Publications by authors named "Wera Hofmann"

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Prospects and challenges for the genetic counsellor profession in the German-speaking countries: report of a workshop.
Gunda Schwaninger, Simone Heidemann, Wera Hofmann, Tamara Maurer, Katharina Mayerhanser

Med Genet· April 2021

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Purification of Circulating Cell-Free DNA from Plasma and Urine Using the Automated Large-Volume Extraction on the QIAsymphony® SP Instrument.
Alexander Wolf, Katharina Beller, Sebastian Groemminger, Wera Hofmann, Matthias Sachse

Adv Exp Med Biol· September 2017

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Evaluation of BRCA1/2 mutational status among German and Austrian women with triple-negative breast cancer.
Axel Muendlein, Bettina H Rohde, Klaus Gasser, Anton Haid, Stephanie Rauch, Wera Hofmann

J Cancer Res Clin Oncol· November 2015

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The influence of low molecular weight heparin medication on plasma DNA in pregnant women.
Sebastian Grömminger, Sanli Erkan, Ulrike Schöck, Kerstin Stangier, Joachim Bonnet, Wera Hofmann

Prenat Diagn· November 2015

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Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins.
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, Sándor Nagy, Ulrike Schöck, Wera Hofmann

J Clin Med· June 2014

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Non-invasive prenatal diagnosis using massively parallel sequencing - first experience in Germany.
Rolf-Dieter Wegner, Markus Stumm, Wera Hofmann

Mol Cytogenet· June 2014

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Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe.
Markus Stumm, Michael Entezami, Karsten Haug, Cornelia Blank, Max Wüstemann, Wera Hofmann

Prenat Diagn· February 2014

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Genetic testing: new challenges in the healthcare of women. Interview by Hannah Branch.
Wera Hofmann, Hannah Branch

Womens Health (Lond)· November 2013

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Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms.
Markus Stumm, Michael Entezami, Nastasja Trunk, Martina Beck, Julia Löcherbach, Wera Hofmann

Prenat Diagn· June 2012

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Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Antonis C Antoniou, Amanda B Spurdle, Olga M Sinilnikova, Sue Healey, Karen A Pooley, Wera Hofmann

Am J Hum Genet· April 2008

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Suppression of polyploidy by the BRCA2 protein.
Evgeny Sagulenko, Larissa Savelyeva, Volker Ehemann, Vitaliya Sagulenko, Wera Hofmann

Cancer Lett· November 2007

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Mutation analysis of BRCA1 and BRCA2 genes in Iranian high risk breast cancer families.
Andrea Pietschmann, Parvin Mehdipour, Parvin Mehdipour, Morteza Atri, Wera Hofmann

J Cancer Res Clin Oncol· August 2005

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Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.
Carolin Hartmann, Anika L John, Rüdiger Klaes, Wera Hofmann, Rainer Bielen

Hum Mutat· December 2004

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Limited relevance of the CHEK2 gene in hereditary breast cancer.
Michael R Dufault, Beate Betz, Barbara Wappenschmidt, Wera Hofmann, Katrin Bandick

Int J Cancer· June 2004

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Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi-quantitative multiplex PCR method.
Wera Hofmann, Heike Görgens, Anika John, Denise Horn, Christine Hüttner

Hum Mutat· July 2003

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