Maren Sullivan

发表

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.

G. Rasp, T. Stöver, K. Zerres, 2009, Cancer research.

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.

C. Eng, I. Harsch, H. Neumann, 2010, The Journal of clinical endocrinology and metabolism.

Systematic comparison of sporadic and syndromic pancreatic islet cell tumors.

M. Fasshauer, L. Fischer, C. Eng, 2010, Endocrine-related cancer.

Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3.

G. Rasp, S. Değer, C. Eng, 2012, Endocrine-related cancer.

Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.

M. Litwin, C. Eng, H. Neumann, 2008, The Journal of clinical endocrinology and metabolism.

Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites.

C. Eng, K. Schmid, H. Neumann, 2011, The Journal of clinical endocrinology and metabolism.

Age‐Related Penetrance of Hereditary Atypical Hemolytic Uremic Syndrome

C. Eng, T. Fehr, K. Budde, 2011, Annals of human genetics.

Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.

C. Eng, H. Neumann, I. Zosin, 2008, Endocrine-related cancer.

Epidemiological Approach to Identifying Genetic Predispositions for Atypical Hemolytic Uremic Syndrome

K. Budde, H. Neumann, M. Zeier, 2010, Annals of human genetics.