Thorsten Marquardt

9.1k citations

156 papers · 5.3k indexed · h-index 40

Co-authors: Ari Helenius Jonas Denecke Kurt Von Figura Hudson H. Freeze Erik Harms Janine Reunert Ineke Braakman Torben Lübke
Topics: Glycosylation and Glycoproteins Research (49 papers)Lysosomal Storage Disorders Research (31 papers)Metabolism and Genetic Disorders (28 papers)
Cited by: Clinical Biochemistry Physiology Cell Biology
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Journal of Clinical Investigation
Partner nations: Germany United States Switzerland

In The Last Decade

Thorsten Marquardt

151 papers receiving 5.2k citations

Peers

Countries citing papers authored by Thorsten Marquardt

Since Specialization

Citations

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

Fields of papers citing papers by Thorsten Marquardt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thorsten Marquardt

This figure shows the co-authorship network connecting the top 25 collaborators of Thorsten Marquardt. A scholar is included among the top collaborators of Thorsten Marquardt 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 Thorsten Marquardt. Thorsten Marquardt 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	Database Analysis of Application Areas and Global Trends in Ketogenic Diets from 2019 to 2024 2025 ·Nutrients ·(unknown),(unknown),(unknown),Thorsten Marquardt,Tobias Fischer	1
2	Expanding the genetic and clinical spectrum of SLC25A42‐associated disorders and testing of pantothenic acid to improve CoA level in vitro 2024 ·JIMD Reports ·(unknown),Arcangela Iuso,Janine Reunert,Marianne Grüneberg,(unknown),Stephan Rust,Giuseppe Fiermonte,Eleonora Paradies,(unknown),Manoj Mannil,Thorsten Marquardt	0
3	Pathogenic Relationships in Cystic Fibrosis and Renal Diseases: CFTR, SLC26A9 and Anoctamins 2023 ·International Journal of Molecular Sciences ·Karl Kunzelmann,Jiraporn Ousingsawat,Andre Kraus,Julien H. Park,Thorsten Marquardt,Rainer Schreiber,Bjoern Buchholz	5
4	Beta-Hydroxybutyrate (BHB), Glucose, Insulin, Octanoate (C8), and Decanoate (C10) Responses to a Medium-Chain Triglyceride (MCT) Oil with and without Glucose: A Single-Center Study in Healthy Adults 2023 ·Nutrients ·(unknown),Manfred Fobker,(unknown),Reinhold Feldmann,Tobias Fischer,Thorsten Marquardt	14
5	Managing type 1 diabetes mellitus with a ketogenic diet 2023 ·Endocrinology Diabetes and Metabolism Case Reports ·(unknown),S E Knowles,Thorsten Marquardt	9
6	Adverse events using shorter MDR-TB regimens: outcomes from Port Moresby, Papua New Guinea 2021 ·Public Health Action ·(unknown),(unknown),(unknown),(unknown),(unknown),Thorsten Marquardt	4
7	The schizophrenia risk locus in SLC39A8 alters brain metal transport and plasma glycosylation 2020 ·Scientific Reports ·Robert G. Mealer,Bruce G. Jenkins,Chia‐Yen Chen,Mark J. Daly,Tian Ge,Sylvain Lehoux,Thorsten Marquardt,Christopher D. Palmer,Julien H. Park,Patrick J. Parsons,Robert Sackstein,Sarah Williams,Richard D. Cummings,Edward M. Scolnick,Jordan W. Smoller	44
8	SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis 2019 ·Brain ·Julien H. Park,(unknown),Janine Reunert,Michael L. McCormick,Julia Mohr,Saskia Biskup,Oliver Schwartz,Stephan Rust,Marianne Grüneberg,(unknown),Ulrike Schara,Eugen Boltshauser,Douglas R. Spitz,Thorsten Marquardt	62
9	Limitations of galactose therapy in phosphoglucomutase 1 deficiency 2017 ·Molecular Genetics and Metabolism Reports ·(unknown),Julien H. Park,(unknown),(unknown),Marianne Grüneberg,Stephan Rust,Janine Reunert,(unknown),Volker Debus,Eric Schulze‐Bahr,Robert C. Baxter,Yoshinao Wada,Christian Thiel,Emile Van Schaftingen,Ralph Fingerhut,Thorsten Marquardt	27
10	Partial correction of neutrophil dysfunction by oral galactose therapy in glycogen storage disease type Ib 2017 ·International Immunopharmacology ·(unknown),Helmut Wittkowski,Aristotelis Antonopoulos,(unknown),Stuart M. Haslam,Dirk Föll,Anne Dell,Thorsten Marquardt	6
11	A novel mutation in PIGW causes glycosylphosphatidylinositol deficiency without hyperphosphatasia 2016 ·American Journal of Medical Genetics Part A ·(unknown),Yoshiko Murakami,Martin K. Wild,Martina Ahlmann,Saskia Biskup,Konstanze Hörtnagel,Marianne Grüneberg,Janine Reunert,Tobias Linden,Taroh Kinoshita,Thorsten Marquardt	19
12	Determination of serum cholestane-3β,5α,6β-triol by gas chromatography–mass spectrometry for identification of Niemann-Pick type C (NPC) disease 2016 ·The Journal of Steroid Biochemistry and Molecular Biology ·Frank Kannenberg,Jerzy–Roch Nofer,Erhard Schulte,Janine Reunert,Thorsten Marquardt,Manfred Fobker	23
13	Outcome of Patients with Classical Infantile Pompe Disease Receiving Enzyme Replacement Therapy in Germany 2014 ·JIMD Reports ·Andreas Hahn,(unknown),Nesrin Karabul,(unknown),Dorle Schmidt,(unknown),Claudia M. Haase,Martina Baethmann,Julia B. Hennermann,Martin Smitka,René Santer,Nicole Muschol,(unknown),Thorsten Marquardt,Martina Huemer,Charlotte Thiels,Marianne Rohrbach,(unknown),Eugen Mengel	47
14	Effects of enzyme replacement therapy in adult patients with Fabry disease on cardiac structure and function: a retrospective cohort study of the Fabry Münster Study (FaMüS) data 2012 ·BMJ Open ·Markus A. Engelen,Eva Brand,(unknown),Thorsten Marquardt,Thomas Duning,Nani Osada,Roland M. Schaefer,Joerg Stypmann	11
15	Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now? 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jonas Denecke,Thorsten Marquardt	18
16	A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy 2007 ·The American Journal of Human Genetics ·Christian Kranz,(unknown),Jonas Denecke,(unknown),(unknown),Volker Debus,Hans-Gerd Kehl,Erik Harms,A. D. Reith,(unknown),H Gröbe,G. Hammersen,(unknown),Thorsten Marquardt	72
17	An activated 5? cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) 2004 ·Human Mutation ·Jonas Denecke,Christian Kranz,Dirk Kemming,Hans-Georg Koch,Thorsten Marquardt	48
18	Hyperinsulinaemic hypoglycaemia—Leading symptom in a patient with congenital disorder of glycosylation Ia (phosphomannomutase deficiency) 2001 ·Journal of Inherited Metabolic Disease ·Hansjosef Böhles,A Sewell,Boris Gebhardt,Axel Reinecke‐Lüthge,Günter Klöppel,Thorsten Marquardt	34
19	A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If) 2001 ·Journal of Clinical Investigation ·Christian Kranz,Jonas Denecke,Mark A. Lehrman,Sutapa Ray,(unknown),(unknown),Dijana Šagi,Jasna Peter‐Katalinić,Hudson H. Freeze,Thomas Schmid,(unknown),Erik Harms,Thorsten Marquardt	104
20	Association of the precursor of cathepsin D with coated membranes. Kinetics and carbohydrate processing 1987 ·European Journal of Biochemistry ·Thorsten Marquardt,Thomas Braulke,Andrej Hasilík,Kurt Von Figura	19

About Thorsten Marquardt

Thorsten Marquardt is a scholar working on Clinical Biochemistry, Physiology and Biochemistry, having authored 156 papers that have together received 5.3k indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (49 papers), Lysosomal Storage Disorders Research (31 papers) and Metabolism and Genetic Disorders (28 papers). The work is most often cited by research in Clinical Biochemistry (621 citations), Physiology (1.6k citations) and Cell Biology (779 citations). Thorsten Marquardt has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Ari Helenius, Jonas Denecke, Kurt Von Figura, Hudson H. Freeze, Erik Harms, Janine Reunert, Ineke Braakman, Torben Lübke, Kerstin Lühn and Dietmar Vestweber. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

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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