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Precision Health Database


Precision Health Database|Search|PHGKB

Heart, Lung, Blood and Sleep Disorders

Last data update: Dec 05, 2023. (Total: 62234 Documents since 2012)
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Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.
Katherine A Martinez et al. J Am Coll Cardiol 2023 82(8) 661-670
Health status and comorbidities of adult patients with phenylketonuria (PKU) in France with a focus on early-diagnosed patients - A nationwide study of health insurance claims data.
Sybil Charrière et al. Mol Genet Metab 2023 139(3) 107625
Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation.
Lieke van den Heuvel et al. J Genet Couns 2023
The role of aldehyde dehydrogenase 2 in cardiovascular disease.
Jian Zhang et al. Nature reviews. Cardiology 2023
Implementing Cardiogenomics in Clinical Practice
Northwestern University and the Jackson Labs, 2023
Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry.
Girolami Francesca et al. Frontiers in cardiovascular medicine 2023 91080608
Finding causal genes underlying risk for coronary artery disease
PL Auer, Nature Genetics, December 6, 2022
Genetic Basis of Childhood Cardiomyopathy.
Bagnall Richard D et al. Circulation. Genomic and precision medicine 2022 e003686
Burden of Rare Genetic Variants in Spontaneous Coronary Artery Dissection With High-risk Features
Y Wang et al, JAMA Cardiology, September 15, 2022
New Cardiovascular Risk Assessment Techniques for Primary Prevention: JACC Review Topic of the Week.
Verma Kunal P et al. Journal of the American College of Cardiology 2022 80(4) 373-387
Everyone deserves a diagnosis
The Family Heart Foundation, July 18, 2022
Lipoprotein (a)
CDC, June 29, 2022
Experiences of athletes with arrhythmogenic cardiac conditions in returning to play.
Shapero Kayle et al. Heart rhythm O2 2022 3(2) 133-140
Association of Lipoprotein (a) in Coronary Artery Disease in Young Individuals.
Patted Aishwarya et al. The Journal of the Association of Physicians of India 2022 70(4) 11-12
Association of Transthyretin Val122Ile Variant With Incident Heart Failure Among Black Individuals
V Parcha et al, JAMA, April 4, 2022
[Sudden cardiac death in young people and in adults: primary and contributing causes. The experience of the multidisciplinary network in Emilia-Romagna].
Leone Ornella et al. Giornale italiano di cardiologia (2006) 2022 23(3) 200-210
Cardiovascular Genetics: The Role of Genetics in Predicting Risk.
Chowns Jessica et al. The Medical clinics of North America 2022 106(2) 313-324
Clinical Features of Aberrations Chromosome 22q: A Pilot Study.
Atli Emine Ikbal et al. Global medical genetics 2022 9(1) 42-50
Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death.
Neves Raquel et al. Circulation. Genomic and precision medicine 2021 CIRCGEN121003497
Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders.
Baban Anwar et al. Heart failure clinics 2021 18(1) 139-153
Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study.
Yeates Laura et al. European journal of human genetics : EJHG 2021
Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study
L Yeates et al, EJHG, September 21, 2021
Monogenic Syndromes with Congenital Heart Diseases in Newborns (Diagnostic Clues for Neonatologists): A Critical Analysis with Systematic Literature Review.
Falsaperla Raffaele et al. Journal of pediatric genetics 2021 10(3) 173-193
Mapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis
P Hariharan et al, Scientific Reports, August 12, 2021
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.
Murdock David R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Return-to-Play for Athletes With Long QT Syndrome or Genetic Heart Diseases Predisposing to Sudden Death.
Tobert Kathryn E et al. Journal of the American College of Cardiology 2021
Clinical Features in a Large Cohort of Patients With 22q11.2 Deletion Syndrome.
Nissan Ella et al. The Journal of pediatrics 2021
Lipoprotein(a) and Cardiovascular Diseases.
Miksenas Hannah et al. JAMA 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
Clinical and genetic findings in patients with congenital cataract and heart diseases.
Li Xinru et al. Orphanet journal of rare diseases 2021 16(1) 242
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