Reiner Caspari

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444

Reiner Caspari, S Olschwang, Waltraut Friedl et al. · Human Molecular Genetics · 1995 · 367 citations

Comparison of Capsule Endoscopy and Magnetic Resonance Imaging for the Detection of Polyps of the Small Intestine in Patients with Familial Adenomatous Polyposis or with Peutz-Jeghers’ Syndrome

Reiner Caspari, M von Falkenhausen, C Krautmacher et al. · Endoscopy · 2004 · 234 citations

Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer

Reiner Caspari, Waltraut Friedl, Marion Mandl et al. · The Lancet · 1994 · 224 citations

Somatic Variant, Cancer Pathology, Early Onset +10

<i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

Stefan Aretz, Siegfried Uhlhaas, Heike Goergens et al. · International Journal of Cancer · 2006 · 194 citations · Full text

Biallelic Mutations, Genetic Disorder, Medicine +11

Attenuated familial adenomatous polyposis due to a mutation in the 3′ part of the APC gene. A clue for understanding the function of the APC protein

Waltraut Friedl, Stephanie Meuschel, C. Lamberti et al. · Human Genetics · 1996 · 168 citations

Genetic Disorder, Familial Adenomatous Polyposis, Genetics +9