J. Farnham

发表

Novel popout with nonsense strings: Effects of predictability of string length and spatial location

Kevin J. Hawley, W. Johnston, K. J. Hawley, 1994, Perception & psychophysics.

Novel popout: Empirical boundaries and tentative theory.

Kevin J. Hawley, W. Johnston, K. J. Hawley, 1993 .

Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

Mark T. W. Ebbert, A. Singleton, N. Price, 2017, Genome Medicine.

Analysis of mutations at the neurofibromatosis 1 (NF1) locus.

J. Farnham, S. Huson, P. Harper, 1992, Human molecular genetics.

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

N. Camp, L. Cannon-Albright, J. Farnham, 2007, The Prostate.

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

J. Farnham, P. Harper, M. Upadhyaya, 1992, American journal of human genetics.

Colorectal cancer risk based on extended family history and body mass index

L. Cannon-Albright, J. Farnham, S. Abdelrahman, 2020, Genetic epidemiology.

Germline Variant in SLCO2B1 and Response to Abiraterone Acetate Plus Prednisone (AA) in New-onset Metastatic Castration-resistant Prostate Cancer (mCRPC)

L. Cannon-Albright, N. Agarwal, J. Farnham, 2018, Molecular Cancer Therapeutics.

Evidence for an Environmental and Inherited Predisposition Contributing to the Risk for Global Tendinopathies or Compression Neuropathies in Patients With Rotator Cuff Tears

L. Cannon-Albright, J. Farnham, C. Teerlink, 2016, Orthopaedic journal of sports medicine.

Increased ProstateCancer Risk

L. Cannon-Albright, N. Agarwal, J. Farnham, 2014 .

Evidence for an inherited predisposition contributing to the risk for rotator cuff disease.

L. Cannon-Albright, J. Farnham, C. Teerlink, 2009, The Journal of bone and joint surgery. American volume.

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

N. Camp, S. Tavtigian, J. Farnham, 2005, Human Genetics.

Strategies for selection of subjects for sequencing after detection of a linkage peak

L. Cannon-Albright, J. Farnham, K. Allen-Brady, 2011, BMC proceedings.

Independent Validation of Effect of HSD3B1 Genotype on Response to Androgen-Deprivation Therapy in Prostate Cancer

L. Cannon-Albright, N. Agarwal, J. Farnham, 2017, JAMA oncology.

Genomic search for prostate cancer predisposition loci in Utah pedigrees

N. Camp, J. Farnham, Lisa A Cannon Albright, 2005, The Prostate.

Inherited Variants in SULT1E1 and Response to Abiraterone Acetate by Men with Metastatic Castration Refractory Prostate Cancer.

L. Cannon-Albright, N. Agarwal, J. Farnham, 2016, The Journal of urology.

Allelic Association in Large Pedigrees

A. Thomas, N. Camp, L. Cannon-Albright, 2001, Genetic epidemiology.

Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study

N. Camp, L. Cannon-Albright, J. Farnham, 2009, Cancer Epidemiology Biomarkers & Prevention.

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21

L. Cannon-Albright, J. Farnham, Alun Thomas, 2012, The Journal of investigative dermatology.

Prostate cancer susceptibility locus HPC1 in Utah high-risk pedigrees.

M. Skolnick, L. Cannon-Albright, S. Tavtigian, 1999, Human molecular genetics.

Identification of Six Loci Associated With Pelvic Organ Prolapse Using Genome-Wide Association Analysis

L. Cannon-Albright, J. Farnham, C. Teerlink, 2011, Obstetrics and gynecology.

Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21.

L. Cannon-Albright, J. Farnham, C. Teerlink, 2009, American journal of human genetics.

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

N. Camp, L. Cannon-Albright, J. Farnham, 2011, Human Genetics.

Population-based risks for cancer in patients with ALS

S. Pulst, L. Cannon-Albright, M. Bromberg, 2016, Neurology.

A candidate prostate cancer susceptibility gene at chromosome 17p

Siavash Ghaffari, Alun Thomas, Nicola J. Camp, 2001, Nature Genetics.

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

A. Whittemore, D. Schaid, J. Carpten, 2007, Human molecular genetics.

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

N. Camp, M. Feolo, S. Neuhausen, 2002, American journal of medical genetics.

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

D. Schaid, R. Eeles, Z. Kote-Jarai, 2016, Human Genetics.

Genome-wide analysis of high-risk primary brain cancer pedigrees identifies PDXDC1 as a candidate brain cancer predisposition gene.

L. Cannon-Albright, J. Farnham, C. Teerlink, 2020, Neuro-oncology.

A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma

L. Cannon-Albright, J. Farnham, Alun Thomas, 2018, Journal of the National Cancer Institute.

Shared Genomic Segment Analysis. Mapping Disease Predisposition Genes in Extended Pedigrees Using SNP Genotype Assays

K Allen-Brady, N J Camp, J M Farnham, 2008, Annals of human genetics.

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

A. Whittemore, D. Schaid, N. Camp, 2005, American journal of human genetics.

Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17.

L. Cannon-Albright, J. Farnham, P. Norton, 2015, American journal of obstetrics and gynecology.

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

A. Whittemore, D. Schaid, J. Carpten, 2012, BMC Medical Genetics.

Prostate cancer risk prediction based on complete prostate cancer family history

W. Lowrance, N. Agarwal, J. Farnham, 2014, The Prostate.

Relative risk for Alzheimer disease based on complete family history

L. Cannon-Albright, N. Foster, J. Kauwe, 2019, Neurology.

Increased risk for other cancers in individuals with Ewing sarcoma and their relatives

L. Cannon-Albright, K. Jones, J. Farnham, 2019, Cancer medicine.

Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.

L. Cannon-Albright, J. Farnham, C. Teerlink, 2016, Journal of shoulder and elbow surgery.

Charcot-Marie-Tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2→12

J. Farnham, A. Clarke, P. Harper, 1993, Human Genetics.

A genealogical assessment of heritable predisposition to aneurysms.

N. Camp, J. Farnham, J. Macdonald, 2003, Journal of neurosurgery.

Linkage analysis of HLA and candidate genes for celiac disease in a North American family-based study

M. Feolo, S. Neuhausen, J. Farnham, 2001, BMC Medical Genetics.

Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees.

N. Camp, L. Cannon-Albright, J. Farnham, 2006, Cancer research.

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

J. Malvehy, S. Puig, J. Farnham, 2018, European Journal of Human Genetics.

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

A. Whittemore, D. Schaid, J. Carpten, 2012, The Prostate.

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

N J Camp, J M Farnham, A. Thomas, 2005, American journal of medical genetics. Part A.

Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer’s Disease: A Population Database Analysis

L. Cannon-Albright, J. Kauwe, J. Farnham, 2022, International journal of environmental research and public health.

Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm

N. Camp, J. Tsuruda, L. Cannon-Albright, 2004, Human Genetics.

A New Nonparametric Linkage Statistic for Mapping Both Qualitative and Quantitative Trait Loci

N. Camp, L. Cannon-Albright, A. Gutin, 2001, Genetic epidemiology.

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

B. Horne, N. Camp, L. Cannon-Albright, 2005, Genetic epidemiology.

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

Kristina Allen-Brady, N. Camp, J. Farnham, 2003, BMC Genetics.

Identification of specific Y chromosomes associated with increased prostate cancer risk

L. Cannon-Albright, N. Agarwal, J. Farnham, 2014, The Prostate.

L. Cannon-Albright, J. Farnham, T. Bowles, 2018, Journal of the American Academy of Dermatology.

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements.

C. Wijmenga, J. Farnham, P. Harper, 1993, Human molecular genetics.

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

N. Camp, L. Cannon-Albright, J. Farnham, 2012, BMC Genomics.

A population‐based study of testicular cancer risk among children and young adults from Norway and Utah, USA

L. Cannon-Albright, P. Nafstad, J. Farnham, 2020, International journal of cancer.

Novel Popout: Effects of Field Unitization and Exposure Duration

W. Johnston, K. J. Hawley, J. Farnham, 1991 .

Correcting for multiple analyses in genomewide linkage studies

N J Camp, J M Farnham, N. Camp, 2001, Annals of human genetics.

Correcting for multiple analyses in genomewide linkage studies.

N. Camp, J. Farnham, 2001 .

Population genealogy resource shows evidence of familial clustering for Alzheimer disease

Sue M. Dintelman, L. Cannon-Albright, J. Kauwe, 2018, Neurology: Genetics.

Association of single nucleotide polymorphisms (SNPs) in ESR1 and PRMT8 and response to treatment with abiraterone acetate (AA) in men with metastatic castration refractory prostate cancer (mCRPC).

L. Cannon-Albright, N. Agarwal, J. Farnham, 2015 .

STUDIES OF PERCEPTUAL MEMORY: FINAL REPORT

Kevin J. Hawley, W. Johnston, K. J. Hawley, 2022 .

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

N. Camp, L. Cannon-Albright, J. Farnham, 2007, The Prostate.

A Robust Multipoint Linkage Statistic (tlod) for Mapping Complex Trait Loci

N. Camp, L. Cannon-Albright, Alun Thomas, 2001, Genetic epidemiology.

Can standard measures identify subclinical markers of autism?

J M Farnham, B. Pennington, S. Rogers, 1993, Journal of autism and developmental disorders.

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

J. Malvehy, S. Puig, J. Farnham, 2018, European Journal of Human Genetics.

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

N. Camp, E. Ostrander, L. Cannon-Albright, 2009, BMC Research Notes.

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

A. Whittemore, D. Schaid, J. Carpten, 2010, The Prostate.