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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Non-invasive prenatal test identifies circulating cell-free DNA chromosomal abnormalities derived from clonal hematopoiesis in aggressive hematological malignancies.
Valentina Giudice et al. Clin Exp Med 2024 24(1) 69
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Peripheral blood DNA methylation profiles predict future development of B-cell Non-Hodgkin Lymphoma
AE Perez et al, NPJ Precision Oncology, July 21, 2022
Can cancer blood tests live up to promise of saving lives?
CK Johnson, AP News, April 11, 2022
High grade B-cell lymphoma with MYC, BCL2 and/or BCL6 rearrangements: unraveling the genetic landscape of a rare aggressive subtype of non-Hodgkin lymphoma.
Ferrari Anna et al. Leukemia & lymphoma 2022 1-7
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Clinicopathological and molecular genomic features of monomorphic epitheliotropic intestinal T-cell lymphoma in the Chinese population: a study of 20 cases.
Chen Chunni et al. Diagnostic pathology 2021 16(1) 114
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Functional multigenic variations associated with hodgkin lymphoma.
Osman Yasser et al. International journal of laboratory hematology 2021
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An overview of genetic predisposition to familial hematological malignancies.
Hamadou Walid Sabri et al. Bulletin du cancer 2021
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New biomarkers in non-Hodgkin lymphoma and acute leukemias.
Rubio-Jurado Benjamín et al. Advances in clinical chemistry 2020 9619-53
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Circulating tumor DNA predicts response in Chinese patients with relapsed or refractory classical hodgkin lymphoma treated with sintilimab.
Shi Yuankai et al. EBioMedicine 2020 Apr 54102731
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Comprehensive Genomic Profiling of Hodgkin Lymphoma Reveals Recurrently Mutated Genes and Increased Mutation Burden.
Liang Winnie S et al. The oncologist 2019 24(2) 219-228
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The application of antigen receptor gene rearrangement of BIOMED-2 in the pathologic diagnosis of 348 cases with non-Hodgkin lymphoma in a single institution in Southwest of China.
Liu Xueni et al. Pathology, research and practice 2019 Nov 215(11) 152615
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Clinical application of thiopurine pharmacogenomics in pediatrics.
Pavlovic Sonja et al. Current drug metabolism 2020 Mar
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Diffuse Large B-Cell Lymphoma and High-Grade B-Cell Lymphoma: Genetic Classification and Its Implications for Prognosis and Treatment.
Crombie Jennifer L et al. Surgical oncology clinics of North America 2020 Jan 29(1) 115-125
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Study Tests Immunotherapy in People with Cancer and Autoimmune Diseases
NCI, August 26, 2019
CMS Finalizes Decision to Cover CAR T-Cell Therapy for Medicare Beneficiaries
ASCO Post, August 8, 2019
Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services
Association of Germline BRCA2 Mutations With the Risk of Pediatric or Adolescent Non-Hodgkin Lymphoma.
Wang Zhaoming et al. JAMA oncology 2019 Jul
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The Use of Optimal Treatment for DLBCL Is Improving in All Age Groups and Is a Key Factor in Overall Survival, but Non-Clinical Factors Influence Treatment.
Wong Doo Nicole et al. Cancers 2019 Jul 11(7)
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NCCN Releases Clinical Practice Guidelines for Pediatric ALL,
by Allison Inserro, AJMC, May 30, 2019
Family History of Breast Cancer Associated with Breast Cancer in Survivors of Hodgkin Lymphoma.
Colonna Sarah et al. International journal of cancer and clinical research 2019 6(1)
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Analysis of circulating tumor DNA by targeted ultra-deep sequencing across various non-Hodgkin lymphoma subtypes.
Shin Seung-Ho et al. Leukemia & lymphoma 2019 Feb 1-10
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Comprehensive Genomic Profiling Reveals Diverse but Actionable Molecular Portfolios across Hematologic Malignancies: Implications for Next Generation Clinical Trials.
Galanina Natalie et al. Cancers 2018 Dec 11(1)
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Circulating tumor DNA: clinical roles in diffuse large B cell lymphoma.
Wu Fang-Tian et al. Annals of hematology 2018 Oct
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Cancer Risk in Families Fulfilling the Amsterdam Criteria for Lynch Syndrome.
Samadder N Jewel et al. JAMA oncology 2017 Aug
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Family history of venous thromboembolism and risk of hospitalized thromboembolism in cancer patients: A nationwide family study.
Zöller Bengt et al. Thrombosis research 2015 Sep 136(3) 573-81
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Familial Risk in Patients With Carcinoma of Unknown Primary.
Samadder N Jewel et al. JAMA oncology 2015 Dec 1-7
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Race and institutional support may play a role in pharmacogenomic trial participation,
ASCO Post, Aug 3
Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.
Amant Frédéric, et al. JAMA oncology 2015 9 0. (6) 814-9
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High familial risk in nodular lymphocyte-predominant Hodgkin lymphoma.
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Perinatal and family risk factors for Hodgkin lymphoma in childhood through young adulthood.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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