Search details
1.
A low-frequency haplotype spanning SLX4/FANCP constitutes a new risk locus for early-onset breast cancer (<60 years) and is associated with reduced DNA repair capacity.
Int J Cancer
; 142(4): 757-768, 2018 02 15.
Article
in English
| MEDLINE | ID: mdl-29044504
2.
Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status.
Hum Mol Genet
; 25(24): 5490-5499, 2016 12 15.
Article
in English
| MEDLINE | ID: mdl-27798103
3.
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.
Hum Mol Genet
; 24(19): 5589-602, 2015 Oct 01.
Article
in English
| MEDLINE | ID: mdl-26025378
4.
MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.
Hum Mutat
; 37(3): 257-68, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26615982
5.
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.
Hum Mol Genet
; 22(2): 408-15, 2013 Jan 15.
Article
in English
| MEDLINE | ID: mdl-23065704
6.
Prediction of individual genetic risk to prostate cancer using a polygenic score.
Prostate
; 75(13): 1467-74, 2015 Sep.
Article
in English
| MEDLINE | ID: mdl-26177737
7.
Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.
Urol Int
; 95(4): 386-9, 2015.
Article
in English
| MEDLINE | ID: mdl-25660097
8.
Do orofacial clefts represent different genetic entities?
Cleft Palate Craniofac J
; 52(1): 115-20, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-24437586
9.
Subgroups of familial and aggressive prostate cancer with considerable frequencies of BRCA2 mutations.
Prostate
; 74(14): 1444-51, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-25111659
10.
Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.
Hum Genet
; 133(3): 347-56, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24162621
11.
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).
Hum Genet
; 132(1): 5-14, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23064873
12.
Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.
Prostate
; 72(4): 410-26, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-21748754
13.
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
Hum Genet
; 131(7): 1095-103, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22198737
14.
Genetic and environmental risk factors for submucous cleft palate.
Eur J Oral Sci
; 120(2): 97-103, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22409215
15.
Heritability of baseline and induced micronucleus frequencies.
Mutagenesis
; 26(1): 111-7, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-21164191
16.
POU5F1P1, a putative cancer susceptibility gene, is overexpressed in prostatic carcinoma.
Prostate
; 70(6): 666-74, 2010 May 01.
Article
in English
| MEDLINE | ID: mdl-20017164
17.
The effect of sample size on polygenic hazard models for prostate cancer.
Eur J Hum Genet
; 28(10): 1467-1475, 2020 10.
Article
in English
| MEDLINE | ID: mdl-32514134
18.
A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data.
Cancer Epidemiol Biomarkers Prev
; 29(9): 1731-1738, 2020 09.
Article
in English
| MEDLINE | ID: mdl-32581112
19.
Reconstruction of a 450-My-old ancestral vertebrate protokaryotype.
Trends Genet
; 22(4): 203-10, 2006 Apr.
Article
in English
| MEDLINE | ID: mdl-16517001
20.
The rate, not the spectrum, of base pair substitutions changes at a GC-content transition in the human NF1 gene region: implications for the evolution of the mammalian genome structure.
Genetics
; 175(1): 421-8, 2007 Jan.
Article
in English
| MEDLINE | ID: mdl-17057231