Judith Melki

1.8k total citations
8 papers, 230 citations indexed

About

Judith Melki is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Judith Melki has authored 8 papers receiving a total of 230 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Judith Melki's work include RNA modifications and cancer (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Judith Melki is often cited by papers focused on RNA modifications and cancer (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Judith Melki collaborates with scholars based in France, Italy and Germany. Judith Melki's co-authors include Solange Bertrandy, Olivier Clermont, Philippe Burlet, Ana Lúcia Brunialti Godard, Arnold Münnich, Louis Viollet, Suzie Lefebvre, Corinne Cruaud, Chiara Franzin and Muriel Coulpier and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Stem Cells.

In The Last Decade

Judith Melki

8 papers receiving 228 citations

Peers

Countries citing papers authored by Judith Melki

Since Specialization

Citations

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

Fields of papers citing papers by Judith Melki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Melki

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	KIF1C Variants Are Associated with Hypomyelination, Ataxia, Tremor, and Dystonia in Fraternal Twins 2019 ·Tremor and Other Hyperkinetic Movements ·(unknown), Aurélie Méneret, Boris Keren, Judith Melki, Christian Denier, Alexandra Dürr, Emmanuelle Apartis, Odile Boespflug‐Tanguy, Fanny Mochel	9
2	KIF1C Variants Are Associated with Hypomyelination, Ataxia, Tremor, and Dystonia in Fraternal Twins 2019 ·SHILAP Revista de lepidopterología ·(unknown), Aurélie Méneret, Boris Keren, Judith Melki, Christian Denier, Alexandra Dürr, Emmanuelle Apartis, Odile Boespflug‐Tanguy, Fanny Mochel	7
3	Amniotic Fluid Stem Cells Restore the Muscle Cell Niche in a HSA‐Cre , Smn ^F7/F7 Mouse Model 2012 ·Stem Cells ·Martina Piccoli, Chiara Franzin, (unknown), Luca Urbani, Bert Blaauw, (unknown), Elisa Taschin, Angelo Cenedese, Giovanni Franco Zanon, Isabelle André‐Schmutz, Antonio Rosato, Judith Melki, Marina Cavazzana, Michela Pozzobon, Paolo De Coppi	47
4	Juvenile‐onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA gene 1997 ·Annals of Neurology ·Ruth Navon, Rami Khosravi, Judith Melki, Liat Drucker, Bertrand Fontaine, (unknown), (unknown), Michel Fardeau, Pierre Rondot, (unknown)	15
5	Spinal muscular atrophy 1997 ·Current Opinion in Neurology ·Judith Melki	78
6	cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn) 1997 ·Genomics ·Louis Viollet, Solange Bertrandy, Ana Lúcia Brunialti Godard, Suzie Lefebvre, Philippe Burlet, Olivier Clermont, Corinne Cruaud, (unknown), Arnold Münnich, Judith Melki	59
7	Early detection of mouse wobbler mutation 1994 ·Neuroreport ·Vincent des Portes, Muriel Coulpier, Judith Melki, Patrick A. Dreyfus	13
8	Machado-Joseph Disease Is Genetically Different from Holguin Dominant Ataxia (SCA2) 1993 ·Genomics ·Isabel Silveira, (unknown), Judith Melki, (unknown), Astrid Lunkes, (unknown), Suzana Gispert, Philippe Burlet, Jean‐Michel Rozet, Paula Coutinho, José Leal Loureiro, Joao C. Guimaraes, Georg Auburger, Arnold Münnich, Jorge Sequeiros	2

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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