I. Oberlé

4.3k total citations · 2 hit papers
37 papers, 3.5k citations indexed

About

I. Oberlé is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, I. Oberlé has authored 37 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 19 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in I. Oberlé's work include Genetics and Neurodevelopmental Disorders (27 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). I. Oberlé is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). I. Oberlé collaborates with scholars based in France, United States and Italy. I. Oberlé's co-authors include Jean‐Louis Mandel, Dominique Heitz, Christine Kretz, Didier Devys, J Boué, André Hanauer, M. F. Bertheas, F. Rousseau, Valérie Biancalana and Giovanna Camerino and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

I. Oberlé

36 papers receiving 3.4k 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, Dominique Heitz et al. profile →
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 →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
I. Oberlé France	25	2.8k	2.2k	1.3k	294	209	37	3.5k
Francesca Mari Italy	34	2.2k 0.8×	2.2k 1.0×	785 0.6×	143 0.5×	239 1.1×	103	3.8k
Ilaria Meloni Italy	29	1.7k 0.6×	1.3k 0.6×	759 0.6×	104 0.4×	91 0.4×	60	2.4k
Francesca Ariani Italy	29	1.6k 0.6×	1.3k 0.6×	581 0.4×	106 0.4×	110 0.5×	70	2.4k
J Boué France	22	1.5k 0.6×	1.4k 0.6×	583 0.4×	224 0.8×	42 0.2×	82	2.6k
Christophe Philippe France	30	1.6k 0.6×	1.5k 0.7×	309 0.2×	135 0.5×	285 1.4×	77	2.7k
Ilaria Longo Italy	24	1.6k 0.6×	1.3k 0.6×	756 0.6×	70 0.2×	115 0.6×	41	2.3k
Ági K. Gedeon Australia	30	2.0k 0.7×	2.5k 1.1×	512 0.4×	404 1.4×	26 0.1×	53	3.5k
Sylvain Briault France	23	1.6k 0.6×	1.8k 0.8×	610 0.5×	426 1.4×	30 0.1×	64	3.1k
Tiziano Pramparo United States	27	1.2k 0.4×	1.7k 0.8×	503 0.4×	173 0.6×	43 0.2×	50	2.7k
Heather E. McDermid Canada	29	2.0k 0.7×	2.1k 1.0×	333 0.3×	177 0.6×	42 0.2×	64	3.3k

Countries citing papers authored by I. Oberlé

Since Specialization

Citations

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

Fields of papers citing papers by I. Oberlé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Oberlé

This figure shows the co-authorship network connecting the top 25 collaborators of I. Oberlé. A scholar is included among the top collaborators of I. Oberlé 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 I. Oberlé. I. Oberlé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Devys, Didier, Valérie Biancalana, François Rousseau, et al.. (1992). Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development. American Journal of Medical Genetics. 43(1-2). 208–216. 139 indexed citations

Rousseau, François, Dominique Heitz, Valérie Biancalana, I. Oberlé, & Jean‐Louis Mandel. (1992). On some technical aspects of direct DNA diagnosis of the fragile X syndrome. American Journal of Medical Genetics. 43(1-2). 197–207. 60 indexed citations

Malmgren, Helena, Karl‐Henrik Gustavson, E Seemanová, et al.. (1992). Methylation and mutation patterns in the fragile X syndrome. American Journal of Medical Genetics. 43(1-2). 268–278. 29 indexed citations

Oberlé, I., J Boué, M. F. Croquette, et al.. (1992). 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. American Journal of Medical Genetics. 43(1-2). 224–231. 16 indexed citations

Rousseau, François, Dominique Heitz, Valérie Biancalana, et al.. (1992). Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation. Obstetrical & Gynecological Survey. 47(5). 306–308. 65 indexed citations

Tejada, Isabel, Étienne Mornet, Valérie Biancalana, et al.. (1992). Direct DNA analysis of fragile X syndrome in Spanish pedigrees. American Journal of Medical Genetics. 43(1-2). 282–290. 21 indexed citations

Malmgren, Helena, Karl‐Henrik Gustavson, E Seemanová, et al.. (1992). METHYLATION AND MUTATION PATTERNS IN THE FRAGILE X SYNDROME. Pediatric Research. 32(5). 621–621. 2 indexed citations

Richards, Brenda, et al.. (1991). Rapid PCR analysis of the St14 (DXS52) VNTR. Nucleic Acids Research. 19(8). 1944–1944. 71 indexed citations

Siniscalco, M., I. Oberlé, Paola Melis, et al.. (1991). Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. American Journal of Medical Genetics. 38(2-3). 357–362. 14 indexed citations

10.

Oberlé, I., Anne Vincent, François Rousseau, et al.. (1991). New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98‐FRAXA Interval. American Journal of Medical Genetics. 38(2-3). 336–342. 12 indexed citations

11.

Vincent, Anne, et al.. (1991). Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis. Nature. 349(6310). 624–626. 179 indexed citations

12.

Suthers, G K, I. Oberlé, J.K. Nancarrow, et al.. (1991). Genetic mapping of new RFLPs at Xq27–q28. Genomics. 9(1). 37–43. 35 indexed citations

13.

Rousseau, François, Dominique Heitz, Valérie Biancalana, et al.. (1991). Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation. New England Journal of Medicine. 325(24). 1673–1681. 540 indexed citations breakdown →

14.

Feil, Robert, Giuseppe Palmieri, Michele D’Urso, et al.. (1990). Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.. Europe PMC (PubMed Central). 46(4). 720–8. 25 indexed citations

15.

Guern, E. Le, P. Couillin, I. Oberlé, N. Ravisé, & J Boué. (1990). More precise localization of the gene for Hunter syndrome. Genomics. 7(3). 358–362. 16 indexed citations

16.

Vincent, Anne, Niklas Dahl, I. Oberlé, et al.. (1989). The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus. Genomics. 5(4). 797–801. 19 indexed citations

17.

Guioli, Silvana, Benoı̂t Arveiler, Barbara Bardoni, et al.. (1989). Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia. Human Genetics. 84(1). 19–21. 49 indexed citations

18.

Voelckel, Marie‐Antoinette, N. Philip, I. Oberlé, et al.. (1989). Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation. Human Genetics. 81(4). 353–357. 25 indexed citations

19.

Heilig, Roland, I. Oberlé, Benoı̂t Arveiler, et al.. (1988). Improved DNA markers for efficient analysis of fragile X families. American Journal of Medical Genetics. 30(1-2). 543–550. 35 indexed citations

20.

Oberlé, I., et al.. (1986). From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.. PubMed. 8. 51–89. 3 indexed citations

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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