Precision Health Database

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Query Trace: all[original query]>>Translation/Implementation Studies[Product Type]

Publication
Controlling the pandemic during the SARS-CoV-2 vaccination rollout J Viana et al, Nat Comms, June 16, 2021
Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent P Lacaze et al, NPJ Genomic Medicine, June 16, 2021
Pan-cancer analysis of SETD2 mutation and its association with the efficacy of immunotherapy M Lu, NPJ Precision Oncology, June 14, 2021
Implantation of a biochemical and genetic screening programme for family hypercholesterolaemia. Collaboration between the clinical laboratory and lipid units: Design of the ARIAN Project. Arrobas Velilla Teresa et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2021 Similar articles in PubMed
Developing a clinical-pathologic model to predict genomic risk of recurrence in patients with hormone receptor positive, human epidermal growth factor receptor-2 negative, node negative breast cancer. Batra Atul et al. Cancer treatment and research communications 2021 28100401 Similar articles in PubMed
Genotyping NUDT15*3 rs1166855232 reveals higher frequency of potential adverse effects of thiopurines in Natives and Mestizos from Mexico. Texis Tomas et al. Pharmacological reports : PR 2021 Similar articles in PubMed
Determinants of Adherence to Diabetes Screening in Iranian Adults With a Positive Family History of Diabetes. Malih Narges et al. Journal of preventive medicine and public health = Yebang Uihakhoe chi 2021 54(3) 190-198 Similar articles in PubMed
Non-Ischemic Sudden Cardiac Arrest: Role of 12 Lead Holter, Family Screening and Genetic Testing. Blich Miry et al. Pacing and clinical electrophysiology : PACE 2021 Similar articles in PubMed
Clinical Utility of Whole Exome Sequencing and Targeted Panels for the Identification of Inborn Errors of Immunity in a Resource-Constrained Setting. Engelbrecht Clair et al. Frontiers in immunology 2021 12665621 Similar articles in PubMed
Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis. Liu Sha et al. Frontiers in genetics 2021 12666648 Similar articles in PubMed
The Cost-Effectiveness of Congenital Adrenal Hyperplasia Newborn Screening in Brazil: A Comparison Between Screened and Unscreened Cohorts. de Miranda Mirela Costa et al. Frontiers in pediatrics 2021 9659492 Similar articles in PubMed
Mutational Landscape of PI3K-AKT-mTOR Pathway in Breast Cancer: Implications for Targeted Therapeutics. Xiao Weikai et al. Journal of Cancer 2021 12(14) 4408-4417 Similar articles in PubMed
Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma. Kim Jung et al. JCO precision oncology 2021 5 Similar articles in PubMed
Electronic Family History Screening Tool for Detection of Inherited Cancer Risk: A Prospective Pilot Study. Le Amy et al. American journal of medical quality : the official journal of the American College of Medical Quality 2021 Similar articles in PubMed
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study. et al. The Lancet. Oncology 2021 Similar articles in PubMed
Genomic Sequencing and Insight into Clinical Heterogeneity and Prognostic Pathway Genes in Patients with Metastatic Colorectal Cancer. Kawaguchi Yoshikuni et al. Journal of the American College of Surgeons 2021 Similar articles in PubMed
Combination chemotherapy versus temozolomide for patients with methylated MGMT (m-MGMT) glioblastoma: results of computational biological modeling to predict the magnitude of treatment benefit. Castro Michael et al. Journal of neuro-oncology 2021 Similar articles in PubMed
Genome sequencing in congenital cataracts improves diagnostic yield. Ma Alan et al. Human mutation 2021 Similar articles in PubMed
Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance. Galbraith Lauren N et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Similar articles in PubMed
Randomized study of remote telehealth genetic services versus usual care in oncology practices without genetic counselors. Cacioppo Cara N et al. Cancer medicine 2021 Similar articles in PubMed
A framework for automated gene selection in genomic applications. Lazo de la Vega L et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Similar articles in PubMed
Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer. Woodward Emma R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Similar articles in PubMed
GenomeDiver: a platform for phenotype-guided medical genomic diagnosis. Pearson Nathaniel M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Similar articles in PubMed
Community research collaboration to develop a promotores-based hereditary breast cancer education program for Spanish-speaking Latinas. Almeida Rebeca et al. Health education research 2021 Similar articles in PubMed
Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples. McConkie-Rosell Allyn et al. Journal of genetic counseling 2021 Similar articles in PubMed
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes. Liu Ge et al. JAMA network open 2021 4(6) e2112820 Similar articles in PubMed
Diverse clinical features and diagnostic delay in monogenic inborn errors of immunity: a call for access to genetic testing. Branch Anna et al. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2021 Similar articles in PubMed
Clinicopathological Features of BRCA1/2 Mutation-Positive Breast Cancer. Paik Hyun-June et al. Oncology 2021 1-8 Similar articles in PubMed
Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. Hale Andrew T et al. Neurosurgery 2021 Similar articles in PubMed
Longitudinal cohorts for harnessing the electronic health record for disease prediction in a US population. Manemann Sheila M et al. BMJ open 2021 11(6) e044353 Similar articles in PubMed