J Boué
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
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- Sexual Differentiation and Disorders 7
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- Prenatal Screening and Diagnostics 18
- Co-authors
- A Boué (46 shared papers)I. Oberlé (4 shared papers)Christine Kretz (2 shared papers)Jean‐Louis Mandel (2 shared papers)M. F. Bertheas (1 shared paper)André Hanauer (1 shared paper)F. Rousseau (1 shared paper)Dominique Heitz (1 shared paper)
- Journals
- Prenatal Diagnosis (13 papers)Human Genetics (6 papers)European Journal of Human Genetics (3 papers)Proceedings of the National Academy of Sciences (3 papers)Cytogenetic and Genome Research (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
J Boué
80 papers receiving 2.4k citations
J Boué's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 1.5k
- Cognitive Neuroscience 583
- Molecular Biology 1.4k
- Pediatrics, Perinatology and Child Health 377
- Clinical Biochemistry 112
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 82 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome Hit paper breakdown → | 1991 | 1202 |
| 2 | Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency. | 1991 | 142 |
| 3 | Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes. | 1993 | 111 |
| 4 | 1986 | 60 | |
| 5 | 1982 | 56 | |
| 6 | 1991 | 54 | |
| 7 | 1988 | 50 | |
| 8 | 1985 | 49 | |
| 9 | Growth characteristics of human embryonic cell lines with chromosomal anomalies. | 1974 | 48 |
| 10 | Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk. | 1992 | 45 |
| 11 | 1988 | 44 | |
| 12 | 1975 | 42 | |
| 13 | 1974 | 34 | |
| 14 | 1982 | 29 | |
| 15 | 1985 | 28 | |
| 16 | 1980 | 26 | |
| 17 | 1985 | 26 | |
| 18 | 1975 | 24 | |
| 19 | Chromosomal anomalies in early spontaneous abortion. (Their consequences on early embryogenesis and in vitro growth of embryonic cells). | 1976 | 23 |
| 20 | Characterization of a variant of beta-hexosaminidase: "hexosaminidase Paris". | 1977 | 23 |
About J Boué
J Boué is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Surgery and Pulmonary and Respiratory Medicine, having authored 82 papers that have together received 2.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (18 papers), Metabolism and Genetic Disorders (9 papers), Congenital Anomalies and Fetal Surgery (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Sexual Differentiation and Disorders (7 papers), Cystic Fibrosis Research Advances (7 papers) and Lysosomal Storage Disorders Research (6 papers). The work is most often cited by research in Genetics (1.5k citations), Cognitive Neuroscience (583 citations), Molecular Biology (1.4k citations), Pediatrics, Perinatology and Child Health (377 citations) and Clinical Biochemistry (112 citations). J Boué has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include A Boué, I. Oberlé, Christine Kretz, Jean‐Louis Mandel, M. F. Bertheas, André Hanauer, F. Rousseau, Dominique Heitz, Didier Devys and Françoise Müller. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, European Journal of Human Genetics, Proceedings of the National Academy of Sciences 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.