Deborah A. Nickerson

According to our database, Deborah A. Nickerson authored at least 8 papers between 2004 and 2021.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2021

Benchmarking association analyses of continuous exposures with RNA-seq in observational studies.

Tamar Sofer, Nuzulul Kurniansyah, François Aguet, Kristin G. Ardlie, Peter Durda, Deborah A. Nickerson, Joshua D. Smith, Yongmei Liu, Sina Gharib, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Kent D. Taylor

Briefings Bioinform., 2021

2017

denovo-db: a compendium of human de novo variants.

Tychele Turner, Qian Yi, Niklas Krumm, John Huddleston, Kendra Hoekzema, Holly A. Stessman, Anna-Lisa Doebley, Raphael A. Bernier, Deborah A. Nickerson, Evan E. Eichler

Nucleic Acids Res., 2017

2016

PRIMUS: improving pedigree reconstruction using mitochondrial and Y haplotypes.

Jeffrey Staples, Lynette Ekunwe, Ethan M. Lange, James G. Wilson, Deborah A. Nickerson, Jennifer E. Below

Bioinform., 2016

2014

Inferring Clonal Composition from Multiple Sections of a Breast Cancer.

Habil Zare, Junfeng Wang, Alex Hu, Kris Weber, Joshua D. Smith, Deborah A. Nickerson, ChaoZhong Song, Daniela M. Witten, C. Anthony Blau, William Stafford Noble

PLoS Comput. Biol., 2014

The contribution of <i>de novo</i> coding mutations to autism spectrum disorder.

Ivan Iossifov, Brian J. O'Roak, Stephan J. Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A. Stessman, Kali T. Witherspoon, Laura Vives, Karynne E. Patterson, Joshua D. Smith, Bryan Paeper, Deborah A. Nickerson, Jeanselle Dea, Shan Dong, Luis E. Gonzalez, Jeffrey D. Mandell, Shrikant M. Mane, Michael T. Murtha, Catherine A. Sullivan, Michael F. Walker, Zainulabedin Waqar, Liping Wei, A. Jeremy Willsey, Boris Yamrom, Yoon-ha Lee, Ewa Grabowska, Ertugrul Dalkic, Zi-Hua Wang, Steven Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C. Schatz, Kenny Ye, W. Richard McCombie, Jay Shendure, Evan E. Eichler, Matthew W. State, Michael Wigler

Nat., 2014

2013

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.

Qing Duan, Eric Yi Liu, Paul L. Auer, Guosheng Zhang, Ethan M. Lange, Goo Jun, Chris Bizon, Shuo Jiao, Steven Buyske, Nora Franceschini, Chris S. Carlson, Li Hsu, Alex P. Reiner, Ulrike Peters, Jeffrey Haessler, Keith Curtis, Christina L. Wassel, Jennifer G. Robinson, Lisa W. Martin, Christopher A. Haiman, Loic Le Marchand, Tara Cox Matise, Lucia A. Hindorff, Dana C. Crawford, Themistocles L. Assimes, Hyun Min Kang, Gerardo Heiss, Rebecca D. Jackson, Charles Kooperberg, James G. Wilson, Gonçalo R. Abecasis, Kari E. North, Deborah A. Nickerson, Leslie A. Lange, Yun Li

Bioinform., 2013

2010

Targeted interrogation of copy number variation using SCIMMkit.

Troy Zerr, Gregory M. Cooper, Evan E. Eichler, Deborah A. Nickerson

Bioinform., 2010

2004

SNPing in the human genome.

Deborah A. Nickerson

Proceedings of the Eighth Annual International Conference on Computational Molecular Biology, 2004