Aziza Lebbar

1.1k total citations
22 papers, 321 citations indexed

About

Aziza Lebbar is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Aziza Lebbar has authored 22 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Aziza Lebbar's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (7 papers). Aziza Lebbar is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (11 papers) and Chromosomal and Genetic Variations (7 papers). Aziza Lebbar collaborates with scholars based in France, Switzerland and Romania. Aziza Lebbar's co-authors include J L Chaussain, Jacques Barbet, Louise Telvi, Jean‐Michel Dupont, Françoise Baverel, Dominique Le Tessier, Géraldine Viot, G. Grangé, F. Lewin and Benjamin L. Morris and has published in prestigious journals such as PEDIATRICS, Psychiatry Research and American Journal of Clinical Pathology.

In The Last Decade

Aziza Lebbar

21 papers receiving 282 citations

Peers

Aziza Lebbar

GENET

PPCH

Capucine Hyon France

M. Crocker United Kingdom

Alaa K. Kamel Egypt

Regine Schubert Germany

Paula R. Martens United States

Florence Amblard France

Geneviève Lefort France

Ingelise Sillesen Denmark

J Boué France

Prochi F. Madon India

Capucine Hyon France

Aziza Lebbar

262 ×1.0

GENET

210 ×1.3

98 ×1.0

PPCH

47 ×0.8

89 ×2.3

Citations per year, relative to Aziza Lebbar Aziza Lebbar (= 1×) peers Capucine Hyon

Countries citing papers authored by Aziza Lebbar

Since Specialization

Citations

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

Fields of papers citing papers by Aziza Lebbar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aziza Lebbar

This figure shows the co-authorship network connecting the top 25 collaborators of Aziza Lebbar. A scholar is included among the top collaborators of Aziza Lebbar 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 Aziza Lebbar. Aziza Lebbar 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

Clément, Arthur, et al.. (2022). A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221). Genes. 14(1). 81–81.

Bourthoumieu, Sylvie, Cécile Laroche, Aziza Lebbar, Jean‐Michel Dupont, & Catherine Yardin. (2014). aCGH may be useful in Case of Dominant Disorders Known to be Caused by Gene Mutations: Two Case Reports. Journal of Molecular and Genetic Medicine. 8(2). 1–2. 1 indexed citations

Khattabi, Laïla El, Laurence Cuisset, Vassilis Tsatsaris, et al.. (2014). Neonatal Silver-Russell Syndrome With Maternal Uniparental Heterodisomy, Trisomy 7 Mosaicism, and Dysplasia of the Cerebellum. American Journal of Clinical Pathology. 142(2). 248–253. 11 indexed citations

Lebbar, Aziza, et al.. (2014). Unusual isochromosome 5p marker chromosome. American Journal of Medical Genetics Part A. 167(2). 455–459. 3 indexed citations

Budișteanu, Magdalena, Sorina Mihaela Papuc, Jean‐Michel Dupont, et al.. (2012). Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture. Psychiatry Research. 197(3). 356–357. 1 indexed citations

Cuisset, Laurence, Vassilis Tsatsaris, Julia Tantau, et al.. (2012). First reported case of interstitial 15 q15.3‐q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur. American Journal of Medical Genetics Part A. 158A(3). 617–621. 1 indexed citations

Morris, Benjamin L., Sylvie Bourthoumieu, Cécile Laroche, et al.. (2012). Dose dependent expression of HDAC4 causes variable expressivity in a novel inherited case of brachydactyly mental retardation syndrome. American Journal of Medical Genetics Part A. 158A(8). 2015–2020. 33 indexed citations

Esvan, Maxime, Jean-Baptiste Meynard, Aziza Lebbar, et al.. (2011). Amniocentesis Performed for Karyotyping after Identified Ultrasonographic Abnormalities: What to Expect?. Fetal Diagnosis and Therapy. 31(1). 55–62. 4 indexed citations

Auger, Jacques, Céline Dupont, Dominique Le Tessier, et al.. (2010). Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management. European Journal of Medical Genetics. 53(3). 127–132. 6 indexed citations

10.

Lebbar, Aziza, Agnès Choiset, Sylvie Girard, et al.. (2009). Is Rapid Aneuploidy Screening Used Alone Acceptable in Prenatal Diagnosis? An Evaluation of the Possible Role of Ultrasound Examination. Fetal Diagnosis and Therapy. 25(2). 285–290. 8 indexed citations

11.

Maincent, Kim, Françoise Baverel, Dominique Le Tessier, et al.. (2009). Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U‐type exchange model. American Journal of Medical Genetics Part A. 149A(3). 437–445. 16 indexed citations

12.

Lebbar, Aziza, et al.. (2008). Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies. Prenatal Diagnosis. 28(4). 313–318. 5 indexed citations

13.

Lebbar, Aziza, Patrick Callier, Françoise Baverel, et al.. (2008). Two cases of mosaicism for complex chromosome rearrangements (CCRM) associated with secondary infertility. American Journal of Medical Genetics Part A. 146A(20). 2651–2656. 4 indexed citations

14.

Grangé, G., Aziza Lebbar, Agnès Choiset, et al.. (2008). Fetal Loss after Amniocentesis in a Series of 5,780 Procedures. Fetal Diagnosis and Therapy. 23(3). 217–221. 15 indexed citations

15.

Dupont, Céline, Aziza Lebbar, Cécile Teinturier, et al.. (2007). First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation. American Journal of Medical Genetics Part A. 143A(11). 1236–1243. 11 indexed citations

16.

Lebbar, Aziza, et al.. (2006). Pure familial 6q21q22.1 duplication in two generations. European Journal of Medical Genetics. 50(1). 60–65. 25 indexed citations

17.

Léger, Juliane, Olivier Dupuy, Mohammed Hassan, et al.. (2003). Translocation (Y;22) resulting in the loss of SHOX and isolated short stature. American Journal of Medical Genetics Part A. 125A(2). 186–190. 17 indexed citations

18.

Lebbar, Aziza, et al.. (2002). Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report. Prenatal Diagnosis. 22(11). 973–975. 3 indexed citations

19.

Tabet, Anne Claude, et al.. (2001). Heteromorphism 18ph+ : with or without reproductive consequences ?. Annales de Génétique. 44(3). 139–142. 2 indexed citations

20.

Telvi, Louise, et al.. (1999). 45,X/46,XY Mosaicism: Report of 27 Cases. PEDIATRICS. 104(2). 304–308. 143 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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