Salah Azzi

2.2k total citations
28 papers, 1.3k citations indexed

About

Salah Azzi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Salah Azzi has authored 28 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 26 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Salah Azzi's work include Genetic Syndromes and Imprinting (27 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (18 papers). Salah Azzi is often cited by papers focused on Genetic Syndromes and Imprinting (27 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (18 papers). Salah Azzi collaborates with scholars based in France, Australia and United Kingdom. Salah Azzi's co-authors include Irène Netchine, Yves Le Bouc, Sylvie Rossignol, Nathalie Thibaud, Walid Abi Habib, Christine Gicquel, Madeleine D. Harbison, Virginie Steunou, Jennifer Ben Salem and Sandra Chantot‐Bastaraud and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Molecular Genetics and Science Advances.

In The Last Decade

Salah Azzi

28 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Salah Azzi France	19	1.0k	930	681	155	62	28	1.3k
Frédéric Brioude France	21	796 0.8×	772 0.8×	462 0.7×	138 0.9×	69 1.1×	49	1.2k
M.J.E. Walenkamp Netherlands	18	515 0.5×	427 0.5×	287 0.4×	715 4.6×	58 0.9×	26	1.2k
David Monk United Kingdom	18	874 0.9×	963 1.0×	646 0.9×	31 0.2×	20 0.3×	23	1.2k
Gail Kirby United Kingdom	9	366 0.4×	345 0.4×	364 0.5×	82 0.5×	13 0.2×	11	693
Jennifer Hughes United Kingdom	6	363 0.4×	563 0.6×	495 0.7×	116 0.7×	7 0.1×	8	991
Boris Utsch Germany	20	391 0.4×	596 0.6×	224 0.3×	54 0.3×	129 2.1×	32	951
Moez Gribaa Tunisia	15	279 0.3×	347 0.4×	162 0.2×	36 0.2×	27 0.4×	51	679
B.M. Lippe United States	10	448 0.4×	501 0.5×	243 0.4×	577 3.7×	20 0.3×	16	1.1k
Hirotaka Wagatsuma Japan	9	490 0.5×	820 0.9×	274 0.4×	40 0.3×	13 0.2×	11	1.0k
Wayne Lam United Kingdom	11	352 0.4×	466 0.5×	143 0.2×	77 0.5×	22 0.4×	22	715

Countries citing papers authored by Salah Azzi

Since Specialization

Citations

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

Fields of papers citing papers by Salah Azzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Salah Azzi

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

Habib, Walid Abi, Frédéric Brioude, Salah Azzi, et al.. (2019). Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders. Science Advances. 5(2). eaau9425–eaau9425. 33 indexed citations

Heide, Solveig, Sandra Chantot‐Bastaraud, Boris Keren, et al.. (2017). Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences. Journal of Medical Genetics. 55(3). 205–213. 34 indexed citations

Habib, Walid Abi, Frédéric Brioude, Thomas Édouard, et al.. (2017). Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction. Genetics in Medicine. 20(2). 250–258. 98 indexed citations

Habib, Walid Abi, Salah Azzi, Frédéric Brioude, et al.. (2014). Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome. Human Molecular Genetics. 23(21). 5763–5773. 51 indexed citations

Azzi, Salah, Frédéric Brioude, Yves Le Bouc, & Irène Netchine. (2014). Human Imprinting Anomalies in Fetal and Childhood Growth Disorders: Clinical Implications and Molecular Mechanisms. Current Pharmaceutical Design. 20(11). 1751–1763. 8 indexed citations

Azzi, Salah, Virginie Steunou, Jörg Tost, et al.. (2014). Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome. Journal of Medical Genetics. 52(1). 53–60. 11 indexed citations

Netchine, Irène, Sylvie Rossignol, Salah Azzi, & Yves Le Bouc. (2013). Epigenetic Anomalies in Childhood Growth Disorders. Nestlé Nutrition Institute Workshop series. 71. 65–73. 7 indexed citations

Azzi, Salah, Theo Sas, Yves Akoli Koudou, et al.. (2013). Degree of methylation ofZAC1(PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort. Epigenetics. 9(3). 338–345. 54 indexed citations

Azzi, Salah, Walid Abi Habib, & Irène Netchine. (2013). Beckwith–Wiedemann and Russell–Silver Syndromes. Current Opinion in Endocrinology Diabetes and Obesity. 21(1). 30–38. 76 indexed citations

10.

Keren, Boris, Sandra Chantot‐Bastaraud, Frédéric Brioude, et al.. (2013). SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy. European Journal of Medical Genetics. 56(10). 546–550. 38 indexed citations

11.

Rossignol, Sylvie, Bruno Delobel, Melita Irving, et al.. (2013). Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver–Russell syndrome. American Journal of Medical Genetics Part A. 161(3). 572–577. 15 indexed citations

12.

Demars, Julie, Sylvie Rossignol, Irène Netchine, et al.. (2011). New insights into the pathogenesis of beckwith-wiedemann and silver-russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects. Human Mutation. 32(10). 1171–1182. 45 indexed citations

13.

Netchine, Irène, Salah Azzi, Yves Le Bouc, & Martin O. Savage. (2011). IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development. Best Practice & Research Clinical Endocrinology & Metabolism. 25(1). 181–190. 77 indexed citations

14.

Bouc, Yves Le, Sylvie Rossignol, Salah Azzi, et al.. (2010). Epigenetics, genomic imprinting and assisted reproductive technology. Annales d Endocrinologie. 71(3). 237–238. 33 indexed citations

15.

Azzi, Salah, Virginie Steunou, Alexandra Rousseau, et al.. (2010). Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes. Human Mutation. 32(2). 249–258. 38 indexed citations

16.

Azzi, Salah, Sylvie Rossignol, Yves Le Bouc, & Irène Netchine. (2010). Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases. Epigenetics. 5(5). 373–377. 19 indexed citations

17.

Bouc, Yves Le, Sylvie Rossignol, Salah Azzi, et al.. (2010). Anomalies épigénétiques et de l’empreinte parentale dans les maladies du développement humain. Bulletin de l Académie Nationale de Médecine. 194(2). 287–300. 3 indexed citations

18.

Demars, Julie, Sylvie Rossignol, Jun Okabe, et al.. (2009). Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders. Human Molecular Genetics. 19(5). 803–814. 92 indexed citations

19.

Azzi, Salah, Sylvie Rossignol, Virginie Steunou, et al.. (2009). Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Human Molecular Genetics. 18(24). 4724–4733. 179 indexed citations

20.

Netchine, Irène, Salah Azzi, Muriel Houang, et al.. (2009). Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated withIGF1Mutation Demonstrates Its Critical Role in Growth and Brain Development. The Journal of Clinical Endocrinology & Metabolism. 94(10). 3913–3921. 107 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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