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Genomics and Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB
Last data update: Apr 21, 2019. (Total: 20772 Documents since 2012)
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Records 1-100 (of 1484 Record(s))
Query Trace: All HLBS[orginal query]>>Reviews/Commentaries[Product Type]
Publication
Stroke genetics: discovery, biology, and clinical applications.
Dichgans Martin et al. The Lancet. Neurology 2019 Apr
Precision health: treating the individual patient with chronic obstructive pulmonary disease.
Obeidat Ma'en et al. The Medical journal of Australia 2019 Apr
Bayesian Networks for Risk Prediction Using Real-World Data: A Tool for Precision Medicine.
Arora Paul et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2019 Apr 22(4) 439-445
Review of Cystic Fibrosis.
Goetz Danielle et al. Pediatric annals 2019 Apr 48(4) e154-e161
FIND FH® Effectively Identified Individuals with Possible Familial Hypercholesterolemia (FH) in Electronic Health Records
Cision PR Newswire, April 11, 2019
Current Status of Familial Hypercholesterolemia in China: A Need for Patient FH Registry Systems.
Chen Peipei et al. Frontiers in physiology 2019 10280
Applications of Machine Learning in Real-Life Digital Health Interventions: Review of the Literature.
Triantafyllidis Andreas K et al. Journal of medical Internet research 2019 Apr 21(4) e12286
Newborn screening for cystic fibrosis: Is there benefit for everyone?
Course C W et al. Paediatric respiratory reviews 2019 Feb
'Precision medicine' and ischaemic heart disease: the stage is set for the new antibody based therapies (lipid lowering and anti-inflammatory).
Prati Francesco et al. European heart journal supplements : journal of the European Society of Cardiology 2019 Mar 21(Suppl B) B73-B75
Identification of biomarkers and genetic approaches toward chronic obstructive pulmonary disease.
Wadhwa Ridhima et al. Journal of cellular physiology 2019 Mar
Pharmacogenomic considerations for antiplatelet agents: the era of precision medicine in stroke prevention and neurointerventional practice.
Bonney Phillip A et al. Cold Spring Harbor molecular case studies 2019 Apr 5(2)
Brugada Syndrome: Progress in Genetics, Risk Stratification and Management.
Romero Jorge et al. Arrhythmia & electrophysiology review 2019 Mar 8(1) 19-27
Pharmacogenomics of chronic obstructive pulmonary disease.
Hersh Craig P et al. Expert review of respiratory medicine 2019 Mar
Precision medicine for cell therapy in acute respiratory distress syndrome.
Zhang Haibo et al. The Lancet. Respiratory medicine 2019 Apr 7(4) e13
Precision medicine for cell therapy in acute respiratory distress syndrome - Authors' reply.
Matthay Michael A et al. The Lancet. Respiratory medicine 2019 Apr 7(4) e14
A review of gene- and cell-based therapies for familial hypercholesterolemia.
Hajighasemi Saeideh et al. Pharmacological research 2019 Mar 143119-132
Genetics of Nonalcoholic Fatty Liver Disease: From Pathogenesis to Therapeutics.
Sookoian Silvia et al. Seminars in liver disease 2019 Mar
Extended Reality in Medical Practice.
Andrews Christopher et al. Current treatment options in cardiovascular medicine 2019 Mar 21(4) 18
Recent understanding of clinical sequencing and gene-based risk stratification in inherited primary arrhythmia syndrome.
Aiba Takeshi et al. Journal of cardiology 2019 May 73(5) 335-342
Diagnosis of Familial Hypercholesterolaemia on First Sight? The Role of the Ophthalmologist in Identifying Patients with Familial Hypercholesterolaemia.
Altschmiedová T et al. Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti 2019 74(4) 127-131
Former Smokers and Their Families Speak Out
CDC, April 2019
Breakthrough study could lead to new treatments for sickle cell disease
J Ives, News Medical, March 29, 2019
Systematic benchmarking of omics computational tools.
Mangul Serghei et al. Nature communications 2019 Mar 10(1) 1393
Systematic benchmarking of omics computational tools.
Mangul Serghei et al. Nature communications 2019 Mar 10(1) 1393
First gene therapy to treat rare blood disease nears European approval
A Feurstein, Stat News, March 29, 2019
How much further do we need to decrease LDL cholesterol levels in heterozygous familial hypercholesterolemia?
Harada-Shiba Mariko et al. Atherosclerosis 2019 Mar
Leveraging Implementation Science to Address Health Disparities in Genomic Medicine: Examples from the Field.
Roberts Megan C et al. Ethnicity & disease 2019 29(Suppl 1) 187-192
Treatment of hereditary and acquired forms of transthyretin amyloidosis in the era of personalized medicine: the role of randomized controlled trials.
Buxbaum Joel N et al. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2019 Mar 1-11
Women with bleeding disorders.
Hermans C et al. Haemophilia : the official journal of the World Federation of Hemophilia 2018 May 24 Suppl 629-36
Clinical relevance of genome-wide polygenic score may be less than claimed.
Curtis David, et al. Annals of human genetics 2019 3 0.
Precision Medicine for Heart Failure: Back to the Future.
Feldman Arthur M et al. Journal of the American College of Cardiology 2019 Mar 73(10) 1185-1188
Familial hypercholesterolemia in China half a century: A review of published literature.
Peng Jie et al. Atherosclerosis. Supplements 2019 Mar 3612-18
Can advanced analytics fix modern medicine's problem of uncertainty, imprecision, and inaccuracy?
Ahmad Tariq et al. European journal of heart failure 2019 21(1) 86-89
Big data analytics in adult congenital heart disease: why coding matters.
Asselbergs Folkert W et al. European heart journal 2019 Mar
Applications of CRISPR systems in respiratory health: Entering a new 'red pen' era in genome editing.
Moses Colette et al. Respirology (Carlton, Vic.) 2019 Mar
Apple Watch Helps Detect AF: Is This the Future?
S Hughes, Medscape, March 16, 2019
Giant study shows Apple Watch can spot heart rhythm changes — but it’s far from ‘medical-grade technology’
M Herper, Stat News, March 16, 2019
Apple Watch Atrial Fibrillation Study Has High Rate of False Positives
M Terry, Biospace, March 18, 2019
Apple Heart Study demonstrates ability of wearable technology to detect atrial fibrillation Stanford researchers presented preliminary findings from a virtual study that enrolled more than 400,000 participants.
Stanford University, March 16, 2019
Getting the Lower List Price for PCSK9 inhibitors
The FH Foundation, March 18, 2019
Women can have hemophilia, too
CDC, 2019
Multiomics Data Triangulation for Asthma Candidate Biomarkers and Precision Medicine.
Pecak Matija et al. Omics : a journal of integrative biology 2018 22(6) 392-409
Germline mutations in lung cancer and personalized medicine.
Cetta Francesco et al. Familial cancer 2018 17(3) 429-430
Big-Data Analysis, Cluster Analysis, and Machine-Learning Approaches.
Alonso-Betanzos Amparo et al. Advances in experimental medicine and biology 1065607-626
Five Feet Apart
CF Foundation, March 2019
Hypertrophic cardiomyopathy: an updated review on diagnosis, prognosis, and treatment.
Makavos George et al. Heart failure reviews 2019 Mar
Could a cure be close for sickle cell anemia?
CBS, 60 Minutes, March 8, 2019
Biology, Genetics and Heart Disease
The FH Foundation, March 14, 2019
Scientists find new approach that shows promise for treating cystic fibrosis
NIH, March 13, 2019
Gene and environmental interactions according to the components of lifestyle modifications in hypertension guidelines.
Kokubo Yoshihiro et al. Environmental health and preventive medicine 2019 Mar 24(1) 19
Your risk for heart disease in a single number,
by Marcus Banks, Science Line, March 5, 2019
New Advances for Newborn Screening of Inborn Errors of Metabolism by Capillary Electrophoresis-Mass Spectrometry (CE-MS).
Shanmuganathan Meera et al. Methods in molecular biology (Clifton, N.J.) 2019 1972139-163
Sickle cell diseases: What can nuclear medicine offer?
Niccoli Asabella Artor et al. Hellenic journal of nuclear medicine 2019 Mar
2018 Langley Award for Basic Research on Nicotine and Tobacco: Bringing Precision Medicine to Smoking Cessation.
Bierut Laura J et al. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2019 Mar
Real Stories from People Living with Hemophilia
CDC, 2019
Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.
Breil Thomas et al. Journal of pediatric endocrinology & metabolism : JPEM 2019 Feb
Blood Biomarkers for Stroke Diagnosis and Management.
Kamtchum-Tatuene Joseph et al. Neuromolecular medicine 2019 Mar
The role of statins in the treatment of familial hypercholesterolemia
S Gilding, The FH Foundation, March 5, 2019
Prepare Your Health: Personal Health Preparedness for People with Bleeding Disorders
CDC A-Z Index ?Ú Public Health Matters Blog, March 4, 2019
Systematic screening in hereditary hemorrhagic telangiectasia: a review.
Kroon Steven et al. Current opinion in pulmonary medicine 2018 24(3) 260-268
The pharmacoepigenomics informatics pipeline defines a pathway of novel and known warfarin pharmacogenomics variants.
Allyn-Feuer Ari et al. Pharmacogenomics 2018 19(5) 413-434
Genetic Risk Factors Are Not Associated with Wet Age-Related Macular Degeneration Treatment Response to Ranibizumab.
Chaudhary Varun et al. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 2018 239(4) 240
Practical Implications of Factor IX Gene Transfer for Individuals with Hemophilia B: A Clinical Perspective.
Miesbach Wolfgang et al. Human gene therapy. Clinical development 2018 29(2) 80-89
Pathways to precision medicine in smoking cessation treatments.
Chen Li-Shiun et al. Neuroscience letters 2018 66983-92
Current and future molecular approaches in the diagnosis of cystic fibrosis.
Bergougnoux Anne et al. Expert review of respiratory medicine 2018 12(5) 415-426
High Blood Pressure During Childhood and Adolescence
CDC, 2019
A Review of the Management of Sporadic Colorectal Adenomas in Young People: Is Surveillance Wasted on the Young?
Bushyhead Daniel et al. Digestive diseases and sciences 2019 Feb
Insomnia tied to depression, cardiovascular disease
M Prize, Science, February 25, 2019
Can Genetic Risk Scoring Predict Atrial Fibrillation Ablation Outcomes?
Lin Chin Yu et al. Korean circulation journal 2019 Feb
Leveraging Genetics to Improve Cardiovascular Health in Diabetes: The 2018 Edwin Bierman Award Lecture.
Doria Alessandro et al. Diabetes 2019 Mar 68(3) 479-489
Risk Stratification in Patients With Nonisquemic Dilated Cardiomyopathy. The Role of Genetic Testing.
Peña-Peña Maria Luisa et al. Revista espanola de cardiologia (English ed.) 2019 Feb
Hemochromatosis: Hereditary hemochromatosis and HFE gene.
Katsarou Martha-Spyridoula et al. Vitamins and hormones 2019 110201-222
Knowledge Deficit of Sickle Cell Trait Status: Can Nurses Help?
Arhin Afua O et al. Critical care nursing quarterly 42(2) 198-201
What Will Become of the Taxpayer Investment in Public Cord Blood Stem Cell Banking?
Harris David T et al. Current stem cell research & therapy 2019 Feb
Are you the one in 200 with haemochromatosis?
Gene in Infamous Experiment on Embryos Points to New Stroke Treatment
K Weintraub, Scientific American, February 20, 2019
Myocardial Infarction in Young Women.
Vaccarino Viola et al. Circulation 2019 Feb 139(8) 1057-1059
Holistic Health and Sickle Cell Disease: A Focus on Mental and Behavioral Health
Office of Minority Health, webinar, February 28, 2019
Genetic profiling for disease stratification in chronic obstructive pulmonary disease and asthma.
Rathnayake Senani N H et al. Current opinion in pulmonary medicine 2019 Feb
Clinical Utility of CYP2C19 Genotyping to Guide Antiplatelet Therapy in Patients With an Acute Coronary Syndrome or Undergoing Percutaneous Coronary Intervention.
Klein Melissa D et al. Arteriosclerosis, thrombosis, and vascular biology 2019 Feb ATVBAHA118311963
Leveraging Implementation Science to Address Health Disparities in Genomic Medicine: Examples from the Field.
Roberts Megan C, et al. Ethnicity & disease 2019 0 0. (Suppl 1) 187-192
How genes affect tobacco and alcohol use Data from 1.2 million people reveal how tobacco and alcohol use may be linked to your genes and to various
Eureka Alert, February 21, 2019
The Potential of 'Omics to Link Lipid Metabolism and Genetic and Comorbidity Risk Factors of Alzheimer's Disease in African Americans.
Stepler Kaitlyn E et al. Advances in experimental medicine and biology 2019 11181-28
Genetic Testing and Risk Scores: Impact on Familial Hypercholesterolemia.
Sarraju Ashish et al. Frontiers in cardiovascular medicine 2019 65
Personalization of therapies in rare diseases: a translational approach for the treatment of cystic fibrosis.
Villella Valeria R et al. Minerva pediatrica 2019 Feb
Cystic fibrosis - an example of personalized and precision medicine.
Skov Marianne et al. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2019 Feb
Familial Hypercholesterolemia: A Prototype for Precision Public Health
Global FH Summit, Atlanta, Georgia, October 20-21, 2019
Familial Hypercholesterolemia: A Prototype for Precision Public Health
FH Foundation, Global FH Summit, October 20-21, 2019, Atlanta, Georgia
Digitising the way to better sleep health.
Jaiswal Stuti J, et al. Lancet (London, England) 2019 0 0. (10172) 639
Utilizing Next-Generation Sequencing for the Diagnosis and Clinical Management of Vascular Ehlers-Danlos Syndrome.
Fujita Daishi et al. International heart journal 59(5) 911-913
Marfan Syndrome and Loeys-Dietz Syndrome in Children: A Multidisciplinary Team Experience.
Manchola-Linero Alejandra et al. Revista espanola de cardiologia (English ed.) 2018 Jul 71(7) 585-587
Towards precision medicine in ischemic stroke and transient ischemic attack.
Lin Yi et al. Frontiers in bioscience (Landmark edition) 2018 231338-1359
Fabry disease: Review and experience during newborn screening.
Hsu Ting-Rong et al. Trends in cardiovascular medicine 2018 28(4) 274-281
Genetic Aspects of Hereditary Arrhythmogenic Syndromes in Children and Adults.
Miranovic Vesna et al. Acta clinica Croatica 2017 Dec 56(4) 749-755
DNA Genome Sequencing in Esophageal Adenocarcinoma.
Pillai Suja et al. Methods in molecular biology (Clifton, N.J.) 2018 1756231-246
Towards precision medicine in severe asthma: Treatment algorithms based on treatable traits.
Papaioannou Andriana I et al. Respiratory medicine 2018 14215-22
Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis.
Sharif Bedra et al. Current opinion in nephrology and hypertension 2018 27(3) 194-200
Using Pharmacogenetic Testing or Platelet Reactivity Testing to Tailor Antiplatelet Therapy: Are Asians different from Caucasians?
Su-Yin Doreen Tan et al. European cardiology 2018 Dec 13(2) 112-114
Awareness of Fabry disease in cardiology: A gap to be filled.
Brito Dulce et al. Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2018 37(6) 457-466
The decision to discontinue screening for carnitine uptake disorder in New Zealand.
Wilson Callum et al. Journal of inherited metabolic disease 2019 Jan 42(1) 86-92
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