Jacques Puechberty
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 32
- Genomic variations and chromosomal abnormalities 24
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genomics and Rare Diseases 4
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- Chromosomal and Genetic Variations 22
- Co-authors
- Franck Pellestor (21 shared papers)Geneviève Lefort (13 shared papers)Thomas Liehr (5 shared papers)Gérard Roizès (7 shared papers)G. Lefort (7 shared papers)P. Sardá (6 shared papers)Vincent Gâtinois (12 shared papers)T. Anahory (3 shared papers)
In The Last Decade
Jacques Puechberty
41 papers receiving 711 citations
Peers
Comparison fields: 5 of 60
- Genetics 458
- Pediatrics, Perinatology and Child Health 221
- Plant Science 311
- Molecular Biology 355
- Developmental Biology 8
Countries citing papers authored by Jacques Puechberty
This map shows the geographic impact of Jacques Puechberty'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 Jacques Puechberty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacques Puechberty more than expected).
Fields of papers citing papers by Jacques Puechberty
This network shows the impact of papers produced by Jacques Puechberty. 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 Jacques Puechberty. The network helps show where Jacques Puechberty may publish in the future.
Co-authors
The 25 scholars most cited alongside Jacques Puechberty, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 127 | |
| 2 | 2014 | 49 | |
| 3 | 2021 | 47 | |
| 4 | 1999 | 40 | |
| 5 | 2011 | 31 | |
| 6 | 2013 | 30 | |
| 7 | 2008 | 29 | |
| 8 | 2006 | 26 | |
| 9 | 2009 | 24 | |
| 10 | 1996 | 24 | |
| 11 | 2017 | 22 | |
| 12 | 1997 | 22 | |
| 13 | 2010 | 22 | |
| 14 | 1999 | 21 | |
| 15 | 2013 | 20 | |
| 16 | 2006 | 19 | |
| 17 | 2012 | 16 | |
| 18 | 2013 | 15 | |
| 19 | 2007 | 15 | |
| 20 | 2008 | 14 |
About Jacques Puechberty
Jacques Puechberty is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 43 papers that have together received 729 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (22 papers), Prenatal Screening and Diagnostics (14 papers), Genomics and Phylogenetic Studies (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Chromatin Dynamics (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (458 citations), Pediatrics, Perinatology and Child Health (221 citations), Plant Science (311 citations), Molecular Biology (355 citations) and Developmental Biology (8 citations). Jacques Puechberty has collaborated with scholars based in France, Germany and Iran. Frequent co-authors include Franck Pellestor, Geneviève Lefort, Thomas Liehr, Gérard Roizès, G. Lefort, P. Sardá, Vincent Gâtinois, T. Anahory, B. Hédon and Pierre Sarda. Their work appears in journals such as European Journal of Human Genetics, Genomics, Human Reproduction, Prenatal Diagnosis and Cytogenetic and Genome Research.
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.