Daniel Hantaı̈

3.5k total citations
63 papers, 1.7k citations indexed

About

Daniel Hantaı̈ is a scholar working on Molecular Biology, Neurology and Cancer Research. According to data from OpenAlex, Daniel Hantaı̈ has authored 63 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 22 papers in Neurology and 21 papers in Cancer Research. Recurrent topics in Daniel Hantaı̈'s work include Protease and Inhibitor Mechanisms (21 papers), Myasthenia Gravis and Thymoma (17 papers) and Blood Coagulation and Thrombosis Mechanisms (13 papers). Daniel Hantaı̈ is often cited by papers focused on Protease and Inhibitor Mechanisms (21 papers), Myasthenia Gravis and Thymoma (17 papers) and Blood Coagulation and Thrombosis Mechanisms (13 papers). Daniel Hantaı̈ collaborates with scholars based in France, United States and Germany. Daniel Hantaı̈'s co-authors include Barry W. Festoff, B. Eymard, Jia‐Sheng Rao, Mohammed Akaaboune, Jeanine Koenig, Frédéric Chevessier, Martine Verdière‐Sahuqué, Pascale Richard, David Beeson and Hanns Lochmüller and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and The Journal of Cell Biology.

In The Last Decade

Daniel Hantaı̈

62 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Hantaı̈ France 26 900 488 400 304 286 63 1.7k
H.J.M. Smeets Netherlands 30 1.5k 1.7× 121 0.2× 100 0.3× 290 1.0× 244 0.9× 63 2.4k
Alessandro Malandrini Italy 26 973 1.1× 577 1.2× 210 0.5× 591 1.9× 216 0.8× 95 2.2k
Craig A. Krekoski Canada 15 606 0.7× 205 0.4× 190 0.5× 598 2.0× 206 0.7× 18 1.8k
Mehrdad Khajavi United States 21 1.5k 1.7× 517 1.1× 219 0.5× 984 3.2× 51 0.2× 31 2.6k
Juan J. Archelos Austria 30 609 0.7× 760 1.6× 109 0.3× 648 2.1× 83 0.3× 45 3.0k
Chaim Jalas United States 23 724 0.8× 191 0.4× 231 0.6× 177 0.6× 60 0.2× 60 1.7k
Ji-Ung Jung United States 20 702 0.8× 209 0.4× 224 0.6× 143 0.5× 94 0.3× 29 1.3k
Gregory L. Bennett United States 17 943 1.0× 61 0.1× 242 0.6× 494 1.6× 153 0.5× 21 2.3k
Melissa C. Colbert United States 26 1.8k 2.0× 39 0.1× 216 0.5× 258 0.8× 372 1.3× 33 2.8k
Anne L. Prieto United States 23 684 0.8× 79 0.2× 515 1.3× 389 1.3× 74 0.3× 30 2.1k

Countries citing papers authored by Daniel Hantaı̈

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Hantaı̈

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Hantaı̈

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

All Works

20 of 20 papers shown
1.
Mussini, Jean‐Marie, Armelle Magot, Daniel Hantaı̈, et al.. (2015). Atypical nuclear abnormalities in a patient with Brody disease. Neuromuscular Disorders. 25(10). 773–779. 4 indexed citations
2.
Eymard, B., Daniel Hantaı̈, Emmanuel Fournier, et al.. (2014). Syndromes myasthéniques congénitaux — L’expérience française. Bulletin de l Académie Nationale de Médecine. 198(2). 257–271. 1 indexed citations
3.
Eymard, B., Daniel Hantaı̈, & B. Estournet. (2013). Congenital myasthenic syndromes. Handbook of clinical neurology. 113. 1469–1480. 39 indexed citations
4.
5.
Bauché, Stéphanie, Delphine Boërio, Claire-Sophie Davoine, et al.. (2013). Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome. Neuromuscular Disorders. 23(12). 998–1009. 14 indexed citations
6.
Chaouch, Amina, David Beeson, Daniel Hantaı̈, & Hanns Lochmüller. (2012). 186th ENMC International Workshop: Congenital myasthenic syndromes 24–26 June 2011, Naarden, The Netherlands. Neuromuscular Disorders. 22(6). 566–576. 29 indexed citations
7.
Wargon, I., Pascale Richard, Thierry Küntzer, et al.. (2011). Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations. Neuromuscular Disorders. 22(4). 318–324. 56 indexed citations
8.
Méjat, Alexandre, V. Decostre, Juan Li, et al.. (2009). Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy. The Journal of Cell Biology. 184(1). 31–44. 96 indexed citations
9.
Rigoard, Philippe, K. Buffenoir, Stéphanie Bauché, et al.. (2009). Modalités et outils d’observation de la jonction neuromusculaire. Neurochirurgie. 55. S43–S48.
10.
Beeson, David, Daniel Hantaı̈, Hanns Lochmüller, & Andrew G. Engel. (2005). 126th International Workshop: Congenital Myasthenic Syndromes, 24–26 September 2004, Naarden, The Netherlands. Neuromuscular Disorders. 15(7). 498–512. 67 indexed citations
11.
Andreux, F., Daniel Hantaı̈, & B. Eymard. (2004). Syndromes myasthéniques congénitaux: Expression phénotypique et caractérisation physiopathologique. Revue Neurologique. 160(2). 163–176. 2 indexed citations
12.
Faraut, Brice, Aymeric Ravel‐Chapuis, Sylvie Bonavaud, et al.. (2004). Thrombin reduces MuSK and acetylcholine receptor expression along with neuromuscular contact size in vitro. European Journal of Neuroscience. 19(8). 2099–2108. 5 indexed citations
13.
Ioos, Christine, A Barois, Pascale Richard, et al.. (2004). Congenital Myasthenic Syndrome due to Rapsyn Deficiency: Three Cases with Arthrogryposis and Bulbar Symptoms. Neuropediatrics. 35(4). 246–249. 19 indexed citations
14.
Ishigaki, Keiko, Delphine Nicolle, Éric Krejci, et al.. (2003). Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency. Neuromuscular Disorders. 13(3). 236–244. 28 indexed citations
15.
Chevessier, Frédéric, Daniel Hantaı̈, & Martine Verdière‐Sahuqué. (2001). Expression of the thrombin receptor (PAR‐1) during rat skeletal muscle differentiation. Journal of Cellular Physiology. 189(2). 152–161. 12 indexed citations
16.
Rohn, Troy T., et al.. (2001). Thrombin Receptor Induction by Injury-Related Factors in Human Skeletal Muscle Cells. Experimental Cell Research. 263(1). 77–87. 28 indexed citations
17.
Festoff, Barry W., et al.. (1998). Thrombin‐induced reversal of astrocyte stellation is mediated by activation of protein kinase C β‐1. European Journal of Biochemistry. 255(3). 766–774. 24 indexed citations
18.
Ho, Gilbert, Irina V. Smirnova, Mohammed Akaaboune, Daniel Hantaı̈, & Barry W. Festoff. (1994). Serine proteases and their serpin inhibitors in Alzheimer's disease. Biomedicine & Pharmacotherapy. 48(7). 296–304. 25 indexed citations
19.
Akaaboune, Mohammed, Marcello Villanova, Barry W. Festoff, Martine Verdière‐Sahuqué, & Daniel Hantaı̈. (1994). Apolipoprotein E expression at neuromuscular junctions in mouse, rat and human skeletal muscle. FEBS Letters. 351(2). 246–248. 30 indexed citations
20.
Akaaboune, Mohammed, et al.. (1993). The influence of denervation on β-amyloid protein precursor and α1-antichymotrypsin in mouse skeletal muscle. Neuromuscular Disorders. 3(5-6). 477–481. 6 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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