Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Danielle LaGrave"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100572- (2023)
Externí odkaz:
https://doaj.org/article/0af056df95334e05a815443d97c9b724
Autor:
Danielle LaGrave, Rachel Lasher, Michelle Bosworth, Amanda Openshaw, Katie Rudd, Erica Andersen
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100654- (2023)
Externí odkaz:
https://doaj.org/article/cbe61dd16c5742eb977c34e352e25feb
Autor:
Nancy C. Rose, Elizabeth S. Barrie, Jennifer Malinowski, Gabrielle P. Jenkins, Monica R. McClain, Danielle LaGrave, Marco L. Leung
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(7)
Noninvasive prenatal screening (NIPS) using cell-free DNA has been assimilated into prenatal care. Prior studies examined clinical validity and technical performance in high-risk populations. This systematic evidence review evaluates NIPS performance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bdaf7d49a87f56839502701854edb8
https://pubmed.ncbi.nlm.nih.gov/36063164
https://pubmed.ncbi.nlm.nih.gov/36063164
Autor:
Kamisha L. Johnson-Davis, Heather A. Reichman, Jonathan R. Genzen, Sonia L. La'ulu, Joshua J.H. Hunsaker, Taylor M. Snow, Wendy Murphy, Gwendolyn A. McMillin, Danielle LaGrave
Publikováno v:
American journal of clinical pathology. 157(1)
Objectives Nicotine (NIC) use during pregnancy can influence markers used in biochemical maternal serum screening. This study was designed to determine prevalence of disclosed tobacco smokers in our patient population and to compare disclosed tobacco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99b6490e3a82356c33bddf67e2937b28
https://pubmed.ncbi.nlm.nih.gov/34508553
https://pubmed.ncbi.nlm.nih.gov/34508553
Autor:
Carole A. Samango-Sprouse, Danielle LaGrave, Daniel Lyons, Hakon Hakonarson, Valerie Kantor, Maria Teresa Trefogli, Irish Balosbalos, Kimberly Martin, Rupin Dhamankar, Paul Billings, Charlly Kao, Elizabeth Valenti
Publikováno v:
American journal of obstetricsgynecology MFM. 2(3)
Background Maternal X chromosome abnormalities may cause discordant results between noninvasive prenatal screening tests and diagnostic evaluation of the fetus/newborn, leading to unnecessary invasive testing. Women with X chromosome abnormalities ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12ed791ab8eb5268eab0baf38ad6a8b
https://pubmed.ncbi.nlm.nih.gov/33345882
https://pubmed.ncbi.nlm.nih.gov/33345882
Autor:
Reha M. Toydemir, Erin E. Baldwin, John Herriges, Ellen M. Arch, Danielle LaGrave, Allen N. Lamb, Pamela A. Burgio
Publikováno v:
Journal of Child Neurology. 34:86-93
To date, 13 patients with interstitial microduplications involving Xq25q26.2 have been reported. Here, we report 6 additional patients from 2 families with duplications involving Xq25q26.2. Family I carries a 5.3-Mb duplication involving 26 genes. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53035b88a85c573ebe8ef0a7754adcbc
https://doi.org/10.1177/0883073818811454
https://doi.org/10.1177/0883073818811454
Publikováno v:
Prenatal Diagnosis. 35:440-446
Objective The aim of this article is to determine the cost effectiveness of cell free DNA (cfDNA) as a replacement forintegrated screening using a societal cost perspective. Method This study used Monte-Carlo simulation with one-way and probabilistic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4988f3c7415a8ff12721f64b9ee339a
https://doi.org/10.1002/pd.4511
https://doi.org/10.1002/pd.4511
Autor:
Danielle LaGrave, Joy B. Redman
In a genetics laboratory, genetic counselors work as part of the larger team of laboratory professionals. This chapter provides details about the many different personnel who work in a genetics laboratory. It discusses their different roles and educa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bdbc20d4eaa3b324ca68a124443b597
https://doi.org/10.1093/med/9780190604929.003.0003
https://doi.org/10.1093/med/9780190604929.003.0003
Autor:
Tatiana Tvrdik, Danielle LaGrave, Erin E. Baldwin, Amanda Openshaw, Christine E. Miller, Patti Krautscheid, Kim Hart
Publikováno v:
American Journal of Medical Genetics Part A. 164:1094-1101
Genetic tests are routinely ordered by health care providers (HCPs) within a wide range of medical specialties. Many providers have limited knowledge or experience with ordering and interpreting genetic tests; thus, test order errors are common. Rigo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99bd18b354275b3845809d9382be0cab
https://doi.org/10.1002/ajmg.a.36453
https://doi.org/10.1002/ajmg.a.36453
Publikováno v:
Prenatal Diagnosis. 33:1201-1206
Objectives In maternal serum screening for Down syndrome, a cutoff of 1 : 270 is often used as a decision point to recommend invasive confirmatory testing. However, it has not been established how well this or any other cutoff relates to patient pref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f42e243ff7fd3b1c05fd27a0c3351e0
https://doi.org/10.1002/pd.4225
https://doi.org/10.1002/pd.4225