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und et, al.
(2015)
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
JAMA 313, S. 1347-1361.
Volltext nicht vorhanden.
Nalleweg, N., Chiriac, M. T., Podstawa, E., Lehmann, Christian
, Rau, Tilmann T., Atreya, R., Krauss, Ekaterina, Hundorfean, G., Fichtner-Feigl, Stefan, et, al., make_name_string expected hash reference und make_name_string expected hash reference
(2015)
L-9 and its receptor are predominantly involved in the pathogenesis of UC.
Gut 64 (5), S. 743-755.
Airapetian, A., Schäfer, Andreas und et, al.
(2014)
Spin density matrix elements in exclusive ω electroproduction on 1 H and 2 H targets at 27.5 GeV beam energy.
The European Physical Journal C - Particles and Fields 74, S. 3110.
Couch, F. J., Wang, X.
, McGuffog, L., Lee, A., Olswold, C., Kuchenbaecker, K. B., Soucy, P., Weber, Bernhard H. F., et, al.
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, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
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, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference
(2013)
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
PLoS Genetics 9 (3), e1003212.
, Wang, C.
, Koboldt, D. C., Sergeev, Y. V., Fulton, R. S., Fulton, L. L., Fronick, C. C., Branham, K. E., Bragg-Gresham, J., Jun, G.
, Hu, Y., Kang, H. M., Liu, D., Weber, Bernhard H. F., et, al., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
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und make_name_string expected hash reference
(2013)
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Nature Genetics 45, S. 1375-1379.
Volltext nicht vorhanden.
, Chen, W., Schu, M., Weber, Bernhard H. F.
und et, al.
(2013)
Seven new loci associated with age-related macular degeneration.
Nature Genetics 45, S. 433-439.
Volltext nicht vorhanden.
, Bunce, C.
, Khan, J. C., Shahid, H., Swaroop, A.
, Abecasis, G.
, Branham, K. E., Zareparsi, S., Bergen, A. A., Klaver, C. C.
, Baas, D. C., Zhang, K., Chen, Y., Gibbs, D., Weber, Bernhard H. F.
, et, al., make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
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, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference
(2012)
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.
International Journal of Epidemiology 41 (1), S. 250-262.
Volltext nicht vorhanden.
Baas, D. C., Ho, L., Tanck, M. W., Fritsche, L. G., Merriam, J. E., van het Slot, R., Koeleman, B. P., Gorgels, T. G., van Duijn, C. M., Uitterlinden, A. G., de Jong, P. T., Hofman, A., ten Brink, J. B., Vingerling, J. R., Klaver, C. C., Dean, M., Weber, Bernhard H. F.
und et, al.
(2012)
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration.
Molecular vision 18, S. 657-674.
, Patterson, C. C., Chakravarthy, U.
, Dasari, S., Klaver, C. C.
, Vingerling, J. R., Ho, L., de Jong, P. T., Fletcher, A. E., Young, I. S.
, Seland, J. H., Rahu, M., Soubrane, G., Tomazzoli, L., Topouzis, F.
, Vioque, J.
, Weber, Bernhard H. F., et, al., make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference
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, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference und make_name_string expected hash reference
(2011)
Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies.
Human Mutation 32 (12), S. 1407-1416.
Volltext nicht vorhanden.
, Silvestri, G., Chakravarthy, U.
, Dasari, S., Fritsche, L. G.
, Weber, Bernhard H. F.
, et, al., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference
, make_name_string expected hash reference und make_name_string expected hash reference
(2011)
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people.
American Journal of Epidemiology 173 (12), S. 1357-1364.
Volltext nicht vorhanden.
, Schlehe, B., Hemminki, K., Sutter, C., Ditsch, N., Blackburn, A.
, Hill, L. Z., Jerry, D. J., Bugert, P., Weber, Bernhard H. F.
, et, al., make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference
(2010)
Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity.
Human Mutation 31 (1), S. 60-66.
Volltext nicht vorhanden.
und et, al.
(2006)
Communicating BRCA1 and BRCA2 genetic test results.
Journal of clinical oncology 24 (18), S. 2969-2970.
Volltext nicht vorhanden.
, DiDonato, S., Gellera, C., Mariotti, C., Lange, H. W., Weirich-Schwaiger, H., Wenning, G. K., Seppi, K., Melegh, B., Havasi, V., Balikó, L., Wieczorek, S. und et, al.
(2006)
Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease.
Human Genetics 120 (2), S. 285-292.
Volltext nicht vorhanden.
, Yashar, B. M., Zareparsi, S., Swaroop, A.
, Iyengar, S. K., Klein, B. E., Klein, R., Lee, K. E., Majewski, J., Schultz, D. W., Klein, M. L., Seddon, J. M., Santangelo, S. L., Weeks, D. E.
, Conley, Y. P., Mah, T. S., Schmidt, S., Weber, Bernhard H. F., et, al., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
und make_name_string expected hash reference
(2005)
Meta-analysis of genome scans of age-related macular degeneration.
Human Molecular Genetics 14 (15), S. 2257-2264.
Volltext nicht vorhanden.
und et, al.
(2002)
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.
European Journal of Human Genetics 10 (3), S. 197-203.
Volltext nicht vorhanden.
und et, al.
(2002)
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype.
Annals of Neurology 51 (5), S. 662.
Volltext nicht vorhanden.
und et, al.
(1997)
SCA2 trinucleotide expansion in German SCA patients.
Neurogenetics 1 (1), S. 59-64.
Volltext nicht vorhanden.
und et, al.
(1996)
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996 - Part 1,2,3.
Cytogenetics and cell genetics 74, S. 1-56.
Volltext nicht vorhanden.
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