Kathryn Roeder

Q: What Schools Are Affiliated With Kathryn Roeder

Kathryn Roeder is affiliated with the following schools: Yale University, Carnegie Mellon University, Stanford University, Pennsylvania State University, University of Idaho

Kathryn Roeder's AcademicInfluence.com Rankings

Kathryn Roeder

Mathematics

#3588

World Rank

#5272

Historical Rank

#1317

USA Rank

Statistics

#215

World Rank

#269

Historical Rank

#86

USA Rank

mathematics Degrees

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Mathematics

Kathryn Roeder's Degrees

PhD Statistics Stanford University
Masters Statistics Stanford University

Why Is Kathryn Roeder Influential?

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According to Wikipedia, Kathryn M. Roeder is an American statistician known for her development of statistical methods to uncover the genetic basis of complex disease and her contributions to mixture models, semiparametric inference, and multiple testing. Roeder holds positions as professor of statistics and professor of computational biology at Carnegie Mellon University, where she leads a project focused on discovering genes associated with autism.

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Kathryn Roeder'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

Genomic Control for Association Studies (1999) (3091)
A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories (2001) (2101)
Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) (2080)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) (1893)
Functional impact of global rare copy number variation in autism spectrum disorders (2010) (1891)
Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) (1645)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism (2011) (1218)
Identification of common genetic risk variants for autism spectrum disorder (2019) (1140)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) (1106)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2018) (1064)
Most genetic risk for autism resides with common variation (2014) (995)
A framework for the interpretation of de novo mutation in human disease (2014) (869)
Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (2016) (831)
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism (2013) (765)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
Genome-wide association identifies multiple ulcerative colitis susceptibility loci (2010) (621)
Testing for an Unusual Distribution of Rare Variants (2011) (595)
Practical Bayesian Density Estimation Using Mixtures of Normals (1997) (579)
HIGH DIMENSIONAL VARIABLE SELECTION. (2007) (575)
A genome-wide scan for common alleles affecting risk for autism (2010) (567)
Genomic control, a new approach to genetic-based association studies. (2001) (505)
Modeling Uncertainty in Latent Class Membership: A Case Study in Criminology (1999) (431)
Stability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models (2010) (420)
The huge Package for High-dimensional Undirected Graph Estimation in R (2012) (399)
Common genetic variants, acting additively, are a major source of risk for autism (2012) (372)
The power of genomic control. (2000) (366)
Individual common variants exert weak effects on the risk for autism spectrum disorders (2012) (346)
False discovery control with p-value weighting (2006) (313)
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis (2012) (308)
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia (2017) (301)
Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples (2016) (296)
Density estimation with confidence sets exemplified by superclusters and voids in the galaxies (1990) (290)
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment (2015) (289)
The heritability of IQ (1997) (252)
Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders (2013) (248)
Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes (2013) (238)
Using linkage genome scans to improve power of association in genome scans. (2006) (217)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. (2012) (202)
Ulcerative colitis loci on chromosomes 1p36 and 12q15 identified by genome-wide association study (2008) (199)
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder (2018) (196)
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder (2018) (194)
The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders (2012) (171)
Genomic Control to the extreme (2004) (158)
Unbiased methods for population‐based association studies (2001) (148)
On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. (2003) (144)
Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls (2013) (143)
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. (2014) (141)
A Graphical Technique for Determining the Number of Components in a Mixture of Normals (1994) (138)
SNP-Based Analysis of Genetic Substructure in the German Population (2006) (137)
No excess of homozygosity at loci used for DNA fingerprinting. (1990) (134)
Pleiotropy and principal components of heritability combine to increase power for association analysis (2008) (133)
Screen and clean: a tool for identifying interactions in genome‐wide association studies (2010) (133)
Association studies for quantitative traits in structured populations (2002) (133)
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. (2008) (126)
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics (2014) (125)
A Semiparametric Mixture Approach to Case-Control Studies with Errors in Covariables (1996) (124)
Genome-Wide Significance Levels and Weighted Hypothesis Testing. (2009) (122)
Characterization of multilocus linkage disequilibrium (2005) (120)
Flexible Parametric Measurement Error Models (1999) (111)
Discovering genetic ancestry using spectral graph theory (2009) (110)
Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families. (2014) (108)
Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes. (2001) (108)
Common risk variants identified in autism spectrum disorder (2017) (106)
Application of Maximum Likelihood Methods to Population Genetic Data for the Estimation of Individual Fertilities (1989) (105)
Fractional paternity assignment: theoretical development and comparison to other methods (1988) (102)
Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS (2018) (100)
Global spectral clustering in dynamic networks (2018) (96)
Do common variants play a role in risk for autism? Evidence and theoretical musings (2011) (96)
Analysis of single‐locus tests to detect gene/disease associations (2005) (95)
Improving power in genome‐wide association studies: weights tip the scale (2007) (94)
Residual diagnostics for mixture models (1992) (92)
Disequilibrium mapping: composite likelihood for pairwise disequilibrium. (1996) (92)
A Bayesian semiparametric model for case-control studies with errors in variables (1997) (92)
Evolutionary-based association analysis using haplotype data. (2002) (88)
African ancestry and lung function in Puerto Rican children. (2012) (86)
DNA Fingerprinting: A Review of the Controversy (1994) (80)
Journal of the American Statistical Association: Comment (2006) (79)
Analysis of multilocus models of association (2003) (78)
A statistical model for locating regulatory regions in genomic DNA. (1997) (75)
Intelligence, Genes, and Success (1997) (74)
APOE and TREM2 regulate amyloid responsive microglia in Alzheimer’s disease (2020) (74)
Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study (2009) (71)
Haplotype fine mapping by evolutionary trees. (2000) (69)
High‐Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men (2009) (66)
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex (2019) (66)
Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau (2002) (61)
Next generation analytic tools for large scale genetic epidemiology studies of complex diseases (2012) (61)
A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA. (2016) (57)
An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders (2018) (56)
Forensic Inference from DNA Fingerprints (1992) (56)
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk (2018) (55)
Genomic control for association studies: a semiparametric test to detect excess-haplotype sharing. (2000) (54)
Statistical evaluation of DNA fingerprinting: a critique of the NRC's report. (1993) (53)
Semisoft clustering of single-cell data (2018) (53)
Candidate Gene Analysis of Femoral Neck Trabecular and Cortical Volumetric Bone Mineral Density in Older Men (2009) (52)
Estimation of allele frequencies for VNTR loci. (1991) (51)
Uniqueness of estimation and identifiability in mixture models (1993) (50)
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022) (49)
Evolutionary‐based association analysis using haplotype data (2003) (48)
The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability. (2017) (45)
Mixture models for linkage analysis of affected sibling pairs and covariates (2002) (45)
A Unified Treatment of Integer Parameter Models (1987) (41)
Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching (2003) (40)
Overdispersion Diagnostics for Generalized Linear Models (1995) (39)
Does Staying in School Make You Smarter (1997) (39)
Of Genes and IQ (1997) (38)
Amino Acid Position 11 of HLA-DRβ1 is a Major Determinant of Chromosome 6p Association with Ulcerative Colitis (2011) (36)
Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men (2011) (35)
Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania (2001) (35)
Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden (2017) (35)
TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease (2011) (35)
Differential Activity of Transcribed Enhancers in the Prefrontal Cortex of 537 cases with Schizophrenia and Controls (2018) (34)
Weighted Hypothesis Testing (2006) (33)
Copy Number Variants for Schizophrenia and Related Psychotic Disorders in Oceanic Palau: Risk and Transmission in Extended Pedigrees (2011) (31)
Positive Semidefinite Rank-Based Correlation Matrix Estimation With Application to Semiparametric Graph Estimation (2014) (31)
NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM. (2015) (30)
Semiparametric Estimation of Normal Mixture Densities (1992) (29)
A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY. (2009) (28)
Statistical Genetics: False discovery or missed discovery? (2003) (25)
GemTools: A fast and efficient approach to estimating genetic ancestry (2011) (25)
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism (2021) (24)
Integration of association statistics over genomic regions using Bayesian adaptive regression splines (2003) (23)
Measuring heterogeneity in forensic databases using hierarchical Bayes models (1998) (22)
Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data (2021) (21)
Genomic Control for Association Studies Author ( s ) : (1999) (21)
Comments on the statistical aspects of the NRC's report on DNA typing. (1994) (21)
TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES. (2016) (20)
Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5 years apart (2020) (20)
Using ancestry matching to combine family‐based and unrelated samples for genome‐wide association studies (2010) (19)
A Bayesian hierarchical model for allele frequencies (2001) (19)
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies. (2016) (17)
Moment-based oscillation properties of mixture models (1997) (17)
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families (2017) (16)
Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression (2019) (16)
Searching for disease susceptibility variants in structured populations. (2009) (16)
Discovery of target genes and pathways of blood trait loci using pooled CRISPR screens and single cell RNA sequencing (2021) (16)
Estimating density from variable circular plot censuses (1987) (15)
False discovery or missed discovery? (2003) (15)
De novo missense variants disrupting protein–protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types (2020) (14)
How rare and common risk variation jointly affect liability for autism spectrum disorder (2020) (14)
A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk (2020) (13)
Intelligence and success: Is it all in the genes? (2002) (13)
ESCO: single cell expression simulation incorporating gene co-expression (2020) (13)
Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart (2020) (13)
H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives (2020) (12)
Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation (2007) (12)
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. (2013) (12)
Integration and transfer learning of single-cell transcriptomes via cFIT (2021) (11)
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder (2021) (11)
STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE. (2010) (11)
Cognitive and default mode networks support developmental stability in functional connectome fingerprinting through adolescence (2019) (10)
H‐MAGMA, inheriting a shaky statistical foundation, yields excess false positives (2020) (10)
New mutations, old statistical challenges (2017) (10)
REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING. (2012) (10)
Constructing local cell-specific networks from single-cell data (2021) (9)
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples (2017) (9)
Not All Autism Genes Are Created Equal: A Response to Myers et al. (2020) (8)
NRC report on DNA typing. (1993) (8)
The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2021) (7)
SCEPTRE improves calibration and sensitivity in single-cell CRISPR screen analysis (2021) (7)
Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth. (2019) (7)
Conditional resampling improves sensitivity and specificity of single cell CRISPR regulatory screens (2020) (7)
Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate (2014) (6)
Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci (2011) (6)
Multi-Stage Variable Selection: Screen and Clean (2007) (6)
Smooth-projected Neighborhood Pursuit for High-dimensional Nonparanormal Graph Estimation (2012) (6)
T9 Combining Autism And Intellectual Disability Exome Data Implicates Disruption Of Neocortical Development In Both Disorders (2017) (5)
Gradient-based Sparse Principal Component Analysis with Extensions to Online Learning (2019) (5)
Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree (2021) (5)
MIRA: mutual information-based reporter algorithm for metabolic networks (2014) (5)
A Unified Statistical Framework for RNA Sequence Data from Individual Cells and Tissue (2016) (5)
Covariance-Based Sample Selection for Heterogeneous Data: Applications to Gene Expression and Autism Risk Gene Detection (2018) (5)
Using multiple measurements of tissue to estimate cell-type-specific gene expression via deconvolution (2018) (5)
Conditional resampling improves calibration in single cell CRISPR screen analysis (2020) (5)
Bayesian estimation of cell-type-specific gene expression per bulk sample with prior derived from single-cell data (2020) (4)
Exponential-family embedding with application to cell developmental trajectories for single-cell RNA-seq data (2020) (4)
The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD (2021) (4)
Wringing The Bell Curve: A Cautionary Tale about the Relationships among Race, Genes, and IQ (1995) (4)
Robust probabilistic modeling for single-cell multimodal mosaic integration and imputation via scVAEIT (2022) (4)
Clustering and Alignment of Polymorphic Sequences for HLA-DRB1 Genotyping (2013) (4)
Corrigendum: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (2009) (4)
“Reply to Olson” (2002) (3)
Testing High Dimensional Differential Matrices, with Application to Detecting Schizophrenia Risk Genes (2016) (3)
Semi-soft Clustering of Single Cell Data (2018) (3)
Model-free prediction test with application to genomics data (2022) (3)
Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31 (2016) (3)
cFIT: Integration and transfer learning of single cell transcriptomes, illustrated by fetal brain cell development (2020) (2)
[DNA Fingerprinting: A Review of the Controversy]: Rejoinder (1994) (2)
Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development (2022) (2)
A United Statistical Framework for Single Cell and Bulk Sequencing Data (2017) (2)
Inequality by Design: Cracking the Bell Curve Myth@@@Intelligence, Genes, and Success: Scientists Respond to The Bell Curve (1999) (2)
Identification of cell-type-specific marker genes from co-expression patterns in tissue samples (2020) (2)
Binning clones by hybridization with complex probes: statistical refinement of an inner product mapping method. (1997) (1)
Gene Expression Deconvolution Implicates Cell-Type-Specific Gene Expression and Co-Expression in Autism (2020) (1)
29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX (2019) (1)
Asymptotic Distribution-Free Independence Test for High Dimension Data (2021) (1)
A method for inferring evolutionary relationships among haplotypes, exemplified by haplotypes at the monoamine oxidase locus (2004) (1)
9 LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES (2019) (1)
Expansion of RNA sequence diversity and RNA editing rates throughout human cortical development (2021) (1)
Application of post-selection inference to multi-omics data yields insights into the etiologies of human diseases (2019) (1)
MIRA: mutual information-based reporter algorithm for metabolic networks (2015) (1)
47. GENE DISCOVERY FROM EXOME SEQUENCING IN AUTISM AND COMPARISON TO DEVELOPMENTAL DELAY AND SCHIZOPHRENIA (2021) (0)
De Novo Insertions and Dele tions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder Graphical (0)
Learning Gene Networks Underlying Clinical Phenotypes Under SNP Perturbations From Genome-Wide Data (2019) (0)
Flexible Parametric Measurement Error Models Short Title. Flexible Models (1997) (0)
Comment (2006) (0)
A pr 2 00 7 Multi-Stage Variable Selection : Screen and Clean (2007) (0)
genomic regions using Bayesian adaptive regression splines (2003) (0)
Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum Disorder (2020) (0)
weighted_FDR.R - a function used to apply weighted false discovery rate for multiple testing. (2006) (0)
S T ] 7 A pr 2 00 6 Weighted Hypothesis Testing (2006) (0)
Supplementary Material for: Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31 (2016) (0)
ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND COMORBID SUBGROUPS (2022) (0)
G-BLUP Prediction of ASD Risk 3 . 1 Linear Random Effects Model (2017) (0)
African Ancestry, SES, FEV1 And Asthma Exacerbations In Puerto Rican Children (2012) (0)
F52. Age-Associated Functional Network Organization in Psychosis (2018) (0)
From local to global gene co-expression estimation using single-cell RNA-seq data (2022) (0)
Testing for an unusual distribution of rare variation (2010) (0)
A data harmonization pipeline to leverage external controls and boost power in GWAS (2020) (0)
A data harmonization pipeline to leverage external controls and boost power in GWAS. (2021) (0)
A method to exploit the structure of genetic ancestry space to enhance case-control studies (2016) (0)
Extrapolated cross-validation for randomized ensembles (2023) (0)
Science mixes it up with statistics (2014) (0)
Response (1991) (0)
An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders (2018) (0)
SCEPTRE improves calibration and sensitivity in single-cell CRISPR screen analysis (2021) (0)
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder (2018) (0)
Autism Sequencing Consortium (ASC) iPSYCH-BROAD Consortium Broad Institute Center for Common Disease Genomics (Broad-CCDG) (2021) (0)
Genetic analysis of schizophrenia in isolated populations (2000) (0)
Acknowledgement to the Reviewers (2009) (0)
De Novo Variation in Coding and Noncoding Regions: What We Can Learn from the Data about Etiological Pathways (2019) (0)
Exponential family measurement error models for single-cell CRISPR screens (2022) (0)
A selective inference approach for FDR control using multi-omics covariates yields insights into disease risk (2019) (0)
Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
Integrative Analyses of Autism And Intellectual Disability Exome Data Reveal Similarities And Divergences And Identify Novel Risk Genes For Both Disorders (2017) (0)
31DISCOVERY AND CHARACTERIZATION OF 102 GENES ASSOCIATED WITH AUTISM FROM EXOME SEQUENCING OF 37,269 INDIVIDUALS (2019) (0)
Contents Vol. 2, 2016 (2017) (0)
Rare De Novo and Common Variations Affect Liability to Autism (2019) (0)
Rejoinder for “Exponential-Family Embedding With Application to Cell Developmental Trajectories for Single-Cell RNA-Seq Data” (2021) (0)
An approach to gene-based testing accounting for dependence of tests among nearby genes (2021) (0)
INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING (2019) (0)
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens. (2023) (0)
Avoiding stratification in association studies (2005) (0)
Neurobiological Clusters Are Associated with Trajectories of Overall Psychopathology in Youth. (2023) (0)

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Kathryn Roeder's Academic­Influence.com Rankings