Cargando…

Significant Evidence of Linkage for a Gene Predisposing to Colorectal Cancer and Multiple Primary Cancers on 22q11

OBJECTIVES: The genetic basis of colorectal cancer (CRC) is not completely specified. Part of the difficulty in mapping predisposition genes for CRC may be because of phenotypic heterogeneity. Using data from a population genealogy of Utah record linked to a statewide cancer registry, we identified...

Descripción completa

Detalles Bibliográficos
Autores principales:	Teerlink, Craig, Nelson, Quentin, Burt, Randall, Cannon-Albright, Lisa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2014
Materias:	Original Contribution
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940837/ https://www.ncbi.nlm.nih.gov/pubmed/24572700 http://dx.doi.org/10.1038/ctg.2014.1

Ejemplares similares

Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
por: Albright, Frederick, et al.
Publicado: (2012)

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21
por: Cannon-Albright, Lisa A, et al.
Publicado: (2012)

A Rare Variant in ERF (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended Pedigree
por: Cannon-Albright, Lisa Anne, et al.
Publicado: (2021)

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
por: Chang, Xiao, et al.
Publicado: (2017)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approach
por: Schneider, Maude, et al.
Publicado: (2013)

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer
por: Neklason, Deborah W, et al.
Publicado: (2010)

Are submicroscopic chromosomal inversions predisposing factors for the t(9;22)(q34;q11.2) translocation in chronic myeloid leukemia?
por: González García, Juan Ramón, et al.
Publicado: (2015)

Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans
por: Yoon, Se Chang, et al.
Publicado: (2016)

Prostate cancer risk prediction based on complete prostate cancer family history
por: Albright, Frederick, et al.
Publicado: (2015)

Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study
por: Schoemaker, Minouk J, et al.
Publicado: (2019)

No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients
por: Guipponi, M, et al.
Publicado: (2017)

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees
por: Cai, Zheng, et al.
Publicado: (2012)

Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q
por: Picelli, Simone, et al.
Publicado: (2008)

High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer
por: Cannon-Albright, Lisa A., et al.
Publicado: (2023)

Extracting disease risk profiles from expression data for linkage analysis: application to prostate cancer
por: Christensen, G Bryce, et al.
Publicado: (2007)

The Danish 22q11 research initiative
por: Schmock, Henriette, et al.
Publicado: (2015)

A population-based analysis of clustering identifies a strong genetic contribution to lethal prostate cancer
por: Nelson, Quentin, et al.
Publicado: (2013)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor
por: Cannon‐Albright, Lisa A., et al.
Publicado: (2020)

The Association of Telomere Length with Colorectal Cancer Differs by the Age of Cancer Onset
por: Boardman, Lisa A, et al.
Publicado: (2014)

Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring
por: Capra, Valeria, et al.
Publicado: (2013)

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

Strategies for selection of subjects for sequencing after detection of a linkage peak
por: Allen-Brady, Kristina, et al.
Publicado: (2011)

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders
por: Jalal, Rhideeta, et al.
Publicado: (2021)

An enhancer variant at 16q22.1 predisposes to hepatocellular carcinoma via regulating PRMT7 expression
por: Shen, Ting, et al.
Publicado: (2022)

Genotypic and phenotypic variability of 22q11.2 microdeletions – an institutional experience
por: Manno, Gabrielle C., et al.
Publicado: (2021)

Quantifying sources of bias in longitudinal data linkage studies of child abuse and neglect: measuring impact of outcome specification, linkage error, and partial cohort follow-up
por: Parrish, Jared W., et al.
Publicado: (2017)

Why Does Obesity as an Inflammatory Condition Predispose to Colorectal Cancer?
por: Rychter, Anna Maria, et al.
Publicado: (2023)

Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands
por: Åberg, Karolina, et al.
Publicado: (2009)

22q11 deletion syndrome: current perspective
por: Hacıhamdioğlu, Bülent, et al.
Publicado: (2015)

22q11 Deletion Syndrome with Vascular Anomalies
por: Maldjian, Pierre, et al.
Publicado: (2018)

Optimising immunisation in children with 22q11 microdeletion
por: Berkhout, Angela, et al.
Publicado: (2020)

The 22q11.2 Low Copy Repeats
por: Vervoort, Lisanne, et al.
Publicado: (2022)

Comorbidity and Cancer Disease Rates among Those at High-Risk for Alzheimer’s Disease: A Population Database Analysis
por: Valentine, David, et al.
Publicado: (2022)

A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?
por: Bertini, Veronica, et al.
Publicado: (2017)

Smoking-Related Risks of Colorectal Cancer by Anatomical Subsite and Sex
por: Gram, Inger T, et al.
Publicado: (2020)

DNA Methylation Identifies Loci Distinguishing Hereditary Nonpolyposis Colorectal Cancer Without Germ-Line MLH1/MSH2 Mutation from Sporadic Colorectal Cancer
por: Chen, Chung-Hsing, et al.
Publicado: (2016)

Prognostic Significance of MRE11 Overexpression in Colorectal Cancer Patients
por: Ho, Vincent, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_c1ssu6228hu5uo6u5sdhoijtrp