Author details

Full Name

Nan M Laird

Affiliation

ORCID

Career Start Year

1979

Papers

242

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36726148	X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study.	Respir Res	2023
33367522	A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests.	Bioinformatics	2021
34159627	Genome-wide association analysis of COVID-19 mortality risk in SARS-CoV-2 genomes identifies mutation in the SARS-CoV-2 spike protein that colocalizes with P.1 of the Brazilian strain.	Genet Epidemiol	2021
32681690	Statistical considerations for the analysis of massively parallel reporter assays data.	Genet Epidemiol	2020
32193444	Identification of Novel Alzheimer's Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data.	Sci Rep	2020
31932770	Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.	Nat Neurosci	2020
30609057	A comparison of popular TDT-generalizations for family-based association analysis.	Genetic Epidemiology	2019
29159827	Family-based tests for associating haplotypes with general phenotype data: Improving the FBAT-haplotype algorithm.	Genetic Epidemiology	2018
28719030	Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia.	Genes Brain Behav	2018
28191685	Gene-based segregation method for identifying rare variants in family-based sequencing studies.	Genet Epidemiol	2017
28296608	Statistical Methods in the Journal - An Update.	N Engl J Med	2017
27854507	Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women.	Am J Respir Cell Mol Biol	2017
27669027	Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution.	Am J Respir Crit Care Med	2017
26771213	Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.	Am J Respir Crit Care Med	2016
26675752	Socioeconomic disadvantage and neural development from infancy through early childhood.	Int J Epidemiol	2015
26343745	Meta-analysis in clinical trials revisited.	Contemporary Clinical Trials	2015
26634245	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	BMC Genet	2015
26111731	Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability.	Hum Hered	2015
26030696	A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.	Am J Respir Crit Care Med	2015
25250875	A novel method for detecting association between DNA methylation and diseases using spatial information.	Genetic Epidemiology	2014
25519381	A comparative analysis of family-based and population-based association tests using whole genome sequence data.	BMC Proc	2014
24621683	Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.	Lancet Respir Med	2014
24964944	Analyzing networks of phenotypes in complex diseases: methodology and applications in COPD.	BMC Syst Biol	2014
25006744	Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.	Am J Respir Crit Care Med	2014
23448186	A general semi-parametric approach to the analysis of genetic association studies in population-based designs.	BMC Genetics	2013
23980521	Distinct quantitative computed tomography emphysema patterns are associated with physiology and function in smokers.	Am J Respir Crit Care Med	2013
23972146	Heritability of chronic obstructive pulmonary disease and related phenotypes in smokers.	Am J Respir Crit Care Med	2013
23341868	Rare variant analysis for family-based design.	PLoS ONE	2013
23379631	Ozone exposure, vitamin C intake, and genetic susceptibility of asthmatic children in Mexico City: a cohort study.	Respiratory Research	2013
22111716	Differentiating population stratification from genotyping error using family data.	Annals of Human Genetics	2012
22549767	Is it rare or common?	Genet Epidemiol	2012
22802602	Prospective association of common eating disorders and adverse outcomes.	Pediatrics	2012
21538986	Alternative methods for testing treatment effects on the basis of multiple outcomes: simulation and case study.	Stat Med	2011
22373362	Identifying rare variants using a Bayesian regression approach.	BMC Proceedings	2011
22373325	Identifying rare variants from exome scans: the GAW17 experience.	BMC Proc	2011
22373204	Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set.	BMC Proceedings	2011
21304886	A new testing strategy to identify rare variants with either risk or protective effect on disease.	PLoS Genet	2011
21480485	Using linkage information to weight a genome-wide association of bipolar disorder.	Am J Med Genet B Neuropsychiatr Genet	2011
21079520	Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel.	Journal of Thoracic Oncology	2011
20726965	Tests for compositional epistasis under single interaction-parameter models.	Annals of Human Genetics	2011
21403520	Estimating the effect of a predictor measured by two informants on a continuous outcome: a comparison of methods.	Epidemiology	2011
21401569	Combining disease models to test for gene-environment interaction in nuclear families.	Biometrics	2011
21659657	The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility.	Am J Respir Cell Mol Biol	2011
20650819	Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures.	Human Genomics	2010
19308960	Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.	Am J Med Genet B Neuropsychiatr Genet	2010
19459833	Estimating disease prevalence using relatives of case and control probands.	Biometrics	2010
20953361	Multivariate logistic regression with incomplete covariate and auxiliary information.	Journal of Multivariate Analysis	2010
20812911	On the optimal design of genetic variant discovery studies.	Statistical Applications in Genetics and Molecular Biology	2010
19996607	Parsing the effects of individual SNPs in candidate genes with family data.	Hum Hered	2010
20459388	Biostatistic tools in pharmacogenomics--advances, challenges, potential.	Current Pharmaceutical Design	2010