Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ignatia Van Den Veyver"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101716- (2024)
Externí odkaz:
https://doaj.org/article/d837fa59ba3f45f593505a8be908c7d2
Autor:
Roni Zemet Lazar, Mohamad Ali Maktabi, Alexandra Tinfow, Jessica Giordano, Thomas Heisler, Qi Yan, Roni Plaschkes, Michal Berkenstadt, Boaz Weisz, David Crosby, Jennifer Walsh, Siobhán Corcoran, Juliana Gebb, Erica Schindewolf, Kendra Miller, Kate Swanson, Teresa Sparks, Asha Talati, Neeta Vora, Ronald Wapner, Ignatia Van Den Veyver
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100651- (2023)
Externí odkaz:
https://doaj.org/article/334da863e04a437ab70514c03fdeac0d
Autor:
Dan Brooks, Roni Zemet Lazar, Sandra Darilek, Grant Bonesteele, Veena Mathur, Ignatia Van Den Veyver, April Adams
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100661- (2023)
Externí odkaz:
https://doaj.org/article/6369f02a9e4643fa831663c837078feb
Autor:
Xinming Zhuo, Qun Wang, Liesbeth Vossaert, Roseen Salman, Adriel Kim, Ignatia Van den Veyver, Amy Breman, Arthur Beaudet
Publikováno v:
PLoS ONE, Vol 16, Iss 4, p e0249695 (2021)
A major challenge for cell-based non-invasive prenatal testing (NIPT) is to distinguish individual presumptive fetal cells from maternal cells in female pregnancies. We have sought a rapid, robust, versatile, and low-cost next-generation sequencing m
Externí odkaz:
https://doaj.org/article/71b7afd547874f3db09b53d76f120a69
Autor:
Jason Ross, Julia Busch, Ellen Mintz, Damian Ng, Alexandra Stanley, David Brafman, V. Reid Sutton, Ignatia Van den Veyver, Karl Willert
Publikováno v:
Cell Reports, Vol 9, Iss 5, Pp 1770-1780 (2014)
Summary: WNT signaling promotes the reprogramming of somatic cells to an induced pluripotent state. We provide genetic evidence that WNT signaling is a requisite step during the induction of pluripotency. Fibroblasts from individuals with focal derma
Externí odkaz:
https://doaj.org/article/8020858f94064fb6b7fad772ff9344d2
Autor:
Kjersti Aagaard, Kevin Riehle, Jun Ma, Nicola Segata, Toni-Ann Mistretta, Cristian Coarfa, Sabeen Raza, Sean Rosenbaum, Ignatia Van den Veyver, Aleksandar Milosavljevic, Dirk Gevers, Curtis Huttenhower, Joseph Petrosino, James Versalovic
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e36466 (2012)
While current major national research efforts (i.e., the NIH Human Microbiome Project) will enable comprehensive metagenomic characterization of the adult human microbiota, how and when these diverse microbial communities take up residence in the hos
Externí odkaz:
https://doaj.org/article/b94e8c9a56314b25b6bd009a5c0197cb
Autor:
Roni Zemet Lazar, Eyal Krispin, Rebecca Johnson, Navya Kumar, Ahmed Nassr, Magdalena Sanz Cortes, Jimmy Espinoza, Michael Belfort, Alireza Shamshirsaz, Ignatia Van Den Veyver
Publikováno v:
Genetics in Medicine. 24:S378-S381
Autor:
Bobby K, Brar, Marisa Gilstrop, Thompson, Neeta L, Vora, Kelly, Gilmore, Karin, Blakemore, Kristen A, Miller, Jessica, Giordano, Andreas, Dufke, Beatrix, Wong, Samantha, Stover, Billie, Lianoglou, Ignatia, Van den Veyver, Esther, Dempsey, Mara, Rosner, Karen, Chong, David, Chitayat, Teresa N, Sparks, Mary E, Norton, Ronald, Wapner, Kristin, Baranano, Angie C, Jelin
Publikováno v:
Prenatal diagnosisREFERENCES. 42(13)
Tubulinopathies refer to conditions caused by genetic variants in isotypes of tubulin resulting in defective neuronal migration. Historically, diagnosis was primarily via postnatal imaging. Our objective was to establish the prenatal phenotype/genoty
Autor:
Brielle Crovetti, Mohamad Ali Maktabi, Hadi Erfani, Tachjaree Panchalee, Qun Wang, Liesbeth Vossaert, Ignatia Van den Veyver
Publikováno v:
Prenatal diagnosis. 42(9)
To explore the potential of circulating trophoblasts (TBs) as a non-invasive tool to assess placental health and predict obstetric complications.We retrospectively reviewed maternal characteristics and pregnancy outcomes of 369 women who enrolled in
Publikováno v:
Journal of genetic counselingREFERENCES. 31(6)
Prenatal exome sequencing (ES) is increasingly used for prenatal diagnosis because emerging data indicate it has incremental diagnostic benefit in pregnancies with fetal anomalies without identified genetic abnormalities by karyotyping and chromosoma