A Munnich
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Craniofacial Disorders and Treatments
Papers in
-
- Mitochondrial Function and Pathology 4
- Retinal Development and Disorders 3
- Genetics 13
- Genomic variations and chromosomal abnormalities 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Neurogenetic and Muscular Disorders Research 3
- Genomics and Rare Diseases 3
- Co-authors
- Stanislas Lyonnet (13 shared papers)Jacky Bonaventure (2 shared papers)Jean Marie Saudubray (2 shared papers)Laurence Legeai‐Mallet (1 shared paper)Catherine Benoist-Lasselin (1 shared paper)Daniel Rabier (3 shared papers)Jean‐Paul Bonnefont (4 shared papers)M. Brivet (2 shared papers)
- Journals
- Journal of Medical Genetics (7 papers)Human Molecular Genetics (3 papers)Clinical Genetics (3 papers)Journal of Clinical Investigation (2 papers)Bone (1 paper)
- Partner nations
- FranceUnited KingdomNetherlands
In The Last Decade
A Munnich
34 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 75
- Clinical Biochemistry 220
- Genetics 344
- Molecular Biology 671
- Surgery 253
- Ophthalmology 50
Countries citing papers authored by A Munnich
This map shows the geographic impact of A Munnich'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 A Munnich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Munnich more than expected).
Fields of papers citing papers by A Munnich
This network shows the impact of papers produced by A Munnich. 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 A Munnich. The network helps show where A Munnich may publish in the future.
Co-authors
The 25 scholars most cited alongside A Munnich, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 147 | |
| 2 | 1992 | 141 | |
| 3 | 1999 | 131 | |
| 4 | 2003 | 90 | |
| 5 | 1998 | 89 | |
| 6 | 1999 | 78 | |
| 7 | 1999 | 66 | |
| 8 | 1994 | 65 | |
| 9 | 2004 | 64 | |
| 10 | 2006 | 45 | |
| 11 | Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria. | 1991 | 37 |
| 12 | 1997 | 36 | |
| 13 | 2012 | 23 | |
| 14 | Approach to the patient with a fatty acid oxidation disorder. | 1992 | 18 |
| 15 | 1993 | 13 | |
| 16 | Site specific screening for point mutations in ornithine transcarbamylase deficiency. | 1992 | 11 |
| 17 | Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity. | 1990 | 9 |
| 18 | 1991 | 8 | |
| 19 | 1991 | 8 | |
| 20 | [Mutations of RET proto-oncogene in Hirschsprung disease]. | 1994 | 8 |
About A Munnich
A Munnich is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Surgery and Cancer Research, having authored 37 papers that have together received 1.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (10 papers), Congenital gastrointestinal and neural anomalies (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Mitochondrial Function and Pathology (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genomics and Rare Diseases (3 papers) and Retinal Development and Disorders (3 papers). The work is most often cited by research in Clinical Biochemistry (220 citations), Genetics (344 citations), Molecular Biology (671 citations), Surgery (253 citations) and Ophthalmology (50 citations). A Munnich has collaborated with scholars based in France, United Kingdom and Netherlands. Frequent co-authors include Stanislas Lyonnet, Jacky Bonaventure, Jean Marie Saudubray, Laurence Legeai‐Mallet, Catherine Benoist-Lasselin, Daniel Rabier, Jean‐Paul Bonnefont, M. Brivet, F Poggi and Ronald J. A. Wanders. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Clinical Genetics, Journal of Clinical Investigation and Bone.
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.