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Precision Health Database


Precision Health Database|Search|PHGKB

Last data update: Sep 26, 2023. (Total: 61648 Documents since 2012)
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The Role of Hyposthenuria in Enuresis Among Paediatric Patients With Sickle Cell Disease.
Jasim N Al-Asadi et al. Sultan Qaboos Univ Med J 2023 23(2) 206-211
Interactions between the lipidome and genetic and environmental factors in autism.
Chloe X Yap et al. Nat Med 29(4) 936-949
Smartphone and Wearable Sensors for the Estimation of Facioscapulohumeral Muscular Dystrophy Disease Severity: Cross-sectional Study.
Ahnjili Zhuparris et al. JMIR formative research 2023 7e41178
A survey exploring caregiver burden and health-related quality of life in hereditary transthyretin amyloidosis.
Sarah Acaster et al. Orphanet journal of rare diseases 2023 18(1) 17
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions.
Chawner Samuel J R A et al. Translational psychiatry 2023 13(1) 7
Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutations.
De Michele Giovanna et al. Acta neurologica Belgica 2023
Personalized Medicine and Obstructive Sleep Apnea
SQ Quy et al, J Per Med, December 2022
Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.
Robinson Jamie R et al. Obesity (Silver Spring, Md.) 2022
Genetics of circadian rhythms and sleep in human health and disease.
Lane Jacqueline M et al. Nature reviews. Genetics 2022
Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients.
Llerena Juan et al. BMC pediatrics 2022 22(1) 492
Causal Association of Cardiovascular Risk Factors and Lifestyle Behaviors With Peripheral Artery Disease: A Mendelian Randomization Approach.
Hoek Anna G et al. Journal of the American Heart Association 2022 e025644
Genetic heterogeneity on sleep disorders in Parkinson's disease: a systematic review and meta-analysis.
Huang Jingxuan et al. Translational neurodegeneration 2022 11(1) 21
A distinctive profile of family genetic risk scores in a Swedish national sample of cases of fibromyalgia, irritable bowel syndrome, and chronic fatigue syndrome compared to rheumatoid arthritis and major depression.
Kendler Kenneth S et al. Psychological medicine 2022 1-8
Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
Birnbaum Rebecca et al. JAMA psychiatry 2022 79(3) 250-259
Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study-a multi-center retrospective cohort study of achondroplasia in the US.
Hoover-Fong Julie E et al. Orphanet journal of rare diseases 2021 16(1) 522
Clinical Trial Design for Disease-Modifying Therapies for Genetic Epilepsies.
Brock Dylan C et al. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 2021
Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
Brunelli Marcela Junqueira et al. The Cochrane database of systematic reviews 2021 9CD009806
Healthcare needs, expectations, utilization, and experienced treatment effects in patients with hereditary spastic paraplegia: a web-based survey in the Netherlands.
Kerstens Hans C J W et al. Orphanet journal of rare diseases 2021 16(1) 283
Childhood adversities are associated with shorter leukocyte telomere length at adult age in a population-based study.
Ämmälä Antti-Jussi et al. Psychoneuroendocrinology 2021 130105276
Obstructive Sleep Apnea and Dementia-Common Gene Associations through Network-Based Identification of Common Driver Genes.
Jeong Hyun-Hwan et al. Genes 2021 12(4)
Social media language of healthcare super-utilizers
SC Guntuku et al, NPJ Digital Medicine, March 25, 2021
Digital Health Applications for Pharmacogenetic Clinical Trials.
Naik Hetanshi et al. Genes 2020 Oct 11(11)
Study on sleep-wake disorders in patients with genetic and non-genetic amyotrophic lateral sclerosis.
Sun Xiaohan et al. Journal of neurology, neurosurgery, and psychiatry 2020 Oct
The impact of the HLA DQB1 gene and amino acids on the development of narcolepsy.
Kachooei-Mohaghegh-Yaghoobi Leila et al. The International journal of neuroscience 2020 Oct 1-11
Short or Long Sleep Duration and CKD: A Mendelian Randomization Study.
Park Sehoon et al. Journal of the American Society of Nephrology : JASN 2020 Oct
An atlas on risk factors for type 2 diabetes: a wide-angled Mendelian randomisation study.
Yuan Shuai et al. Diabetologia 2020 Sep
Increased frequency of sleep problems in children and adolescents with familial Mediterranean fever: The role of anxiety and depression.
Durcan Gizem et al. International journal of rheumatic diseases 2020 Aug
Characterization of genetic and phenotypic heterogeneity of obstructive sleep apnea using electronic health records.
Veatch Olivia J et al. BMC medical genomics 2020 Jul 13(1) 105
How Will Genetics Inform the Clinical Care of Atrial Fibrillation?
Shoemaker M Benjamin et al. Circulation research 2020 Jun 127(1) 111-127
Clinical Practice Guidelines for Achondroplasia.
Kubota Takuo et al. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2020 29(1) 25-42
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