N. Laird

Aribert Rothenberger, Christoph Lange, Herbert Roeyers, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Testing for association in genetic studies

N. Laird, P. Kraft, C. Lange, 2005 .

A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information

Daniel Rabinowitz, N. Laird, D. Rabinowitz, 2000, Human Heredity.

A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.

Raúl San José Estépar, Edwin K Silverman, Terri H Beaty, 2015, American journal of respiratory and critical care medicine.

Generalized linear mixture models for handling nonignorable dropouts in longitudinal studies.

N M Laird, N. Laird, G. Fitzmaurice, 2000, Biostatistics.

Binge-eating disorder as a distinct familial phenotype in obese individuals.

N. Laird, S. McElroy, M. Tsuang, 2006, Archives of general psychiatry.

Effect of the hemodialysis prescription of patient morbidity: report from the National Cooperative Dialysis Study.

N. Laird, E. Lowrie, J. Sargent, 1981, The New England journal of medicine.

Nonlinear growth curve analysis: estimating the population parameters.

N. Laird, C. Berkey, 1986, Annals of human biology.

Using the General Linear Mixed Model to Analyse Unbalanced Repeated Measures and Longitudinal Data

Nan M. Laird, N. Laird, A. Cnaan, 1997 .

Random-effects models for longitudinal data.

J. Ware, N. Laird, 1982, Biometrics.

Regression methods for assessing familial aggregation of disease

N. Laird, K. Cuenco, 2003, Statistics in medicine.

Multivariate logistic regression for familial aggregation of two disorders. II. Analysis of studies of eating and mood disorders.

N. Laird, P. Keck, R. Betensky, 2001, American journal of epidemiology.

Statistical Challenges in Sequence-Based Association Studies with Population- and Family-Based Designs

N. Laird, I. Ionita-Laza, M. Cho, 2013 .

Mortality associated with depression

N. Laird, N. Horton, R. Monson, 2008, Social Psychiatry and Psychiatric Epidemiology.

Heritability of chronic obstructive pulmonary disease and related phenotypes in smokers.

N. Laird, E. Silverman, M. Cho, 2013, American journal of respiratory and critical care medicine.

Discussion of "Adjusting for nonignorable drop-out using semiparametric nonresponse models" by DO Scharfstein, A Rotnitzky and JM Robins

Nan M. Laird, Donna K. Pauler, N. Laird, 1999 .

Relation between malpractice claims and adverse events due to negligence. Results of the Harvard Medical Practice Study III.

Ann G. Lawthers, Joseph P. Newhouse, Troyen A. Brennan, 1991 .

Sex‐Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women

N. Laird, D. DeMeo, J. Hokanson, 2017, American journal of respiratory cell and molecular biology.

The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD).

N. Laird, D. DeMeo, E. Silverman, 2004, Human molecular genetics.

Perioperative red blood cell transfusion

N. Laird, J. Buckwalter, S. Oparil, 1988 .

Assessment of nutritional status of the National Cooperative Dialysis Study population.

N. Laird, D. Roxe, P. Schoenfeld, 1983, Kidney international. Supplement.

Statistical Applications in Genetics and Molecular Biology

N. Laird, I. Ionita-Laza, 2010 .

An algorithmic approach for the fitting of a general mixed ANOVA model appropriate in longitudinal settings

N. Laird, D. Stram, James H. jWare, 1986 .

Adjusting for Nonignorable Drop-Out Using Semiparametric Nonresponse Models: Comment

N. Laird, D. Pauler, 1999 .

Family study of the aggregation of eating disorders and mood disorders

N. Laird, M. Tsuang, A. Hausmann, 2003, Psychological Medicine.

Multivariate logistic regression for familial aggregation of two disorders. I. Development of models and methods.

N. Laird, R. Betensky, J. Hudson, 2001, American journal of epidemiology.

Identifying rare variants from exome scans: the GAW17 experience

R. Cantor, N. Laird, I. König, 2011, BMC proceedings.

Genomic screening in family-based association testing

N. Laird, K. Van Steen, P. Kraft, 2005, BMC Genetics.

Self‐Consistency—I

N. Laird, 2006 .

Modeling success or failure of dialysis therapy: the National Cooperative Dialysis Study.

N. Laird, C. Berkey, E. Lowrie, 1983, Kidney international. Supplement.

Protocol for the National Cooperative Dialysis Study.

N. Laird, E. Lowrie, R. Henry, 1983, Kidney international. Supplement.

Comparison of the study groups in the National Cooperative Dialysis Study and a description of morbidity, mortality, and patient withdrawal.

N. Laird, E. Lowrie, Lowrie Eg, 1983, Kidney international. Supplement.

Aggregation, Heritability and Segregation Analysis: Modeling Genetic Inheritance Without Genetic Data

N. Laird, C. Lange, 2011 .

Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures

Nan M Laird, Isabelle Romieu, N. Laird, 2010, Human Genomics.

The Association Of Genome-Wide Significant Spirometric Loci With COPD Susceptibility

N. Laird, J. Hokanson, T. Beaty, 2011, ATS 2011.

A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry

N. Laird, E. Regan, D. DeMeo, 2015, BMC Genetics.

Tracing aerosol pollution.

N. Laird, G. Thurston, 1985, Science.

Family-based association analysis of beta2-adrenergic receptor polymorphisms in the childhood asthma management program.

N. Laird, E. Silverman, J. Drazen, 2003, The Journal of allergy and clinical immunology.

Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability

Christoph Lange, Michael H. Cho, Edwin K. Silverman, 2015, Human Heredity.

Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.

P. Paré, N. Laird, T. Beaty, 2016, American journal of respiratory and critical care medicine.

On the analysis of copy‐number variations in genome‐wide association studies: a translation of the family‐based association test

Iuliana Ionita-Laza, Christoph Lange, Scott T Weiss, 2008, Genetic epidemiology.

Selection modelling versus mixture modelling with nonignorable nonresponse

Donald B. Rubin, Nan M. Laird, Robert J. Glynn, 1986 .

Exome Sequencing In Severe COPD Cases And Resistant Smoking Controls From COPDGene

N. Laird, J. Hokanson, E. Silverman, 2012, ATS 2012.

Incidence of adverse events and negligence in hospitalized patients: results of the Harvard Medical Practice Study I*

T. Brennan, L. Leape, A. Localio, 2004, Quality and Safety in Health Care.

Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia

S. Mccarroll, N. Laird, B. Neale, 2018, Genes, brain, and behavior.

Genome‐Wide Association Study of the Genetic Determinants of Emphysema Distribution

N. Laird, D. DeMeo, R. Bowler, 2016, American journal of respiratory and critical care medicine.

Maximum likelihood computations with repeated measures: application of the EM algorithm

N. Laird, D. Stram, N. Lange, 1987 .

Statistical analysis of longitudinal studies

N. Laird, 2022, International Statistical Review.

A Study of how Socioeconomic Status Moderates the Relationship between SNPs Encompassing BDNF and ADHD Symptom Counts in ADHD Families

N. Laird, J. Smoller, S. Faraone, 2007, Behavior genetics.

Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.

Raúl San José Estépar, Edwin K Silverman, Terri H Beaty, 2014, American journal of respiratory and critical care medicine.

A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men.

Tianhua Niu, Xiping Xu, Xin Xu, 2004, American journal of human genetics.

A candidate gene association study on preterm delivery: application of high-throughput genotyping technology and advanced statistical methods.

Tianhua Niu, Xiping Xu, Xin Xu, 2004, Human molecular genetics.

Some Statistical Methods for Combining Experimental Results

F Mosteller, N M Laird, F. Mosteller, 1990, International Journal of Technology Assessment in Health Care.

The Basics of Genetic Association Analysis

N. Laird, C. Lange, 2011 .

Evaluating the Effect of Coaching on SAT Scores: A Meta-Analysis

Nan M. Laird, N. Laird, R. Dersimonian, 1983 .

A 40-year perspective on the prevalence of depression: the Stirling County Study.

N. Laird, R. Monson, A. Sobol, 2000, Archives of general psychiatry.

Penalized solutions to functional regression problems

Jaroslaw Harezlak, Brent A. Coull, Shannon R. Magari, 2007, Comput. Stat. Data Anal..

Model-based approaches to analysing incomplete longitudinal and failure time data.

N M Laird, J W Hogan, N. Laird, 1997, Statistics in medicine.

Multivariate logistic regression with incomplete covariate and auxiliary information

Garrett M. Fitzmaurice, Nan M. Laird, Sanjoy K. Sinha, 2010, J. Multivar. Anal..

15 The analysis of case-control data: Epidemiologic studies of familial aggregation

Nan M. Laird, Garrett M. Fitzmaurice, Ann G. Schwartz, 2000, Bioenvironmental and public health statistics.

Meta-analysis in clinical trials revisited.

N. Laird, R. Dersimonian, Nan Laird, 2015, Contemporary clinical trials.

A simulation study of estimators for rates of change in longitudinal studies with attrition.

James H. Ware, Nan M. Laird, J. Ware, 1991, Statistics in medicine.

Modelling adolescent blood pressure patterns and their prediction of adult pressures.

N M Laird, C S Berkey, N. Laird, 1991, Biometrics.

Longitudinal analysis of incomplete adolescent data.

N. Laird, C. Berkey, J. Gardner, 1991, Annals of human biology.

Genetic polymorphisms of estrogen metabolizing enzyme and breast cancer risk in Thai women

N. Laird, P. Brennan, S. Sangrajrang, 2009, International journal of cancer.

Nonparametric mixed-effects models for repeated binary data arising in serial dilution assays : An application to estimating viral burden in AIDS

N. Laird, V. Gruttola, R. Zackin, 1996 .

Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

A Family-Based Association Test for Repeatedly Measured Quantitative Traits Adjusting for Unknown Environmental and/or Polygenic Effects

Christoph Lange, Edwin K Silverman, Scott T Weiss, 2004, Statistical applications in genetics and molecular biology.

Schizophrenia risk conferred by protein-coding de novo mutations

M. Daly, S. Mccarroll, N. Laird, 2018 .

Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2

N. Laird, Winston A Hide, R. Tanzi, 2021, Molecular Psychiatry.

A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests

Scott T. Weiss, Christoph Lange, Michael H. Cho, 2020, Bioinform..

Identification of Novel Alzheimer’s Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data

N. Laird, R. Tanzi, C. Lange, 2020, Scientific Reports.

An exact, unifying framework for region-based association testing in family-based designs, including higher criticism approaches, SKATs, multivariate and burden tests

Scott T. Weiss, Christoph Lange, Michael H. Cho, 2019, bioRxiv.

A comparison of popular TDT‐generalizations for family‐based association analysis

Christoph Lange, Julian Hecker, N. Laird, 2019, Genetic epidemiology.

Rare Variant Analysis for Family-Based Design

Iuliana Ionita-Laza, Wai-Ki Yip, N. Laird, 2013, PloS one.

Combining Disease Models to Test for Gene–Environment Interaction in Nuclear Families

Christoph Lange, Edwin K Silverman, Stijn Vansteelandt, 2011, Biometrics.

Tests for Compositional Epistasis under Single Interaction‐Parameter Models

Tyler J VanderWeele, Nan M Laird, N. Laird, 2011, Annals of human genetics.

Gene‐environment interaction tests for dichotomous traits in trios and sibships

Christoph Lange, Stijn Vansteelandt, Nan M Laird, 2009, Genetic epidemiology.

The Role of Family-Based Designs in Genome-Wide Association Studies

Christoph Lange, Nan M. Laird, N. Laird, 2009, 1010.4629.

New Powerful Approaches for Family‐based Association Tests with Longitudinal Measurements

Christoph Lange, Xin Xu, N. Laird, 2009, Annals of human genetics.

Impact of Population Stratification on Family-Based Association Tests with Longitudinal Measurements

N. Laird, C. Lange, B. Raby, 2009, Statistical applications in genetics and molecular biology.

On the parsing of statistical information in family-based association testing

N. Laird, C. Lange, M. McQueen, 2007, Nature Genetics.

Exact family‐based association tests for biallelic data

Kady Schneiter, Nan Laird, Chris Corcoran, 2005, Genetic epidemiology.

Genomic screening and replication using the same data set in family-based association testing

Christoph Lange, Kristel Van Steen, Edwin K Silverman, 2005, Nature Genetics.

PBAT: tools for family-based association studies.

Christoph Lange, Edwin K Silverman, Dawn DeMeo, 2004, American journal of human genetics.

Family‐based association tests for survival and times‐to‐onset analysis

Christoph Lange, Deborah Blacker, Nan M Laird, 2004, Statistics in medicine.

Family‐based tests for associating haplotypes with general phenotype data: Application to asthma genetics

Xin Xu, Steve Horvath, S. Horvath, 2004, Genetic epidemiology.

Using the noninformative families in family-based association tests: a powerful new testing strategy.

Christoph Lange, Edwin K Silverman, Dawn DeMeo, 2003, American journal of human genetics.

On a general class of conditional tests for family‐based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations

Christoph Lange, N. Laird, C. Lange, 2002, Genetic epidemiology.

Family-based tests of association in the presence of linkage.

N M Laird, N. Laird, D. Blacker, 2000, American journal of human genetics.

Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions.

N M Laird, K. Lunetta, N. Laird, 2000, American journal of human genetics.

Implementing a unified approach to family‐based tests of association

Xin Xu, N. Laird, S. Horvath, 2000, Genetic epidemiology.

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

Iuliana Ionita-Laza, Christoph Lange, Nan M. Laird, 2011, PLoS genetics.

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

M. Daly, S. Mccarroll, N. Laird, 2019, Nature Neuroscience.

Positively Selected G6PD-Mahidol Mutation Reduces Plasmodium vivax Density in Southeast Asians

N. Laird, L. Quintana-Murci, E. Patin, 2009, Science.

X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study

N. Laird, T. Beaty, E. Silverman, 2023, Respiratory Research.

Introduction to Statistical Genetics and Background in Molecular Genetics

N. Laird, C. Lange, 2011 .

Genetic association analysis of behavioral inhibition using candidate loci from mouse models.

N. Laird, J. Kagan, J. Rosenbaum, 2001, American journal of medical genetics.

The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility.

N. Laird, J. Hokanson, T. Beaty, 2011, American journal of respiratory cell and molecular biology.

The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts

Xiaofeng Zhu, Thomas Meitinger, Christoph Lange, 2007, PLoS genetics.

On the frequency of copy number variants

Iuliana Ionita-Laza, Scott T. Weiss, Nan M. Laird, 2008, Bioinform..

IL10 gene polymorphisms are associated with asthma phenotypes in children

N. Laird, E. Silverman, A. Randolph, 2004, Genetic epidemiology.

Methods for Analysis of Longitudinal Data: Blood-Lead Concentrations and Cognitive Development

Christine Waternaux, James H. Ware, Nan M. Laird, 1989 .

Family‐based tests for associating haplotypes with general phenotype data

Christoph Lange, Julian Hecker, Xin Xu, 2018, Genetic epidemiology.

Improving the FBAT-haplotype algorithm

F. W. Townes, N. Laird, C. Lange, 2018 .

Parameter estimation in variance component models for binary response data.

N. Laird, M. Knuiman, 1990 .

Analysis of longitudinal and cluster-correlated data

Nan M. Laird, N. Laird, 2004 .

Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia.

Matcheri Keshavan, Ellen Frank, David J Miklowitz, 2009, Bipolar disorders.

Estimation and Tests of Haplotype-Environment Interaction when Linkage Phase Is Ambiguous

N. Laird, E. Silverman, D. Schaid, 2003, Human Heredity.

Regression models for mixed discrete and continuous responses with potentially missing values.

N M Laird, N. Laird, G. Fitzmaurice, 1997, Biometrics.

Regression Models for a Bivariate Discrete and Continuous Outcome with Clustering

Nan M. Laird, Garrett M. Fitzmaurice, N. Laird, 1995 .

Analyzing networks of phenotypes in complex diseases: methodology and applications in COPD

Russell Bowler, John Quackenbush, Joseph Loscalzo, 2014, BMC Systems Biology.

Mixture models for the joint distribution of repeated measures and event times.

N M Laird, J W Hogan, N. Laird, 1997, Statistics in medicine.

Genome‐wide association scan of the time to onset of attention deficit hyperactivity disorder

M. Daly, B. Franke, M. Gill, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Statistical Challenges in Sequence-Based Association Studies with Population- and Family-Based Designs

N. Laird, I. Ionita-Laza, M. Cho, 2012, Statistics in Biosciences.

Evidence for an Association of the Dopamine D5 Receptor Gene on Age at Onset of Attention Deficit Hyperactivity Disorder

N. Laird, J. Smoller, S. Faraone, 2007, Annals of human genetics.

The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group

David W. Bates, Laura A. Petersen, Nan M. Laird, 1997 .

Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan.

Iuliana Ionita-Laza, Christoph Lange, Nan M Laird, 2007, American journal of human genetics.

Linkage disequilibrium mapping of the chromosome 6q21–22.31 bipolar I disorder susceptibility locus

B. Devlin, N. Laird, J. Calabrese, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

N. Laird, E. Silverman, S. Haneuse, 2021, Genetic epidemiology.

Mutations in SARS-CoV-2 spike protein and RNA polymerase complex are associated with COVID-19 mortality risk

N. Laird, E. Silverman, S. Haneuse, 2020, bioRxiv.

Using the jackknife to estimate the variance of regression estimators from repeated measures studies

Stuart R. Lipsitz, David P. Harrington, Nan M. Laird, 1990 .

Population Genetics Considerations

N. Laird, 2015 .

The Fundamentals of Modern Statistical Genetics

Christoph Lange, Nan M. Laird, N. Laird, 2010 .

A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry

N. Laird, E. Regan, R. Casaburi, 2015, BMC Genetics.

An alternative parameterization of the general linear mixture model for longitudinal data with non‐ignorable drop‐outs

N M Laird, N. Laird, G. Fitzmaurice, 2001, Statistics in medicine.

Vitamin D deficiency is associated with respiratory symptoms and airway wall thickening in smokers with and without COPD: a prospective cohort study

Raúl San José Estépar, Camille M. Moore, N. Laird, 2020, BMC Pulmonary Medicine.

A new statistical screening approach for finding pharmacokinetics-related genes in genome-wide studies

N. Laird, H. Ueno, N. Saijo, 2009, The Pharmacogenomics Journal.

Self-Consistency - Basic†

N. Laird, 2014 .

A Mixture Model for Longitudinal Data with Application to Assessment of Noncompliance

N. Laird, D. Pauler, 2000, Biometrics.

Smoothing the non-parametric estimate of a prior distribution by roughening: A computational study

T. Louis, N. Laird, 1991 .

Analysis of Linear and Non-Linear Growth Models with Random Parameters

N. Laird, 1990 .

A study of medical injury and medical malpractice.

N M Laird, A R Localio, L L Leape, 1989, The New England journal of medicine.

Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design?

F. Kronenberg, M. McCarthy, F. Hu, 2009, PLoS genetics.

Obesity and Weight Gain in Relation to Depression: Findings from the Stirling County Study

N. Laird, N. Horton, R. Monson, 2008, International Journal of Obesity.

Studying the incidence of depression: an ‘interval’ effect

N. Laird, R. Monson, A. Sobol, 2000 .

Incidence of depression in the Stirling County Study: historical and comparative perspectives

N. Laird, R. Monson, A. Sobol, 2000, Psychological Medicine.

Variance calculations for identity-by-descent estimation.

Deborah Blacker, Nan M Laird, Matthew B McQueen, 2006, American journal of human genetics.

Association of a genetic marker at the corticotropin-releasing hormone locus with behavioral inhibition

N. Laird, J. Kagan, J. Rosenbaum, 2003, Biological Psychiatry.

The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group.

S D Small, D W Bates, L L Leape, 1998, JAMA.

A Structural Approach to the Familial Coaggregation of Disorders

N. Laird, M. Hernán, T. VanderWeele, 2008, Epidemiology.

Genome-Wide Association Study on Overall Survival of Advanced Non-small Cell Lung Cancer Patients Treated with Carboplatin and Paclitaxel

Yasunori Sato, Noriko Katori, Hiromi Sakamoto, 2011, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Effects of dialysis prescription on bone and mineral metabolism: the National Cooperative Dialysis Study.

N. Laird, H. Harter, B. Teehan, 1983, Kidney international. Supplement.

Alpha-2 macroglobulin is genetically associated with Alzheimer disease

Steven M. Horvath, Bradley T. Hyman, Deborah Blacker, 1998, Nature Genetics.

Adversary social roles: Their effects on witnesses' communication of evidence and the assessments of adjudicators.

N. Laird, N. Vidmar, 1983 .

Population Substructure in Association Studies

N. Laird, C. Lange, 2011 .

Identifying rare variants using a Bayesian regression approach

N. Laird, Cheng Li, Aimin Yan, 2011, BMC proceedings.

Association Analysis in Family Designs

N. Laird, C. Lange, 2011 .

Is It Rare or Common?

N. Laird, K. Adhikari, C. Lange, 2012, Genetic epidemiology.

Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin.

M. Daly, M. Albert, N. Laird, 2003, Human molecular genetics.

Blood eosinophil count thresholds and exacerbations in patients with chronic obstructive pulmonary disease

Camille M. Moore, Stephanie A. Santorico, Joyce D. Schroeder, 2018, The Journal of allergy and clinical immunology.

A comparison of diagnostic interviews for depression in the Stirling County study: challenges for psychiatric epidemiology.

N. Laird, R. Monson, A. Sobol, 2000, Archives of general psychiatry.

Lobar Emphysema Distribution Is Associated With 5‐Year Radiological Disease Progression

Eric A. Hoffman, Russell Bowler, Philip F. Judy, 2018, Chest.

Meta-analysis: Heterogeneity can be a good thing

N. Laird, 2013 .

Comments on ‘Empirical vs natural weighting in random effects meta‐analysis’

Garrett Fitzmaurice, N. Laird, G. Fitzmaurice, 2010, Statistics in Medicine.

Alternative methods for testing treatment effects on the basis of multiple outcomes: Simulation and case study

Sharon-Lise T Normand, Stuart R Lipsitz, Nicholas J Horton, 2011, Statistics in medicine.

Maximum Likelihood Analysis of Logistic Regression Models with Incomplete Covariate Data and Auxiliary Information

N M Laird, N. Laird, N. Horton, 2001, Biometrics.

Relation between malpractice claims and adverse events due to negligence. Results of the Harvard Medical Practice Study III.

N M Laird, A R Localio, H H Hiatt, 1991, The New England journal of medicine.

Mln Clinics in London 1996 Multilevel Unit Specific and Population Average Generalised Linear Models ——————————————————- the Effects of Centering in Multilevel Analysis ——————————————————- a Multilevel Analysis for Screening Data Accumulated from a Number of Studies ——————————————————- Some New Publ

David B. Rose, Rubin, C. Morris, 2022 .

Ozone exposure, vitamin C intake, and genetic susceptibility of asthmatic children in Mexico City: a cohort study

J. Schwartz, D. Dockery, N. Laird, 2013, Respiratory Research.

Cigarette smoking in relation to depression: historical trends from the Stirling County Study.

N. Laird, N. Horton, R. Monson, 2003, The American journal of psychiatry.

Polymorphism in maternal LRP8 gene is associated with fetal growth.

N. Laird, B. Zuckerman, Xin Xu, 2006, American journal of human genetics.

Familiality and heritability of binge eating disorder: results of a case-control family study and a twin study.

Nan M Laird, N. Laird, C. Bulik, 2008, The International journal of eating disorders.

Missing data in longitudinal studies.

N M Laird, N. Laird, 1988, Statistics in medicine.

Review papers : Longitudinal studies with continuous responses

Christl A. Donnelly, James H. Ware, Nan M. Laird, 1992 .

Estimating Disease Prevalence Using Relatives of Case and Control Probands

B. Ripley, N. Laird, James I Hudson, 2010, Biometrics.

Analysing incomplete longitudinal binary responses: a likelihood-based approach.

N M Laird, S R Lipsitz, S. Lipsitz, 1994, Biometrics.

Maximum likelihood regression methods for paired binary data.

N M Laird, D P Harrington, S R Lipsitz, 1990, Statistics in medicine.

Bivariate logistic regression analysis of childhood psychopathology ratings using multiple informants.

N M Laird, N. Laird, G. Fitzmaurice, 1995, American journal of epidemiology.

Em algorithm reconstruction of particle size distributions from diffusion battery data

Nan M. Laird, Edward F. Maher, N. Laird, 1985 .

Bias due to misclassification of personal exposures in epidemiologic studies of indoor and outdoor air pollution

John D. Spengler, Halûk Özkaynak, N. Laird, 1986 .

Empirical Bayes Ranking Methods

Thomas A. Louis, Nan M. Laird, T. Louis, 1989 .

14 The EM algorithm

Nan M. Laird, N. Laird, 1993, Computational Statistics.

Selection Modeling Versus Mixture Modeling with Nonignorable Nonresponse

Donald B. Rubin, Nan M. Laird, Robert J. Glynn, 1986 .

Further Comparative Analyses of Pretest-Posttest Research Designs

Nan M. Laird, N. Laird, 1983 .

Using linkage information to weight a genome‐wide association of bipolar disorder

B. Devlin, N. Laird, D. Howrigan, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Finding the design matrix for the marginal homogeneity model

S. Lipsitz, D. Harrington, N. Laird, 1990 .

Inter-laboratory variability in Ames assay results.

T. Louis, N. Laird, M. Knuiman, 1987, Mutation research.

A general semi-parametric approach to the analysis of genetic association studies in population-based designs

N. Laird, J. Hokanson, C. Lange, 2013, BMC Genetics.

Systems Analysis of Adverse Drug Events

David W. Bates, Laura A. Petersen, Lucian L. Leape, 2008 .

An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease (reply)

N. Laird, D. Blacker, R. Tanzi, 1999, Nature Genetics.

Bayes Analysis of Model-Based Methods for Nonignorable Nonresponse in the Harvard Medical Practice Survey

William G. Johnson, Nan M. Laird, N. Laird, 1993 .

Sample-size estimation: a sensitivity analysis in the context of a clinical trial for treatment of mild hypertension.

N. Laird, M. Weinstein, W. Stason, 1979, American Journal of Epidemiology.

Estimating the Effect of a Predictor Measured by Two Informants on a Continuous Outcome: A Comparison of Methods

N. Laird, H. Goldsmith, K. Javaras, 2011, Epidemiology.

Longitudinal studies with continuous responses.

N M Laird, J. Ware, N. Laird, 1992, Statistical methods in medical research.

Multiple informants: mortality associated with psychiatric disorders in the Stirling County Study.

N M Laird, N. Laird, N. Horton, 2001, American journal of epidemiology.

Incorporating missingness for estimation of marginal regression models with multiple source predictors

Nicholas J Horton, Nan M Laird, Bernardo Hernández, 2007, Statistics in medicine.

Use of multiple informant data as a predictor in psychiatric epidemiology

N. Laird, N. Horton, G. Zahner, 1999 .

The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers.

N M Laird, M Knapp, N. Laird, 2000, American journal of human genetics.

A new multimarker test for family‐based association studies

Xin Xu, Ross Lazarus, Deborah Blacker, 2007, Genetic epidemiology.

Simple moment estimates of the κ-coefficient and its variance

Stuart R. Lipsitz, Troyen A. Brennan, Nan M. Laird, 1994 .

Power estimation of multiple SNP association test of case‐control study and application

Xiping Xu, Xin Xu, Xiping Xu, 2004, Genetic epidemiology.

A Reanalysis of the Stanford Heart Transplant Data

Murray Aitkin, Nan M. Laird, Brian Francis, 1983 .

Multiple imputation in mixture models for nonignorable nonresponse with follow-ups

Donald B. Rubin, Nan M. Laird, Robert J. Glynn, 1993 .

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set

N. Laird, B. Raby, Gourab De, 2011, BMC proceedings.

Correcting for non-compliance in randomized trials: an application to the ATBC Study.

N M Laird, J Palmgren, N. Laird, 1999, Statistics in medicine.

Gene‐based segregation method for identifying rare variants in family‐based sequencing studies

Ingo Ruczinski, Christoph Lange, Sungho Won, 2017, Genetic epidemiology.

Tutorial in Biostatistics: Evaluating the impact of 'critical periods' in longitudinal studies of growth using piecewise mixed effects models.

N M Laird, N. Laird, A. Must, 2001, International journal of epidemiology.

Regression analysis of multiple-source longitudinal outcomes: a "Stirling County" depression study.

Constantine Daskalakis, Nan M Laird, N. Laird, 2002, American journal of epidemiology.

Estimating rates of change in randomized clinical trials.

N M Laird, N. Laird, F Wang, 1990, Controlled clinical trials.

Family‐based association analysis of a statistically derived quantitative traits for ADHD reveal an association in DRD4 with inattentive symptoms in ADHD individuals

N. Laird, J. Smoller, S. Faraone, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Incidence of major depression: prediction from subthreshold categories in the Stirling County Study.

N. Laird, A. Nierenberg, R. Monson, 2002, Journal of affective disorders.

Increasing efficiency from censored survival data by using random effects to model longitudinal covariates

N M Laird, J W Hogan, N. Laird, 1998, Statistical methods in medical research.

INCIDENCE OF ADVERSE EVENTS AND NEGLIGENCE IN HOSPITALIZED PATIENTS

T. Brennan, L. Leape, N. Laird, 2008 .

Marginal regression models with a time to event outcome and discrete multiple source predictors

N. Laird, N. Horton, H. Litman, 2006, Lifetime data analysis.

10 – Estimation of Marginal Regression Models with Multiple Source Predictors

N. Laird, N. Horton, H. Litman, 2010 .

25 Estimation of Marginal Regression Models with Multiple Source Predictors

N. Laird, N. Horton, H. Litman, 2007 .