Perrine Malzac

1.5k total citations
28 papers, 881 citations indexed

About

Perrine Malzac is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Perrine Malzac has authored 28 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Perrine Malzac's work include Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (8 papers) and Prenatal Screening and Diagnostics (6 papers). Perrine Malzac is often cited by papers focused on Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (8 papers) and Prenatal Screening and Diagnostics (6 papers). Perrine Malzac collaborates with scholars based in France, United States and Switzerland. Perrine Malzac's co-authors include Anne Moncla, A. Moncla, Marie‐Antoinette Voelckel, Marc Lalande, Nathalie Roëckel, Marie‐Geneviève Mattéi, Nicole Philip, Philippe Jay, Sylvie Taviaux and Françoise Muscatelli and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Perrine Malzac

28 papers receiving 848 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Perrine Malzac France 13 574 519 214 81 63 28 881
Elisabetta Lapi Italy 18 477 0.8× 534 1.0× 131 0.6× 49 0.6× 80 1.3× 48 957
Mary Z. Pelias United States 17 238 0.4× 536 1.0× 157 0.7× 82 1.0× 55 0.9× 35 1.1k
Judith P. Willner United States 14 527 0.9× 631 1.2× 191 0.9× 44 0.5× 59 0.9× 33 1.2k
Patricia I. Bader United States 18 584 1.0× 619 1.2× 180 0.8× 29 0.4× 77 1.2× 32 1.1k
Abdul Noor Canada 20 620 1.1× 823 1.6× 118 0.6× 40 0.5× 85 1.3× 42 1.4k
Sheila Youings United Kingdom 15 831 1.4× 428 0.8× 166 0.8× 49 0.6× 46 0.7× 18 978
Joan Atkin United States 13 342 0.6× 356 0.7× 228 1.1× 83 1.0× 44 0.7× 19 776
Bernard N. Chodirker Canada 15 293 0.5× 280 0.5× 152 0.7× 31 0.4× 64 1.0× 44 752
Nicholas R. Dennis United Kingdom 16 640 1.1× 368 0.7× 353 1.6× 144 1.8× 38 0.6× 23 1.0k
B. P. Hauffa Germany 16 635 1.1× 599 1.2× 209 1.0× 59 0.7× 22 0.3× 43 1.2k

Countries citing papers authored by Perrine Malzac

Since Specialization
Citations

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

Fields of papers citing papers by Perrine Malzac

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Perrine Malzac

This figure shows the co-authorship network connecting the top 25 collaborators of Perrine Malzac. A scholar is included among the top collaborators of Perrine Malzac 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 Perrine Malzac. Perrine Malzac 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.
Cano, N., et al.. (2019). Mise en place et évaluation de séances d’éthique appliquée dans un service de psychiatrie générale en France. Annales Médico-psychologiques revue psychiatrique. 178(9). 884–890. 2 indexed citations
2.
Perrin, Jeanne, J. Saïas‐Magnan, Gérard Karsenty, et al.. (2012). Case report of apoptosis in testis of four AZFc-deleted patients: increased DNA fragmentation during meiosis, but decreased apoptotic markers in post-meiotic germ cells. Human Reproduction. 27(7). 1939–1945. 6 indexed citations
3.
Gorincour, G., Sébastien Tassy, Antoine Payot, et al.. (2011). Décision d’interruption médicale de grossesse : le point de vue des soignants français. Gynécologie Obstétrique & Fertilité. 39(4). 198–204. 9 indexed citations
4.
Coz, Pierre Le, et al.. (2010). Parental experience following perinatal death: exploring the issues to make progress. European Journal of Obstetrics & Gynecology and Reproductive Biology. 151(2). 143–148. 36 indexed citations
5.
Figarella‐Branger, Dominique, et al.. (2002). Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation. Neuromuscular Disorders. 12(1). 4–12. 20 indexed citations
6.
Bernard, Rafaëlle, Amandine Boyer, Perrine Malzac, et al.. (2002). Prenatal detection of the 17p11.2 duplication in Charcot-Marie-Tooth disease type 1A: necessity of a multidisciplinary approach for heterogeneous disorders. European Journal of Human Genetics. 10(5). 297–302. 7 indexed citations
7.
Bernard, Rafaëlle, Véronique Labelle, Sandrine Tardieu, et al.. (2000). Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A. European Journal of Human Genetics. 8(3). 229–235. 3 indexed citations
8.
Missirian, Chantal, Perrine Malzac, Jean-Michel Guys, et al.. (2000). Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French family. American Journal of Medical Genetics. 95(1). 10–12. 14 indexed citations
9.
Tauber, M., Béatrice Jouret, Catherine Pienkowski, et al.. (2000). Auxological and Endocrine Evolution of 28 Children with Prader-Willi Syndrome: Effect of GH Therapy in 14 Children. Hormone Research in Paediatrics. 53(6). 279–287. 66 indexed citations
10.
Moncla, Anne, Perrine Malzac, Marie‐Antoinette Voelckel, et al.. (1999). Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients. European Journal of Human Genetics. 7(2). 131–139. 78 indexed citations
11.
Piétu, Geneviève, Martine Le Cunff, Perrine Malzac, et al.. (1999). Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes. Neuromuscular Disorders. 9(1). 3–10. 21 indexed citations
12.
Malzac, Perrine, Hayley Webber, A. Moncla, et al.. (1998). Mutation Analysis of UBE3A in Angelman Syndrome Patients. The American Journal of Human Genetics. 62(6). 1353–1360. 121 indexed citations
13.
Lacombe, Didier, A. Moncla, Perrine Malzac, Marie‐Geneviève Mattéi, & J Battin. (1997). Syndrome de Smith-Magenis. Archives de Pédiatrie. 4(5). 438–442. 1 indexed citations
14.
Jay, Philippe, Claire Rougeulle, Annick Massacrier, et al.. (1997). The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17(3). 357–361. 205 indexed citations
15.
Mignon, C., Perrine Malzac, A. Moncla, et al.. (1996). Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect. European Journal of Human Genetics. 4(2). 88–100. 54 indexed citations
16.
17.
Boccaccio, Irène, et al.. (1996). Unexpected Inheritance of the(CGG)(n) Trinucleotide Expansion in aFragile X Syndrome Family. European Journal of Human Genetics. 4(1). 8–12. 9 indexed citations
18.
Desgeorges, Marie, et al.. (1994). A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patient. Human Molecular Genetics. 3(2). 369–370. 6 indexed citations
19.
Romey, Marie‐Catherine, et al.. (1994). Homozygosity for a novel missense mutation (1175V) in exon 5 of the CFTR gene in a family of Armenian descent. Human Molecular Genetics. 3(4). 661–662. 4 indexed citations
20.
Sorrentino, Vincenzo, Giuseppe Giannini, Perrine Malzac, & Marie‐Geneviève Mattéi. (1993). Localization of a Novel Ryanodine Receptor Gene (RYR3) to Human Chromosome 15q14-q15 by in Situ Hybridization. Genomics. 18(1). 163–165. 28 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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