| human | Q5 |
| P496 | ORCID iD | 0000-0002-8213-949X |
| P1153 | Scopus author ID | 35375069400 |
| P69 | educated at | University of Utah | Q168515 |
| P108 | employer | University of Utah | Q168515 |
| Strand Life Sciences | Q7621233 | ||
| University of Utah School of Medicine | Q7896521 | ||
| P735 | given name | James | Q677191 |
| James | Q677191 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q34015399 | A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics |
| Q59548815 | A simple diagnostic index for asthma |
| Q53237784 | A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. |
| Q34308746 | Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families |
| Q59548776 | Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses:ELAC2 and familial early-onset prostate cancer |
| Q36599631 | Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG |
| Q37121925 | Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics |
| Q59548803 | Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm |
| Q59548777 | Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees |
| Q36796431 | Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears |
| Q41947566 | Evidence for an inherited predisposition contributing to the risk for rotator cuff disease |
| Q35688980 | Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17. |
| Q59548778 | Examination of ELN as a Candidate Gene in the Utah Intracranial Aneurysm Pedigrees |
| Q40718874 | Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. |
| Q40561180 | Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms |
| Q59548761 | Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees |
| Q36190531 | Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses |
| Q45105954 | Genomic search for prostate cancer predisposition loci in Utah pedigrees |
| Q59548787 | Identification and study of Utah pseudo-isolate populations—prospects for gene identification |
| Q35599982 | Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis |
| Q33944643 | Identification of specific Y chromosomes associated with increased prostate cancer risk |
| Q59548819 | Impact of Correlated Factors on Bone Density in Individuals with a Family History of Osteoporosis |
| Q36502322 | Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21. |
| Q59548773 | Localization of a Prostate Cancer Predisposition Gene to an 880-kb Region on Chromosome 22q12.3 in Utah High-Risk Pedigrees |
| Q33454990 | No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees |
| Q52218044 | Novel popout with nonsense strings: effects of predictability of string length and spatial location. |
| Q34494526 | Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees |
| Q43791618 | Population-based risk assessment for other cancers in relatives of hereditary prostate cancer (HPC) cases |
| Q37113358 | Population-based risks for cancer in patients with ALS. |
| Q34944738 | Prostate cancer risk prediction based on complete prostate cancer family history |
| Q37229978 | Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study |
| Q29417074 | Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study |
| Q34241688 | Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays. |
| Q37189147 | Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. |
| Q40190172 | Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. |
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