Amale Ichkou

455 total citations
6 papers, 79 citations indexed

About

Amale Ichkou is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Amale Ichkou has authored 6 papers receiving a total of 79 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Amale Ichkou's work include Fetal and Pediatric Neurological Disorders (5 papers), Genetic and Kidney Cyst Diseases (4 papers) and Hedgehog Signaling Pathway Studies (2 papers). Amale Ichkou is often cited by papers focused on Fetal and Pediatric Neurological Disorders (5 papers), Genetic and Kidney Cyst Diseases (4 papers) and Hedgehog Signaling Pathway Studies (2 papers). Amale Ichkou collaborates with scholars based in France, Switzerland and India. Amale Ichkou's co-authors include Tania Attié‐Bitach, Nadia Elkhartoufi, Michel Vekemans, Sophie Thomas, Férechté Encha‐Razavi, Lucile Boutaud, Caroline Alby, A. Millischer, Nadia Bahi‐Buisson and Bettina Bessières and has published in prestigious journals such as Journal of Medical Genetics, Acta Neuropathologica Communications and Birth Defects Research Part A Clinical and Molecular Teratology.

In The Last Decade

Amale Ichkou

5 papers receiving 78 citations

Peers

Amale Ichkou

MB

PPCH

GENET

ID

CB

Matthieu Décamp France

Pierre Sinajon Canada

Francesca Benini Italy

Stacy Gabriel United States

Nadia Elkhartoufi France

Leigh Anne Flore United States

H. Melanie Bedford Canada

Julie McCarrier United States

Rosa Baldinger Switzerland

Christian Marshall Canada

Matthieu Décamp France

Amale Ichkou

60 ×1.4

MB

55 ×1.5

PPCH

89 ×2.5

GENET

6 ×0.7

ID

7 ×0.8

CB

Citations per year, relative to Amale Ichkou Amale Ichkou (= 1×) peers Matthieu Décamp

Countries citing papers authored by Amale Ichkou

Since Specialization

Citations

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

Fields of papers citing papers by Amale Ichkou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amale Ichkou

This figure shows the co-authorship network connecting the top 25 collaborators of Amale Ichkou. A scholar is included among the top collaborators of Amale Ichkou 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 Amale Ichkou. Amale Ichkou 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:

6 of 6 papers shown

1.

Tessier, Aude, Lucile Boutaud, Mélanie Parisot, et al.. (2023). Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathologica Communications. 11(1). 29–29. 7 indexed citations

2.

Bacrot, Séverine, Charlotte Mechler, Dominique Martin‐Coignard, et al.. (2018). Whole exome sequencing diagnoses the first fetal case of Bainbridge‐Ropers syndrome presenting as pontocerebellar hypoplasia type 1. Birth Defects Research. 110(6). 538–542. 11 indexed citations

3.

Karaer, Kadri, Zafer Yüksel, Amale Ichkou, Cüneyt Çalışır, & Tania Attié‐Bitach. (2015). A novel KIF7 mutation in two affected siblings with acrocallosal syndrome. Clinical Dysmorphology. 24(2). 61–64. 5 indexed citations

4.

Alby, Caroline, Valérie Malan, Lucile Boutaud, et al.. (2015). Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation. Birth Defects Research Part A Clinical and Molecular Teratology. 106(1). 36–46. 30 indexed citations

5.

Krajewska‐Walasek, Małgorzata, et al.. (2015). MOLAR TOOTH SIGN AND ACROCALLOSAL SYNDROME--A REPORT ON A POLISH FAMILY AND REVIEW OF KIF7 SYNDROMOLOGY.. PubMed. 26(2). 171–9.

6.

Putoux, Audrey, Sheela Nampoothiri, Nicole Laurent, et al.. (2012). Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome. Journal of Medical Genetics. 49(11). 713–720. 26 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.

Explore authors with similar magnitude of impact