Nada Houcinat
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Metabolism and Genetic Disorders
Papers in
- Genetics 5
- Genetics and Neurodevelopmental Disorders 3
- Connective tissue disorders research 2
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
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- RNA Research and Splicing 1
- Metabolomics and Mass Spectrometry Studies 1
- Co-authors
- Sébastien Moutton (3 shared papers)Christophe Philippe (3 shared papers)Christian Combe (1 shared paper)Jérôme Toutain (2 shared papers)Laurence Faivre (3 shared papers)Brigitte Llanas (1 shared paper)Mirna Assoum (2 shared papers)Ange‐Line Bruel (3 shared papers)
- Journals
- Human Mutation (1 paper)Clinical Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)European Journal of Human Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- FranceMartiniqueUnited States
In The Last Decade
Nada Houcinat
6 papers receiving 85 citations
Peers
Comparison fields: 5 of 31
- Genetics 70
- Clinical Biochemistry 16
- Pediatrics, Perinatology and Child Health 16
- Biochemistry 5
- Cancer Research 10
Countries citing papers authored by Nada Houcinat
This map shows the geographic impact of Nada Houcinat'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 Nada Houcinat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nada Houcinat more than expected).
Fields of papers citing papers by Nada Houcinat
This network shows the impact of papers produced by Nada Houcinat. 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 Nada Houcinat. The network helps show where Nada Houcinat may publish in the future.
Co-authors
The 25 scholars most cited alongside Nada Houcinat, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 39 | |
| 2 | 2015 | 21 | |
| 3 | 2018 | 17 | |
| 4 | 2017 | 11 | |
| 5 | 2019 | 7 | |
| 6 | 2017 | 1 |
About Nada Houcinat
Nada Houcinat is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Infectious Diseases, having authored 6 papers that have together received 96 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Connective tissue disorders research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Metabolism and Genetic Disorders (1 paper), Fetal and Pediatric Neurological Disorders (1 paper), RNA Research and Splicing (1 paper), Genomics and Rare Diseases (1 paper) and Metabolomics and Mass Spectrometry Studies (1 paper). The work is most often cited by research in Genetics (70 citations), Clinical Biochemistry (16 citations), Pediatrics, Perinatology and Child Health (16 citations), Biochemistry (5 citations) and Cancer Research (10 citations). Nada Houcinat has collaborated with scholars based in France, Martinique and United States. Frequent co-authors include Sébastien Moutton, Christophe Philippe, Christian Combe, Jérôme Toutain, Laurence Faivre, Brigitte Llanas, Mirna Assoum, Ange‐Line Bruel, Antonio Vitobello and Yannis Duffourd. Their work appears in journals such as Human Mutation, Clinical Genetics, Journal of Inherited Metabolic Disease, European Journal of Human Genetics and American Journal of Medical Genetics Part A.
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.