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期刊名:Genetics in medicine open

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e-ISSN:2949-7744

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共收录本刊相关文章索引199
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Khalsa Al-Kharusi,Chantel Van Wyk,Mariya Al Hinai et al. Khalsa Al-Kharusi et al.
Genetic counseling as an emerging profession has seen an expansion around the world. In the Sultanate of Oman, the profession has developed with the establishment of clinical and biochemical genetic services in 2010 and genetic counseling s...
Gunda Schwaninger,Kathrin Taxer,Sabrina Marti et al. Gunda Schwaninger et al.
In spring 2022, the inaugural cohort of Genetic and Genomic Counseling MSc students graduated from the Medical University of Innsbruck, representing a significant milestone for the establishment of the genetic counselor (GC) profession in t...
Kirsten Boggs,Fiona Lynch,Michelle Ward et al. Kirsten Boggs et al.
Genetic counselors (GCs) face unique challenges in the acute care setting. Acute care environments-such as neonatal and pediatric intensive care units-are characterized by urgency, complexity, and rapid decision making. These settings requi...
Holly Canton,Rebecca Macintosh,Joanna Sweeting et al. Holly Canton et al.
Purpose: In Australia and New Zealand, one third of genetic counselors have less than 5 years' experience. Sharing experienced practitioners' professional knowledge is needed as the profession grows. Formal mentoring is a...
Anaita Kanga-Parabia,Lucas Mitchell,Renee Smyth et al. Anaita Kanga-Parabia et al.
Purpose: To understand diversity, inclusion, and capacity of genetic counselors (GCs) in Australasia (Australia and New Zealand). Methods: ...
Markus A Feufel,Dorothee Speiser,Stephen Schüürhuis et al. Markus A Feufel et al.
Purpose: We developed the online-based counseling tool iKNOW for women with a pathogenic germline variant in BRCA1/2 to improve risk understanding and quality of life. ...
Reema W Aljassar,Qianyi Shen,Buthaina Albash et al. Reema W Aljassar et al.
Functional investigation of genetic variants found in long QT syndrome can provide evidence that is needed to confirm the genetic diagnosis and establish the cause of the condition. We performed functional assessment to determine the z-scor...