Joëlle Augé

954 total citations
9 papers, 583 citations indexed

About

Joëlle Augé is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Joëlle Augé has authored 9 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Surgery. Recurrent topics in Joëlle Augé's work include Hedgehog Signaling Pathway Studies (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Renal and related cancers (2 papers). Joëlle Augé is often cited by papers focused on Hedgehog Signaling Pathway Studies (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Renal and related cancers (2 papers). Joëlle Augé collaborates with scholars based in France, Belarus and Switzerland. Joëlle Augé's co-authors include Tania Attié‐Bitach, Michel Vekemans, Arnold Münnich, Heather Etchevers, Paul Czernichow, Michel Polak, Stanislas Lyonnet, Férechté Encha‐Razavi, Florence Molinari and Virginia Meskenaïte and has published in prestigious journals such as Science, The Journal of Clinical Endocrinology & Metabolism and Biochemical and Biophysical Research Communications.

In The Last Decade

Joëlle Augé

9 papers receiving 570 citations

Peers

Countries citing papers authored by Joëlle Augé

Since Specialization

Citations

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

Fields of papers citing papers by Joëlle Augé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joëlle Augé

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	PAX8,TITF1, andFOXE1Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations 2005 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Joëlle Augé, (unknown), Heather Etchevers, (unknown), Paul Czernichow, Michel Vekemans, Michel Polak, Tania Attié‐Bitach	151
2	Gene expression in pharyngeal arch 1 during human embryonic development 2005 ·Human Molecular Genetics ·Juanliang Cai, David E. Ash, Lori E. Kotch, Ethylin Wang Jabs, Tania Attié‐Bitach, Joëlle Augé, (unknown), Heather Etchevers, Michel Vekemans, (unknown), Rose M. Tidwell, D. Messina, (unknown), Michael Lovett	28
3	Expression of the SMADIP1 gene during early human development 2002 ·Mechanisms of Development ·Yolanda Espinosa‐Parrilla, Jeanne Amiel, Joëlle Augé, Férechté Encha‐Razavi, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Tania Attié‐Bitach	27
4	Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation 2002 ·Science ·Florence Molinari, Marlène Rio, Virginia Meskenaïte, (unknown), Joëlle Augé, Delphine Bacq, Sylvain Briault, Michel Vekemans, Arnold Münnich, Tania Attié‐Bitach, P. Sonderegger, Laurence Colleaux	138
5	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain 2000 ·The American Journal of Human Genetics ·Renaud Touraine, Tania Attié‐Bitach, E. Manceau, Eckhard Korsch, Pierre Sarda, Véronique Pingault, Férechté Encha‐Razavi, Anna Pelet, Joëlle Augé, A Nivelon‐Chevallier, A. M. Holschneider, Marc Munnes, (unknown), Michel Goossens, Arnold Munnich, (unknown), Stanislas Lyonnet	124
6	PAX2 mutations in renal–coloboma syndrome: mutational hotspot and germline mosaicism 2000 ·European Journal of Human Genetics ·Jeanne Amiel, Sophie Audollent, Dominique Joly, P. Dureau, Rémi Salomon, (unknown), Joëlle Augé, François Bouissou, Corinne Antignac, Marie-Claire Gübler, (unknown), Arnold Münnich, Michel Vekemans, Stanislas Lyonnet, Tania Attié‐Bitach	58
7	Expression of the Sonic Hedgehog gene in human embryos with neural tube defects 2000 ·Teratology ·I A Kirillova, (unknown), Joëlle Augé, Sophie Audollent, (unknown), Férechté Encha‐Razavi, G. I. Lazjuk, Tania Attié‐Bitach, Michel Vekemans	2
8	Expression of the Sonic Hedgehog gene in human embryos with neural tube defects 2000 ·Teratology ·I A Kirillova, (unknown), Joëlle Augé, Sophie Audollent, (unknown), Férechté Encha‐Razavi, G. I. Lazjuk, Tania Attié‐Bitach, Michel Vekemans	36
9	Salvage of 5′-deoxy-5′-methylthioadenosine and L-homocysteine into methionine in cells cultured in a methionine-free medium: A study of “methionine-dependence” 1986 ·Biochemical and Biophysical Research Communications ·Laurence Christa, Joëlle Kersual, Joëlle Augé, Jean‐Louis Pérignon	19

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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