Daniela Karall

7.7k citations

124 papers · 2.6k indexed · 1 hit paper · h-index 26

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Biochemistry top 1%
- Amino Acid Enzymes and Metabolism

Papers in ⓘ

Clinical Biochemistry 65
- Metabolism and Genetic Disorders 65
Biochemistry 14
- Amino Acid Enzymes and Metabolism 12

Co-authors: Sabine Scholl‐Bürgi (81 shared papers)Edda Haberlandt (27 shared papers)Martina Huemer (12 shared papers)Johannes Häberle (11 shared papers)Marjorie Dixon (3 shared papers)Carlo Dionisi‐Vici (2 shared papers)Anupam Chakrapani (2 shared papers)Vicente Rubio (2 shared papers)
Journals: Journal of Inherited Metabolic Disease (14 papers)Orphanet Journal of Rare Diseases (9 papers)Neuropediatrics (6 papers)Scientific Reports (3 papers)Journal of Breath Research (3 papers)
Partner nations: Austria Germany Switzerland

In The Last Decade

Daniela Karall

114 papers receiving 2.5k citations

Hit Papers

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Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision 2019 · 268 citations

Peers

Countries citing papers authored by Daniela Karall

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Karall

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Daniela Karall, 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 Daniela Karall Line = papers co-authored together Daniela Karall links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 124 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Suggested guidelines for the diagnosis and management of urea cycle disorders Orphanet Journal of Rare Diseases ·Johannes Häberle, Nathalie Boddaert, Alberto Burlina, Anupam Chakrapani, Marjorie Dixon, Martina Huemer, Daniela Karall, Diego Martinelli, Pablo Crespo, René Santer, Aude Servais, Vassili Valayannopoulos, Martin Lindner, Vicente Rubio, Carlo Dionisi‐Vici	2012	399
2	Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision Journal of Inherited Metabolic Disease ·Johannes Häberle, Alberto Burlina, Anupam Chakrapani, Marjorie Dixon, Daniela Karall, Martin Lindner, Hanna Mandel, Diego Martinelli, Guillem Pintos‐Morell, René Santer, Anastasia Skouma, Aude Servais, Galit Tal, Vicente Rubio, Martina Huemer, Carlo Dionisi‐Vici Hit paper breakdown →	2019	268
3	Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision Journal of Inherited Metabolic Disease ·Nikolas Boy, Chris Mühlhausen, Esther M. Maier, Jana Herınger, Birgit Assmann, Peter Burgard, Marjorie Dixon, Sandra Fleissner, Cheryl R. Greenberg, Inga Harting, Georg F. Hoffmann, Daniela Karall, David M. Koeller, Michael Krawinkel, Jürgen G. Okun, Thomas Opladen, Roland Posset, Katja Sahm, Johannes Zschocke, Stefan Kölker, (unknown)	2016	147
4	The enigmatic role of tafazzin in cardiolipin metabolism Biochimica et Biophysica Acta (BBA) - Biomembranes ·Riekelt H. Houtkooper, Marjolein Turkenburg, Bwee Tien Poll‐The, Daniela Karall, Celia Pérez‐Cerdá, Amelia Morrone, Sabrina Malvagia, Ronald J. A. Wanders, Willem Kulik, Frédéric M. Vaz	2009	124
5	Spectrum of combined respiratory chain defects Journal of Inherited Metabolic Disease ·Johannes A. Mayr, Tobias B. Haack, Peter Freisinger, Daniela Karall, Christine Makowski, Johannes Koch, René G. Feichtinger, Franz Zimmermann, Boris Rolinski, Uwe Ahting, Thomas Meitinger, Holger Prokisch, Wolfgang Sperl	2015	76
6	Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy Orphanet Journal of Rare Diseases ·Martina Huemer, Sabine Scholl‐Bürgi, Karine Hadaya, Ilse Kern, Ronny Beer, Klaus Seppi, Brian Fowler, Matthias R. Baumgartner, Daniela Karall	2014	75
7	Prolonged QTc Intervals and Decreased Left Ventricular Contractility in Patients with Propionic Acidemia The Journal of Pediatrics ·Daniela Baumgartner, Sabine Scholl‐Bürgi, Jörn Oliver Sass, Wolfgang Sperl, Ulrich Schweigmann, Jörg-Ingolf Stein, Daniela Karall	2007	65
8	Impact of age at onset and newborn screening on outcome in organic acidurias Journal of Inherited Metabolic Disease ·Jana Herınger, Vassili Valayannopoulos, Allan M. Lund, Frits A. Wijburg, Peter Freisinger, Ivo Barić, Matthias R. Baumgartner, Peter Burgard, Alberto Burlina, Kimberly A. Chapman, Elisenda Cortès i Saladelafont, Daniela Karall, Chris Mühlhausen, Victoria Riches, Manuel Schiff, Jolanta Sykut‐Cegielska, John H. Walter, Jiri Zeman, B. Chabrol, Stefan Kölker	2015	64
9	3-Heptanone as a potential new marker for valproic acid therapy Journal of Breath Research ·Stefanie Erhart, A Amann, Edda Haberlandt, G Edlinger, Angela Schmid, Wojciech Filipiak, Konrad Schwarz, Paweł Mochalski, Kevin Rostásy, Daniela Karall, Sabine Scholl‐Bürgi	2009	59
10	Ketogenic diets in patients with inherited metabolic disorders Journal of Inherited Metabolic Disease ·Sabine Scholl‐Bürgi, Alexander Höller, Karin Pichler, Miriam Michel, Edda Haberlandt, Daniela Karall	2015	47
11	Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD) Orphanet Journal of Rare Diseases ·Daniela Karall, Michaela Brunner‐Krainz, Katharina Kogelnig, Vassiliki Konstantopoulou, Esther M. Maier, Dorothea Möslinger, Barbara Plecko, Wolfgang Sperl, Barbara Volkmar, Sabine Scholl‐Bürgi	2015	43
12	Incidence, disease onset and short-term outcome in urea cycle disorders –cross-border surveillance in Germany, Austria and Switzerland Orphanet Journal of Rare Diseases ·(unknown), Susanne Nettesheim, Stefan Kölker, Daniela Karall, Johannes Häberle, Roland Posset, Georg F. Hoffmann, B. Heinrich, Florian Gleich, Sven F. Garbade	2017	41
13	Effect of valproic acid treatment on body composition, leptin and the soluble leptin receptor in epileptic children Epilepsy Research ·Markus Rauchenzauner, Edda Haberlandt, Sabine Scholl‐Bürgi, Daniela Karall, Elisabeth Schoenherr, T. Tatarczyk, Julia Engl, Markus Laimer, Gerhard Luef, Christoph Ebenbichler	2008	39
14	Predictive validity of attentional functions in differentiating children with and without ADHD: a componential analysis Developmental Medicine & Child Neurology ·Liane Kaufmann, Nikola Zieren, Sibylle Zotter, Daniela Karall, Sabine Scholl‐Bürgi, Edda Haberlandt, Bruno Fimm	2010	38
15	Adrenocorticotropic Hormone versus Pulsatile Dexamethasone in the Treatment of Infantile Epilepsy Syndromes Pediatric Neurology ·Edda Haberlandt, Christine de Weger, S. Baumgartner Sigl, Markus Rauchenzauner, Sabine Scholl‐Bürgi, Kevin Rostásy, Daniela Karall	2009	38
16	Amino Acid Cerebrospinal Fluid/Plasma Ratios in Children: Influence of Age, Gender, and Antiepileptic Medication PEDIATRICS ·Sabine Scholl‐Bürgi, Edda Haberlandt, Peter Heinz‐Erian, Florian Deisenhammer, Ursula Albrecht, S. Baumgartner Sigl, Markus Rauchenzauner, Hanno Ulmer, Daniela Karall	2008	37
17	ALG8-CDG: novel patients and review of the literature Orphanet Journal of Rare Diseases ·Michaela Höck, K. Wegleiter, Elisabeth Ralser, Ursula Kiechl‐Kohlendorfer, Sabine Scholl‐Bürgi, Christine Fauth, Elisabeth Steichen, Karin Pichler, Dirk J. Lefeber, Gert Matthjis, Liesbeth Keldermans, Kathrin Maurer, Johannes Zschocke, Daniela Karall	2015	34
18	A recurrent germline mutation in the PIGA gene causes Simpson‐Golabi‐Behmel syndrome type 2 American Journal of Medical Genetics Part A ·Christine Fauth, Katharina Steindl, Annick Toutain, Sandra A. Farrell, Martina Witsch‐Baumgartner, Daniela Karall, Pascal Joset, Sebastian Böhm, Alessandra Baumer, Oliver Maier, Johannes Zschocke, Rosanna Weksberg, Christian R. Marshall, Anita Rauch	2015	30
19	Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency Journal of Inherited Metabolic Disease ·Martina Huemer, Daniel R. Carvalho, Jaime Moritz Brum, Özlem Ünal, Turgay Coşkun, James D. Weisfeld‐Adams, Nina L. Schrager, Sabine Scholl‐Bürgi, Andrea Schlune, Markus G. Donner, Martin Hersberger, Claudio Gemperle, Brunhilde Riesner, Hanno Ulmer, Johannes Häberle, Daniela Karall	2016	30
20	Amino acid metabolism in patients with propionic acidaemia Journal of Inherited Metabolic Disease ·Sabine Scholl‐Bürgi, Jörn Oliver Sass, Johannes Zschocke, Daniela Karall	2010	29

About Daniela Karall

Daniela Karall is a scholar working on Clinical Biochemistry, Biochemistry, Pediatrics, Perinatology and Child Health, Physiology and Genetics, having authored 124 papers that have together received 2.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (65 papers), Mitochondrial Function and Pathology (29 papers), Diet and metabolism studies (21 papers), Amino Acid Enzymes and Metabolism (12 papers), Neonatal Health and Biochemistry (11 papers), Pharmacological Effects and Toxicity Studies (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Glycogen Storage Diseases and Myoclonus (7 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Biochemistry (364 citations), Pediatrics, Perinatology and Child Health (478 citations), Rheumatology (328 citations) and Physiology (479 citations). Daniela Karall has collaborated with scholars based in Austria, Germany and Switzerland. Frequent co-authors include Sabine Scholl‐Bürgi, Edda Haberlandt, Martina Huemer, Johannes Häberle, Marjorie Dixon, Carlo Dionisi‐Vici, Anupam Chakrapani, Vicente Rubio, Aude Servais and Martin Lindner. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Neuropediatrics, Scientific Reports and Journal of Breath Research.

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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