Author

Susanne Rondot

Observed names: Rondot, Susanne, S Rondot, S. Rondot, S. Rondot

Observed institution: Heidelberg University

OpenAlex ID: A5037873612

Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotype

2006 · K Frank-Raue, H Buhr, et al. · European Journal of Endocrinology · 130

Prevalence and Clinical Spectrum of Nonsecretory Medullary Thyroid Carcinoma in a Series of 839 Patients with Sporadic Medullary Thyroid Carcinoma

2012 · Karin Frank-Raue, Andreas Machens, et al. · Thyroid · 119

Molecular genetics and phenomics of RET mutations: Impact on prognosis of MTC

2010 · Karin Frank-Raue, Susanne Rondot, et al. · Molecular and Cellular Endocrinology · 108

Mutational Spectrum of the Steroid 21-Hydroxylase Gene in Austria: Identification of a Novel Missense Mutation

2001 · S. M. Baumgartner-Parzer, E. Schulze, et al. · The Journal of Clinical Endocrinology & Metabolism · 74

Characterization of the RET protooncogene transmembrane domain mutation S649L associated with nonaggressive medullary thyroid carcinoma.

2008 · Mario Colombo-Benkmann, Zhenpeng Li, et al. · European Journal of Endocrinology · 46

Clinical relevance of RET variants G691S, L769L, S836S and S904S to sporadic medullary thyroid cancer

2011 · Andreas Machens, Karin Frank‐Raue, et al. · Clinical Endocrinology · 36

Change in the spectrum of RET mutations diagnosed between 1994 and 2006.

2007 · Karin Frank-Raue, Susanne Rondot, et al. · PubMed · 35

Coincidence of Multiple Endocrine Neoplasia Types 1 and 2: Mutations in theRETProtooncogene andMEN1Tumor Suppressor Gene in a Family Presenting with Recurrent Primary Hyperparathyroidism

2005 · Karin Frank-Raue, Susanne Rondot, et al. · The Journal of Clinical Endocrinology & Metabolism · 26

New Mutations in the RET Protooncogene-L881V – Associated with Medullary Thyroid Carcinoma and -R770Q – in a Patient with Mixed Medullar/Follicular Thyroid Tumour

2009 · K. Frank-Raue, J. Döhring, et al. · Experimental and Clinical Endocrinology & Diabetes · 21

Primary Hyperparathyroidism as the Leading Symptom in a Patient with a Y791F RET Mutation

2005 · H. Vierhapper, S. Rondot, et al. · Thyroid · 16

Hereditäre Formen des primären Hyperparathyreoidismus

2011 · K Frank-Raue, G Leidig-Bruckner, et al. · DMW - Deutsche Medizinische Wochenschrift · 13

Hereditäres medulläres Schilddrüsenkarzinom - Genotyp - Phänotyp Charakterisierung

2003 · K. Frank-Raue, C. Heimbach, et al. · DMW - Deutsche Medizinische Wochenschrift · 13

Multiple endocrine neoplasia type 1 associated with a new germline Men1 mutation in a family with atypical tumor phenotype

2015 · Nikolaos Perakakis, Felix Flohr, et al. · HORMONES · 11

[Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT].

2011 · K Frank-Raue, G Leidig-Bruckner, et al. · PubMed · 7

Clinical utility gene card for: multiple endocrine neoplasia type 2

2011 · Friedhelm Raue, Susanne Rondot, et al. · European Journal of Human Genetics · 7

PDF

Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation

2022 · Christoph Welsch, Anna Katharina Flügel, et al. · BMC Endocrine Disorders · 4

PDF

Hereditäre Formen des primären Hyperparathyreoidismus

2006 · F. Raue, C. Haag, et al. · Osteologie/Osteology · 2

Pitfalls in the genetic diagnosis of MEN 2

2004 · S Rondot, H Vierhapper, et al. · Experimental and Clinical Endocrinology & Diabetes · 1

Men1 gene novel mutation caused bilaterral parathyroid carcinomas : case reports

2008 · Juodelė, Linas, Kučinskas, Laimutis, et al. · Lithuanian University of Health Sciences

Two new mutations in the RET protooncogene: R770Q in coincidence with Y791N in the same family with medullary thyroid carcinoma

2008 · Susanne Rondot, Angela Lorenz, et al. · 10th European Congress of Endocrinology

Men1 Mutation Caused Bilateral Parathyroide Carcinomas: Case Report

2008 · Linas Juodelė, Laimutis Kučinskas, et al. · Lithuanian University of Health Sciences

First Expierence of Men2 Syndrome Genetic Diagnosis in Lithuania

2008 · Linas Juodelė, Laimutis Kučinskas, et al. · Lithuanian University of Health Sciences

Case report: A 49y-old female patient with MEN 1 syndrome shows a new mutation in the MEN 1 gene

2007 · E Spilcke-Liss, S Rondot, et al. · Experimental and Clinical Endocrinology & Diabetes

Genetic analysis of multiple endocrine neoplasia type 1 by direct sequencing and multiplex ligation dependent probe amplification (MLPA)

2007 · S Rondot, K Frank-Raue, et al. · Experimental and Clinical Endocrinology & Diabetes

Molekulargenetische Diagnostik in der Osteologie - Ein Überblick über die angewandten Methoden

2006 · S. Clausmeyer, Ch. Haag, et al. · Osteologie/Osteology

Works count: 28

Citation count: 669

H-index: 12

I10-index: 13