Janine Reunert

2.1k citations

45 papers · 880 indexed · h-index 20

Co-authors: Thorsten Marquardt Stephan Rust Marianne Grüneberg Julien H. Park Manfred Fobker Saskia Biskup Frank Kannenberg Eugen Mengel
Topics: Glycosylation and Glycoproteins Research (16 papers)Lysosomal Storage Disorders Research (11 papers)Carbohydrate Chemistry and Synthesis (10 papers)
Cited by: Clinical Biochemistry Physiology Hematology
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Brain
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 of co-authors of Janine Reunert

This figure shows the co-authorship network connecting the top 25 collaborators of Janine Reunert. A scholar is included among the top collaborators of Janine Reunert 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 Janine Reunert. Janine Reunert 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	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
2	Enteric-Coated Cysteamine Bitartrate in Cystinosis Patients 2023 ·Pharmaceutics ·(unknown),(unknown),Marianne Grüneberg,Chris Ottolenghi,(unknown),(unknown),Janine Reunert,Erik Harms,Thorsten Marquardt	4
3	A comparison of immediate release and delayed release cysteamine in 17 patients with nephropathic cystinosis 2021 ·Orphanet Journal of Rare Diseases ·(unknown),(unknown),Marianne Grüneberg,Chris Ottolenghi,(unknown),Janine Reunert,Erik Harms,Thorsten Marquardt	13
4	Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy—A Case Report 2021 ·Frontiers in Neurology ·(unknown),Janine Reunert,(unknown),Lambert van den Heuvel,Richard J. Rodenburg,(unknown),Stephan Rust,Astrid Jeibmann,Michael Frosch,Thorsten Marquardt	5
5	Application of N-palmitoyl-O-phosphocholineserine for diagnosis and assessment of response to treatment in Niemann-Pick type C disease 2020 ·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,(unknown),Jean E. Schaffer,Daniel Ory,Xuntian Jiang	22
6	Application of a glycinated bile acid biomarker for diagnosis and assessment of response to treatment in Niemann-pick disease type C1 2020 ·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,(unknown),Jean E. Schaffer,Daniel Ory,Xuntian Jiang	11
7	Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG) 2020 ·Orphanet Journal of Rare Diseases ·(unknown),Marianne Grüneberg,Ingrid DuChesne,Janine Reunert,Thorsten Marquardt	11
8	SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation 2020 ·Molecular Genetics and Metabolism Reports ·Thorsten Marquardt,Vladimı́r Bzdúch,(unknown),Stephan Rust,Janine Reunert,Marianne Grüneberg,Julien H. Park,Nico Callewaert,Robin Lachmann,Yoshinao Wada,Thomas Engel	5
9	L-Fucose treatment of FUT8-CDG 2020 ·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	19
10	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
11	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
12	SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapy 2017 ·Genetics in Medicine ·Julien H. Park,(unknown),Manfred Fobker,(unknown),Barbara Fiedler,Janine Reunert,Stephan Rust,Konstantinos Tsiakas,René Santer,Marianne Grüneberg,Thorsten Marquardt	57
13	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
14	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
15	Rapid Diagnosis of 83 Patients with Niemann Pick Type C Disease and Related Cholesterol Transport Disorders by Cholestantriol Screening 2015 ·EBioMedicine ·Janine Reunert,Manfred Fobker,Frank Kannenberg,(unknown),(unknown),(unknown),Stephan Rust,Thorsten Marquardt	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 2015 ·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	36
17	TMEM165 Deficiency: Postnatal Changes in Glycosylation 2015 ·JIMD Reports ·(unknown),Marianne Grüneberg,Janine Reunert,Julien H. Park,Stephan Rust,Chris Mühlhausen,Yoshinao Wada,René Santer,Thorsten Marquardt	23
18	Transferrin variants: Pitfalls in the diagnostics of Congenital disorders of glycosylation 2014 ·Clinical Biochemistry ·(unknown),Julien H. Park,Yoshinao Wada,Stephan Rust,Janine Reunert,Ingrid DuChesne,Marianne Grüneberg,Thorsten Marquardt	23
19	Life with too much polyprenol: polyprenol reductase deficiency 2011 ·Molecular Genetics and Metabolism ·(unknown),Ziqiang Guan,Stephan Rust,Janine Reunert,Boje Müller,(unknown),Klaus Zerres,Sabine Rudnik‐Schöneborn,Nadina Ortiz‐Brüchle,Martin Häusler,(unknown),Ewa Świeżewska,Christian R.H. Raetz,Thorsten Marquardt	39
20	Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih 2009 ·Molecular Genetics and Metabolism ·(unknown),Heymut Omran,(unknown),Jonas Denecke,Janine Reunert,Thorsten Marquardt	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) and Carbohydrate Chemistry and Synthesis (10 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.

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