Hereditary cancer risk assessment: challenges for the next-gen sequencing era

Hereditary cancer risk assessment: challenges for the next-gen sequencing era

Bibliographic Details
Main Authors:	Hugo ePinheiro, Patrícia eOliveira, Carla eOliveira
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2015-03-01
Series:	Frontiers in Oncology
Subjects:	Genetic Testing Hereditary cancer next-gen sequencing Clinical Criteria Multi-gene panel Whole exome/genome
Online Access:	http://journal.frontiersin.org/Journal/10.3389/fonc.2015.00062/full

Similar Items

Extracellular Vesicles – powerful markers of cancer EVolution
by: Joana eCarvalho, et al.
Published: (2015-01-01)

Corrigendum: Importance of adhesins in virulence of Paracoccidioides spp.
by: Haroldo eOliveira
Published: (2015-05-01)

Evaluation of Next-Generation Sequencing as a clinical and research modality in the diagnosis of hereditary breast cancer
by: Dougherty, Kristen Elizabeth
Published: (2016)

Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
by: Yan Lu, et al.
Published: (2018-05-01)

Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
by: Yan Lu, et al.
Published: (2018-08-01)

The immune response to sand fly salivary proteins and its influence on Leishmania immunity
by: Regis eGomes, et al.
Published: (2012-05-01)

Insights into the neural mechanisms underlying hand praxis: implications for the neurocognitive rehabilitation of apraxia
by: Jorge eOliveira, et al.
Published: (2014-12-01)

Recombinant production of plant lectins in microbial systems for biomedical application – the frutalin case study
by: Carla eOliveira, et al.
Published: (2014-08-01)

Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes
by: Paul Dunn, et al.
Published: (2018-02-01)

Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing
by: Antiñolo, G., et al.
Published: (2023)

Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies
by: Michael Seleman, et al.
Published: (2017-07-01)

Clinical application of multigene panels: challenges of next generation counseling and cancer risk management
by: Thomas Paul Slavin, et al.
Published: (2015-09-01)

NAPG mutation in family members with hereditary hemorrhagic telangiectasia in China
by: Yu Xu, et al.
Published: (2021-06-01)

Novel heterozygous BPIFC variant in a Chinese pedigree with hereditary trichilemmal cysts
by: Xian‐Guo Fu, et al.
Published: (2019-06-01)

Cross-comparison of exome analysis, next-generation sequencing of amplicons, and the iPLEX® ADME PGx Panel for pharmacogenomic profiling
by: Eng Wee eChua, et al.
Published: (2016-01-01)

Obesity and endocrine dysfunction programmed by maternal smoking in pregnancy and lactation
by: Patricia Cristina Lisboa, et al.
Published: (2012-11-01)

Whole‐Exome Sequencing of Germline Variants in Non‐BRCA Families with Hereditary Breast Cancer
by: Bajalica‐lagercrantz, S., et al.
Published: (2022)

Differences in exercise intensity seems to influence the affective responses in self-selected and imposed exercise: a meta-analysis
by: Bruno eOliveira, et al.
Published: (2015-08-01)

Development and validation of next generation sequencing based 35-gene hereditary cancer panel
by: Wing Chan, et al.
Published: (2020-04-01)

Effects of Different Carbohydrate Sources on Fructan Metabolism in Plants of Chrysolaena obovata Grown in vitro
by: Flavio eTrevisan, et al.
Published: (2015-09-01)

Hereditary cancer risk assessment: insights and perspectives for the Next-Generation Sequencing era
by: Israel Gomy, et al.
Published: (2016-01-01)

Detection of Genomic Structural Variants from Next-Generation Sequencing Data
by: Lorenzo eTattini, et al.
Published: (2015-06-01)

Applicability of next generation genetic testing in epilepsy through whole exome sequencing
by: Daniela Catereniuc, et al.
Published: (2020-10-01)

La próxima Next-Gen
by: María del Mar Marcos Molano, et al.
Published: (2009-01-01)

Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature
by: Dong Wang, et al.
Published: (2021-07-01)

Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases
by: Morgane Plutino, et al.
Published: (2018-04-01)

Applications of Next Generation Sequencing to the Analysis of Familial Breast/Ovarian Cancer
by: Veronica Zelli, et al.
Published: (2020-01-01)

Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing
by: Debora Mancini-DiNardo, et al.
Published: (2019-10-01)

Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report
by: Senmao Chai, et al.
Published: (2020-11-01)

Next generation sequencing identifies mutations in Colombian patients with primary immunodeficiency diseases
by: Carlos Andrés Arango-Franco, et al.
Published: (2018-06-01)

Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole‐Exome Sequencing
by: Chao Liang, et al.
Published: (2020-06-01)

Sand-fly saliva-Leishmania-man: the trigger trio
by: Camila I. De Oliveira, et al.
Published: (2013-11-01)

NGS in Hereditary Ataxia: When Rare Becomes Frequent
by: Daniele Galatolo, et al.
Published: (2021-08-01)

Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
by: Valentina S. Vysotskaia, et al.
Published: (2017-02-01)

Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients
by: Jihye Park, et al.
Published: (2019-10-01)

A germline mutation in Rab43 gene identified from a cancer family predisposes to a hereditary liver-colon cancer syndrome
by: Yanting Jiang, et al.
Published: (2019-06-01)

Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification
by: Rick Kamps, et al.
Published: (2017-01-01)

Clinical impact and cost-effectiveness of whole exome sequencing as a diagnostic tool: a pediatric center’s experience
by: C. Alexander Valencia, et al.
Published: (2015-08-01)

Targeted Next Generation Sequencing (NGS) to Diagnose Hereditary Hemolytic Anemias
by: Rishab Bharadwaj, et al.
Published: (2020-07-01)

Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes
by: Hongwei Shen, et al.
Published: (2019-05-01)

Cannot write session to /tmp/vufind_sessions/sess_sm7798mv5pl9nlhr7m181vs5so