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10q26 is associated with increased risk of age-related macular degeneration in the Utah population

artículo científico publicado en 2008

21-gene recurrence score testing utilization among older women from different races: A population-based study

artículo científico publicado en 2020

A Meta-analysis of Multiple Myeloma Risk Regions in African and European Ancestry Populations Identifies Putatively Functional Loci

artículo científico publicado en 2016

A Pooled Analysis of Reproductive Factors, Exogenous Hormone Use, and Risk of Multiple Myeloma among Women in the International Multiple Myeloma Consortium

artículo científico publicado en 2015

A Role for XRCC4 in Age at Diagnosis and Breast Cancer Risk

scientific article published on 01 July 2006

A candidate prostate cancer susceptibility gene at chromosome 17p

artículo científico publicado en 2001

A cautionary note on the appropriateness of using a linkage resource for an association study

artículo científico publicado en 2003

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 comprehensive study of polymorphisms in the ABCB1, ABCC2, ABCG2, NR1I2 genes and lymphoma risk

artículo científico publicado en 2011

A family‐based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia ⬇️

artículo científico publicado el 19 de noviembre de 2012

A genealogical assessment of heritable predisposition to aneurysms ⬇️

artículo científico publicado el 1 de octubre de 2003

A low density genome-wide search for loci involved in alcohol dependence using the transmission/disequilibrium test, sib-TDT, and two combined tests

artículo científico publicado en 1999

A new nonparametric linkage statistic for mapping both qualitative and quantitative trait loci

artículo científico publicado en 2001

A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease

artículo científico publicado en 2008

A pooled analysis of alcohol consumption and risk of multiple myeloma in the international multiple myeloma consortium

artículo científico publicado en 2013

A pooled analysis of cigarette smoking and risk of multiple myeloma from the international multiple myeloma consortium

artículo científico publicado en 2014

A robust multipoint linkage statistic (tlod) for mapping complex trait loci

artículo científico publicado en 2001

A role for XRCC2 gene polymorphisms in breast cancer risk and survival

artículo científico publicado en 2011

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

artículo científico publicado en 2011

A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration

artículo científico publicado en 2006

Allelic association in large pedigrees

artículo científico publicado en 2001

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

artículo científico publicado el 19 de junio de 2012

Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis

artículo científico publicado en 2007

Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13.

artículo científico publicado en 2003

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

artículo científico publicado en 2020

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

artículo científico publicado en 2013

Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

artículo científico publicado en 2002

Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis

artículo científico publicado en 2019

Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis

artículo científico publicado en 2018

Associations of ATR and CHEK1 single nucleotide polymorphisms with breast cancer

artículo científico publicado en 2013

Automated construction and testing of multi-locus gene–gene associations ⬇️

artículo científico publicado el 13 de noviembre de 2010

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses:ELAC2 and familial early-onset prostate cancer

artículo científico publicado en 2005

Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes

artículo científico publicado en 2005

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

Classification tree analysis: a statistical tool to investigate risk factor interactions with an example for colon cancer (United States)

artículo científico publicado en 2002

Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance

scientific article published on 01 June 2020

Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids ⬇️

artículo científico publicado el 10 de julio de 2011

Common occurrence of monoclonal B-cell lymphocytosis among members of high-risk CLL families

artículo científico publicado en 2010

Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes

artículo científico publicado en 2012

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

artículo científico publicado en 2012

Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study

artículo científico publicado en 2003

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

artículo científico publicado en 2007

Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm

artículo científico publicado en 2003

Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees

artículo científico publicado en 2004

Consensus Analysis of Whole Transcriptome Profiles from Two Breast Cancer Patient Cohorts Reveals Long Non-Coding RNAs Associated with Intrinsic Subtype and the Tumour Microenvironment

artículo científico publicado en 2016

Correcting for multiple analyses in genomewide linkage studies

artículo científico publicado en 2001

Correction: Consensus Analysis of Whole Transcriptome Profiles from Two Breast Cancer Patient Cohorts Reveals Long Non-Coding RNAs Associated with Intrinsic Subtype and the Tumour Microenvironment

artículo científico publicado en 2018

Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients

artículo científico publicado en 2015

Discordant Haplotype Sequencing Identifies Functional Variants at the 2q33 Breast Cancer Risk Locus

artículo científico publicado en 2016

Dissecting the genetic etiology of major depressive disorder using linkage analysis

artículo científico publicado en 2005

Elevated IgM and abnormal free light chain ratio are increased in relatives from high-risk chronic lymphocytic leukemia pedigrees

artículo científico publicado en 2019

Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study

artículo científico publicado en 2009

Evidence for a heritable component in death resulting from aortic and mitral valve diseases.

artículo científico publicado en 2004

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree

artículo científico publicado en 2005

Examination of ELN as a Candidate Gene in the Utah Intracranial Aneurysm Pedigrees

article

Extracting disease risk profiles from expression data for linkage analysis: application to prostate cancer

artículo científico publicado en 2007

Familial Myeloma

artículo científico publicado en 2008

Family Study Designs Informed by Tumor Heterogeneity and Multi-Cancer Pleiotropies: The Power of the Utah Population Database

artículo científico publicado en 2020

Fine-Scale Structure of the Genome and Markers Used in Association Mapping ⬇️

artículo científico publicado el 1 de enero de 2011

Fine-mapping CASP8 risk variants in breast cancer

artículo científico publicado en 2011

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

artículo científico publicado en 2009

Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration.

artículo científico publicado en 2008

Genetic Distance and Markers Used in Linkage Mapping ⬇️

artículo científico publicado el 1 de enero de 2011

Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia

artículo científico publicado en 2013

Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes

artículo científico publicado en 2019

Genetic risk factors in two Utah pedigrees at high risk for suicide

artículo científico publicado en 2013

Genetic susceptibility variants for chronic lymphocytic leukemia

artículo científico publicado en 2010

Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis

artículo científico publicado en 2009

Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility

artículo científico publicado en 2008

Genetic variation at the interleukin-1 locus is a determinant of changes in soluble endothelial factors in patients with acute coronary syndromes

Genetically Determined Height and Risk of Non-hodgkin Lymphoma

artículo científico publicado en 2019

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

artículo científico publicado en 2016

Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia

artículo científico publicado en 2017

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL

scientific journal article

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

artículo científico publicado en 2013

Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.

artículo científico publicado en 2015

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

artículo científico publicado en 2010

Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders

artículo científico publicado en 2005

Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees

artículo científico publicado en 2007

Genome-wide linkage analysis for celiac disease in North American families

artículo científico publicado en 2002

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

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees ⬇️

artículo científico publicado el 8 de abril de 2010

Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees

artículo científico publicado en 2003

Genome-wide scans meta-analysis for pulse pressure

scientific article published on 16 July 2007

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

article

Genomewide Multipoint Linkage Analysis of Seven Extended Palauan Pedigrees with Schizophrenia, by a Markov-Chain Monte Carlo Method ⬇️

artículo científico publicado el 19 de octubre de 2001

Genomic search for prostate cancer predisposition loci in Utah pedigrees

artículo científico publicado en 2005

Germline mutations in lysine specific demethylase 1 (LSD1/KDM1A) confer susceptibility to multiple myeloma

artículo científico publicado en 2018

Graphical modeling of the joint distribution of alleles at associated loci

artículo científico publicado en 2004

HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease

artículo científico publicado en 2002

HLA class I and II diversity contributes to the etiologic heterogeneity of non-Hodgkin lymphoma subtypes.

artículo científico publicado en 2018

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

artículo científico publicado en 2012

Haplotype association analyses in resources of mixed structure using Monte Carlo testing ⬇️

artículo científico publicado el 9 de diciembre de 2010

Harnessing Population Pedigree Data and Machine Learning Methods to Identify Patterns of Familial Bladder Cancer Risk

artículo científico publicado en 2020

High-Resolution Characterization of Linkage Disequilibrium Structure and Selection of Tagging Single Nucleotide Polymorphisms: Application to the Cholesteryl Ester Transfer Protein Gene

article

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

artículo científico publicado en 2014

Identification and study of Utah pseudo-isolate populations—prospects for gene identification

article

Identification of a major susceptibility locus for lethal graft-versus-host disease in MHC-matched mice

artículo científico publicado en 2009

Identification of excess clustering of coronary heart diseases among extended pedigrees in a genealogical population database

artículo científico publicado en 2006

Identification of regions of positive selection using Shared Genomic Segment analysis

artículo científico publicado en 2011

Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma

artículo científico publicado en 2014

Immunophenotypic and gene expression analysis of monoclonal B-cell lymphocytosis shows biologic characteristics associated with good prognosis CLL.

artículo científico publicado en 2011

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

artículo científico publicado en 2022

Interleukin 1 receptor antagonist gene polymorphism and restenosis after coronary angioplasty

artículo científico publicado en 2001

Interleukin-1 receptor antagonist gene polymorphism and coronary artery disease

artículo científico publicado en 1999

Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery disease ⬇️

artículo científico publicado el 1 de agosto de 2010

Linkage analysis of Tourette syndrome in a large Utah pedigree

artículo científico publicado en 2010

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

artículo científico publicado en 2002

Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees

artículo científico publicado en 2004

Lipid Trait Variants and the Risk of Non-Hodgkin Lymphoma Subtypes: A Mendelian Randomization Study

artículo científico publicado en 2020

Lobular breast cancer: Excess familiality observed in the Utah Population Database

artículo científico publicado en 2005

Localization of a Prostate Cancer Predisposition Gene to an 880-kb Region on Chromosome 22q12.3 in Utah High-Risk Pedigrees

article

Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypes

artículo científico publicado en 2013

Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting

artículo científico publicado en 2006

Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21

artículo científico publicado en 2009

Meta-analysis of associations of the Ser217Leu and Ala541Thr variants in ELAC2 (HPC2) and prostate cancer

artículo científico publicado en 2002

Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia

artículo científico publicado en 2016

Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1.

artículo científico publicado en 2007

Model-fitting and linkage analysis of sodium–lithium countertransport

article

Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease

scientific article published on 04 May 2007

Multiple myeloma and family history of lymphohaematopoietic cancers: Results from the International Multiple Myeloma Consortium

artículo científico publicado en 2016

Multiple-polymorphism associations of 7 matrix metalloproteinase and tissue inhibitor metalloproteinase genes with myocardial infarction and angiographic coronary artery disease

artículo científico publicado en 2007

National Cancer Institute Prostate Cancer Genetics Workshop

artículo científico publicado en 2011

No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

artículo científico publicado en 2009

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

artículo científico publicado en 2018

Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

artículo científico publicado en 2011

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees

artículo científico publicado en 2012

Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families.

artículo científico publicado en 2017

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

artículo científico publicado en 2022

PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size

artículo científico publicado en 2006

PedGenie: meta genetic association testing in mixed family and case-control designs

artículo científico publicado en 2007

Pedigree association: assigning individual weights to pedigree members for genetic association analysis

artículo científico publicado en 2009

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

artículo científico publicado en 2006

Pooled study of occupational exposure to aromatic hydrocarbon solvents and risk of multiple myeloma

scientific article published on 18 August 2018

Population-based risk assessment for other cancers in relatives of hereditary prostate cancer (HPC) cases

artículo científico publicado en 2005

Predictors of Response Outcomes for Research Recruitment Through a Central Cancer Registry: Evidence From 17 Recruitment Efforts for Population-Based Studies

artículo científico publicado en 2019

Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2 ⬇️

artículo científico publicado el 5 de noviembre de 2003

Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation

artículo científico publicado en 2004

Re-interpretation of PAM50 gene expression as quantitative tumor dimensions shows utility for clinical trials: application to prognosis and response to paclitaxel in breast cancer

article

Reparameterization of PAM50 expression identifies novel breast tumor dimensions and leads to discovery of a genomewide significant breast cancer locus at 12q15.

artículo científico publicado en 2018

Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study

artículo científico publicado en 2009

Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

artículo científico publicado en 2007

Shared genomic segment analysis: the power to find rare disease variants

artículo científico publicado en 2012

Shared genomic segments in high-risk multigenerational pedigrees with gastroschisis

artículo científico publicado en 2019

Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource

artículo científico publicado en 2008

Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb.

artículo científico publicado en 2007

The effect of selective sampling on mapping quantitative trait loci ⬇️

artículo científico publicado el 1 de enero de 1997

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)

artículo científico publicado en 2011

Validity and power of association testing in family-based sampling designs: evidence for and against the common wisdom ⬇️

artículo científico publicado el 16 de febrero de 2011

Whole transcriptome profiling of patient-derived xenograft models as a tool to identify both tumor and stromal specific biomarkers

scientific article published on 09 March 2016

Young Adult and Usual Adult Body Mass Index and Multiple Myeloma Risk: A Pooled Analysis in the International Multiple Myeloma Consortium (IMMC).

artículo científico publicado en 2017

hapConstructor: automatic construction and testing of haplotypes in a Monte Carlo framework

artículo científico publicado en 2008

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