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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

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

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

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

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

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

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

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

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

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.

Blood (2009) 114 (22): 4048.

https://doi.org/10.1182/blood.V114.22.4048.4048

Published: 2009

NARROW

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

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

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

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

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

TCIRG1 Associated Congenital Neutropenia

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

Massively parallel sequencing: the new frontier of hematologic genomics

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

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

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American Society of Hematology

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ASH Publications

American Society of Hematology

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