Katrin Hoffmann

2.6k citations

31 papers · 1.7k indexed · h-index 19

Impact in

Endocrinology top 5%
- Infections and bacterial resistance
Developmental Neuroscience top 5%

Papers in ⓘ

Molecular Biology 13
- RNA Research and Splicing 3
- RNA modifications and cancer 3
- Gene expression and cancer classification 3
- Nuclear Structure and Function 2
Genetics 12
- Genetic Associations and Epidemiology 4
- Genetic Syndromes and Imprinting 2

Co-authors: Wolfgang Löscher (5 shared papers)Ina Gröticke (3 shared papers)Donald E. Olins (2 shared papers)Richard P. Wenzel (1 shared paper)Allan J. Morrison (1 shared paper)Karl Sperling (3 shared papers)Ada L. Olins (2 shared papers)Stefan Mundlos (6 shared papers)
Journals: European Journal of Human Genetics (6 papers)Experimental Neurology (3 papers)Human Mutation (2 papers)Neuropharmacology (2 papers)Nature Genetics (1 paper)
Partner nations: Germany United States Switzerland

In The Last Decade

Katrin Hoffmann

29 papers receiving 1.6k citations

Peers

Countries citing papers authored by Katrin Hoffmann

Since Specialization

Citations

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

Fields of papers citing papers by Katrin Hoffmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Katrin 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 Katrin Hoffmann Line = papers co-authored together Katrin 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 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly) Nature Genetics ·Katrin Hoffmann, Christine Karin Dreger, Ada L. Olins, Donald E. Olins, Leonard D. Shultz, Barbara Lucke, H.-G Karl, Reinhard Kaps, Dietmar Müller, Amparo Vayá, Justo Aznar, Russell E. Ware, Norberto Sotelo Cruz, Tom H. Lindner, Harald Herrmann, André Reis, Karl Sperling	2002	261
2	Behavioral alterations in the pilocarpine model of temporal lobe epilepsy in mice Experimental Neurology ·Ina Gröticke, Katrin Hoffmann, Wolfgang Löscher	2007	168
3	Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations Human Mutation ·Georg C. Schwabe, Katrin Hoffmann, Niki T. Loges, Daniel Birker, Colette Rossier, Margherita M. de Santi, Heike Olbrich, Manfred Fliegauf, Mike Failly, Uta Liebers, Mirella Collura, Gerhard Gaedicke, Stefan Mundlos, U. Wahn, Jean‐Louis Blouin, B. Niggemann, Heymut Omran, Stylianos E. Antonarakis, Lucia Bartoloni	2007	163
4	Behavioral alterations in a mouse model of temporal lobe epilepsy induced by intrahippocampal injection of kainate Experimental Neurology ·Ina Gröticke, Katrin Hoffmann, Wolfgang Löscher	2008	119
5	Associated mortality and clinical characteristics of nosocomial Pseudomonas maltophilia in a university hospital Journal of Clinical Microbiology ·Allan J. Morrison, Katrin Hoffmann, Richard P. Wenzel	1986	116
6	CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait PLoS Genetics ·Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J. Alshalah, Claudia Mischung, Andreas W. Kuß, Nicholas Humphrey, Stefan Mundlos, Peter N. Robinson	2009	109
7	The granulocyte nucleus and lamin B receptor: avoiding the ovoid Chromosoma ·Katrin Hoffmann, Karl Sperling, Ada L. Olins, Donald E. Olins	2007	94
8	Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene European Journal of Human Genetics ·Stefanie Weber, Katrin Hoffmann, Nikola Jeck, Kathrin Saar, Martin Boeswald, Eberhard Kuwertz-Broeking, Ivan IC Meij, Nine Knoers, Pierre Cochat, Tereza Šuláková, Klaus E. Bonzel, Marianne Soergel, Friedrich Manz, K Schaerer, Hannsjoerg W. Seyberth, André Reis, Martin Konrad	2000	78
9	Cryopreservation does not alter main characteristics of Good Manufacturing Process–grade human multipotent mesenchymal stromal cells including immunomodulating potential and lack of malignant transformation Cytotherapy ·Jana Luetzkendorf, Katrin Nerger, Julian Hering, Angelika Moegel, Katrin Hoffmann, Christiane Hoefers, Carsten Müller‐Tidow, Lutz Peter Mueller	2015	70
10	Epileptic seizures and hippocampal damage after cuprizone-induced demyelination in C57BL/6 mice Experimental Neurology ·Katrin Hoffmann, Maren Lindner, Ina Gröticke, Martin Stangel, Wolfgang Löscher	2007	69
11	Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany European Journal of Human Genetics ·Anke Tönjes, Eleftheria Zeggini, Péter Kovács, Yvonne Böttcher, Dorit Schleinitz, Kerstin Dietrich, Andrew P. Morris, Beate Enigk, Nigel W. Rayner, Moritz Koriath, Markus Eszlinger, Anu Kemppinen, Inga Prokopenko, Katrin Hoffmann, Daniel Teupser, Joachim Thiery, Knut Krohn, Mark I. McCarthy, Michael Stümvoll	2009	64
12	Glutamate is critically involved in seizure-induced overexpression of P-glycoprotein in the brain Neuropharmacology ·Jens P. Bankstahl, Katrin Hoffmann, Kerstin Bethmann, Wolfgang Löscher	2008	59
13	Mutation in the ARH Gene and a Chromosome 13q Locus Influence Cholesterol Levels in a New Form of Digenic-Recessive Familial Hypercholesterolemia Circulation Research ·Hussam Al‐Kateb, Sylvia Bähring, Katrin Hoffmann, Konstantin Strauch, Andreas Busjahn, Gudrun Nürnberg, Muhidien Jouma, Eckehard K.F. Bautz, H. A. Dresel, Friedrich C. Luft	2002	51
14	Uniparental disomies 7 and 14 Best Practice & Research Clinical Endocrinology & Metabolism ·Katrin Hoffmann, Raoul Heller	2011	43
15	Expression of the multidrug transporter MRP2 in the blood–brain barrier after pilocarpine-induced seizures in rats Epilepsy Research ·Katrin Hoffmann, Alexandra M. Gastens, Holger A. Volk, Wolfgang Löscher	2006	41
16	CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs’ dystrophy Graefe s Archive for Clinical and Experimental Ophthalmology ·Sabine Foja, Mirjam Luther, Katrin Hoffmann, Andreas Rupprecht, Claudia Gruenauer‐Kloevekorn	2017	32
17	Familial Gordon syndrome associated with a PIEZO2 mutation American Journal of Medical Genetics Part A ·Franz Alisch, Alexander Weichert, Karim D. Kalache, Viola Paradiso, Ann Carolin Longardt, Christof Dame, Katrin Hoffmann, Denise Horn	2016	25
18	HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing European Journal of Human Genetics ·Wenke Seifert, Julia Beninde, Katrin Hoffmann, Tom H. Lindner, C. Bassir, Fuat Aksu, Christoph Hübner, Nienke E. Verbeek, Stefan Mundlos, Denise Horn	2009	22
19	Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family BMC Medical Genetics ·Sevjidmaa Baasanjav, Aleksander Jamsheer, Mateusz Kolanczyk, Denise Horn, Tomasz Latos, Katrin Hoffmann, Anna Latos‐Bieleńska, Stefan Mundlos	2010	19
20	High-throughput sequencing of microdissected chromosomal regions European Journal of Human Genetics ·Anja Weise, Bernd Timmermann, Manfred Grabherr, Martin Werber, Patricia Heyn, Nadezda Kosyakova, Thomas Liehr, Heidemarie Neitzel, Kateryna Konrat, Christiane Bommer, Carola Dietrich, Anna Rajab, Richard Reinhardt, Stefan Mundlos, Tom H. Lindner, Katrin Hoffmann	2009	18

About Katrin Hoffmann

Katrin Hoffmann is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Psychiatry and Mental health, having authored 31 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), Pharmacological Effects and Toxicity Studies (4 papers), Epilepsy research and treatment (4 papers), RNA Research and Splicing (3 papers), RNA modifications and cancer (3 papers), Gene expression and cancer classification (3 papers), Nuclear Structure and Function (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Endocrinology (110 citations), Developmental Neuroscience (81 citations), Cellular and Molecular Neuroscience (338 citations), Neurology (126 citations) and Psychiatry and Mental health (219 citations). Katrin Hoffmann has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Wolfgang Löscher, Ina Gröticke, Donald E. Olins, Richard P. Wenzel, Allan J. Morrison, Karl Sperling, Ada L. Olins, Stefan Mundlos, Raoul Heller and Tom H. Lindner. Their work appears in journals such as European Journal of Human Genetics, Experimental Neurology, Human Mutation, Neuropharmacology and Nature Genetics.

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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