Malte Spielmann - Concepedia

Author

Malte Spielmann

Max Planck Institute for Molecular Genetics ORCID

Also Known As

B. Scheffer, M Spielmann, M. Spielmann, Malte Spielmann, Spielmann M, Spielmann, M, Spielmann, Malte, Varun K.A. Sreenivasan

198

Publications

15.3K

Citations

H-Index

143

Concepts

All Affiliations

Max Planck Institute for Molecular Genetics Charité - Universitätsmedizin Berlin University of Lübeck Berlin Institute of Health at Charité - Universitätsmedizin Berlin Berlin-Brandenburger Centrum für Regenerative Therapien

About

Malte Spielmann is an author at Max Planck Institute for Molecular Genetics specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	33	10K
2	Natural Sciences	6	6	3.1K
3	Engineering	4	4	810
4	Public Health	4	4	399
5	Social Sciences	2	2	60

Malte Spielmann

Publications

13.6K

Citations

H-Index

Page 1

	Year	Citations
The single-cell transcriptional landscape of mammalian organogenesis Junyue Cao, Malte Spielmann, Xiaojie Qiu, Nature Cell LineageDevelopmental BiologySingle Cell SequencingMedicineSingle-cell Transcriptional Landscape	2019	4.4K
Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions Darío G. Lupiáñez, Katerina Kraft, Verena Heinrich, Cell ChromatinChromatin StructureChromatin RemodelingNatural SciencesEpigenetic Change	2015	2.2K
A human cell atlas of fetal gene expression Junyue Cao, Diana R. O’Day, Hannah A. Pliner, Science	2020	780
Formation of new chromatin domains determines pathogenicity of genomic duplications Martin Franke, Daniel M. Ibrahim, Guillaume Andrey, Nature ChromatinGenome InstabilityChromatin StructureChromatin RemodelingNatural Sciences	2016	701
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state Semra Smajić, Cesar A. Prada‐Medina, Zied Landoulsi, Brain Idiopathic ParkinsonEngineeringGeneticsNeurochemical BiomarkersDisease Gene Identification	2021	525
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease Damian Smedley, Max Schubach, Julius O.B. Jacobsen, The American Journal of Human Genetics BiologyBioinformaticsGenetic AnalysisWhole-genome Analysis FrameworkMendelian Disorder	2016	285
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome Tomasz Żemojtel, Sebastian Köhler, Luisa Mackenroth, Science Translational Medicine	2014	259
Embryo-scale, single-cell spatial transcriptomics Sanjay Srivatsan, Mary C. Regier, Eliza Barkan, Science Body Axis PatterningEngineeringSpatial OmicsTrajectory AnalysisSingle Cell Sequencing	2021	258
Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein‐Coding Regions Stefan H. Lelieveld, Malte Spielmann, Stefan Mundlos, Human Mutation	2015	227
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice Katerina Kraft, Sinje Geuer, Anja J. Will, Cell Reports	2015	227

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