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J

Juul Wijnen

john hunter hospital
H指数:66
被引数:1.7万

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Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes
2018-10-038
OAAI
Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue

卵巢肿瘤组织中BRCA1/2变异筛查的验证与实施

2018-09-0121
OAAI
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

鉴定与雌激素受体阴性乳腺癌风险相关的十种变异

2017-10-23270
OAAI
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (vol 117, pg 1215, 2017)
2017-10-121
OAAI
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
2017-07-2510
OAAI
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

疑似Lynch综合征或体质错配修复缺陷综合征的大量先证者中PMS2的综合突变分析

2016-08-2148
OAAI
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
2016-04-0116
OAAI
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms
2016-03-2365
OAAI
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
2015-11-1028
OAAI
Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyl tripeptide in combination with interferon-γ
2014-03-1078
OAAI
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
2013-12-22382
OA
Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

11q23和15q13上的结直肠癌风险变异与无法解释的腺瘤性息肉病相关

2013-11-1923
OA