Azarnouche Ardalan

400 citations
9 papers · 244 · h-index 9

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Cystic Fibrosis Research Advances

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Congenital Ear and Nasal Anomalies 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
    • Genetic Syndromes and Imprinting 1

Azarnouche Ardalan

9 papers receiving 231 citations

Peers

Azarnouche Ardalan
Comparison fields: 5 of 35
  • Genetics 122
  • Pulmonary and Respiratory Medicine 57
  • Molecular Biology 121
  • Genetics 14
  • Pediatrics, Perinatology and Child Health 20
Replace Társis Paiva Vieira with:
Társis Paiva Vieira Brazil
Milena Simioni Brazil
Hitisha P. Zaveri United States
H. J. Eussen Netherlands
Molly B. Sheridan United States
Cindy Pham Lorentz United States
Fernando Santos Spain
Cinthya Zepeda‐Mendoza United States
S.W. Cheung United States
Koen Devriendt Belgium
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Citations per field
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Társis Paiva Vieira · 1×
Citations per year

Countries citing papers authored by Azarnouche Ardalan

Since Specialization
Citations

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

Fields of papers citing papers by Azarnouche Ardalan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Azarnouche Ardalan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Azarnouche Ardalan Line = papers co-authored together Azarnouche Ardalan links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 200574
2 200437
3 200531
4 200629
5 200518
6 200017
7 200016
8
A new case of a severe clinical phenotype of the cat-eye syndrome.
200414
9 20158

About Azarnouche Ardalan

Azarnouche Ardalan is a scholar working on Genetics, Molecular Biology, Genetics, Pulmonary and Respiratory Medicine and Plant Science, having authored 9 papers that have together received 244 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital Ear and Nasal Anomalies (2 papers), Chromosomal and Genetic Variations (2 papers), Cystic Fibrosis Research Advances (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Congenital Anomalies and Fetal Surgery (1 paper), Genetic Syndromes and Imprinting (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (122 citations), Pulmonary and Respiratory Medicine (57 citations), Molecular Biology (121 citations), Genetics (14 citations) and Pediatrics, Perinatology and Child Health (20 citations). Azarnouche Ardalan has collaborated with scholars based in France, Portugal and Switzerland. Frequent co-authors include Jean‐Louis Taillemite, Marie‐France Portnoï, Valérie Malan, Sarah Ducrocq, Nicolas Gruchy, Gilles Roger, Sandrine Marlin, Marguerite Prieur, Françoise Goutières and Florence Niel. Their work appears in journals such as Clinical Genetics, Clinical Chemistry, Molecular Cytogenetics, Human Reproduction and Multiple Sclerosis Journal.

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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