Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kristine N. Jinnett"'
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionPreeclampsia (PE) is a leading cause of maternal and perinatal morbidity worldwide. However, current methods of screening are complicated and require special skill sets. In this observational study of prospectively collected samples, we w
Externí odkaz:
https://doaj.org/article/85e341fbea1445619111c4337e5758db
Autor:
Eser Kirkizlar, Bernhard Zimmermann, Tudor Constantin, Ryan Swenerton, Bin Hoang, Nicholas Wayham, Joshua E. Babiarz, Zachary Demko, Robert J. Pelham, Stephanie Kareht, Alexander L. Simon, Kristine N. Jinnett, Matthew Rabinowitz, Styrmir Sigurjonsson, Matthew Hill
Publikováno v:
Translational Oncology, Vol 8, Iss 5, Pp 407-416 (2015)
We demonstrate proof-of-concept for the use of massively multiplexed PCR and next-generation sequencing (mmPCR-NGS) to identify both clonal and subclonal copy-number variants (CNVs) in circulating tumor DNA. This is the first report of a targeted met
Externí odkaz:
https://doaj.org/article/7d066fbaf8d04bb1b6461ca5636564b1
Autor:
Melissa Stosic, Joshua E. Babiarz, Katie Kobara, Rupin Dhamankar, Allison M. Ryan, Eser Kirkizlar, Zachary Demko, Anne S. Bassett, Bernhard Zimmermann, Nicholas Wayham, Peter Benn, Kristine N. Jinnett, Donna M. McDonald-McGinn, Anna Norvez, Susan J. Gross
Publikováno v:
Ultrasound in Obstetrics & Gynecology
Objectives To evaluate the performance of a single-nucleotide polymorphism (SNP)-based non-invasive prenatal test (NIPT) for the detection of fetal 22q11.2 deletion syndrome in clinical practice, assess clinical follow-up and review patient choices f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::391f5054aabb6fb0d417ad168e83a016
https://doi.org/10.1002/uog.15754
https://doi.org/10.1002/uog.15754
Autor:
Nathan M. Hunkapiller, Allison Ryan, Naresh Vankayalapati, Bernhard Zimmermann, Milena Banjevic, Nicole L. Fong, Matthew Hill, Susan J. Gross, Zachary Demko, Styrmir Sigurjonsson, Kristine N. Jinnett
Publikováno v:
Fetal diagnosis and therapy. 40(3)
Objective: To validate an updated version (Version 2) of a single-nucleotide polymorphism (SNP)-based noninvasive prenatal test (NIPT) and to determine the likelihood of success when testing for fetal aneuploidies following a redraw. Methods: Version
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be1977ddc27dc2be26bfcfa9732f5be3
https://pubmed.ncbi.nlm.nih.gov/27028530
https://pubmed.ncbi.nlm.nih.gov/27028530
Autor:
Ryan Swenerton, Alexander Simon, Nicholas Wayham, Robert J. Pelham, Bernhard Zimmermann, Joshua E. Babiarz, Kristine N. Jinnett, Zachary Demko, Tudor Constantin, Bin Hoang, Styrmir Sigurjonsson, Eser Kirkizlar, Matthew Hill, Matthew Rabinowitz, Stephanie Kareht
Publikováno v:
Translational Oncology
Translational Oncology, Vol 8, Iss 5, Pp 407-416 (2015)
Translational Oncology, Vol 8, Iss 5, Pp 407-416 (2015)
We demonstrate proof-of-concept for the use of massively multiplexed PCR and next-generation sequencing (mmPCR-NGS) to identify both clonal and subclonal copy-number variants (CNVs) in circulating tumor DNA. This is the first report of a targeted met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e890e74bc5ef4dbbc19431a4b50a2937