Valérie Malan

5.7k total citations
69 papers, 1.4k citations indexed

About

Valérie Malan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Valérie Malan has authored 69 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 27 papers in Pediatrics, Perinatology and Child Health and 25 papers in Molecular Biology. Recurrent topics in Valérie Malan's work include Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (24 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Valérie Malan is often cited by papers focused on Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (24 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Valérie Malan collaborates with scholars based in France, Belgium and Switzerland. Valérie Malan's co-authors include Michel Vekemans, Arnold Münnich, Laurence Colleaux, C Turleau, Nathalie Boddaert, Marlène Rio, Jeanne Amiel, Stanislas Lyonnet, Loïc de Pontual and Nigel P. Carter and has published in prestigious journals such as JAMA, Nucleic Acids Research and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Valérie Malan

66 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Valérie Malan France	20	923	733	333	148	135	69	1.4k
Fabiola Quintero‐Rivera United States	16	907 1.0×	634 0.9×	357 1.1×	83 0.6×	99 0.7×	54	1.4k
Francesca Forzano Italy	22	675 0.7×	505 0.7×	282 0.8×	136 0.9×	144 1.1×	64	1.4k
Griet Van Buggenhout Belgium	20	1.2k 1.3×	1.0k 1.4×	444 1.3×	171 1.2×	112 0.8×	63	1.9k
Beth S. Torchia United States	23	1.2k 1.3×	693 0.9×	686 2.1×	88 0.6×	109 0.8×	34	1.6k
Fady M. Mikhail United States	19	551 0.6×	700 1.0×	338 1.0×	80 0.5×	62 0.5×	61	1.5k
Beata Nowakowska Poland	21	741 0.8×	563 0.8×	218 0.7×	160 1.1×	242 1.8×	87	1.5k
Gordana Raca United States	18	1.1k 1.1×	586 0.8×	490 1.5×	88 0.6×	94 0.7×	62	1.7k
Suzanna G.M. Frints Netherlands	21	1.1k 1.1×	878 1.2×	416 1.2×	90 0.6×	95 0.7×	39	1.9k
Antonie D. Kline United States	23	936 1.0×	1.5k 2.1×	211 0.6×	100 0.7×	135 1.0×	49	2.0k
Jean‐Pierre Fryns Belgium	18	635 0.7×	664 0.9×	185 0.6×	182 1.2×	249 1.8×	72	1.3k

Countries citing papers authored by Valérie Malan

Since Specialization

Citations

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

Fields of papers citing papers by Valérie Malan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Malan

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

All Works

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20 of 20 papers shown

Siquier-Pernet, Karine, Geoffroy Delplancq, Marlène Rio, et al.. (2025). Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech. Molecular Autism. 16(1). 10–10.

Siquier-Pernet, Karine, Pauline Marzin, Christine Bôle‐Feysot, et al.. (2024). LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy. Human Genetics and Genomics Advances. 6(1). 100372–100372.

Huber, Céline, Geneviève Baujat, Caroline Michot, et al.. (2022). Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. Journal of Medical Genetics. 60(4). 337–345. 8 indexed citations

Ranza, Emmanuelle, Anne Guimier, Sylvie Beaudoın, et al.. (2022). Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia. American Journal of Medical Genetics Part A. 191(1). 77–83. 2 indexed citations

Silvente, Francisco Requena, et al.. (2021). CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients. Nucleic Acids Research. 49(W1). W93–W103. 16 indexed citations

Bras, Alicia Le, Laurent Salomon, L. Bussières, et al.. (2019). Cost‐effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model‐based analysis. Ultrasound in Obstetrics and Gynecology. 54(5). 596–603. 4 indexed citations

Malan, Valérie, L. Bussières, Norbert Winer, et al.. (2019). Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial. Obstetrical & Gynecological Survey. 74(1). 16–17. 3 indexed citations

Münnich, Arnold, Caroline Demily, Valérie Malan, et al.. (2019). Vingt ans de consultations de génétique clinique sur site dans les hôpitaux de jour pour les personnes atteintes de troubles du spectre autistique de la région parisienne. médecine/sciences. 35(11). 843–851. 1 indexed citations

Münnich, Arnold, Caroline Demily, Valérie Malan, et al.. (2019). Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder. Molecular Autism. 10(1). 33–33. 26 indexed citations

10.

Gomot, Marie, Romuald Blanc, Catherine Barthélémy, et al.. (2018). 22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype. Translational Psychiatry. 8(1). 146–146. 26 indexed citations

11.

Jackson, Carolyn C., Alain Lefèvre‐Utile, Anne Guimier, et al.. (2017). Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34‐q36.3 heterozygous terminal deletion. American Journal of Medical Genetics Part A. 173(7). 1858–1865. 4 indexed citations

12.

Spazzapan, Peter, Éric Arnaud, Geneviève Baujat, et al.. (2015). Clinical and neuroradiological features of the 9p deletion syndrome. Child s Nervous System. 32(2). 327–335. 31 indexed citations

13.

Wells, Constance, Emmanuel Spaggiari, Valérie Malan, et al.. (2015). First fetal case of the 8q24.3 contiguous genes syndrome. American Journal of Medical Genetics Part A. 170(1). 239–242. 18 indexed citations

14.

Philippe, Anne, Valérie Malan, Marie‐Line Jacquemont, et al.. (2013). Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X‐linked intellectual disability with distinctive facial appearance. American Journal of Medical Genetics Part A. 161(6). 1370–1375. 19 indexed citations

15.

Essaoui, M., Mathilde Nizon, Julia Tantau, et al.. (2013). Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid. European Journal of Medical Genetics. 56(9). 502–505. 12 indexed citations

16.

Malan, Valérie & Serge Romana. (2012). Analyse chromosomique sur puce à ADN (CGH array) : principe et application en diagnostic prénatal. Revue de médecine périnatale. 4(2). 67–73. 2 indexed citations

17.

Rio, Marlène, Valérie Malan, Sarah Boissel, et al.. (2009). Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition. European Journal of Human Genetics. 18(3). 285–290. 29 indexed citations

18.

Malan, Valérie, N. Morichon-Delvallez, Alexandra Benachi, et al.. (2007). Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: A Case Report. Human Reproduction. 22(4). 1037–1041. 32 indexed citations

19.

Amiel, Jeanne, Marlène Rio, Loïc de Pontual, et al.. (2007). Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Autonomic Dysfunction. The American Journal of Human Genetics. 80(5). 988–993. 212 indexed citations

20.

Malan, Valérie, Christian Grillon, Damien Sanlaville, et al.. (2004). A new case of a severe clinical phenotype of the cat-eye syndrome.. PubMed. 15(4). 443–8. 14 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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