang Xia, 2014, Genetic epidemiology.

Space Oriented Rank-Based Data Integration

Shili Lin, 2010, Statistical applications in genetics and molecular biology.

Regularization in Finite Mixture of Regression Models with Diverging Number of Parameters

Shili Lin, Abbas Khalili, 2013, Biometrics.

Integrative genome-wide chromatin signature analysis using finite mixture models

Shili Lin, T. Huang, Kun Huang, 2012, BMC Genomics.

Gamma-Normal-Gamma Mixture Model for Detecting Differentially Methylated Loci in Three Breast Cancer Cell Lines

J. Gray, Lang Li, Shili Lin, 2007 .

Gamma-Normal-Gamma Mixture Model for Detecting Differentially Methylated Loci in Three Breast Cancer Cell Lines

J. Gray, Lang Li, Shili Lin, 2007, Cancer informatics.

Microarray analysis of gene expression: considerations in data mining and statistical treatment.

Vincent F. Melfi, J. Verducci, Shili Lin, 2006, Physiological genomics.

Multilocus LD measure and tagging SNP selection with generalized mutual information

Shili Lin, Zhenqiu Liu, Shili Lin, 2005, Genetic epidemiology.

Logistic Bayesian LASSO for Identifying Association with Rare Haplotypes and Application to Age‐Related Macular Degeneration

Shili Lin, S. Biswas, Shili Lin, 2012, Biometrics.

A Bayesian Approach for Incorporating Variable Rates of Heterogeneity in Linkage Analysis

Shili Lin, S. Biswas, Shili Lin, 2006 .

DNA methylation as a molecular relic to recapitulate tumor progression in breast cancer

Shili Lin, C. Eng, T. Huang, 2022 .

Breast cancer-associated fibroblasts confer AKT1-mediated epigenetic silencing of Cystatin M in epithelial cells.

Sandya Liyanarachchi, Shuying Sun, Michael C. Ostrowski, 2008, Cancer research.

Temporal dynamic reorganization of 3D chromatin architecture in hormone-induced breast cancer and endocrine resistance

R. Schiff, S. Frietze, Shili Lin, 2019, Nature Communications.

Classification of tissue samples using mixture modeling of microarray gene expression data

Roxana Alexandridis, Shili Lin, Shili Lin, 2003 .

A new Bayesian approach incorporating covariate information for heterogeneity and its comparison with HLOD

Donald A Berry, D. Berry, Shili Lin, 2005, BMC Genetics.

On modeling locus heterogeneity using mixture distributions

Shili Lin, S. Biswas, Shili Lin, 2004, BMC Genetics.

ON THE PERFORMANCE OF MARKOV CHAIN MONTE CARLO METHODS ON PEDIGREE DATA AND A NEW ALGORITHM

Shili Lin, Shili Lin, 1992 .

A quantitative proteomic workflow for characterization of frozen clinical biopsies: laser capture microdissection coupled with label-free mass spectrometry.

Anjali A. Satoskar, Sashwati Roy, Chandan K. Sen, 2012, Journal of proteomics.

ADAMTS13 activity and antigen during therapy and follow-up of patients with idiopathic thrombotic thrombocytopenic purpura: correlation with clinical outcome

Shili Lin, M. Jin, S. Cataland, 2011, Haematologica.

Testing for Associations of Opposite Directionality in a Heterogeneous Population

Shili Lin, Fangyuan Zhang, Jie Ding, 2017 .

Block-based association tests for rare variants using Kullback–Leibler divergence

Yue-Qing Hu, Shili Lin, Degang Zhu, 2016, Journal of Human Genetics.

A Bayesian mixture model for chromatin interaction data

Liang Niu, Shili Lin, L. Niu, 2015, Statistical applications in genetics and molecular biology.

Three‐dimensional analysis reveals altered chromatin interaction by enhancer inhibitors harbors TCF7L2‐regulated cancer gene signature

P. Farnham, S. Frietze, Shili Lin, 2018, Journal of cellular biochemistry.

The advent of the cDNA and oligonucleotide microarray accelerated the rate of discovery of genetic interplay by simultaneously monitoring thousands of genes in a single experiment (12,

Vincent F. Melfi, J. Verducci, Shili Lin, 2006 .

Detecting X‐linked common and rare variant effects in family‐based sequencing studies

Shili Lin, A. Turkmen, 2020, Genetic epidemiology.

An adaptive and robust method for multi-trait analysis of genome-wide association studies using summary statistics.

Shili Lin, C. Song, Q. Deng, 2022, European journal of human genetics : EJHG.

Classification Using Mass Spectrometry Proteomic Data with Kernel-Based Algorithms

Shili Lin, Zhenqiu Liu, Shili Lin, 2006 .

Construction of a Confidence Set of Markers for the Location of a Disease Gene Using Affected Sib Pair Data

Shili Lin, Shili Lin, 2002, Human Heredity.

A comparison of methods for intermediate fine mapping

Shili Lin, Charalampos Papachristou, 2006, Genetic epidemiology.

Detection of parent-of-origin effects for quantitative traits in complete and incomplete nuclear families with multiple children.

Ji-Yuan Zhou, Yue-Qing Hu, Wing Kam Fung, 2011, American journal of epidemiology.

Detection of imprinting and heterogeneous maternal effects on high blood pressure using Framingham Heart Study data

Shili Lin, Jingyuan Yang, 2009, BMC proceedings.

Methylation analysis by microarray.

Daniel E. Deatherage, Shili Lin, T. Huang, 2009, Methods in molecular biology.

An Adaptive and Robust Test for Microbial Community Analysis

Shili Lin, Qingyu Chen, C. Song, 2022, Frontiers in Genetics.

Demographic and ADAMTS13 biomarker data as predictors of early recurrences of idiopathic thrombotic thrombocytopenic purpura

J. George, Shili Lin, E. Kraut, 2009, European journal of haematology.

Likelihood Approach for Detecting Imprinting and In Utero Maternal Effects Using General Pedigrees from Prospective Family‐Based Association Studies

Shili Lin, Jingyuan Yang, 2012, Biometrics.

Rare disease and other assumptions in statistical analysis of genetic data : the good , the bad , and the ugly

Shili Lin, 2015 .

A Family-Based Rare Haplotype Association Method for Quantitative Traits

Shili Lin, S. Biswas, Ananda S. Datta, 2019, Human Heredity.

Evaluation of Recent Statistical Methods for Detecting Differential Methylation Using BS-seq Data

Shili Lin, Chenggong Han, Hancong Tang, 2018, OBM Genetics.

Detection of Differentially Methylated Regions Using Bayesian Curve Credible Bands

Jincheol Park, Shili Lin, 2016, Statistics in Biosciences.

Early Pregnancy Maternal Blood DNA Methylation in Repeat Pregnancies and Change in Gestational Diabetes Mellitus Status—A Pilot Study

M. Tadesse, Shili Lin, Michelle A. Williams, 2015, Reproductive Sciences.

BOG: R-package for Bacterium and virus analysis of Orthologous Groups

Jincheol Park, Shili Lin, C. Taslim, 2015, Computational and structural biotechnology journal.

Incorporating information from markers in LD with test locus for detecting imprinting and maternal effects

Shili Lin, Fangyuan Zhang, 2020, European Journal of Human Genetics.

Haplotype association analysis of North American Rheumatoid Arthritis Consortium data using a generalized linear model with regularization

Shili Lin, W. Guo, C. Liang, 2009, BMC proceedings.

Sample Size Requirement for Detecting Interference under the Chi-Square Model

Shili Lin, 2001, Human Heredity.

Human alveolar macrophage response to Mycobacterium tuberculosis: immune characteristics underlying large inter-individual variability

W. Sadee, Shili Lin, A. Azad, 2022, bioRxiv.

Confidence intervals for putative quantitative trait loci – development and applications of new linkage methods

M. Abney, Shili Lin, Charalampos Papachristou, 2007, BMC proceedings.

Ciclosporin and plasma exchange in thrombotic thrombocytopenic purpura: long‐term follow‐up with serial analysis of ADAMTS13 activity

J. George, Shili Lin, E. Kraut, 2007, British journal of haematology.

Effect of prophylactic cyclosporine therapy on ADAMTS13 biomarkers in patients with idiopathic thrombotic thrombocytopenic purpura

J. George, Shili Lin, E. Kraut, 2008, American journal of hematology.

Photoperiod reverses the effects of estrogens on male aggression via genomic and nongenomic pathways

Shili Lin, R. Nelson, B. Trainor, 2007, Proceedings of the National Academy of Sciences.

Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data

Shili Lin, Fangyuan Zhang, 2014, Journal of Human Genetics.

Two‐Locus Modeling of Asthma in a Hutterite Pedigree via Markov Chain Monte Carlo

S Lin, M. Irwin, Shili Lin, 2001, Genetic Epidemiology.

Relationship between ADAMTS13 activity in clinical remission and the risk of TTP relapse

Shili Lin, M. Jin, S. Cataland, 2008, British journal of haematology.

Joint detection of association, imprinting and maternal effects using all children and their parents

Yue-Qing Hu, Yue-Qing Hu, Shili Lin, 2013, European Journal of Human Genetics.

Evaluation and comparison of methods for recapitulation of 3D spatial chromatin structures

Shili Lin, Jincheol Park, Jincheol Park, 2019, Briefings Bioinform..

Impact of data resolution on three-dimensional structure inference methods

Shili Lin, Jincheol Park, Jincheol Park, 2016, BMC Bioinformatics.

Monte Carlo Methods in Genetic Analysis

Shili Lin, Shili Lin, 1996 .

Linkage analysis with sequential imputation

Shili Lin, Zachary Skrivanek, Mark Irwin, 2003, Genetic epidemiology.

Integration of Ranked Lists via Cross Entropy Monte Carlo with Applications to mRNA and microRNA Studies

Jie Ding, Shili Lin, Shili Lin, 2009, Biometrics.

Comparative study on ChIP-seq data: normalization and binding pattern characterization

Pearlly Yan, Tim Hui-Ming Huang, Kun Huang, 2009, Bioinform..

Logistic Bayesian LASSO for detecting association combining family and case-control data

Shili Lin, W. Stewart, Han Zhang, 2018, BMC Proceedings.

FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triads

Meng Wang, Shili Lin, M. Wang, 2014, Bioinform..

Blocking Approach for Identification of Rare Variants in Family-Based Association Studies

Asuman S. Turkmen, Shili Lin, A. Turkmen, 2014, PloS one.

An Optimum Projection and Noise Reduction Approach for Detecting Rare and Common Variants Associated with Complex Diseases

Asuman Turkmen, Shili Lin, A. Turkmen, 2012, Human Heredity.

Modeling and analysis of Hi-C data by HiSIF identifies characteristic promoter-distal loops

Xiaolong Cheng, Shili Lin, V. Jin, 2020, Genome Medicine.

PrEMeR-CG: inferring nucleotide level DNA methylation values from MethylCap-seq data

Pearlly Yan, Ralf Bundschuh, Shili Lin, 2014, Bioinform..

CD24 is a genetic modifier for risk and progression of multiple sclerosis

Yang Liu, Ming You, Xingluo Liu, 2003, Proceedings of the National Academy of Sciences of the United States of America.

A Dinucleotide Deletion in CD24 Confers Protection against Autoimmune Diseases

Yang Liu, Xincheng Zheng, Pan Zheng, 2007, PLoS genetics.

Epithelial Cells in Cystatin M AKT 1-Mediated Epigenetic Silencing of Associated Fibroblasts Confer − Breast Cancer

Michael C. Ostrowski, Daniel E. Deatherage, Shuying Sun, 2008 .

Original Article A hypermorphic SP1-binding CD24 variant associates with risk and progression of multiple sclerosis

Shili Lin, Lizhong Wang, Dongling Li, 2012 .

A hypermorphic SP1-binding CD24 variant associates with risk and progression of multiple sclerosis.

Yang Liu, Pan Zheng, Shili Lin, 2012, American journal of translational research.

Identifying differentially methylated genes using mixed effect and generalized least square models

Pearlly Yan, Tim Hui-Ming Huang, Shili Lin, 2009, BMC Bioinformatics.

GrammR: graphical representation and modeling of count data with application in metagenomics

Shili Lin, Deepak Nag Ayyala, Shili Lin, 2015, Bioinform..

Detection of Differentially Methylated Regions Using Bayesian Curve Credible Bands

Jincheol Park, Shili Lin, 2016, Statistics in Biosciences.

Statistical methods for detecting differentially methylated regions based on MethylCap-seq data

Pearlly Yan, Ralf Bundschuh, Shili Lin, 2016, Briefings Bioinform..

MicroRNA expression profiles for the NCI-60 cancer cell panel

John N Weinstein, Wolfgang Sadee, Philip L Lorenzi, 2007, Molecular Cancer Therapeutics.

MicroRNAs modulate the chemosensitivity of tumor cells

William C Reinhold, John N Weinstein, Wolfgang Sadee, 2008, Molecular Cancer Therapeutics.

Composite MicroRNA Target Predictions and Comparisons of Several Prediction Algorithms

Vincent F. Melfi, J. Verducci, Shili Lin, 2006 .

Chromatin signature analysis and prediction of genome-wide novel promoters using finite mixture model

Tim Hui-Ming Huang, Kun Huang, Shili Lin, 2011, 2011 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS).

Bayestrat: Population Stratification Correction Using Bayesian Shrinkage Prior for Genetic Association Studies

Shili Lin, A. Turkmen, Zilu Liu, 2021, bioRxiv.

Linkage analysis of the simulated data – evaluations and comparisons of methods

Charalampos Papachristou, M. Irwin, Shili Lin, 2003, BMC Genetics.

Network construction and structure detection with metagenomic count data

Shili Lin, Steve Piantadosi, Zhenqiu Liu, 2015, BioData Mining.

Kullback–Leibler Distance Methods for Detecting Disease Association with Rare Variants from Sequencing Data

Shili Lin, Yue-Qing Hu, Asuman S Turkmen, 2015, Annals of human genetics.

Microsatellites versus single‐nucleotide polymorphisms in confidence interval estimation of disease loci

Charalampos Papachristou, Shili Lin, Shili Lin, 2006, Genetic epidemiology.

Robust partial likelihood approach for detecting imprinting and maternal effects using case-control families

Shili Lin, Shili Lin, Jingyuan Yang, 2013, 1304.4799.

Analyzing ChIP-seq data: preprocessing, normalization, differential identification, and binding pattern characterization.

Kun Huang, Shili Lin, Cenny Taslim, 2012, Methods in molecular biology.

Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein

Liang Niu, Guoliang Li, Guoliang Li, 2014, PloS one.

Identifying hypermethylated CpG islands using a quantile regression model

Pearlly Yan, Tim Hui-Ming Huang, Shili Lin, 2011, BMC Bioinformatics.

A two‐step procedure for constructing confidence intervals of trait loci with application to a rheumatoid arthritis dataset

Shili Lin, Charalampos Papachristou, Shili Lin, 2006, Genetic epidemiology.

Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers.

Ming D. Li, R. Elston, F. Wright, 2003, Genetics.

Differential methylation hybridization: profiling DNA methylation with a high-density CpG island microarray.

Shili Lin, Pearlly S Yan, Dustin Potter, 2009, Methods in molecular biology.

Preprocessing differential methylation hybridization microarray data

Pearlly Yan, Tim Hui-Ming Huang, Shili Lin, 2011, BioData Mining.

Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data

Dustin P. Potter, Pearlly Yan, Tim Hui-Ming Huang, 2007, BMC Bioinformatics.

Heritable Clustering Algorithms for Recapturing Epigenetic Progression in Breast Cancer

Shili Lin, C. Eng, T. Huang, 2006 .

Clinical presentations of naturally occurring canine seizures: similarities to human seizures

Shili Lin, J. J. Curtin, Kristen S. Willard, 2002, Epilepsy & Behavior.

A Confidence Set Inference Method for Identifying SNPs That Regulate Quantitative Phenotypes

Charalampos Papachristou, Shili Lin, Shili Lin, 2012, Human Heredity.

Assessing the Effects of Imprinting and Maternal Genotypes on Complex Genetic Traits

Shili Lin, 2013 .

Modeling and Analysis of Multi‐Library, Multi‐Group SAGE Data with Application to a Study of Mouse Cerebellum

Shili Lin, Zailong Wang, Magdalena Popesco, 2007, Biometrics.

Modeling and Analysis of SAGE Libraries

Shili Lin, Zailong Wang, Shili Lin, 2005 .

Rank aggregation methods

Shili Lin, Shili Lin, 2010 .

Incorporating covariates in mapping heterogeneous traits: a hierarchical model using empirical Bayes estimation

Shili Lin, Swati Biswas, Shili Lin, 2007, Genetic epidemiology.

Evaluations of maximization procedures for estimating linkage parameters under heterogeneity

Swati Biswas, Shili Lin, Shili Lin, 2004, Genetic epidemiology.

Serial analysis of gene expression profiles of adult and aged mouse cerebellum

A. Rotter, Shili Lin, L. Friedman, 2008, Neurobiology of Aging.

Using the partitioning principle to construct confidence sets for the location of a disease gene

J. Hsu, Shili Lin, J. Rogers, 2004 .

Detecting rare haplotypes associated with complex diseases using both population and family data: Combined logistic Bayesian Lasso

Shili Lin, Xiaofei Zhou, Meng Wang, 2020, Statistical methods in medical research.

Gender Differences in Pulmonary Function, Respiratory Symptoms, and Macrophage Proteomics among HIV-Infected Smokers

Shili Lin, K. Wood, P. Diaz, 2014, Scientifica.

Generalized linear modeling with regularization for detecting common disease rare haplotype association

Wei Guo, Shili Lin, W. Guo, 2009, Genetic epidemiology.

A robust unified approach to analyzing methylation and gene expression data

Tim Hui-Ming Huang, Shili Lin, Abbas Khalili, 2009, Comput. Stat. Data Anal..

Class discovery and classification of tumor samples using mixture modeling of gene expression data - a unified approach

Shili Lin, Roxana Alexandridis, Mark Irwin, 2004, Bioinform..

Are rare variants really independent?

Shili Lin, A. Turkmen, 2017, Genetic epidemiology.

A random effect model for reconstruction of spatial chromatin structure

Shili Lin, Jincheol Park, Jincheol Park, 2017, Biometrics.

DIME: R-package for identifying differential ChIP-seq based on an ensemble of mixture models

Tim Hui-Ming Huang, Shili Lin, Cenny Taslim, 2011, Bioinform..

Logistic Bayesian LASSO for Genetic Association Analysis of Data from Complex Sampling Designs

Yuan Zhang, Mark P. Purdue, Jonathan N. Hofmann, 2017, Journal of Human Genetics.

The Association of ARMC5 with the Renin-Angiotensin-Aldosterone System, Blood Pressure and Glycemia in African Americans.

W. Hsueh, Shili Lin, James G. Wilson, 2020, The Journal of clinical endocrinology and metabolism.

Clinical characteristics and mode of inheritance of familial focal seizures in Standard Poodles.

Shili Lin, Yuqun Luo, Linda L. Hyson, 2007, Journal of the American Veterinary Medical Association.

Detection of parent‐of‐origin effects using general pedigree data

W. Fung, Shili Lin, Jie Ding, 2010, Genetic epidemiology.

Detection of Parent-of-Origin Effects Based on Complete and Incomplete Nuclear Families with Multiple Affected Children

Ji-Yuan Zhou, Wing K. Fung, Yue-Qing Hu, 2008, Human Heredity.

Sparse Inverse Covariance Estimation with L0 Penalty for Network Construction with Omics Data

Zhenqiu Liu, Shili Lin, Nan Deng, 2016, J. Comput. Biol..

scHiCSRS: A Self-Representation Smoothing Method with Gaussian Mixture Model for Imputing single cell Hi-C Data

Shili Lin, Qing Xie, 2021, bioRxiv.

HiCImpute: A Bayesian hierarchical model for identifying structural zeros and enhancing single cell Hi-C data

Shili Lin, V. Jin, Qing Xie, 2021, bioRxiv.

Are dropout imputation methods for scRNA-seq effective for scHi-C data?

Shili Lin, Chenggong Han, Qing Xie, 2020, Briefings Bioinform..

Handbook on analyzing human genetic data : computational approaches and software

Shili Lin, Shili Lin, Hongyu Zhao, 2010 .

TopKLists: a comprehensive R package for statistical inference, stochastic aggregation, and visualization of multiple omics ranked lists

Shili Lin, Michael G Schimek, Eva Budinská, 2015, Statistical applications in genetics and molecular biology.

Genome-Wide Tagging SNPs with Entropy-Based Monte Carlo Method

Ming Tan, Shili Lin, Zhenqiu Liu, 2006, J. Comput. Biol..

Capturing heterogeneity of covariate effects in hidden subpopulations in the presence of censoring and large number of covariates

Shili Lin, Abbas Khalili, M. Asgharian, 2019, The Annals of Applied Statistics.

Imprinting and Maternal Effect Detection Using Partial Likelihood Based on Discordant Sibpair Data

Shili Lin, Abbas Khalili, Fangyuan Zhang, 2019, Statistica Sinica.

Optimum study design for detecting imprinting and maternal effects based on partial likelihood

Shili Lin, Abbas Khalili, Fangyuan Zhang, 2016, Biometrics.

nongenomic pathways Photoperiod reverses the effects of estrogens on male aggression via genomic and

Shili Lin, R. Nelson, B. Trainor, 2007 .

Clinical presentations of naturally occurring canine seizures: similarities to human seizures.

Shili Lin, Kristen S. Willard, Linda L. Hyson, 2002, Epilepsy & behavior : E&B.

Impact of data resolution on three-dimensional structure inference methods

Jincheol Park, Shili Lin, 2016, BMC Bioinformatics.

Statistical Inference on Three-Dimensional Structure of Genome by Truncated Poisson Architecture Model

Shili Lin, Jincheol Park, Jincheol Park, 2015 .

An algorithm for haplotype analysis

Terence P. Speed, Shili Lin, T. Speed, 1997, RECOMB '97.

Incorporating information from markers in LD with test locus for detecting imprinting and maternal effects

Shili Lin, Fangyuan Zhang, 2020, European Journal of Human Genetics.

Feature selection in finite mixture of sparse normal linear models in high-dimensional feature space.

Shili Lin, Jiahua Chen, Abbas Khalili, 2011, Biostatistics.

Markov Chain Monte Carlo Linkage Analysis Methods

Shili Lin, Robert P. Igo, Yuqun Luo, 2009 .

Monte Carlo analysis on a large pedigree

E A Thompson, S Lin, A B Olshen, 1993, Genetic epidemiology.

Interrelationship between ADAMTS13 activity, von Willebrand factor, and complement activation in remission from immune‐mediated trhrombotic thrombocytopenic purpura

Shili Lin, S. Cataland, Shangbin Yang, 2020, British journal of haematology.

Probe signal correction for differential methylation hybridization experiments

Dustin P. Potter, Pearlly Yan, Tim Hui-Ming Huang, 2008, BMC Bioinformatics.

data mining and statistical treatment Microarray analysis of gene expression: considerations in

Shili Lin, Joseph S. Verducci, Sashwati Roy, 2016 .

Demographic and ADAMTS13 biomarker data as predictors of early recurrences of idiopathic thrombotic thrombocytopenic purpura

J. George, Shili Lin, E. Kraut, 2009, European Journal of Haematology.

A Mixture Modeling Framework for Differential Analysis of High-Throughput Data

Shili Lin, Cenny Taslim, Shili Lin, 2014, Comput. Math. Methods Medicine.

Detecting associations of rare variants with common diseases: collapsing or haplotyping?

Meng Wang, Shili Lin, M. Wang, 2015, Briefings Bioinform..

Detection of Parent-of-Origin Effects in Complete and Incomplete Nuclear Families with Multiple Affected Children Using Multiple Tightly Linked Markers

W. Fung, Yue-Qing Hu, Shili Lin, 2008, Human Heredity.

Sparse estimation in semiparametric finite mixture of varying coefficient regression models

Shili Lin, Abbas Khalili, M. Asgharian, 2023, Biometrics.

Identifying rare variant associations in population-based and family-based designs

Asuman S Turkmen, Shili Lin, A. Turkmen, 2014, BMC Proceedings.

Regularization in Finite Mixture of Regression Models with Diverging Number of Parameters

Shili Lin, Abbas Khalili, 2013, Biometrics.