Geneviève Pierquin
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- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 2
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- Prenatal Screening and Diagnostics 4
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- Congenital heart defects research 3
- Mitochondrial Function and Pathology 2
- RNA regulation and disease 2
- Renal and related cancers 2
- RNA modifications and cancer 2
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- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Léon MutesaVincent BoursNicole Van RegemorterMarc AbramowiczFrédérick LibertAnne LefortAudrey KillianAnna Genin
- Partner nations
- BelgiumUnited StatesFrance
In The Last Decade
Geneviève Pierquin
23 papers receiving 308 citations
Peers
Comparison fields: 5 of 52
- Genetics 173
- Cell Biology 59
- Pediatrics, Perinatology and Child Health 59
- Molecular Biology 188
- Genetics 23
Countries citing papers authored by Geneviève Pierquin
This map shows the geographic impact of Geneviève Pierquin'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 Geneviève Pierquin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Geneviève Pierquin more than expected).
Fields of papers citing papers by Geneviève Pierquin
This network shows the impact of papers produced by Geneviève Pierquin. 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 Geneviève Pierquin. The network helps show where Geneviève Pierquin may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Geneviève Pierquin, 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 | 2016 | 6 | |
| 2 | Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. | 2013 | 6 |
| 3 | IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign | 2012 | 1 |
| 4 | 2012 | 80 | |
| 5 | 2012 | 6 | |
| 6 | 2010 | 18 | |
| 7 | 2008 | 22 | |
| 8 | 2008 | 12 | |
| 9 | 2007 | 5 | |
| 10 | Precocious puberty associated with partial trisomy 18q and monosomy 11q. | 2007 | 3 |
| 11 | 2005 | 48 | |
| 12 | 1995 | 9 | |
| 13 | Familial occurrence of Summitt syndrome or a variant example of Carpenter syndrome? | 1992 | 1 |
| 14 | 1991 | 29 | |
| 15 | 1991 | 4 | |
| 16 | 1989 | 9 | |
| 17 | 1989 | 5 | |
| 18 | 1988 | 15 | |
| 19 | [Supravalvular aortic stenosis. Autosomal dominant form of congenital cardiopathy]. | 1988 | 2 |
| 20 | [Fetal or neonatal autopsy and genetic counseling. Experience of the Human Genetic Service of Liège]. | 1985 | 0 |
About Geneviève Pierquin
Geneviève Pierquin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 24 papers that have together received 318 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (4 papers), Congenital heart defects research (3 papers), Mitochondrial Function and Pathology (2 papers), RNA regulation and disease (2 papers), Renal and related cancers (2 papers), RNA modifications and cancer (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (173 citations), Cell Biology (59 citations) and Pediatrics, Perinatology and Child Health (59 citations). Geneviève Pierquin has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Léon Mutesa, Vincent Bours, Nicole Van Regemorter, Marc Abramowicz, Frédérick Libert, Anne Lefort, Audrey Killian, Anna Genin, Martine Biervliet and Nathalie Van der Aa. Their work appears in journals such as Human Mutation, Clinical Genetics, Human Molecular Genetics, Human Genetics and Prenatal Diagnosis.
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.