Novel approach for parallelizing pairwise comparison problems as applied to detecting segments identical by decent in whole-genome data

por Sapin, Emmanuel, Keller, Matthew C
Publicado 2021

Bias and Precision of Parameter Estimates from Models Using Polygenic Scores to Estimate Environmental and Genetic Parental Influences

por Kim, Yongkang, Balbona, Jared V., Keller, Matthew C.
Publicado 2020

Estimation of Parental Effects Using Polygenic Scores

por Balbona, Jared V., Kim, Yongkang, Keller, Matthew C.
Publicado 2021

Quantification of Inbreeding Due to Distant Ancestors and Its Detection Using Dense Single Nucleotide Polymorphism Data

por Keller, Matthew C., Visscher, Peter M., Goddard, Michael E.
Publicado 2011

Detecting autozygosity through runs of homozygosity: A comparison of three autozygosity detection algorithms

por Howrigan, Daniel P, Simonson, Matthew A, Keller, Matthew C
Publicado 2011

Relationships between estimated autozygosity and complex traits in the UK Biobank

por Johnson, Emma C., Evans, Luke M., Keller, Matthew C.
Publicado 2018

Whole-Genome Pathway Analysis on 132,497 Individuals Identifies Novel Gene-Sets Associated with Body Mass Index

por Simonson, Matthew A., McQueen, Matthew B., Keller, Matthew C.
Publicado 2014

Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk

por Simonson, Matthew A, Wills, Amanda G, Keller, Matthew C, McQueen, Matthew B
Publicado 2011

The Association of Genotype-Based Inbreeding Coefficient with a Range of Physical and Psychological Human Traits

por Verweij, Karin J. H., Abdellaoui, Abdel, Veijola, Juha, Sebert, Sylvain, Koiranen, Markku, Keller, Matthew C., Järvelin, Marjo-Riitta, Zietsch, Brendan P.
Publicado 2014

Assortative mating biases marker-based heritability estimators

por Border, Richard, O’Rourke, Sean, de Candia, Teresa, Goddard, Michael E., Visscher, Peter M., Yengo, Loic, Jones, Matt, Keller, Matthew C.
Publicado 2022

Author Correction: Assortative mating biases marker-based heritability estimators

por Border, Richard, O’Rourke, Sean, de Candia, Teresa, Goddard, Michael E., Visscher, Peter M., Yengo, Loic, Jones, Matt, Keller, Matthew C.
Publicado 2022

Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals

por Kemper, Kathryn E., Yengo, Loic, Zheng, Zhili, Abdellaoui, Abdel, Keller, Matthew C., Goddard, Michael E., Wray, Naomi R., Yang, Jian, Visscher, Peter M.
Publicado 2021

Mutational load analysis of unrelated individuals

por Howrigan, Daniel P, Simonson, Matthew A, Kamens, Helen M, Stephens, Sarah H, Wills, Amanda G, Ehringer, Marissa A, Keller, Matthew C, McQueen, Matthew B
Publicado 2011

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

por Lee, S Hong, DeCandia, Teresa R, Ripke, Stephan, Yang, Jian, Sullivan, Patrick F, Goddard, Michael E, Keller, Matthew C, Visscher, Peter M, Wray, Naomi R
Publicado 2012

The Genetic Correlation between Height and IQ: Shared Genes or Assortative Mating?

por Keller, Matthew C., Garver-Apgar, Christine E., Wright, Margaret J., Martin, Nicholas G., Corley, Robin P., Stallings, Michael C., Hewitt, John K., Zietsch, Brendan P.
Publicado 2013

Genetic influences on the human oral microbiome

por Demmitt, Brittany A., Corley, Robin P., Huibregtse, Brooke M., Keller, Matthew C., Hewitt, John K., McQueen, Matthew B., Knight, Rob, McDermott, Ivy, Krauter, Kenneth S.
Publicado 2017

Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor

por Keller, Matthew C., Simonson, Matthew A., Ripke, Stephan, Neale, Ben M., Gejman, Pablo V., Howrigan, Daniel P., Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F., Sullivan, Patrick F., The Schizophrenia Psychiatric Genome-Wide Association Study Consortium
Publicado 2012

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

por Evans, Luke M., Tahmasbi, Rasool, Vrieze, Scott I., Abecasis, Gonçalo R., Das, Sayantan, Gazal, Steven, Bjelland, Douglas W., de Candia, Teresa R., Goddard, Michael E., Neale, Benjamin M., Yang, Jian, Visscher, Peter M., Keller, Matthew C.
Publicado 2018

Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities

por Mallard, Travis T., Karlsson Linnér, Richard, Grotzinger, Andrew D., Sanchez-Roige, Sandra, Seidlitz, Jakob, Okbay, Aysu, de Vlaming, Ronald, Meddens, S. Fleur W., Palmer, Abraham A., Davis, Lea K., Tucker-Drob, Elliot M., Kendler, Kenneth S., Keller, Matthew C., Koellinger, Philipp D., Harden, K. Paige
Publicado 2022

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

por Yang, Jian, Bakshi, Andrew, Zhu, Zhihong, Hemani, Gibran, Vinkhuyzen, Anna A.E., Lee, Sang Hong, Robinson, Matthew R., Perry, John R.B., Nolte, Ilja M., van Vliet-Ostaptchouk, Jana V., Snieder, Harold, Esko, Tonu, Milani, Lili, Mägi, Reedik, Metspalu, Andres, Hamsten, Anders, Magnusson, Patrik K.E., Pedersen, Nancy L., Ingelsson, Erik, Soranzo, Nicole, Keller, Matthew C., Wray, Naomi R., Goddard, Michael E., Visscher, Peter M.
Publicado 2015