Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Amy Breman"'
Autor:
Khurram Liaqat, Francesco Vetrini, Erin Conboy, Kayla Treat, Lili Mantcheva, Marco Abreu, Tae-Hwi Schwantes-An, Kevin Booth, Reynold Ly, Amy Breman, Marwan Tayeh, Benjamin Helm, Brett Graham, Stephanie Ware
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101434- (2024)
Externí odkaz:
https://doaj.org/article/3961cf0b9fbc499db7946db2fe4eb974
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
Publikováno v:
Journal of genetic counselingREFERENCES.
Genetic counselors have skills and expertise in genetics and patient care that make them an asset to research and research teams. However, the National Society of Genetic Counselors (NSGC) found in 2020 that more than half of practicing genetic couns
Autor:
Amy Breman, Karlla Welch Brigatti, Maria Chahrour, Giusy Della Gatta, Bracha Erlanger Avigdor, Lauretta El Hayek, Claudia Gonzaga-Jauregui, Maria Kousi, Ikeoluwa A. Osei-Owusu, Jonathan Pevsner, Jennifer E. Posey, Erik G. Puffenberger, Paweł Stankiewicz, Cristopher V. Van Hout, Cinthya J. Zepeda Mendoza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bed5d9524c599bca75790773a96c654
https://doi.org/10.1016/b978-0-12-820140-4.00021-1
https://doi.org/10.1016/b978-0-12-820140-4.00021-1
Autor:
Nichole Owen, Volkan Okur, Stephanie Anderson, Janice Smith, Carlos Bacino, Patricia Ward, Sau Cheung, Amy Breman, Ignatia Van Den Veyver, Weimin Bi
Publikováno v:
Genetics in Medicine. 24:S291
Autor:
Elizabeth, Normand, Sadeem, Qdaisat, Weimin, Bi, Chad, Shaw, Ignatia, Van den Veyver, Arthur, Beaudet, Amy, Breman
Publikováno v:
Prenatal diagnosis. 36(9)
Detection of genomic copy number abnormalities in a single cell using array comparative genomic hybridization (CGH) offers a promising non-invasive alternative for prenatal diagnosis. Our objective was to compare three commercially available whole-ge
Autor:
Weimin, Bi, Amy, Breman, Chad A, Shaw, Pawel, Stankiewicz, Tomasz, Gambin, Xinyan, Lu, Sau Wai, Cheung, Laird G, Jackson, James R, Lupski, Ignatia B, Van den Veyver, Arthur L, Beaudet
Publikováno v:
Prenatal diagnosis. 32(1)
High resolution detection of genomic copy number abnormalities in a single cell is relevant to preimplantation genetic diagnosis and potentially to noninvasive prenatal diagnosis. Our objective is to develop a reliable array comparative genomic hybri
Autor:
Amy, Breman, Amber N, Pursley, Patricia, Hixson, Weimin, Bi, Patricia, Ward, Carlos A, Bacino, Chad, Shaw, James R, Lupski, Arthur, Beaudet, Ankita, Patel, Sau W, Cheung, Ignatia, Van den Veyver
Publikováno v:
Prenatal diagnosis. 32(4)
To evaluate the results of prenatal chromosomal microarray analysis (CMA) on1000 fetal samples referred for testing at our institution and to compare these data to published reports.High resolution CMA was offered to women undergoing amniocentesis or
Autor:
Amy Breman, Brenda Grimes
Publikováno v:
Transgenic Research; Oct2008, Vol. 17 Issue 5, p979-983, 5p
Autor:
Ripudaman Singh, Lotte Hatt, Katarina Ravn, Ida Vogel, Rikke Christensen, Else Marie Vestergaard, Niels Uldbjerg, Elizabeth Normand, Sadeem Qdaisat, Den Veyver, Ignatia B., Laird Jackson, Li Zhao, Rui Chen, Shaw, Chad A., Amy Breman, Arthur Beaudet, Palle Schelde
Publikováno v:
Aarhus University
Singh, R, Hatt, L, Ravn, K, Vogel, I, Christensen, R, Vestergaard, E M, Uldbjerg, N, Normand, E, Qdaisat, S, B. van den Veyver, I, Jackson, L, Zhao, L, Chen, R, Shaw, C A, Breman, A, Beaudet, A & Schelde, P 2016, ' Cell Based NIPT (cbNIPT)-Using Fetal Cells in Pregnant Women’s Blood for Genome Analyses ', IISPD Congress on prenatal diagnosis and therapy, Berlin, Germany, 01/07/2016-08/07/2016 .
Singh, R, Hatt, L, Ravn, K, Vogel, I, Christensen, R, Vestergaard, E M, Uldbjerg, N, Normand, E, Qdaisat, S, B. van den Veyver, I, Jackson, L, Zhao, L, Chen, R, Shaw, C A, Breman, A, Beaudet, A & Schelde, P 2016, ' Cell Based NIPT (cbNIPT)-Using Fetal Cells in Pregnant Women’s Blood for Genome Analyses ', IISPD Congress on prenatal diagnosis and therapy, Berlin, Germany, 01/07/2016-08/07/2016 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::31da25b4050ef433785bb75974589e00
https://pure.au.dk/portal/en/publications/cell-based-nipt-cbnipt-using-fetal-cells-in-pregnant-womens-blood-for-genome-analyses(862644e4-f9af-420a-9ed9-84db555a6eb5).html
https://pure.au.dk/portal/en/publications/cell-based-nipt-cbnipt-using-fetal-cells-in-pregnant-womens-blood-for-genome-analyses(862644e4-f9af-420a-9ed9-84db555a6eb5).html