Novel Y-chromosome Short Tandem Repeat Variants Detected Through the Use of Massively Parallel Sequencing

Por Warshauer, David H., Churchill, Jennifer D., Novroski, Nicole, King, Jonathan L., Budowle, Bruce
Publicado no Genomics Proteomics Bioinformatics (2015)

More comprehensive forensic genetic marker analyses for accurate human remains identification using massively parallel DNA sequencing

Por Ambers, Angie D., Churchill, Jennifer D., King, Jonathan L., Stoljarova, Monika, Gill-King, Harrell, Assidi, Mourad, Abu-Elmagd, Muhammad, Buhmeida, Abdelbaset, Budowle, Bruce
Publicado no BMC Genomics (2016)

Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing

Por Churchill, Jennifer D., Chang, Joseph, Ge, Jianye, Rajagopalan, Narasimhan, Wootton, Sharon C., Chang, Chien-Wei, Lagacé, Robert, Liao, Wenchi, King, Jonathan L., Budowle, Bruce
Publicado no Croat Med J (2015)

Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa

Por Churchill, Jennifer D., Bowne, Sara J., Sullivan, Lori S., Lewis, Richard Alan, Wheaton, Dianna K., Birch, David G., Branham, Kari E., Heckenlively, John R., Daiger, Stephen P.
Publicado em 2013

Erratum to: More Comprehensive Forensic Genetic Marker Analyses for Accurate Human Remains Identification Using Massively Parallel DNA Sequencing

Por Ambers, Angie D., Churchill, Jennifer D., King, Jonathan L., Stoljarova, Monika, Gill-King, Harrell, Assidi, Mourad, Abu-Elmagd, Muhammad, Buhmeida, Abdelbaset, Al-Qahtani, Mohammed, Budowle, Bruce
Publicado no BMC Genomics (2017)

Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders

Por Koboldt, Daniel C., Larson, David E., Sullivan, Lori S., Bowne, Sara J., Steinberg, Karyn M., Churchill, Jennifer D., Buhr, Aimee C., Nutter, Nathan, Pierce, Eric A., Blanton, Susan H., Weinstock, George M., Wilson, Richard K., Daiger, Stephen P.
Publicado em 2014