引用次数
引用: 6,519
H-指数: 38
I10-指数 : 82
出版物: 186
Working memory-relevant gray matter in the left pSTG relates to genetic risk and diagnostic status in Developmental Dyslexia: a VBM study
Angela D. Friederici , Arndt Wilcke , Arndt Wilcke , Claudia Männel
42nd Annual Meeting of the Society for Neuroscience
2012
Genetic Screening Test for Dyslexia: A Survey on Acceptance
Arndt Wilcke , Claudia Männel , Johannes Boltze , Holger Kirsten
WCRM 2011: World Conference on Regenerative Medicine
2011
Genetic modulators of dyslexia related MMR
Arndt Wilcke , Johannes Boltze , Holger Kirsten , Bent Müller
22nd World Congress of Psychiatric Genetics (WCPG)
2014
In vitro Selektion von DNA-Molekülen für Schimmelpilz-Biosensoren
Beate Strehlitz , Regina Stoltenburg , Holger Kirsten
Universität Tübingen
2001
Dyslexia risk variant rs11100040 alters brain connectivity profiles affecting phonological awareness
Angela D. Friederici , Arndt Wilcke , Michael A. Skeide , Johannes Boltze
20th Annual Meeting of the Organization for Human Brain Mapping (OHBM)
2014
No Association Between Systemic Sclerosis and C77G Polymorphism in the Human PTPRC (CD45) Gene
Rita Rzepka , Holger Kirsten , Peter Ahnert , Inga Melchers
The Journal of Rheumatology 35 ( 9) 1817 -1819
8
2008
Covid-19 in outpatients-Is fever a useful indicator for SARS-CoV-2 infection?
Christoph Lübbert , Florian Lordick , Holger Kirsten , Amrei von Braun
PLOS ONE 16 ( 2)
1
2021
Evaluation of phosphodiesterase 9A as a novel biomarker in heart failure with preserved ejection fraction.
Volker Adams , Holger Kirsten , Philipp Lurz , Petra Büttner
Esc Heart Failure 8 ( 3) 1861 -1872
2021
Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL.
Markus Scholz , Michael Kluge , Arno Villringer , Dirk Alexander Wittekind
European Journal of Endocrinology 184 ( 6) 847 -856
2021
Correction: Covid-19 in outpatients-Is fever a useful indicator for SARS-CoV-2 infection?
Christoph Lübbert , Florian Lordick , Holger Kirsten , Amrei von Braun
PLOS ONE 16 ( 5)
2021
Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes.
Janne Pott , Valentin Schlegel , Andrej Teren , Katrin Horn
Circulation: Genomic and Precision Medicine 11 ( 5)
34
2018
Cellular Adhesion Gene SELP Is Associated with Rheumatoid Arthritis and Displays Differential Allelic Expression
Jana Burkhardt , Mechthild Blume , Elisabeth Petit-Teixeira , Vitor Hugo Teixeira
PLOS ONE 9 ( 8) 1 -10
18
2014
Common variants in glyoxalase I do not increase chronic pancreatitis risk.
Tom Kaune , Marcus Hollenbach , Bettina Keil , Jian-Min Chen
PLOS ONE 14 ( 10)
2019
Dyslexia risk gene relates to representation of sound in the auditory brainstem
Nicole E. Neef , Bent Müller , Johanna Liebig , Gesa Schaadt
Developmental Cognitive Neuroscience 24 63 -71
53
2017
Effectiveness of different central venous catheter fixation suture techniques: An in vitro crossover study.
Manuel Florian Struck , Lars Friedrich , Stefan Schleifenbaum , Holger Kirsten
PLOS ONE 14 ( 9)
3
2019
Comparison of scoring methods for the detection of causal genes with or without rare variants
Markus Scholz , Holger Kirsten
BMC Proceedings 5 ( 9) 1 -7
5
2011
Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.
Janek Spada , Markus Scholz , Holger Kirsten , Tilman Hensch
Journal of Sleep Research 25 ( 6) 690 -701
46
2016
Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.
Bent Müller , Johannes Boltze , Ivonne Czepezauer , Volker Hesse
Genetics and Molecular Biology 41 ( 1) 41 -49
2018
Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children
Michael A. Skeide , Holger Kirsten , Indra Kraft , Gesa Schaadt
NeuroImage 118 414 -421
33
2015
Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood
Ralph Burkhardt , Holger Kirsten , Frank Beutner , Lesca M. Holdt
PLOS Genetics 11 ( 9) e1005510
29
2015