Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jennifer Czerwinski"'
Autor:
Sarah Mayes, Syed Hashmi, Mark A. Turrentine, Sandra Darilek, Lara A. Friel, Jennifer Czerwinski
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 01, Pp e18-e24 (2016)
Abstract Objective Noninvasive prenatal testing (NIPT) enables the detection of common fetal aneuploidies such as trisomy 21, trisomy 18, trisomy 13, and sex chromosome abnormalities via analysis of cell-free fetal DNA circulating in maternal serum
Externí odkaz:
https://doaj.org/article/ae13ae5137b3413792640bc2ddc15bb5
Autor:
Kathleen, Shields, Jennifer, Czerwinski, Tracie, Dauwe, Syed, Hashmi, Paul, Hillman, Kate, Mowrey, Kathryn, Gunther
Publikováno v:
The Journal of Continuing Education in Nursing. 54:16-24
Background Many infants admitted to the neonatal intensive care unit (NICU) have genetic conditions. Previous research has shown that gaps exist in the genetics knowledge of nurses and that they lack comfort applying genetics information to clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f808a82e9da9f4fb93719807a2baa36d
https://doi.org/10.3928/00220124-20221207-06
https://doi.org/10.3928/00220124-20221207-06
Autor:
Claire N. Singletary, Patricia McCarthy Veach, Lauren Murphy, Chelsea Wagner, Maureen E. Mork, Jennifer Czerwinski, Kaitlyn Amos
Publikováno v:
Journal of Genetic Counseling. 31:663-676
A personal or family medical history is inherently part of a genetic counselor's life story. Yet, the degree to which this history influences counselors' clinical specialty choice and professional psychosocial practice is unexplored. A medical diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41eed22e44b7614a7dec15d565573df8
https://doi.org/10.1002/jgc4.1533
https://doi.org/10.1002/jgc4.1533
Autor:
Sarah Jane Noblin, Lara A. Friel, Jennifer Czerwinski, Chelsea Wagner, Blair Stevens, Han-Yang Chen
Publikováno v:
Journal of Genetic Counseling. 28:692-699
The introduction of cell-free DNA screening, or non-invasive prenatal testing (NIPT), for chromosome abnormalities has greatly impacted prenatal care since its introduction in late 2011. We aimed to evaluate the association between the introduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1b7cae302a6583ea2e433b18dcfdd47
https://doi.org/10.1002/jgc4.1095
https://doi.org/10.1002/jgc4.1095
Autor:
Jennifer Czerwinski, Claire N. Singletary, Meagan Giles Choates, Chelsea Wagner, Nevena Krstić
Publikováno v:
Prenatal Diagnosis. 38:748-754
OBJECTIVE Characterize the uptake of chromosomal microarray analysis (CMA) among women undergoing invasive prenatal diagnosis at a large academic institution over a 4-year time period. METHODS Retrospective database review of women who underwent inva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac9cf5d3e5d9b0128a46d855ed9632c
https://doi.org/10.1002/pd.5324
https://doi.org/10.1002/pd.5324
Autor:
Leslie Dunnington, Jessica M. Davis, Maggie Clifford, Erica M. Bednar, S. Shahrukh Hashmi, Jennifer Czerwinski, Sarah A. Bannon, Courtney D. DiNardo
Publikováno v:
Leuk Lymphoma
Multiple genes have been identified to cause hereditary predispositions to hematologic malignancies, and characterized by an increased risk to develop myelodysplastic syndromes (MDS), acute myeloid leukemia (AML), and/or aplastic anemia (AA). Referra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae11e9c6180cf0d10bf2cc84efa972fc
https://pubmed.ncbi.nlm.nih.gov/31274040
https://pubmed.ncbi.nlm.nih.gov/31274040
Autor:
Eric J. Thomas, Patricia A. Heale, Jennifer Czerwinski, Susan Lesser, Kuogen Tsao, Madelene J. Ottosen
Publikováno v:
Journal of Obstetric, Gynecologic & Neonatal Nursing. 49:S85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d4ea51d0cab7f642d388494502b9ab8
https://doi.org/10.1016/j.jogn.2020.09.149
https://doi.org/10.1016/j.jogn.2020.09.149
Autor:
Jennifer Czerwinski, Helen Gould, Katie Stoll, S. Shahrukh Hashmi, Victoria F. Wagner, Kathryn K. Ostermaier
Publikováno v:
Journal of genetic counselingREFERENCES. 28(6)
Genetic counselors have a unique role in healthcare that requires a balance between being a patient educator and patient advocate when discussing disability. This study aimed to determine genetic counselors' implicit attitudes toward disability, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::410e0bcdd0ee3bd1e17801c1c760c979
https://pubmed.ncbi.nlm.nih.gov/31442365
https://pubmed.ncbi.nlm.nih.gov/31442365
Publikováno v:
Journal of Genetic Counseling. 24:952-960
With the rapidly evolving field of prenatal testing, there is a growing need to provide support for women pursuing termination of pregnancy following the discovery of a fetal anomaly. Previous studies have documented that women in this situation ofte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffb17aaa64a95e3de7199531d032e15b
https://doi.org/10.1007/s10897-015-9832-x
https://doi.org/10.1007/s10897-015-9832-x
Autor:
Jennifer Czerwinski, Kathryn M. Reese, Claire N. Singletary, Anthony Johnson, Sandra Darilek, Malorie Jones
Publikováno v:
Journal of genetic counseling. 27(5)
The rate of twinning is rising and since the introduction of non-invasive prenatal testing, interest in and uptake of genetic screening and testing in twin pregnancies has not been investigated. This study aimed to explore the attitudes toward and up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db93bdf267ae6e5e2bcb869afa77d09
https://pubmed.ncbi.nlm.nih.gov/29525932
https://pubmed.ncbi.nlm.nih.gov/29525932