Julia Vodopiutz

1.5k total citations
28 papers, 520 citations indexed

About

Julia Vodopiutz is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Julia Vodopiutz has authored 28 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Julia Vodopiutz's work include Connective tissue disorders research (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Proteoglycans and glycosaminoglycans research (4 papers). Julia Vodopiutz is often cited by papers focused on Connective tissue disorders research (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Proteoglycans and glycosaminoglycans research (4 papers). Julia Vodopiutz collaborates with scholars based in Austria, United States and Germany. Julia Vodopiutz's co-authors include Andreas Janecke, Thomas Müller, Munis Dündar, Olaf A. Bodamer, Jacques Baenziger, Beat Steinmann, Qi Zhang, Kazuyuki Sugahara, Gerd Utermann and Birgit Krabichler and has published in prestigious journals such as PEDIATRICS, Gut and The American Journal of Human Genetics.

In The Last Decade

Julia Vodopiutz

26 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia Vodopiutz Austria 13 309 241 171 59 49 28 520
Elena Schnabel‐Besson Germany 8 348 1.1× 110 0.5× 69 0.4× 62 1.1× 43 0.9× 17 582
Hagit Baris Feldman Israel 11 131 0.4× 71 0.3× 33 0.2× 45 0.8× 34 0.7× 42 366
Nausheen J. Shervani Japan 10 204 0.7× 166 0.7× 77 0.5× 312 5.3× 48 1.0× 11 548
Nick Giannoukakis United States 8 146 0.5× 129 0.5× 33 0.2× 85 1.4× 55 1.1× 14 362
Kathryn E. Dickerson United States 10 602 1.9× 119 0.5× 41 0.2× 52 0.9× 51 1.0× 23 786
Jonathan A. Cohn United States 8 333 1.1× 166 0.7× 124 0.7× 306 5.2× 29 0.6× 10 1.0k
François‐Xavier Mauvais France 13 121 0.4× 27 0.1× 56 0.3× 74 1.3× 125 2.6× 27 378
Chee-Wai Woon United States 10 452 1.5× 40 0.2× 101 0.6× 172 2.9× 39 0.8× 14 642
Robin Butler United Kingdom 12 350 1.1× 233 1.0× 58 0.3× 37 0.6× 33 0.7× 14 579
Anastasia Fedick United States 12 217 0.7× 139 0.6× 45 0.3× 32 0.5× 30 0.6× 20 426

Countries citing papers authored by Julia Vodopiutz

Since Specialization
Citations

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

Fields of papers citing papers by Julia Vodopiutz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Vodopiutz

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Vodopiutz. A scholar is included among the top collaborators of Julia Vodopiutz 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 Vodopiutz. Julia Vodopiutz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Boero, Silvio, Julia Vodopiutz, Mohamad Maghnie, et al.. (2024). International expert opinion on the considerations for combining vosoritide and limb surgery: a modified delphi study. Orphanet Journal of Rare Diseases. 19(1). 347–347. 1 indexed citations
2.
Vogel, Georg F., Dietmar Rieder, H. Sälzer, et al.. (2024). Kinesin family member 12 ‐related hepatopathy: A generally indolent disorder with elevated gamma‐glutamyl‐transferase activity. Clinical Genetics. 106(3). 224–233.
3.
Vodopiutz, Julia, et al.. (2023). Leri–Weill Dyschondrosteosis Caused by a Leaky Homozygous SHOX Splice-Site Variant. Genes. 14(4). 877–877. 2 indexed citations
4.
Siegert, Sandy, Gabriel T. Mindler, Christof Brücke, et al.. (2021). Expanding the Phenotype of the FAM149B1-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single Family. Genes. 12(11). 1648–1648. 2 indexed citations
5.
Breu, Markus, Petra Trimmel‐Schwahofer, Wolfgang M. Schmidt, et al.. (2021). The relation of etiology based on the 2017 ILAE classification to the effectiveness of the ketogenic diet in drug‐resistant epilepsy in childhood. Epilepsia. 62(11). 2814–2825. 6 indexed citations
6.
Vodopiutz, Julia, et al.. (2021). Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management. Wiener Medizinische Wochenschrift. 171(5-6). 94–101.
7.
Brunner‐Krainz, Michaela, Gérard Cortina, René G. Feichtinger, et al.. (2018). Severe Deoxyguanosine Kinase Deficiency in Austria. Journal of Pediatric Gastroenterology and Nutrition. 68(1). e1–e6. 11 indexed citations
8.
Vodopiutz, Julia, Jan de Laffolie, Victorien M. Wolters, et al.. (2018). SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptase. Human Molecular Genetics. 28(5). 828–841. 24 indexed citations
9.
Vodopiutz, Julia, Maria T. Schmook, Vassiliki Konstantopoulou, et al.. (2014). MED20 mutation associated with infantile basal ganglia degeneration and brain atrophy. European Journal of Pediatrics. 174(1). 113–118. 11 indexed citations
10.
Braunholz, Diana, Ilaria Parenti, Jelena Pozojevic, et al.. (2014). Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics. Human Mutation. 36(1). 26–29. 19 indexed citations
11.
Müller, Thomas, Shuji Mizumoto, Julia Vodopiutz, et al.. (2013). Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers–Danlos syndrome. Human Molecular Genetics. 22(18). 3761–3772. 69 indexed citations
12.
Vodopiutz, Julia, Heinz Zoller, Maximilian Schmid, et al.. (2013). Homozygous SALL1 mutation causes a novel multiple congenital anomaly mental retardation syndrome. Neuropediatrics. 44(S 01). 1 indexed citations
13.
Ritter, Markus, Julia Vodopiutz, Silvia Lechner, et al.. (2012). Coexistence ofKCNV2associated cone dystrophy with supernormal rod electroretinogram andMFRPrelated oculopathy in a Turkish family. British Journal of Ophthalmology. 97(2). 169–173. 3 indexed citations
14.
Morava, Éva, Julia Vodopiutz, Dirk J. Lefeber, et al.. (2012). Defining the Phenotype in Congenital Disorder of Glycosylation Due to ALG1 Mutations. PEDIATRICS. 130(4). e1034–e1039. 26 indexed citations
15.
Vodopiutz, Julia, Heinz Zoller, Aimée L Fenwick, et al.. (2012). Homozygous SALL1 Mutation Causes a Novel Multiple Congenital Anomaly—Mental Retardation Syndrome. The Journal of Pediatrics. 162(3). 612–617. 22 indexed citations
16.
Dündar, Munis, Thomas Müller, Qi Zhang, et al.. (2009). Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome. The American Journal of Human Genetics. 85(6). 873–882. 110 indexed citations
17.
Weber, Benedikt, Anton H. Schwabegger, Julia Vodopiutz, et al.. (2009). Prenatal Diagnosis of Apert Syndrome with Cloverleaf Skull Deformity Using Ultrasound, Fetal Magnetic Resonance Imaging and Genetic Analysis. Fetal Diagnosis and Therapy. 27(1). 51–56. 10 indexed citations
18.
Item, Chike Bellarmine, Ivana Mihalek, Anil Jalan, et al.. (2007). Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III. Molecular Genetics and Metabolism. 91(4). 379–383. 12 indexed citations
19.
Vodopiutz, Julia, et al.. (2007). Severe Speech Delay as the Presenting Symptom of Guanidinoacetate Methyltransferase Deficiency. Journal of Child Neurology. 22(6). 773–774. 12 indexed citations
20.
Vodopiutz, Julia, et al.. (2002). Chest Pain in Hospitalized Patients: Cause-Specific and Gender-Specific Differences. Journal of Women s Health. 11(8). 719–727. 23 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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