Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Por Hindorff, Lucia A., Sethupathy, Praveen, Junkins, Heather A., Ramos, Erin M., Mehta, Jayashri P., Collins, Francis S., Manolio, Teri A.
Publicado em 2009

Phenotype–Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

Por Ramos, Erin M, Hoffman, Douglas, Junkins, Heather A, Maglott, Donna, Phan, Lon, Sherry, Stephen T, Feolo, Mike, Hindorff, Lucia A
Publicado em 2014

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

Por Welter, Danielle, MacArthur, Jacqueline, Morales, Joannella, Burdett, Tony, Hall, Peggy, Junkins, Heather, Klemm, Alan, Flicek, Paul, Manolio, Teri, Hindorff, Lucia, Parkinson, Helen
Publicado em 2014

The PhenX Toolkit pregnancy and birth collections

Por Whitehead, Nedra S., Hammond, Jane A., Williams, Michelle A., Huggins, Wayne, Hoover, Sonja, Hamilton, Carol M., Ramos, Erin M., Junkins, Heather A., Harlan, William R., Hogue, Carol J.
Publicado no Ann Epidemiol (2012)

Using PhenX Measures to Identify Opportunities for Cross-Study Analysis

Por Pan, Huaqin, Tryka, Kimberly A., Vreeman, Daniel J., Huggins, Wayne, Phillips, Michael J., Mehta, Jayashri P., Phillips, Jacqueline H., McDonald, Clement J., Junkins, Heather A., Ramos, Erin M., Hamilton, Carol M.
Publicado em 2012

PhenX RISING: real world implementation and sharing of PhenX measures

Por McCarty, Catherine A, Huggins, Wayne, Aiello, Allison E, Bilder, Robert M, Hariri, Ahmad, Jernigan, Terry L, Newman, Erik, Sanghera, Dharambir K, Strauman, Timothy J, Zeng, Yi, Ramos, Erin M, Junkins, Heather A
Publicado em 2014

The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

Por MacArthur, Jacqueline, Bowler, Emily, Cerezo, Maria, Gil, Laurent, Hall, Peggy, Hastings, Emma, Junkins, Heather, McMahon, Aoife, Milano, Annalisa, Morales, Joannella, Pendlington, Zoe May, Welter, Danielle, Burdett, Tony, Hindorff, Lucia, Flicek, Paul, Cunningham, Fiona, Parkinson, Helen
Publicado no Nucleic Acids Res (2017)

A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog

Por Morales, Joannella, Welter, Danielle, Bowler, Emily H., Cerezo, Maria, Harris, Laura W., McMahon, Aoife C., Hall, Peggy, Junkins, Heather A., Milano, Annalisa, Hastings, Emma, Malangone, Cinzia, Buniello, Annalisa, Burdett, Tony, Flicek, Paul, Parkinson, Helen, Cunningham, Fiona, Hindorff, Lucia A., MacArthur, Jacqueline A. L.
Publicado no Genome Biol (2018)

Data Compatibility in the Addiction Sciences: An Examination of Measure Commonality()

Por Conway, Kevin P., Vullo, Genevieve C., Kennedy, Ashley P., Finger, Matthew S., Agrawal, Arpana, Bjork, James M., Farrer, Lindsay A., Hancock, Dana B., Hussong, Andrea, Wakim, Paul, Huggins, Wayne, Hendershot, Tabitha, Nettles, Destiney S., Pratt, Joseph, Maiese, Deborah, Junkins, Heather A., Ramos, Erin M., Strader, Lisa C., Hamilton, Carol M., Sher, Kenneth J.
Publicado em 2014

The PhenX Toolkit: Get the Most From Your Measures

Por Hamilton, Carol M., Strader, Lisa C., Pratt, Joseph G., Maiese, Deborah, Hendershot, Tabitha, Kwok, Richard K., Hammond, Jane A., Huggins, Wayne, Jackman, Dean, Pan, Huaqin, Nettles, Destiney S., Beaty, Terri H., Farrer, Lindsay A., Kraft, Peter, Marazita, Mary L., Ordovas, Jose M., Pato, Carlos N., Spitz, Margaret R., Wagener, Diane, Williams, Michelle, Junkins, Heather A., Harlan, William R., Ramos, Erin M., Haines, Jonathan
Publicado em 2011

The IGNITE network: a model for genomic medicine implementation and research

Por Weitzel, Kristin Wiisanen, Alexander, Madeline, Bernhardt, Barbara A., Calman, Neil, Carey, David J., Cavallari, Larisa H., Field, Julie R., Hauser, Diane, Junkins, Heather A., Levin, Phillip A., Levy, Kenneth, Madden, Ebony B., Manolio, Teri A., Odgis, Jacqueline, Orlando, Lori A., Pyeritz, Reed, Wu, R. Ryanne, Shuldiner, Alan R., Bottinger, Erwin P., Denny, Joshua C., Dexter, Paul R., Flockhart, David A., Horowitz, Carol R., Johnson, Julie A., Kimmel, Stephen E., Levy, Mia A., Pollin, Toni I., Ginsburg, Geoffrey S.
Publicado no BMC Med Genomics (2016)