Lung Diseases - HLBS-PopOmics -

Specific PHGKB|HLBS|PHGKB

Lung Diseases

- HLBS-PopOmics -

What's New

Last Posted: Dec 13, 2018

---

• 2019 Digital Toolkit: NATIONAL BIRTH DEFECTS PREVENTION MONTH  
• Health professionals' involvement and information provision in genetic counseling following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong.  
  So Po Lam et al. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2018 Dec
• Metabolic Signatures of Cystic Fibrosis Identified in Dried Blood Spots For Newborn Screening Without Carrier Identification.  
  DiBattista Alicia et al. Journal of proteome research 2018 Dec
• Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis.  
  Gill Harinder et al. Annals of hematology 2018 Dec
• Polygenic risk score identifies associations between sleep duration and diseases determined from an electronic medical record biobank.  
  Dashti Hassan S et al. Sleep 2018 Dec
• Prenatal Diagnosis of Cystic Fibrosis.  
  Fedick Anastasia M et al. Methods in molecular biology (Clifton, N.J.) 2019 1885221-231
• Can You Inherit Pulmonary Hypertension? Here’s What You Should Know  
  Cleveland Clinic, December 10, 2018
• A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults  
  M. Murray and the Genomics and Population Health Action Collaborative, National Academies of Medicine, December 3, 2018
• Cardiac MRI biomarkers for Duchenne muscular dystrophy.  
  Magrath Patrick et al. Biomarkers in medicine 2018 Nov
• Gene therapy for sickle cell disease.  
  Olowoyeye Abiola et al. The Cochrane database of systematic reviews 2018 Nov 11CD007652
• Genomics, microbiomics, proteomics, and metabolomics in bronchopulmonary dysplasia.  
  Lal Charitharth Vivek et al. Seminars in perinatology 2018 Nov 42(7) 425-431
• Implementing Genomics-Based Screening Programs for Healthy Adults: A Proposed Evidence-based Approach from the Genomics and Population Health Action Collaborative
  Khoury MJ et al, Blog Post, December 3, 2018
• The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratories.  
  Charest-Morin Xavier et al. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2018 1483
• A Case-control Study Supporting the Use of Liquid Biopsy in the Targeted Therapy for Lung Cancer  
  Dai Li-Jun et al. Asian Pacific journal of cancer prevention : APJCP 2018 Jul 19(7) 1761-1766
• Clinical Impact of Single Nucleotide Polymorphism in PD-L1 on Response to Nivolumab for Advanced Non-Small-Cell Lung Cancer Patients.  
  Nomizo Takashi et al. Scientific reports 2017 745124