Janine Reunert

2.1k citations

45 papers · 880 indexed · h-index 20

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 8
Physiology top 10%
- Lysosomal Storage Disorders Research 11
Hematology top 10%
- Autoimmune and Inflammatory Disorders Research 4
Molecular Biology
- Glycosylation and Glycoproteins Research 16
Organic Chemistry top 10%
- Carbohydrate Chemistry and Synthesis 10
Immunology
- Galectins and Cancer Biology 6
Biochemistry
- Amino Acid Enzymes and Metabolism 5
Genetics
- Genetics and Neurodevelopmental Disorders 5

Co-authors: Thorsten Marquardt Stephan Rust Marianne Grüneberg Julien H. Park Manfred Fobker Saskia Biskup Frank Kannenberg Eugen Mengel
Cited by: Clinical Biochemistry Physiology Hematology
Journals: SHILAP Revista de lepidopterología (1 paper)PLoS ONE (1 paper)Brain (1 paper)
Partner nations: Germany Japan Switzerland

In The Last Decade

Janine Reunert

42 papers receiving 876 citations

Peers

Countries citing papers authored by Janine Reunert

Since Specialization

Citations

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

Fields of papers citing papers by Janine Reunert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Janine Reunert, 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 Janine Reunert Line = papers co-authored together Janine Reunert 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	Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy—A Case Report Frontiers in Neurology ·Aziza Miriam Belkheir,Janine Reunert,Christiane Elpers,Lambert van den Heuvel,Richard J. Rodenburg,Anja Seelhöfer,Stephan Rust,Astrid Jeibmann,Michael Frosch,Thorsten Marquardt	2021	5
5	Application of N-palmitoyl-O-phosphocholineserine for diagnosis and assessment of response to treatment in Niemann-Pick type C disease Molecular Genetics and Metabolism ·Rohini Sidhu,Pamela Kell,Dennis J. Dietzen,Nicole Y. Farhat,An Dang,Forbes D. Porter,Elizabeth Berry‐Kravis,Charles H. Vite,Janine Reunert,Thorsten Marquardt,Roberto Giugliani,Charles Marques Lourenço,Olaf A. Bodamer,Raymond Wang,Ellen Plummer,Jean E. Schaffer,Daniel Ory,Xuntian Jiang	2020	22
6	Application of a glycinated bile acid biomarker for diagnosis and assessment of response to treatment in Niemann-pick disease type C1 Molecular Genetics and Metabolism ·Rohini Sidhu,Pamela Kell,Dennis J. Dietzen,Nicole Y. Farhat,An Dang,Forbes D. Porter,Elizabeth Berry‐Kravis,Janine Reunert,Thorsten Marquardt,Roberto Giugliani,Charles Marques Lourenço,Raymond Wang,Nina Movsesyan,Ellen Plummer,Jean E. Schaffer,Daniel Ory,Xuntian Jiang	2020	11
7	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
8	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
9	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
10	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
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	Determination of serum cholestane-3β,5α,6β-triol by gas chromatography–mass spectrometry for identification of Niemann-Pick type C (NPC) disease The Journal of Steroid Biochemistry and Molecular Biology ·Frank Kannenberg,Jerzy–Roch Nofer,Erhard Schulte,Janine Reunert,Thorsten Marquardt,Manfred Fobker	2016	23
15	Rapid Diagnosis of 83 Patients with Niemann Pick Type C Disease and Related Cholesterol Transport Disorders by Cholestantriol Screening EBioMedicine ·Janine Reunert,Manfred Fobker,Frank Kannenberg,Ingrid Du Chesne,Maria Plate,Judith Wellhausen,Stephan Rust,Thorsten Marquardt	2015	53
16	Niemann-Pick Type C-2 Disease: Identification by Analysis of Plasma Cholestane-3β,5α,6β-Triol and Further Insight into the Clinical Phenotype JIMD Reports ·Janine Reunert,Amelie S. Lotz‐Havla,Giulia Polo,Frank Kannenberg,Manfred Fobker,Matthias Griese,Eugen Mengel,Ania C. Muntau,Philipp A. Schnabel,Olaf Sommerburg,Ingo Borggraefe,Andrea Dardis,Alessandro P. Burlina,Marcus Mall,Giovanni Ciana,Bruno Bembi,Alberto Burlina,Thorsten Marquardt	2015	36
17	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
18	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
19	Life with too much polyprenol: polyprenol reductase deficiency Molecular Genetics and Metabolism ·J.E.H. Gründahl,Ziqiang Guan,Stephan Rust,Janine Reunert,Boje Müller,Ingrid Du Chesne,Klaus Zerres,Sabine Rudnik‐Schöneborn,Nadina Ortiz‐Brüchle,Martin Häusler,Joanna Siedlecka,Ewa Świeżewska,Christian R.H. Raetz,Thorsten Marquardt	2011	39
20	Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih Molecular Genetics and Metabolism ·Torsten Stölting,Heymut Omran,Anne Erlekotte,Jonas Denecke,Janine Reunert,Thorsten Marquardt	2009	19

About Janine Reunert

Janine Reunert is a scholar working on Clinical Biochemistry, Biochemistry and Physiology, having authored 45 papers that have together received 880 indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (16 papers), Lysosomal Storage Disorders Research (11 papers), Carbohydrate Chemistry and Synthesis (10 papers), Metabolism and Genetic Disorders (8 papers), Galectins and Cancer Biology (6 papers), Amino Acid Enzymes and Metabolism (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autoimmune and Inflammatory Disorders Research (4 papers). The work is most often cited by research in Clinical Biochemistry (90 citations), Physiology (342 citations) and Hematology (83 citations). Janine Reunert has collaborated with scholars based in Germany, Japan and Switzerland. Frequent co-authors include Thorsten Marquardt, Stephan Rust, Marianne Grüneberg, Julien H. Park, Manfred Fobker, Saskia Biskup, Frank Kannenberg, Eugen Mengel, Charles Marques Lourenço and Peter Groenen. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

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