Patrick Thierry

645 total citations
8 papers, 310 citations indexed

About

Patrick Thierry is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pharmacy. According to data from OpenAlex, Patrick Thierry has authored 8 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Pharmacy. Recurrent topics in Patrick Thierry's work include Axon Guidance and Neuronal Signaling (2 papers), Oral and gingival health research (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Patrick Thierry is often cited by papers focused on Axon Guidance and Neuronal Signaling (2 papers), Oral and gingival health research (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Patrick Thierry collaborates with scholars based in France, Germany and United States. Patrick Thierry's co-authors include Giovanni Castelnovo, Anne Ducros, Elisabeth Tournier‐Lasserve, Christian Denier, A Autret, Anne Joutel, Patrick Van Bogaert, Sonia Alamowitch, E Roullet and T Deonna and has published in prestigious journals such as Neurology, Human Mutation and Human Genetics.

In The Last Decade

Patrick Thierry

8 papers receiving 304 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Patrick Thierry France 7 206 152 62 56 39 8 310
Emily V. Fletcher United States 10 195 0.9× 114 0.8× 21 0.3× 35 0.6× 26 0.7× 14 381
Tara Newcomb United States 10 263 1.3× 119 0.8× 116 1.9× 63 1.1× 37 0.9× 12 454
Neven Maksemous Australia 12 121 0.6× 89 0.6× 134 2.2× 81 1.4× 124 3.2× 28 362
M. Pérez-Pérez Spain 7 89 0.4× 183 1.2× 14 0.2× 38 0.7× 12 0.3× 7 335
Isabel Espinosa-Medina United States 9 225 1.1× 97 0.6× 34 0.5× 35 0.6× 19 0.5× 11 452
Anahí Hurtado‐Chong Switzerland 11 231 1.1× 150 1.0× 48 0.8× 9 0.2× 10 0.3× 17 475
Kohji Kato Japan 9 130 0.6× 187 1.2× 50 0.8× 138 2.5× 7 0.2× 21 384
Raoul van de Graaf Netherlands 6 240 1.2× 129 0.8× 81 1.3× 80 1.4× 10 0.3× 9 362
Maurizio Giorelli Italy 13 84 0.4× 87 0.6× 18 0.3× 129 2.3× 25 0.6× 28 439
Marina Lai Italy 10 79 0.4× 66 0.4× 58 0.9× 57 1.0× 36 0.9× 12 420

Countries citing papers authored by Patrick Thierry

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Thierry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Thierry

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

All Works

8 of 8 papers shown
1.
Borck, Guntram, Liat de Vries, Pola Smirin‐Yosef, et al.. (2014). Homozygous truncating PTPRF mutation causes athelia. Human Genetics. 133(8). 1041–1047. 6 indexed citations
2.
Feldmann, Delphine, Cédric Le Maréchal, Laurence Jonard, et al.. (2008). A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss. European Journal of Medical Genetics. 52(4). 195–200. 38 indexed citations
3.
Canún, Sonia, Martin B. Delatycki, Gabriele Gillessen‐Kaesbach, et al.. (2008). No mutation in genes of the WNT signaling pathway in patients with Zimmermann–Laband syndrome. Clinical Dysmorphology. 17(3). 181–185. 10 indexed citations
4.
Wieland, Ilse, William Reardon, Sigrid Tinschert, et al.. (2007). Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic. European Journal of Human Genetics. 16(2). 184–191. 20 indexed citations
5.
Bohring, Axel, et al.. (2006). New cases of Bohring–Opitz syndrome, update, and critical review of the literature. American Journal of Medical Genetics Part A. 140A(12). 1257–1263. 22 indexed citations
6.
Wieland, Ilse, William Reardon, Sibylle Jakubiczka, et al.. (2005). Twenty-six novelEFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS). Human Mutation. 26(2). 113–118. 53 indexed citations
7.
Douard, M.C., Mario Di Palma, Sylvie Chevret, et al.. (2005). Prospective, double-blind, randomized trial of equimolar mixture of nitrous oxide/oxygen to prevent pain induced by insertion of venous access ports in cancer patients. Supportive Care in Cancer. 14(2). 161–166. 10 indexed citations
8.
Denier, Christian, Anne Ducros, Katayoun Vahedi, et al.. (1999). High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2. Neurology. 52(9). 1816–1816. 151 indexed citations

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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