Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Beverly M. Yashar"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract The “diagnostic odyssey” describes the process those with undiagnosed conditions undergo to identify a diagnosis. Throughout this process, families of children with undiagnosed conditions have multiple opportunities to decide whether to
Externí odkaz:
https://doaj.org/article/5528a44c15a94ff5a1871c88d347d0cb
Autor:
Shane C Quinonez, Bridget C O'Connor, Michelle F Jacobs, Atnafu Mekonnen Tekleab, Ayalew Marye, Delayehu Bekele, Beverly M Yashar, Erika Hanson, Abate Yeshidinber, Getahun Wedaje
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0255278 (2021)
BackgroundOver the past two decades non-communicable diseases (NCDs) have steadily increased as a cause of worldwide disability and mortality with a concomitant decrease in disease burden from communicable, maternal, neonatal and nutritional conditio
Externí odkaz:
https://doaj.org/article/5777e7f451944c409f15e9cba94845b1
Publikováno v:
Journal of Genetic Counseling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4284dc213968c98fadad4b498fedc68
https://doi.org/10.1002/jgc4.1712
https://doi.org/10.1002/jgc4.1712
Publikováno v:
Journal of Genetic Counseling
The COVID‐19 pandemic has upended genetic counseling (GC) graduate students’ lives, as they have been forced to transition, manage, and acclimate to life during a pandemic. The current study is a first step in understanding their lived experience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723ff8309c93494099a1772e8fedb6a2
https://doi.org/10.1002/jgc4.1501
https://doi.org/10.1002/jgc4.1501
Publikováno v:
Journal of genetic counselingREFERENCES. 31(6)
Pharmacogenomic (PGx) testing is an increasingly utilized technology that offers the potential for precision drug selection to treat depression. Though PGx-guided therapy is associated with increased rates of remission of depression symptoms, for man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a530229cf3ae4fda506c0e75399dc664
https://pubmed.ncbi.nlm.nih.gov/35900228
https://pubmed.ncbi.nlm.nih.gov/35900228
Autor:
Ken Resnicow, Emerson Delacroix, Gabriela Chen, Sarah Austin, Elena Stoffel, Erika N. Hanson, Lynette Hammond Gerido, Kimberly A. Kaphingst, Beverly M. Yashar, Monica Marvin, Jennifer J. Griggs, Deborah Cragun
Publikováno v:
Journal of genetic counseling. 31(5)
Genetic counselors (GCs) have traditionally been trained to adopt a position of equipoise or clinical neutrality. They provide information, answer questions, address barriers, and engage in shared decision-making, but generally, they do not prescribe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc53082805eb62974afc59dc6f69dbae
https://pubmed.ncbi.nlm.nih.gov/35906848
https://pubmed.ncbi.nlm.nih.gov/35906848
Publikováno v:
Journal of Huntington's disease. 11(3)
Background: Health information-seeking is a coping strategy used globally by individuals with a personal or family history of a medical condition, including Huntington’s disease (HD). Objective: We sought to ascertain information-seeking practices
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::660819a728cd733ff46340a27464c01a
https://pubmed.ncbi.nlm.nih.gov/35570496
https://pubmed.ncbi.nlm.nih.gov/35570496
Publikováno v:
Journal of genetic counseling. 31(5)
Transgender and/or gender non-binary (TGNB) individuals face significant health care disparities, including deficiencies in provider knowledge. To address this knowledge gap for genetic counselors, we developed, implemented, and analyzed an education
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23be52cee06dfb2928331231eb0197f
https://pubmed.ncbi.nlm.nih.gov/35460542
https://pubmed.ncbi.nlm.nih.gov/35460542
Publikováno v:
Journal of Genetic Counseling. 29:67-77
This study assessed genetic counselors' (GCs) perceptions of delegation as a tool to increase workforce efficiency and help meet the current gap between the number of genetic service providers and the number of patients. GCs were recruited to partici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8de070d21cdb1eab39eb7f38769fd1e3
https://doi.org/10.1002/jgc4.1181
https://doi.org/10.1002/jgc4.1181
Publikováno v:
Journal of Perinatal & Neonatal Nursing. 33:E3-E14
Prenatal genetic screening (GS) for the most common autosomal aneuploidies encompasses maternal serum screening (MSS) and noninvasive prenatal testing (NIPT, or cell-free fetal DNA testing). In the United States, most maternity care is provided by ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c181fda257515e39bc46a057f6858fbc
https://doi.org/10.1097/jpn.0000000000000440
https://doi.org/10.1097/jpn.0000000000000440