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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 Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

PLoS genetics, 2016-02, Vol.12 (2), p.e1005850-e1005850

2016

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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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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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Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

Cancer research (Chicago, Ill.), 2017-08, Vol.77 (15), p.4078-4088

2017

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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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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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KSHV-Initiated Notch Activation Leads to Membrane-Type-1 Matrix Metalloproteinase-Dependent Lymphatic Endothelial-to-Mesenchymal Transition

Cell host & microbe, 2011-12, Vol.10 (6), p.577-590

2011

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Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure

Genes and environment, 2024-05, Vol.46 (1), p.12-12, Article 12

2024

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Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma

Blood, 2011-07, Vol.118 (3), p.493-498

2011

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Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcoma

PloS one, 2013-01, Vol.8 (1), p.e55209-e55209

2013

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Aberrations of chromosome 19 in asbestos-associated lung cancer and in asbestos-induced micronuclei of bronchial epithelial cells in vitro

Carcinogenesis (New York), 2008-05, Vol.29 (5), p.913-917

2008

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Molecular Alterations at 9q33.1 and Polyploidy in Asbestos-Related Lung Cancer

Clinical cancer research, 2009-01, Vol.15 (2), p.468-475

2009

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MED12, the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

Science (American Association for the Advancement of Science), 2011-10, Vol.334 (6053), p.252-255

2011

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The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Nature communications, 2020-12, Vol.11 (1), p.6383-6383, Article 6383

2020

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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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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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Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

Gastroenterology (New York, N.Y. 1943), 2023-10, Vol.165 (4), p.861-873

2023

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Abstract 68: Exomic landscape of uterine leiomyosarcomas

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.68-68

2015

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Candidate susceptibility variants for esophageal squamous cell carcinoma

Genes chromosomes & cancer, 2017-06, Vol.56 (6), p.453-459

2017

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Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

Familial cancer, 2024-06

2024

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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 Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

Mutations in BRIP1 confer high risk of ovarian cancer

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

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

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

Sex-specific familial aggregation of cancers in Finland

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

KSHV-Initiated Notch Activation Leads to Membrane-Type-1 Matrix Metalloproteinase-Dependent Lymphatic Endothelial-to-Mesenchymal Transition

Contribution of allelic imbalance to colorectal cancer

Genome-wide somatic mutation analysis of sinonasal adenocarcinoma with and without wood dust exposure

Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma

Comprehensive evaluation of coding region point mutations in microsatellite‐unstable colorectal cancer

Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcoma

Aberrations of chromosome 19 in asbestos-associated lung cancer and in asbestos-induced micronuclei of bronchial epithelial cells in vitro

Molecular Alterations at 9q33.1 and Polyploidy in Asbestos-Related Lung Cancer

MED12, the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Germline mutations in young non-smoking women with lung adenocarcinoma

Loss of SUFU Function in Familial Multiple Meningioma

Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

Abstract 68: Exomic landscape of uterine leiomyosarcomas

Candidate susceptibility variants for esophageal squamous cell carcinoma

Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

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