Annett Böddrich

1.1k total citations
12 papers, 737 citations indexed

About

Annett Böddrich is a scholar working on Molecular Biology, Physiology and Neurology. According to data from OpenAlex, Annett Böddrich has authored 12 papers receiving a total of 737 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Physiology and 3 papers in Neurology. Recurrent topics in Annett Böddrich's work include Alzheimer's disease research and treatments (4 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Connective tissue disorders research (2 papers). Annett Böddrich is often cited by papers focused on Alzheimer's disease research and treatments (4 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Connective tissue disorders research (2 papers). Annett Böddrich collaborates with scholars based in Germany, United States and Belgium. Annett Böddrich's co-authors include Erich E. Wanker, Fiona Francis, Tim M. Strom, Hans Lehrach, Michael J. Econs, Bettina Lorenz, Thomas Meitinger, Andrea N. Albrecht, Sigmar Stricker and Stefan Mundlos and has published in prestigious journals such as Chemical Communications, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Annett Böddrich

12 papers receiving 731 citations

Peers

Countries citing papers authored by Annett Böddrich

Since Specialization

Citations

This map shows the geographic impact of Annett Böddrich's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Annett Böddrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annett Böddrich more than expected).

Fields of papers citing papers by Annett Böddrich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annett Böddrich. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Annett Böddrich. The network helps show where Annett Böddrich may publish in the future.

Co-authorship network of co-authors of Annett Böddrich

This figure shows the co-authorship network connecting the top 25 collaborators of Annett Böddrich. A scholar is included among the top collaborators of Annett Böddrich based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Annett Böddrich. Annett Böddrich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Mixing Aβ(1–40) and Aβ(1–42) peptides generates unique amyloid fibrils 2020 ·Chemical Communications ·Linda Cerofolini, Enrico Ravera, Sara Bologna, Thomas Wiglenda, Annett Böddrich, Bettina Purfürst, Iryna Benilova, (unknown), (unknown), (unknown), Leonardo Gonnelli, Marco Fragai, Bart De Strooper, Erich E. Wanker, Claudio Luchinat	49
2	Interleukin‐12/23 deficiency differentially affects pathology in male and female Alzheimer's disease‐like mice 2020 ·EMBO Reports ·Pascale Eede, Juliane Obst, (unknown), Genevieve Yvon‐Durocher, Bernhard Clemens Richard, Niclas Gimber, Jan Schmoranzer, Annett Böddrich, Erich E. Wanker, Stefan Prokop, Frank L. Heppner	26
3	Epigallocatechin gallate (EGCG) reduces the intensity of pancreatic amyloid fibrils in human islet amyloid polypeptide (hIAPP) transgenic mice 2018 ·Scientific Reports ·András Frankó, Diana C. Rodriguez Camargo, Annett Böddrich, Divita Garg, Andrés Rodríguez‐Camargo, Birgit Rathkolb, Dirk Janik, Michaela Aichler, Annette Feuchtinger, Frauke Neff, Helmut Fuchs, Erich E. Wanker, Bernd Reif, Hans‐Ulrich Häring, Andreas Peter, Martin Hrabě de Angelis	54
4	The redox environment triggers conformational changes and aggregation of hIAPP in Type II Diabetes 2017 ·Scientific Reports ·Diana C. Rodriguez Camargo, Konstantinos Tripsianes, Katalin Buday, András Frankó, Christoph Göbl, Christoph Hartlmüller, Riddhiman Sarkar, Michaela Aichler, (unknown), Michael Schulz, Annett Böddrich, Christian Erck, Henrik Martens, Axel Walch, Tobias Madl, Erich E. Wanker, Marcus Conrad, Martin Hrabě de Angelis, Bernd Reif	81
5	Identification of VCP/p97, Carboxyl Terminus of Hsp70-interacting Protein (CHIP), and Amphiphysin II Interaction Partners Using Membrane-based Human Proteome Arrays 2005 ·Molecular & Cellular Proteomics ·Gerlinde Grelle, Susanne Kostka, Albrecht Otto, Birgit Kersten, K. Genser, Eva‐Christina Müller, Stephanie Wälter, Annett Böddrich, Ulrich Stelzl, (unknown), Rudolf Volkmer, Christiane Landgraf, Simon Alberti, Jörg Höhfeld, (unknown), Erich E. Wanker	46
6	A molecular pathogenesis for transcription factor associated poly-alanine tract expansions 2004 ·Human Molecular Genetics ·Andrea N. Albrecht, Uwe Kornak, Annett Böddrich, (unknown), Peter N. Robinson, Asita C. Stiege, Rudi Lurz, Sigmar Stricker, Erich E. Wanker, Stefan Mundlos	124
7	The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage elements 2002 ·Mechanisms of Development ·Andrea N. Albrecht, Georg C. Schwabe, Sigmar Stricker, Annett Böddrich, Erich E. Wanker, Stefan Mundlos	40
8	Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets 1997 ·Genome Research ·Fiona Francis, Tim M. Strom, Steffen Hennig, Annett Böddrich, Bettina Lorenz, Oliver Brandau, Klaus Mohnike, (unknown), (unknown), Sven Klages, Katja Borzym, Thomas Pohl, C Oudet, Michael J. Econs, Peter Rowe, Richard Reinhardt, Thomas Meitinger, Hans Lehrach	129
9	Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia 1997 ·Human Molecular Genetics ·Tim M. Strom, Fiona Francis, Bettina Lorenz, Annett Böddrich, Hans Lehrach, Michael J. Econs, Thomas Meitinger	155
10	New evidence for a mutation hotspot in exon 37 of the NF1 gene 1997 ·Human Mutation ·Annett Böddrich, Peter N. Robinson, (unknown), Annegret Buske, Sigrid Tinschert, Peter Nürnberg	12
11	Three novel mutations of the NF1 gene detected by temperature gradient gel electrophoresis of exons 5 and 8 1996 ·Electrophoresis ·Denise Horn, Peter N. Robinson, Annett Böddrich, Annegret Buske, Sigrid Tinschert, (unknown)	9
12	Reduced Neurofibromin Content but Normal Gap Activity in a Patient with Neurofibromatosis Type 1 Caused by a Five-Base-Pair Duplication in Exon 12B of the NF1 Gene 1995 ·Biochemical and Biophysical Research Communications ·Annett Böddrich, (unknown), Denise Horn, Dieter Kaufmann, W. Krone, Peter Nürnberg	12

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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