Published on 12/21/2020
Human Genomics across the Lifespan
Birth Defects and Child Health
Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate.
Velázquez-Aragón José A et al. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2020 Dec 1055665620980238
Cetuximab plus irinotecan administered biweekly with reduced infusion time to heavily pretreated patients with metastatic colorectal cancer and related RAS and BRAF mutation status.
Jensen Benny V et al. International journal of cancer 2020 Dec
Impact of Commercialized Genomic Tests on Adjuvant Treatment Decisions in Early Stage Breast Cancer Patients.
Assi Hazem I et al. Journal of oncology 2020 20209238084
Defining Clinical Utility of Tumor Biomarker Tests: A Clinician's Viewpoint.
Hayes Daniel F et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2020 Dec JCO2001572
Clinical Application of the FoundationOne CDx Assay to Therapeutic Decision-Making for Patients with Advanced Solid Tumors.
Takeda Masayuki et al. The oncologist 2020 Dec
Development and Validation of a Machine Learning Model to Explore Tyrosine Kinase Inhibitor Response in Patients With Stage IV EGFR Variant-Positive Non-Small Cell Lung Cancer.
Song Jiangdian et al. JAMA network open 2020 Dec 3(12) e2030442
Development and validation of a prognostic nomogram for patients with triple-negative breast cancer with histology of infiltrating duct carcinoma.
Jing Na et al. Annals of translational medicine 2020 Nov 8(21) 1447
Genomic profiling reveals high frequency of DNA repair genetic aberrations in gallbladder cancer.
Abdel-Wahab Reham et al. Scientific reports 2020 Dec 10(1) 22087
Population-based Screening for Hereditary Colorectal Cancer Variants in Japan.
Fujita Masashi et al. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2020 Dec
CanRisk Tool - A web interface for the prediction of breast and ovarian cancer risk and the likelihood of carrying genetic pathogenic variants.
Carver Tim et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 Dec
A Breast Radiology Department-operated, Proactive Same-day Program Identifies Pathogenic Breast Cancer Mutations in Unaffected Women.
Loving Vilert A et al. Academic radiology 2020 Dec
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high frequency of cancer prone syndromes.
Byrjalsen Anna et al. PLoS genetics 2020 Dec 16(12) e1009231
Germline TP53 Testing in Breast Cancers: Why, When and How?
Evans D Gareth et al. Cancers 2020 Dec 12(12)
Should the risk for uterine cancer influence decision making for prophylactic hysterectomy in BRCA1/2 mutated patients- a systematic review and meta-analysis.
Nahshon Chen et al. Gynecologic oncology 2020 Dec
Inequalities and risk factors related to non-participation in colorectal cancer screening programmes: a systematic review.
Unanue-Arza Saloa et al. European journal of public health 2020 Dec
Polygenic Risk Scoring is an Effective Approach to Predict Those Individuals Most Likely to Decline Cognitively Due to Alzheimer's Disease.
Daunt P et al. The journal of prevention of Alzheimer's disease 2021 8(1) 78-83
Communicating 5-Year Risk of Alzheimer's Disease Dementia: Development and Evaluation of Materials that Incorporate Multiple Genetic and Biomarker Research Results.
Mozersky Jessica et al. Journal of Alzheimer's disease : JAD 2020 Dec
Integrative Analysis of Genomics and Transcriptome Data to Identify Regulation Networks in Female Osteoporosis.
Zhang Xianzuo et al. Frontiers in genetics 2020 11600097
Recommendations to researchers for aiding in increasing American Indian representation in genetic research and personalized medicine.
Carroll Dana M et al. Personalized medicine 2020 Dec
Texas health educators' practice in basic genomics education and services.
Chen Lei-Shih et al. Personalized medicine 2020 Dec
Study design and implementation of the PRecision Medicine In MEntal health Care (PRIME Care) Trial.
Oslin David W et al. Contemporary clinical trials 2020 Dec 106247
Use of Genomic Information in Health Impact Assessment is Yet to Come: A Systematic Review.
Ádám Balázs et al. International journal of environmental research and public health 2020 Dec 17(24)
Heart, Lung, Blood and Sleep Diseases
Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter data.
Myers Kelly D et al. The Lancet. Digital health 2019 Dec 1(8) e393-e402
Characterizing Pharmacogenetic Testing Among Children's Hospitals.
Brown Jacob T et al. Clinical and translational science 2020 Dec
Considerations When Applying Pharmacogenomics to Your Practice.
Nicholson Wayne T et al. Mayo Clinic proceedings 2020 Dec
Prescribing Prevalence of Medications With Potential Genotype-Guided Dosing in Pediatric Patients.
Ramsey Laura B et al. JAMA network open 2020 Dec 3(12) e2029411
Pharmacist Consult Reports to Support Pharmacogenomics Report Interpretation.
Bright David et al. Pharmacogenomics and personalized medicine 2020 13719-724
Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A three-year implementation results in a public tertiary academic referral hospital.
Tanner Laura M et al. Prenatal diagnosis 2020 Dec
The Influence of Chromosomal Polymorphism on Embryo Development and Embryonic Molecular Karyotype in Preimplantation Genetic Testing for Chromosomal Translocation.
Li Gang et al. Frontiers in physiology 2020 11543188