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

A catalog of curated breast cancer genes

精选乳腺癌基因目录

Bose, Muthiah; Benada, Jan; Thatte, Jayashree Vijay; Kinalis, Savvas; Ejlertsen, Bent; Nielsen, Finn Cilius; Sørensen, Claus Storgaard; Rossing, Maria

A Gain-of-Function p53-Mutant Oncogene Promotes Cell Fate Plasticity and Myeloid Leukemia through the Pluripotency Factor FOXH1

获得功能的 p53 突变致癌基因通过多能性因子 FOXH1 促进细胞命运可塑性和髓系白血病

Evangelia Loizou, Ana Banito, Geulah Livshits, Yu-Jui Ho, Richard P Koche, Francisco J Sánchez-Rivera, Allison Mayle, Chi-Chao Chen, Savvas Kinalis, Frederik O Bagger, Edward R Kastenhuber, Benjamin H Durham, Scott W Lowe

BloodSpot: a database of healthy and malignant haematopoiesis updated with purified and single cell mRNA sequencing profiles

BloodSpot:一个包含健康和恶性造血信息的数据库,并已更新纯化和单细胞mRNA测序谱。

Bagger, Frederik Otzen; Kinalis, Savvas; Rapin, Nicolas

Deep targeted sequencing of TP53 in chronic lymphocytic leukemia: clinical impact at diagnosis and at time of treatment

慢性淋巴细胞白血病中TP53的深度靶向测序:诊断和治疗时的临床意义

Brieghel, Christian; Kinalis, Savvas; Yde, Christina W; Schmidt, Ane Y; Jønson, Lars; Andersen, Michael A; da Cunha-Bang, Caspar; Pedersen, Lone B; Geisler, Christian H; Nielsen, Finn C; Niemann, Carsten U

High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer

晚期癌症患者同源重组修复中致病性种系变异的发生率较高

Bertelsen, Birgitte; Tuxen, Ida Viller; Yde, Christina Westmose; Gabrielaite, Migle; Torp, Mathias Husted; Kinalis, Savvas; Oestrup, Olga; Rohrberg, Kristoffer; Spangaard, Iben; Santoni-Rugiu, Eric; Wadt, Karin; Mau-Sorensen, Morten; Lassen, Ulrik; Nielsen, Finn Cilius

Deconvolution of autoencoders to learn biological regulatory modules from single cell mRNA sequencing data

利用自编码器反卷积从单细胞mRNA测序数据中学习生物调控模块

Kinalis, Savvas; Nielsen, Finn Cilius; Winther, Ole; Bagger, Frederik Otzen

Circulating tumor DNA as a marker of treatment response in BRAF V600E mutated non-melanoma solid tumors

循环肿瘤DNA作为BRAF V600E突变型非黑色素瘤实体瘤治疗反应的标志物

Ahlborn, Lise Barlebo; Tuxen, Ida Viller; Mouliere, Florent; Kinalis, Savvas; Schmidt, Ane Y; Rohrberg, Kristoffer Staal; Santoni-Rugiu, Eric; Nielsen, Finn Cilius; Lassen, Ulrik; Yde, Christina Westmose; Oestrup, Olga; Mau-Sorensen, Morten

Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia

应用全外显子组测序指导对斯堪的纳维亚半岛厄勒海峡地区患者进行罕见遗传性出血性疾病的特定功能检测和诊断

Eva Leinøe, Eva Zetterberg, Savvas Kinalis, Olga Østrup, Peter Kampmann, Eva Norström, Nadine Andersson, Jenny Klintman, Klaus Qvortrup, Finn Cilius Nielsen, Maria Rossing