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

An artificial intelligence-assisted clinical framework to facilitate diagnostics and translational discovery in hematologic neoplasia

人工智能辅助临床框架,促进血液系统肿瘤的诊断和转化发现

Ming Tang, Željko Antić, Pedram Fardzadeh, Stefan Pietzsch, Charlotte Schröder, Adrian Eberhardt, Alena van Bömmel, Gabriele Escherich, Winfried Hofmann, Martin A Horstmann, Thomas Illig, J Matt McCrary, Jana Lentes, Markus Metzler, Wolfgang Nejdl, Brigitte Schlegelberger, Martin Schrappe, Martin Zi

Major Problems in Clinical Psychological Science and How to Address them. Introducing a Multimodal Dynamical Network Approach

临床心理科学中的主要问题及其解决方法:引入多模态动态网络方法

Westhoff, Marlon; Berg, Max; Reif, Andreas; Rief, Winfried; Hofmann, Stefan G

CTLA-4 Insufficiency due to a Novel CTLA-4 Deletion, Identified through Copy Number Variation Analysis

通过拷贝数变异分析确定 CTLA-4 缺陷是由于新的 CTLA-4 缺失所致

Lisa Olfe, Sandra von Hardenberg, Winfried Hofmann, Bernd Auber, Ulrich Baumann, Rita Beier, Ignatius Ryan Adriawan, Faranaz Atschekzei, Torsten Witte, Georgios Sogkas

Do We Need a Novel Framework for Classifying Psychopathology? A Discussion Paper

我们是否需要一种新的精神病理学分类框架?一份讨论文件

Rief, Winfried; Hofmann, Stefan G; Berg, Max; Forbes, Miriam K; Pizzagalli, Diego A; Zimmermann, Johannes; Fried, Eiko; Reed, Geoffrey M

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing

通过全外显子组测序鉴定出与分枝杆菌感染易感性相关的候选基因和序列变异。

Alexander Varzari ,Igor V Deyneko ,Gitte Hoffmann Bruun ,Maja Dembic ,Winfried Hofmann ,Victor M Cebotari ,Sergei S Ginda ,Brage S Andresen ,Thomas Illig

Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair

PNKP 的病理突变会引发 DNA 单链断裂修复缺陷,但不会导致 DNA 双链断裂修复缺陷

Ilona Kalasova, Richard Hailstone, Janin Bublitz, Jovel Bogantes, Winfried Hofmann, Alejandro Leal, Hana Hanzlikova, Keith W Caldecott

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

疑似李-弗劳梅尼综合征的乳腺癌患者:突变谱、候选基因和未解释的遗传

Judith Penkert ,Gunnar Schmidt ,Winfried Hofmann ,Stephanie Schubert ,Maximilian Schieck ,Bernd Auber ,Tim Ripperger ,Karl Hackmann ,Marc Sturm ,Holger Prokisch ,Ursula Hille-Betz ,Dorothea Mark ,Thomas Illig ,Brigitte Schlegelberger ,Doris Steinemann