Detalhe da pesquisa
1.
Systematic molecular and clinical analysis of uterine leiomyomas from fertile-aged women undergoing myomectomy.
Hum Reprod
; 35(10): 2237-2244, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32829387
2.
Mutation analysis of components of the Mediator kinase module in MED12 mutation-negative uterine leiomyomas.
Br J Cancer
; 110(9): 2246-9, 2014 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-24642626
3.
Identification of 33 candidate oncogenes by screening for base-specific mutations.
Br J Cancer
; 111(8): 1657-62, 2014 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-25117815
4.
Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer.
Br J Cancer
; 107(10): 1761-5, 2012 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23132392
5.
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer.
J Endocrinol Invest
; 32(5): 426-9, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19794292
6.
Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition.
J Endocrinol Invest
; 32(6): 512-8, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19474519
7.
Blood-derived gene-expression profiling in unravelling susceptibility to recessive disease.
J Med Genet
; 44(11): 718-20, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17660462
8.
No evidence of somatic aryl hydrocarbon receptor interacting protein mutations in sporadic endocrine neoplasia.
Endocr Relat Cancer
; 14(3): 901-6, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17914118
9.
CHEK2 I157T associates with familial and sporadic colorectal cancer.
J Med Genet
; 43(7): e34, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16816021
10.
No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer.
J Med Genet
; 42(4): e22, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15805151
11.
The MDM2 promoter polymorphism SNP309T-->G and the risk of uterine leiomyosarcoma, colorectal cancer, and squamous cell carcinoma of the head and neck.
J Med Genet
; 42(9): 694-8, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16141004
12.
Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32.
Cancer Res
; 58(13): 2715-9, 1998 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-9661879
13.
p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.
Cancer Res
; 61(15): 5718-22, 2001 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11479205
14.
BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients.
Eur J Hum Genet
; 9(6): 424-30, 2001 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-11436123
15.
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
Eur J Hum Genet
; 8(10): 757-63, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11039575
16.
Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients.
J Natl Cancer Inst
; 92(18): 1529-31, 2000 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-10995809
17.
Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers.
Br J Cancer
; 96(2): 352-6, 2007 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-17242703
18.
Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families.
Clin Genet
; 72(4): 311-20, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17850627
19.
A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families.
Br J Cancer
; 84(5): 704-8, 2001 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-11237395
20.
Survival of breast cancer patients in BRCA1, BRCA2, and non-BRCA1/2 breast cancer families: a relative survival analysis from Finland.
Int J Cancer
; 93(3): 368-72, 2001 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11433401