J Boué
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Papers in
- Surgery 7
- Congenital Anomalies and Fetal Surgery 6
- Pediatric Hepatobiliary Diseases and Treatments 3
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- DNA Repair Mechanisms 2
- Porphyrin Metabolism and Disorders 2
- Co-authors
- A Boué (13 shared papers)I. Oberlé (1 shared paper)Jean‐Louis Mandel (1 shared paper)Valérie Biancalana (1 shared paper)François Rousseau (1 shared paper)Didier Devys (1 shared paper)Dicky Halley (1 shared paper)N.G.J. Jaspers (1 shared paper)
- Journals
- Clinical Genetics (1 paper)Fetal Diagnosis and Therapy (1 paper)The Lancet (1 paper)Journal of Inherited Metabolic Disease (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- FranceNetherlandsSwitzerland
In The Last Decade
J Boué
23 papers receiving 315 citations
Peers
Comparison fields: 5 of 55
- Genetics 160
- Pediatrics, Perinatology and Child Health 85
- Reproductive Medicine 28
- Cognitive Neuroscience 57
- Clinical Biochemistry 18
Countries citing papers authored by J Boué
This map shows the geographic impact of J Boué'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 J Boué with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J Boué more than expected).
Fields of papers citing papers by J Boué
This network shows the impact of papers produced by J Boué. 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 J Boué. The network helps show where J Boué may publish in the future.
Co-authors
The 25 scholars most cited alongside J Boué, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 138 | |
| 2 | 1973 | 72 | |
| 3 | 1979 | 34 | |
| 4 | 1975 | 17 | |
| 5 | 1981 | 14 | |
| 6 | 2009 | 12 | |
| 7 | 1985 | 9 | |
| 8 | 1987 | 6 | |
| 9 | Actions of steroid contraceptives on gametic material. | 1973 | 6 |
| 10 | Etudes chromosomiques et anatomiques des grossesses suivant l'arrêt de contraceptifs stéroïdes | 1973 | 5 |
| 11 | [HLA and molar pregnancies (triploidies, hydatidiform moles and choriocarcinoma). Etiological and epidemiological study]. | 1987 | 5 |
| 12 | [Accidental ultrasonographic disclosure of isolated intra-abdominal fetal hyperechogenicity. Apropos of a series of 87 cases]. | 1992 | 4 |
| 13 | Intestinal dysfunction in CF affected fetuses. Results of 240 prenatal diagnoses based on microvillar enzyme activities. | 1987 | 2 |
| 14 | [Chromosomal and anatomic studies of pregnancies after discontinuation of steroid contraceptives]. | 1973 | 2 |
| 15 | [Fortuitous discovery in echography of an isolated fetal intra-abdominal hyperechogenic mass. 87 cases]. | 1991 | 2 |
| 16 | [Prenatal diagnosis: results of 1530 amniotic taps and prospective study of 1023 cases (author's transl)]. | 1979 | 2 |
| 17 | [Prenatal diagnosis of chromosome abnormalities. Three years of experience]. | 1977 | 1 |
| 18 | [Antenatal diagnosis of structural chromosome anomalies. 226 cases (author's transl)]. | 1981 | 1 |
| 19 | 1988 | 1 | |
| 20 | [Prenatal diagnosis of Fanconi's anemia]. | 1985 | 1 |
About J Boué
J Boué is a scholar working on Surgery, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Clinical Biochemistry, having authored 23 papers that have together received 337 indexed citations. Recurring topics across this work include Congenital Anomalies and Fetal Surgery (6 papers), Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Pediatric Hepatobiliary Diseases and Treatments (3 papers), DNA Repair Mechanisms (2 papers), Metabolism and Genetic Disorders (2 papers), Porphyrin Metabolism and Disorders (2 papers) and Folate and B Vitamins Research (1 paper). The work is most often cited by research in Genetics (160 citations), Pediatrics, Perinatology and Child Health (85 citations), Reproductive Medicine (28 citations), Cognitive Neuroscience (57 citations) and Clinical Biochemistry (18 citations). J Boué has collaborated with scholars based in France, Netherlands and Switzerland. Frequent co-authors include A Boué, I. Oberlé, Jean‐Louis Mandel, Valérie Biancalana, François Rousseau, Didier Devys, Dicky Halley, N.G.J. Jaspers, W. Keijzer and D. Bootsma. Their work appears in journals such as Clinical Genetics, Fetal Diagnosis and Therapy, The Lancet, Journal of Inherited Metabolic Disease and Journal of Medical 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.