Kathryn Roeder - Concepedia

Author

Kathryn Roeder

Also Known As

Aaron Topol, Alan F. Schatzberg, Bernie Devlin, C. M. Kammerer, Darina Czamara , Elise B. Robinson, Elise Robinson, Howard J Edenberg, Jeffrey C. Barrett, Joseph Buxbaum

342

Publications

51.5K

Citations

H-Index

207

Concepts

All Affiliations

Carnegie Mellon University University of Pittsburgh Yale University Harvard University Icahn School of Medicine at Mount Sinai

About

Kathryn Roeder is an author at Carnegie Mellon University specializing in medicine, genetics, and biostatistics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	42	65	17.9K
2	Engineering	19	26	2.1K
3	Education	5	5	2.6K
4	Business	3	3	608
5	Health Sciences	1	1	63

Kathryn Roeder

158

Publications

37.7K

Citations

H-Index

Page 1

	Year	Citations
Genomic Control for Association Studies Bernie Devlin, Kathryn Roeder Biometrics	1999	3.2K
A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories Bobby L. Jones, Daniel S. Nagin, Kathryn Roeder Sociological Methods & Research EducationSocial SciencesDevelopmental PsychologyDevelopmental TrajectoriesMixture Analysis	2001	2.3K
De novo mutations revealed by whole-exome sequencing are strongly associated with autism Stephan Sanders, Michael T. Murtha, Abha R. Gupta, Nature Neurodevelopmental DisordersSyndromic AutismWhole-exome SequencingGeneticsGenetic Disorder	2012	2.1K
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Patterns and rates of exonic de novo mutations in autism spectrum disorders Benjamin M. Neale, Yan Kou, Li Liu, Nature Neurodevelopmental DisordersAutism Spectrum DisordersSyndromic AutismGeneticsGenetic Disorder	2012	1.8K
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci Stephan Sanders, Xin He, A. Jeremy Willsey, Neuron Genome-wide Association StudySyndromic AutismGeneticsRisk LociMolecular Biology	2015	1.5K
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Phil H. Lee, Verneri Anttila, Hyejung Won, Cell PsychiatryPsychiatric DisordersGenetic DisorderGeneticsPsychiatric Genetics	2019	1.4K
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Neuron Neurodevelopmental DisordersWilliams Syndrome RegionSyndromic AutismGenetic DisorderGenetics	2011	1.3K
Most genetic risk for autism resides with common variation Trent Gaugler, Lambertus Klei, Stephan Sanders, Nature Genetics Syndromic AutismGeneticsGenetic EpidemiologyAutismNeurodiversity	2014	1.3K
Gene expression elucidates functional impact of polygenic risk for schizophrenia Menachem Fromer, Panos Roussos, Solveig K. Sieberts, Nature Neuroscience PsychiatryRisk PredictionGeneticsPolygenic RiskSchizophrenia	2016	1.2K

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