Holger Kirsten
Holger Kirsten
Senior Researcher, Universität Leipzig
Verified email at - Homepage
Cited by
Cited by
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
BioRxiv, 447367, 2018
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
A catalog of genetic loci associated with kidney function from analyses of a million individuals
M Wuttke, Y Li, M Li, KB Sieber, MF Feitosa, M Gorski, A Tin, L Wang, ...
Nature genetics 51 (6), 957-972, 2019
A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis
K Fjeld, FU Weiss, D Lasher, J Rosendahl, JM Chen, BB Johansson, ...
Nature genetics 47 (5), 518-522, 2015
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
A Tin, J Marten, VL Halperin Kuhns, Y Li, M Wuttke, H Kirsten, KB Sieber, ...
Nature genetics 51 (10), 1459-1474, 2019
The role of HPV RNA transcription, immune response‐related gene expression and disruptive TP53 mutations in diagnostic and prognostic profiling of head and …
G Wichmann, M Rosolowski, K Krohn, M Kreuz, A Boehm, A Reiche, ...
International journal of cancer 137 (12), 2846-2857, 2015
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
E Porcu, S Rüeger, K Lepik, FA Santoni, A Reymond, Z Kutalik
Nature communications 10 (1), 1-12, 2019
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci
H Kirsten, H Al-Hasani, L Holdt, A Gross, F Beutner, K Krohn, K Horn, ...
Human molecular genetics 24 (16), 4746-4763, 2015
The role of gene DCDC2 in German dyslexics
A Wilcke, J Weissfuss, H Kirsten, G Wolfram, J Boltze, P Ahnert
Annals of dyslexia 59 (1), 1-11, 2009
Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis
J Rosendahl, H Kirsten, E Hegyi, P Kovacs, FU Weiss, H Laumen, ...
Gut 67 (10), 1855-1863, 2018
Large-scale cis-and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
Nature genetics 53 (9), 1300-1310, 2021
Imaging genetics of FOXP2 in dyslexia
A Wilcke, C Ligges, J Burkhardt, M Alexander, C Wolf, E Quente, P Ahnert, ...
European Journal of Human Genetics 20 (2), 224-229, 2012
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A Teumer, Y Li, S Ghasemi, BP Prins, M Wuttke, T Hermle, A Giri, ...
Nature communications 10 (1), 1-19, 2019
Association of MICA with rheumatoid arthritis independent of known HLA-DRB1risk alleles in a family-based and a case control study
H Kirsten, E Petit-Teixeira, M Scholz, D Hasenclever, H Hantmann, ...
Arthritis research & therapy 11 (3), 1-11, 2009
Predicting early signs of dyslexia at a preliterate age by combining behavioral assessment with structural MRI
I Kraft, J Schreiber, R Cafiero, R Metere, G Schaadt, J Brauer, NE Neef, ...
Neuroimage 143, 378-386, 2016
Genome‐wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study
J Spada, M Scholz, H Kirsten, T Hensch, K Horn, P Jawinski, C Ulke, ...
Journal of Sleep Research 25 (6), 690-701, 2016
Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children
MA Skeide, H Kirsten, I Kraft, G Schaadt, B Müller, N Neef, J Brauer, ...
Neuroimage 118, 414-421, 2015
A stereotaxic, population-averaged T1w ovine brain atlas including cerebral morphology and tissue volumes
B Nitzsche, S Frey, LD Collins, J Seeger, D Lobsien, A Dreyer, H Kirsten, ...
Frontiers in neuroanatomy 9, 69, 2015
Comprehensive cytogenetic characterization of an esthesioneuroblastoma
H Holland, R Koschny, W Krupp, J Meixensberger, M Bauer, H Kirsten, ...
Cancer genetics and cytogenetics 173 (2), 89-96, 2007
Dyslexia risk gene relates to representation of sound in the auditory brainstem
NE Neef, B Müller, J Liebig, G Schaadt, M Grigutsch, TC Gunter, A Wilcke, ...
Developmental cognitive neuroscience 24, 63-71, 2017
The system can't perform the operation now. Try again later.
Articles 1–20