Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests

Por Zawistowski, Matthew, Reppell, Mark, Wegmann, Daniel, St Jean, Pamela L, Ehm, Margaret G, Nelson, Matthew R, Novembre, John, Zöllner, Sebastian
Publicado em 2014

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

Por Schaibley, Valerie M., Zawistowski, Matthew, Wegmann, Daniel, Ehm, Margaret G., Nelson, Matthew R., St. Jean, Pamela L., Abecasis, Gonçalo R., Novembre, John, Zöllner, Sebastian, Li, Jun Z.
Publicado em 2013

Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial

Por St Jean, Pamela L., Xue, Zhengyu, Carter, Nick, Koh, Gavin C. K. W., Duparc, Stephan, Taylor, Maxine, Beaumont, Claire, Llanos-Cuentas, Alejandro, Rueangweerayut, Ronnatrai, Krudsood, Srivicha, Green, Justin A., Rubio, Justin P.
Publicado no Malar J (2016)

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe

Por Rubio, Justin P., Topp, Simon, Warren, Liling, St Jean, Pamela L., Wegmann, Daniel, Kessner, Darren, Novembre, John, Shen, Judong, Fraser, Dana, Aponte, Jennifer, Nangle, Keith, Cardon, Lon R., Ehm, Margaret G., Chissoe, Stephanie L., Whittaker, John C., Nelson, Matthew R., Mooser, Vincent E.
Publicado em 2012

An 18-kDa Translocator Protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28

Por Owen, David R, Yeo, Astrid J, Gunn, Roger N, Song, Kijoung, Wadsworth, Graham, Lewis, Andrew, Rhodes, Chris, Pulford, David J, Bennacef, Idriss, Parker, Christine A, StJean, Pamela L, Cardon, Lon R, Mooser, Vincent E, Matthews, Paul M, Rabiner, Eugenii A, Rubio, Justin P
Publicado em 2012

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Por Need, Anna C., Ge, Dongliang, Weale, Michael E., Maia, Jessica, Feng, Sheng, Heinzen, Erin L., Shianna, Kevin V., Yoon, Woohyun, Kasperavičiūtė, Dalia, Gennarelli, Massimo, Strittmatter, Warren J., Bonvicini, Cristian, Rossi, Giuseppe, Jayathilake, Karu, Cola, Philip A., McEvoy, Joseph P., Keefe, Richard S. E., Fisher, Elizabeth M. C., St. Jean, Pamela L., Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Ruppert, Andreas, Fraser, Gillian, Crombie, Caroline, Middleton, Lefkos T., St. Clair, David, Roses, Allen D., Muglia, Pierandrea, Francks, Clyde, Rujescu, Dan, Meltzer, Herbert Y., Goldstein, David B.
Publicado em 2009

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Por Need, Anna C., Ge, Dongliang, Weale, Michael E., Maia, Jessica, Feng, Sheng, Heinzen, Erin L., Shianna, Kevin V., Yoon, Woohyun, Kasperavičiūtė, Dalia, Gennarelli, Massimo, Strittmatter, Warren J., Bonvicini, Cristian, Rossi, Giuseppe, Jayathilake, Karu, Cola, Philip A., McEvoy, Joseph P., Keefe, Richard S. E., Fisher, Elizabeth M. C., St. Jean, Pamela L., Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Ruppert, Andreas, Fraser, Gillian, Crombie, Caroline, Middleton, Lefkos T., St. Clair, David, Roses, Allen D., Muglia, Pierandrea, Francks, Clyde, Rujescu, Dan, Meltzer, Herbert Y., Goldstein, David B.
Publicado em 2009