Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. (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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1 August 2017

Richie Soong

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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

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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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Comprehensive comparison of three commercial human whole-exome capture platforms

1 August 2017

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A genome-wide association study of testicular germ cell tumor

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

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

21 January 2018

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

21 January 2018

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

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A PALB2 germline mutation associated with hereditary breast cancer in Italy

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

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Common disorders are quantitative traits

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

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

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

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

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

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Update on familial pancreatic cancer

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

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Identifiers

DOI

1 reference

Dimensions Publication ID

1 August 2017

1006551337

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1 reference