日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Whole-miRNome sequencing: a panel for the targeted sequencing of all human miRNA genes.

全 miRNA 组测序:用于对所有人类 miRNA 基因进行靶向测序的检测方法

Galka-Marciniak Paulina, Urbanek-Trzeciak Martyna Olga, Kuznicki Daniel, Szostak Natalia, Tire Adrian, Nawrocka-Muszynska Paulina Maria, Chojnacka Katarzyna, Suszynska Malwina, Klonowska Katarzyna, Czubak Karol, Machowska Magdalena, Philips Anna, Maksin Konstantin, Susok Laura, Sand Michael, Rys Janusz, Jura Jolanta, Ratajska Magdalena, Dams-Kozlowska Hanna, Kowalewski Janusz, Lewandowska Marzena Anna, Kozlowski Piotr

Editorial: 365 days of progress in cancer genetics

社论:癌症遗传学365天的进展

Ratajska, Magdalena; Sette, Claudio; Cunliffe, Heather E

Diagnostic Accuracy of Liquid Biopsy in Endometrial Cancer

液体活检在子宫内膜癌诊断中的准确性

Łukasiewicz, Marta; Pastuszak, Krzysztof; Łapińska-Szumczyk, Sylwia; Różański, Robert; Veld, Sjors G J G In 't; Bieńkowski, Michał; Stokowy, Tomasz; Ratajska, Magdalena; Best, Myron G; Würdinger, Thomas; Żaczek, Anna J; Supernat, Anna; Jassem, Jacek

BARD1 Autoantibody Blood Test for Early Detection of Ovarian Cancer

BARD1自身抗体血液检测用于卵巢癌的早期诊断

Pilyugin, Maxim; Ratajska, Magdalena; Stukan, Maciej; Concin, Nicole; Zeillinger, Robert; Irminger-Finger, Irmgard

BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases

BRIP1、RAD51C 和 RAD51D 基因突变与卵巢癌高易感性相关:基于约 30,000 例病例汇总分析的突变患病率和精确风险估计

Suszynska, Malwina; Ratajska, Magdalena; Kozlowski, Piotr

BARD1 is A Low/Moderate Breast Cancer Risk Gene: Evidence Based on An Association Study of the Central European p.Q564X Recurrent Mutation

BARD1 是一个低/中等乳腺癌风险基因:基于中欧 p.Q564X 复发突变关联研究的证据

Suszynska, Malwina; Kluzniak, Wojciech; Wokolorczyk, Dominika; Jakubowska, Anna; Huzarski, Tomasz; Gronwald, Jacek; Debniak, Tadeusz; Szwiec, Marek; Ratajska, Magdalena; Klonowska, Katarzyna; Narod, Steven; Bogdanova, Natalia; Dörk, Thilo; Lubinski, Jan; Cybulski, Cezary; Kozlowski, Piotr

Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer

检测卵巢癌患者循环肿瘤DNA中的BRCA1/2突变

Ratajska, Magdalena; Koczkowska, Magdalena; Żuk, Monika; Gorczyński, Adam; Kuźniacka, Alina; Stukan, Maciej; Biernat, Wojciech; Limon, Janusz; Wasąg, Bartosz

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example.

对乳腺癌和/或卵巢癌患者 BARD1 基因大突变的分析:以波兰人群为例

Klonowska Katarzyna, Ratajska Magdalena, Czubak Karol, Kuzniacka Alina, Brozek Izabela, Koczkowska Magdalena, Sniadecki Marcin, Debniak Jaroslaw, Wydra Dariusz, Balut Magdalena, Stukan Maciej, Zmienko Agnieszka, Nowakowska Beata, Irminger-Finger Irmgard, Limon Janusz, Kozlowski Piotr

Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing

对134例连续卵巢癌患者进行BRCA1/2基因突变分析。通过二代测序检测到新的和复发的BRCA1/2基因改变。

Ratajska, Magdalena; Krygier, Magdalena; Stukan, Maciej; Kuźniacka, Alina; Koczkowska, Magdalena; Dudziak, Mirosław; Śniadecki, Marcin; Dębniak, Jarosław; Wydra, Dariusz; Brozek, Izabela; Biernat, Wojciech; Borg, Ake; Limon, Janusz; Wasąg, Bartosz

Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

波兰科内莉亚·德·兰格综合征患者中NIPBL基因突变的谱系

Kuzniacka, Alina; Wierzba, Jolanta; Ratajska, Magdalena; Lipska, Beata S; Koczkowska, Magdalena; Malinowska, Monika; Limon, Janusz