Caroline Paternotte

1.3k total citations
19 papers, 887 citations indexed

About

Caroline Paternotte is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Caroline Paternotte has authored 19 papers receiving a total of 887 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 12 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Caroline Paternotte's work include Neurological diseases and metabolism (13 papers), Hereditary Neurological Disorders (11 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Caroline Paternotte is often cited by papers focused on Neurological diseases and metabolism (13 papers), Hereditary Neurological Disorders (11 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Caroline Paternotte collaborates with scholars based in France, United Kingdom and United States. Caroline Paternotte's co-authors include Jamïlé Hazan, Alexis Brice, Jean Weissenbach, Jean‐Marc Burgunder, Delphine Samson, Corinne Cruaud, Núria Fonknechten, Alexandra Dürr, Jean-François Prud'homme and Laurence Cattolico and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Caroline Paternotte

19 papers receiving 876 citations

Peers

Countries citing papers authored by Caroline Paternotte

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Paternotte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Paternotte

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

#	Work	Indexed citations
1	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Stephan Klebe, Alexandra Dürr, Naïma Bouslam, Djamel Grid, Caroline Paternotte, Christel Depienne, Sylvain Hanein, Ahmed Bouhouche, Nizar Elleuch, Hamid Azzedine, Sandrine Poëa‐Guyon, Sylvie Forlani, (unknown), Céline Charon, Jamïlé Hazan, Alexis Brice, Giovanni Stévanin	14
2	A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21 2007 ·Neurology ·Giovanni Stévanin, Caroline Paternotte, Paula Coutinho, Stephan Klebe, N. Elleuch, José Leal Loureiro, Erwan Denis, Vítor Tedim Cruz, A. Dürr, J Prudhomme, Jean Weissenbach, Alexis Brice, Jamïlé Hazan	21
3	Analysis of the planar cell polarity gene Vangl2 and its co‐expressed paralog Vangl1 in neural tube defect patients (Am J Med Genet 136A: 90–92, 2005) 2005 ·American Journal of Medical Genetics Part A ·Kit Doudney, Gudrun E. Moore, Philip Stanier, Patricia Ybot‐González, Caroline Paternotte, Nicholas D. E. Greene, Andrew J. Copp, Roger E. Stevenson	3
4	Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia 2003 ·Molecular and Cellular Neuroscience ·J. Murdoch, Kit Doudney, Dianne Gerrelli, Noel C. Wortham, Caroline Paternotte, Philip Stanier, Andrew J. Copp	9
5	Cloning and Characterization of Igsf9 in Mouse and Human: A New Member of the Immunoglobulin Superfamily Expressed in the Developing Nervous System 2002 ·Genomics ·Kit Doudney, J. Murdoch, Claire Braybrook, Caroline Paternotte, (unknown), Andrew J. Copp, Philip Stanier	26
6	Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Unrelated Turkish Families 2001 ·Neuropediatrics ·(unknown), Rıza Köksal Özgül, Caroline Paternotte, Hayat Erdem‐Yurter, J Prudhomme, Meral Özgüç, Haluk Topaloğlu	24
7	Comparative Physical and Transcript Maps of ∼1 Mb around loop-tail, a Gene for Severe Neural Tube Defects on Distal Mouse Chromosome 1 and Human Chromosome 1q22–q23 2001 ·Genomics ·Kit Doudney, J. Murdoch, Caroline Paternotte, (unknown), Simon G. Gregory, Andrew J. Copp, Philip Stanier	13
8	A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34 2000 ·The American Journal of Human Genetics ·Bertrand Fontaine, Claire-Sophie Davoine, Alexandra Dürr, Caroline Paternotte, Imed Feki, Jean Weissenbach, Jamïlé Hazan, Alexis Brice	65
9	Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia 1999 ·Nature Genetics ·Jamïlé Hazan, Núria Fonknechten, (unknown), Caroline Paternotte, Delphine Samson, (unknown), (unknown), Corinne Cruaud, Alexandra Dürr, (unknown), Philippe Brottier, Laurence Cattolico, Valérie Barbe, Jean‐Marc Burgunder, Jean-François Prud'homme, Alexis Brice, Bertrand Fontaine, (unknown), Jean Weissenbach	464
10	Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias 1999 ·Archives of Neurology ·Paula Coutinho, José Barros, (unknown), (unknown), Cristina Alves, (unknown), (unknown), (unknown), José Leal Loureiro, João Vasco Santos, Abdelmadjid Hamri, Caroline Paternotte, Jamïlé Hazan, Carolina Silva, J Prudhomme, Djamel Grid	56
11	Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation 1999 ·Genes Chromosomes and Cancer ·Iwona Włodarska, Licia Selleri, Roberta La Starza, Caroline Paternotte, Glen A. Evans, Marc Boogaerts, Herman Van den Berghe, Cristina Mecucci	11
12	A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia 1999 ·Genomics ·Jamïlé Hazan, Claire-Sophie Davoine, (unknown), Núria Fonknechten, Caroline Paternotte, Cécile Fizames, Corinne Cruaud, Delphine Samson, Delphine Muselet, (unknown), Alexis Brice, Gàbor Gyapay, Roland Heilig, Bertrand Fontaine, Jean Weissenbach	10
13	Quality Assessment of Whole Genome Mapping Data in the Refined Familial Spastic Paraplegia Interval on Chromosome 14q 1998 ·Genome Research ·Caroline Paternotte, (unknown), Cécile Fizames, (unknown), (unknown), Alexandra Dürr, Delphine Samson, (unknown), Delphine Muselet, (unknown), Nathalie Drouot, Thomas Voit, Bertrand Fontaine, Gàbor Gyapay, Georg Auburger, Jean Weissenbach, Jamïlé Hazan	14
14	Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. 1998 ·Journal of Medical Genetics ·O. Heinzlef, Caroline Paternotte, Florence Mahieux, Jean-François Prud’homme, (unknown), M Madigand, Jean Pouget, J. Weissenbach, E Roullet, Jamïlé Hazan	50
15	[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis]. 1998 ·PubMed ·(unknown), Caroline Paternotte, Jean-François Prud’homme, J. Weissenbach, Jamïlé Hazan, Jean‐Marc Burgunder	2
16	FISH characterization of two new meyloid breakpoints in t(11;21)(q24;q11.2) translocaton associated wit Myelodysplastic Syndromes (MDS) 1996 ·British Journal of Haematology ·Iwona Włodarska, Licia Selleri, Caroline Paternotte, (unknown), D. Gareth Evans, Marc Boogaerts, Herman Van den Berghe	2
17	Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family 1996 ·Human Genetics ·Joachim Bürger, (unknown), Caroline Paternotte, (unknown), Jamïlé Hazan, André Reis	28
18	Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2 1996 ·Brain ·Alexandra Dürr, (unknown), Caroline Paternotte, (unknown), (unknown), Paula Coutinho, Catherine Lamy, Stéphane Bourgeois, J Prudhomme, Clotilde Penet, J.‐L. Mas, Jean‐Marc Burgunder, Jamïlé Hazan, J. Weissenbach, Alexis Brice, Bertrand Fontaine	67
19	High-resolution physical mapping of a 250-kb region of human chromosome 11q24 by genomic sequence sampling (GSS) 1995 ·Genomics ·Licia Selleri, Michael W. Smith, (unknown), Anthony J. Romo, (unknown), Caroline Paternotte, (unknown), (unknown), Glen A. Evans	8

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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