Ingrid Haußer

10.1k total citations
164 papers, 5.6k citations indexed

About

Ingrid Haußer is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Ingrid Haußer has authored 164 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Cell Biology, 62 papers in Molecular Biology and 59 papers in Genetics. Recurrent topics in Ingrid Haußer's work include Skin and Cellular Biology Research (70 papers), Connective tissue disorders research (41 papers) and Dermatological and Skeletal Disorders (27 papers). Ingrid Haußer is often cited by papers focused on Skin and Cellular Biology Research (70 papers), Connective tissue disorders research (41 papers) and Dermatological and Skeletal Disorders (27 papers). Ingrid Haußer collaborates with scholars based in Germany, United States and Switzerland. Ingrid Haußer's co-authors include I. Anton‐Lamprecht, Tobias Brandt, Leena Bruckner‐Tuderman, Anne De Paepe, Vinzenz Oji, Caspar Grond‐Ginsbach, E. Orberk, Heiko Traupe, Wolfgang Hartschuh and R. Weber and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Ingrid Haußer

159 papers receiving 5.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Ingrid Haußer 2.0k 1.9k 1.6k 809 773 164 5.6k
Heiko Traupe 2.0k 1.0× 2.0k 1.1× 1.3k 0.8× 495 0.6× 542 0.7× 166 5.5k
Peter M. Steijlen 1.4k 0.7× 1.9k 1.0× 1.2k 0.7× 237 0.3× 460 0.6× 140 5.1k
Satoshi Itami 1.6k 0.8× 2.6k 1.4× 724 0.4× 428 0.5× 495 0.6× 194 8.1k
Jung San Huang 1.0k 0.5× 4.1k 2.2× 869 0.5× 240 0.3× 205 0.3× 93 7.3k
Aleksander Hinek 1.6k 0.8× 2.6k 1.4× 2.4k 1.4× 619 0.8× 156 0.2× 143 6.8k
Maria Trojanowska 1.4k 0.7× 4.6k 2.4× 908 0.6× 902 1.1× 4.0k 5.2× 171 10.0k
Mark D. Sternlicht 651 0.3× 3.0k 1.6× 618 0.4× 280 0.3× 323 0.4× 45 7.2k
Marikki Laiho 638 0.3× 6.8k 3.6× 572 0.3× 356 0.4× 574 0.7× 116 9.2k
George Bou–Gharios 449 0.2× 3.4k 1.8× 714 0.4× 509 0.6× 842 1.1× 158 6.6k
Adam B. Glick 903 0.5× 4.6k 2.4× 734 0.4× 216 0.3× 441 0.6× 109 7.4k

Countries citing papers authored by Ingrid Haußer

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Haußer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Haußer

This figure shows the co-authorship network connecting the top 25 collaborators of Ingrid Haußer. A scholar is included among the top collaborators of Ingrid Haußer 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 Ingrid Haußer. Ingrid Haußer 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.
Zhang, Xin, Katrin Bennewitz, Xiaogang Li, et al.. (2025). Endogenous acrolein accumulation in akr7a3 mutants causes microvascular dysfunction due to increased arachidonic acid metabolism. Redox Biology. 83. 103639–103639.
3.
Jahn, Denise, Willy Morelle, Ingrid Haußer, et al.. (2024). Golgi pH elevation due to loss of V-ATPase subunit V0a2 function correlates with tissue-specific glycosylation changes and globozoospermia. Cellular and Molecular Life Sciences. 82(1). 4–4. 3 indexed citations
4.
Byers, Peter H., Neeti Ghali, Juliette Harris, et al.. (2024). The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series. American Journal of Medical Genetics Part A. 197(4). e63957–e63957. 1 indexed citations
5.
Xin, Qian, Stephan Klatt, Katrin Bennewitz, et al.. (2023). Impaired Detoxification of Trans, Trans‐2,4‐Decadienal, an Oxidation Product from Omega‐6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular Disease. Advanced Science. 11(4). e2302325–e2302325. 6 indexed citations
6.
Haußer, Ingrid, et al.. (2023). Epidermal or Dermal Collagen VII Is Sufficient for Skin Integrity: Insights to Anchoring Fibril Homeostasis. Journal of Investigative Dermatology. 144(6). 1301–1310.e7. 6 indexed citations
7.
Lavallee, Mark E., Ingrid Haußer, F M Pope, et al.. (2023). Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review. Journal of the American Academy of Dermatology. 89(3). 551–559. 4 indexed citations
8.
Bennewitz, Katrin, Ingrid Haußer, Carsten Sticht, et al.. (2022). pdx1 Knockout Leads to a Diabetic Nephropathy– Like Phenotype in Zebrafish and Identifies Phosphatidylethanolamine as Metabolite Promoting Early Diabetic Kidney Damage. Diabetes. 71(5). 1073–1080. 20 indexed citations
9.
Nyström, Alexander, Cameron J. Nowell, Ingrid Haußer, et al.. (2021). Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease. Disease Models & Mechanisms. 14(6). 5 indexed citations
10.
Bornert, Olivier, Pauline Nauroy, Johannes Bischof, et al.. (2020). QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical Study. Journal of Investigative Dermatology. 141(4). 883–893.e6. 40 indexed citations
11.
He, Yinghong, Kerstin Thriene, Melanie Boerries, et al.. (2018). Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytes. Matrix Biology. 74. 62–76. 15 indexed citations
12.
Mencía, Ángeles, Cristina Chamorro, Blanca Duarte, et al.. (2018). Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells. Molecular Therapy — Nucleic Acids. 11. 68–78. 34 indexed citations
13.
Gruber, Robert, Elke Rodríguez, Heiko Traupe, et al.. (2017). Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination. Journal of Investigative Dermatology. 138(3). 709–711. 12 indexed citations
14.
He, Yinghong, Ingrid Haußer, Agnes Schwieger‐Briel, et al.. (2016). Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility. The American Journal of Human Genetics. 99(6). 1395–1404. 54 indexed citations
15.
Kühl, Tobias, Markus Mezger, Ingrid Haußer, et al.. (2016). Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses. Journal of Investigative Dermatology. 136(6). 1116–1123. 37 indexed citations
16.
Weingart, Christiane, Ingrid Haußer, Olivia Kershaw, & Barbara Kohn. (2014). Ehlers-Danlos-like-Syndrom bei einer Katze. Schweizer Archiv für Tierheilkunde. 156(11). 543–548. 4 indexed citations
17.
Eckl, Katja‐Martina, Rotem Tidhar, Holger Thiele, et al.. (2013). Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length. Journal of Investigative Dermatology. 133(9). 2202–2211. 130 indexed citations
18.
Krieg, Peter, Sabine Rosenberger, Jin Hou, et al.. (2012). Aloxe3 Knockout Mice Reveal a Function of Epidermal Lipoxygenase-3 as Hepoxilin Synthase and Its Pivotal Role in Barrier Formation. Journal of Investigative Dermatology. 133(1). 172–180. 104 indexed citations
19.
Malfait, Fransiska, et al.. (2003). The natural history of human dermatosparaxis : a report of two cases. Ghent University Academic Bibliography (Ghent University). 1 indexed citations
20.
Haußer, Ingrid, et al.. (2003). Heterozygous carriers of Pseudoxanthoma elasticum were not found among patients with cervical artery dissections. Journal of Neurology. 250(8). 983–986. 17 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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