Birke Bausch

University of Freiburg — Germany

Medicine · Health Sciences

26h-index3.8kcitations60works0.02yr avg
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Research Topics

Adrenal and Paraganglionic Tumors(37), Cancer, Hypoxia, and Metabolism(22), Pituitary Gland Disorders and Treatments(19), Hormonal Regulation and Hypertension(14), Neuroblastoma Research and Treatments(12)

Publications59 total

Genotype-specific neoplastic risk profiles in patients with VHL disease
Endocrine Related Cancer·2025Open Access
Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency
Journal of Clinical Immunology·2022· 14 citedOpen Access
<i>SDHB</i> variant type impacts phenotype and malignancy in pheochromocytoma-paraganglioma
Journal of Medical Genetics·2021· 15 cited
Clinical decision making in small non-functioning VHL-related incidentalomas
Endocrine Connections·2020· 3 citedOpen Access
Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment
Child s Nervous System·2020· 65 citedOpen Access
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma
Journal of Medical Genetics·2019· 26 citedOpen Access
Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy
JAMA Network Open·2019· 128 citedOpen Access
OR29-4 Pregnancy Outcomes in Women with Pheochromocytoma and Paraganglioma: An International Multi-Center Study
Journal of the Endocrine Society·2019Open Access
Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study
The Lancet Diabetes & Endocrinology·2019· 144 citedOpen Access
65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma
Endocrine Related Cancer·2018· 70 citedOpen Access
Preventive medicine of von Hippel–Lindau disease-associated pancreatic neuroendocrine tumors
Endocrine Related Cancer·2018· 67 citedOpen Access
Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 Patients
World Journal of Surgery·2018· 35 cited
Prevention Medicine in Bilateral Phaeochromocytoma
SSRN Electronic Journal·2018Open Access
Max Schottelius: Pioneer in Pheochromocytoma
Journal of the Endocrine Society·2017· 23 citedOpen Access
The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations
Endocrine Related Cancer·2017· 31 citedOpen Access
Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes <i>SDHA</i>, <i>TMEM127</i>, <i>MAX</i>, and <i>SDHAF2</i> for Gene-Informed Prevention
JAMA Oncology·2017· 195 citedOpen Access
Characterization of endolymphatic sac tumors and von Hippel–Lindau disease in the International Endolymphatic Sac Tumor Registry
Head & Neck·2015· 65 citedOpen Access
Fibroscan der Leber
DMW - Deutsche Medizinische Wochenschrift·2015
A registry-based study of thyroid paraganglioma: histological and genetic characteristics
Endocrine Related Cancer·2015· 32 citedOpen Access
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study
The Lancet Oncology·2014· 178 citedOpen Access
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Frequent Co-authors

Hartmut P.H. Neumann(32), Charis Eng(22), Martin K. Walz(14), Mariola Pęczkowska(14), Andrzej Januszewicz(12), Francesca Schiavi(11), Giuseppe Opocher(11), Oliver Gimm(9), Kornelia Hasse-Lazar(9), Carsten C. Boedeker(9), Thera P. Links(9), Attila Patócs(8), Frédéric Castinetti(8), Nelson Wohllk(8), Marta Barontini(8), Tobias Krauß(8), Angelica Malinoc(7), Barbara Jarząb(7), Ernst von Dobschuetz(7), Claudio Letizia(7)