| Year |
Citation |
Score |
| 2019 |
Sander C, Wallenborn M, Brandt VP, Ahnert P, Reuschel V, Eisenlöffel C, Krupp W, Meixensberger J, Holland H. Central neurocytoma: SNP array analyses, subtel FISH, and review of the literature. Pathology, Research and Practice. PMID 31000381 DOI: 10.1016/J.Prp.2019.03.025 |
0.3 |
|
| 2019 |
Huber R, Kirsten H, Näkki A, Pohlers D, Thude H, Eidner T, Heinig M, Brand K, Ahnert P, Kinne RW. Association of Human Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study. International Journal of Molecular Sciences. 20. PMID 30893847 DOI: 10.3390/Ijms20061382 |
0.309 |
|
| 2016 |
Müller B, Wilcke A, Czepezauer I, Ahnert P, Boltze J, Kirsten H. Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort. Scientific Reports. 6: 27901. PMID 27312598 DOI: 10.1038/Srep27901 |
0.308 |
|
| 2015 |
Kirsten H, Al-Hasani H, Holdt L, Gross A, Beutner F, Krohn K, Horn K, Ahnert P, Burkhardt R, Reiche K, Hackermüller J, Löffler M, Teupser D, Thiery J, Scholz M. Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†. Human Molecular Genetics. PMID 26019233 DOI: 10.1093/Hmg/Ddv194 |
0.306 |
|
| 2015 |
Xu LX, Holland H, Kirsten H, Ahnert P, Krupp W, Bauer M, Schober R, Mueller W, Fritzsch D, Meixensberger J, Koschny R. Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 35: 148-57. PMID 25376146 DOI: 10.1111/Neup.12176 |
0.347 |
|
| 2014 |
Burkhardt J, Blume M, Petit-Teixeira E, Hugo Teixeira V, Steiner A, Quente E, Wolfram G, Scholz M, Pierlot C, Migliorini P, Bombardieri S, Balsa A, Westhovens R, Barrera P, Radstake TR, ... ... Ahnert P, et al. Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression. Plos One. 9: e103872. PMID 25147926 DOI: 10.1371/Journal.Pone.0103872 |
0.308 |
|
| 2014 |
Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H. Genetic risk variants for dyslexia on chromosome 18 in a German cohort. Genes, Brain, and Behavior. 13: 350-6. PMID 24373531 DOI: 10.1111/Gbb.12118 |
0.317 |
|
| 2011 |
Holland H, Mocker K, Ahnert P, Kirsten H, Hantmann H, Koschny R, Bauer M, Schober R, Scholz M, Meixensberger J, Krupp W. High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas. Cancer Genetics. 204: 541-9. PMID 22137484 DOI: 10.1016/J.Cancergen.2011.10.007 |
0.31 |
|
| 2011 |
Holland H, Livrea M, Ahnert P, Koschny R, Kirsten H, Meixensberger J, Bauer M, Schober R, Fritzsch D, Krupp W. Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis. Pathology, Research and Practice. 207: 310-6. PMID 21306833 DOI: 10.1016/J.Prp.2010.12.010 |
0.303 |
|
| 2011 |
Mocker K, Holland H, Ahnert P, Schober R, Bauer M, Kirsten H, Koschny R, Meixensberger J, Krupp W. Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics. Pathology, Research and Practice. 207: 67-72. PMID 20926204 DOI: 10.1016/J.Prp.2010.09.001 |
0.301 |
|
| 2009 |
Burkhardt J, Petit-Teixeira E, Teixeira VH, Kirsten H, Garnier S, Ruehle S, Oeser C, Wolfram G, Scholz M, Migliorini P, Balsa A, Westhovens R, Barrera P, Alves H, Pascual-Salcedo D, ... ... Ahnert P, et al. Association of the X-chromosomal genes TIMP1 and IL9R with rheumatoid arthritis. The Journal of Rheumatology. 36: 2149-57. PMID 19723899 DOI: 10.3899/Jrheum.090059 |
0.307 |
|
| 2009 |
Kirsten H, Burkhardt J, Hantmann H, Hunzelmann N, Vaith P, Ahnert P, Melchers I. 5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population. Arthritis Research & Therapy. 11: 403; author reply 40. PMID 19435465 DOI: 10.1186/Ar2606 |
0.305 |
|
| 2009 |
Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P. The role of gene DCDC2 in German dyslexics. Annals of Dyslexia. 59: 1-11. PMID 19238550 DOI: 10.1007/S11881-008-0020-7 |
0.317 |
|
| 2008 |
Krupp W, Holland H, Koschny R, Bauer M, Schober R, Kirsten H, Livrea M, Meixensberger J, Ahnert P. Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics. Cancer Genetics and Cytogenetics. 184: 87-93. PMID 18617056 DOI: 10.1016/J.Cancergencyto.2008.03.015 |
0.303 |
|
| 2007 |
Ahnert P, Kirsten H. Association of ITGAV supports a role of angiogenesis in rheumatoid arthritis. Arthritis Research & Therapy. 9: 108. PMID 18001496 DOI: 10.1186/Ar2313 |
0.3 |
|
| 2007 |
Kirsten H, Teupser D, Weissfuss J, Wolfram G, Emmrich F, Ahnert P. Robustness of single-base extension against mismatches at the site of primer attachment in a clinical assay. Journal of Molecular Medicine (Berlin, Germany). 85: 361-9. PMID 17160404 DOI: 10.1007/S00109-006-0129-2 |
0.329 |
|
| 2000 |
Ahnert P, Picha KM, Patel SS. A ring-opening mechanism for DNA binding in the central channel of the T7 helicase-primase protein. The Embo Journal. 19: 3418-27. PMID 10880454 DOI: 10.1093/Emboj/19.13.3418 |
0.679 |
|
| 2000 |
Picha KM, Ahnert P, Patel SS. DNA binding in the central channel of bacteriophage T7 helicase-primase is a multistep process. Nucleotide hydrolysis is not required. Biochemistry. 39: 6401-9. PMID 10828954 DOI: 10.1021/Bi992857I |
0.68 |
|
| 1997 |
Ahnert P, Patel SS. Asymmetric interactions of hexameric bacteriophage T7 DNA helicase with the 5'- and 3'-tails of the forked DNA substrate. The Journal of Biological Chemistry. 272: 32267-73. PMID 9405431 DOI: 10.1074/Jbc.272.51.32267 |
0.507 |
|
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