Cargando…

Association between germline pathogenic variants in cancer‐predisposing genes and lymphoma risk

The application of advanced molecular technology has significantly expanded lymphoma classification, allowing risk stratification and treatment optimization. Limited evidence suggests the presence of a genetic predisposition in lymphoma, indicating the potential for better individualized clinical ma...

Descripción completa

Detalles Bibliográficos
Autores principales:	Usui, Yoshiaki, Iwasaki, Yusuke, Matsuo, Keitaro, Endo, Mikiko, Kamatani, Yoichiro, Hirata, Makoto, Sugano, Kokichi, Yoshida, Teruhiko, Matsuda, Koichi, Murakami, Yoshinori, Maeda, Yoshinobu, Nakagawa, Hidewaki, Momozawa, Yukihide
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633290/ https://www.ncbi.nlm.nih.gov/pubmed/36065483 http://dx.doi.org/10.1111/cas.15522

Ejemplares similares

Genetic characterization of pancreatic cancer patients and prediction of carrier status of germline pathogenic variants in cancer-predisposing genes
por: Mizukami, Keijiro, et al.
Publicado: (2020)

Germline Pathogenic Variants in 7636 Japanese Patients With Prostate Cancer and 12 366 Controls
por: Momozawa, Yukihide, et al.
Publicado: (2019)

Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants
por: Momozawa, Yukihide, et al.
Publicado: (2022)

Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls
por: Momozawa, Yukihide, et al.
Publicado: (2018)

Personalized medicine with germline pathogenic variants: Importance of population‐ and region‐wide evidence
por: Usui, Yoshiaki, et al.
Publicado: (2023)

Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population
por: Yamamoto, Kenichi, et al.
Publicado: (2020)

Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals
por: Akiyama, Masato, et al.
Publicado: (2023)

Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report
por: Nakagawa, Makoto, et al.
Publicado: (2021)

Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing
por: Kosugi, Shunichi, et al.
Publicado: (2019)

GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation
por: Terao, Chikashi, et al.
Publicado: (2019)

Trends in non‐Hodgkin lymphoma mortality rate in Japan and the United States: A population‐based study
por: Usui, Yoshiaki, et al.
Publicado: (2023)

Detection of trait-associated structural variations using short-read sequencing
por: Kosugi, Shunichi, et al.
Publicado: (2023)

Genome‐wide association study identifies gastric cancer susceptibility loci at 12q24.11‐12 and 20q11.21
por: Tanikawa, Chizu, et al.
Publicado: (2018)

Endogenization and excision of human herpesvirus 6 in human genomes
por: Liu, Xiaoxi, et al.
Publicado: (2020)

Germline PMS2 mutation screened by mismatch repair protein immunohistochemistry of colorectal cancer in Japan
por: Sugano, Kokichi, et al.
Publicado: (2016)

A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation
por: Iida, Aritoshi, et al.
Publicado: (2018)

Functional variants in ADH1B and ALDH2 are non-additively associated with all-cause mortality in Japanese population
por: Sakaue, Saori, et al.
Publicado: (2019)

Empirical evaluation of variant calling accuracy using ultra-deep whole-genome sequencing data
por: Kishikawa, Toshihiro, et al.
Publicado: (2019)

Diabetes and cancer risk: A Mendelian randomization study
por: Goto, Atsushi, et al.
Publicado: (2019)

Genome-wide association study (GWAS) of ovarian cancer in Japanese predicted regulatory variants in 22q13.1
por: Yodsurang, Varalee, et al.
Publicado: (2018)

Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population
por: Low, Siew-Kee, et al.
Publicado: (2019)

12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population
por: Takata, Ryo, et al.
Publicado: (2019)

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes
por: Mutai, Hideki, et al.
Publicado: (2022)

Ancestry-specific predisposing germline variants in cancer
por: Oak, Ninad, et al.
Publicado: (2020)

Germline Whole-Gene Deletion of FH Diagnosed from Tumor Profiling
por: Ueki, Arisa, et al.
Publicado: (2021)

An X chromosome-wide meta-analysis based on Japanese cohorts revealed that non-autosomal variations are associated with serum urate
por: Nakatochi, Masahiro, et al.
Publicado: (2021)

Clinical Utility of Germline Genetic Testing in Japanese Men Undergoing Prostate Biopsy
por: Akamatsu, Shusuke, et al.
Publicado: (2022)

Germline BAP1 mutations predispose to malignant mesothelioma
por: Testa, Joseph R., et al.
Publicado: (2011)

Germline mutations in BAP1 predispose to melanocytic tumors
por: Wiesner, Thomas, et al.
Publicado: (2011)

Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma
por: Begemann, Matthias, et al.
Publicado: (2020)

MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years
por: Momma, Tomoyuki, et al.
Publicado: (2019)

Association between germline pathogenic variants and breast cancer risk in Japanese women: The HERPACC study
por: Kasugai, Yumiko, et al.
Publicado: (2022)

Identification of a novel uterine leiomyoma GWAS locus in a Japanese population
por: Sakai, Kensuke, et al.
Publicado: (2020)

Genome-Wide Natural Selection Signatures Are Linked to Genetic Risk of Modern Phenotypes in the Japanese Population
por: Yasumizu, Yoshiaki, et al.
Publicado: (2020)

A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature
por: Iida, Aritoshi, et al.
Publicado: (2019)

Germline mutations predisposing to diffuse large B-cell lymphoma
por: Leeksma, O C, et al.
Publicado: (2017)

Germline mutations predisposing to diffuse large B-cell lymphoma
por: Leeksma, O C, et al.
Publicado: (2017)

Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects
por: Ito, Shuji, et al.
Publicado: (2023)

Characterizing rare and low-frequency height-associated variants in the Japanese population
por: Akiyama, Masato, et al.
Publicado: (2019)

Author Correction: Characterizing rare and low-frequency height-associated variants in the Japanese population
por: Akiyama, Masato, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_j1km1s11qirffeeoo530gmhr88