C. Fallet

616 total citations
15 papers, 444 citations indexed

About

C. Fallet is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, C. Fallet has authored 15 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 4 papers in Molecular Biology and 3 papers in Developmental Neuroscience. Recurrent topics in C. Fallet's work include Fetal and Pediatric Neurological Disorders (6 papers), Neonatal and fetal brain pathology (4 papers) and Prenatal Screening and Diagnostics (3 papers). C. Fallet is often cited by papers focused on Fetal and Pediatric Neurological Disorders (6 papers), Neonatal and fetal brain pathology (4 papers) and Prenatal Screening and Diagnostics (3 papers). C. Fallet collaborates with scholars based in France, Brazil and Germany. C. Fallet's co-authors include Roberto Lent, C. Daumas‐Duport, Vivaldo Moura‐Neto, Leonardo C. deAzevedo, Cecilia Hedin‐Pereira, G. Sebag, Hervé J. Brisse, Philippe Blot, C Nessmann and Nadine Girard and has published in prestigious journals such as The Journal of Comparative Neurology, Molecular Psychiatry and Experimental Neurology.

In The Last Decade

C. Fallet

14 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Fallet France	10	174	145	102	96	53	15	444
Matthew J. Anzivino United States	11	64 0.4×	128 0.9×	116 1.1×	153 1.6×	17 0.3×	14	443
Kuniyasu Takada Japan	9	103 0.6×	271 1.9×	24 0.2×	128 1.3×	16 0.3×	15	391
Kristine D. Baerwald United States	7	48 0.3×	172 1.2×	143 1.4×	68 0.7×	9 0.2×	9	578
Tianci Chu China	13	46 0.3×	117 0.8×	102 1.0×	99 1.0×	12 0.2×	20	396
Philip H. Iffland United States	11	51 0.3×	181 1.2×	17 0.2×	93 1.0×	15 0.3×	17	377
Yee Ping Yip United States	12	52 0.3×	127 0.9×	180 1.8×	192 2.0×	40 0.8×	21	393
Sara Loddo Italy	13	123 0.7×	277 1.9×	13 0.1×	54 0.6×	8 0.2×	39	639
Arjang Salehi United States	7	27 0.2×	246 1.7×	27 0.3×	50 0.5×	23 0.4×	10	490
Loan Nguyen United States	3	200 1.1×	89 0.6×	25 0.2×	161 1.7×	19 0.4×	8	457
Benjamin Wheaton Australia	11	30 0.2×	80 0.6×	52 0.5×	87 0.9×	21 0.4×	16	325

Countries citing papers authored by C. Fallet

Since Specialization

Citations

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

Fields of papers citing papers by C. Fallet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Fallet

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

15 of 15 papers shown

1.

Isidor, Bertrand, Norbert Winer, Madeleine Joubert, et al.. (2008). Inherited 18q23 duplication in a fetus with multiple congenital anomalies. European Journal of Medical Genetics. 51(3). 231–238. 4 indexed citations

2.

Lahutte, M., C. Bordarier, Clémentine André, C. Fallet, & C. Adamsbaum. (2008). L’infarctus veineux hemorragique du nouveau-ne, une pathologie mal connue. Journal de Radiologie. 89(10). 1489–1489. 1 indexed citations

3.

Leroy, Jules G., Gilles Lyon, C. Fallet, et al.. (2007). Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype. Acta Neuropathologica. 114(4). 387–399. 6 indexed citations

4.

Bouchet, C, Sandrine Vuillaumier‐Barrot, M. Gonzalés, et al.. (2006). Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families. Molecular Genetics and Metabolism. 90(1). 93–96. 17 indexed citations

5.

Lent, Roberto, Daniela Uziel, M. Baudrimont, & C. Fallet. (2005). Cellular and molecular tunnels surrounding the forebrain commissures of human fetuses. The Journal of Comparative Neurology. 483(4). 375–382. 32 indexed citations

6.

Kultas‐Ilinsky, Kristy, C. Fallet, & Catherine Verney. (2004). Development of the human motor‐related thalamic nuclei during the first half of gestation, with special emphasis on GABAergic circuits. The Journal of Comparative Neurology. 476(3). 267–289. 12 indexed citations

7.

Funalot, Benoît, Tanja Ouimet, Audrey Clapéron, et al.. (2004). Endothelin-converting enzyme-1 is expressed in human cerebral cortex and protects against Alzheimer's disease. Molecular Psychiatry. 9(12). 1122–1128. 49 indexed citations

8.

Funalot, Benoît, Tanja Ouimet, Audrey Clapéron, et al.. (2004). Endothelin-converting enzyme-1 is expressed in human cerebral cortex and protects against Alzheimer's disease. Molecular Psychiatry. 9(12). 1059–1059. 9 indexed citations

9.

deAzevedo, Leonardo C., C. Fallet, Vivaldo Moura‐Neto, et al.. (2003). Cortical radial glial cells in human fetuses: Depth‐correlated transformation into astrocytes. Journal of Neurobiology. 55(3). 288–298. 121 indexed citations

10.

Tawk, Marcel, Matthias Titeux, C. Fallet, et al.. (2003). Synemin expression in developing normal and pathological human retina and lens. Experimental Neurology. 183(2). 499–507. 24 indexed citations

11.

Moura, Cláudia, Y. Hillion, Farida Daïkha-Dahmane, et al.. (2002). Isolated non-compaction of the myocardium diagnosed in the fetus: two sporadic and two familial cases. Cardiology in the Young. 12(3). 278–283. 29 indexed citations

12.

Kesrouani, Assaad, C. Fallet, E. Vuillard, et al.. (2001). Pathologic and laboratory correlation in microcephaly associated with prenatal cocaine exposure. Early Human Development. 63(2). 79–81. 6 indexed citations

13.

Brisse, Hervé J., G. Sebag, C. Fallet, et al.. (1998). [Prenatal MRI of corpus callosum agenesis. Study of 20 cases with neuropathological correlations].. PubMed. 79(7). 659–66. 16 indexed citations

14.

Brisse, Hervé J., et al.. (1997). Supratentorial parenchyma in the developing fetal brain: in vitro MR study with histologic comparison.. American Journal of Neuroradiology. 18(8). 1491–7. 75 indexed citations

15.

Larroche, Jeanne‐Claudie, et al.. (1994). Abnormal Cortical Plate (Polymicrogyria), Heterotopias and Brain Damage in Monozygous Twins. Neonatology. 65(6). 343–352. 43 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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