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Increased risk of cancer in patients with fumarate hydratase germline mutation

Journal of medical genetics, 2006-06, Vol.43 (6), p.523-526

2006

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LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Journal of medical genetics, 2006-05, Vol.43 (5), p.e18-e18

2006

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Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC)

Cancer research (Chicago, Ill.), 2001-06, Vol.61 (11), p.4545-4549

2001

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Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers

British journal of cancer, 2007-01, Vol.96 (2), p.352-356

2007

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Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Gut, 2002-07, Vol.51 (1), p.56-59

2002

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No evidence of somatic aryl hydrocarbon receptor interacting protein mutations in sporadic endocrine neoplasia

Endocrine-related cancer, 2007-09, Vol.14 (3), p.901-906

2007

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Mutation analysis of the CHK2 gene in families with hereditary breast cancer

British journal of cancer, 2001-07, Vol.85 (2), p.209-212

2001

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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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Inherited Susceptibility to Uterine Leiomyomas and Renal Cell Cancer

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (6), p.3387-3392

2001

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No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer

Oncogene, 2007-04, Vol.26 (17), p.2513-2517

2007

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

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Germline and Somatic Mutation Analysis of MLH3 in MSI-Positive Colorectal Cancer

The American journal of pathology, 2000-08, Vol.157 (2), p.347-352

2000

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Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer

Journal of endocrinological investigation, 2009-05, Vol.32 (5), p.426-429

2009

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No SMAD4 hypermethylation in colorectal cancer

British journal of cancer, 2000-10, Vol.83 (8), p.1015-1019

2000

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Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

American journal of human genetics, 1998-06, Vol.62 (6), p.1544-1548

1998

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Screening for microsatellite instability target genes in colorectal cancers

Journal of medical genetics, 2002-11, Vol.39 (11), p.785-789

2002

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E-cadherin is not frequently mutated in hereditary gastric cancer

Journal of medical genetics, 2001, Vol.38 (1), p.49-52

2001

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Chromosome 11q22.3-q25 LOH in Ovarian Cancer: Association with a More Aggressive Disease Course and Involved Subregions

Gynecologic oncology, 1998-11, Vol.71 (2), p.299-304

1998

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DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Human molecular genetics, 2001-12, Vol.10 (26), p.3001-3007

2001

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The Expression of AIP -Related Molecules in Elucidation of Cellular Pathways in Pituitary Adenomas

The American journal of pathology, 2009-12, Vol.175 (6), p.2501-2507

2009

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Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

The American journal of pathology, 2001-09, Vol.159 (3), p.825-829

2001

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Mutation and LOH analysis of ACO2 in colorectal cancer: no evidence of biallelic genetic inactivation

Journal of medical genetics, 2003-05, Vol.40 (5), p.e73-73

2003

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ATM mutations in Finnish breast cancer patients

Journal of medical genetics, 2002-03, Vol.39 (3), p.192-196

2002

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Induction of Cyclooxygenase-2 in a Mouse Model of Peutz-Jeghers Polyposis

Proceedings of the National Academy of Sciences - PNAS, 2002-09, Vol.99 (19), p.12327-12332

2002

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Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414del4 found in male breast cancer

European journal of cancer (1990), 1999-05, Vol.35 (5), p.707-710

1999

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Increased risk of cancer in patients with fumarate hydratase germline mutation

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC)

Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

No evidence of somatic aryl hydrocarbon receptor interacting protein mutations in sporadic endocrine neoplasia

Mutation analysis of the CHK2 gene in families with hereditary breast cancer

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

Inherited Susceptibility to Uterine Leiomyomas and Renal Cell Cancer

No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

Germline and Somatic Mutation Analysis of MLH3 in MSI-Positive Colorectal Cancer

Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer

No SMAD4 hypermethylation in colorectal cancer

Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

Screening for microsatellite instability target genes in colorectal cancers

E-cadherin is not frequently mutated in hereditary gastric cancer

Chromosome 11q22.3-q25 LOH in Ovarian Cancer: Association with a More Aggressive Disease Course and Involved Subregions

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

The Expression of AIP -Related Molecules in Elucidation of Cellular Pathways in Pituitary Adenomas

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

Mutation and LOH analysis of ACO2 in colorectal cancer: no evidence of biallelic genetic inactivation

ATM mutations in Finnish breast cancer patients

Induction of Cyclooxygenase-2 in a Mouse Model of Peutz-Jeghers Polyposis

Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414del4 found in male breast cancer

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