User profiles for Stephen J Chanock
Stephen ChanockNIH Verified email at mail.nih.gov Cited by 157178 |
Genome-wide association study reveals genetic risk underlying Parkinson's disease
We performed a genome-wide association study (GWAS) in 1,713 individuals of European
ancestry with Parkinson's disease (PD) and 3,978 controls. After replication in 3,361 cases …
ancestry with Parkinson's disease (PD) and 3,978 controls. After replication in 3,361 cases …
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
…, JF Fraumeni Jr, RN Hoover, G Thomas, SJ Chanock - Nature …, 2007 - nature.com
We conducted a genome-wide association study (GWAS) of breast cancer by genotyping
528,173 SNPs in 1,145 postmenopausal women of European ancestry with invasive breast …
528,173 SNPs in 1,145 postmenopausal women of European ancestry with invasive breast …
LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants
MJ Machiela, SJ Chanock - Bioinformatics, 2015 - academic.oup.com
Assessing linkage disequilibrium (LD) across ancestral populations is a powerful approach
for investigating population-specific genetic structure as well as functionally mapping regions …
for investigating population-specific genetic structure as well as functionally mapping regions …
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
…, JF Fraumeni Jr, R Hoover, DJ Hunter, SJ Chanock… - Nature …, 2007 - nature.com
Recently, common variants on human chromosome 8q24 were found to be associated with
prostate cancer risk. While conducting a genome-wide association study in the Cancer …
prostate cancer risk. While conducting a genome-wide association study in the Cancer …
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
…, AG Uitterlinden, A Hofman, DJ Hunter, SJ Chanock… - Nature …, 2013 - nature.com
Breast cancer is the most common cancer among women. Common variants at 27 loci have
been identified as associated with susceptibility to breast cancer, and these account for ∼9…
been identified as associated with susceptibility to breast cancer, and these account for ∼9…
Multiple loci identified in a genome-wide association study of prostate cancer
We followed our initial genome-wide association study (GWAS) of 527,869 SNPs on 1,172
individuals with prostate cancer and 1,157 controls of European origin—nested in the Prostate…
individuals with prostate cancer and 1,157 controls of European origin—nested in the Prostate…
[PDF][PDF] Polygenic risk scores for prediction of breast cancer and breast cancer subtypes
…, D Campa, BD Carter, JE Castelao, SJ Chanock… - The American Journal of …, 2019 - cell.com
Stratification of women according to their risk of breast cancer based on polygenic risk scores
(PRSs) could improve screening and prevention strategies. Our aim was to develop PRSs, …
(PRSs) could improve screening and prevention strategies. Our aim was to develop PRSs, …
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
We conducted a two-stage genome-wide association study of pancreatic cancer, a cancer
with one of the lowest survival rates worldwide. We genotyped 558,542 SNPs in 1,896 …
with one of the lowest survival rates worldwide. We genotyped 558,542 SNPs in 1,896 …
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
Using a multistage genetic association approach comprising 7,480 affected individuals and
7,779 controls, we identified markers in chromosomal region 8q24 associated with colorectal …
7,779 controls, we identified markers in chromosomal region 8q24 associated with colorectal …
[HTML][HTML] Mutations in TERT, the Gene for Telomerase Reverse Transcriptase, in Aplastic Anemia
…, S Kajigaya, GM Baerlocher, SJ Chanock… - … England Journal of …, 2005 - Mass Medical Soc
Background Mutations in TERC, the gene for the RNA component of telomerase, cause
short telomeres in congenital aplastic anemia and in some cases of apparently acquired …
short telomeres in congenital aplastic anemia and in some cases of apparently acquired …