Oliver Gimm

Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene

Jenny Welander, Gerald Goh, Stefano Caramuta, 2015, Genes, chromosomes & cancer.

Caveolin-1 and caveolin-2,together with three bone morphogenetic protein-related genes, may encode novel tumor suppressors down-regulated in sporadic follicular thyroid carcinogenesis.

Charis Eng, Christoph Plass, Sissy M Jhiang, 2003, Cancer research.

TFF3-based candidate gene discrimination of benign and malignant thyroid tumors in a region with borderline iodine deficiency.

M. Eszlinger, K. Krause, D. Fuhrer, 2008, The Journal of clinical endocrinology and metabolism.

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.

Louise Izatt, Marc Tischkowitz, Anneke Lucassen, 2007, The Journal of clinical endocrinology and metabolism.

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Jenny Welander, Diana E. Benn, Patricia L. M. Dahia, 2017, Nature Reviews Endocrinology.

Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.

Jenny Welander, Adam Andreasson, C. Larsson, 2014, The Journal of clinical endocrinology and metabolism.

Risk factors of paralysis and functional outcome after recurrent laryngeal nerve monitoring in thyroid surgery.

Johannes Haerting, Hans Lippert, J. Haerting, 2004, Surgery.

Timing and Extent of Surgery in Patients with Familial Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia 2A-related RET Mutations Not Affecting Codon 634

Phuong Nguyen Thanh, H. Dralle, B. Niederle, 2004, World Journal of Surgery.