A. Moncla

1.7k total citations
29 papers, 1.1k citations indexed

About

A. Moncla is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Moncla has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Moncla's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Syndromes and Imprinting (6 papers). A. Moncla is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Syndromes and Imprinting (6 papers). A. Moncla collaborates with scholars based in France, United Kingdom and Italy. A. Moncla's co-authors include Perrine Malzac, Marie‐Geneviève Mattéi, N. Philip, D. Depétris, Laurent Villard, Cécile Mignon‐Ravix, Marie‐Antoinette Voelckel, André Mégarbané, Mark C. Hirst and A Flannery and has published in prestigious journals such as Neurology, Journal of Cell Science and The American Journal of Human Genetics.

In The Last Decade

A. Moncla

28 papers receiving 1.1k citations

Peers

Countries citing papers authored by A. Moncla

Since Specialization

Citations

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

Fields of papers citing papers by A. Moncla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Moncla

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

#	Work	Indexed citations
1	Novel FOXG1 mutations associated with the congenital variant of Rett syndrome 2009 ·Journal of Medical Genetics ·Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, (unknown), Roberta De Filippis, Nadia Bahi‐Buisson, Juliette Nectoux, (unknown), Thierry Bienvenu, A. Moncla, B. Chabrol, Laurent Villard, Zita Krūmiņa, Judith Armstrong, (unknown), M. Pineda, Eva Gak, Francesca Mari, Francesca Ariani, Alessandra Renieri	74
2	Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update 2005 ·European Journal of Medical Genetics ·Christophe Philippe, Laurent Villard, Nicolás de Roux, Martine Raynaud, (unknown), Laurent Pasquier, Gaëtan Lesca, Julien Mancini, Philippe Jonveaux, A. Moncla, Jamel Chelly, Thierry Bienvenu	57
3	Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation 2005 ·American Journal of Medical Genetics Part A ·N. Philip, Laurence Colleaux, Sabine Sigaudy, Tania Attié‐Bitach, Chantal Missirian, A. Moncla, Marie‐Geneviève Mattéi, G. Bollini	4
4	Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene 2005 ·Reproductive BioMedicine Online ·Anne Girardet, A. Moncla, S. Hamamah, Mireille Claustres	2
5	DNMT3B mutations and DNA methylation defect define two types of ICF syndrome 2004 ·Human Mutation ·(unknown), Muriel Rigolet, Déborah Bourc’his, Fabienne Nigon, Işık Bökesoy, J P Fryns, Maj Hultén, Philippe Jonveaux, P Maraschio, André Mégarbané, A. Moncla, E. Viégas-Pèquignot	88
6	Phénotypes neuropsychologiques des génopathies 2000 ·Archives de Pédiatrie ·Marie-Odile Livet, (unknown), A. Moncla, Julien Mancini	1
7	Auxological and Endocrine Evolution of 28 Children with Prader-Willi Syndrome: Effect of GH Therapy in 14 Children 2000 ·Hormone Research in Paediatrics ·M. Tauber, (unknown), Béatrice Jouret, Catherine Pienkowski, Perrine Malzac, A. Moncla, P Rochiccioli	66
8	Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcoma 2000 ·European Journal of Pediatrics ·Sabine Sigaudy, (unknown), A. David, J. Vigneron, Didier Lacombe, A. Moncla, Elisabeth Flori, N. Philip	23
9	SHOX gene mutations and deletions in dyschondrosteosis or Leri‐Weill syndrome 1999 ·Acta Paediatrica ·Valérie Cormier‐Daire, (unknown), Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, A. Moncla, Michel Vekemans, M. Le Merrer, Arnold Münnich	20
10	Mutation Analysis of UBE3A in Angelman Syndrome Patients 1998 ·The American Journal of Human Genetics ·Perrine Malzac, Hayley Webber, A. Moncla, John M. Graham, Mary K. Kukolich, Charles A. Williams, Roberta A Pagon, Linda Ramsdell, Tatsuya Kishino, Joseph Wagstaff	121
11	Congenital bowing of the long bones in two fetuses presenting features of Stuve-Wiedemann syndrome and Schwartz- Jampel syndrome type 2 1998 ·Clinical Dysmorphology ·Sabine Sigaudy, A. Moncla, C. Fredouille, (unknown), Jérôme Lambert, N. Philip	9
12	Syndrome de Smith-Magenis 1997 ·Archives de Pédiatrie ·Didier Lacombe, A. Moncla, Perrine Malzac, Marie‐Geneviève Mattéi, J Battin	1
13	Le syndrome de Smith-Magenis 1997 ·Archives de Pédiatrie ·(unknown), A. Moncla, B Delobel, M. F. Croquette, N. Philip, Louis Vallée	0
14	Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect 1996 ·European Journal of Human Genetics ·C. Mignon, Perrine Malzac, A. Moncla, D. Depétris, Nathalie Roëckel, Marie‐Françoise Croquette, Marie‐Geneviève Mattéi	54
15	Unexpected Inheritance of the(CGG)(n) Trinucleotide Expansion in aFragile X Syndrome Family 1996 ·European Journal of Human Genetics ·Irène Boccaccio, (unknown), Perrine Malzac, (unknown), Marie‐Antoinette Voelckel, A. Moncla, (unknown)	9
16	Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome 1995 ·Clinical Dysmorphology ·N. Philip, (unknown), A. Moncla, Sabine Sigaudy, Nelci Zanon, G. Léna, M Choux	29
17	Ondine-Hirschsprung syndrome (Haddad syndrome) 1993 ·European Journal of Pediatrics ·Alain Verloès, (unknown), Didier Lacombe, (unknown), E. Rebuffat, J L Demarquez, A. Moncla, E Adám	42
18	Prader-Willi syndrome: Diagnostic strategy with a cytogenetic and molecular approach 1993 ·Neuromuscular Disorders ·Perrine Malzac, A. Moncla, Marie‐Antoinette Voelckel, M.O. Livet, (unknown), Marie‐Geneviève Mattéi, J. F. Mattéi	1
19	Physical mapping of an Xq-proximal interstitial duplication in a male 1992 ·Human Genetics ·Françoise Muscatelli, (unknown), N. Philip, A. Moncla, Marie‐Geneviève Mattéi, J. F. Mattéi, Michel Fontés	11
20	Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases. 1991 ·Journal of Medical Genetics ·A. Moncla, M.O. Livet, (unknown), J. F. Mattéi, Marie‐Geneviève Mattéi, F Giraud	32

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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