Anke Busch - Concepedia

Author

Anke Busch

Institute of Molecular Biology ORCID

Also Known As

Anke Busch, Busch, Anke

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

Institute of Molecular Biology Goethe University Frankfurt University of California, Irvine University of Freiburg Helmholtz Zentrum München

About

Anke Busch is an author at Institute of Molecular Biology specializing in medicine, gene expression, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	1.3K
2	Natural Sciences	10	10	464
3	Cell Biology	10	10	520
4	Engineering	5	5	534
5	Biology	1	1	19

Anke Busch

Publications

Citations

H-Index

Page 1

	Year	Citations
IntaRNA: efficient prediction of bacterial sRNA targets incorporating target site accessibility and seed regions Anke Busch, Andreas S. Richter, Rolf Backofen Bioinformatics	2008	551
Position-dependent splicing activation and repression by SR and hnRNP proteins rely on common mechanisms Steffen Erkelenz, William F. Mueller, Melanie S. Evans, RNA	2012	238
The chromatin regulator Brg1 suppresses formation of intraductal papillary mucinous neoplasm and pancreatic ductal adenocarcinoma Guido von Figura, Akihisa Fukuda, Nilotpal Roy, Nature Cell Biology Tumor BiologyChromatinOncologyPancreatic CancerChromatin Regulator Brg1	2014	185
Using RNA secondary structures to guide sequence motif finding towards single-stranded regions Michael Hiller, Rainer Pudimat, Anke Busch, Nucleic Acids Research EngineeringStructural BioinformaticsGeneticsMolecular BiologyGene Recognition	2006	172
Freiburg RNA tools: a central online resource for RNA-focused research and teaching Martin Raden, Syed Mohsin Ali, Omer S. Alkhnbashi, Nucleic Acids Research EngineeringGeneticsMolecular BiologyRna-focused ResearchGenomics	2018	166
INFO-RNA—a fast approach to inverse RNA folding Anke Busch, Rolf Backofen Bioinformatics	2006	146
Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome Mariella Simon, Élodie M. Richard, Xinjian Wang, PLoS Genetics Neurodegenerative DiseasesMendelian DisorderMitochondrial BiogenesisMitochondrial FunctionGenetic Disorder	2015	113
Deep and accurate detection of m6A RNA modifications using miCLIP2 and m6Aboost machine learning Nadine Körtel, Cornelia Rücklé, You Zhou, Nucleic Acids Research	2021	109
Improved library preparation with the new iCLIP2 protocol Andreas Buchbender, Holger Mutter, F.X. Reymond Sutandy, Methods EngineeringLibrary PreparationMolecular BiologySoftware EngineeringProtocol Compliance	2019	106
A splice donor mutation in <i>NAA10</i> results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome Taraneh Esmailpour, Hamidreza Riazifar, Linan Liu, Journal of Medical Genetics	2014	104

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