Louise Telvi

928 total citations
31 papers, 600 citations indexed

About

Louise Telvi is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Louise Telvi has authored 31 papers receiving a total of 600 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Immunology. Recurrent topics in Louise Telvi's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Sexual Differentiation and Disorders (5 papers). Louise Telvi is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Sexual Differentiation and Disorders (5 papers). Louise Telvi collaborates with scholars based in France, Italy and Japan. Louise Telvi's co-authors include Jacques Barbet, Aziza Lebbar, J L Chaussain, Jean Gogusev, Alexandra Ion, Ken McElreavey, Stanislas du Manoir, M Levardon, Jean‐Louis Chaussain and A Pompidou and has published in prestigious journals such as PEDIATRICS, Journal of the American Society of Nephrology and Thorax.

In The Last Decade

Louise Telvi

31 papers receiving 569 citations

Peers

Countries citing papers authored by Louise Telvi

Since Specialization

Citations

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

Fields of papers citing papers by Louise Telvi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Telvi

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Telvi. A scholar is included among the top collaborators of Louise Telvi 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 Louise Telvi. Louise Telvi 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	Establishment and characterization of a human parathyroid carcinoma derived cell line 2014 ·Pathology - Research and Practice ·Jean Gogusev, Ichiro Murakami, Louise Telvi, (unknown), E. Sarfati, Francis Jaubert	2
2	Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia 2008 ·Cancer Genetics and Cytogenetics ·(unknown), Ichiro Murakami, (unknown), Louise Telvi, Marc Jeanpierre, C Nézelof, Francis Jaubert, Jean Gogusev	7
3	Pure proximal deletion of chromosome 21 and kyphosis 2007 ·European Journal of Medical Genetics ·Boris Keren, (unknown), Annick Toutain, Delphine Héron, B. Fouquet, Béatrice Laudier, Louise Telvi, Serge Romana, Michel Vekemans, Damien Sanlaville	4
4	Early Pattern of Epilepsy in the Ring Chromosome 20 Syndrome 2006 ·Epilepsia ·Dorothée Ville, Anna Kamińska, Nadia Bahi‐Buisson, Arnaud Biraben, Perrine Plouin, Louise Telvi, Olivier Dulac, Catherine Chiron	31
5	DOR-1, A novel CD10+ stromal cell line derived from progressive Langerhans cell histiocytosis of bone 2004 ·Pediatric Blood & Cancer ·Jean Gogusev, Louise Telvi, Ichiro Murakami, Yves Lepelletier, C Nézelof, (unknown), Christophe Glorion, Francis Jaubert	4
6	Molecular Cytogenetic Aberrations in Autosomal Dominant Polycystic Kidney Disease Tissue 2003 ·Journal of the American Society of Nephrology ·Jean Gogusev, Ichiro Murakami, (unknown), Louise Telvi, (unknown), Philippe Lesavre, D Droz	28
7	Molecular cytogenetic aberrations in CD30+ anaplastic large cell lymphoma cell lines 2002 ·Cancer Genetics and Cytogenetics ·Jean Gogusev, Louise Telvi, C Nézelof	12
8	A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient. 2002 ·PubMed ·Antonio Pizzuti, Giuseppe Calabrese, Maura Bozzali, Louise Telvi, Elisena Morizio, Valentina Guida, Valentina Gatta, Liborio Stuppia, Alexandra Ion, Giandomenico Palka, Bruno Dallapiccola	30
9	Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 2000 ·European Journal of Human Genetics ·G Calabrese, Louise Telvi, (unknown), Elisena Morizio, Antonio Pizzuti, Liborio Stuppia, Roberta Bordoni, Alexandra Ion, Donatella Fantasia, Rita Mingarelli, Giandomenico Palka	30
10	Detection of DNA copy number changes in human endometriosis by comparative genomic hybridization 1999 ·Human Genetics ·Jean Gogusev, (unknown), Louise Telvi, (unknown), Stanislas du Manoir, (unknown), M Levardon	63
11	45,X/46,XY Mosaicism: Report of 27 Cases 1999 ·PEDIATRICS ·Louise Telvi, Aziza Lebbar, (unknown), Jacques Barbet, J L Chaussain	143
12	Detection of DNA copy number changes in human endometriosis by comparative genomic hybridization 1999 ·Human Genetics ·Jean Gogusev, (unknown), Louise Telvi, (unknown), Stanislas du Manoir, (unknown), M Levardon	20
13	Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene 1998 ·Human Genetics ·(unknown), Louise Telvi, Jean-Louis Chaussain, Jacques Barbet, (unknown), (unknown), (unknown), Marc Fellous, Ken McElreavey	19
14	A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome. 1996 ·PubMed ·Alexandra Ion, Louise Telvi, Jean‐Louis Chaussain, Frederic Galactéros, (unknown), M Fellous, Ken McElreavey	47
15	Gonadal dysgenesis in del(18p) syndrome 1995 ·American Journal of Medical Genetics ·Louise Telvi, (unknown), Alexandra Ion, Françoise Fouquet, Yves Le Bouc, Jean‐Louis Chaussain	16
16	Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion 1995 ·Human Genetics ·Attila Tar, (unknown), (unknown), Alexandra Ion, Louise Telvi, Sandrine Barbaux, (unknown), Éric Vilain, Marc Fellous, Ken McElreavey	15
17	Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21) 1992 ·American Journal of Medical Genetics ·Louise Telvi, (unknown), O Raoul, Josué Feingold, G Ponsot, A Pompidou, (unknown), J Lejeune	3
18	CASE REPORT Lesch-Nyhan syndrome in a girl 1992 ·Patrick Van Bogaert, I. Ceballos, Isabelle Desguerre, Louise Telvi, P. Kamoun, G Ponsot	1
19	De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome. 1992 ·Journal of Medical Genetics ·Louise Telvi, J.-M. Pinard, (unknown), Pierre‐Marie Sinet, Annie Nicole, J Feingold, Olivier Dulac, A Pompidou, G Ponsot	4
20	Study of immunoglobulins in pleura and pleural effusions. 1979 ·Thorax ·Louise Telvi, Francis Jaubert, A Eyquem, J P Andreux, François Labrousse, J Chrétien	17

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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