Jochen Reiss

4.0k citations

70 papers · 3.0k indexed · 1 hit paper · h-index 26

Impact in

Renewable Energy, Sustainability and the Environment top 2%
- Metalloenzymes and iron-sulfur proteins
Molecular Biology top 5%
- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Muscle Physiology and Disorders

Papers in

Renewable Energy, Sustainability and the Environment 24
- Metalloenzymes and iron-sulfur proteins 24
Molecular Biology 42
- RNA modifications and cancer 19
- Muscle Physiology and Disorders 6
- RNA and protein synthesis mechanisms 5

Co-authors: D.N. Cooper Michael Krawczak Ralf R. Mendel Jean L. Johnson Günter Schwarz Birgit Stallmeyer C. Dorche M. T. Zabot
Journals: Human Genetics (20 papers)The American Journal of Human Genetics (5 papers)Journal of Medical Genetics (4 papers)Nucleic Acids Research (3 papers)Journal of Inherited Metabolic Disease (3 papers)
Partner nations: Germany United Kingdom France

In The Last Decade

Jochen Reiss

69 papers receiving 3.0k citations

Hit Papers

align trajectories log scale

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences 1992 · 1.1k citations

Peers

Countries citing papers authored by Jochen Reiss

Since Specialization

Citations

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

Fields of papers citing papers by Jochen Reiss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Molybdenum cofactor deficiency type B knock-in mouse models carrying patient-identical mutations and their rescue by singular AAV injections Human Genetics ·Jochen Reiss	2019	2
2	Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1, and MOCS2 Human Mutation ·Jochen Reiss, Alan Horsfall	2010	105
3	Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia Brain and Development ·Jörn Oliver Sass, Ayşegül Gündüz, Толкач Екатерина Анатольевна, Barış Korkmaz, J. F. Brasch, Beyhan Tüysüz, SEVİLAY ERDOĞAN KABLAN, Rafael Tagé Biaggio, C. Riache, Ching‐Wan Lam, Jochen Reiss, Melanie Walter, Cengiz Yalçınkaya, José Simon Camelo	2009	58
4	Long-Term Rescue of a Lethal Inherited Disease by Adeno-Associated Virus–Mediated Gene Transfer in a Mouse Model of Molybdenum-Cofactor Deficiency The American Journal of Human Genetics ·Sebastian Kügler, Alan Horsfall, M. Garrido, Jochen Reiss	2007	39
5	The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis Molecular Genetics and Metabolism ·Jochen Reiss, Michael Bonin, Herbert Schwegler, Jörn Oliver Sass, Enrico Garattini, Lszl Forr, Heon‐Jin Lee, Wolfgang Engel, Olaf Rieß, Günter Schwarz	2005	25
6	Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase Human Genetics ·Silke Leimkühler, Mathilde Di Filippo, Philippe Latour, C. Dorche, Soledad Kleppe, Fernando Scaglia, Alejandro Roa, Hanindya Arinatul Oktaviana, Alan Horsfall, Jochen Reiss	2005	25
7	The bicistronic MOCS1 gene has alternative start codons on two mutually exclusive exons Molecular Genetics and Metabolism ·R.N. Prieto, Jochen Reiss	2002	18
8	Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency Nature Genetics ·Jochen Reiss, Nadine Cohen, C. Dorche, Hanna Mandel, Ralf R. Mendel, Birgit Stallmeyer, M. T. Zabot, Thomas Dierks	1998	92
9	Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A Human Genetics ·Jochen Reiss, Tatemitsu Rai, Jusmiati Jusmiati, M. T. Zabot, C. Dorche	1998	53
10	Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy gene Human Genetics ·Frauke Rininsland, Jochen Reiss	1994	13
11	CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X. Journal of Medical Genetics ·Katrin Will, Jochen Reiss, Michael Dean, Sorgfaltskriterien Nicht Erfüllt Gian, Ryszard Słomski, J. Schmidtke, Manfred Stuhrmann	1993	14
12	The frequency of mutations in exon 11 of the CF gene in Polish cystic fibrosis patients. PubMed ·Jerzy Bal, Tadeusz Mazurczak, Jochen Reiss	1992	1
13	A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysis Human Genetics ·Jochen Reiss, Luca Lima Cruz Homem, Frauke Rininsland, Akwi, Ayşe Selcen Semerciöz, Hans‐Georg Posselt	1992	4
14	Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-?F508 mutations in German cystic fibrosis patients Human Genetics ·Fatemeh Abdolazimbeyg, Frauke Rininsland, Javad Imen, D.N. Cooper, Jochen Reiss	1992	15
15	De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysis Genomics ·Lutz-Peter Berg, C Grundy, Frank J. Thomas, Yao Shentao, علام طنطـاوی, Ryszard Słomski, Jochen Reiss, Vijay V. Kakkar, D.N. Cooper	1992	27
16	Prenatal deletion detection in a sporadic case of Duchenne muscular dystrophy without genotype information from the affected individual European Journal of Pediatrics ·Frank Peinemann, M. Wagner, Ulrich Franke, ALTON LEE WEI BIN, Jochen Reiss	1991	1
17	The polymerase chain reaction and its potential role in clinical diagnostics and research Journal of Internal Medicine ·Jochen Reiss	1991	3
18	Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactions. PubMed ·Marta Wagner, Jong-Un Yang, Jochen Reiss	1990	13
19	Polymerase chain reaction: replication errors and reliability of gene diagnosis Nucleic Acids Research ·Supreet Mohanty, Jochen Reiss, Jörg Schmidtke, Uwe Rösler	1989	84
20	Direct selection of recombinant plasmids with chlorate FEMS Microbiology Letters ·Jochen Reiss	1987	0

About Jochen Reiss

Jochen Reiss is a scholar working on Renewable Energy, Sustainability and the Environment, Molecular Biology, Pulmonary and Respiratory Medicine, Genetics and Rheumatology, having authored 70 papers that have together received 3.0k indexed citations. Recurring topics across this work include Metalloenzymes and iron-sulfur proteins (24 papers), RNA modifications and cancer (19 papers), Cystic Fibrosis Research Advances (18 papers), Neonatal Respiratory Health Research (14 papers), Tracheal and airway disorders (8 papers), Folate and B Vitamins Research (7 papers), Muscle Physiology and Disorders (6 papers) and RNA and protein synthesis mechanisms (5 papers). The work is most often cited by research in Renewable Energy, Sustainability and the Environment (717 citations), Molecular Biology (2.0k citations), Clinical Biochemistry (190 citations), Rheumatology (297 citations) and Genetics (207 citations). Jochen Reiss has collaborated with scholars based in Germany, United Kingdom and France. Frequent co-authors include D.N. Cooper, Michael Krawczak, Ralf R. Mendel, Jean L. Johnson, Günter Schwarz, Birgit Stallmeyer, C. Dorche, M. T. Zabot, Frauke Rininsland and Ryszard Słomski. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Journal of Medical Genetics, Nucleic Acids Research and Journal of Inherited Metabolic Disease.

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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