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Oncogene|October 19, 2002
Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patientsAurel Perren, André Barghorn, Sonja Schmid, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|May 27, 2003
PTEN as a molecular marker to distinguish metastatic from primary synchronous endometrioid carcinomas of the ovary and uterusRomeo Ricci, Paul Komminoth, Fridolin Bannwart, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 26, 2003
DPC4/Smad4: no mutations, rare allelic imbalances, and retained protein expression in pancreatic endocrine tumorsAurel Perren, Parvin Saremaslani, Sonja Schmid, et al.
Anticancer Research|March 16, 2004
CGH analysis shows genetic similarities and differences in atypical fibroxanthoma and undifferentiated high grade pleomorphic sarcomaDaniela Mihic-Probst, Jianming Zhao, Parvin Saremaslani, et al.
Virchows Archiv : an International Journal of Pathology|August 9, 2007
Hereditary neuroendocrine tumors of the gastroenteropancreatic systemMartin Anlauf, Nele Garbrecht, Juliane Bauersfeld, et al.
Virchows Archiv : an International Journal of Pathology|April 11, 2002
Loss of heterozygosity at chromosome 6q23-25 correlates with clinical and histologic parameters in salivary gland adenoid cystic carcinomaIngrid Stallmach, Petra Zenklusen, Paul Komminoth, et al.
The American Journal of Surgical Pathology|February 28, 2008
Islet 1 (Isl1) expression is a reliable marker for pancreatic endocrine tumors and their metastasesAnja M Schmitt, Florian Riniker, Martin Anlauf, et al.
The American Journal of Pathology|March 14, 2002
High frequency of t(14;18)-translocation breakpoints outside of major breakpoint and minor cluster regions in follicular lymphomas: improved polymerase chain reaction protocols for their detectionAndrea Albinger-Hegyi, Bernhard Hochreutener, Marie-Therese Abdou, et al.
Gastroenterology|May 12, 2005
Precursor lesions in patients with multiple endocrine neoplasia type 1-associated duodenal gastrinomasMartin Anlauf, Aurel Perren, Cora Lu Meyer, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2004
A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomasMargarete Maier-Woelfle, Michael Brändle, Paul Komminoth, et al.
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