Klaus Zerres

Germ-Line Mutations in Nonsyndromic Pheochromocytoma

Hartmut P.H. Neumann, Birke Bausch, Sarah R. McWhinney et al. · New England Journal of Medicine · 2002 · 1.4K citations · Full text

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3

Linda M. Brzustowicz, Thomas Lehner, Lucio H. Castilla et al. · Nature · 1990 · 617 citations

Developmental Biology, Genetic Disorder, Genetics +5

Natural History in Proximal Spinal Muscular Atrophy

Klaus Zerres · Archives of Neurology · 1995 · 541 citations

PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats

Luiz F. Onuchic, Laszlo Furu, Yasuyuki Nagasawa et al. · The American Journal of Human Genetics · 2002 · 506 citations · Full text

Signaling Pathway, Autoimmune Disease, Disease Mechanism +13

Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype Correlation, and Implications for Genetic Counseling

Brunhilde Wirth, Micaela A. Godoy Herz, A Wetter et al. · The American Journal of Human Genetics · 1999 · 361 citations · Full text

Rare Diseases, Genetic Disorder, Genetics +9