Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancerUnregulated smooth-muscle myosin in human intestinal neoplasiaGenetic reconstruction of individual colorectal tumor historiesNumbers of mutations to different types of colorectal cancerGermline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instabilityMultiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYHMutations in BRIP1 confer high risk of ovarian cancerMutations in the circadian gene CLOCK in colorectal cancerLocalization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysisColorectal adenoma and cancer divergence. Evidence of multilineage progressionMeta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancerCommon variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis.Clusterin expression in normal mucosa and colorectal cancer.Somatic mutation analysis of MYH11 in breast and prostate cancerMutation analysis of components of the Mediator kinase module in MED12 mutation-negative uterine leiomyomas.Mixed lineage kinase 3 gene mutations in mismatch repair deficient gastrointestinal tumours.COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancerUterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3H.Low-penetrance susceptibility variants in familial colorectal cancer.Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma.Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.Metastasis-Associated Gene Expression Changes Predict Poor Outcomes in Patients with Dukes Stage B and C Colorectal CancerGermline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis.Mice with inactivation of aryl hydrocarbon receptor-interacting protein (Aip) display complete penetrance of pituitary adenomas with aberrant ARNT expressionLittle evidence for involvement of MLH3 in colorectal cancer predisposition.MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas.Strong family history of uterine leiomyomatosis warrants fumarate hydratase mutation screening.Founding mutations and Alu-mediated recombination in hereditary colon cancer.Identification of 33 candidate oncogenes by screening for base-specific mutations.Molecular staging for survival prediction of colorectal cancer patients.A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.Screening of Finnish RAD51C founder mutations in prostate and colorectal cancer patients.Cancer risk in mutation carriers of DNA-mismatch-repair genes.
P50
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P50
description
finnischer Universität Helsinki und Akademie von Finnland
@de
kasvaingenonomiikan professori ...... iaprofessori (Suomen Akatemia)
@fi
professor of tumor genomics (b ...... professor (Academy of Finland)
@en
name
Lauri Aaltonen
@ast
Lauri Aaltonen
@ca
Lauri Aaltonen
@da
Lauri Aaltonen
@de
Lauri Aaltonen
@en
Lauri Aaltonen
@es
Lauri Aaltonen
@fi
Lauri Aaltonen
@fr
Lauri Aaltonen
@ga
Lauri Aaltonen
@nb
type
label
Lauri Aaltonen
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Lauri Aaltonen
@ca
Lauri Aaltonen
@da
Lauri Aaltonen
@de
Lauri Aaltonen
@en
Lauri Aaltonen
@es
Lauri Aaltonen
@fi
Lauri Aaltonen
@fr
Lauri Aaltonen
@ga
Lauri Aaltonen
@nb
altLabel
Lauri Antti Aaltonen
@en
prefLabel
Lauri Aaltonen
@ast
Lauri Aaltonen
@ca
Lauri Aaltonen
@da
Lauri Aaltonen
@de
Lauri Aaltonen
@en
Lauri Aaltonen
@es
Lauri Aaltonen
@fi
Lauri Aaltonen
@fr
Lauri Aaltonen
@ga
Lauri Aaltonen
@nb
P1006
P1015
P214
P244
P269
P1006
P1015
P1053
A-5375-2010
P1207
n2004078921
P19
P21
P213
0000 0001 1603 2769
P214
P244
nb2001003959