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A Germline DNA Polymorphism Enhances Alternative Splicing of theKLF6Tumor Suppressor Gene and Is Associated with Increased Prostate Cancer Risk

article

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

artículo científico publicado en 2005

A phenome-wide association study to discover pleiotropic effects of , , and

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families

artículo científico publicado en 2012

Androgen receptor gene polymorphisms and increased risk of urologic measures of benign prostatic hyperplasia

artículo científico publicado en 2004

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

artículo científico publicado en 2020

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

artículo científico publicado en 2011

Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2007

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network

FKBP5 genetic variation: association with selective serotonin reuptake inhibitor treatment outcomes in major depressive disorder

artículo científico publicado en 2013

Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.

artículo científico publicado en 2007

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy

artículo científico publicado en 2015

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

artículo científico publicado en 2010

Glutathione S-transferase T1 and M1: gene sequence variation and functional genomics

artículo científico

Growth factor, cytokine, and vitamin D receptor polymorphisms and risk of benign prostatic hyperplasia in a community-based cohort of men.

artículo científico publicado en 2006

Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlation

artículo científico publicado en 2012

Identifying genetically driven clinical phenotypes using linear mixed models

artículo científico publicado en 2016

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

artículo científico publicado en 2014

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.

artículo científico publicado en 2017

Phenotype risk scores identify patients with unrecognized Mendelian disease patterns

scientific article published in Science

Polymorphisms in genes involved in sex hormone metabolism may increase risk of benign prostatic hyperplasia

article

Polymorphisms in the 5alpha reductase type 2 gene and urologic measures of BPH.

artículo científico publicado en 2005

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2006

The All of Us Research Program: Data quality, utility, and diversity

artículo científico publicado en 2022

The phenotypic legacy of admixture between modern humans and Neandertals

artículo científico publicado en 2016

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

artículo científico publicado en 2016

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