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

Structured neurological soft signs examination reveals motor coordination deficits in adults diagnosed with high-functioning autism

结构化的神经系统软体征检查揭示了被诊断为高功能自闭症的成年人的运动协调缺陷

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-66723-5
Wieting, Jelte; Baumann, Madita Vanessa; Deest-Gaubatz, Stephanie; Bleich, Stefan; Eberlein, Christian Karl; Frieling, Helge; Deest, Maximilian
自闭症
神经科学
发表日期：2024
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Sex differences in MAGEL2 gene promoter methylation in high functioning autism - trends from a pilot study using nanopore Cas9 targeted long read sequencing

高功能自闭症患者MAGEL2基因启动子甲基化水平的性别差异——基于纳米孔Cas9靶向长读测序的初步研究趋势

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-02053-9
Wieting, Jelte; Jahn, Kirsten; Bleich, Stefan; Deest, Maximilian; Frieling, Helge
MAG
自闭症
表观遗传
神经科学
发表日期：2024
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A targeted long-read sequencing approach questions the association of OXTR methylation with high-functioning autism

一项针对性的长读长测序方法对OXTR甲基化与高功能自闭症之间的关联提出了质疑

期刊:Clinical Epigenetics
影响因子:4.4
doi:10.1186/s13148-023-01616-4
Wieting, Jelte; Jahn, Kirsten; Bleich, Stefan; Frieling, Helge; Deest, Maximilian
自闭症
表观遗传
神经科学
发表日期：2023
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Neurological soft signs are increased in major depressive disorder irrespective of treatment

重度抑郁症患者的神经系统软体征增多，且与治疗无关。

期刊:Journal of Neural Transmission
影响因子:4
doi:10.1007/s00702-023-02602-z
Schülke, Rasmus; Liepach, Kyra; Brömstrup, Anna Lena; Folsche, Thorsten; Deest, Maximilian; Bleich, Stefan; Neyazi, Alexandra; Frieling, Helge; Maier, Hannah B
抑郁症
神经科学
发表日期：2023
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Bifrontal electroconvulsive therapy leads to improvement of cerebral glucose hypometabolism in frontotemporal dementia with comorbid psychotic depression - a case report

双额叶电休克疗法可改善伴有精神病性抑郁症的前颞叶痴呆患者的脑葡萄糖代谢减退——病例报告

期刊:BMC Psychiatry
影响因子:3.6
doi:10.1186/s12888-023-04759-z
Schröder, Sebastian; Bönig, Lena; Proskynitopoulos, Phileas Johannes; Janke, Eva; Heck, Johannes; Mahmoudi, Nima; Groh, Adrian; Berding, Georg; Wedegärtner, Felix; Deest-Gaubatz, Stephanie; Maier, Hannah Benedictine; Bleich, Stefan; Frieling, Helge; Schulze Westhoff, Martin
抑郁症
神经科学
代谢
发表日期：2023
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Comparison of methylation estimates obtained via MinION nanopore sequencing and sanger bisulfite sequencing in the TRPA1 promoter region

比较通过 MinION 纳米孔测序和 Sanger 亚硫酸氢盐测序获得的 TRPA1 启动子区域甲基化水平的估计值

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-023-01694-6
Gombert, Sara; Jahn, Kirsten; Pathak, Hansi; Burkert, Alexandra; Schmidt, Gunnar; Wiehlmann, Lutz; Davenport, Colin; Brändl, Björn; Müller, Franz-Josef; Leffler, Andreas; Deest, Maximilian; Frieling, Helge
RPA1
表观遗传
TRPA1
发表日期：2023
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Adverse drug reactions in geriatric psychiatry-retrospective cohort study of a 6-year period

老年精神病学中药物不良反应——一项为期6年的回顾性队列研究

期刊:Irish Journal of Medical Science
影响因子:1.6
doi:10.1007/s11845-023-03300-1
Heck, Johannes; Noltemeyer, Nina; Schulze Westhoff, Martin; Deest-Gaubatz, Stephanie; Schröder, Sebastian; Krichevsky, Benjamin; Simon, Nicolas; Gerbel, Swetlana; Friedrich, Maximilian; Stichtenoth, Dirk O; Bleich, Stefan; Frieling, Helge; Groh, Adrian
发表日期：2023
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Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis

在普拉德-威利综合征和普拉德-威利综合征相关精神病中，催产素受体基因的特定启动子区域存在低甲基化。

期刊:Translational Psychiatry
影响因子:6.2
doi:10.1038/s41398-022-02014-9
Heseding, Hannah M; Jahn, Kirsten; Eberlein, Christian K; Wieting, Jelte; Maier, Hannah B; Proskynitopoulos, Phileas J; Glahn, Alexander; Bleich, Stefan; Frieling, Helge; Deest, Maximilian
信号转导
表观遗传
发表日期：2022
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Methylation pattern and mRNA expression of synapse-relevant genes in the MAM model of schizophrenia in the time-course of adolescence

在青春期MAM精神分裂症模型中，突触相关基因的甲基化模式和mRNA表达随时间的变化

期刊:npj Schizophrenia
影响因子:4.1
doi:10.1038/s41537-022-00319-8
Khan, Abdul Qayyum; Thielen, Lukas; Le Pen, Gwenaëlle; Krebs, Marie-Odile; Kebir, Oussama; Groh, Adrian; Deest, Maximilian; Bleich, Stefan; Frieling, Helge; Jahn, Kirsten
精神分裂症
表观遗传
神经科学
DNA甲基化
发表日期：2022
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Aripiprazole treatment for temper outbursts in Prader-Willi syndrome

阿立哌唑治疗普拉德-威利综合征的暴怒症状

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-022-02470-y
Deest, Maximilian; Wieting, Jelte; Jakob, Maximilian Michael; Deest-Gaubatz, Stephanie; Groh, Adrian; Seifert, Johanna; Toto, Sermin; Bleich, Stefan; Frieling, Helge; Eberlein, Christian K
发表日期：2022
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