Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Wera, Hofmann"'
Autor:
Gunda Schwaninger, Simone Heidemann, Wera Hofmann, Tamara Maurer, Katharina Mayerhanser, Joelle Ronez, Herdit Schüler, Katharina Steinmüller, Sabine Rudnik-Schöneborn, Johannes Zschocke
Publikováno v:
Medizinische Genetik. 33:35-44
The genetic counsellor profession has not yet been established in the German-speaking countries. In 2019 the Medical University of Innsbruck inaugurated the first German-taught Master’s degree programme in Genetic and Genomic Counselling. In order
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2012d57f62a422f00ecaa76f52fb20e
https://doi.org/10.1515/medgen-2021-2055
https://doi.org/10.1515/medgen-2021-2055
Autor:
Ulrike Schöck, Angela Schubert, Eva Christina Prott, Christof von Kalle, Joachim Bonnet, Kerstin A. Stangier, Ute Knoll, Rüdiger Schloo, Sanli Erkan, Sebastian Grömminger, Wera Hofmann, Markus Stumm
Publikováno v:
Prenatal Diagnosis. 35:1155-1157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb867b871285ce241f6cb69f2173aaf
https://doi.org/10.1002/pd.4668
https://doi.org/10.1002/pd.4668
Autor:
Ulrike Schöck, Cornelia Blank, Patricia Smerdka, Max Wüstemann, Tilo Burkhardt, Bernt Schulze, Yadhu Kumar, Sabine Langer-Freitag, Michael Entezami, Roland Zimmermann, Gisela Raabe-Meyer, Maja Hempel, E. Ostermayer, Tina Schleicher, Wera Hofmann, Bernd Weil, Markus Schelling, Sebastian Grömminger, Markus Stumm, Karsten Haug
Publikováno v:
Prenatal Diagnosis. 34:185-191
Objective The objective of this study is to validate the diagnostic accuracy of a non-invasive prenatal test for detecting trisomies 13, 18, and 21 for a population in Germany and Switzerland. Methods Random massively parallel sequencing was applied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b3aef9d7103846c5ce52e467009d5ce
https://doi.org/10.1002/pd.4278
https://doi.org/10.1002/pd.4278
Autor:
Alexander, Wolf, Katharina, Beller, Sebastian, Groemminger, Wera, Hofmann, Matthias, Sachse, Jana, Fassunke
Publikováno v:
Advances in experimental medicine and biology. 924
Increasing sample numbers for screening and diagnostics using circulating cell-free DNA (ccfDNA) as analyte demands an automated solution for ccfDNA extraction. The efficiency of a new, automated, large volume ccfDNA extraction method was evaluated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::455d63c39c3363dcc1f54f25f8008cbb
https://pubmed.ncbi.nlm.nih.gov/27753041
https://pubmed.ncbi.nlm.nih.gov/27753041
Autor:
Sebastian Groemminger, Katharina Beller, Matthias Sachse, Jana Fassunke, Alexander Wolf, Wera Hofmann
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783319420424
Increasing sample numbers for screening and diagnostics using circulating cell-free DNA (ccfDNA) as analyte demands an automated solution for ccfDNA extraction. The efficiency of a new, automated, large volume ccfDNA extraction method was evaluated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10d4249031a3bf26458e940f5ccba4d7
https://doi.org/10.1007/978-3-319-42044-8_33
https://doi.org/10.1007/978-3-319-42044-8_33
Autor:
Wera Hofmann, Nastasja Trunk, Michael Entezami, Markus Stumm, Julia Löcherbach, Martina Beck, Rolf-Dieter Wegner, Rolf Becker, Andreas Hagen
Publikováno v:
Prenatal Diagnosis. 32:569-577
Objective Here we describe the successful application of massively parallel sequencing for noninvasive prenatal detection of trisomy 21. In addition, for the detection of a broader spectrum of fetal aneuploidies, a target enrichment approach was succ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::401534be1da387207b798ac29998a551
https://doi.org/10.1002/pd.3862
https://doi.org/10.1002/pd.3862
Autor:
Sebastian, Grömminger, Sanli, Erkan, Ulrike, Schöck, Kerstin, Stangier, Joachim, Bonnet, Rüdiger, Schloo, Angela, Schubert, Eva-Christina, Prott, Ute, Knoll, Markus, Stumm, Christof, von Kalle, Wera, Hofmann
Publikováno v:
Prenatal diagnosis. 35(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3296b97080b91abfb07b06ec6edc2a6f
https://pubmed.ncbi.nlm.nih.gov/26248743
https://pubmed.ncbi.nlm.nih.gov/26248743
Autor:
Wera Hofmann
Publikováno v:
Women's Health. 9:513-515
Dr Wera Hofmann is an expert in biochemistry and has over 12 years of human genetic diagnostics experience. Until 2006, she supervised a diagnostic unit for BRCA gene testing at the Interdisciplinary Center for Hereditary Breast Cancer (Max Delbrück
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53c52f33f5346e7e4c5f571777b68d0b
https://doi.org/10.2217/whe.13.56
https://doi.org/10.2217/whe.13.56
Autor:
Ulrike Schöck, Sanli Erkan, Sándor Nagy, Wera Hofmann, Markus Stumm, Sebastian Grömminger, Mathias Ehrich, Joachim Bonnet, Rolf-Dieter Wegner, Patricia Smerdka, Erbil Yagmur
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 679-692 (2014)
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 679-692 (2014)
Non-invasive prenatal testing (NIPT) by random massively parallel sequencing of maternal plasma DNA for multiple pregnancies is a promising new option for prenatal care since conventional non-invasive screening for fetal trisomies 21, 18 and 13 has l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc11afd3ba95a30977e8e7fe57e019e
https://pubmed.ncbi.nlm.nih.gov/26237471
https://pubmed.ncbi.nlm.nih.gov/26237471
Autor:
Siegfried Scherneck, Wera Hofmann
Publikováno v:
Der Chirurg. 70:373-379
Bei 5–10 % aller an Mammacarcinom erkrankten Frauen ist die Erkrankung auf eine genetische Disposition zuruckzufuhren. Innerhalb der letzten 10 Jahre sind die wichtigsten disponierenden Gene fur Mammacarcinom, BRCA1 und BRCA2, identifiziert worden.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e7f77aa935d16ab0dbb0a3a110676b5
https://doi.org/10.1007/s001040050659
https://doi.org/10.1007/s001040050659