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孙洁基因检测

孙洁主治医师

北京大学肿瘤医院家族遗传性肿瘤中心

孙洁,主治医师,博士。从事家族遗传性乳腺癌的临床工作与研究,擅长家族遗传性乳腺癌的遗传咨询、基因检测解读与风险评估。现为北京抗癌协会家族遗传性肿瘤专委会秘书。以第一作者身份在《J Clin Oncol》、《Clin Can Res》等国际主流肿瘤刊物发表SCI论文6篇,影响因子累积84分。授权发明专利1项。主持国自然青年基金1项,主持院内基金1项。参与编译/编写《哈里森内科学:肿瘤疾病分册》、《整合肿瘤学》等书籍。发表论文:,1. Sun J#, Chu F#, Pan J#, Zhang Y, Yao L, Chen J, Hu L, Zhang J, Xu Y, Wang X et al: BRCA-CRisk: A Contralateral Breast Cancer Risk Prediction Model for BRCA Carriers. J Clin Oncol 2023,41(5):991-999,2. Hu L#, Sun J#, Li Z, Qu Z, Liu Y, Wan Q, Liu J, Ding X, Zang F, Zhang J et al: Clinical Relevance of Pathogenic Germline Variants in Mismatch Repair Genes in Chinese Breast Cancer Patients. NPJ Breast Cancer 2022, 8(1):52.,3. Fu F#, Zhang Y#, Sun J#, Zhang C, Zhang D, Xie L, Chu F, Yu X, Xie Y: Predictors of Sentinel Lymph Node Metastasis in Chinese Women with Clinical T1-T2 N0 Breast Cancer and a Normal Axillary Ultrasound. Acta Radiol 2022, 63(11):1463-1468.,4. Sun J#, Meng H#, Yao L, Lv M, Bai J, Zhang J, Wang L, Ouyang T, Li J, Wang T et al: Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. Clin Cancer Res 2017, 23(20):6113-6119.,5. Zhang J#, Sun J#, Chen J#, Yao L#, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B et al: Comprehensive Analysis of BRCA1 and BRCA2 Germline Mutations in A Large Cohort of 5931 Chinese Women with Breast Cancer. Breast Cancer Res Treat 2016, 158(3):455-462.,6. Sun J#, Wang Y#, Xia Y#, Xu Y, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B et al: Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer. PLoS Genet 2015, 11(5):e1005228.
孙洁 —— 专家简介
孙洁,主治医师,博士。从事家族遗传性乳腺癌的临床工作与研究,擅长家族遗传性乳腺癌的遗传咨询、基因检测解读与风险评估。现为北京抗癌协会家族遗传性肿瘤专委会秘书。以第一作者身份在《J Clin Oncol》、《Clin Can Res》等国际主流肿瘤刊物发表SCI论文6篇,影响因子累积84分。授权发明专利1项。主持国自然青年基金1项,主持院内基金1项。参与编译/编写《哈里森内科学:肿瘤疾病分册》、《整合肿瘤学》等书籍。发表论文:,1. Sun J#, Chu F#, Pan J#, Zhang Y, Yao L, Chen J, Hu L, Zhang J, Xu Y, Wang X et al: BRCA-CRisk: A Contralateral Breast Cancer Risk Prediction Model for BRCA Carriers. J Clin Oncol 2023,41(5):991-999,2. Hu L#, Sun J#, Li Z, Qu Z, Liu Y, Wan Q, Liu J, Ding X, Zang F, Zhang J et al: Clinical Relevance of Pathogenic Germline Variants in Mismatch Repair Genes in Chinese Breast Cancer Patients. NPJ Breast Cancer 2022, 8(1):52.,3. Fu F#, Zhang Y#, Sun J#, Zhang C, Zhang D, Xie L, Chu F, Yu X, Xie Y: Predictors of Sentinel Lymph Node Metastasis in Chinese Women with Clinical T1-T2 N0 Breast Cancer and a Normal Axillary Ultrasound. Acta Radiol 2022, 63(11):1463-1468.,4. Sun J#, Meng H#, Yao L, Lv M, Bai J, Zhang J, Wang L, Ouyang T, Li J, Wang T et al: Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. Clin Cancer Res 2017, 23(20):6113-6119.,5. Zhang J#, Sun J#, Chen J#, Yao L#, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B et al: Comprehensive Analysis of BRCA1 and BRCA2 Germline Mutations in A Large Cohort of 5931 Chinese Women with Breast Cancer. Breast Cancer Res Treat 2016, 158(3):455-462.,6. Sun J#, Wang Y#, Xia Y#, Xu Y, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B et al: Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer. PLoS Genet 2015, 11(5):e1005228.

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