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Hartmut P. H. Neumann

Hartmut P. H. Neumann

D-Index & Metrics

Medicine

D-Index
89
Citations
27454
World Ranking
12753
National Ranking
683

Overview

Hartmut P. H. Neumann is affiliated with the University of Freiburg in Germany. Their research primarily spans the fields of Medicine and Biochemistry, Genetics, and Molecular Biology, with a focus on subfields including Endocrinology, Diabetes and Metabolism, Cancer Research, Surgery, Molecular Biology, and Oncology.

Their work addresses several main topics, notably:

  • Cancer, Hypoxia, and Metabolism
  • Adrenal and Paraganglionic Tumors
  • Hormonal Regulation and Hypertension
  • Pituitary Gland Disorders and Treatments
  • Neuroblastoma Research and Treatments
  • Glioma Diagnosis and Treatment
  • Neuroendocrine Tumor Research Advances

Recent publications by Neumann include:

  • "Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature," 2020, The Lancet Diabetes & Endocrinology
  • "Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment," 2020, Child's Nervous System
  • "Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicine," 2020, Human Molecular Genetics
  • "Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study," 2020, Endocrine Connections
  • "SDHB variant type impacts phenotype and malignancy in pheochromocytoma-paraganglioma," 2021, Journal of Medical Genetics

Across their career, Neumann has published frequently in venues such as Endocrine Connections, The Lancet Diabetes & Endocrinology, Child's Nervous System, Human Molecular Genetics, and the Journal of Medical Genetics.

Their collaboration network includes frequent co-authors:

  • Birke Bausch
  • Charis Eng
  • Nelson Wohllk
  • Thera P. Links
  • Mariola Pęczkowska

Neumann's research often intersects clinical medicine and molecular biology, emphasizing genetic and phenotypic characterization of endocrine tumors and related metabolic disorders. Their studies contribute to understanding the genetic underpinnings and clinical manifestations of diseases such as phaeochromocytoma, paraganglioma, multiple endocrine neoplasia, and von Hippel-Lindau disease.

Best Publications

  • Germ-line mutations in nonsyndromic pheochromocytoma.

    Hartmut P.H. Neumann;Birke Bausch;Sarah R. McWhinney;Bernhard U. Bender

  • Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.

    Hartmut P. H. Neumann;Christian Pawlu;Mariola Pęczkowska;Birke Bausch

  • Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.

    Lois M. Mulligan;Lois M. Mulligan;Charis Eng;Catherine S. Healey;David Clayton

  • von Hippel–Lindau disease: A clinical and scientific review

    Eamonn R. Maher;Hartmut P.H. Neumann;Stéphane Richard

  • Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.

    Berton Zbar;Takeshi Kishida;Fan Chen;Laura Schmidt

  • Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau Disease

    Hartmut Neumann;Dietmar P. Berger;Gunther Sigmund;Ulrich Blum

  • Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

    L. Schmidt;K. Junker;N. Nakaigawa;T. Kinjerski

  • Pheochromocytoma and Paraganglioma.

    Hartmut P H Neumann;William F Young;Charis Eng

  • Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome.

    Hartmut P. H. Neumann;Hans R. Eggert;Klaus Weigel;Hartmut Friedburg

  • Posterior retroperitoneoscopic adrenalectomy--results of 560 procedures in 520 patients.

    Martin K. Walz;Piero F. Alesina;Frank A. Wenger;Anastasios Deligiannis

  • Malignant pheochromocytoma: Current status and initiatives for future progress

    Graeme Eisenhofer;Stefan R. Bornstein;Frederieke M. Brouwers;Nai Kong V. Cheung

  • Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma

    Sakari Vanharanta;Mary Buchta;Sarah R. McWhinney;Sanna K. Virta

  • Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

    Tamara Manuelian;Jens Hellwage;Seppo Meri;Jessica Caprioli

  • Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.

    Francesca Schiavi;Carsten C. Boedeker;Birke Bausch;Mariola Peçzkowska

  • Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus.

    H.P.H. Neumann;O.D. Wiestler

  • Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

    Edgar A Otto;Toby W Hurd;Rannar Airik;Moumita Chaki

  • Pheochromocytomas: detection with 18F DOPA whole body PET--initial results..

    Stefan Hoegerle;Egbert Nitzsche;Carsten Altehoefer;Nadir Ghanem

  • LAPAROSCOPIC SURGERY FOR PHEOCHROMOCYTOMA: ADRENALECTOMY, PARTIAL RESECTION, EXCISION OF PARAGANGLIOMAS

    Gunter Janetschek;Gerd Finkenstedt;Rudolph Gasser;Ursula G. Waibel

  • Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

    H P H Neumann;M Salzmann;B Bohnert-Iwan;T Mannuelian

  • Pheochromocytoma: presentation, diagnosis and treatment

    Nicole Reisch;Mariola Peczkowska;Andrzej Januszewicz;Hartmut P H Neumann

Frequent Co-Authors

Charis Eng
Charis Eng Cleveland Clinic Lerner College of Medicine
Kurt Werner Schmid
Kurt Werner Schmid University of Duisburg-Essen
Eamonn R. Maher
Eamonn R. Maher University of Cambridge
Hiltrud Brauch
Hiltrud Brauch German Cancer Research Center
Klaus Zerres
Klaus Zerres RWTH Aachen University
William F. Young
William F. Young Mayo Clinic
Lois M. Mulligan
Lois M. Mulligan Queen's University
Berton Zbar
Berton Zbar National Institutes of Health
Massimo Mannelli
Massimo Mannelli University of Florence

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