Marianne Grüneberg

1.0k citations

30 papers · 553 indexed · h-index 14

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 7
Biochemistry
- Amino Acid Enzymes and Metabolism 5
Molecular Biology
- Glycosylation and Glycoproteins Research 11
Physiology
Nutrition and Dietetics
Pathology and Forensic Medicine
- Biomedical Research and Pathophysiology 4
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 4
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 3
Immunology
- Galectins and Cancer Biology 3
Rheumatology
- Glycogen Storage Diseases and Myoclonus 2

Co-authors: Thorsten Marquardt Janine Reunert Stephan Rust Julien H. Park Saskia Biskup Manfred Fobker Yoshinao Wada Ingrid DuChesne
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: Brain (1 paper)Clinica Chimica Acta (1 paper)Genomics (1 paper)
Partner nations: Germany Japan Switzerland

In The Last Decade

Marianne Grüneberg

28 papers receiving 550 citations

Peers

Countries citing papers authored by Marianne Grüneberg

Since Specialization

Citations

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

Fields of papers citing papers by Marianne Grüneberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Marianne Grüneberg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marianne Grüneberg Line = papers co-authored together Marianne Grüneberg links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Expanding the genetic and clinical spectrum of SLC25A42‐associated disorders and testing of pantothenic acid to improve CoA level in vitro JIMD Reports ·K. Heckmann,Arcangela Iuso,Janine Reunert,Marianne Grüneberg,Anja Seelhöfer,Stephan Rust,Giuseppe Fiermonte,Eleonora Paradies,Carmela Piazzolla,Manoj Mannil,Thorsten Marquardt	2024	0
2	Enteric-Coated Cysteamine Bitartrate in Cystinosis Patients Pharmaceutics ·Sabrina Klank,Christina van Stein,Marianne Grüneberg,Chris Ottolenghi,Kerstin K. Rauwolf,Jürgen Grebe,Janine Reunert,Erik Harms,Thorsten Marquardt	2023	4
3	A comparison of immediate release and delayed release cysteamine in 17 patients with nephropathic cystinosis Orphanet Journal of Rare Diseases ·Christina Esther van Stein,Sabrina Klank,Marianne Grüneberg,Chris Ottolenghi,J. Grebe,Janine Reunert,Erik Harms,Thorsten Marquardt	2021	13
4	Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG) Orphanet Journal of Rare Diseases ·Roman Taday,Marianne Grüneberg,Ingrid DuChesne,Janine Reunert,Thorsten Marquardt	2020	11
5	SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation Molecular Genetics and Metabolism Reports ·Thorsten Marquardt,Vladimı́r Bzdúch,Max Hogrebe,Stephan Rust,Janine Reunert,Marianne Grüneberg,Julien H. Park,Nico Callewaert,Robin Lachmann,Yoshinao Wada,Thomas Engel	2020	5
6	L-Fucose treatment of FUT8-CDG Molecular Genetics and Metabolism Reports ·Julien H. Park,Janine Reunert,Miao He,Robert G. Mealer,Maxence Noël,Yoshinao Wada,Marianne Grüneberg,Judit Horváth,Richard D. Cummings,Oliver Schwartz,Thorsten Marquardt	2020	19
7	Incidental diagnosis of leukocyte adhesion deficiency type II following ABO typing Clinical Immunology ·N. John Cooper,Yu‐Tung Li,Anette Torvin Møller,Nelly Schulz‐Weidner,Ulrich J. Sachs,Franz F. Wagner,Holger Hackstein,Sandra Wienzek‐Lischka,Marianne Grüneberg,Martin K. Wild,Gregor Bein,Thorsten Marquardt	2020	5
8	SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis Brain ·Julien H. Park,Christiane Elpers,Janine Reunert,Michael L. McCormick,Julia Mohr,Saskia Biskup,Oliver Schwartz,Stephan Rust,Marianne Grüneberg,Anja Seelhöfer,Ulrike Schara,Eugen Boltshauser,Douglas R. Spitz,Thorsten Marquardt	2019	62
9	Transferrin glycosylation analysis from dried blood spot cards and capillary blood samples Journal of Chromatography B ·Anna B. Wolking,Julien H. Park,Marianne Grüneberg,Janine Reunert,Ralph Fingerhut,Manfred Fobker,Thorsten Marquardt	2019	7
10	QIL1-dependent assembly of MICOS complex–lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation Journal of Human Genetics ·Juliana Gödiker,Marianne Grüneberg,Ingrid DuChesne,Janine Reunert,Stephan Rust,Cordula Westermann,Yoshiro Wada,Georg Classen,Claus‐Dieter Langhans,Karl P. Schlingmann,Richard J. Rodenburg,Regina Pohlmann,Thorsten Marquardt	2018	33
11	Limitations of galactose therapy in phosphoglucomutase 1 deficiency Molecular Genetics and Metabolism Reports ·Kristine Nolting,Julien H. Park,Laura C. Tegtmeyer,Andrea Zühlsdorf,Marianne Grüneberg,Stephan Rust,Janine Reunert,Ingrid Du Chesne,Volker Debus,Eric Schulze‐Bahr,Robert C. Baxter,Yoshinao Wada,Christian Thiel,Emile Van Schaftingen,Ralph Fingerhut,Thorsten Marquardt	2017	27
12	SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapy Genetics in Medicine ·Julien H. Park,Max Hogrebe,Manfred Fobker,Renate Brackmann,Barbara Fiedler,Janine Reunert,Stephan Rust,Konstantinos Tsiakas,René Santer,Marianne Grüneberg,Thorsten Marquardt	2017	57
13	A novel mutation in PIGW causes glycosylphosphatidylinositol deficiency without hyperphosphatasia American Journal of Medical Genetics Part A ·Max Hogrebe,Yoshiko Murakami,Martin K. Wild,Martina Ahlmann,Saskia Biskup,Konstanze Hörtnagel,Marianne Grüneberg,Janine Reunert,Tobias Linden,Taroh Kinoshita,Thorsten Marquardt	2016	19
14	TMEM165 Deficiency: Postnatal Changes in Glycosylation JIMD Reports ·S. Schulte Althoff,Marianne Grüneberg,Janine Reunert,Julien H. Park,Stephan Rust,Chris Mühlhausen,Yoshinao Wada,René Santer,Thorsten Marquardt	2015	23
15	Transferrin variants: Pitfalls in the diagnostics of Congenital disorders of glycosylation Clinical Biochemistry ·Andrea Zühlsdorf,Julien H. Park,Yoshinao Wada,Stephan Rust,Janine Reunert,Ingrid DuChesne,Marianne Grüneberg,Thorsten Marquardt	2014	23
16	The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation Clinica Chimica Acta ·Julien H. Park,Andrea Zühlsdorf,Yoshinao Wada,Claudia Roll,Stephan Rust,Ingrid Du Chesne,Marianne Grüneberg,Janine Reunert,Thorsten Marquardt	2014	10
17	Patientenklassifikation und Risikoprofilanalysen bei Typ-2-Diabetikern in der Schwerpunktpraxis DMW - Deutsche Medizinische Wochenschrift ·B Lippmann-Grob,R. Bierwirth,Philipp Kron,B Leinhos,Katja Funke,M Huptas,Marianne Grüneberg,K Weich,C Münscher,F Potthoff	2004	6
18	Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samples Acta Paediatrica ·R. Rossi,Sigrid Danzebrink,Katrin Linnenbürger,Dirk Hillebrand,Marianne Grüneberg,V Sablitzky,Thomas Deufel,Kurt Ullrich,Erik Harms	1994	37
19	Disturbance of GABA Metabolism in Pyridoxine-Dependent Seizures Neuropediatrics ·Gerhard Kurlemann,Ralph Ziegler,Marianne Grüneberg,T. Bömelburg,K. J. Ullrich,D. Palm	1992	22
20	A long-range repeat cluster in chromosome 1 of the house mouse, Mus musculus, and its relation to a germline homogeneously staining region Genomics ·L. Purmann,Christoph Plass,Marianne Grüneberg,Heinz Winking,Walther Traut	1992	16

About Marianne Grüneberg

Marianne Grüneberg is a scholar working on Clinical Biochemistry, Biochemistry and Cell Biology, having authored 30 papers that have together received 553 indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (11 papers), Metabolism and Genetic Disorders (7 papers), Amino Acid Enzymes and Metabolism (5 papers), Biomedical Research and Pathophysiology (4 papers), Carbohydrate Chemistry and Synthesis (4 papers), Neonatal Health and Biochemistry (3 papers), Galectins and Cancer Biology (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). The work is most often cited by research in Clinical Biochemistry (97 citations), Biochemistry (38 citations) and Molecular Biology (335 citations). Marianne Grüneberg has collaborated with scholars based in Germany, Japan and Switzerland. Frequent co-authors include Thorsten Marquardt, Janine Reunert, Stephan Rust, Julien H. Park, Saskia Biskup, Manfred Fobker, Yoshinao Wada, Ingrid DuChesne, Yoshiro Wada and Konstanze Hörtnagel. Their work appears in journals such as Brain, Clinica Chimica Acta and Genomics.

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.

Explore authors with similar magnitude of impact