Fallen : roman /

Por Auer, Paul
Publicado em 2020

Mauern : roman /

Por Auer, Paul
Publicado em 2022

Rare variant association studies: considerations, challenges and opportunities

Por Auer, Paul L, Lettre, Guillaume
Publicado no Genome Med (2015)

Statistical Design and Analysis of RNA Sequencing Data

Por Auer, Paul L., Doerge, R. W.
Publicado em 2010

From exomes to genomes: challenges and solutions in population-based genetic association studies

Por Auer, Paul L, Leal, Suzanne M
Publicado no Eur J Hum Genet (2017)

Genetic association studies in cardiovascular diseases: do we have enough power?

Por Auer, Paul L., Stitziel, Nathan O.
Publicado no Trends Cardiovasc Med (2017)

Functional Annotation of Putative Regulatory Elements at Cancer Susceptibility Loci

Por Rosse, Stephanie A, Auer, Paul L, Carlson, Christopher S
Publicado em 2014

Classification, Predictive Modelling, and Statistical Analysis of Cancer Data (A)

Por Jiang, Hongmei, An, Lingling, Baladandayuthapani, Veerabhadran, Auer, Paul Livermore
Publicado em 2014

Testing for Rare Variant Associations in the Presence of Missing Data

Por Auer, Paul L., Wang, Gao, Leal, Suzanne M.
Publicado no Genet Epidemiol (2013)

The effect of phenotypic outliers and non-normality on rare-variant association testing

Por Auer, Paul L, Reiner, Alex P, Leal, Suzanne M
Publicado no Eur J Hum Genet (2016)

Capturing microRNA targets using an RNA-induced silencing complex (RISC)-trap approach

Por Cambronne, Xiaolu A., Shen, Rongkun, Auer, Paul L., Goodman, Richard H.
Publicado em 2012

Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations

Por Hu, Yi-Juan, Li, Yun, Auer, Paul L., Lin, Dan-Yu
Publicado no Proc Natl Acad Sci U S A (2015)

Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women

Por Reiner, Alex P., Beleza, Sandra, Franceschini, Nora, Auer, Paul L., Robinson, Jennifer G., Kooperberg, Charles, Peters, Ulrike, Tang, Hua
Publicado em 2012

Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project

Por Auer, Paul L., Reiner, Alex P., Wang, Gao, Kang, Hyun Min, Abecasis, Goncalo R., Altshuler, David, Bamshad, Michael J., Nickerson, Deborah A., Tracy, Russell P., Rich, Stephen S., Leal, Suzanne M.
Publicado no Am J Hum Genet (2016)

Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

Por Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.
Publicado em 2014

Rare coding variants pinpoint genes that control human hematological traits

Por Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E., Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M., Auer, Paul L., Johnson, Andrew D., Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P.
Publicado no PLoS Genet (2017)

Rare Variation Facilitates Inferences of Fine-Scale Population Structure in Humans

Por O’Connor, Timothy D., Fu, Wenqing, Mychaleckyj, Josyf C., Logsdon, Benjamin, Auer, Paul, Carlson, Christopher S., Leal, Suzanne M., Smith, Joshua D., Rieder, Mark J., Bamshad, Michael J., Nickerson, Deborah A., Akey, Joshua M.
Publicado no Mol Biol Evol (2015)

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

Por Johnsen, Jill M., Auer, Paul L., Morrison, Alanna C., Jiao, Shuo, Wei, Peng, Haessler, Jeffrey, Fox, Keolu, McGee, Sean R., Smith, Joshua D., Carlson, Christopher S., Smith, Nicholas, Boerwinkle, Eric, Kooperberg, Charles, Nickerson, Deborah A., Rich, Stephen S., Green, David, Peters, Ulrike, Cushman, Mary, Reiner, Alex P.
Publicado em 2013

Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project

Por Kim, Daniel Seung, Crosslin, David R., Auer, Paul L., Suzuki, Stephanie M., Marsillach, Judit, Burt, Amber A., Gordon, Adam S., Meschia, James F., Nalls, Mike A., Worrall, Bradford B., Longstreth, W. T., Gottesman, Rebecca F., Furlong, Clement E., Peters, Ulrike, Rich, Stephen S., Nickerson, Deborah A., Jarvik, Gail P.
Publicado em 2014

Meta-Analysis of Gene Level Tests for Rare Variant Association

Por Liu, Dajiang J., Peloso, Gina M., Zhan, Xiaowei, Holmen, Oddgeir L., Zawistowski, Matthew, Feng, Shuang, Nikpay, Majid, Auer, Paul L., Goel, Anuj, Zhang, He, Peters, Ulrike, Farrall, Martin, Orho-Melander, Marju, Kooperberg, Charles, McPherson, Ruth, Watkins, Hugh, Willer, Cristen J., Hveem, Kristian, Melander, Olle, Kathiresan, Sekar, Abecasis, Gonçalo R.
Publicado em 2013