Imputation Aware Meta-Analysis of Genome-Wide Association Studies

Por Zaitlen, Noah, Eskin, Eleazar
Publicado em 2010

Heritability in the genome-wide association era

Por Zaitlen, Noah, Kraft, Peter
Publicado em 2012

A Novel Test for Detecting SNP–SNP Interactions in Case-Only Trio Studies

Por Balliu, Brunilda, Zaitlen, Noah
Publicado no Genetics (2016)

Linkage Effects and Analysis of Finite Sample Errors in the HapMap

Por Zaitlen, Noah, Min Kang, Hyun, Eskin, Eleazar
Publicado em 2009

EMINIM: An Adaptive and Memory-Efficient Algorithm for Genotype Imputation

Por Kang, Hyun Min, Zaitlen, Noah A., Eskin, Eleazar
Publicado em 2010

Variation in predictive ability of common genetic variants by established strata - The example of breast cancer and age

Por Aschard, Hugues, Zaitlen, Noah, Lindström, Sara, Kraft, Peter
Publicado no Epidemiology (2015)

Leveraging the HapMap Correlation Structure in Association Studies

Por Zaitlen, Noah, Kang, Hyun Min, Eskin, Eleazar, Halperin, Eran
Publicado em 2007

Leveraging Genetic Variability across Populations for the Identification of Causal Variants

Por Zaitlen, Noah, Paşaniuc, Bogdan, Gur, Tom, Ziv, Elad, Halperin, Eran
Publicado em 2010

New approaches to population stratification in genome-wide association studies

Por Price, Alkes L., Zaitlen, Noah A., Reich, David, Patterson, Nick
Publicado em 2010

Genotyping common and rare variation using overlapping pool sequencing

Por He, Dan, Zaitlen, Noah, Pasaniuc, Bogdan, Eskin, Eleazar, Halperin, Eran
Publicado em 2011

A non-parametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes

Por Aschard, Hugues, Zaitlen, Noah, Tamimi, Rulla M., Lindström, Sara, Kraft, Peter
Publicado em 2013

Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies

Por Brown, Brielin C., Price, Alkes L., Patsopoulos, Nikolaos A., Zaitlen, Noah
Publicado no Genetics (2016)

Transethnic Genetic-Correlation Estimates from Summary Statistics

Por Brown, Brielin C., Ye, Chun Jimmie, Price, Alkes L., Zaitlen, Noah
Publicado no Am J Hum Genet (2016)

efficient association study design via power-optimized tag SNP selection

Por HAN, BUHM, KANG, HYUN MIN, SEO, MYEONG SEONG, ZAITLEN, NOAH, ESKIN, ELEAZAR
Publicado em 2008

Combining effects from rare and common genetic variants in an exome-wide association study of sequence data

Por Aschard, Hugues, Qiu, Weiliang, Pasaniuc, Bogdan, Zaitlen, Noah, Cho, Michael H, Carey, Vincent
Publicado em 2011

Genetic and environmental components of family history in type 2 diabetes

Por Cornelis, Marilyn C, Zaitlen, Noah, Hu, Frank B., Kraft, Peter, Price, Alkes L.
Publicado no Hum Genet (2014)

Massively Parallel Identification of Regulatory Variants in Asthma

Por Biton, Anne, Torgerson, Dara, Letonqueze, Olivier, Zhao, Wenxue, Zaitlen, Noah, Erle, David J.
Publicado no Ann Am Thorac Soc (2016)

Advantages and pitfalls in the application of mixed model association methods

Por Yang, Jian, Zaitlen, Noah A., Goddard, Michael E., Visscher, Peter M., Price, Alkes L.
Publicado em 2014

Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants

Por Uricchio, Lawrence H., Zaitlen, Noah A., Ye, Chun Jimmie, Witte, John S., Hernandez, Ryan D.
Publicado no Genome Res (2016)

Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

Por Zaitlen, Noah A., Kang, Hyun Min, Feolo, Michael L., Sherry, Stephen T., Halperin, Eran, Eskin, Eleazar
Publicado em 2005