Françoise Narcy

1.0k total citations
22 papers, 541 citations indexed

About

Françoise Narcy is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Françoise Narcy has authored 22 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Françoise Narcy's work include Prenatal Screening and Diagnostics (6 papers), Cleft Lip and Palate Research (6 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Françoise Narcy is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Cleft Lip and Palate Research (6 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Françoise Narcy collaborates with scholars based in France, Belgium and India. Françoise Narcy's co-authors include Marc Dommergues, Marie-Claire Gübler, Yves Dumez, Mireille Lacoste, Anne‐Lise Delezoide, Françoise Müller, Yi Cai, Jeanne‐Claudie Larroche, D. Mahieu‐Caputo and Marie Gonzalès and has published in prestigious journals such as Kidney International, American Journal of Obstetrics and Gynecology and American Journal Of Pathology.

In The Last Decade

Françoise Narcy

22 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Françoise Narcy France 12 294 139 135 129 101 22 541
Peter Nicolaidis United Kingdom 13 486 1.7× 129 0.9× 77 0.6× 142 1.1× 97 1.0× 25 716
Gareth Seaward Canada 8 418 1.4× 108 0.8× 112 0.8× 470 3.6× 65 0.6× 16 679
C. V. Isaksen Norway 17 390 1.3× 172 1.2× 136 1.0× 190 1.5× 35 0.3× 27 733
Pietro Cignini Italy 15 252 0.9× 176 1.3× 51 0.4× 311 2.4× 42 0.4× 49 721
Dick van Velzen United Kingdom 10 115 0.4× 125 0.9× 79 0.6× 40 0.3× 119 1.2× 24 415
Farida Daïkha-Dahmane France 8 203 0.7× 48 0.3× 109 0.8× 45 0.3× 37 0.4× 9 292
Peter Warren Australia 11 261 0.9× 91 0.7× 35 0.3× 218 1.7× 81 0.8× 22 599
I. Tekesin Germany 12 173 0.6× 88 0.6× 56 0.4× 92 0.7× 73 0.7× 33 432
J.F. Oury France 12 221 0.8× 108 0.8× 30 0.2× 64 0.5× 24 0.2× 19 392
P Vanlieferinghen France 10 89 0.3× 132 0.9× 68 0.5× 32 0.2× 71 0.7× 40 404

Countries citing papers authored by Françoise Narcy

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Narcy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Narcy

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

All Works

20 of 20 papers shown
1.
Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21: À propos de 101 cas fcetopathologiques. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 2 indexed citations
2.
Grangé, G., et al.. (2006). Fréquence des malformations associées à la trisomie 21. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 35(5). 477–482. 4 indexed citations
3.
Daïkha-Dahmane, Farida, Marc Dommergues, Françoise Narcy, et al.. (2001). Congenital Erythropoietic Porphyria: Prenatal Diagnosis and Autopsy Findings in Two Sibling Fetuses. Pediatric and Developmental Pathology. 4(2). 180–184. 9 indexed citations
4.
Mahieu‐Caputo, D., Marc Dommergues, Anne‐Lise Delezoide, et al.. (2000). Twin-to-Twin Transfusion Syndrome: Role of the Fetal Renin-Angiotensin System. Obstetrical & Gynecological Survey. 55(9). 542–543. 5 indexed citations
5.
Mahieu‐Caputo, D., Marc Dommergues, Anne‐Lise Delezoide, et al.. (2000). Twin-to-Twin Transfusion Syndrome. American Journal Of Pathology. 156(2). 629–636. 150 indexed citations
6.
Faivre, Laurence, N. Morichon-Delvallez, Géraldine Viot, et al.. (1998). Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature. Prenatal Diagnosis. 18(10). 1055–1060. 41 indexed citations
7.
Mandarim‐de‐Lacerda, Carlos Alberto, et al.. (1997). Stereology of the myocardium in human foetuses. Early Human Development. 48(3). 249–259. 25 indexed citations
8.
Daïkha-Dahmane, Farida, Françoise Narcy, Marc Dommergues, et al.. (1997). Distribution of α-integrin subunits in fetal polycystic kidney diseases. Pediatric Nephrology. 11(3). 267–273. 19 indexed citations
9.
Daïkha-Dahmane, Farida, Marc Dommergues, Françoise Müller, et al.. (1997). Development of human fetal kidney in obstructive uropathy: Correlations with ultrasonography and urine biochemistry. Kidney International. 52(1). 21–32. 67 indexed citations
10.
Gübler, Marie-Claire, et al.. (1997). [Prenatal diagnosis of renal malformations and diseases].. PubMed. 17(4). 240–50. 6 indexed citations
11.
Labrune, Philippe, Pascale Trioche, Catherine Fallet‐Bianco, et al.. (1997). Severe brain and limb defects with possible autosomal recessive inheritance: A series of six cases and review of the literature. American Journal of Medical Genetics. 73(2). 144–149. 4 indexed citations
12.
Verloès, Alain, Françoise Narcy, & Catherine Fallet‐Bianco. (1995). Syndromal hypothalamic hamartoblastoma with holoprosencephaly sequence, microphthalmia, pulmonary malformations, radial hypoplasia and müllerian regression: further delineation of a new syndrome?. PubMed. 4(1). 33–7. 11 indexed citations
13.
Müller, Françoise, Marie-Cécile Aubry, Brigitte Simon‐Bouy, et al.. (1995). Hyperechogenic fetal bowel: An ultrasonographic marker for adverse fetal and neonatal outcome. American Journal of Obstetrics and Gynecology. 173(2). 508–513. 58 indexed citations
14.
Narcy, Françoise, et al.. (1995). Syndromal hypothalamic hamartoblastoma with holoprosencecephaly sequence, microphthalmia, pulmonary malformation, radial hypoplasia and M??llerian regression. Clinical Dysmorphology. 4(1). 33???37–33???37. 1 indexed citations
15.
Daïkha-Dahmane, Farida, et al.. (1995). Distribution and ontogenesis of tenascin in normal and cystic human fetal kidneys.. PubMed. 73(4). 547–57. 12 indexed citations
16.
Larroche, Jeanne‐Claudie, et al.. (1995). Contents, Vol. 10, No. 4, 1995. Fetal Diagnosis and Therapy. 10(4). 211–213. 50 indexed citations
17.
Dumez, Yves, Marc Dommergues, Marie-Claire Gübler, et al.. (1994). Meckel‐Gruber syndrome: Prenatal diagnosis at 10 menstrual weeks using embryoscopy. Prenatal Diagnosis. 14(2). 141–144. 9 indexed citations
18.
Dumez, Yves, Laurent Mandelbrot, N. Radunovic, et al.. (1993). Prenatal management of congenital cystic adenomatoid malformation of the lung. Journal of Pediatric Surgery. 28(1). 36–41. 34 indexed citations
19.
Delezoide, Anne‐Lise, Françoise Narcy, & Jeanne‐Claudie Larroche. (1990). Cerebral midline developmental anomalies: spectrum and associated features.. PubMed. 1(3-4). 197–210. 11 indexed citations
20.
Drake, Amelia F., P Contencin, Françoise Narcy, & Robin T. Cotton. (1989). Lateral cricoid cuts as an adjunctive measure to enlarge the stenotic subglottic airway: an anatomic study. International Journal of Pediatric Otorhinolaryngology. 18(2). 129–137. 13 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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