Katrin Hinderhofer

3.2k total citations
74 papers, 1.5k citations indexed

About

Katrin Hinderhofer is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Katrin Hinderhofer has authored 74 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 27 papers in Genetics and 20 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Katrin Hinderhofer's work include Pulmonary Hypertension Research and Treatments (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Genomics and Rare Diseases (12 papers). Katrin Hinderhofer is often cited by papers focused on Pulmonary Hypertension Research and Treatments (17 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Genomics and Rare Diseases (12 papers). Katrin Hinderhofer collaborates with scholars based in Germany, Poland and United States. Katrin Hinderhofer's co-authors include Ulrike Zentgraf, F. Schöffl, Ralf Prändl, Christine Fischer, Ute Moog, Ekkehard Grünig, Christina A. Eichstaedt, Christina Evers, Martin Granzow and Nicola Benjamin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Katrin Hinderhofer

71 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Katrin Hinderhofer Germany 23 905 371 342 272 107 74 1.5k
Claudia Gonzaga‐Jauregui United States 21 744 0.8× 97 0.3× 736 2.2× 95 0.3× 154 1.4× 61 1.6k
Fides D. Lay United States 16 1.8k 2.0× 102 0.3× 306 0.9× 152 0.6× 60 0.6× 20 2.1k
Kyoichi Isono Japan 29 2.2k 2.4× 249 0.7× 357 1.0× 62 0.2× 27 0.3× 58 2.6k
Jessica X. Chong United States 19 769 0.8× 46 0.1× 687 2.0× 88 0.3× 62 0.6× 44 1.4k
P. Pearson Netherlands 21 879 1.0× 276 0.7× 710 2.1× 81 0.3× 25 0.2× 50 1.6k
Melanie M. Mahtani United States 14 818 0.9× 252 0.7× 705 2.1× 68 0.3× 27 0.3× 18 1.4k
Digamber S. Borgaonkar United States 20 1.1k 1.3× 268 0.7× 955 2.8× 163 0.6× 96 0.9× 66 2.4k
Gerard Merkx Netherlands 25 1.6k 1.7× 219 0.6× 570 1.7× 262 1.0× 27 0.3× 52 2.2k
Saya Ito Japan 20 1.4k 1.5× 70 0.2× 208 0.6× 257 0.9× 27 0.3× 62 1.9k
Sergi Aranda Spain 16 1.8k 2.0× 88 0.2× 318 0.9× 161 0.6× 154 1.4× 30 2.3k

Countries citing papers authored by Katrin Hinderhofer

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Hinderhofer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Hinderhofer

This figure shows the co-authorship network connecting the top 25 collaborators of Katrin Hinderhofer. A scholar is included among the top collaborators of Katrin Hinderhofer 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 Katrin Hinderhofer. Katrin Hinderhofer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kaufmann, Lilian, et al.. (2025). Phenotypical and Genotypical Expansion of Autosomal‐Dominant KDM1A ‐Related Neurodevelopmental Disorder Spectrum: A Case Report. American Journal of Medical Genetics Part A. 197(11). e64144–e64144.
2.
Evers, Christina, et al.. (2023). Compilation of Genotype and Phenotype Data in GCDH-LOVD for Variant Classification and Further Application. Genes. 14(12). 2218–2218. 1 indexed citations
3.
Grünig, Ekkehard, Nicola Benjamin, Hans‐Jürgen Seyfarth, et al.. (2023). Is iron deficiency caused by BMPR2 mutations or dysfunction in pulmonary arterial hypertension patients?. Pulmonary Circulation. 13(2). e12242–e12242. 4 indexed citations
4.
Gläser, Dieter, et al.. (2021). Leitlinien zur molekulargenetischen Diagnostik: Fragiles-X-Syndrom und andere FMR1-assoziierte Syndrome. Medizinische Genetik. 33(1). 65–73.
5.
Ungerer, Matthias N., Ernst Hund, Jan Purrucker, et al.. (2020). Real-world outcomes in non-endemic hereditary transthyretin amyloidosis with polyneuropathy: a 20-year German single-referral centre experience. Amyloid. 28(2). 91–99. 12 indexed citations
6.
Eichstaedt, Christina A., Heimo Mairbäurl, Jie Song, et al.. (2020). Genetic Predisposition to High-Altitude Pulmonary Edema. High Altitude Medicine & Biology. 21(1). 28–36. 22 indexed citations
7.
Ott, Tim, Lilian Kaufmann, Martin Granzow, et al.. (2019). The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1. Frontiers in Physiology. 10. 134–134. 14 indexed citations
8.
Brum, Ilma Simoni, et al.. (2018). FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve. Reproductive Biology and Endocrinology. 16(1). 65–65. 24 indexed citations
9.
Grund, Kerstin, Dominik Sturm, Christian Sutter, et al.. (2017). Next Generation Sequencing and Pediatric Brain Tumors: Detection of Cancer Predisposition Syndromes in Patients and Their Families. 1(4). 1–1. 36 indexed citations
10.
Brum, Ilma Simoni, et al.. (2017). FMR1 and AKT/mTOR signalling pathways: potential functional interactions controlling folliculogenesis in human granulosa cells. Reproductive BioMedicine Online. 35(5). 485–493. 19 indexed citations
11.
Evers, Christina, Christian Staufner, Martin Granzow, et al.. (2017). Impact of clinical exomes in neurodevelopmental and neurometabolic disorders. Molecular Genetics and Metabolism. 121(4). 297–307. 34 indexed citations
12.
Hartung, Benno, et al.. (2016). Ornithine transcarbamylase deficiency of a male newborn with fatal outcome. International Journal of Legal Medicine. 130(3). 783–785. 3 indexed citations
13.
Viales, Rebecca R., Christina A. Eichstaedt, Nicola Ehlken, et al.. (2015). Mutation in BMPR2 Promoter: A ‘Second Hit’ for Manifestation of Pulmonary Arterial Hypertension?. PLoS ONE. 10(7). e0133042–e0133042. 22 indexed citations
14.
Klinke, Olaf, Gouri Baldwin, Brigitte Bancel, et al.. (2015). KIT Mutation and Loss of 14q May Be Sufficient for the Development of Clinically Symptomatic Very Low-Risk GIST. PLoS ONE. 10(6). e0130149–e0130149. 6 indexed citations
15.
Dikow, Nicola, Stephanie Karch, Martin Granzow, et al.. (2014). 3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior. American Journal of Medical Genetics Part A. 164(12). 3061–3068. 29 indexed citations
16.
Kristen, Arnt V., Katrin Scherer, Sebastian J. Buss, et al.. (2014). Noninvasive Risk Stratification of Patients With Transthyretin Amyloidosis. JACC. Cardiovascular imaging. 7(5). 502–510. 51 indexed citations
17.
Sutter, Christian, et al.. (2014). Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia. European Journal of Human Genetics. 23(5). 704–707. 11 indexed citations
18.
Ebrahimi‐Fakhari, Darius, et al.. (2014). Disruption of SOX6 Is Associated With a Rapid-Onset Dopa-Responsive Movement Disorder, Delayed Development, and Dysmorphic Features. Pediatric Neurology. 52(1). 115–118. 10 indexed citations
19.
Dikow, Nicola, Harald Gaspar, Martina Kreiß‐Nachtsheim, et al.. (2013). The phenotypic spectrum of duplication 5q35.2–q35.3 encompassing NSD1: Is it really a reversed sotos syndrome?. American Journal of Medical Genetics Part A. 161(9). 2158–2166. 35 indexed citations
20.
Prändl, Ralf, et al.. (1998). HSF3, a new heat shock factor from Arabidopsis thaliana, derepresses the heat shock response and confers thermotolerance when overexpressed in transgenic plants. Molecular and General Genetics MGG. 258(3). 269–278. 142 indexed citations

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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