FastMap: Fast eQTL mapping in homozygous populations

por Gatti, Daniel M., Shabalin, Andrey A., Lam, Tieu-Chong, Wright, Fred A., Rusyn, Ivan, Nobel, Andrew B.
Publicado 2009

The Set2/Rpd3S Pathway Suppresses Cryptic Transcription without Regard to Gene Length or Transcription Frequency

por Lickwar, Colin R., Rao, Bhargavi, Shabalin, Andrey A., Nobel, Andrew B., Strahl, Brian D., Lieb, Jason D.
Publicado 2009

Harnessing changes in open chromatin determined by ATAC-seq to generate insulin-responsive reporter constructs

por Merrill, Collin B., Montgomery, Austin B., Pabon, Miguel A., Shabalin, Andrey A., Rodan, Aylin R., Rothenfluh, Adrian
Publicado 2022

Genome-wide association study meta-analysis of suicide death and suicidal behavior

por Li, Qingqin S., Shabalin, Andrey A., DiBlasi, Emily, Gopal, Srihari, Canuso, Carla M., Palotie, Aarno, Drevets, Wayne C., Docherty, Anna R., Coon, Hilary
Publicado 2022

seeQTL: a searchable database for human eQTLs

por Xia, Kai, Shabalin, Andrey A., Huang, Shunping, Madar, Vered, Zhou, Yi-Hui, Wang, Wei, Zou, Fei, Sun, Wei, Sullivan, Patrick F., Wright, Fred A.
Publicado 2012

Polygenic association of glomerular filtration rate decline in world trade center responders

por Koraishy, Farrukh M., Mann, Frank D., Waszczuk, Monika A., Kuan, Pei-Fen, Jonas, Katherine, Yang, Xiaohua, Docherty, Anna, Shabalin, Andrey, Clouston, Sean, Kotov, Roman, Luft, Benjamin
Publicado 2022

Test-statistic inflation in methylome-wide association studies

por Guintivano, Jerry, Shabalin, Andrey A, Chan, Robin F., Rubinow, David R., Sullivan, Patrick F., Meltzer-Brody, Samantha, Aberg, Karolina a, van den Oord, Edwin J. C. G.
Publicado 2020

Polygenic risk scores for asthma and allergic disease associate with COVID-19 severity in 9/11 responders

por Waszczuk, Monika A., Morozova, Olga, Lhuillier, Elizabeth, Docherty, Anna R., Shabalin, Andrey A., Yang, Xiaohua, Carr, Melissa A., Clouston, Sean A. P., Kotov, Roman, Luft, Benjamin J.
Publicado 2023

Enrichment methods provide a feasible approach to comprehensive and adequately powered investigations of the brain methylome

por Chan, Robin F., Shabalin, Andrey A., Xie, Lin Y., Adkins, Daniel E., Zhao, Min, Turecki, Gustavo, Clark, Shaunna L., Aberg, Karolina A., van den Oord, Edwin J.C.G.
Publicado 2017

Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach

por Monson, Eric T., Shabalin, Andrey A., Docherty, Anna R., DiBlasi, Emily, Bakian, Amanda V., Li, Qingqin S., Gray, Douglas, Keeshin, Brooks, Crowell, Sheila E., Mullins, Niamh, Willour, Virginia L., Coon, Hilary
Publicado 2021

Quantitative Trait Locus Mapping Methods for Diversity Outbred Mice

por Gatti, Daniel M., Svenson, Karen L., Shabalin, Andrey, Wu, Long-Yang, Valdar, William, Simecek, Petr, Goodwin, Neal, Cheng, Riyan, Pomp, Daniel, Palmer, Abraham, Chesler, Elissa J., Broman, Karl W., Churchill, Gary A.
Publicado 2014

Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder

por Aberg, Karolina A., Shabalin, Andrey A., Chan, Robin F., Zhao, Min, Kumar, Gaurav, van Grootheest, Gerard, Clark, Shaunna L., Xie, Lin Y., Milaneschi, Yuri, Penninx, Brenda W. J. H., van den Oord, Edwin J. C. G.
Publicado 2018

Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival

por Weigman, Victor J., Chao, Hann-Hsiang, Shabalin, Andrey A., He, Xiaping, Parker, Joel S., Nordgard, Silje H., Grushko, Tatyana, Huo, Dezheng, Nwachukwu, Chika, Nobel, Andrew, Kristensen, Vessela N., Børresen-Dale, Anne-Lise, Olopade, Olufunmilayo I., Perou, Charles M.
Publicado 2011

Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

por Ramasamy, Adaikalavan, Trabzuni, Daniah, Gibbs, J. Raphael, Dillman, Allissa, Hernandez, Dena G., Arepalli, Sampath, Walker, Robert, Smith, Colin, Ilori, Gigaloluwa Peter, Shabalin, Andrey A., Li, Yun, Singleton, Andrew B., Cookson, Mark R., Hardy, John, Ryten, Mina, Weale, Michael E.
Publicado 2013

A methylation study of long term depression risk

por Clark, Shaunna L, Hattab, Mohammad W, Chan, Robin F, Shabalin, Andrey A, Han, Laura KM, Zhao, Min, Smit, Johannes H, Jansen, Rick, Milaneschi, Yuri, Xie, Lin Ying, van Grootheest, Gerard, Penninx, Brenda WJH, Aberg, Karolina A, van den Oord, Edwin JCG
Publicado 2019

High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction

por McClay, Joseph L., Shabalin, Andrey A., Dozmorov, Mikhail G., Adkins, Daniel E., Kumar, Gaurav, Nerella, Srilaxmi, Clark, Shaunna L., Bergen, Sarah E., Hultman, Christina M., Magnusson, Patrik K. E., Sullivan, Patrick F., Aberg, Karolina A., van den Oord, Edwin J. C. G.
Publicado 2015

Methylome-wide association findings for major depressive disorder overlap in blood and brain and replicate in independent brain samples

por Aberg, Karolina A., Dean, Brian, Shabalin, Andrey A., Chan, Robin F., Han, Laura K.M., Zhao, Min, van Grootheest, Gerard, Xie, Lin Y., Milaneschi, Yuri, Clark, Shaunna L., Turecki, Gustavo, Penninx, Brenda W.J.H., van den Oord, Edwin J.C.G.
Publicado 2018

Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide

por Coon, Hilary, Shabalin, Andrey, Bakian, Amanda V., DiBlasi, Emily, Monson, Eric T., Kirby, Anne, Chen, Danli, Fraser, Alison, Yu, Zhe, Staley, Michael, Callor, William Brandon, Christensen, Erik D., Crowell, Sheila E., Gray, Douglas, Crockett, David K., Li, Qingqin S., Keeshin, Brooks, Docherty, Anna R.
Publicado 2022

Correcting for cell-type effects in DNA methylation studies: reference-based method outperforms latent variable approaches in empirical studies

por Hattab, Mohammad W., Shabalin, Andrey A., Clark, Shaunna L., Zhao, Min, Kumar, Gaurav, Chan, Robin F., Xie, Lin Ying, Jansen, Rick, Han, Laura K. M., Magnusson, Patrik K. E., van Grootheest, Gerard, Hultman, Christina M., Penninx, Brenda W. J. H., Aberg, Karolina A., van den Oord, Edwin J. C. G.
Publicado 2017

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

por Coon, Hilary, Darlington, Todd M., DiBlasi, Emily, Callor, W. Brandon, Ferris, Elliott, Fraser, Alison, Yu, Zhe, William, Nancy, Das, Sujan C., Crowell, Sheila E., Chen, Danli, Anderson, John S., Klein, Michael, Jerominski, Leslie, Cannon, Dale, Shabalin, Andrey, Docherty, Anna, Williams, Megan, Smith, Ken R., Keeshin, Brooks, Bakian, Amanda V., Christensen, Erik, Li, Qingqin S., Camp, Nicola J., Gray, Douglas
Publicado 2018