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Familial Isolated Pituitary Adenomas (FIPA) and the Pituitary Adenoma Predisposition due to Mutations in the Aryl Hydrocarbon Receptor Interacting Protein (AIP) Gene

Endocrine reviews, 2013-04, Vol.34 (2), p.239-277

2013

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Genomics of uterine leiomyomas: insights from high-throughput sequencing

Fertility and sterility, 2014-09, Vol.102 (3), p.621-629

2014

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Colibactin DNA-damage signature indicates mutational impact in colorectal cancer

Nature medicine, 2020-07, Vol.26 (7), p.1063-1069

2020

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Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease–Associated Colorectal Cancer

Gastroenterology (New York, N.Y. 1943), 2021-08, Vol.161 (2), p.592-607

2021

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Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (5), p.1315-1320

2016

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Exome-wide somatic mutation characterization of small bowel adenocarcinoma

PLoS genetics, 2018-03, Vol.14 (3), p.e1007200-e1007200

2018

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Transposable elements as tissue-specific enhancers in cancers of endodermal lineage

Nature communications, 2023-09, Vol.14 (1), p.5313-5313, Article 5313

2023

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Mutational processes of distinct POLE exonuclease domain mutants drive an enrichment of a specific TP53 mutation in colorectal cancer

PLoS genetics, 2020-02, Vol.16 (2), p.e1008572-e1008572

2020

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Characterization of Uterine Leiomyomas by Whole-Genome Sequencing

The New England journal of medicine, 2013-07, Vol.369 (1), p.43-53

2013

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Cancer incidence following non-neoplastic medical conditions: a prospective population-based cohort study

Acta oncologica, 2024-11, Vol.63 (1), p.841-849

2024

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From APC to the genetics of hereditary and familial colon cancer syndromes

Human molecular genetics, 2021-10, Vol.30 (R2), p.R206-R224

2021

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Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity

Cell reports (Cambridge), 2014-05, Vol.7 (3), p.654-660

2014

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CTCF/cohesin-binding sites are frequently mutated in cancer

Nature genetics, 2015-07, Vol.47 (7), p.818-821

2015

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Germline mutations in young non-smoking women with lung adenocarcinoma

Lung cancer (Amsterdam, Netherlands), 2018-08, Vol.122, p.76-82

2018

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Mutations in BRIP1 confer high risk of ovarian cancer

Nature genetics, 2011-11, Vol.43 (11), p.1104-1107

2011

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Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Journal of clinical oncology, 2009-10, Vol.27 (28), p.4793-4797

2009

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Metastasis-Associated Gene Expression Changes Predict Poor Outcomes in Patients with Dukes Stage B and C Colorectal Cancer

Clinical cancer research, 2009-12, Vol.15 (24), p.7642-7651

2009

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Loss of SUFU Function in Familial Multiple Meningioma

American journal of human genetics, 2012-09, Vol.91 (3), p.520-526

2012

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Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

Nature communications, 2019-09, Vol.10 (1), p.4022-9, Article 4022

2019

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Sex-specific familial aggregation of cancers in Finland

Scientific reports, 2022-09, Vol.12 (1), p.1-9, Article 15126

2022

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Identification of Lynch syndrome among patients with colorectal cancer

JAMA : the journal of the American Medical Association, 2012-10, Vol.308 (15), p.1555

2012

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The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling

Nature genetics, 2009-08, Vol.41 (8), p.885-890

2009

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Mice Lacking a Myc Enhancer That Includes Human SNP rs6983267 Are Resistant to Intestinal Tumors

Science (American Association for the Advancement of Science), 2012-12, Vol.338 (6112), p.1360-1363

2012

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Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma

Nature (London), 2021-08, Vol.596 (7872), p.398-403

2021

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Eleven candidate susceptibility genes for common familial colorectal cancer

PLoS genetics, 2013-10, Vol.9 (10), p.e1003876-e1003876

2013

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Familial Isolated Pituitary Adenomas (FIPA) and the Pituitary Adenoma Predisposition due to Mutations in the Aryl Hydrocarbon Receptor Interacting Protein (AIP) Gene

Genomics of uterine leiomyomas: insights from high-throughput sequencing

Colibactin DNA-damage signature indicates mutational impact in colorectal cancer

Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease–Associated Colorectal Cancer

Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers

Exome-wide somatic mutation characterization of small bowel adenocarcinoma

Transposable elements as tissue-specific enhancers in cancers of endodermal lineage

Mutational processes of distinct POLE exonuclease domain mutants drive an enrichment of a specific TP53 mutation in colorectal cancer

Characterization of Uterine Leiomyomas by Whole-Genome Sequencing

Cancer incidence following non-neoplastic medical conditions: a prospective population-based cohort study

From APC to the genetics of hereditary and familial colon cancer syndromes

Uterine Leiomyoma-Linked MED12 Mutations Disrupt Mediator-Associated CDK Activity

CTCF/cohesin-binding sites are frequently mutated in cancer

Germline mutations in young non-smoking women with lung adenocarcinoma

Mutations in BRIP1 confer high risk of ovarian cancer

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

Metastasis-Associated Gene Expression Changes Predict Poor Outcomes in Patients with Dukes Stage B and C Colorectal Cancer

Loss of SUFU Function in Familial Multiple Meningioma

Retrotransposon insertions can initiate colorectal cancer and are associated with poor survival

Sex-specific familial aggregation of cancers in Finland

Identification of Lynch syndrome among patients with colorectal cancer

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling

Mice Lacking a Myc Enhancer That Includes Human SNP rs6983267 Are Resistant to Intestinal Tumors

Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma

Eleven candidate susceptibility genes for common familial colorectal cancer

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