Per Hoffmann

48.2k citations

158 papers · 3.6k indexed · h-index 34

Impact in

Developmental Neuroscience top 2%
- Neurogenesis and neuroplasticity mechanisms
Developmental and Educational Psychology top 2%
- Reading and Literacy Development

Papers in ⓘ

Genetics 59
- Genetic Associations and Epidemiology 23
- Genetics and Neurodevelopmental Disorders 19
- Genomic variations and chromosomal abnormalities 11
- Cleft Lip and Palate Research 7
Statistics and Probability 10
- Cognitive and developmental aspects of mathematical skills 9

Co-authors: Markus M. Nöthen (66 shared papers)Stefan Herms (28 shared papers)Gerd Schulte‐Körne (12 shared papers)Oliver Brüstle (2 shared papers)Johannes Schumacher (7 shared papers)Bertram Müller‐Myhsok (11 shared papers)Kerstin U. Ludwig (15 shared papers)Philipp Wörsdörfer (1 shared paper)
Journals: Scientific Reports (6 papers)Studies in Conservation (6 papers)The International Journal of Nautical Archaeology (6 papers)Stem Cell Research (5 papers)Translational Psychiatry (5 papers)
Partner nations: Germany Switzerland United States

In The Last Decade

Per Hoffmann

149 papers receiving 3.4k citations

Peers

Countries citing papers authored by Per Hoffmann

Since Specialization

Citations

This map shows the geographic impact of Per Hoffmann'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 Per Hoffmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Per Hoffmann more than expected).

Fields of papers citing papers by Per Hoffmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Per Hoffmann. 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 Per Hoffmann. The network helps show where Per Hoffmann may publish in the future.

Co-authors

The 25 scholars most cited alongside Per Hoffmann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Per Hoffmann Line = papers co-authored together Per Hoffmann links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 158 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells Cell stem cell ·Marc Thier, Philipp Wörsdörfer, Yenal B. Lakes, Raphaela Gorris, Stefan Herms, Thoralf Opitz, Dominic Seiferling, Tamara Quandel, Per Hoffmann, Markus M. Nöthen, Oliver Brüstle, Frank Edenhofer	2012	402
2	Excitation-induced ataxin-3 aggregation in neurons from patients with Machado–Joseph disease Nature ·Philipp Koch, Péter Breuer, Michael Peitz, Johannes Jungverdorben, Jaideep Kesavan, Daniel Poppe, Jonas Doerr, Julia Ladewig, Jérôme Mertens, Thomas Tüting, Per Hoffmann, Thomas Klockgether, Bernd O. Evert, Ullrich Wüllner, Oliver Brüstle	2011	248
3	Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas International Journal of Cancer ·Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Stefanie Vogt, Sophia Chen, Monika Morak, Susanne Raeder, Katrin Kayser, Dietlinde Stienen, R. Adam, Peter Nürnberg, Guido Plotz, Elke Holinski‐Feder, Richard P. Lifton, Hölger Thiele, Per Hoffmann, Verena Steinke, Stefan Aretz	2014	103
4	Genetics of dyslexia: the evolving landscape Journal of Medical Genetics ·Johannes Schumacher, Per Hoffmann, Christine Schmäl, Gerd Schulte‐Körne, Markus M. Nöthen	2007	97
5	A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia Human Molecular Genetics ·Heidi Anthoni, Marco Zucchelli, Hans Matsson, Bertram Müller‐Myhsok, Ingegerd Fransson, Johannes Schumacher, Satu Massinen, Päivi Onkamo, Andreas Warnke, Heide Griesemann, Per Hoffmann, Jaana Nopola‐Hemmi, Heikki Lyytinen, Gerd Schulte‐Körne, Juha Kere, Markus M. Nöthen, Myriam Peyrard‐Janvid	2007	91
6	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children Molecular Psychiatry ·Darina Roeske, Kerstin U. Ludwig, Nina Neuhoff, Jessica Becker, Jürgen Bartling, Jennifer Bruder, F.F. Brockschmidt, Andreas Warnke, Helmut Remschmidt, Per Hoffmann, Bertram Müller‐Myhsok, Markus M. Nöthen, Gerd Schulte‐Körne	2009	77
7	TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue Seizure ·Katharina Pernhorst, Stefan Herms, Per Hoffmann, Sven Cichon, Herbert Schulz, Thomas Sander, Susanne Schoch, Albert J. Becker, Alexander Grote	2013	72
8	The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis Journal Of Clinical Periodontology ·Annika Kröger, Claudia Hülsmann, Stefan Fickl, Thomas Spinell, Fabian Hüttig, Frederic Kaufmann, André Heimbach, Per Hoffmann, Norbert Enkling, Stefan Renvert, Frank Schwarz, Ryan T. Demmer, Panos N. Papapanou, Søren Jepsen, Moritz Kebschull	2018	69
9	The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations Human Molecular Genetics ·Johannes Schumacher, Gonzalo Laje, Rami Abou Jamra, Tim Becker, Thomas W. Mühleisen, Catalina Vasilescu, Manuel Mattheisen, Stefan Herms, Per Hoffmann, Axel M. Hillmer, Alexander Georgi, Christine Herold, Thomas G. Schulze, Peter Propping, Marcella Rietschel, Francis J. McMahon, Markus M. Nöthen, Sven Cichon	2009	67
10	Hippo Signaling Mediates Proliferation, Invasiveness, and Metastatic Potential of Clear Cell Renal Cell Carcinoma Translational Oncology ·Ute Schütte, Savita Bisht, Lukas C. Heukamp, Moritz Kebschull, Alexandra Florin, Jens Haarmann, Per Hoffmann, Gerd Bendas, Reinhard Buettner, Peter Brossart, Georg Feldmann	2014	66
11	Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells Scientific Reports ·Eduardo Fernández‐Rebollo, Birgit Mentrup, Regina Ebert, Julia Franzen, Giulio Abagnale, Torsten Sieben, Alina Ostrowska, Per Hoffmann, Pierre‐François Roux, Björn Rath, Michèle Goodhardt, Jean-Marc Lemaı̂tre, Oliver Bischof, Franz Jakob, Wolfgang Wagner	2017	65
12	DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations Clinical Epigenetics ·Amit Sharma, Muhammad Ahmer Jamil, Nicole Nuesgen, Felix Schreiner, Lutz Priebe, Per Hoffmann, Stefan Herns, Markus M. Nöthen, Holger Fröhlich, Johannes Oldenburg, Joachim Woelfle, Osman El‐Maarri	2015	58
13	αCaMKII Autophosphorylation Controls the Establishment of Alcohol Drinking Behavior Neuropsychopharmacology ·Alanna C. Easton, Walter Lucchesi, Anbarasu Lourdusamy, Bernd Lenz, Jalal Solati, Yulia Golub, Piotr Lewczuk, Cathy Fernandes, Sylvane Desrivières, Ralph R. Dawirs, Gunther H. Moll, Johannes Kornhuber, Josef Frank, Per Hoffmann, Michael Soyka, Falk Kiefer, Günter Schumann, Karl-Peter Giese, Christian P. Müller	2013	54
14	BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma PLoS Genetics ·Daniel Nettersheim, Sina Jostes, Rakesh Sharma, Simon Schneider, Andrea Hofmann, Humberto J. Ferreira, Per Hoffmann, Glen Kristiansen, Manel Esteller, Hubert Schorle	2015	54
15	Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Human Mutation ·Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski‐Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz	2012	54
16	Aberrant NMDA receptor DNA methylation detected by epigenome-wide analysis of hippocampus and prefrontal cortex in major depression European Archives of Psychiatry and Clinical Neuroscience ·Oliver Kaut, Ina Schmitt, Andrea Hofmann, Per Hoffmann, Thomas E. Schläepfer, Ullrich Wüllner, René Hurlemann	2015	52
17	On the Ultrastructural Localization of Hemicelluloses within Delignified Tracheids of Spruce Holzforschung ·Per Hoffmann, N. Parameswaran	1976	50
18	Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy European Journal of Medical Genetics ·Markus Draaken, Heiko Reutter, Charlotte Schramm, Enrika Bartels, Thomas M. Boemers, Anne‐Karoline Ebert, Wolfgang Rösch, Annette Schröder, Raimund Stein, Susanne Moebus, Dietlinde Stienen, Per Hoffmann, Markus M. Nöthen, Michael Ludwig	2010	48
19	Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample Psychiatric Genetics ·Kerstin U. Ludwig, Johannes Schumacher, Gerd Schulte‐Körne, Inke R. König, Andreas Warnke, Ellen Plume, Heidi Anthoni, Myriam Peyrard‐Janvid, Haiying Meng, Andreas Ziegler, Helmut Remschmidt, Juha Kere, Jeffrey R. Gruen, Bertram Müller‐Myhsok, Markus M. Nöthen, Per Hoffmann	2008	46
20	Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia Behavior Genetics ·Darina Czamara, Jennifer Bruder, Jessica Becker, Jürgen Bartling, Per Hoffmann, Kerstin U. Ludwig, Bertram Müller‐Myhsok, Gerd Schulte‐Körne	2010	44

About Per Hoffmann

Per Hoffmann is a scholar working on Genetics, Statistics and Probability, Developmental and Educational Psychology, Archeology and Archeology, having authored 158 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (23 papers), Genetics and Neurodevelopmental Disorders (19 papers), Epigenetics and DNA Methylation (12 papers), Reading and Literacy Development (12 papers), Genomic variations and chromosomal abnormalities (11 papers), Cognitive and developmental aspects of mathematical skills (9 papers), DNA Repair Mechanisms (7 papers) and Cleft Lip and Palate Research (7 papers). The work is most often cited by research in Developmental Neuroscience (194 citations), Developmental and Educational Psychology (425 citations), Genetics (845 citations), Periodontics (129 citations) and Cellular and Molecular Neuroscience (459 citations). Per Hoffmann has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Markus M. Nöthen, Stefan Herms, Gerd Schulte‐Körne, Oliver Brüstle, Johannes Schumacher, Bertram Müller‐Myhsok, Kerstin U. Ludwig, Philipp Wörsdörfer, Marc Thier and Frank Edenhofer. Their work appears in journals such as Scientific Reports, Studies in Conservation, The International Journal of Nautical Archaeology, Stem Cell Research and Translational Psychiatry.

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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