Barbara Plecko

10.0k total citations
138 papers, 4.6k citations indexed

About

Barbara Plecko is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Barbara Plecko has authored 138 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 61 papers in Clinical Biochemistry and 24 papers in Genetics. Recurrent topics in Barbara Plecko's work include Metabolism and Genetic Disorders (61 papers), Biochemical and Molecular Research (24 papers) and Mitochondrial Function and Pathology (21 papers). Barbara Plecko is often cited by papers focused on Metabolism and Genetic Disorders (61 papers), Biochemical and Molecular Research (24 papers) and Mitochondrial Function and Pathology (21 papers). Barbara Plecko collaborates with scholars based in Austria, Switzerland and Germany. Barbara Plecko's co-authors include Peter T. Clayton, Cornelis Jakobs, Philippa B. Mills, Eduard A. Struys, P. G. Barth, P. Vreken, Fredoen Valianpour, Sylvia Stöckler, Leo Nijtmans and Les Grivell and has published in prestigious journals such as Nature Medicine, PLoS ONE and NeuroImage.

In The Last Decade

Barbara Plecko

128 papers receiving 4.5k citations

Peers

Countries citing papers authored by Barbara Plecko

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Plecko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Plecko

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Plecko. A scholar is included among the top collaborators of Barbara Plecko 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 Barbara Plecko. Barbara Plecko 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	Inherited disorders of vitamin metabolism 2025 ·European Journal of Paediatric Neurology ·Barbara Plecko	0
2	Lipidomics—Paving the Road towards Better Insight and Precision Medicine in Rare Metabolic Diseases 2023 ·International Journal of Molecular Sciences ·Martina Zandl‐Lang, Barbara Plecko, Harald Köfeler	7
3	Metabolomics analysis of antiquitin deficiency in cultured human cells and plasma: Relevance to pyridoxine‐dependent epilepsy 2022 ·Journal of Inherited Metabolic Disease ·Lisa M. Crowther, (unknown), Martina Zandl‐Lang, Lucia Abela, Hans Hartmann, Michelle Seiler, Déborah Mathis, Barbara Plecko	6
4	A Case of Vitamin-B6-Dependent Disorder Presenting with Abnormal Eye–Head Movements and Infantile Spasms without Hypsarrhythmia 2022 ·Neuropediatrics ·Judith Kalser, Barbara Plecko, (unknown), Bigna K. Bölsterli	1
5	Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive 2021 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Nadja Ehmke, (unknown), (unknown), Barbara Plecko, Manuel Holtgrewe, Dominik Seelow, (unknown), Michael R. Speicher, Uwe Kornak, Denise Horn, Stefan Mundlos, Björn Fischer‐Zirnsak, Felix Boschann	12
6	A retrospective study on disease management in children and adolescents with phenylketonuria during the Covid-19 pandemic lockdown in Austria 2021 ·Orphanet Journal of Rare Diseases ·Marion Herle, Michaela Brunner‐Krainz, Daniela Karall, (unknown), Dorothea Möslinger, (unknown), Barbara Plecko, Sabine Scholl‐Bürgi, (unknown), Saskia B. Wortmann, Martina Huemer	4
7	Lethal Encephalopathy in an Infant with Hypophosphatasia despite Enzyme Replacement Therapy 2021 ·Hormone Research in Paediatrics ·Adalbert Raimann, Christine Haberler, Janina Patsch, (unknown), Kambis Sadeghi, Michael Freilinger, Susanna Lang, Maria T. Schmook, Barbara Plecko, G. Haeusler	2
8	Childhood-onset epileptic encephalopathy due to FGF12 exon 1–4 tandem duplication 2020 ·Neurology Genetics ·(unknown), Michael R. Speicher, (unknown), Barbara Plecko	3
9	N⁸‐acetylspermidine as a potential plasma biomarker for Snyder‐Robinson syndrome identified by clinical metabolomics 2015 ·Journal of Inherited Metabolic Disease ·Lucia Abela, (unknown), Katharina Steindl, Bernhard Schmitt, Massimo Mastrangelo, Pascal Joset, Sorina Mihaela Papuc, Heinrich Sticht, Alessandra Baumer, Lisa M. Crowther, Déborah Mathis, Anita Rauch, Barbara Plecko	26
10	Sensory stimulus‐sensitive drop attacks and basal ganglia calcification: new findings in a patient with FOLR1 deficiency 2014 ·Epileptic Disorders ·Sandra P. Toelle, (unknown), Bernhard Schmitt, Ianina Scheer, Beat Thöny, Barbara Plecko	20
11	Fatal Outcome of Rhino-orbital-cerebral Mucormycosis Due to Bilateral Internal Carotid Occlusion in a Child After Hematopoietic Stem Cell Transplantation 2013 ·The Pediatric Infectious Disease Journal ·Lucia Abela, Sandra P. Toelle, Annette Hackenberg, Ianina Scheer, Tayfun Güngör, Barbara Plecko	8
12	Status epilepticus in a neonate treated with pyridoxine because of a familial recurrence risk for antiquitin deficiency: pyridoxine toxicity? 2011 ·Developmental Medicine & Child Neurology ·Hans Hartmann, (unknown), Cornelis Jakobs, Barbara Plecko	18
13	Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase 2010 ·Journal of Pediatric Rehabilitation Medicine ·Celeste Decker, Zi‐Fan Yu, Roberto Giugliani, Ida Vanessa Döederlein Schwartz, Nathalie Guffon, Elisa Leão Teles, Clara Sá-Miranda, J. E. Wraith, Michael Beck, Laila Arash, Maurizio Scarpa, David Ketteridge, John J. Hopwood, Barbara Plecko, Robert D. Steiner, Chester B. Whitley, Paige Kaplan, Stuart J. Swiedler, Susan E. Conrad, Paul Harmatz	52
14	Urinary Total Globotriaosylceramide and Isoforms to Identify Women With Fabry Disease: A Diagnostic Test Study 2010 ·American Journal of Kidney Diseases ·Eduard Paschke, Günter Fauler, (unknown), Axel Schlagenhauf, Barbara Plecko, Wolfgang Erwa, Frank Breunig, (unknown), Bojan Vujkovac, Gere Sunder‐Plassmann, Peter Kotanko	15
15	Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase 2008 ·Molecular Genetics and Metabolism ·Paul Harmatz, Roberto Giugliani, Ida Vanessa Döederlein Schwartz, Nathalie Guffon, Elisa Leão Teles, Clara Sá-Miranda, J. E. Wraith, Michael Beck, Laila Arash, Maurizio Scarpa, David Ketteridge, John J. Hopwood, Barbara Plecko, Robert D. Steiner, Chester B. Whitley, Paige Kaplan, (unknown), Stuart J. Swiedler, Celeste Decker	159
16	Mutations in antiquitin in individuals with pyridoxine-dependent seizures 2006 ·Nature Medicine ·Philippa B. Mills, Eduard A. Struys, Cornelis Jakobs, Barbara Plecko, Peter Baxter, Matthias R. Baumgartner, Michèl A.A.P. Willemsen, Heymut Omran, Uta Tacke, Birgit Uhlenberg, Bernhard Weschke, Peter T. Clayton	392
17	eIF2B-Related Disorders: Antenatal Onset and Involvement of Multiple Organs 2003 ·The American Journal of Human Genetics ·Marjo S. van der Knaap, Carola G.M. van Berkel, Jochen Herms, Rudy Van Coster, Martina Baethmann, Sakkubai Naidu, Eugen Boltshauser, Michèl A.A.P. Willemsen, Barbara Plecko, Georg F. Hoffmann, Christopher G. Proud, Gert C. Scheper, Jan C. Pronk	114
18	Mutation analysis in patients with N-acetylglutamate synthase deficiency 2003 ·Human Mutation ·Johannes Häberle, Éva Schmidt, Silke Pauli, Joachim Kreuder, Barbara Plecko, (unknown), (unknown), Erik Harms, Hans Georg Koch	39
19	Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate 1998 ·European Journal of Pediatrics ·Barbara Plecko, Wolfgang Erwa, Bendicht Wermuth	27
20	Liposomal amphotericin-B (AmBisome) for treatment of cutaneous widespread candidosis in an infant with methylmalonic acidaemia 1993 ·European Journal of Pediatrics ·Sylvia Stöckler, Herwig Lackner, (unknown), Wolfgang Schwinger, Barbara Plecko, Werner Müller	5

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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