Arnold Münnich
Impact in
- Clinical Biochemistry top 0.01%
- Metabolism and Genetic Disorders
- Genetics top 0.05%
- Neurogenetic and Muscular Disorders Research
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Metabolism and Genetic Disorders 151
- Genetics 238
- Genetics and Neurodevelopmental Disorders 59
- Neurogenetic and Muscular Disorders Research 47
- Connective tissue disorders research 42
- Genomic variations and chromosomal abnormalities 40
- Co-authors
- Agnès Rötig (163 shared papers)Pierre Rustin (90 shared papers)Dominique Chrétien (77 shared papers)Stanislas Lyonnet (128 shared papers)Valérie Cormier‐Daire (115 shared papers)Jeanne Amiel (62 shared papers)Martine Le Merrer (42 shared papers)Judith Melki (23 shared papers)
- Journals
- The American Journal of Human Genetics (63 papers)Human Mutation (52 papers)European Journal of Human Genetics (42 papers)Journal of Medical Genetics (36 papers)Nature Genetics (34 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Arnold Münnich
771 papers receiving 53.3k citations
Arnold Münnich's Hit Papers
Peers
Comparison fields: 5 of 181
- Clinical Biochemistry 6.9k
- Genetics 7.0k
- Molecular Biology 33.5k
- Genetics 13.3k
- Cellular and Molecular Neuroscience 4.4k
Countries citing papers authored by Arnold Münnich
This map shows the geographic impact of Arnold Münnich'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 Arnold Münnich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arnold Münnich more than expected).
Fields of papers citing papers by Arnold Münnich
This network shows the impact of papers produced by Arnold Münnich. 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 Arnold Münnich. The network helps show where Arnold Münnich may publish in the future.
Co-authors
The 25 scholars most cited alongside Arnold Münnich, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 787 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and characterization of a spinal muscular atrophy-determining gene Hit paper breakdown → | 1995 | 3348 |
| 2 | Lamin A Truncation in Hutchinson-Gilford Progeria Hit paper breakdown → | 2003 | 1195 |
| 3 | Biochemical and molecular investigations in respiratory chain deficiencies Hit paper breakdown → | 1994 | 1127 |
| 4 | Correlation between severity and SMN protein level in spinal muscular atrophy Hit paper breakdown → | 1997 | 935 |
| 5 | Defective myosin VIIA gene responsible for Usher syndrome type IB Hit paper breakdown → | 1995 | 919 |
| 6 | Hirschsprung disease, associated syndromes and genetics: a review Hit paper breakdown → | 2007 | 880 |
| 7 | Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia Hit paper breakdown → | 1997 | 864 |
| 8 | Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis Hit paper breakdown → | 2011 | 802 |
| 9 | Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia Hit paper breakdown → | 1994 | 777 |
| 10 | Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome Hit paper breakdown → | 2003 | 694 |
| 11 | 2001 | 685 | |
| 12 | Mutations of the RET proto-oncogene in Hirschsprung's disease Hit paper breakdown → | 1994 | 645 |
| 13 | Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency Hit paper breakdown → | 1995 | 623 |
| 14 | 1997 | 554 | |
| 15 | Mitochondrial double-stranded RNA triggers antiviral signalling in humans Hit paper breakdown → | 2018 | 482 |
| 16 | 2007 | 458 | |
| 17 | 2012 | 400 | |
| 18 | 1996 | 373 | |
| 19 | 2007 | 352 | |
| 20 | 2009 | 336 |
About Arnold Münnich
Arnold Münnich is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Genetics and Cell Biology, having authored 787 papers that have together received 55.7k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (185 papers), Metabolism and Genetic Disorders (151 papers), RNA modifications and cancer (70 papers), Genetics and Neurodevelopmental Disorders (59 papers), Neurogenetic and Muscular Disorders Research (47 papers), Connective tissue disorders research (42 papers), ATP Synthase and ATPases Research (41 papers) and Genomic variations and chromosomal abnormalities (40 papers). The work is most often cited by research in Clinical Biochemistry (6.9k citations), Genetics (7.0k citations), Molecular Biology (33.5k citations), Genetics (13.3k citations) and Cellular and Molecular Neuroscience (4.4k citations). Arnold Münnich has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Agnès Rötig, Pierre Rustin, Dominique Chrétien, Stanislas Lyonnet, Valérie Cormier‐Daire, Jeanne Amiel, Martine Le Merrer, Judith Melki, Thomas Bourgeron and Olivier Clermont. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, European Journal of Human Genetics, Journal of Medical Genetics and Nature Genetics.
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.