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CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v8.8)
PHGKB
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Public Health Genomics Branch
Genomics and Precision Health Update
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Last data update: Nov 30, 2023
. (Total: 62283 Documents since 2012)
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all[original query]>>Reviews/Commentaries[Product Type]
Machine Learning in Cardiovascular Risk Prediction and Precision Preventive Approaches.
Nitesh Gautam et al. Curr Atheroscler Rep 2023
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Cystic Fibrosis.
Hartmut Grasemann et al. N Engl J Med 2023 389(18) 1693-1707
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Screening for haemoglobin disorders: One size may not fit all.
Lisa M Shook et al. Br J Haematol 2023
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Etranacogene dezaparvovec for the treatment of adult patients with severe and moderately severe hemophilia B.
Giancarlo Castaman et al. Expert Rev Hematol 2023
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The past 10 years of cystic fibrosis treatment: the road to cure.
Claudio Castaños et al. Lancet Respir Med 2023 11(10) 864-865
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Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review.
Linda Koshy et al. Indian J Med Res 2023 158(2) 119-135
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How and Why to Organize Family-Based Screening Clinics for Hypertrophic Cardiomyopathy.
Bryana J Rivers et al. Can J Cardiol 2023
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Outcomes and long-term effects of hematopoietic stem cell transplant in sickle cell disease.
Zaina Inam et al. Expert Rev Hematol 2023
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Machine learning applications in stroke medicine: advancements, challenges, and future prospectives.
Mario Daidone et al. Neural Regen Res 2023 19(4) 769-773
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Deep learning for ECG Arrhythmia detection and classification: an overview of progress for period 2017-2023.
Yaqoob Ansari et al. Front Physiol 2023 141246746
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Mobile Health and Preventive Medicine.
Jill Waalen et al. Med Clin North Am 2023 107(6) 1097-1108
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Current challenges and new approaches to implementing optimal management of sickle cell disease in sub-Saharan Africa.
Mwashungi Ally et al. Semin Hematol 2023
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Premature atherosclerosis: An analysis over 39 years in the Netherlands. Implications for young individuals in high-risk families.
Juliette Crooijmans et al. Atherosclerosis 2023 117267
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A proposed methodology of health education for inherited genetic disorders: Bag and Ball technique.
Sam Marconi David et al. Trop Doct 2023 494755231204633
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Standards for the care of people with cystic fibrosis (CF): A timely and accurate diagnosis.
Carlo Castellani et al. J Cyst Fibros 2023
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How do people inherit hemophilia?
Medical News Today, September 2023
Gene therapy for Hemoglobinopathies.
Maria Rosa Lidonnici et al. Hum Gene Ther 2023
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Experts say Found’s story highlights the extraordinary complexity of the problem for pregnant people living with SCD – and the critical importance of receiving proper, specialized care as early as possible. This is especially true now that medical advances in care and disease-modifying therapies have helped many people living with SCD survive well through their reproductive years. For parents-to-be, that means awareness is key. Individuals with SCD are at higher risk than the general population for preeclampsia, as Found discovered; but those with preeclampsia can go on to develop a condition called eclampsia, which can lead to seizures and even coma. People with SCD are also at higher risk for sepsis and blood clots. And there are risks for the fetus, such as lower-than-normal growth in the womb, preterm delivery, and stillbirth.
K Miller, Self, September 2023
Pregnant and Living with Sickle Cell Disease: A Push for Better Outcomes
NIH, September 2023
Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
Justine Cole et al. J Clin Med 2023 12(17)
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Diagnostic challenges in CFTR-related metabolic syndrome: Where the guidelines fall short.
Erin F Kallam et al. Paediatr Respir Rev 2023
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The use of artificial intelligence in interventional cardiology.
Hakan Göçer et al. Turk Gogus Kalp Damar Cerrahisi Derg 2023 31(3) 420-421
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Hemostasis - A Balancing Act.
H Marijke van den Berg et al. N Engl J Med 2023 389(9) 853-856
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Primary aldosteronism: molecular medicine meets public health.
Elena A B Azizan et al. Nat Rev Nephrol 2023
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Why cystic fibrosis newborn screening programs have failed to meet original expectations… thus far.
Philip M Farrell et al. Mol Genet Metab 2023 107679
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Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death.
Sahil Zaveri et al. Front Cardiovasc Med 2023 101253479
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Familial Hyperlipidemia Caused by Apolipoprotein B Mutation in the Pediatric Amish Population: A Mini Review.
Corey Snyder et al. Interv Cardiol (Lond) 2023 15(Suppl 17) 433-437
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Children with cystic fibrosis are still receiving inconclusive diagnosis despite undergoing newborn screening.
Ioanna Loukou et al. Acta Paediatr 2023
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Researchers uncover mysteries behind immune response to hemophilia A treatment
Medical XPress, August 2023
A Practical Guide to Genetic Testing in Inherited Heart Disease.
Emily E Brown et al. Card Electrophysiol Clin 2023 15(3) 241-247
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Page last reviewed:
Oct 1, 2023
Page last updated:
Nov 30, 2023
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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