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Bernd Auber
Bernd Auber
Unknown affiliation
Verified email at mh-hannover.de
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Cited by
Cited by
Year
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
RL Milne, KB Kuchenbaecker, K Michailidou, J Beesley, S Kar, ...
Nature genetics 49 (12), 1767-1778, 2017
3542017
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
K Kast, K Rhiem, B Wappenschmidt, E Hahnen, J Hauke, B Bluemcke, ...
Journal of medical genetics 53 (7), 465-471, 2016
2662016
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
CP Kratz, L Franke, H Peters, N Kohlschmidt, B Kazmierczak, U Finckh, ...
British journal of cancer 112 (8), 1392-1397, 2015
2162015
Gene panel testing of 5589 BRCA1/2‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary …
J Hauke, J Horvath, E Groß, A Gehrig, E Honisch, K Hackmann, ...
Cancer medicine 7 (4), 1349-1358, 2018
1682018
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
L Fachal, H Aschard, J Beesley, DR Barnes, J Allen, S Kar, KA Pooley, ...
Nature genetics 52 (1), 56-73, 2020
1492020
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
X Yang, H Song, G Leslie, C Engel, E Hahnen, B Auber, J Horváth, K Kast, ...
JNCI: Journal of the National Cancer Institute 112 (12), 1242-1250, 2020
1402020
BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer
N Weber-Lassalle, J Hauke, J Ramser, L Richters, E Groß, B Blümcke, ...
Breast Cancer Research 20, 1-6, 2018
1222018
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
MT Parsons, E Tudini, H Li, E Hahnen, B Wappenschmidt, L Feliubadaló, ...
Human mutation 40 (9), 1557-1578, 2019
1192019
Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
M Shoukier, N Klein, B Auber, J Wickert, J Schröder, B Zoll, P Burfeind, ...
Clinical genetics 83 (1), 53-65, 2013
992013
Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness
VL Patel, EL Busch, TM Friebel, A Cronin, G Leslie, L McGuffog, J Adlard, ...
Cancer research 80 (3), 624-638, 2020
542020
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic …
S Schubert, JL van Luttikhuizen, B Auber, G Schmidt, W Hofmann, ...
International journal of cancer 144 (11), 2683-2694, 2019
542019
MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies
T Ripperger, W Hofmann, JC Koch, K Shirneshan, D Haase, G Wulf, ...
Haematologica 103 (2), e55, 2018
512018
FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study
A Osmanovic, I Rangnau, A Kosfeld, S Abdulla, C Janssen, B Auber, ...
European Journal of Human Genetics 25 (3), 324-331, 2017
492017
Leupaxin, a novel coactivator of the androgen receptor, is expressed in prostate cancer and plays a role in adhesion and invasion of prostate carcinoma cells
S Kaulfuss, M Grzmil, B Hemmerlein, P Thelen, S Schweyer, J Neesen, ...
Molecular endocrinology 22 (7), 1606-1621, 2008
462008
German Consortium for Hereditary Breast and Ovarian Cancer (GC-HBOC). Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
K Kast, K Rhiem, B Wappenschmidt, E Hahnen, J Hauke, B Bluemcke, ...
J Med Genet 53 (7), 465-71, 2016
412016
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion
GM Stettner, M Shoukier, C Höger, K Brockmann, B Auber
American Journal of Medical Genetics Part A 155 (8), 2003-2007, 2011
372011
Increased cancer prevalence in peripartum cardiomyopathy
TJ Pfeffer, S Schlothauer, S Pietzsch, M Schaufelberger, B Auber, ...
Cardio Oncology 1 (2), 196-205, 2019
362019
The FANCM: p. Arg658* truncating variant is associated with risk of triple-negative breast cancer
G Figlioli, M Bogliolo, I Catucci, L Caleca, SV Lasheras, R Pujol, JI Kiiski, ...
NPJ breast cancer 5 (1), 1-14, 2019
322019
A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome
B Auber, P Burfeind, S Herold, K Schoner, G Simson, R Rauskolb, ...
Clinical genetics 72 (5), 454-459, 2007
312007
Borna disease virus multiplication in mouse organotypic slice cultures is site-specifically inhibited by gamma interferon but not by interleukin-12
G Friedl, M Hofer, B Auber, C Sauder, J Hausmann, P Staeheli, ...
Journal of virology 78 (3), 1212-1218, 2004
312004
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