Férechté Razavi

915 total citations
15 papers, 194 citations indexed

About

Férechté Razavi is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Férechté Razavi has authored 15 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Genetics. Recurrent topics in Férechté Razavi's work include Fetal and Pediatric Neurological Disorders (4 papers), Neonatal and fetal brain pathology (2 papers) and Genetic Syndromes and Imprinting (2 papers). Férechté Razavi is often cited by papers focused on Fetal and Pediatric Neurological Disorders (4 papers), Neonatal and fetal brain pathology (2 papers) and Genetic Syndromes and Imprinting (2 papers). Férechté Razavi collaborates with scholars based in France, Germany and Martinique. Férechté Razavi's co-authors include Jelena Martinović, Arnold Münnich, Dominique Chrétien, Tania Attié‐Bitach, Agnès Rötig, Limor Minai, Dominique Hénin, Marie‐Christine Dauge, Katell Peoc’h and Homa Adle‐Biassette and has published in prestigious journals such as Journal of Neuropathology & Experimental Neurology, Neurobiology of Disease and Journal of Medical Genetics.

In The Last Decade

Férechté Razavi

15 papers receiving 187 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Férechté Razavi France 8 130 53 35 25 21 15 194
Mohammad Yahya Vahidi Mehrjardi Iran 13 184 1.4× 68 1.3× 22 0.6× 21 0.8× 14 0.7× 38 323
Urania Kotzaeridou Germany 11 285 2.2× 68 1.3× 58 1.7× 20 0.8× 12 0.6× 15 404
Ajith Sreekantan-Nair United Kingdom 3 66 0.5× 22 0.4× 15 0.4× 13 0.5× 24 1.1× 3 141
Ofra Sabag Israel 10 243 1.9× 64 1.2× 38 1.1× 30 1.2× 5 0.2× 18 330
Huifang Yan China 9 108 0.8× 79 1.5× 7 0.2× 24 1.0× 10 0.5× 23 201
Ruud van der Breggen Netherlands 6 153 1.2× 63 1.2× 40 1.1× 82 3.3× 7 0.3× 7 321
Ilya Kanivets Russia 7 91 0.7× 61 1.2× 26 0.7× 13 0.5× 19 0.9× 39 162
Patricia Galvin‐Parton United States 11 192 1.5× 84 1.6× 45 1.3× 47 1.9× 4 0.2× 13 313
Sue Forrest Australia 9 293 2.3× 172 3.2× 43 1.2× 40 1.6× 8 0.4× 12 395
Minal Menezes Australia 10 195 1.5× 65 1.2× 8 0.2× 27 1.1× 9 0.4× 17 290

Countries citing papers authored by Férechté Razavi

Since Specialization
Citations

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

Fields of papers citing papers by Férechté Razavi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Férechté Razavi

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

All Works

15 of 15 papers shown
1.
Lœuillet, Laurence, Juliette Nectoux, E. Pannier, et al.. (2022). Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth Defects Research. 115(5). 563–571. 1 indexed citations
2.
Marguet, Florent, Fabien Guimiot, Jelena Martinović, et al.. (2021). Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome. European Journal of Medical Genetics. 64(9). 104282–104282. 7 indexed citations
3.
Calmels, Nadège, Maryse Bonnière, Suzanne Chartier, et al.. (2020). Prenatal diagnosis of cerebro‐oculo‐facio‐skeletal syndrome: Report of three fetuses and review of the literature. American Journal of Medical Genetics Part A. 182(5). 1236–1242. 5 indexed citations
4.
Heide, Solveig, Sandrine Poëa‐Guyon, Véronique Rousseau, et al.. (2019). PAK3 mutations responsible for severe intellectual disability and callosal agenesis inhibit cell migration. Neurobiology of Disease. 136. 104709–104709. 14 indexed citations
5.
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
6.
Bèaufrere, Aurélie, Maryse Bonnière, Julia Tantau, et al.. (2018). Corpus Callosum Abnormalities and Short Femurs in Beckwith–Wiedemann Syndrome: A Report of Two Fetal Cases. Fetal and Pediatric Pathology. 37(6). 411–417. 3 indexed citations
7.
Chartier, Suzanne, Caroline Alby, Lucile Boutaud, et al.. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth Defects Research. 110(7). 598–602. 7 indexed citations
8.
Alby, Caroline, Bettina Bessières, Éric Bieth, et al.. (2013). Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt‐oram and ulnar‐mammary syndromes. American Journal of Medical Genetics Part A. 161(7). 1797–1802. 9 indexed citations
9.
Dupré, Thierry, Sandrine Vuillaumier‐Barrot, Pascale de Lonlay, et al.. (2010). Should PMM2-deficiency (CDG Ia) be searched in every case of unexplained hydrops fetalis?. Molecular Genetics and Metabolism. 101(2-3). 253–257. 18 indexed citations
10.
Martinović, Jelena, et al.. (2008). Prenatal cortical hyperostosis with COL1A1 gene mutation. American Journal of Medical Genetics Part A. 146A(14). 1820–1824. 19 indexed citations
11.
Minai, Limor, Jelena Martinović, Dominique Chrétien, et al.. (2008). Mitochondrial respiratory chain complex assembly and function during human fetal development. Molecular Genetics and Metabolism. 94(1). 120–126. 43 indexed citations
12.
Adle‐Biassette, Homa, Catherine Verney, Katell Peoc’h, et al.. (2006). Immunohistochemical Expression of Prion Protein (PrPC) in the Human Forebrain During Development. Journal of Neuropathology & Experimental Neurology. 65(7). 698–706. 38 indexed citations
13.
Faivre, Laurence, Anne‐Lise Delezoide, Françoise Narcy, et al.. (1999). A new lethal syndrome of exomphalos, short limbs, and macrogonadism. Journal of Medical Genetics. 36(2). 131–136. 1 indexed citations
14.
Razavi, Férechté, et al.. (1996). Lethal familial fetal akinesia sequence (FAS) with distinct neuropathological pattern: Type III lissencephaly syndrome. American Journal of Medical Genetics. 62(1). 16–22. 17 indexed citations
15.
Razavi, Férechté, et al.. (1996). Lethal familial fetal akinesia sequence (FAS) with distinct neuropathological pattern: Type III lissencephaly syndrome. American Journal of Medical Genetics. 62(1). 16–22. 1 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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