Lucia Laugwitz

713 total citations
15 papers, 97 citations indexed

About

Lucia Laugwitz is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Lucia Laugwitz has authored 15 papers receiving a total of 97 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Physiology, 5 papers in Cell Biology and 4 papers in Molecular Biology. Recurrent topics in Lucia Laugwitz's work include Lysosomal Storage Disorders Research (7 papers), Cellular transport and secretion (5 papers) and Advanced Neuroimaging Techniques and Applications (3 papers). Lucia Laugwitz is often cited by papers focused on Lysosomal Storage Disorders Research (7 papers), Cellular transport and secretion (5 papers) and Advanced Neuroimaging Techniques and Applications (3 papers). Lucia Laugwitz collaborates with scholars based in Germany, Austria and United States. Lucia Laugwitz's co-authors include Tobias B. Haack, Samuel Groeschel, Ingeborg Krägeloh‐Mann, K. Harzer, Christiane Kehrer, Felix Distelmaier, Stefanie Beck‐Wödl, Rebecca Buchert, Lüdger Schöls and Laimdota Zizmare and has published in prestigious journals such as Brain, Movement Disorders and Antioxidants.

In The Last Decade

Lucia Laugwitz

14 papers receiving 97 citations

Peers

Countries citing papers authored by Lucia Laugwitz

Since Specialization

Citations

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

Fields of papers citing papers by Lucia Laugwitz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Laugwitz

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences 2024 ·Disease Models & Mechanisms ·(unknown), Stefan Hauser, (unknown), Lucia Laugwitz, Samuel Groeschel, Wibke G. Janzarik, (unknown), (unknown), Lüdger Schöls, Ingeborg Krägeloh‐Mann, Simone Mayer	5
2	Late‐onset Krabbe disease presenting as spastic paraplegia – implications of GCase and CTSB/D 2024 ·Annals of Clinical and Translational Neurology ·(unknown), (unknown), Ute Hehr, Alexander Weiß, Matthias Kettwig, Lucia Laugwitz, Samuel Groeschel, Manuel Schmidt, Philipp Arnold, Martin Regensburger, Friederike Zunke	0
3	Elevated cholesterol is a common phenotype for dominant and recessive ATAD3-associated disorders 2024 ·Brain ·(unknown), Lucia Laugwitz, Rebecca Buchert, Mona Grimmel, (unknown), Marc Sturm, Selina Reich, Martje G. Pauly, Norbert Brüggemann, Alexander Münchau, (unknown), Matthis Synofzik, (unknown), Susana Peralta	1
4	Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders 2023 ·Antioxidants ·(unknown), Jannik Prasuhn, Lucia Laugwitz, Cheuk‐Wing Fung, Brian Hon‐Yin Chung, Marcello Bellusci, Ertan Mayatepek, Dirk Klee, Felix Distelmaier	6
5	Hematopoietic Stem Cell Transplantation with Mesenchymal Stromal Cells in Children with Metachromatic Leukodystrophy 2022 ·Stem Cells and Development ·(unknown), Judith Böhringer, (unknown), Samuel Groeschel, (unknown), (unknown), Christiane Kehrer, Lucia Laugwitz, Andrea Bevot, (unknown), Michael Schumm, Peter Lang, Rupert Handgretinger, Ingeborg Krägeloh‐Mann, Ingo Müller, Michaela Döring	8
6	Bi‐Allelic COQ4 Variants Cause Adult‐Onset Ataxia‐Spasticity Spectrum Disease 2022 ·Movement Disorders ·Isabell Cordts, (unknown), Jannik Prasuhn, Annette Seibt, Diran Herebıan, (unknown), Joohyun Park, (unknown), Lucia Laugwitz, Sophia Göricke, Paul Lingor, Norbert Brüggemann, Alexander Münchau, Matthis Synofzik, Dagmar Timmann, Johannes A. Mayr, Tobias B. Haack, Felix Distelmaier, Marcus Deschauer	9
7	MR-spectroscopy in metachromatic leukodystrophy: A model free approach and clinical correlation 2022 ·NeuroImage Clinical ·(unknown), Pascal Martin, Benjamin Bender, Lucia Laugwitz, Laimdota Zizmare, Christoph Trautwein, Ingeborg Krägeloh‐Mann, Uwe Klose, Samuel Groeschel	3
8	Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? – Chances and challenges 2022 ·Molecular Genetics and Metabolism ·(unknown), Samuel Groeschel, K. Harzer, Christiane Kehrer, (unknown), Stefanie Beck‐Wödl, Holger Hengel, Lüdger Schöls, Tobias B. Haack, Ingeborg Krägeloh‐Mann, Lucia Laugwitz	15
9	Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR‐based urinary metabolomics 2022 ·JIMD Reports ·Lucia Laugwitz, Laimdota Zizmare, (unknown), Claire Cannet, Judith Böhringer, Jürgen G. Okun, Manfred Spraul, Ingeborg Krägeloh‐Mann, Samuel Groeschel, Christoph Trautwein	5
10	Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long‐term follow‐up and review of the literature 2022 ·JIMD Reports ·Lucia Laugwitz, (unknown), (unknown), (unknown), Benjamin Bender, Volkmar Gieselmann, Stefanie Beck‐Woedl, Gernot Bruchelt, K. Harzer, (unknown), Samuel Groeschel	7
11	Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy 2021 ·Clinical Genetics ·Christina Rapp, (unknown), Lucia Laugwitz, Mieke Boon, George Briassoulis, Stavroula Ilia, Birgit Kammer, Simone Reu, (unknown), Rebecca Buchert, (unknown), Tawfiq Froukh, Peter Witters, Daisy Rymen, Tobias B. Haack, Marijke Proesmans, Matthias Griese	12
12	Challenges in Biochemical Diagnosis of Krabbe and Gaucher Disease 2021 ·Neuropediatrics ·(unknown), (unknown), (unknown), (unknown), Judith Böhringer, K. Harzer, Lucia Laugwitz, Stefanie Beck‐Wödl, Ingeborg Krägeloh‐Mann, Samuel Groeschel	1
13	Paroxysmal and non-paroxysmal dystonia in 3 patients with biallelic ECHS1 variants: Expanding the neurological spectrum and therapeutic approaches 2020 ·European Journal of Medical Genetics ·Sabine Illsinger, Georg Christoph Korenke, Sylvia Boesch, Michael Nocker, Daniela Karall, Jean‐Marc Nuoffer, Lucia Laugwitz, Johannes A. Mayr, Sabine Scholl‐Bürgi, Peter Freisinger, (unknown), Stefan Kölker, Holger Prokisch, Tobias B. Haack	12
14	Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology? 2020 ·European Journal of Medical Genetics ·Lucia Laugwitz, Rebecca Buchert, Samuel Groeschel, Angelika Rieß, Mona Grimmel, Stefanie Beck‐Wödl, Marc Sturm, (unknown), (unknown), Ingeborg Krägeloh‐Mann, Tobias B. Haack	5
15	Isolated PREPL deficiency associated with congenital myasthenic syndrome-22 2018 ·Klinische Pädiatrie ·Lucia Laugwitz, Silke Redler, Rebecca Buchert, Marc Sturm, (unknown), Ulrike Schara, Dagmar Wieczorek, Tobias B. Haack, Felix Distelmaier	8

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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