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Hereditary Cancer in Clinical Practice 封面图

Hereditary Cancer in Clinical Practice

IF2.4
论文数24
被引数593
期刊论文 24
发表时间
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Renal cell carcinoma risk among individuals heterozygous for fumarate hydratase variants: further insights into genotype-phenotype correlations异柠檬酸脱氢酶变异杂合子个体中肾细胞癌的风险：对基因型-表型相关性的进一步认识
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-05-12
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PREAI
deleteHoffman, Trevor L.; Wirio, Sony; Sethumadhavan, Vivek
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Breast cancer specialists' experiences and attitudes towards mainstream genetic testing for patients with breast cancer
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-04-24
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PREAI
deleteAllan, Kirsten; Cicciarelli, Linda; Beard, Catherine; Lindeman, Geoffrey J.; Mann, G. Bruce; James, Paul A.; Forrest, Laura E.
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Monitoring and treatment patterns of von Hippel-Lindau disease-associated central nervous system hemangioblastomas监测和治疗von Hippel-Lindau病相关的中枢神经系统血管母细胞瘤的模式
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-04-20
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PREAI
deleteJonasch, Eric; Song, Yan; Freimark, Jonathan; Mohan, Manasi; Signorovitch, James; Sundaram, Murali
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Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis胚系MMR基因变异对MSI-H/dMMR消化道癌患者免疫检查点抑制剂反应的影响：一项回顾性队列分析
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-04-18
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PREAI
deleteDardenne, Antoine; Loisel, Camille; Pellat, Anna; Perrier, Alexandre; Metras, Julie; Samaille, Thomas; Parc, Yann; Leclerc, Julie; Cohen, Romain; Andre, Thierry
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Importance of genetic testing in childhood cancer survivors for hereditary cancer predisposition syndromes儿童癌症幸存者进行遗传癌症易感综合征基因检测的重要性
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-04-15
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PREAI
deleteUrbas, Anja; Usaj, Polona; Seruga, Bostjan; Krajc, Mateja; Hotujec, Simona; Stegel, Vida; Zaletel, Lorna Zadravec
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Meeting abstracts from the Annual Conference Clinical Genetics of Cancer 2024 Abstracts2024年癌症临床遗传学年会摘要集
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-05
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PREAI
deleteBialkowska, Katarzyna; Jakubowska, Anna
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Challenging interpretation of low-level PTCH1 mosaicism in patients with clinically diagnosed Gorlin syndrome: a case series and review of the literature临床诊断戈林综合征患者中低水平PTCH1嵌合现象的解读挑战：病例系列分析及文献综述
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-01
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PREAI
deleteDwarte, Tanya M.; Alli, Rozanna; Srinivasa, Shweta; Noon, Fallon; Kimmantudawage, Sumudu Perera; Gordon, Lisa; Beshay, Victoria; Joshua, Anthony M.; Araujo, Raquel Ruiz; Jalilian, Chris; Thomas, David M.; Smith, Miriam J.; Winship, Ingrid; Ballinger, Mandy L.; Li, Minmin; Tucker, Katherine M.; Courtney, Eliza K.
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Case report: a rare BRCA1 de novo variant in a female with breast cancer病例报告：一名乳腺癌女性患者中罕见的BRCA1新发变异
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-01
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PREAI
deleteDencker, Carlotta; Strehlow, Vincent; Aktas, Bahriye; Lemke, Johannes; Hentschel, Julia
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A retrospective analysis of risk-reducing salpingo-oophorectomy performed in women diagnosed with hereditary breast and ovarian cancer at our institution对在本机构进行的风险降低性输卵管卵巢切除术的回顾性分析：针对被诊断为遗传性乳腺癌和卵巢癌的女性
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-01
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PREAI
deleteShimizu, Yusaku; Kitai, Miho; Akada, Masashi; Maeda, Michihide; Yamabe, Eri; Kakubari, Reisa; Hisa, Tsuyoshi; Kamiura, Shoji
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Utilization of care and alignment of screening with NCCN guidelines for patients with Lynch syndrome: a retrospective cohort study利用护理和筛查与NCCN指南的契合度对林奇综合征患者的研究：一项回顾性队列研究
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-01
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PREAI
deleteLowry, Christina; Laurent, Cecile; Bindra, Ameek K.; Powell, C. Bethan; Garcia, Christine
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Genomic profiling in Bulgarian women with ovarian cancer: a dual-sample NGS approach保加利亚卵巢癌女性患者的基因组分析：一种双样本NGS方法
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-03-01
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PREAI
deleteKamburova, Zornitsa; Popovska, Savelina; Tsvetkov, Chavdar
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Two novel multiple endocrine neoplasia type 1 variants caused thymic neuroendocrine tumor: a case report两种新型多发性内分泌腺瘤病1型变异导致胸腺神经内分泌肿瘤：病例报告
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-02-24
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PREAI
deleteDai, Zi; Zhang, Jing; Wang, Jing; Ma, Leshi; Liao, Pei; Deng, Xiaojie; Li, Zhenxiang; Luo, Zhijie; Guan, Jieshan
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Primary and metastatic brain tumours in hereditary cancer syndromes: case reports with and literature review遗传性癌综合征中的原发性与转移性脑肿瘤：病例报告与文献综述
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-01-29
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PREAI
deleteRobaczynska, Joanna; Kiljanczyk, Milena; Stachowski, Adam; Lubinski, Krzysztof; Dodopoulos, Angelos; Benali, Rayane; Kiljanczyk, Adam; Becht, Rafal; Cybulski, Cezary; Gronwald, Jacek; Lubinski, Jan
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Decisional conflict in women with a BRCA1 or BRCA2 pathogenic variant who have not elected for risk-reducing salpingo-oophorectomyBRCA1或BRCA2致病性变异且未选择风险降低性输卵管卵巢切除术的女性的决策冲突
deleteHereditary Cancer in Clinical Practice
IF2.4
delete2026-01-17
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PREAI
deleteMetcalfe, Kelly A.; Kinney, Anita Y.; Narod, Steven A.; Poll, Aletta; Armel, Susan; Lombardi, Lucia; Tavangar, Farideh; Pal, Tuya
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Skin cancer risk in hereditary mixed cancer syndromes遗传性混合癌综合征中的皮肤癌风险
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-12-02
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PREAI
deleteNikkola, Veera; Alakoski, Anna; Mecklin, Jukka-Pekka; Seppala, Toni T.; Nikkola, Jussi; Schrader, Kashmintan
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Clinical characteristics and healthcare burden of neurofibromatosis type 1 in Saudi Arabia: a single centre experience神经纤维瘤病1型的临床特征及医疗负担：沙特阿拉伯单一中心经验
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-11-26
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deleteAlmuqbil, Mohammed A.; Al Ammari, Maha; Al Dhayyan, Nada S.; Kaithathara, Seena Thomas; Al Balwi, Mohamed
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Contribution of MLH1, MSH2, and MSH6 large genomic rearrangements to Pakistani colorectal cancer patientsMLH1、MSH2和MSH6大片段基因组重排对巴基斯坦结直肠癌患者的贡献
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-11-19
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deleteNaeemi, Humaira; Muhammad, Noor; Loya, Asif; Yusuf, Muhammed Aasim; Rashid, Muhammad Usman
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The genetic puzzle of FAP: exploring novel diagnostic approaches for APC/MUTYH-negative caseFAP的遗传之谜：探索APC/MUTYH阴性病例的新型诊断方法
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-11-07
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deleteGrot, Natalia; Kazimierczyk, Marek; Szuman, Marcin; Kaczmarek-Rys, Marta; Kryszczynska, Alicja; Dziechciowska, Iga; Knaur, Monika; Hnatyszyn, Andrzej; Hryhorowicz, Szymon; Plawski, Andrzej
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Molecular markers associated with elevated colorectal cancer risk: a mini review
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-11-05
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deleteSzuman, Marcin; Kazimierczyk, Marek; Grot, Natalia; Kaczmarek-Rys, Marta; Kryszczynska, Alicja; Dziechciowska, Iga; Knaur, Monika; Hnatyszyn, Andrzej; Hryhorowicz, Szymon; Plawski, Andrzej
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Tumour spectrum, distinguishing features and management recommendations for NTHL1-associated tumour syndrome: a systematic review肿瘤谱系、鉴别特征以及NTHL1相关肿瘤综合征的管理建议：一项系统综述
deleteHEREDITARY CANCER IN CLINICAL PRACTICE
IF2.4
delete2025-10-17
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deleteGao, Weilun; Liao, Chuyi; Buchanan, Daniel D.; Macrae, Finlay; de Voer, Richarda M.
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