Nan Laird

Q: What Schools Are Affiliated With Nan Laird

Nan Laird is affiliated with the following schools: University of California, Berkeley, Boston University, Seoul National University, Harvard University

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Nan Laird

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#865

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#1532

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#379

USA Rank

Statistics

#27

World Rank

#39

Historical Rank

#16

USA Rank

Measure Theory

#34

World Rank

#60

Historical Rank

#20

USA Rank

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Mathematics

Nan Laird's Degrees

Bachelors Mathematics University of California, Berkeley

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Why Is Nan Laird Influential?

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According to Wikipedia, Nan McKenzie Laird is the Harvey V. Fineberg Professor of Public Health, Emerita in Biostatistics at the Harvard T.H. Chan School of Public Health. She served as Chair of the Department from 1990 to 1999. She was the Henry Pickering Walcott Professor of Biostatistics from 1991 to 1999. Laird is a Fellow of the American Statistical Association, as well as the Institute of Mathematical Statistics. She is a member of the International Statistical Institute.

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Nan Laird's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper (1977) (50586)
Meta-analysis in clinical trials. (1986) (33548)
Random-effects models for longitudinal data. (1982) (8540)
Incidence of Adverse Drug Events and Potential Adverse Drug Events: Implications for Prevention (1995) (3183)
Applied Longitudinal Analysis (2004) (2613)
Effect of computerized physician order entry and a team intervention on prevention of serious medication errors. (1998) (2191)
The Costs of Adverse Drug Events in Hospitalized Patients (1997) (1810)
Systems analysis of adverse drug events. ADE Prevention Study Group. (1995) (1733)
Meta-analysis in clinical trials revisited. (2015) (1686)
Reducing obesity via a school-based interdisciplinary intervention among youth: Planet Health. (1999) (1470)
Max-imum Likelihood from Incomplete Data (1972) (1210)
Incidence of adverse drug events and potential adverse drug events. Implications for prevention. ADE Prevention Study Group. (1995) (1066)
Incidence of adverse drug events and potential adverse drug events (1995) (934)
Implementing a unified approach to family‐based tests of association (2000) (915)
Nonparametric Maximum Likelihood Estimation of a Mixing Distribution (1978) (800)
Random-effects models for serial observations with binary response. (1984) (781)
The family based association test method: strategies for studying general genotype–phenotype associations (2001) (777)
Missing data in longitudinal studies. (1988) (741)
A Common Genetic Variant Is Associated with Adult and Childhood Obesity (2006) (739)
Relation between malpractice claims and adverse events due to negligence. Results of the Harvard Medical Practice Study III. (1991) (730)
Effect of the hemodialysis prescription of patient morbidity: report from the National Cooperative Dialysis Study. (1981) (680)
Using the general linear mixed model to analyse unbalanced repeated measures and longitudinal data. (2005) (675)
Alpha-2 macroglobulin is genetically associated with Alzheimer disease (1998) (665)
A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information (2000) (635)
Incidence of adverse events and negligence in hospitalized patients: results of the Harvard Medical Practice Study I* (2004) (599)
Perioperative red blood cell transfusion (1988) (569)
The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group. (1998) (565)
Some Statistical Methods for Combining Experimental Results (1990) (563)
The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group (1997) (544)
Using the General Linear Mixed Model to Analyse Unbalanced Repeated Measures and Longitudinal Data (1997) (543)
Covariance Analysis of Censored Survival Data Using Log-Linear Analysis Techniques (1981) (491)
Systems Analysis of Adverse Drug Events (2008) (485)
Family-based designs in the age of large-scale gene-association studies (2006) (464)
Estimation and Tests of Haplotype-Environment Interaction when Linkage Phase Is Ambiguous (2003) (461)
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. (2008) (455)
Generalized estimating equations for correlated binary data: Using the odds ratio as a measure of association (1991) (451)
Association of obesity with physical activity, television programs and other forms of video viewing among children in Mexico City (1999) (436)
Maximum likelihood computations with repeated measures: application of the EM algorithm (1987) (418)
Impact of a school-based interdisciplinary intervention on diet and physical activity among urban primary school children: eat well and keep moving. (1999) (413)
Family‐based tests for associating haplotypes with general phenotype data: Application to asthma genetics (2004) (410)
Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations (2008) (377)
Mixture models for the joint distribution of repeated measures and event times. (1997) (362)
Patient risk factors for adverse drug events in hospitalized patients. ADE Prevention Study Group. (1999) (357)
A likelihood-based method for analysing longitudinal binary responses (1993) (345)
A 40-year perspective on the prevalence of depression: the Stirling County Study. (2000) (316)
PBAT: tools for family-based association studies. (2004) (288)
Family-based tests of association in the presence of linkage. (2000) (284)
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. (2014) (280)
Genome‐wide association scan of attention deficit hyperactivity disorder (2008) (271)
Hospital characteristics associated with adverse events and substandard care. (1991) (267)
Model-based approaches to analysing incomplete longitudinal and failure time data. (1997) (265)
Regression Models for Discrete Longitudinal Responses (1993) (260)
Empirical Bayes Confidence Intervals Based on Bootstrap Samples (1987) (244)
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. (2005) (235)
Co-occurrence of binge eating disorder with psychiatric and medical disorders. (2008) (231)
Regression Analysis for Categorical Variables with Outcome Subject to Nonignorable Nonresponse (1988) (228)
Assessment of nutritional status of the National Cooperative Dialysis Study population. (1983) (223)
A discordant-sibship test for disequilibrium and linkage: no need for parental data. (1998) (222)
Performance of generalized estimating equations in practical situations. (1994) (210)
The transforming growth factor-β1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD) (2004) (210)
Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations. (2005) (202)
A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men. (2004) (198)
Family study of affective spectrum disorder. (2003) (197)
A multivariate family-based association test using generalized estimating equations: FBAT-GEE. (2003) (195)
Cigarette smoking in relation to depression: historical trends from the Stirling County Study. (2003) (184)
Regression Models for a Bivariate Discrete and Continuous Outcome with Clustering (1995) (184)
A study of medical injury and medical malpractice. (1989) (180)
Genomic screening and replication using the same data set in family-based association testing (2005) (178)
A Random-Effects Model for Multiple Characteristics with Possibly Missing Data (1997) (172)
Binge-eating disorder as a distinct familial phenotype in obese individuals. (2006) (170)
The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts (2007) (163)
Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions. (2000) (161)
Tutorial in Biostatistics: Evaluating the impact of 'critical periods' in longitudinal studies of growth using piecewise mixed effects models. (2001) (161)
Modeling success or failure of dialysis therapy: the National Cooperative Dialysis Study. (1983) (157)
Positively Selected G6PD-Mahidol Mutation Reduces Plasmodium vivax Density in Southeast Asians (2009) (157)
Selection Modeling Versus Mixture Modeling with Nonignorable Nonresponse (1986) (156)
A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease (2011) (155)
Further Comparative Analyses of Pretest-Posttest Research Designs (1983) (147)
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. (2009) (145)
Power and design considerations for a general class of family-based association tests: quantitative traits. (2002) (141)
Multiple imputation in mixture models for nonignorable nonresponse with follow-ups (1993) (140)
Association of a genetic marker at the corticotropin-releasing hormone locus with behavioral inhibition (2003) (138)
Familiality and heritability of binge eating disorder: results of a case-control family study and a twin study. (2008) (136)
On the replication of genetic associations: timing can be everything! (2008) (135)
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry (2015) (132)
Maximum likelihood analysis of generalized linear models with missing covariates (1999) (129)
Family-based association analysis of beta2-adrenergic receptor polymorphisms in the childhood asthma management program. (2003) (125)
The Fundamentals of Modern Statistical Genetics (2010) (123)
Empirical Bayes methods for two-way contingency tables (1978) (122)
Genome‐wide association scan of the time to onset of attention deficit hyperactivity disorder (2008) (121)
Power calculations for a general class of family-based association tests: dichotomous traits. (2002) (119)
Evaluating the Effect of Coaching on SAT Scores: A Meta-Analysis (1983) (118)
A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes. (2015) (118)
Methods for Analysis of Longitudinal Data: Blood-Lead Concentrations and Cognitive Development (1989) (118)
The Effect of Covariance Structure on Variance Estimation in Balanced Growth-Curve Models with Random Parameters (1989) (118)
Anxiety and depression: a 40‐year perspective on relationships regarding prevalence, distribution, and comorbidity (2004) (117)
Rare Variant Analysis for Family-Based Design (2013) (115)
Distinct quantitative computed tomography emphysema patterns are associated with physiology and function in smokers. (2013) (110)
IL10 gene polymorphisms are associated with asthma phenotypes in children (2004) (110)
Empirical Bayes Ranking Methods (1989) (108)
On a general class of conditional tests for family‐based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations (2002) (108)
Heritability of chronic obstructive pulmonary disease and related phenotypes in smokers. (2013) (107)
Incidence of depression in the Stirling County Study: historical and comparative perspectives (2000) (105)
Genetic polymorphisms of estrogen metabolizing enzyme and breast cancer risk in Thai women (2009) (103)
The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility. (2011) (102)
Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan. (2007) (100)
A Reanalysis of the Stanford Heart Transplant Data (1983) (99)
Comparison of the study groups in the National Cooperative Dialysis Study and a description of morbidity, mortality, and patient withdrawal. (1983) (98)
The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD). (2004) (98)
Em algorithm reconstruction of particle size distributions from diffusion battery data (1985) (97)
A candidate gene association study on preterm delivery: application of high-throughput genotyping technology and advanced statistical methods. (2004) (95)
Multivariate Logistic Models for Incomplete Binary Responses (1996) (95)
A Family-Based Association Test for Repeatedly Measured Quantitative Traits Adjusting for Unknown Environmental and/or Polygenic Effects (2004) (94)
Bivariate logistic regression analysis of childhood psychopathology ratings using multiple informants. (1995) (92)
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations (2019) (92)
Regression models for mixed discrete and continuous responses with potentially missing values. (1997) (92)
Genome-Wide Association Study on Overall Survival of Advanced Non-small Cell Lung Cancer Patients Treated with Carboplatin and Paclitaxel (2011) (86)
Using the noninformative families in family-based association tests: a powerful new testing strategy. (2003) (86)
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design? (2009) (85)
Blood eosinophil count thresholds and exacerbations in patients with chronic obstructive pulmonary disease (2018) (82)
A comparison of diagnostic interviews for depression in the Stirling County study: challenges for psychiatric epidemiology. (2000) (82)
Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation (2010) (80)
Family-based methods for linkage and association analysis. (2008) (79)
Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin. (2003) (79)
Generalized linear mixture models for handling nonignorable dropouts in longitudinal studies. (2000) (79)
Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns. (2014) (78)
Review papers : Longitudinal studies with continuous responses (1992) (73)
Family study of the aggregation of eating disorders and mood disorders (2003) (73)
Obesity and Weight Gain in Relation to Depression: Findings from the Stirling County Study (2008) (70)
Use of multiple informant data as a predictor in psychiatric epidemiology (1999) (68)
An alternative parameterization of the general linear mixture model for longitudinal data with non‐ignorable drop‐outs (2001) (67)
Polymorphism in maternal LRP8 gene is associated with fetal growth. (2006) (65)
The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers. (2000) (62)
Penalized solutions to functional regression problems (2007) (60)
A Mixture Model for Longitudinal Data with Application to Assessment of Noncompliance (2000) (59)
Genetic association analysis of behavioral inhibition using candidate loci from mouse models. (2001) (57)
On the analysis of copy‐number variations in genome‐wide association studies: a translation of the family‐based association test (2008) (57)
Tests for homogeneity of the risk difference when data are sparse. (1998) (57)
Analysing incomplete longitudinal binary responses: a likelihood-based approach. (1994) (55)
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease. (2016) (53)
Protocol for the National Cooperative Dialysis Study. (1983) (53)
A Study of how Socioeconomic Status Moderates the Relationship between SNPs Encompassing BDNF and ADHD Symptom Counts in ADHD Families (2007) (53)
Selection modelling versus mixture modelling with nonignorable nonresponse (1986) (52)
Using the jackknife to estimate the variance of regression estimators from repeated measures studies (1990) (52)
Computation of variance components using the em algorithm (1982) (52)
A new multimarker test for family‐based association studies (2007) (51)
Family‐based association analysis of a statistically derived quantitative traits for ADHD reveal an association in DRD4 with inattentive symptoms in ADHD individuals (2008) (51)
A simulation study of estimators for rates of change in longitudinal studies with attrition. (1991) (50)
Maximum likelihood regression methods for paired binary data. (1990) (50)
Increasing efficiency from censored survival data by using random effects to model longitudinal covariates (1998) (49)
Mortality associated with depression (2008) (49)
Maximum Likelihood Analysis of Logistic Regression Models with Incomplete Covariate Data and Auxiliary Information (2001) (47)
Multivariate logistic regression for familial aggregation of two disorders. I. Development of models and methods. (2001) (47)
An efficient family‐based association test using multiple markers (2006) (46)
Ozone exposure, vitamin C intake, and genetic susceptibility of asthmatic children in Mexico City: a cohort study (2013) (45)
Nonlinear growth curve analysis: estimating the population parameters. (1986) (45)
Multiple informants: mortality associated with psychiatric disorders in the Stirling County Study. (2001) (44)
Family‐based association tests for survival and times‐to‐onset analysis (2004) (43)
Tests of Gene‐Environment Interaction for Case‐Parent Triads with General Environmental Exposures (2004) (43)
Estimating rates of change in randomized clinical trials. (1990) (43)
Intention-to-treat analyses for incomplete repeated measures data. (1996) (42)
Genome‐Wide Association Study of the Genetic Determinants of Emphysema Distribution (2016) (40)
Power estimation of multiple SNP association test of case‐control study and application (2004) (40)
Lobar Emphysema Distribution Is Associated With 5‐Year Radiological Disease Progression (2018) (40)
Longitudinal studies with continuous responses. (1992) (40)
A Structural Approach to the Familial Coaggregation of Disorders (2008) (39)
Correcting for non-compliance in randomized trials: an application to the ATBC Study. (1999) (38)
Simple moment estimates of the κ-coefficient and its variance (1994) (38)
Incidence of major depression: prediction from subthreshold categories in the Stirling County Study. (2002) (36)
Empirical bayes estimates using the nonparametric maximum likelihood estimate for the priort (1982) (35)
Analyzing networks of phenotypes in complex diseases: methodology and applications in COPD (2014) (35)
Empirical Bayes confidence intervals for a series of related experiments (1989) (35)
Self-disparagement as feature and forerunner of depression: findings from the Stirling County Study. (2002) (33)
[Validity and reproducibility of a questionnaire on physical activity and non-activity for school children in Mexico City]. (2000) (31)
Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia (2018) (31)
Statistical Methods in the Journal - An Update. (2017) (31)
Multivariate logistic regression for familial aggregation of two disorders. II. Analysis of studies of eating and mood disorders. (2001) (31)
Smoothing the non-parametric estimate of a prior distribution by roughening: A computational study (1991) (31)
[Regression Models for Discrete Longitudinal Responses]: Rejoinder (1993) (31)
Sex‐Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women (2017) (30)
An analysis of two-period crossover designs with carry-over effects. (1992) (30)
Gene‐environment interaction tests for dichotomous traits in trios and sibships (2009) (29)
Bias due to misclassification of personal exposures in epidemiologic studies of indoor and outdoor air pollution (1986) (29)
The sib transmission/disequilibrium test is a Mantel-Haenszel test. (1998) (28)
The Role of Family-Based Designs in Genome-Wide Association Studies (2009) (28)
Weighted least squares analysis of repeated categorical measurements with outcomes subject to nonresponse. (1994) (28)
Approximate Posterior Distributions for Incomplete Data Problems (1982) (27)
Nonparametric mixed-effects models for repeated binary data arising in serial dilution assays : An application to estimating viral burden in AIDS (1996) (26)
Identification of Novel Alzheimer’s Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data (2020) (25)
Modelling adolescent blood pressure patterns and their prediction of adult pressures. (1991) (24)
Analysis of longitudinal and cluster-correlated data (2004) (24)
Prediction and creation of smooth curves for temporally correlated longitudinal data (1995) (23)
Alternative methods for testing treatment effects on the basis of multiple outcomes: Simulation and case study (2011) (22)
Evidence for an Association of the Dopamine D5 Receptor Gene on Age at Onset of Attention Deficit Hyperactivity Disorder (2007) (21)
A Three-stage Estimator for Studies with Repeated and Possibly Missing Binary Outcomes (1992) (20)
On the Optimal Design of Genetic Variant Discovery Studies (2010) (20)
The Association Of Genome-Wide Significant Spirometric Loci With COPD Susceptibility (2011) (19)
Regression analysis of multiple-source longitudinal outcomes: a "Stirling County" depression study. (2002) (19)
Parameter estimation in variance component models for binary response data. (1990) (18)
fgui: A Method for Automatically Creating Graphical User Interfaces for Command-Line R Packages. (2009) (18)
Regression methods for assessing familial aggregation of disease (2003) (17)
Effect of dialysis therapy on the hematopoietic system: the National Cooperative Dialysis Study. (1983) (17)
Adversary social roles: Their effects on witnesses' communication of evidence and the assessments of adjudicators. (1983) (17)
A Bayesian framework for intent-to-treat analysis with missing data. (1998) (17)
Exact family‐based association tests for biallelic data (2005) (16)
Multivariate Analysis: Discrete Variables (Logistic Regression) (2001) (16)
Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability (2015) (16)
Incorporating missingness for estimation of marginal regression models with multiple source predictors (2007) (16)
Tests for Compositional Epistasis under Single Interaction‐Parameter Models (2011) (16)
Using linkage information to weight a genome‐wide association of bipolar disorder (2011) (16)
Linkage disequilibrium mapping of the chromosome 6q21–22.31 bipolar I disorder susceptibility locus (2009) (15)
Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set (2011) (15)
A new statistical screening approach for finding pharmacokinetics-related genes in genome-wide studies (2009) (14)
Gene‐based segregation method for identifying rare variants in family‐based sequencing studies (2017) (13)
Fitting ACE structural equation models to case‐control family data (2009) (13)
Inter-laboratory variability in Ames assay results. (1987) (13)
Long𝒞ri𝒮𝒫: a test for bump hunting in longitudinal data (2007) (12)
Thyroid cancer risk from exposure to ionizing radiation: a case study in the comparative potency model. (1987) (12)
Joint models for efficient estimation in proportional hazards regression models (2003) (12)
Family‐based Association Test (FBAT) (2011) (12)
Studying the incidence of depression: an ‘interval’ effect (2000) (12)
New Powerful Approaches for Family‐based Association Tests with Longitudinal Measurements (2009) (11)
A Conversation with F. N. David (1989) (11)
Discussion of "Adjusting for nonignorable drop-out using semiparametric nonresponse models" by DO Scharfstein, A Rotnitzky and JM Robins (1999) (11)
Multivariate logistic regression with incomplete covariate and auxiliary information (2010) (10)
Statistical Challenges in Sequence-Based Association Studies with Population- and Family-Based Designs (2013) (10)
Non‐linear hierarchical models for monitoring compliance (2002) (10)
15 The analysis of case-control data: Epidemiologic studies of familial aggregation (2000) (10)
The EM Algorithm in Genetics, Genomics and Public Health (2010) (9)
Vitamin D deficiency is associated with respiratory symptoms and airway wall thickening in smokers with and without COPD: a prospective cohort study (2020) (9)
Identifying rare variants from exome scans: the GAW17 experience (2011) (9)
A comparative analysis of family-based and population-based association tests using whole genome sequence data (2014) (9)
Comments on ‘Empirical vs natural weighting in random effects meta‐analysis’ (2010) (9)
Longitudinal panel data: an overview of current methodology (1996) (9)
Tracing aerosol pollution. (1985) (9)
Biostatistic tools in pharmacogenomics--advances, challenges, potential. (2010) (9)
Finding the design matrix for the marginal homogeneity model (1990) (8)
A Method for Modeling Utilization Data from Multiple Sources: Application in a Study of Linkage to Primary Care (2002) (8)
On the frequency of copy number variants (2008) (8)
An algorithmic approach for the fitting of a general mixed ANOVA model appropriate in longitudinal settings (1986) (8)
FBAT-SNP-PC: An Approach for Multiple Markers and Single Trait in Family-Based Association Tests (2008) (8)
Estimating the Effect of a Predictor Measured by Two Informants on a Continuous Outcome: A Comparison of Methods (2011) (8)
Mutations in SARS-CoV-2 spike protein and RNA polymerase complex are associated with COVID-19 mortality risk (2020) (8)
No bias in linkage analysis. (2004) (8)
An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease (reply) (1999) (8)
Correction: Regression Analysis for Categorical Variables with Outcome Subject to Nonignorable Nonresponse (1988) (8)
Genomic screening in family-based association testing (2005) (8)
Schizophrenia risk conferred by protein-coding de novo mutations (2018) (7)
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 (2021) (7)
Comparison of linkage and association strategies for quantitative traits using the COGA dataset (2005) (7)
EFBAT: exact family-based association tests (2007) (7)
Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" (2007) (7)
Effects of dialysis prescription on bone and mineral metabolism: the National Cooperative Dialysis Study. (1983) (7)
Differentiating Population Stratification from Genotyping Error Using Family Data (2012) (7)
[Selection Models and the File Drawer Problem]: Comment (1988) (7)
Estimating Disease Prevalence Using Relatives of Case and Control Probands (2010) (7)
Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures (2010) (7)
[Prediction of Future Observations in Growth Curve Models]: Comment (1987) (7)
Combining Disease Models to Test for Gene–Environment Interaction in Nuclear Families (2011) (6)
Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2 (2021) (6)
14 The EM algorithm (1993) (6)
Identifying rare variants using a Bayesian regression approach (2011) (6)
Bayes Analysis of Model-Based Methods for Nonignorable Nonresponse in the Harvard Medical Practice Survey (1993) (6)
Missing Information Principle (2006) (6)
25 Estimation of Marginal Regression Models with Multiple Source Predictors (2007) (5)
Is It Rare or Common? (2012) (5)
Binary Response Models and Logistic Regression (2015) (5)
A comparison of popular TDT‐generalizations for family‐based association analysis (2019) (5)
Hemodynamic and cardiac correlates of different hemodialysis regimes: the National Cooperative Dialysis Study. (1983) (5)
Empirical Bayes Confidence Intervals Based on Bootstrap Samples: Rejoinder (1987) (5)
Adjusting for Nonignorable Drop-Out Using Semiparametric Nonresponse Models: Comment (1999) (5)
Self‐Consistency—I (2006) (5)
Power evaluations for family-based tests of association with incomplete parental genotypes. (2003) (4)
A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information (2014) (4)
Family‐based tests for associating haplotypes with general phenotype data (2018) (4)
A reanalysis of the Stanford heart transplant data:a rejoinder (1983) (4)
Longitudinal analysis of incomplete adolescent data. (1991) (4)
Approaches to Handling Incomplete Data in Family‐based Association Testing (2007) (4)
Estimating rates of change in clinical studies (1992) (4)
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests (2020) (4)
Family-Based Association Tests with Longitudinal Measurements: Handling Missing Data (2009) (4)
A NOTE ON CLASSIFYING ORDINAL-SCALE DATA (1979) (4)
Variance calculations for identity-by-descent estimation. (2006) (3)
Testing for association in genetic studies (2005) (3)
Sample-size estimation: a sensitivity analysis in the context of a clinical trial for treatment of mild hypertension. (1979) (3)
Influences of dialysis prescription on electrolyte and acid-base metabolism: the National Cooperative Dialysis Study. (1983) (3)
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry (2015) (3)
INCIDENCE OF OF ADVERSE EVENTS AND NEGLIGENCE IN HOSPITALIZED PATIENTS. REPLY (1991) (3)
On the parsing of statistical information in family-based association testing (2007) (3)
Principles of Inheritance: Mendel’s Laws and Genetic Models (2011) (3)
10 – Estimation of Marginal Regression Models with Multiple Source Predictors (2010) (3)
Impact of Population Stratification on Family-Based Association Tests with Longitudinal Measurements (2009) (3)
Marginal regression models with a time to event outcome and discrete multiple source predictors (2006) (2)
Introduction to Statistical Genetics and Background in Molecular Genetics (2011) (2)
The General Concepts of Gene Mapping: Linkage, Association, Linkage Disequilibrium and Marker Maps (2011) (2)
Estimating the Prevalence of Disease Using Relatives of Case and Control Probands (2007) (2)
19 Regression analysis of spatially correlated data: The kanawha county health study (1994) (2)
Family‐based association for quantitative traits. (2014) (2)
Response to Macgregor (2008) (2)
Longitudinal Data Modeling (2013) (2)
Chapter 5: Random effects and the linear mixed model (2004) (2)
A general semi-parametric approach to the analysis of genetic association studies in population-based designs (2013) (2)
Analysis of Linear and Non-Linear Growth Models with Random Parameters (1990) (2)
Analysis of data with missing values: discussion following meeting (1988) (1)
An exact, unifying framework for region-based association testing in family-based designs, including higher criticism approaches, SKATs, multivariate and burden tests (2019) (1)
Parsing the Effects of Individual SNPs in Candidate Genes with Family Data (2009) (1)
Raphson and Em Algorithms for Linear Mixed- Eeects Models for Repeated-measures Data, Journal of the American Statistical Association Where L Represents the Full Likelihood for the Complete Data, Deened in Section 4.2, And (1997) (1)
X Chromosome Genetic Associations in COPD (2019) (1)
Family-based Association for Quantitative Traits (2005) (1)
Statistical analysis of longitudinal studies (2022) (1)
Meta-analysis: Heterogeneity can be a good thing (2013) (1)
Exome Sequencing In Severe COPD Cases And Resistant Smoking Controls From COPDGene (2012) (1)
Probabilistic diagnosis in linkage analysis of bipolar disorder: Putting weights on the fringe (1997) (1)
The Basics of Genetic Association Analysis (2011) (1)
Estimating the κ‐coefficient from a Selected Sample (2001) (1)
Basic Concepts of Linkage Analysis (2011) (1)
Association Analysis in Family Designs (2011) (1)
Identification of Adverse Events Occurring during Hospitalization (2020) (1)
Chapter 7: Likelihood models for repeated binary data (2004) (0)
A Statistical Model for Positron Emission Tomography: Comment (1985) (0)
Population Substructure in Association Studies (2011) (0)
Some Basic Concepts from Population Genetics (2011) (0)
Chapter 2: Estimation in the LMCD assuming normally distributed errors and complete data (2004) (0)
Chapter 1: Introduction to longitudinal data analysis (2004) (0)
Statistical Applications in Genetics and Molecular Biology (2010) (0)
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 (0)
Whole Exome Sequencing Analysis Of Severe COPD (2017) (0)
Neural ExpectationMaximization (2017) (0)
Statistical Screening Method for Genetic Factors Influencing Susceptibility to Common Diseases in a Two-Stage Genome-Wide Association Study (2009) (0)
Collection of Biostatistics Research Archive (2006) (0)
·P-46 Estimating rates of change in randomized studies (1990) (0)
Association strategies in Alzheimer's disease: Findings from the NIMH genetics initiative (2000) (0)
Genome Wide Association Studies (2011) (0)
Harvard University Department of Biostatistics (2012) (0)
Chapter 3: Estimation in the LMCD assuming normally distributed errors with unbalanced designs/missing data (2004) (0)
Isolation of Brain Tumor Segment using HMGMM (2017) (0)
Comment: Bayes, Oracle Bayes, and Empirical Bayes (2019) (0)
Categorical Auxiliary Data in the Discrete Time Proportional Hazards Model (2003) (0)
American Educational Research Association Empirical Bayes Ranking Methods (2007) (0)
Exome Array Analysis Identifies Il27 As A Susceptibility Locus For Chronic Obstructive Pulmonary Disease (2016) (0)
Statistical Challenges in Sequence-Based Association Studies with Population- and Family-Based Designs (2012) (0)
Looking Toward the Future (2011) (0)
Chapter 8: Random effects models for repeated binary data (2004) (0)
Chapter 4: Semi-parametric estimation in the linear model for correlated data (2004) (0)
Book reviews (1995) (0)
Population Genetics Considerations (2015) (0)
X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study (2023) (0)
Genetics and population analysis On the frequency of copy number variants (2008) (0)
Aggregation, Heritability and Segregation Analysis: Modeling Genetic Inheritance Without Genetic Data (2011) (0)
Linear Mixed Models (2015) (0)
Self-Consistency - Basic† (2014) (0)
Genomic screening and replication in one data set in family-based association testing (2005) (0)
ABSTRACTS FROM THE TWENTY-SECOND ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY (2013) (0)
Chapter 6: Longitudinal data analysis for counts and binary outcomes: generalized estimating equations (GEE) (2004) (0)

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