Wulf Röschinger

2.9k citations

48 papers · 1.6k indexed · h-index 21

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Genetics top 5%
- Neurogenetic and Muscular Disorders Research

Papers in

Clinical Biochemistry 31
- Metabolism and Genetic Disorders 31
Biochemistry 7
- Amino Acid Enzymes and Metabolism 6

Co-authors: Adelbert A. Roscher Ania C. Muntau Bernhard Olgemöller Ralph Fingerhut Uta Nennstiel Federica Deodato Carlo Dionisi‐Vici Bridget Wilcken
Journals: Molecular Genetics and Metabolism (4 papers)International Journal of Neonatal Screening (3 papers)Journal of Inherited Metabolic Disease (3 papers)Clinical Chemistry (3 papers)Clinica Chimica Acta (3 papers)
Partner nations: Germany Switzerland United States

In The Last Decade

Wulf Röschinger

45 papers receiving 1.6k citations

Peers

Countries citing papers authored by Wulf Röschinger

Since Specialization

Citations

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

Fields of papers citing papers by Wulf Röschinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Wulf Röschinger, 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 Wulf Röschinger Line = papers co-authored together Wulf Röschinger 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	Vitamin B12 Deficiency Newborn Screening PEDIATRICS ·Ulrike Mütze, Florian Gleich, Dorothea Haas, Michael S. Urschitz, Wulf Röschinger, Nils Janzen, Georg F. Hoffmann, Sven F. Garbade, Steffen Syrbe, Stefan Kölker	2024	2
2	Single-centre prospective evaluation of the first 5 years of cystic fibrosis newborn screening in Germany ERJ Open Research ·Shao Zhuze, 顾明, M. Elizabeth Foster, Wulf Röschinger, Florian Gothe, L. V. Eremeeva, Maria Feilcke, Carolin Kröner, Tianyu Zhu, Alejandra Juana Torres Pérez, Elias Seidl, Matthias Griese, Matthias Kappler	2024	0
3	A Modular Genetic Approach to Newborn Screening from Spinal Muscular Atrophy to Sickle Cell Disease—Results from Six Years of Genetic Newborn Screening Genes ·H. Jesse Smith, Ludwig Czibere, Siegfried Burggraf, Clare Norris, Esther M. Maier, Wulf Röschinger, Marc Becker, Jürgen Durner	2024	4
4	Newborn screening for aromatic l-amino acid decarboxylase deficiency – Strategies, results, and implication for prevalence calculations Molecular Genetics and Metabolism ·孝美山本, Jürgen G. Okun, Dirk Kohlmüller, Georgi Manukjan, Licenia Córdoba Oñate, Jürgen Durner, Nadya Clarrisha Sompotan, Friederike Hörster, Ulrike Mütze, Patrik Feyh, Georg F. Hoffmann, Wulf Röschinger, Nils Janzen, Thomas Opladen	2024	3
5	Quality considerations and major pitfalls for high throughput DNA-based newborn screening for severe combined immunodeficiency and spinal muscular atrophy PLoS ONE ·H. Jesse Smith, Ludwig Czibere, Siegfried Burggraf, Olfert Landt, Esther M. Maier, Wulf Röschinger, Michael H. Albert, Licenia Córdoba Oñate, Nils Janzen, Marc Becker, Jürgen Durner	2024	1
6	Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria Nutrients ·Elena Schnabel‐Besson, Stefan Kölker, Florian Gleich, Patrik Feyh, Friederike Hörster, Dorothea Haas, Junmin Fang‐Hoffmann, Marina Morath, Gwendolyn Gramer, Wulf Röschinger, Sven F. Garbade, Georg F. Hoffmann, Jürgen G. Okun, Ulrike Mütze	2023	15
7	Neugeborenenscreeningprogramm für die spinale Muskelatrophie Der Nervenarzt ·Heike Kölbel, Katharina Vill, Oliver Schwartz, Astrid Blaschek, Uta Nennstiel, Ulrike Schara‐Schmidt, Georg F. Hoffmann, Dieter Gläser, Wulf Röschinger, Günther Bernert, Andrea Klein, Wolfgang Müller‐Felber	2021	2
8	Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening – Opportunity or Burden? Journal of Neuromuscular Diseases ·Wolfgang Müller‐Felber, Katharina Vill, Oliver Schwartz, Dieter Gläser, Uta Nennstiel, Brunhilde Wirth, Siegfried Burggraf, Wulf Röschinger, Marc Becker, Jürgen Durner, Katja Eggermann, Christine Müller, Iris Hannibal, B. Olgemöller, Ulrike Schara, Astrid Blaschek, Heike Kölbel	2020	42
9	Diagnostic Challenges Using a 2-Tier Strategy for Methylmalonic Acidurias: Data from 1.2 Million Dried Blood Spots Annals of Nutrition and Metabolism ·Ben-Hur Albuquerque Silva, Wulf Röschinger, Holger Blessing, Amelie S. Lotz‐Havla, 孙科全, Esther M. Maier	2020	10
10	One Year of Newborn Screening for SMA – Results of a German Pilot Project Journal of Neuromuscular Diseases ·Katharina Vill, Heike Kölbel, Oliver Schwartz, Astrid Blaschek, Bernhard Olgemöller, Erik Harms, Siegfried Burggraf, Wulf Röschinger, Jürgen Durner, Dieter Gläser, Uta Nennstiel, Brunhilde Wirth, Ulrike Schara, Pooja S Hegde, Marc Becker, Katharina Hohenfellner, Wolfgang Müller‐Felber	2019	108
11	Fatal pitfalls in newborn screening for mitochondrial trifunctional protein (MTP)/long-chain 3-Hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency Orphanet Journal of Rare Diseases ·Amelie S. Lotz‐Havla, Wulf Röschinger, 孙科全, Ayvazli Aykhan Nizami, Daniela Karall, Vassiliki Konstantopoulou, Saskia B. Wortmann, Esther M. Maier	2018	18
12	In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranes Journal of Lipid Research ·Regina Ensenauer, Ralph Fingerhut, Sonja C. Schriever, Barbara Fink, Marc Becker, 谢柠, Philipp Pagel, A. Kirschner, Torsten Dame, Bernhard Olgemöller, Wulf Röschinger, Adelbert A. Roscher	2012	13
13	2-Methylbutyryl-coenzyme A dehydrogenase deficiency: Functional and molecular studies on a defect in isoleucine catabolism Molecular Genetics and Metabolism ·Jörn Oliver Sass, Regina Ensenauer, Wulf Röschinger, K. Fleury, Ulrike Steuerwald, Vamsi N.K. Mypati, Katharina Engel, Johannes Häberle, Brage Storstein Andresen, André Mégarbané, W. Lehnert, Johannes Zschocke	2007	35
14	Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase Biochemical and Biophysical Research Communications ·Sonja C. Stadler, Ying Chen, Stephan Meier, Peter Mayerhofer, Johannes M. Herrmann, Katja Anslinger, Adelbert A. Roscher, Wulf Röschinger, Andreas Holzinger	2005	7
15	Population spectrum ofACADMgenotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency Human Mutation ·Esther M. Maier, Bernhard Liebl, Wulf Röschinger, Uta Nennstiel, Ralph Fingerhut, Bernhard Olgemöller, Ulrich Busch, Nils Krone, Rüdiger von Kries, Adelbert A. Roscher	2005	92
16	T-cell-depleted peripheral blood stem cell transplantation for α-mannosidosis Bone Marrow Transplantation ·Michael H. Albert, Friedhelm R. Schuster, Christina Peters, Sandra Schulze, B. F. Pontz, Ania C. Muntau, Wulf Röschinger, Daniel Stachel, 梁灿兴, R. Haas, Irene Schmid	2003	12
17	Characteristics of l-ornithine: 2-oxoacid aminotransferase and potential prenatal diagnosis of gyrate atrophy of the choroid and retina by first trimester chorionic villus sampling Clinica Chimica Acta ·Wulf Röschinger, W. Endres, Yoon S. Shin	2000	0
18	Modellprojekt zur Neuordnung des Neugeborenen-Screenings in Bayern: Konzeption und erste Ergebnisse Das Gesundheitswesen ·Bernhard Liebl, Ralph Fingerhut, Wulf Röschinger, Ania C. Muntau, Ina Knerr, B. Olgemöller, Andreas Zapf, A. Roscher	2000	13
19	Dorfman-Chanarin-Syndrom - Eine Neutrallipidspeicherkrankheit Der Hautarzt ·Andreas Wollenberg, Martin Schaller, Wulf Röschinger, Carl Georg Schirren, Hans Wolff	1997	8
20	3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylase Clinica Chimica Acta ·Wulf Röschinger, David S. Millington, Douglas A. Gage, Aa Vanheuzen, Takeo Iwamoto, Shoji Yano, Seymour Packman, Denise Simoneaux, Susan A. Berry, Lawrence Sweetman	1995	25

About Wulf Röschinger

Wulf Röschinger is a scholar working on Clinical Biochemistry, Biochemistry, Genetics, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 48 papers that have together received 1.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (31 papers), Mitochondrial Function and Pathology (14 papers), Neonatal Health and Biochemistry (11 papers), Folate and B Vitamins Research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers), Diet and metabolism studies (8 papers), Biochemical and Molecular Research (7 papers) and Amino Acid Enzymes and Metabolism (6 papers). The work is most often cited by research in Clinical Biochemistry (955 citations), Genetics (276 citations), Pediatrics, Perinatology and Child Health (375 citations), Biochemistry (135 citations) and Rheumatology (250 citations). Wulf Röschinger has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Adelbert A. Roscher, Ania C. Muntau, Bernhard Olgemöller, Ralph Fingerhut, Uta Nennstiel, Federica Deodato, Carlo Dionisi‐Vici, Bridget Wilcken, William J. Rhead and Hans Demmelmair. Their work appears in journals such as Molecular Genetics and Metabolism, International Journal of Neonatal Screening, Journal of Inherited Metabolic Disease, Clinical Chemistry and Clinica Chimica Acta.

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