|Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement …|
A Rivera, SA Fisher, LG Fritsche, CN Keilhauer, P Lichtner, T Meitinger, ...
Human molecular genetics 14 (21), 3227-3236, 2005
|A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants|
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
|Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy|
BHF Weber, G Vogt, RC Pruett, H Stöhr, U Felbor
Nature genetics 8 (4), 352-356, 1994
|Seven new loci associated with age-related macular degeneration|
AMD Gene Consortium
Nature genetics 45 (4), 433, 2013
|An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness|
TM Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, ...
Nature genetics 19 (3), 260-263, 1998
|Positional cloning of the gene associated with X-linked juvenile retinoschisis|
CG Sauer, A Gehrig, R Warneke-Wittstock, A Marquardt, CC Ewing, ...
Nature genetics 17 (2), 164-170, 1997
|Silk properties determined by gland-specific expression of a spider fibroin gene family|
PA Guerette, DG Ginzinger, BHF Weber, JM Gosline
Science 272 (5258), 112-115, 1996
|Microglia activation in retinal degeneration|
Journal of leukocyte biology 81 (6), 1345-1351, 2007
|Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA|
LG Fritsche, T Loenhardt, A Janssen, SA Fisher, A Rivera, CN Keilhauer, ...
Nature genetics 40 (7), 892-896, 2008
|Systemic complement activation in age-related macular degeneration|
HPN Scholl, PC Issa, M Walier, S Janzer, B Pollok-Kopp, F Börncke, ...
PloS one 3 (7), e2593, 2008
|Mutations in a Novel Gene, VMD2; Encoding a Protein of Unknown Properties Cause Juvenile-Onset Vitelliform Macular Dystrophy (Best's Disease)|
A Marquardt, H Stöhr, LA Passmore, F Krämer, A Rivera, BHF Weber
Human molecular genetics 7 (9), 1517-1525, 1998
|Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer|
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
|A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration|
A Rivera, K White, H Stöhr, K Steiner, N Hemmrich, T Grimm, B Jurklies, ...
The American Journal of Human Genetics 67 (4), 800-813, 2000
|cDNA cloning, genomic structure, and chromosomal localization of three members of the human fatty acid desaturase family|
A Marquardt, H Stöhr, K White, BHF Weber
Genomics 66 (2), 175-183, 2000
|Meta-analysis of genome scans of age-related macular degeneration|
SA Fisher, GR Abecasis, BM Yashar, S Zareparsi, A Swaroop, SK Iyengar, ...
Human molecular genetics 14 (15), 2257-2264, 2005
|Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk|
FJ Couch, X Wang, L McGuffog, A Lee, C Olswold, KB Kuchenbaecker, ...
PLoS Genet 9 (3), e1003212, 2013
|Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular …|
F Krämer, K White, D Pauleikhoff, A Gehrig, L Passmore, A Rivera, ...
European Journal of Human Genetics 8 (4), 286-292, 2000
|Characterization of ATM Gene Mutations in 66 Ataxia Telangiectasia Families|
N Sandoval, M Platzer, A Rosenthal, T Dörk, R Bendix, B Skawran, ...
Human molecular genetics 8 (1), 69-79, 1999
|The CREATE project: development of certified reference materials for allergenic products and validation of methods for their quantification|
R Van Ree, MD Chapman, F Ferreira, S Vieths, D Bryan, O Cromwell, ...
Multidisciplinary Approaches to Allergies, 149-179, 2012
|TMEM16B, a novel protein with calcium-dependent chloride channel activity, associates with a presynaptic protein complex in photoreceptor terminals|
H Stöhr, JB Heisig, PM Benz, S Schöberl, VM Milenkovic, O Strauss, ...
Journal of Neuroscience 29 (21), 6809-6818, 2009