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Journal Articles

Association between Sleep Traits and Risk of Non-Hodgkin's Lymphoma Subtypes: A Mendelian Randomization Study in the International Lymphoma (InterLymph) Epidemiology Consortium

Blood (2024) 144 (Supplement 1): 6182.

https://doi.org/10.1182/blood-2024-199373

Published: 2024

Journal Articles

HBB rs334 , ABO R s8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

Hyokyoung G Hong, Mateus H Gouveia, Martin Ogwang, Patrick Kerchan, Steven Reynolds, Constance N Tenge, Pamela A Were, Robert T Kuremu, Walter N Wekesa, Nestory Masalu, Esther Kawira, Tobias Kinyera, Xunde Wang, Jiefu Zhou, Isaac Otim, Ismail D Legason, Hadijah Nabalende, Herry Dhudha, Mediatrix Mumia, Francine G Baker, Temi Okusolubo, Leona W Ayers, Kishor Bhatia, James J Goedert, Joshua G Woo, Nathan Cole, Wen Luo, Belynda Hicks, Adebowale A Adeyemo, Ludmila Prokunina-Olsson, Daniel N. Shriner, Charles N Rotimi, George Chagaluka, W Thomas Johnston, Nora Mutalima, Eric Borgstein, George N Liomba, Steve Kamiza, Nyengo Mkandawire, Collins Mitambo, Collins Mitambo, Elizabeth Molyneux, Robert Newton, Michelle Manning, Joseph F Fraumeni, Jr., Ruth M Pfeiffer, Amy Hutchinson, Meredith Yeager, Swee Lay Thein, Stephen J. Chanock, Sam M. Mbulaiteye

Blood (2022) 140 (Supplement 1): 9314–9316.

https://doi.org/10.1182/blood-2022-170410

Published: 2022

Journal Articles

Increased Frequency of Mosaic Chromosomal Alterations in Peripheral Blood Samples of Sub-Saharan African Children with Endemic Burkitt Lymphoma

Blood (2022) 140 (Supplement 1): 9240–9241.

https://doi.org/10.1182/blood-2022-169500

Published: 2022

Journal Articles

Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study

Blood (2022) 140 (Supplement 1): 9233–9235.

https://doi.org/10.1182/blood-2022-169911

Published: 2022

Journal Articles

Germline-Somatic Interactions in Myelofibrosis Susceptibility

Blood (2021) 138 (Supplement 1): 313.

https://doi.org/10.1182/blood-2021-150634

Published: 2021

Journal Articles

Pre-Transplant Clonal Mosaicism Is Associated with Increased Relapse and Lower Survival in Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Cell Transplant

Blood (2020) 136 (Supplement 1): 9–10.

https://doi.org/10.1182/blood-2020-140342

Published: 2020

Journal Articles

Chromosomal Aberrations in Pre-HCT Blood Samples and Outcomes after Transplantation in Patients with Myelofibrosis

Youjin Wang, PhD, Derek W Brown, PhD, Weiyin Zhou, MS, Tao Wang, PhD, Meredith Yeager, PhD, Andrew St. Martin, MS, Stephen R. Spellman, MS, Stephanie J. Lee, MDMPH, Stephen J. Chanock, MD, Wael Saber, MD MS, Mitchell Machiela, PhD, Shahinaz Gadalla, MD PhD

Blood (2020) 136 (Supplement 1): 4–5.

https://doi.org/10.1182/blood-2020-142418

Published: 2020

Journal Articles

Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia

Blood (2019) 134 (Supplement_1): 1224.

https://doi.org/10.1182/blood-2019-128235

Published: 2019

Journal Articles

De Novo and Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome: Similarities and Differences in SNP-Array Detected Chromosomal Aberrations in Pre-Transplant Blood Samples

Blood (2019) 134 (Supplement_1): 1430.

https://doi.org/10.1182/blood-2019-129110

Published: 2019

Journal Articles

Chromosome 6 Loss-of-Heterozygosity in Pre-Transplant Blood Samples of Patients with Severe Aplastic Anemia Is Associated with Lower Risk of Acute Graft- Versus -Host Disease

Shahinaz M Gadalla, MD PhD, Weiyin Zhou, MS, Tao Wang, PhD, Yoshitaka Zaimoku, MD, Shinji Nakao, MD PhD, Laurie Burdette, PhD, Amanda Willis, BS, Medhat Askar, MD PhD, Michael Haagenson, MS, Meredith Yeager, PhD, Youjin Wang, Stephen R. Spellman, Stephen J Chanock, MD, Stephanie J. Lee, MD PhD, Sharon A Savage, MD

Blood (2017) 130 (Supplement 1): 4479.

https://doi.org/10.1182/blood.V130.Suppl_1.4479.4479

Published: 2017

Journal Articles

Novel and Known Ribosomal Causes of Diamond-Blackfan Anemia Identified through Comprehensive Genomic Characterization

Payal Khincha, MD, Lisa Mirabello, PhD, Steven R Ellis, PhD, Neelam Giri, MD, Seth Brodie, Settara Chandrasekharappa, PhD, Frank Donovan, Weiyin Zhou, MS, Belynda Hicks, Joseph Boland, Meredith Yeager, PhD, Kristine Jones, Bin Zhu, PhD, Mingyi Wang, Blanche P. Alter, MD MPH, Sharon A Savage, MD

Blood (2016) 128 (22): 1495.

https://doi.org/10.1182/blood.V128.22.1495.1495

Published: 2016

Journal Articles

Germline Mutations in Patients Receiving Unrelated Donor Hematopoietic Cell Transplant for Severe Aplastic Anemia

Shahinaz M. Gadalla, MD PhD MSC, Bari J Ballew, PhD, Michael D Haagenson, MS, Stephen R. Spellman, MBS, Belynda Hicks, Blanche P Alter, MD MPH, Bin Zhu, PhD, Weiyin Zhou, MS, Meredith Yeager, PhD, Tao Wang, PhD, Katharina Fleischhauer, MD, Katharine C. Hsu, MD PhD, Michael R. Verneris, MD, Neal Freedman, PhD MPH, Stephanie J. Lee, MD, Sharon A Savage, MD FAAP

Blood (2016) 128 (22): 68.

https://doi.org/10.1182/blood.V128.22.68.68

Published: 2016

Journal Articles

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

Lynn R. Goldin, Mary L. McMaster, Melissa Rotunno, Sarah E. M. Herman, Kristine Jones, Bin Zhu, Joseph Boland, Laurie Burdett, Belynda Hicks, Sarangan Ravichandran, Brian T. Luke, Meredith Yeager, Laura Fontaine, Alisa M. Goldstein, Stephen J. Chanock, Margaret A. Tucker, Adrian Wiestner, Gerald Marti, Neil E. Caporaso

Blood (2016) 128 (18): 2261–2263.

https://doi.org/10.1182/blood-2016-02-697771

Published: 2016

Includes: Supplemental data

Journal Articles

Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

Lisa Mirabello, Elizabeth R. Macari, Lea Jessop, Steven R. Ellis, Timothy Myers, Neelam Giri, Alison M. Taylor, Katherine E. McGrath, Jessica M. Humphries, Bari J. Ballew, Meredith Yeager, Joseph F. Boland, Ji He, Belynda D. Hicks, Laurie Burdett, Blanche P. Alter, Leonard Zon, Sharon A. Savage

Blood (2014) 124 (1): 24–32.

https://doi.org/10.1182/blood-2013-11-540278

Published: 2014

Includes: Supplemental data

Journal Articles

Functional Consequences Of RPS29 Germline Mutations In Diamond-Blackfan Anemia

Lisa Mirabello, PhD, Elizabeth R Macari, PhD, Lea Jessop, PhD, Timothy Myers, PhD, Neelam Giri, MD, Alison M. Taylor, PhD, Katherine E. McGrath, Jessica M. Humphries, Bari J Ballew, PhD, Meredith Yeager, PhD, Joseph F Boland, Ji He, Belynda D Hicks, Laurie Burdett, PhD, Blanche P Alter, MD, MPH, Leonard I. Zon, MD, Sharon A Savage, MD

Blood (2013) 122 (21): 2465.

https://doi.org/10.1182/blood.V122.21.2465.2465

Published: 2013

Journal Articles

Germline Mutations in RTEL1 cause Dyskeratosis Congenita

Bari J. Ballew, PhD, Kevin B. Jacobs, M.S., Meredith Yeager, PhD, Neelam Giri, MD, Joseph F. Boland, Belynda D. Hicks, Laurie Burdett, PhD, Amy A. Hutchinson, Blanche P. Alter, MD, MPH, Sharon A. Savage, MD

Blood (2012) 120 (21): 515.

https://doi.org/10.1182/blood.V120.21.515.515

Published: 2012

Journal Articles

RPS29 is Mutated in a Multi-Case Diamond Blackfan Anemia Family

Lisa Mirabello, PhD, Bari J. Ballew, PhD, Neelam Giri, MD, Kevin B. Jacobs, M.S., Meredith Yeager, PhD, Joseph F. Boland, Belynda D. Hicks, Laurie Burdett, PhD, Amy A. Hutchinson, Blanche P. Alter, MD, MPH, Sharon A. Savage, MD

Blood (2012) 120 (21): 511.

https://doi.org/10.1182/blood.V120.21.511.511

Published: 2012

Journal Articles

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

Blood (2009) 114 (2): 264–267.

https://doi.org/10.1182/blood-2009-01-198697

Published: 2009

Includes: Supplemental data

Journal Articles

Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes

Deirdre A. Hill, Sophia S. Wang, James R. Cerhan, Scott Davis, Wendy Cozen, Richard K. Severson, Patricia Hartge, Sholom Wacholder, Meredith Yeager, Stephen J. Chanock, Nathaniel Rothman

Blood (2006) 108 (9): 3161–3167.

https://doi.org/10.1182/blood-2005-01-026690

Published: 2006

Includes: Supplemental data

Journal Articles

Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma

Qing Lan, Tongzhang Zheng, Nathaniel Rothman, Yawei Zhang, Sophia S. Wang, Min Shen, Sonja I. Berndt, Shelia H. Zahm, Theodore R. Holford, Brian Leaderer, Meredith Yeager, Robert Welch, Peter Boyle, Bing Zhang, Kaiyong Zou, Yong Zhu, Stephen Chanock

Blood (2006) 107 (10): 4101–4108.

https://doi.org/10.1182/blood-2005-10-4160

Published: 2006

Includes: Supplemental data

NARROW

Association between Sleep Traits and Risk of Non-Hodgkin's Lymphoma Subtypes: A Mendelian Randomization Study in the International Lymphoma (InterLymph) Epidemiology Consortium

HBB rs334 , ABO R s8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

Increased Frequency of Mosaic Chromosomal Alterations in Peripheral Blood Samples of Sub-Saharan African Children with Endemic Burkitt Lymphoma

Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study

Germline-Somatic Interactions in Myelofibrosis Susceptibility

Pre-Transplant Clonal Mosaicism Is Associated with Increased Relapse and Lower Survival in Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Cell Transplant

Chromosomal Aberrations in Pre-HCT Blood Samples and Outcomes after Transplantation in Patients with Myelofibrosis

Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia

De Novo and Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome: Similarities and Differences in SNP-Array Detected Chromosomal Aberrations in Pre-Transplant Blood Samples

Chromosome 6 Loss-of-Heterozygosity in Pre-Transplant Blood Samples of Patients with Severe Aplastic Anemia Is Associated with Lower Risk of Acute Graft- Versus -Host Disease

Novel and Known Ribosomal Causes of Diamond-Blackfan Anemia Identified through Comprehensive Genomic Characterization

Germline Mutations in Patients Receiving Unrelated Donor Hematopoietic Cell Transplant for Severe Aplastic Anemia

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

Functional Consequences Of RPS29 Germline Mutations In Diamond-Blackfan Anemia

Germline Mutations in RTEL1 cause Dyskeratosis Congenita

RPS29 is Mutated in a Multi-Case Diamond Blackfan Anemia Family

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes

Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma

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American Society of Hematology

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ASH Publications

American Society of Hematology

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