Marie‐Pierre Moizard

2.1k total citations · 1 hit paper
19 papers, 1.1k citations indexed

About

Marie‐Pierre Moizard is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Marie‐Pierre Moizard has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Marie‐Pierre Moizard's work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic Syndromes and Imprinting (5 papers) and RNA modifications and cancer (5 papers). Marie‐Pierre Moizard is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genetic Syndromes and Imprinting (5 papers) and RNA modifications and cancer (5 papers). Marie‐Pierre Moizard collaborates with scholars based in France, Germany and Netherlands. Marie‐Pierre Moizard's co-authors include Claude Moraine, Martine Raynaud, Christian Andrés, Annick Toutain, Nathalie Ronce, Sylvain Briault, Hans‐Hilger Ropers, Frédéric Laumonnier, Jamel Chelly and Marie Gomot and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and Human Genetics.

In The Last Decade

Marie‐Pierre Moizard

17 papers receiving 1.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marie‐Pierre Moizard France	11	697	569	331	173	90	19	1.1k
Paolo Alfieri Italy	20	648 0.9×	327 0.6×	187 0.6×	144 0.8×	65 0.7×	69	1.1k
Genila Bibat United States	20	552 0.8×	495 0.9×	351 1.1×	71 0.4×	52 0.6×	35	925
Sahana Nagabhushan Kalburgi United States	10	417 0.6×	397 0.7×	137 0.4×	140 0.8×	106 1.2×	16	740
Tracey Flint Denmark	20	900 1.3×	768 1.3×	245 0.7×	188 1.1×	90 1.0×	44	1.4k
Seda S. Tolu United States	9	349 0.5×	421 0.7×	473 1.4×	212 1.2×	41 0.5×	34	992
Sabrina Buoni Italy	20	611 0.9×	745 1.3×	312 0.9×	165 1.0×	156 1.7×	56	1.4k
Judith St‐Onge Canada	17	534 0.8×	581 1.0×	379 1.1×	141 0.8×	62 0.7×	32	1.3k
Valeswara‐Rao Gazula United States	10	667 1.0×	356 0.6×	145 0.4×	407 2.4×	79 0.9×	11	1.1k
Srihari C. Sampath United States	13	1.2k 1.7×	322 0.6×	90 0.3×	238 1.4×	172 1.9×	17	1.6k
SakkuBai Naidu United States	15	483 0.7×	643 1.1×	354 1.1×	87 0.5×	45 0.5×	18	991

Countries citing papers authored by Marie‐Pierre Moizard

Since Specialization

Citations

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

Fields of papers citing papers by Marie‐Pierre Moizard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie‐Pierre Moizard. 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 Marie‐Pierre Moizard. The network helps show where Marie‐Pierre Moizard may publish in the future.

Co-authorship network of co-authors of Marie‐Pierre Moizard

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

All Works

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19 of 19 papers shown

Moizard, Marie‐Pierre, Nathalie Ronce, Paul Guéguen, et al.. (2025). Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2. American Journal of Medical Genetics Part A. 200(3). 744–748.

Ronce, Nathalie, Benjamin Cogné, Thomas Besnard, et al.. (2024). Identification of a Rare Branch Point Variant in the SMS Gene in a Large Family With a Severe Form of Snyder–Robinson Syndrome. Clinical Genetics. 107(2). 231–233.

Jeanne, Médéric, Marie‐Laure Vuillaume, Valerie E. Vancollie, et al.. (2021). Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. Human Genetics. 140(6). 885–896. 14 indexed citations

Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Alessandra Baumer, et al.. (2019). CUGC for Simpson-Golabi-Behmel syndrome (SGBS). European Journal of Human Genetics. 27(4). 663–668. 10 indexed citations

Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Jean‐Luc Alessandri, et al.. (2018). Mutation update for theGPC3gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Human Mutation. 39(6). 790–805. 22 indexed citations

Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations

Jedraszak, Guillaume, M Girard, D. Djeddi, et al.. (2013). A patient with Simpson–Golabi–Behmel syndrome, biliary cirrhosis and successful liver transplantation. American Journal of Medical Genetics Part A. 164(3). 774–777. 5 indexed citations

Ratbi, Ilham, Siham Chafai Elalaoui, Marie‐Pierre Moizard, Martine Raynaud, & Abdelaziz Sefiani. (2011). Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome.. PubMed. 52(5). 525–8. 2 indexed citations

Pénisson-Besnier, I., Thibaud Lebouvier, Marie‐Pierre Moizard, et al.. (2008). Carotid artery dissection in an adult with the Simpson–Golabi–Behmel syndrome. American Journal of Medical Genetics Part A. 146A(4). 464–467. 15 indexed citations

10.

Béroud, Christophe, Sylvie Tuffery‐Giraud, Masafumi Matsuo, et al.. (2006). Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy. Human Mutation. 28(2). 196–202. 156 indexed citations

11.

Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

12.

Gomot, Marie, Nathalie Ronce, Ramzi Zemni, et al.. (2002). TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment. American Journal of Medical Genetics. 112(4). 400–404. 9 indexed citations

13.

Moizard, Marie‐Pierre, Annick Toutain, Martine Raynaud, et al.. (2000). Severe cognitive impairment in DMD: obvious clinical evidence for Dp71 isoform point mutations screening. European Journal of Human Genetics. 8(7). 552–556. 86 indexed citations

14.

Raynaud, Martine, Marie‐Pierre Moizard, Sylvain Briault, et al.. (2000). Systematic analysis of X-inactivation in 19 XLMR families: extremely skewed profiles in carriers in three families. European Journal of Human Genetics. 8(4). 253–258. 17 indexed citations

15.

Ronce, Nathalie, Martine Raynaud, Annick Toutain, et al.. (1999). Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinical and molecular data in one family. American Journal of Medical Genetics. 83(2). 132–137. 10 indexed citations

16.

Moizard, Marie‐Pierre, et al.. (1998). Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy?. American Journal of Medical Genetics. 80(1). 32–41. 97 indexed citations

17.

Ronce, Nathalie, Marie‐Pierre Moizard, Laura Robb, et al.. (1997). A C2055T Transition in Exon 8 of the ATP7A Gene Is Associated with Exon Skipping in an Occipital Horn Syndrome Family. The American Journal of Human Genetics. 61(1). 233–238. 4 indexed citations

18.

Raynaud, Martine, Chantal Gendrot, Anne Moncla, et al.. (1996). X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1. American Journal of Medical Genetics. 64(1). 97–106. 12 indexed citations

19.

Gendrot, Chantal, Nathalie Ronce, Annick Toutain, et al.. (1994). X‐linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region. Clinical Genetics. 45(3). 145–153. 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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