Weber, Bernhard H.F.

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., Burdon, K. P., Hebbring, S. J., Wen, C., Gorski, M., et al. (2016) · Nature Genetics

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 1,544

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

Rivera, A., Fisher, S. A., Fritsche, L. G., Keilhauer, C. N., Lichtner, P., Meitinger, T., & Weber, B. H. F. (2005) · Human Molecular Genetics

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 788

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy

Weber, B. H. F., Vogt, G., Pruett, R. C., Stöhr, H., & Felbor, U. (1994) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 656

Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

Rebbeck, T. R., Mitra, N., Wan, F., Sinilnikova, O. M., Healey, S., McGuffog, L., Mazoyer, S., Chenevix-Trench, G., Easton, D. F., Antoniou, A. C., et al. (2015) · JAMA

BRCA gene mutations in cancerMultiple and Secondary Primary Cancers

Cited by 521

Positional cloning of the gene associated with X-linked juvenile retinoschisis

Sauer, C. G., Gehrig, A., Warneke-Wittstock, R., Marquardt, A., Ewing, C. C., Gibson, A., Lorenz, B., Jurklies, B., & Weber, B. H. F. (1997) · Nature Genetics

Retinal Development and DisordersOcular Disorders and Treatments

Cited by 497

Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA

Fritsche, L. G., Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N., & Weber, B. H. F. (2008) · Nature Genetics

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 400

Meta-analysis of genome scans of age-related macular degeneration

Fisher, S. A., Abecasis, G. R., Yashar, B. M., Zareparsi, S., Swaroop, A., Iyengar, S. K., Klein, B. E. K., Klein, R., Lee, K. E., Majewski, J., et al. (2005) · Human Molecular Genetics

Genetic Associations and EpidemiologyRetinal Diseases and Treatments

Cited by 239

CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors

Corbo, J. C., Lawrence, K. A., Karlstetter, M., Myers, C. A., Abdelaziz, M., Dirkes, W., Weigelt, K., Seifert, M., Benes, V., Fritsche, L. G., et al. (2010) · Genome Research

Retinal Development and DisordersGenomics and Chromatin Dynamics

Cited by 219

TMEM16B, a novel protein with calcium-dependent chloride channel activity, associates with a presynaptic protein complex in photoreceptor terminals

Stöhr, H., Heisig, J. B., Benz, P. M., Schöberl, S., Milenkovic, V. M., Strauss, O., Aartsen, W. M., Wijnholds, J., Weber, B. H. F., & Schulz, H. L. (2009) · The Journal of Neuroscience

Ion channel regulation and functionNeuroscience and Neuropharmacology Research

Cited by 216

An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)

Fritsche, L. G., Lauer, N., Hartmann, A., Stippa, S., Keilhauer, C. N., Oppermann, M., Pandey, M. K., Köhl, J., Zipfel, P. F., Weber, B. H. F., et al. (2010) · Human Molecular Genetics

Complement system in diseasesRetinal Diseases and Treatments

Cited by 203

Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies

McKay, G. J., Patterson, C. C., Chakravarthy, U., Dasari, S., Klaver, C. C., Vingerling, J. R., Ho, L., de Jong, P. T. V. M., Fletcher, A. E., Young, I. S., et al. (2011) · Human Mutation

Retinal Diseases and TreatmentsRetinal Imaging and Analysis

Cited by 151

Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease

Winkler, T. W., Grassmann, F., Brandl, C., Kiel, C., Günther, F., Strunz, T., Weidner, L., Zimmermann, M. E., Korb, C. A., Poplawski, A., et al. (2020) · BMC Medical Genomics

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 138

Variations in Apolipoprotein E Frequency With Age in a Pooled Analysis of a Large Group of Older People

McKay, G. J., Silvestri, G., Chakravarthy, U., Dasari, S., Fritsche, L. G., Weber, B. H., Keilhauer, C. N., Klein, M. L., Francis, P. J., Klaver, C. C., et al. (2011) · American Journal of Epidemiology

Lipoproteins and Cardiovascular HealthRetinal Diseases and Treatments

Cited by 105

Sorsby Fundus Dystrophy: Novel Mutations, Novel Phenotypic Characteristics, and Treatment Outcomes

Gliem, M., Müller, P. L., Mangold, E., Holz, F. G., Bolz, H. J., Stöhr, H., Weber, B. H. F., & Charbel Issa, P. (2015) · Investigative Opthalmology & Visual Science

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 67

Correction: Systemic Complement Activation in Age-Related Macular Degeneration

Scholl, H. P. N., Charbel Issa, P., Walier, M., Janzer, S., Pollok-Kopp, B., Börncke, F., Fritsche, L. G., Chong, N. V., Fimmers, R., Wienker, T., et al. (2008) · PLoS ONE

Complement system in diseasesRetinal Diseases and Treatments

Cited by 39

Dap12 expression in activated microglia from retinoschisin-deficient retina and its PU.1-dependent promoter regulation

Weigelt, K., Ernst, W., Walczak, Y., Ebert, S., Loenhardt, T., Klug, M., Rehli, M., Weber, B. H. F., & Langmann, T. (2007) · Journal of Leukocyte Biology

Neuroinflammation and Neurodegeneration MechanismsRetinal Development and Disorders

Cited by 38

Genetic Association Analysis of Anti-VEGF Treatment Response in Neovascular Age-Related Macular Degeneration

Strunz, T., Pöllmann, M., Gamulescu, M.-A., Tamm, S., & Weber, B. H. F. (2022) · International Journal of Molecular Sciences

Retinal Diseases and TreatmentsRetinal Imaging and Analysis

Cited by 10