Julia B. Hennermann

4.9k total citations
95 papers, 2.1k citations indexed

About

Julia B. Hennermann is a scholar working on Physiology, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, Julia B. Hennermann has authored 95 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Physiology, 33 papers in Clinical Biochemistry and 32 papers in Molecular Biology. Recurrent topics in Julia B. Hennermann's work include Lysosomal Storage Disorders Research (51 papers), Metabolism and Genetic Disorders (33 papers) and Folate and B Vitamins Research (14 papers). Julia B. Hennermann is often cited by papers focused on Lysosomal Storage Disorders Research (51 papers), Metabolism and Genetic Disorders (33 papers) and Folate and B Vitamins Research (14 papers). Julia B. Hennermann collaborates with scholars based in Germany, United States and Switzerland. Julia B. Hennermann's co-authors include Nenad Blau, Uta Lichter‐Konecki, Ulrich Langenbeck, Barbara Vetter, E. Mönch, Christoph Bührer, Johan L.K. Van Hove, Eugen Mengel, Maja von der Hagen and Gunter Scharer and has published in prestigious journals such as The Lancet, PLoS ONE and Brain.

In The Last Decade

Julia B. Hennermann

90 papers receiving 2.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Julia B. Hennermann Germany	27	1.0k	1.0k	892	368	288	95	2.1k
Can Fıçıcıoğlu United States	23	790 0.8×	890 0.9×	551 0.6×	289 0.8×	295 1.0×	102	1.7k
Maria Alice Donati Italy	31	2.5k 2.4×	1.4k 1.4×	915 1.0×	475 1.3×	319 1.1×	136	3.9k
M. Estela Rubio‐Gozalbo Netherlands	33	1.2k 1.2×	1.6k 1.6×	806 0.9×	454 1.2×	641 2.2×	114	2.8k
G. T. N. Besley United Kingdom	26	948 0.9×	510 0.5×	904 1.0×	254 0.7×	174 0.6×	87	1.9k
Randall A. Heidenreich United States	25	722 0.7×	353 0.4×	798 0.9×	199 0.5×	131 0.5×	46	2.0k
Ivo Barić Croatia	25	1.1k 1.1×	980 1.0×	240 0.3×	503 1.4×	223 0.8×	81	1.8k
Bénédicte Héron France	23	527 0.5×	263 0.3×	554 0.6×	165 0.4×	102 0.4×	65	1.6k
Roy A. Gravel Canada	32	1.8k 1.7×	741 0.7×	535 0.6×	1.4k 3.7×	502 1.7×	69	3.4k
Ronen Spiegel Israel	26	884 0.9×	338 0.3×	314 0.4×	200 0.5×	70 0.2×	97	1.9k
George H. Thomas United States	28	925 0.9×	361 0.4×	411 0.5×	148 0.4×	353 1.2×	55	1.9k

Countries citing papers authored by Julia B. Hennermann

Since Specialization

Citations

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

Fields of papers citing papers by Julia B. Hennermann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia B. Hennermann. 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 Julia B. Hennermann. The network helps show where Julia B. Hennermann may publish in the future.

Co-authorship network of co-authors of Julia B. Hennermann

This figure shows the co-authorship network connecting the top 25 collaborators of Julia B. Hennermann. A scholar is included among the top collaborators of Julia B. Hennermann 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 Julia B. Hennermann. Julia B. Hennermann 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

Mütze, Ulrike, Florian Gleich, Sarah C. Grünert, et al.. (2025). Long-Term Outcomes of Adolescents and Young Adults Identified by Metabolic Newborn Screening. PEDIATRICS. 155(4). 2 indexed citations

Werner, Helene, Markus A. Landolt, Andreas Hahn, et al.. (2024). Living with Pompe disease: results from a qualitative interview study with children and adolescents and their caregivers. Orphanet Journal of Rare Diseases. 19(1). 358–358.

Kampmann, Christoph, Christina Lampe, Christiane M. Wiethoff, et al.. (2024). Natural history of valve disease in patients with mucopolysaccharidosis II and the impact of enzyme replacement therapy. Journal of Inherited Metabolic Disease. 48(1). e12808–e12808.

Schnabel‐Besson, Elena, Sven F. Garbade, Florian Gleich, et al.. (2024). Parental and child's psychosocial and financial burden living with an inherited metabolic disease identified by newborn screening. Journal of Inherited Metabolic Disease. 48(1). e12784–e12784. 4 indexed citations

Guffon, Nathalie, Vassiliki Konstantopoulou, Julia B. Hennermann, et al.. (2023). Long‐term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha‐mannosidosis: A phase 2, open label, multicenter study. Journal of Inherited Metabolic Disease. 46(4). 705–719. 10 indexed citations

Halfmann, Moritz C., U. Joseph Schoepf, Julia B. Hennermann, et al.. (2022). Left atrial strain correlates with severity of cardiac involvement in Anderson-Fabry disease. European Radiology. 33(3). 2039–2051. 15 indexed citations

Cacicedo, Maximiliano L., Beate K. Straub, Jürgen G. Okun, et al.. (2022). mRNA-based therapy proves superior to the standard of care for treating hereditary tyrosinemia 1 in a mouse model. Molecular Therapy — Methods & Clinical Development. 26. 294–308. 11 indexed citations

Gramer, Gwendolyn, Georg F. Hoffmann, & Julia B. Hennermann. (2021). Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening. Molecular Genetics and Metabolism Reports. 27. 100738–100738. 2 indexed citations

Baerwald, Christoph, Martin Schwarz, Frank Rutsch, et al.. (2020). Everyday Life, Dietary Practices, and Health Conditions of Adult PKU Patients: A Multicenter, Cross-Sectional Study. Annals of Nutrition and Metabolism. 76(4). 251–258. 12 indexed citations

10.

Guffon, Nathalie, Anna Tylki‐Szymańska, Lise Borgwardt, et al.. (2019). Recognition of alpha-mannosidosis in paediatric and adult patients: Presentation of a diagnostic algorithm from an international working group. Molecular Genetics and Metabolism. 126(4). 470–474. 23 indexed citations

11.

Kampmann, Christoph, Christina Lampe, Jörg Reinke, et al.. (2016). Heart and Cardiovascular Involvement in Patients with Mucopolysaccharidosis Type IVA (Morquio-A Syndrome). PLoS ONE. 11(9). e0162612–e0162612. 34 indexed citations

12.

Lenders, Malte, Julia B. Hennermann, Christine Kurschat, et al.. (2016). Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease. Orphanet Journal of Rare Diseases. 11(1). 88–88. 36 indexed citations

13.

Hennermann, Julia B., et al.. (2015). Eight-Year Follow-Up of Neuropsychiatric Symptoms and Brain Structural Changes in Fabry Disease. PLoS ONE. 10(9). e0137603–e0137603. 36 indexed citations

14.

Hahn, Andreas, Nesrin Karabul, Dorle Schmidt, et al.. (2014). Outcome of Patients with Classical Infantile Pompe Disease Receiving Enzyme Replacement Therapy in Germany. JIMD Reports. 20. 65–75. 47 indexed citations

15.

Blau, Nenad, Julia B. Hennermann, Ulrich Langenbeck, & Uta Lichter‐Konecki. (2011). Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies. Molecular Genetics and Metabolism. 104. S2–S9. 177 indexed citations

16.

Trefz, Friedrich K., Barbara K. Burton, Nicola Longo, et al.. (2009). Efficacy of Sapropterin Dihydrochloride in Increasing Phenylalanine Tolerance in Children with Phenylketonuria: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study. The Journal of Pediatrics. 154(5). 700–707.e1. 156 indexed citations

17.

Busche, Andreas, Julia B. Hennermann, Friederike Bürger, et al.. (2008). Neonatal manifestation of multiple sulfatase deficiency. European Journal of Pediatrics. 168(8). 969–973. 19 indexed citations

18.

Zavadáková, Petra, Brian Fowler, Terttu Suormala, et al.. (2005). cblEType of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression. Human Mutation. 25(3). 239–247. 33 indexed citations

19.

Hennermann, Julia B., A Loui, Astrid Weber, & E. Mönch. (2004). Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria. Journal of Perinatal Medicine. 32(4). 383–5. 6 indexed citations

20.

Hennermann, Julia B., et al.. (1998). Lipid and lipoprotein profiles in children with familial hypercholesterolaemia: effects of therapy. European Journal of Pediatrics. 157(11). 912–918. 12 indexed citations

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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