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Martin Bäckdahl

Associated

About me

Visiting address: 

L1:00

Karolinska University Hospital Solna 

Publications

Genetic and epigenetic background and protein expression profiles in relation to telomerase activation in medullary thyroid carcinoma
Wang N, Kjellin H, Sofiadis A, Fotouhi O, Juhlin Cc, Bäckdahl M, et al
Oncotarget 2016;7(16):21332-46

HRAS mutation prevalence and associated expression patterns in pheochromocytoma
Stenman A, Welander J, Gustavsson I, Brunaud L, Bäckdahl M, Söderkvist P, et al
Genes, chromosomes & cancer 2016;55(5):452-9

Novel somatic mutations and distinct molecular signature in aldosterone-producing adenomas
Åkerström T, Willenberg Hs, Cupisti K, Ip J, Backman S, Moser A, et al
Endocrine-related cancer 2015;22(5):735-44

Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinoma
Juhlin Cc, Goh G, Healy Jm, Fonseca Al, Scholl Ui, Stenman A, et al
The Journal of clinical endocrinology and metabolism 2015;100(3):E493-502

Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene
Juhlin Cc, Stenman A, Haglund F, Clark Ve, Brown Tc, Baranoski J, et al
Genes, chromosomes & cancer 2015;54(9):542-54

Frequent EPAS1/HIF2α exons 9 and 12 mutations in non-familial pheochromocytoma
Welander J, Andreasson A, Brauckhoff M, Bäckdahl M, Larsson C, Gimm O, et al
Endocrine-related cancer 2014;21(3):495-504

MicroRNA expression patterns associated with hyperfunctioning and non-hyperfunctioning phenotypes in adrenocortical adenomas
Velázquez-fernández D, Caramuta S, Özata Dm, Lu M, Höög A, Bäckdahl M, et al
European journal of endocrinology 2014;170(4):583-91

Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma
Welander J, Andreasson A, Juhlin Cc, Wiseman Rw, Bäckdahl M, Höög A, et al
The Journal of clinical endocrinology and metabolism 2014;99(7):E1352-60

Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas
Kugelberg J, Welander J, Schiavi F, Fassina A, Bäckdahl M, Larsson C, et al
World journal of surgery 2014;38(3):724-32

Telomerase-dependent and independent telomere maintenance and its clinical implications in medullary thyroid carcinoma
Wang N, Xu D, Sofiadis A, Höög A, Vukojević V, Bäckdahl M, et al
The Journal of clinical endocrinology and metabolism 2014;99(8):E1571-9

The activating TERT promoter mutation C228T is recurrent in subsets of adrenal tumors
Liu T, Brown Tc, Juhlin Cc, Andreasson A, Wang N, Bäckdahl M, et al
Endocrine-related cancer 2014;21(3):427-34

Acquired hypermethylation of the P16INK4A promoter in abdominal paraganglioma: relation to adverse tumor phenotype and predisposing mutation
Kiss Nb, Muth A, Andreasson A, Juhlin Cc, Geli J, Bäckdahl M, et al
Endocrine-related cancer 2013;20(1):65-78

Clinical and functional impact of TARBP2 over-expression in adrenocortical carcinoma
Caramuta S, Lee L, Ozata Dm, Akçakaya P, Xie H, Höög A, et al
Endocrine-related cancer 2013;20(4):551-64

The VHL gene is epigenetically inactivated in pheochromocytomas and abdominal paragangliomas
Andreasson A, Kiss Nb, Caramuta S, Sulaiman L, Svahn F, Bäckdahl M, et al
Epigenetics 2013;8(12):1347-54

Anaplastic carcinoma of the thyroid gland: treatment and outcome over 13 years at one institution
Segerhammar I, Larsson C, Nilsson Il, Bäckdahl M, Höög A, Wallin G, et al
Journal of surgical oncology 2012;106(8):981-6

Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter
Åkerström T, Crona J, Delgado Verdugo A, Starker Lf, Cupisti K, Willenberg Hs, et al
PloS one 2012;7(7):e41926-

Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas
Welander J, Larsson C, Bäckdahl M, Hareni N, Sivlér T, Brauckhoff M, et al
Human molecular genetics 2012;21(26):5406-16

The role of microRNA deregulation in the pathogenesis of adrenocortical carcinoma
Ozata Dm, Caramuta S, Velazquez-fernandez D, Akcakaya P, Xie H, Hoog A, et al
ENDOCRINE-RELATED CANCER 2011;18(6):643-55

Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis
Sandgren J, De Stahl Td, Andersson R, Menzel U, Piotrowski A, Nord H, et al
ENDOCRINE-RELATED CANCER 2010;17(3):561-79

The involvement of miR-483 and its host gene IGF2 in development of adrenal cortical carcinoma
Ozata D, Caramuta S, Akcakaya P, Xie Hong, Backdahl M, Larsson C, et al
EJC SUPPLEMENTS 2010;8(5):224-224

Preoperative Tc-99(m)-sestamibi scintigraphy with SPECT localizes most pathologic parathyroid glands
Lindqvist V, Jacobsson H, Chandanos E, Backdahl M, Kjellman M, Wallin G
LANGENBECKS ARCHIVES OF SURGERY 2009;394(5):811-5

Transcriptional profiling enables molecular classification of adrenocortical tumours
Laurell C, Velazquez-fernandez D, Lindsten K, Juhlin C, Enberg U, Geli J, et al
EUROPEAN JOURNAL OF ENDOCRINOLOGY 2009;161(1):141-52

Global and regional CpG methylation in pheochromocytomas and abdominal paragangliomas: Association to malignant behavior
Geli J, Kiss N, Karimi M, Lee Jj, Backdahl M, Ekstrom Tj, et al
CLINICAL CANCER RESEARCH 2008;14(9):2551-9

Methylation of the p16(INK4A) promoter is associated with malignant behavior in abdominal extra-adrenal paragangliomas but not pheochromocytomas
Kiss Nb, Geli J, Lundberg F, Avci C, Velazquez-fernandez D, Hashemi J, et al
ENDOCRINE-RELATED CANCER 2008;15(2):609-21

Operation for primary hyperparathyroidism: The new versus the old order - A randomised controlled trial of preoperative localisation
Aarum S, Nordenstrom J, Reihner E, Zedenius J, Jacobsson H, Danielsson R, et al
SCANDINAVIAN JOURNAL OF SURGERY 2007;96(1):26-30

The Ras effectors NORE1A and RASSF1A are frequently inactivated in pheochromocytoma and abdominal paraganglioma
Geli J, Kiss N, Lanner F, Foukakis T, Natalishvili N, Larsson O, et al
ENDOCRINE-RELATED CANCER 2007;14(1):125-34

Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH
Jarbo C, Buckley Pg, Piotrowski A, Mantripragada Kk, Benetkiewicz M, De Stahl Td, et al
INTERNATIONAL JOURNAL OF CANCER 2006;118(5):1159-64

Predictors of outcome in patients with papillary thyroid carcinoma
Kjellman P, Zedenius J, Lundell G, Backdahl M, Farnebo Lo, Hamberger B, et al
EJSO 2006;32(3):345-52

Deletions and altered expression of the RIZ1 tumour suppressor gene in 1p36 in pheochromocytomas and abdominal paragangliomas
Geli J, Nord B, Frisk T, Elder Ee, Ekstrom Tj, Carling T, et al
INTERNATIONAL JOURNAL OF ONCOLOGY 2005;26(5):1385-91

Expression profiling of adrenocortical neoplasms suggests a molecular signature of malignancy
Velazquez-fernandez D, Laurell C, Geli J, Hoog A, Odeberg J, Kjellman M, et al
SURGERY 2005;138(6):1087-94

Nimodipine and microsurgery induced recovery of the vocal cord after recurrent laryngeal nerve resection
Mattsson P, Bjorck G, Remahl S, Backdahl M, Hamberger B, Hydman J, et al
LARYNGOSCOPE 2005;115(10):1863-5

Ki-67 and hTERT expression can aid in the distinction between malignant and benign pheochromocytoma and paraganglioma
Elder Ee, Xu D, Hoog A, Enberg U, Pisa P, Gruber A, et al
MODERN PATHOLOGY 2003;16(3):246-55

Loss of heterozygosity on the short arm of chromosome 1 in pheochromocytoma and abdominal paraganglioma
Elder Ee, Nord B, Carling T, Juhlin C, Backdahl M, Hoog A, et al
WORLD JOURNAL OF SURGERY 2002;26(8):965-71

Genetic background of adrenocortical tumor development
Kjellman M, Larsson C, Backdahl M
WORLD JOURNAL OF SURGERY 2001;25(7):948-56

In vitro release of aldosterone and cortisol in human adrenal adenomas correlates to mRNA expression of steroidogenic enzymes for genes CYP11B2 and CYP17
Enberg U, Farnebo Lo, Wedell A, Grondal S, Thoren M, Grimelius L, et al
WORLD JOURNAL OF SURGERY 2001;25(7):957-66

Malignant Fibrous Histiocytoma, Aggressive Fibromatosis and Benign Fibrous Tumors Express mRNA for the Metalloproteinase Inducer EMMPRIN and the Metalloproteinases MMP-2 and MT1-MMP
Ahlén J, Enberg U, Larsson C, Larsson O, Frisk T, Brosjö O, et al
Sarcoma 2001;5(3):143-9

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology
Edstrom E, Mahlamaki E, Nord B, Kjellman M, Karhu R, Hoog A, et al
AMERICAN JOURNAL OF PATHOLOGY 2000;156(2):651-9

Expression analysis of RET and the GDNF/GFRa-1 and NTN/GFRa-2 ligand complexes in pheochromocytomas and paragangliomas
Edstrom E, Frisk T, Farnebo F, Hoog A, Backdahl M, Larsson C
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 2000;6(4):469-74

Gelatinase A, membrane type 1 matrix metalloproteinase, and extracellular matrix metalloproteinase inducer mRNA expression: Correlation with invasive growth of breast cancer
Dalberg K, Eriksson E, Enberg U, Kjellman M, Backdahl M
WORLD JOURNAL OF SURGERY 2000;24(3):334-40

Expression of matrix metalloproteinase gelatinase A messenger ribonucleic acid in parathyroid carcinomas
Farnebo F, Svensson A, Thompson Nw, Backdahl M, Grimelius L, Larsson C, et al
SURGERY 1999;126(6):1183-7

Gelatinase A and membrane-type 1 matrix metalloproteinase mRNA: Expressed in adrenocortical cancers but not in adenomas
Kjellman M, Enberg U, Hoog A, Larsson C, Holst M, Farnebo Lo, et al
WORLD JOURNAL OF SURGERY 1999;23(3):237-42

Genotyping of adrenocortical tumors: Very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16
Kjellman M, Roshani L, Teh Bt, Kallioniemi Op, Hoog A, Gray S, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 1999;84(2):730-5

No overrepresentation of congenital adrenal hyperplasia in patients with adrenocortical tumours
Kjellman M, Holst M, Backdahl M, Larsson C, Farnebo Lo, Wedell A
CLINICAL ENDOCRINOLOGY 1999;50(3):343-6

A rapid method for DNA extraction from fine-needle aspiration biopsies of thyroid tumors, and subsequent RET mutation analysis
Zedenius J, Dwight T, Robinson Bg, Delbridge L, Backdahl M, Wallin G, et al
CANCER DETECTION AND PREVENTION 1998;22(6):544-8

Telomerase activity in lesions of the thyroid: Application to diagnosis of clinical samples including fine-needle aspirates
Aogi K, Kitahara K, Buley I, Backdahl M, Tahara H, Sugino T, et al
CLINICAL CANCER RESEARCH 1998;4(8):1965-70

Tumor-specific decreased expression of calcium sensing receptor messenger ribonucleic acid in sporadic primary hyperparathyroidism
Farnebo F, Enberg U, Grimelius L, Backdahl M, Schalling M, Larsson C, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 1997;82(10):3481-6

Alterations of p53 and expression of WAF1/p21 in human thyroid tumors
Zedenius J, Larsson C, Wallin G, Backdahl M, Aspenblad U, Hoog A, et al
THYROID 1996;6(1):1-9

Deletions of the long arm of chromosome 10 in progression of follicular thyroid tumors
Zedenius J, Wallin G, Svensson A, Bovee J, Hoog A, Backdahl M, et al
HUMAN GENETICS 1996;97(3):299-303

Genetic aberrations in adrenocortical tumors detected using comparative genomic hybridization correlate with tumor size and malignancy
Kjellman M, Kallioniemi Op, Karhu R, Hoog A, Farnebo Lo, Auer G, et al
CANCER RESEARCH 1996;56(18):4219-23

Stromal fibroblasts adjacent to invasive thyroid tumors: Expression of gelatinase a but not stromelysin 3 mRNA
Zedenius J, Stahlebackdahl M, Enberg U, Grimelius L, Larsson C, Wallin G, et al
WORLD JOURNAL OF SURGERY 1996;20(1):101-6

ALLELOTYPING OF FOLLICULAR THYROID-TUMORS
Zedenius J, Wallin G, Svensson A, Grimelius L, Hoog A, Lundell G, et al
HUMAN GENETICS 1995;96(1):27-32

ESTROGEN TARGET TISSUE DETERMINES ALTERNATIVE PROMOTER UTILIZATION OF THE HUMAN ESTROGEN-RECEPTOR GENE IN OSTEOBLASTS AND TUMOR-CELL LINES
Grandien K, Backdahl M, Ljunggren O, Gustafsson Ja, Berkenstam A
ENDOCRINOLOGY 1995;136(5):2223-9

MUTATIONS OF CODON-918 IN THE RET PROTOONCOGENE CORRELATE TO POOR-PROGNOSIS IN SPORADIC MEDULLARY-THYROID CARCINOMAS
Zedenius J, Larsson C, Bergholm U, Bovee J, Svensson A, Hallengren B, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 1995;80(10):3088-90

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