B. Weber

A BRCA2 germ‐line mutation in familial pancreatic carcinoma

K. White, K. Held, Bernhard Weber, 2001, International journal of cancer.

Assessment of RS1 in X‐linked juvenile retinoschisis and sporadic senile retinoschisis

B. Lorenz, B. Weber, A. Gehrig, 1999, Clinical genetics.

VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies

A. Marquardt, K. White, B. Weber, 2000, Human mutation.

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 degeneration

B. Lorenz, B. Jurklies, F. Holz, 2000, European Journal of Human Genetics.

Sorsby fundus dystrophy mutation Timp3S156C affects the morphological and biochemical phenotype but not metalloproteinase homeostasis

H. Schrewe, B. Weber, G. Soboleva, 2003, Journal of cellular physiology.

Membrane‐associated guanylate kinase proteins MPP4 and MPP5 associate with Veli3 at distinct intercellular junctions of the neurosensory retina

H. Stöhr, A. Reichenbach, L. Molday, 2005, The Journal of comparative neurology.

Characterization of ATM gene mutations in 66 ataxia telangiectasia families.

T. Dörk, Y. Shiloh, A. Rosenthal, 1999, Human molecular genetics.