1-10 of 10
Deborah A Nickerson
Close
Sort by
Journal Articles

A Multi-Omics Approach to X-Chromosome Inactivation (XCI) Identifies Severe Xci Skewing in Female Genetic Carriers of Hemophilia

Marsha M Wheeler, PhD, Kathryn Sheldon, Shelley N Fletcher, Angela Dove, Kerry W Lannert, Chris Frazar, Barbara A. Konkle, MD, Deborah A Nickerson, Jill M Johnsen, MD
Journal: Blood
Blood (2020) 136 (Supplement 1): 19–20.
https://doi.org/10.1182/blood-2020-143066
Published: 2020
Journal Articles

Novel Structural Variants Originating in F8 N on-Coding Regions in Previously Unresolved Cases of Severe Hemophilia A

Marsha M Wheeler, PhD, Barbara A Konkle, Crystal Watson, Glenn F. Pierce, Deborah A Nickerson, Jill M Johnsen, MD
Journal: Blood
Blood (2018) 132 (Supplement 1): 379.
https://doi.org/10.1182/blood-2018-99-112690
Published: 2018
Journal Articles

Next Generation DNA Sequencing of the RH Locus in 1135 Donors Implicates RHCE-RHD(2)-RHCE Hybrid Alleles As Causative of C+ Antigen

Marsha M Wheeler, PhD, Kerry W Lannert, Haley Huston, Shelley N Fletcher, Samantha Harris, Gayle Teramura, Chris Frazar, Jason G Underwood, PhD, Tristan Schaffer, Meghan Delaney, D.O., Deborah A Nickerson, PhD, Jill M Johnsen, MD
Journal: Blood
Blood (2017) 130 (Supplement 1): 1118.
https://doi.org/10.1182/blood.V130.Suppl_1.1118.1118
Published: 2017
Journal Articles

Association of Helicobacter Pylori Infection with Iron Deficiency in Asians and Pacific Islanders but not in Caucasians, African Americans, or Hispanics

Gordon D. McLaren, MD, Joseph A. Murray, MD, Stela McLachlan, PhD, Paul C. Adams, MD, John H. Eckfeldt, MD, Chris D. Vulpe, MD, Victor R. Gordeuk, MD, Tricia Brantner, Catherine Leiendecker-Foster, M.S., CLSp(MB), Wen-Pin Chen, MS, Anthony A. Killeen, MD, Ronald T. Acton, PhD, Lisa F. Barcellos, PhD, Deborah A. Nickerson, PhD, Kenneth B. Beckman, PhD, Christine E. McLaren, PhD
Journal: Blood
Blood (2015) 126 (23): 4556.
https://doi.org/10.1182/blood.V126.23.4556.4556
Published: 2015
Journal Articles

Exome Sequencing Identifies a GNPAT Variant Associated with Severe Iron Overload in HFE C282Y Homozygous Men with Extreme Phenotypes; Possible Role in Regulation of Hepcidin Expression

Gordon D. McLaren, MD, Mary J. Emond, PhD, V. Nathan Subramaniam, PhD, Pradyumna D. Phatak, MD, James C. Barton, MD, Paul C. Adams, MD, Justin B. Goh, PhD, Cameron J. McDonald, PhD, Lawrie W. Powell, MD PhD, Lyle C. Gurrin, PhD, Katrina J. Allen, MBBS, PhD, Deborah A. Nickerson, PhD, Tin Louie, MS, Grant A. Ramm, PhD, Gregory J. Anderson, PhD, Christine E. McLaren, PhD
Journal: Blood
Blood (2014) 124 (21): 745.
https://doi.org/10.1182/blood.V124.21.745.745
Published: 2014
Journal Articles

TCIRG1 Associated Congenital Neutropenia

Vahagn Makaryan, MD, Elisabeth Rosenthal, PhD, Audrey Anna Bolyard, RN, BS, Merideth L. Kelley, MS, BS, Jennifer Below, PhD, Michael Bamshad, MD, Kathryn M. Bofferding, BS, Joshua D. Smith, Kati Buckingham, BS, Laurence A. Boxer, MD, Julia Skokowa, Karl Welte, Deborah A. Nickerson, PhD, Gail P. Jarvik, MD, PhD, David C. Dale, MD, For the UW Center for Mendelian Genomics
Journal: Blood
Blood (2013) 122 (21): 440.
https://doi.org/10.1182/blood.V122.21.440.440
Published: 2013
Journal Articles

Exome Sequencing Identifies Genes and Variant Alleles Associated With Severity Of Iron Overload In Hemochromatosis HFE C282Y Homozygotes

Christine E. McLaren, PhD, Mary J. Emond, PhD, Pradyumna D. Phatak, MD, Paul C. Adams, MD, V. Nathan Subramaniam, PhD, James C. Barton, MD, Lawrie W. Powell, MD, PhD, Lyle C. Gurrin, PhD, Katrina J. Allen, MBBS, PhD, Deborah A. Nickerson, PhD, Tin Louie, MS, Grant A. Ramm, PhD, Gregory J. Anderson, PhD, Gordon D. McLaren, MD
Journal: Blood
Blood (2013) 122 (21): 179.
https://doi.org/10.1182/blood.V122.21.179.179
Published: 2013
Journal Articles

Massively parallel sequencing: the new frontier of hematologic genomics

Jill M. Johnsen, Deborah A. Nickerson, Alex P. Reiner
Journal: Blood
Blood (2013) 122 (19): 3268–3275.
https://doi.org/10.1182/blood-2013-07-460287
Published: 2013
Journal Articles

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

Jill M. Johnsen, Paul L. Auer, Alanna C. Morrison, Shuo Jiao, Peng Wei, Jeffrey Haessler, Keolu Fox, Sean R. McGee, Joshua D. Smith, Christopher S. Carlson, Nicholas Smith, Eric Boerwinkle, Charles Kooperberg, Deborah A. Nickerson, Stephen S. Rich, David Green, Ulrike Peters, Mary Cushman, Alex P. Reiner
Journal: Blood
Blood (2013) 122 (4): 590–597.
https://doi.org/10.1182/blood-2013-02-485094
Published: 2013
Includes: Supplemental data
Journal Articles

Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency.

Christine E. McLaren, Ph.D., Chad P. Garner, Ph.D., Clare C. Constantine, Ph.D., Stela Masle, Ph.D., Christopher D. Vulpe, M.D., Ph.D., Beverly M. Snively, Ph.D., James D. Cook, MD, Deborah A. Nickerson, Ph.D., Catherine Leiendecker-Foster, M.S., Kenneth B. Beckman, Ph.D., John H. Eckfeldt, M.D., Ph.D., Victor R. Gordeuk, M.D., Joseph A. Murray, M.D., Paul C. Adams, M.D., Lisa F. Barcellos, Ph.D., Anthony A. Killeen, MD, Katrina Goddard, Ph.D., David M. Reboussin, Ph.D., Gordon D. McLaren, M.D.
Journal: Blood
Blood (2009) 114 (22): 4048.
https://doi.org/10.1182/blood.V114.22.4048.4048
Published: 2009