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Genomics and Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB
Last data update: Dec 28, 2020. (Total: 37862 Documents since 2012)
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Records 1-30 (of 2062 Record(s))
Query Trace: all[original query]>>Reviews/Commentaries[Product Type]
Publication
Germline TP53 Testing in Breast Cancers: Why, When and How?
Evans D Gareth et al. Cancers 2020 Dec 12(12)
Germline Variation and Somatic Alterations in Ewing Sarcoma.
Machiela Mitchell J et al. Methods in molecular biology (Clifton, N.J.) 2021 22263-14
Transcription strikes back: clinical utility of lung adenocarcinoma subtypes.
Skoulidis Ferdinandos et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Dec
Using artificial intelligence for pulmonary TB prevention, diagnosis, and treatment.
Jain Manoj et al. The Indian journal of tuberculosis 2020 67(4S) S119-S121
Current Application of Digital Diagnosing Systems for Retinopathy of Prematurity.
Bao Yuekun et al. Computer methods and programs in biomedicine 2020 Nov 105871
Current Clinical Applications of in vivo Gene Therapy with AAVs.
Mendell Jerry R et al. Molecular therapy : the journal of the American Society of Gene Therapy 2020 Dec
A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients.
Soltani Saber et al. Tropical medicine and health 2020 Dec 48(1) 96
Organoids for personalized treatment of Cystic Fibrosis: Professional perspectives on the ethics and governance of organoid biobanking.
Lensink Michael A et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2020 Dec
[Significance of Targeted Sequencing Assay for Patients with Suspected Myeloid Malignancies].
Zhang Li-Juan et al. Zhongguo shi yan xue ye xue za zhi 2020 Dec 28(6) 1985-1990
Severity-adjusted evaluation of newborn screening on the metabolic disease course in individuals with cytosolic urea cycle disorders.
Posset Roland et al. Molecular genetics and metabolism 2020 Nov
Gene therapy for sickle cell disease.
Olowoyeye Abiola et al. The Cochrane database of systematic reviews 2020 Nov 11CD007652
The Genetic Basis of Primary Myelofibrosis and Its Clinical Relevance.
Rumi Elisa et al. International journal of molecular sciences 2020 Nov 21(23)
Pituitary stalk interruption syndrome is characterized by genetic heterogeneity.
Brauner Raja et al. PloS one 2020 15(12) e0242358
Informed consent for genetic testing in hematology.
Marron Jonathan M et al. Hematology. American Society of Hematology. Education Program 2020 2020(1) 213-218
Newborn Screening for Congenital Adrenal Hyperplasia: Review of Factors Affecting Screening Accuracy.
Held Patrice K et al. International journal of neonatal screening 2020 Aug 6(3)
Challenges in Assessing the Cost-Effectiveness of Newborn Screening: The Example of Congenital Adrenal Hyperplasia.
Grosse Scott D et al. International journal of neonatal screening 2020 Oct 6(4)
Reimbursing the value of gene therapy care in an era of uncertainty.
Noone Declan et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Nov
Addressing patient education priorities in the era of gene therapy for haemophilia: Towards evidence-informed shared decision-making.
Woollard Laurence et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Nov
Landscape of Congenital Adrenal Hyperplasia Newborn Screening in the United States.
Edelman Sari et al. International journal of neonatal screening 2020 Aug 6(3)
The Changing Face of Cystic Fibrosis and Its Implications for Screening.
Naehrlich Lutz et al. International journal of neonatal screening 2020 Jul 6(3)
The International Radiomics Platform - An Initiative of the German and Austrian Radiological Societies.
Overhoff Daniel et al. RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin 2020 Nov
A review of inherited cancer susceptibility syndromes.
Brown Gina R et al. JAAPA : official journal of the American Academy of Physician Assistants 2020 Dec 33(12) 10-16
Emerging Alternatives to Conventional Clinic Visits in the Era of COVID-19: Adoption of Telehealth at VCU Adult Cystic Fibrosis Center.
Womack Caitlin et al. International journal of general medicine 2020 131175-1186
Why Do We Screen Newborn Infants for Cystic Fibrosis?
Barben Jürg et al. International journal of neonatal screening 2020 Jul 6(3)
Newborn Screening for Cystic Fibrosis: Over the Hump, Still Need to Fine-Tune It.
Castellani Carlo et al. International journal of neonatal screening 2020 Jul 6(3)
Neonatal Screening on Tandem Mass Spectrometry as a Powerful Tool for the Reassessment of the Prevalence of Underestimated Diseases in Newborns and Their Family Members: A Focus on Short Chain Acyl-CoA Dehydrogenase Deficiency.
Messina MariaAnna et al. International journal of neonatal screening 2020 Jul 6(3)
Clinical and Pathologic Implications of Tumor Genomics of Predominant Histologic Subtypes in Lung Adenocarcinoma.
Xu Xuejun et al. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2020 Dec 15(12) e187-e188
Diving Deep into Deep Learning: An Update on Artificial Intelligence in Retina.
Goldhagen Brian E et al. Current ophthalmology reports 2020 Sep 8(3) 121-128
[Clinical pathway for cardiomyopathies: a genetic testing strategy proposed by ANMCO in Tuscany].
Girolami Francesca et al. Giornale italiano di cardiologia (2006) 2020 Dec 21(12) 926-934
Transparency, trust, and community welfare: towards a precision public health ethics framework for the genomics era.
Juengst Eric T et al. Genome medicine 2020 Nov 12(1) 98
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