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Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing

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Harvard

Rohlin, A, Rambech, E, Kvist, A, Törngren, T, Eiengård, F, Lundstam, U, Zagoras, T, Gebre-Medhin, S, Borg, Å, Björk, J, Nilbert, M & Nordling, M 2017, 'Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing', Familial Cancer, bind 16, nr. 2, s. 195-203. https://doi.org/10.1007/s10689-016-9934-0

APA

Rohlin, A., Rambech, E., Kvist, A., Törngren, T., Eiengård, F., Lundstam, U., Zagoras, T., Gebre-Medhin, S., Borg, Å., Björk, J., Nilbert, M., & Nordling, M. (2017). Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing. Familial Cancer, 16(2), 195-203. https://doi.org/10.1007/s10689-016-9934-0

CBE

Rohlin A, Rambech E, Kvist A, Törngren T, Eiengård F, Lundstam U, Zagoras T, Gebre-Medhin S, Borg Å, Björk J, Nilbert M, Nordling M. 2017. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing. Familial Cancer. 16(2):195-203. https://doi.org/10.1007/s10689-016-9934-0

MLA

Vancouver

Author

Rohlin, Anna ; Rambech, Eva ; Kvist, Anders ; Törngren, Therese ; Eiengård, Frida ; Lundstam, Ulf ; Zagoras, Theofanis ; Gebre-Medhin, Samuel ; Borg, Åke ; Björk, Jan ; Nilbert, Mef ; Nordling, Margareta. / Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing. I: Familial Cancer. 2017 ; Bind 16, Nr. 2. s. 195-203.

Bibtex

@article{ac62ffa6a0b244ba94185b42d07705e2,
title = "Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing",
abstract = "Hereditary syndromes causing colorectal cancer include both polyposis and non-polyposis syndromes. Overlapping phenotypes between the syndromes have been recognized and this make targeted molecular testing for single genes less favorable, instead there is a gaining interest for multi-gene panel-based approaches detecting both SNVs, indels and CNVs in the same assay. We applied a panel including 19 CRC susceptibility genes to 91 individuals of six phenotypic subgroups. Targeted NGS-based sequencing of the whole gene regions including introns of the 19 genes was used. The individuals had a family history of CRC or had a phenotype consistent with a known CRC syndrome. The purpose of the study was to demonstrate the diagnostic difficulties linked to genotype-phenotype diversity and the benefits of using a gene panel. Pathogenicity classification was carried out on 46 detected variants. In total we detected sixteen pathogenic or likely pathogenic variants and 30 variants of unknown clinical significance. Four of the pathogenic or likely pathogenic variants were found in BMPR1A in patients with unexplained familial adenomatous polyposis or atypical adenomatous polyposis, which extends the genotype-phenotype spectrum for this gene. Nine patients had more than one variant remaining after the filtration, including three with truncating mutations in BMPR1A, PMS2 and AXIN2. CNVs were found in three patients, in upstream regions of SMAD4, MSH3 and CTNNB1, and one additional individual harbored a 24.2 kb duplication in CDH1 intron1.",
author = "Anna Rohlin and Eva Rambech and Anders Kvist and Therese T{\"o}rngren and Frida Eieng{\aa}rd and Ulf Lundstam and Theofanis Zagoras and Samuel Gebre-Medhin and {\AA}ke Borg and Jan Bj{\"o}rk and Mef Nilbert and Margareta Nordling",
year = "2017",
month = apr,
doi = "10.1007/s10689-016-9934-0",
language = "English",
volume = "16",
pages = "195--203",
journal = "Familial Cancer",
issn = "1389-9600",
publisher = "Springer Netherlands",
number = "2",

}

RIS

TY - JOUR

T1 - Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing

AU - Rohlin, Anna

AU - Rambech, Eva

AU - Kvist, Anders

AU - Törngren, Therese

AU - Eiengård, Frida

AU - Lundstam, Ulf

AU - Zagoras, Theofanis

AU - Gebre-Medhin, Samuel

AU - Borg, Åke

AU - Björk, Jan

AU - Nilbert, Mef

AU - Nordling, Margareta

PY - 2017/4

Y1 - 2017/4

N2 - Hereditary syndromes causing colorectal cancer include both polyposis and non-polyposis syndromes. Overlapping phenotypes between the syndromes have been recognized and this make targeted molecular testing for single genes less favorable, instead there is a gaining interest for multi-gene panel-based approaches detecting both SNVs, indels and CNVs in the same assay. We applied a panel including 19 CRC susceptibility genes to 91 individuals of six phenotypic subgroups. Targeted NGS-based sequencing of the whole gene regions including introns of the 19 genes was used. The individuals had a family history of CRC or had a phenotype consistent with a known CRC syndrome. The purpose of the study was to demonstrate the diagnostic difficulties linked to genotype-phenotype diversity and the benefits of using a gene panel. Pathogenicity classification was carried out on 46 detected variants. In total we detected sixteen pathogenic or likely pathogenic variants and 30 variants of unknown clinical significance. Four of the pathogenic or likely pathogenic variants were found in BMPR1A in patients with unexplained familial adenomatous polyposis or atypical adenomatous polyposis, which extends the genotype-phenotype spectrum for this gene. Nine patients had more than one variant remaining after the filtration, including three with truncating mutations in BMPR1A, PMS2 and AXIN2. CNVs were found in three patients, in upstream regions of SMAD4, MSH3 and CTNNB1, and one additional individual harbored a 24.2 kb duplication in CDH1 intron1.

AB - Hereditary syndromes causing colorectal cancer include both polyposis and non-polyposis syndromes. Overlapping phenotypes between the syndromes have been recognized and this make targeted molecular testing for single genes less favorable, instead there is a gaining interest for multi-gene panel-based approaches detecting both SNVs, indels and CNVs in the same assay. We applied a panel including 19 CRC susceptibility genes to 91 individuals of six phenotypic subgroups. Targeted NGS-based sequencing of the whole gene regions including introns of the 19 genes was used. The individuals had a family history of CRC or had a phenotype consistent with a known CRC syndrome. The purpose of the study was to demonstrate the diagnostic difficulties linked to genotype-phenotype diversity and the benefits of using a gene panel. Pathogenicity classification was carried out on 46 detected variants. In total we detected sixteen pathogenic or likely pathogenic variants and 30 variants of unknown clinical significance. Four of the pathogenic or likely pathogenic variants were found in BMPR1A in patients with unexplained familial adenomatous polyposis or atypical adenomatous polyposis, which extends the genotype-phenotype spectrum for this gene. Nine patients had more than one variant remaining after the filtration, including three with truncating mutations in BMPR1A, PMS2 and AXIN2. CNVs were found in three patients, in upstream regions of SMAD4, MSH3 and CTNNB1, and one additional individual harbored a 24.2 kb duplication in CDH1 intron1.

U2 - 10.1007/s10689-016-9934-0

DO - 10.1007/s10689-016-9934-0

M3 - Journal article

C2 - 27696107

VL - 16

SP - 195

EP - 203

JO - Familial Cancer

JF - Familial Cancer

SN - 1389-9600

IS - 2

ER -

ID: 49102425