Katja‐Martina Eckl

1.7k citations

23 papers · 951 indexed · h-index 14

Co-authors: Hans Christian Hennies Heiko Traupe Vinzenz Oji Ingrid Haußer Monika Schäfer‐Korting Sarah Hedtrich Peter Krieg Gudrun Nürnberg
Topics: Skin and Cellular Biology Research (15 papers)Dermatology and Skin Diseases (5 papers)Wnt/β-catenin signaling in development and cancer (4 papers)
Cited by: Dermatology Pharmaceutical Science Cell Biology
Journals: International Journal of Molecular Sciences Journal of Controlled Release The American Journal of Human Genetics
Partner nations: Germany Austria United Kingdom

In The Last Decade

Katja‐Martina Eckl

23 papers receiving 920 citations

Peers

Countries citing papers authored by Katja‐Martina Eckl

Since Specialization

Citations

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

Fields of papers citing papers by Katja‐Martina Eckl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katja‐Martina Eckl. 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 Katja‐Martina Eckl. The network helps show where Katja‐Martina Eckl may publish in the future.

Co-authorship network of co-authors of Katja‐Martina Eckl

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers 2021 ·International Journal of Molecular Sciences ·Dulce Lima Cunha,(unknown),Robert Gruber,(unknown),Arno Lingenhel,Manoj Kumar Gupta,Janine Altmüller,Peter Nürnberg,Matthias Schmuth,Johannes Zschocke,Tomo Šarić,Katja‐Martina Eckl,Hans Christian Hennies	5
2	Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling 2021 ·Acta Dermato Venereologica ·Mee‐Ran Kim,Vinzenz Oji,(unknown),Heiko Traupe,Jerzy–Roch Nofer,Ingrid Haußer,(unknown),Katja‐Martina Eckl,Stefan A. Wudy,Alberto Sánchez‐Guijo,Laura Kerschke,Judith Fischer,(unknown)	4
3	Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V 2021 ·Frontiers in Genetics ·Katja‐Martina Eckl,Robert Gruber,(unknown),Andrew S. Marriott,(unknown),Verena Moosbrugger‐Martinz,Stefan Blunder,Anna Schossig,Janine Altmüller,Holger Thiele,Peter Nürnberg,Johannes Zschocke,Hans Christian Hennies,Matthias Schmuth	5
4	Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan 2019 ·Molecular Genetics & Genomic Medicine ·Dulce Lima Cunha,Omar M Alakloby,Robert Gruber,Naseebullah Kakar,Jamil Ahmad,(unknown),(unknown),Katja‐Martina Eckl,Birgit Krabichler,Janine Altmüller,Peter Nürnberg,Johannes Zschocke,Guntram Borck,Matthias Schmuth,(unknown),(unknown),Hans Christian Hennies	7
5	Thermosensitive dendritic polyglycerol-based nanogels for cutaneous delivery of biomacromolecules 2015 ·Nanomedicine Nanotechnology Biology and Medicine ·Madeleine Witting,María Molina,(unknown),(unknown),Katja‐Martina Eckl,Hans Christian Hennies,Marcelo Calderón,Wolfgang Frieß,Sarah Hedtrich	69
6	Penetration of normal, damaged and diseased skin — An in vitro study on dendritic core–multishell nanotransporters 2014 ·Journal of Controlled Release ·(unknown),Christian Zoschke,Emanuel Fleige,Robert Brodwolf,Alexander Boreham,E. Rühl,Katja‐Martina Eckl,(unknown),Hans Christian Hennies,Ulrike Alexiev,Rainer Haag,Sarah Hedtrich,Monika Schäfer‐Korting	60
7	Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation inCSTA 2014 ·British Journal of Dermatology ·Verena Moosbrugger‐Martinz,Ahmad Jalili,(unknown),(unknown),Johannes Zschocke,Matthias Schmuth,Georg Stingl,Katja‐Martina Eckl,(unknown),Robert Gruber	13
8	Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length 2013 ·Journal of Investigative Dermatology ·Katja‐Martina Eckl,Rotem Tidhar,Holger Thiele,Vinzenz Oji,Ingrid Haußer,Susanne Brodesser,(unknown),(unknown),Friedrich Stock,Dietmar Müller,Kerstin Becker,(unknown),Gudrun Nürnberg,Janine Altmüller,Peter Nürnberg,Heiko Traupe,Anthony H. Futerman,Hans Christian Hennies	130
9	Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion 2011 ·The American Journal of Human Genetics ·Diana C. Blaydon,Daniela Nitoiu,Katja‐Martina Eckl,Rita Cabral,Philip Bland,Ingrid Haußer,David A. van Heel,Shefali Rajpopat,Judith Fischer,Vinzenz Oji,Alex Zvulunov,Heiko Traupe,(unknown),David P. Kelsell	67
10	Hallmarks of Atopic Skin Mimicked In Vitro by Means of a Skin Disease Model Based on FLG Knock-down 2011 ·Alternatives to Laboratory Animals ·Sarah Hedtrich,(unknown),Katja‐Martina Eckl,(unknown),Johanna Plendl,(unknown),Hans-Christian Hennies,Monika Schäfer‐Korting	52
11	Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease 2010 ·The American Journal of Human Genetics ·Vinzenz Oji,Katja‐Martina Eckl,Karin Aufenvenne,(unknown),(unknown),(unknown),(unknown),Dieter Metze,Gudrun Nürnberg,Regina Fölster‐Holst,Monika Schäfer‐Korting,Ingrid Haußer,Heiko Traupe,Hans Christian Hennies	146
12	CEDNIK syndrome results from loss-of-function mutations in SNAP29 2010 ·British Journal of Dermatology ·Dana Fuchs‐Telem,Helen Stewart,David Rapaport,Janna Nousbeck,Andrea Gat,(unknown),(unknown),Steffen Emmert,Katja‐Martina Eckl,(unknown),Ofer Sarig,Dorith Goldsher,(unknown),Akemi Ishida‐Yamamoto,Mia Horowitz,Eli Sprecher	64
13	Molecular Analysis of 250 Patients with Autosomal Recessive Congenital Ichthyosis: Evidence for Mutation Hotspots in ALOXE3 and Allelic Heterogeneity in ALOX12B 2009 ·Journal of Investigative Dermatology ·Katja‐Martina Eckl,(unknown),(unknown),(unknown),(unknown),Vinzenz Oji,Heiko Traupe,(unknown),Francisco Martı́nez,Josef Smolle,Avikam Harel,Peter Krieg,Eli Sprecher,Hans Christian Hennies	79
14	Role of epidermis-type lipoxygenases for skin barrier function and adipocyte differentiation 2006 ·Prostaglandins & Other Lipid Mediators ·Gerhard Fürstenberger,(unknown),Katja‐Martina Eckl,Hans Christian Hennies,Claus Jørgensen,Philip Hallenborg,Karsten Kristiansen,Peter Krieg	31
15	Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies 2005 ·Archives of Dermatological Research ·Robert Pichler,(unknown),Jörg Berg,(unknown),Katja‐Martina Eckl,Hans Christian Hennies,Josef Auböck	2
16	Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis 2005 ·Human Mutation ·Katja‐Martina Eckl,Peter Krieg,Wolfgang Küster,Heiko Traupe,Françoise André,(unknown),Gerhard Fürstenberger,Hans Christian Hennies	70
17	Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome 2004 ·The American Journal of Human Genetics ·Hans Christian Hennies,Anita Rauch,Wenke Seifert,(unknown),Elisabeth Moser,(unknown),Gholamali Tariverdian,Krystyńa Chrzańowska,Małgorzata Krajewska‐Walasek,Anna Rajab,Roberto Giugliani,Thomas Neumann,Katja‐Martina Eckl,Mohsen Karbasiyan,André Reis,Denise Horn	55
18	Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates 2003 ·Human Genetics ·Katja‐Martina Eckl,Howard P. Stevens,(unknown),(unknown),Heiko Traupe,(unknown),Philippe Frossard,Rudolf Stadler,Irene M. Leigh,Peter Nürnberg,André Reis,Hans Christian Hennies	44
19	Pharmacokinetics of temocapril and temocaprilat after 14 once daily oral doses of temocapril in hypertensive patients with varying degrees of renal impairment 1997 ·British Journal of Clinical Pharmacology ·Kurt Püchler,Katja‐Martina Eckl,Lutz Fritsche,(unknown),Hans‐Hellmut Neumayer,(unknown),(unknown),T. Thomsen,Ivar Roots	5
20	The pharmacokinetics of paroxetine in patients with liver cirrhosis 1989 ·Acta Psychiatrica Scandinavica ·(unknown),(unknown),(unknown),(unknown),W. H. Greb,Katja‐Martina Eckl,(unknown),David S. Wolf	25

About Katja‐Martina Eckl

Katja‐Martina Eckl is a scholar working on Cell Biology, Dermatology and Pharmaceutical Science, having authored 23 papers that have together received 951 indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (15 papers), Dermatology and Skin Diseases (5 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). The work is most often cited by research in Dermatology (239 citations), Pharmaceutical Science (162 citations) and Cell Biology (378 citations). Katja‐Martina Eckl has collaborated with scholars based in Germany, Austria and United Kingdom. Frequent co-authors include Hans Christian Hennies, Heiko Traupe, Vinzenz Oji, Ingrid Haußer, Monika Schäfer‐Korting, Sarah Hedtrich, Peter Krieg, Gudrun Nürnberg, Gerhard Fürstenberger and Peter Nürnberg. Their work appears in journals such as International Journal of Molecular Sciences, Journal of Controlled Release and The American Journal of Human 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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