Joëlle Boué

2.8k total citations · 2 hit papers
36 papers, 1.9k citations indexed

About

Joëlle Boué is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Joëlle Boué has authored 36 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Joëlle Boué's work include Prenatal Screening and Diagnostics (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Joëlle Boué is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Joëlle Boué collaborates with scholars based in France, United States and Denmark. Joëlle Boué's co-authors include A Boué, Philippe Lazar, A. Gropp, Jean‐Louis Mandel, I. Oberlé, Valérie Biancalana, P Jalbert, Marie‐Antoinette Voelckel, Dominique Heitz and Christine Kretz and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Nucleic Acids Research.

In The Last Decade

Joëlle Boué

36 papers receiving 1.8k 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.

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation

1991 540 citations François Rousseau, Dominique Heitz et al. New England Journal of Medicine profile →
Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions

1975 467 citations Joëlle Boué, A Boué et al. profile →

Peers

Countries citing papers authored by Joëlle Boué

Since Specialization

Citations

This map shows the geographic impact of Joëlle 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 Joëlle Boué with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joëlle Boué more than expected).

Fields of papers citing papers by Joëlle Boué

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joëlle 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 Joëlle Boué. The network helps show where Joëlle Boué may publish in the future.

Co-authorship network of co-authors of Joëlle Boué

This figure shows the co-authorship network connecting the top 25 collaborators of Joëlle Boué. A scholar is included among the top collaborators of Joëlle 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 Joëlle Boué. Joëlle 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	Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia typeII 1998 ·Human Genetics ·(unknown), (unknown), (unknown), (unknown), A. Fois, (unknown), Maja Di Rocco, Joëlle Boué, J M Kirk, Rosalind Coleman, Gerd Scherer	44
2	Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24 1997 ·American Journal of Medical Genetics ·Vincent des Portes, Nadem Soufir, Alain Carrié, Pierre Billuart, T Bienvenu, Marie Claude Vinet, Chérif Beldjord, G Ponsot, Axel Kahn, Joëlle Boué, Jamel Chelly	29
3	Parental origin and mechanisms of formation of three eases of 12p tetrasomy 1996 ·Clinical Genetics ·C Turleau, Brigitte Simon‐Bouy, (unknown), (unknown), (unknown), Denise Molina‐Gomes, Jean‐Pierre Siffroi, Joëlle Boué	20
4	Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency 1995 ·Human Mutation ·(unknown), (unknown), M C Raux-Demay, (unknown), Joëlle Boué, Brigitte Simon‐Bouy, (unknown), A Boué, Étienne Mornet	62
5	Le syndrome de l'X fragile 1994 ·SHILAP Revista de lepidopterología ·Joëlle Boué	1
6	Molecular analysis of a ring chromosome X in a family with fragile X syndrome 1993 ·Human Genetics ·Étienne Mornet, (unknown), (unknown), Brigitte Simon‐Bouy, Michèle Mathieu, (unknown), (unknown), Éric Leguern, Joëlle Boué, A Boué	4
7	Affected sibs with fragde X syndrome exhibit an age‐dependent decrease in the size of the fragile X full mutation 1993 ·Clinical Genetics ·Étienne Mornet, (unknown), (unknown), Isabel Tejada, (unknown), Joëlle Boué, A Boué	9
8	Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation 1992 ·Obstetrical & Gynecological Survey ·François Rousseau, Dominique Heitz, Valérie Biancalana, (unknown), Christine Kretz, Joëlle Boué, Niels Tommerup, (unknown), C.D. DeLozier-Blanchet, (unknown), (unknown), P Jalbert, Marie‐Antoinette Voelckel, I. Oberlé, Jean‐Louis Mandel	65
9	Direct DNA analysis of fragile X syndrome in Spanish pedigrees 1992 ·American Journal of Medical Genetics ·Isabel Tejada, Étienne Mornet, Valérie Biancalana, I. Oberlé, Joëlle Boué, Jean‐Louis Mandel, A Boué	21
10	First‐trimester diagnosis of hypophosphatasia. Importance of gestational age and of purity of CV samples 1991 ·Prenatal Diagnosis ·Françoise Müller, (unknown), P. Bussière, F. Lewin, Joëlle Boué	8
11	The ΔF508 mutation in mild adult forms of cystic fibrosis (CF) 1991 ·Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, A. Taillandier, Jean‐Louis Serre, Joëlle Boué, A Boué	3
12	Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation breakdown → 1991 ·New England Journal of Medicine ·François Rousseau, Dominique Heitz, Valérie Biancalana, (unknown), Christine Kretz, Joëlle Boué, Niels Tommerup, (unknown), C.D. DeLozier-Blanchet, Marie‐Françoise Croquette, S Gilgenkrantz, P Jalbert, Marie‐Antoinette Voelckel, I. Oberlé, Jean‐Louis Mandel	540
13	Prenatal diagnosis of mucolipidosis type II on first‐trimester amniotic fluid 1990 ·Prenatal Diagnosis ·Livia Poënaru, Christine Mézard, Saïd Akli, Jean‐François Oury, Yves Dumez, Joëlle Boué	6
14	GENETIC DIFFERENCES BETWEEN CYSTIC FIBROSIS WITH AND WITHOUT MECONIUM ILEUS 1989 ·The Lancet ·Brigitte Simon‐Bouy, Jean‐Louis Serre, Étienne Mornet, (unknown), Joëlle Boué, A Boué	5
15	Prenatal Diagnosis in 200 Pregnancies with a 1-in-4 Risk of Cystic Fibrosis 1987 ·Obstetrical & Gynecological Survey ·A Boué, Françoise Müller, C Nézelof, J.F. Oury, (unknown), (unknown), M. C. Aubry, Joëlle Boué	4
16	Human triploidy: Association with partial hydatidiform moles and nonmolar conceptuses 1981 ·Human Pathology ·Aron E. Szulman, Emile Philippe, Joëlle Boué, A Boué	131
17	Aspects génétiques des arrêts précoces du développement 1980 ·annales de biologie animale biochimie biophysique ·A Boué, Joëlle Boué, (unknown)	2
18	Genetic Counselling and Prenatal Diagnosis for Chromosome Anomalies 1976 ·International Journal of Gynecology & Obstetrics ·Joëlle Boué, A Boué	2
19	In vitro cultivation of cells from aneuploid human embryos. Initiation of cell lines and longevity of the cultures 1975 ·In Vitro Cellular & Developmental Biology - Plant ·A Boué, Joëlle Boué, Susan Cure, (unknown), (unknown)	23
20	Outcome of pregnancies following a spontaneous abortion with chromosomal anomalies 1973 ·American Journal of Obstetrics and Gynecology ·Joëlle Boué, A Boué, P Lazăr, Sonia Guéguen	30

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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