(Q34269998)

1 August 2017

title

Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. (English)

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1 August 2017

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2

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1 August 2017

Richie Soong

6

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Dimitrios H. Roukos

object named as

Dimitrios H Roukos

4

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Yudi Pawitan

5

object named as

Yudi Pawitan

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1 August 2017

Chee-Seng Ku

1

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1 August 2017

Mengchu Wu

3

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1 August 2017

Barry Iacopetta

7

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1 August 2017

publication date

20 April 2012

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1 August 2017

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1 August 2017

volume

25

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1 August 2017

issue

8

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1 August 2017

page(s)

1055-1068

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https://scigraph.springernature.com/pub.10.1038/modpathol.2012.62

1 August 2017

exact match

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cites work

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Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.

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Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

21 January 2018

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Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

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PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

21 January 2018

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PALB2: a novel inactivating mutation in a Italian breast cancer family.

21 January 2018

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21 January 2018

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Somatic hypermethylation of MSH2 is a frequent event in Lynch Syndrome colorectal cancers

21 January 2018

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Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Hereditary gastric cancer

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Clinical cancer genetics: Part I: Gastrointestinal

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Hereditary colorectal cancer diagnostics: morphological features of familial colorectal cancer type X versus Lynch syndrome.

21 January 2018

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21 January 2018

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21 January 2018

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CpG island methylator phenotype-low (CIMP-low) in colorectal cancer: possible associations with male sex and KRAS mutations

21 January 2018

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Three DNA methylation epigenotypes in human colorectal cancer

21 January 2018

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Genome-scale analysis of aberrant DNA methylation in colorectal cancer

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Molecular correlates with MGMT promoter methylation and silencing support CpG island methylator phenotype-low (CIMP-low) in colorectal cancer.

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

CpG island methylator phenotype-low (CIMP-low) colorectal cancer shows not only few methylated CIMP-high-specific CpG islands, but also low-level methylation at individual loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Aberrant DNA methylation in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency

21 January 2018

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Epigenomic diversity of colorectal cancer indicated by LINE-1 methylation in a database of 869 tumors

21 January 2018

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A cohort study of tumoral LINE-1 hypomethylation and prognosis in colon cancer

21 January 2018

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DNA methylation predicts recurrence from resected stage III proximal colon cancer

21 January 2018

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Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

A compendium of genome-wide associations for cancer: critical synopsis and reappraisal

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Low-penetrance susceptibility variants in familial colorectal cancer

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Molecular pathological epidemiology of colorectal neoplasia: an emerging transdisciplinary and interdisciplinary field

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Familial nasopharyngeal carcinoma

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Familial testicular germ cell tumors in adults: 2010 summary of genetic risk factors and clinical phenotype

21 January 2018

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Familial chronic lymphocytic leukemia

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

A genome-wide association study of testicular germ cell tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

A PALB2 germline mutation associated with hereditary breast cancer in Italy

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

Breast cancer genome-wide association studies: there is strength in numbers

21 January 2018

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Common disorders are quantitative traits

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Familial colorectal cancer type X syndrome: two distinct molecular entities?

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Differential features of colorectal cancers fulfilling Amsterdam criteria without involvement of the mutator pathway

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Complex segregation analysis of nasopharyngeal carcinoma in Guangdong, China: evidence for a multifactorial mode of inheritance (complex segregation analysis of NPC in China)

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

A genome-wide scan suggests a susceptibility locus on 5p 13 for nasopharyngeal carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Update on familial pancreatic cancer

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https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

Increased frequency of 20q gain and copy-neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.2012.62

7 January 2021

10.1038/MODPATHOL.2012.62

Identifiers

DOI

1 reference

Dimensions Publication ID

1 August 2017

1006551337

0 references

1 reference