Samuel Backman
ST-läkare vid Institutionen för kirurgiska vetenskaper; Endokrinkirurgi
- Telefon:
- 018-471 47 06
- E-post:
- samuel.backman@uu.se
- Besöksadress:
- Akademiska sjukhuset, ingång 70, 1 tr
751 85 UPPSALA - Postadress:
- Akademiska sjukhuset, ingång 70, 1 tr
751 85 UPPSALA
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Publikationer
Urval av publikationer
- Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause (2021)
- Whole genome sequencing of apparently mutation-negative MEN1 patients (2020)
- Spatiotemporal Heterogeneity Characterizes the Genetic Landscape of Pheochromocytoma and Defines Early Events in Tumorigenesis. (2015)
Senaste publikationer
- Pan-genomic characterization of high-risk pediatric papillary thyroid carcinoma (2021)
- Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause (2021)
- Molecular studies of endocrine tumors (2020)
- Whole genome sequencing of apparently mutation-negative MEN1 patients (2020)
- Whole‐genome sequencing of synchronous thyroid carcinomas identifies aberrant DNA repair in thyroid cancer dedifferentiation (2020)
Alla publikationer
Artiklar
- Pan-genomic characterization of high-risk pediatric papillary thyroid carcinoma (2021)
- Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause (2021)
- Whole genome sequencing of apparently mutation-negative MEN1 patients (2020)
- Whole‐genome sequencing of synchronous thyroid carcinomas identifies aberrant DNA repair in thyroid cancer dedifferentiation (2020)
- RNA Sequencing Provides Novel Insights into the Transcriptome of Aldosterone Producing Adenomas (2019)
- Epigenetics of pheochromocytoma and paraganglioma (2018)
- RNA-Sequencing Analysis of Adrenocortical Carcinoma, Pheochromocytoma and Paraganglioma from a Pan-Cancer Perspective (2018)
- Comprehensive analysis of CTNNB1 in adrenocortical carcinomas (2018)
- Global DNA Methylation Analysis Identifies Two Discrete clusters of Pheochromocytoma with Distinct Genomic and Genetic Alterations (2017)
- Detection of Somatic Mutations in Gastroenteropancreatic Neuroendocrine Tumors Using Targeted Deep Sequencing (2017)
- Spatiotemporal Heterogeneity Characterizes the Genetic Landscape of Pheochromocytoma and Defines Early Events in Tumorigenesis. (2015)
- Novel somatic mutations and distinct molecular signature in aldosterone-producing adenomas. (2015)
- Potential prognostic markers and candidate genetic drivers in small intestine neuroendocrine tumours
- TFF3 in primary tumours has a negative impact on survival in small intestinal neuroendocrine tumours
Böcker
Konferenser
