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N

Norbert Arnold

humboldt university of berlin
H指数:59
被引数:1.3万

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A critical spotlight on the paradigms of FFPE-DNA sequencing

Ffpe-dna测序范式的关键焦点

2023-06-2315
OAAI
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers

多基因风险评分表明女性BRCA1/2致病变异携带者乳腺癌发病的极端年龄

2022-06-277
OAAI
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

基于313变异的多基因风险评分对具有杂合BRCA1或BRCA2致病变异的欧洲血统女性对侧乳腺癌风险预测的预测能力

2021-09-0120
OAAI
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

使用多基因风险评分的男性BRCA1和BRCA2致病性变异携带者的乳腺癌和前列腺癌风险

2021-07-2829
OAAI
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

仅病例研究,以确定BRCA1/BRCA2突变携带者的乳腺癌风险的遗传调节剂 (第12卷,1078,2021)

2021-05-140
OAAI
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

仅针对病例的研究,以确定BRCA1/BRCA2突变携带者的乳腺癌风险的遗传调节剂

2021-02-1724
OAAI
Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers
2020-12-2919
OA
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

BRCA1和BRCA2致病变异携带者的多基因风险评分和乳腺癌和上皮性卵巢癌风险

2020-10-0179
OAAI
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

种系HOXB13突变p.G84E和p.R217C不增加乳腺癌风险

2020-06-163
OAAI
Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

BRCA1和BRCA2基因组域与前列腺癌风险和侵袭性的关系

2020-02-0336
OAAI
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
2019-08-0811
OAAI
Breast cancer risk inBRCA1/2mutation carriers and noncarriers under prospective intensified surveillance

前瞻性强化监测下brca1/2突变携带者和非携带者的乳腺癌风险

2019-05-2232
OAAI
Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

BARD1基因种系功能缺失变异与早发家族性乳腺癌相关,但与卵巢癌无关

2019-04-2947
OAAI
The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers
2019-01-066
OAAI
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history

无癌症家族史的802例单侧三阴性乳腺癌妇女中致病性BRCA1/2种系突变的发生率

2018-03-0780
OAAI