Rare variant association studies: considerations, challenges and opportunities von Auer, Paul L, Lettre, Guillaume

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fate of duplicated genes in a polyploid plant genome von Roulin, Anne, Auer, Paul L, Libault, Marc, Schlueter, Jessica, Farmer, Andrew, May, Greg, Stacey, Gary, Doerge, Rebecca W, Jackson, Scott A

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Comparison of multiple imputation and other methods for the analysis of imputed genotypes von Auer, Paul L, Wang, Gao, Li, Guangyou, DeWan, Andrew T, Leal, Suzanne M

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Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women von Reiner, Alex P., Beleza, Sandra, Franceschini, Nora, Auer, Paul L., Robinson, Jennifer G., Kooperberg, Charles, Peters, Ulrike, Tang, Hua

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

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

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Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI von Sun, Quan, Rowland, Bryce T., Chen, Jiawen, Mikhaylova, Anna V., Avery, Christy, Peters, Ulrike, Lundin, Jessica, Matise, Tara, Buyske, Steve, Tao, Ran, Mathias, Rasika A., Reiner, Alexander P., Auer, Paul L., Cox, Nancy J., Kooperberg, Charles, Thornton, Timothy A., Raffield, Laura M., Li, Yun

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Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality von Hong, Yun Soo, Battle, Stephanie L., Shi, Wen, Puiu, Daniela, Pillalamarri, Vamsee, Xie, Jiaqi, Pankratz, Nathan, Lake, Nicole J., Lek, Monkol, Rotter, Jerome I., Rich, Stephen S., Kooperberg, Charles, Reiner, Alex P., Auer, Paul L., Heard-Costa, Nancy, Liu, Chunyu, Lai, Meng, Murabito, Joanne M., Levy, Daniel, Grove, Megan L., Alonso, Alvaro, Gibbs, Richard, Dugan-Perez, Shannon, Gondek, Lukasz P., Guallar, Eliseo, Arking, Dan E.

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Rare coding variants pinpoint genes that control human hematological traits von 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

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Finding causal genes underlying risk for coronary artery disease von Auer, Paul L.

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Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans von Schick, Ursula M., Jain, Deepti, Hodonsky, Chani J., Morrison, Jean V., Davis, James P., Brown, Lisa, Sofer, Tamar, Conomos, Matthew P., Schurmann, Claudia, McHugh, Caitlin P., Nelson, Sarah C., Vadlamudi, Swarooparani, Stilp, Adrienne, Plantinga, Anna, Baier, Leslie, Bien, Stephanie A., Gogarten, Stephanie M., Laurie, Cecelia A., Taylor, Kent D., Liu, Yongmei, Auer, Paul L., Franceschini, Nora, Szpiro, Adam, Rice, Ken, Kerr, Kathleen F., Rotter, Jerome I., Hanson, Robert L., Papanicolaou, George, Rich, Stephen S., Loos, Ruth J.F., Browning, Brian L., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C., Mohlke, Karen L., North, Kari E., Thornton, Timothy A., Reiner, Alex P.

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Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study von Simanek, Amanda M., Manansala, Regina, Woo, Jennifer M.P., Meier, Helen C. S., Needham, Belinda L., Auer, Paul L.

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Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project von AUER, Paul L, JOHNSEN, Jill M, RICH, Stephen S, O'DONNELL, Christopher J, JACKSON, Rebecca D, WALLACE, Robert B, ZHAO CHEN, GRAUBERT, Timothy A, WILSON, James G, HUA TANG, LETTRE, Guillaume, REINER, Alex P, JOHNSON, Andrew D, GANESH, Santhi K, YUN LI, LOGSDON, Benjamin A, LANGE, Leslie A, NALLS, Michael A, GUOSHENG ZHANG, FRANCESCHINI, Nora, FOX, Keolu, LANGE, Ethan M

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Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study von Hu, Yao, Bien, Stephanie A., Nishimura, Katherine K., Haessler, Jeffrey, Hodonsky, Chani J., Baldassari, Antoine R., Highland, Heather M., Wang, Zhe, Preuss, Michael, Sitlani, Colleen M., Wojcik, Genevieve L., Tao, Ran, Graff, Mariaelisa, Huckins, Laura M., Sun, Quan, Chen, Ming-Huei, Mousas, Abdou, Auer, Paul L., Lettre, Guillaume, Kooperberg, Charles

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Capturing microRNA targets using an RNA-induced silencing complex (RISC)-trap approach von Cambronne, Xiaolu A., Shen, Rongkun, Auer, Paul L., Goodman, Richard H.

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

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Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations von Hu, Yi-Juan, Li, Yun, Auer, Paul L., Lin, Dan-Yu

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Statistical design and analysis of RNA sequencing data von Auer, Paul L, Doerge, R W

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Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study von Hu, Yao, Bien, Stephanie A, Nishimura, Katherine K, Haessler, Jeffrey, Hodonsky, Chani J, Baldassari, Antoine R, Highland, Heather M, Wang, Zhe, Preuss, Michael, Sitlani, Colleen M, Wojcik, Genevieve L, Tao, Ran, Graff, Mariaelisa, Huckins, Laura M, Sun, Quan, Chen, Ming-Huei, Mousas, Abdou, Auer, Paul L, Lettre, Guillaume, Tang, Weihong, Qi, Lihong, Thyagarajan, Bharat, Buyske, Steve, Fornage, Myriam, Hindorff, Lucia A, Li, Yun, Lin, Danyu, Reiner, Alexander P, North, Kari E, Loos, Ruth J. F, Raffield, Laura M, Peters, Ulrike, Avery, Christy L, Kooperberg, Charles

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Regeneration Rosetta: An Interactive Web Application To Explore Regeneration-Associated Gene Expression and Chromatin Accessibility von Rau, Andrea, Dhara, Sumona P, Udvadia, Ava J, Auer, Paul L

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