J Boué

3.4k total citations · 1 hit paper
82 papers, 2.6k citations indexed

About

J Boué is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, J Boué has authored 82 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 23 papers in Pediatrics, Perinatology and Child Health and 21 papers in Genetics. Recurrent topics in J Boué's work include Prenatal Screening and Diagnostics (18 papers), Metabolism and Genetic Disorders (9 papers) and Congenital Anomalies and Fetal Surgery (9 papers). J Boué is often cited by papers focused on Prenatal Screening and Diagnostics (18 papers), Metabolism and Genetic Disorders (9 papers) and Congenital Anomalies and Fetal Surgery (9 papers). J Boué collaborates with scholars based in France, United States and United Kingdom. J Boué's co-authors include A Boué, Christine Kretz, I. Oberlé, Jean‐Louis Mandel, M. F. Bertheas, André Hanauer, Didier Devys, F. Rousseau, Dominique Heitz and Françoise Müller and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

J Boué

80 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

1991 1.2k citations I. Oberlé, J Boué et al. profile →

Peers

Countries citing papers authored by J Boué

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of J Boué

This figure shows the co-authorship network connecting the top 25 collaborators of J Boué. A scholar is included among the top collaborators of J Boué based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J Boué. J Boué is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	[Blood groups ABO A1 A2 BO, Rh, MN and P in Russians]. 2002 ·PubMed ·(unknown), J Moullec, (unknown), J Boué	0
2	Transition from Normal toPremutated Alleles inFragile X Syndrome Resultsfrom a Multistep Process 1994 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Mladen Jokić, (unknown), A. Taillandier, Fran Thomas, Brigitte Simon‐Bouy, J Boué, J.L. Serre, (unknown), (unknown)	8
3	General Cystic Fibrosis Mutations Are Usually Missense Mutations Affecting Two Specific Protein Domains and Associated with a Specific RFLP Marker Haplotype 1993 ·European Journal of Human Genetics ·J.L. Serre, (unknown), Brigitte Simon‐Bouy, J Boué, A Boué	2
4	Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR‐1 CpG Island, and no clear phenotypic association 1992 ·American Journal of Medical Genetics ·I. Oberlé, J Boué, M. F. Croquette, Marie‐Antoinette Voelckel, Marie‐Geneviève Mattéi, Jean‐Louis Mandel	16
5	Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk. 1992 ·PubMed ·M. T. Vanier, Claire Rodriguez‐Lafrasse, Robert Rousson, (unknown), J Boué, Agnès Choiset, (unknown), (unknown), (unknown), P. G. Pentchev	45
6	Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients 1991 ·Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, A. Taillandier, J Boué, A Boué	7
7	Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected children 1991 ·Prenatal Diagnosis ·J Boué, Françoise Müller, Brigitte Simon‐Bouy, Céline Faure, A Boué	14
8	Nearly 80% of cystic fibrosis heterozygotes and 64% of couples at risk may be detected through a unique screening of four mutations by ASO reverse dot blot 1991 ·Genomics ·J.L. Serre, A. Taillandier, Étienne Mornet, Brigitte Simon‐Bouy, J Boué, A Boué	6
9	More precise localization of the gene for Hunter syndrome 1990 ·Genomics ·E. Le Guern, P. Couillin, I. Oberlé, N. Ravisé, J Boué	16
10	Glycine/serine ratio and the prenatal diagnosis of non‐ketotic hyperglycinaemia 1990 ·Prenatal Diagnosis ·P Parvy, Daniel Rabier, J Boué, J. M. Saudubray, P Kamoun	2
11	The cystic fibrosis ΔF508 mutation in the French population 1990 ·Human Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, (unknown), J Boué, A Boué	6
12	Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development 1988 ·Prenatal Diagnosis ·Françoise Müller, J.-F. Oury, Yves Dumez, J Boué, A Boué	50
13	A variant of mucolipidosis 1988 ·European Journal of Pediatrics ·Livia Poënaru, L. Castelnau, Franca Tomé, J Boué, P Maroteaux	4
14	Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia by Simultaneous Radioimmunoassay of 21-Deoxycortisol and 17-Hydroxyprogesterone in Amniotic Fluid 1988 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Jean Fiet, P. Couillin, M C Raux-Demay, (unknown), Hervé Galons, Jean‐Marie Villette, J Boué, C Dreux	19
15	Prenatal diagnosis of propionic acidemia in chorionic villi by direct assay of propionyl CoA carboxylase 1988 ·Prenatal Diagnosis ·B. Chadefaux, (unknown), Daniel Rabier, F. Rocchiccioli, J Boué, J.-F. Oury, P. Kamoun	9
16	Interest of Biology in the Management of Pregnancies where a Fetal Malformation Has Been Detected by Ultrasonography 1988 ·Fetal Diagnosis and Therapy ·A Boué, Françoise Müller, (unknown), J Boué	13
17	[Oocyte meiosis in a trisomy 18 fetus. Behavior of the supernumerary chromosome and identification of the 18 bivalent]. 1978 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·(unknown), M. Devictor, J Boué, (unknown), A Boué, (unknown)	5
18	The meiotic behavior of triploidy in a human 69,XXX fetus 1978 ·Cytogenetic and Genome Research ·J. M. Luciani, M. Devictor, J Boué, Mathias Freund, (unknown)	2
19	[Pericentric inversions and reproductive loss]. 1975 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·J Boué, (unknown), (unknown), Christopher J. Leonard	1
20	[Development and retention durations of 716 zygotes, products of precocious spontaneous abortions]. 1971 ·PubMed ·J Boué, A Boué, P Lazăr, (unknown)	2

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.

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