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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Apr 23, 2024
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Records 1 - 29 (of 29 Records)
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Retinoblastoma[original query]>>Original Studies[Product Type]
Automatic retinoblastoma screening and surveillance using deep learning.
Ruiheng Zhang et al. Br J Cancer 2023
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Circulating tumor DNA reveals complex biological features with clinical relevance in metastatic breast cancer.
Aleix Prat et al. Nature communications 2023 14(1) 1157
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A Multi-Thresholding-Based Discriminative Neural Classifier for Detection of Retinoblastoma Using CNN Models.
Parmod Kumar et al. BioMed research international 2023 20235803661
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Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a Neoplasm.
Jette J Bakhuizen et al. JAMA network open 2023 6(2) e2254157
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Landscape of RB1 alterations in 22,432 Chinese solid tumor patients.
Xu Guanghui et al. Annals of translational medicine 2022 10(16) 885
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Immune Checkpoint Blockade Outcome in Small-Cell Lung Cancer and Its Relationship With Retinoblastoma Mutation Status and Function.
Dowlati Afshin et al. JCO precision oncology 2022 6e2200257
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Cancer predisposing syndrome: a retrospective cohort analysis in a pediatric and multidisciplinary genetic cancer counseling unit.
Escudero Adela et al. International journal of clinical oncology 2022
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Next-generation Sequencing of Cerebrospinal Fluid for Clinical Molecular Diagnostics in Pediatric, Adolescent and Young Adult (AYA) Brain Tumor Patients.
Miller Alexandra M et al. Neuro-oncology 2022
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Monitoring Retinoblastoma by Machine Learning of Aqueous Humor Metabolic Fingerprinting.
Liu Wanshan et al. Small methods 2022 6(1) e2101220
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Long-read nanopore DNA sequencing can resolve complex intragenic duplication/deletion variants, providing information to enable preimplantation genetic diagnosis.
Watson Christopher M et al. Prenatal diagnosis 2022
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Parental age and retinoblastoma-a retrospective study of demographic data and genetic analysis.
Tanwar Meghana et al. Eye (London, England) 2021
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Retinoblastoma genetics screening and clinical management.
Gupta Himika et al. BMC medical genomics 2021 14(1) 188
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Clinical features and survival of Chinese children with trilateral retinoblastoma during 2006-2019: A retrospective multicenter study.
Fang Xiaolian et al. American journal of ophthalmology 2020 Oct
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Travel burden and clinical presentation of retinoblastoma: analysis of 1024 patients from 43 African countries and 518 patients from 40 European countries.
Fabian Ido Didi et al. The British journal of ophthalmology 2020 Sep
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Parent Knowledge of Screening and Genetic Testing in Retinoblastoma.
Xiao Wei et al. Journal of ophthalmology 2020 20203839792
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Genetic testing for inherited ocular conditions in a developing country.
Zanolli Mario et al. Ophthalmic genetics 2020 Mar 1-5
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A gene expression signature of Retinoblastoma loss-of-function predicts resistance to neoadjuvant chemotherapy in ER-positive/HER2-positive breast cancer patients.
Risi Emanuela et al. Breast cancer research and treatment 2018 Jul 170(2) 329-341
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Detection and reporting of RB1 promoter hypermethylation in diagnostic screening.
Price Elizabeth A et al. Ophthalmic genetics 2018 May 1-6
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Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease.
Yahalom Claudia et al. Ophthalmic genetics 2018 May 1-7
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Knowledge, experiences and attitudes concerning genetics among retinoblastoma survivors and parents.
Hill Jessica A et al. European journal of human genetics : EJHG 2018 Jan
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"Where Does it Come from?" Experiences Among Survivors and Parents of Children with Retinoblastoma in Kenya.
Gedleh Amal et al. Journal of genetic counseling 2017 Nov
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A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.
Li Wenhui L et al. The Journal of molecular diagnostics : JMD 2016 Jul 18(4) 480-93
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Patient understanding of genetic information influences reproductive decision making in retinoblastoma.
Foster A et al. Clinical genetics 2017 Apr
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Familial Retinoblastoma: Raised Awareness Improves Early Diagnosis and Outcome.
Al-Nawaiseh Ibrahim et al. Journal of ophthalmology 2017 20175053961
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Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
Dommering Charlotte J et al. Familial cancer 2016 Nov
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Prenatal versus Postnatal Screening for Familial Retinoblastoma.
Soliman Sameh E et al. Ophthalmology 2016 Oct
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Knowledge of genetics in familial retinoblastoma.
Soliman Sameh E et al. Ophthalmic genetics 2016 Jul 1-7
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Cancer Genetics Education in a Low- to Middle-Income Country: Evaluation of an Interactive Workshop for Clinicians in Kenya.
Hill Jessica A et al. PLoS ONE 10(6) e0129852
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Genetic screening in patients with Retinoblastoma in Israel.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 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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