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Epidemiological, clinical and molecular characterization of Lynch‐like syndrome: A population‐based study

International journal of cancer, 2019-07, Vol.145 (1), p.87-98

2019

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Somatic mutation profiles as molecular classifiers of ulcerative colitis‐associated colorectal cancer

International journal of cancer, 2021-06, Vol.148 (12), p.2997-3007

2021

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Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Journal of surgical oncology, 2016-02, Vol.113 (2), p.209-212

2016

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Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Genes chromosomes & cancer, 2014-10, Vol.53 (10), p.857-864

2014

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Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.776-787

2015

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Distinct molecular profiles in Lynch syndrome‐associated and sporadic ovarian carcinomas

International journal of cancer, 2013-12, Vol.133 (11), p.2596-2608

2013

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Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma

International journal of cancer, 2007-08, Vol.121 (4), p.915-920

2007

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Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous β-catenin

Human mutation, 2008-03, Vol.29 (3), p.390-397

2008

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Genome profiles of familial/bilateral and sporadic testicular germ cell tumors

Genes chromosomes & cancer, 2002-06, Vol.34 (2), p.168-174

2002

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Cutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer

Genes chromosomes & cancer, 2008-02, Vol.47 (2), p.107-117

2008

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Molecular mapping of the putative gonadoblastoma locus on the Y chromosome

Genes chromosomes & cancer, 1995-11, Vol.14 (3), p.210-214

1995

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Deletion of 1p loci and microsatellite instability in colorectal polyps

Genes chromosomes & cancer, 1995-11, Vol.14 (3), p.182-188

1995

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Cancer risk in mutation carriers of DNA‐mismatch‐repair genes

International journal of cancer, 1999-04, Vol.81 (2), p.214-218

1999

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Distinct molecular profiles in Lynch syndrome-associated and sporadic ovarian carcinomas: LS-associated and sporadic ovarian carcinomas

International journal of cancer, 2013-06, p.n/a

2013

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Large genomic rearrangements and germline epimutations in Lynch syndrome

International journal of cancer, 2009-05, Vol.124 (10), p.2333-2340

2009

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Microsatellite instability and hereditary non-polyposis colon cancer

The Journal of pathology, 1995-08, Vol.176 (4), p.329-330

Peltomäki, PäIvi

1995

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Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction

International journal of cancer, 2000-01, Vol.89 (1), p.44-50

2000

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Little evidence for involvement of MLH3 in colorectal cancer predisposition

International journal of cancer, 2003-08, Vol.106 (2), p.292-296

2003

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MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis

Genes chromosomes & cancer, 1997-04, Vol.18 (4), p.269-278

1997

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Sporadic gastric carcinomas with microsatellite instability display a particular clinicopathologic profile

International journal of cancer, 1995-02, Vol.64 (1), p.32-36

1995

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Hereditary colorectal cancer: risk assessment and management

Clinical genetics, 2000-08, Vol.58 (2), p.89-97

2000

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Microsatellite instability in cervical and endometrial carcinomas

International journal of cancer, 1997-03, Vol.70 (5), p.499-501

1997

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Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds

Genes chromosomes & cancer, 1999-12, Vol.26 (4), p.372-375

1999

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Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

Genes chromosomes & cancer, 2000-04, Vol.27 (4), p.424-429

2000

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HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1

Genes chromosomes & cancer, 2004-07, Vol.40 (3), p.261-265

2004

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Epidemiological, clinical and molecular characterization of Lynch‐like syndrome: A population‐based study

Somatic mutation profiles as molecular classifiers of ulcerative colitis‐associated colorectal cancer

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Distinct molecular profiles in Lynch syndrome‐associated and sporadic ovarian carcinomas

Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma

Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous β-catenin

Genome profiles of familial/bilateral and sporadic testicular germ cell tumors

Cutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer

Molecular mapping of the putative gonadoblastoma locus on the Y chromosome

Deletion of 1p loci and microsatellite instability in colorectal polyps

Cancer risk in mutation carriers of DNA‐mismatch‐repair genes

Distinct molecular profiles in Lynch syndrome-associated and sporadic ovarian carcinomas: LS-associated and sporadic ovarian carcinomas

Large genomic rearrangements and germline epimutations in Lynch syndrome

Microsatellite instability and hereditary non-polyposis colon cancer

Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction

Little evidence for involvement of MLH3 in colorectal cancer predisposition

MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis

Sporadic gastric carcinomas with microsatellite instability display a particular clinicopathologic profile

Hereditary colorectal cancer: risk assessment and management

Microsatellite instability in cervical and endometrial carcinomas

Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds

Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1

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