H. Luque

847 total citations
11 papers, 265 citations indexed

About

H. Luque is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, H. Luque has authored 11 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in H. Luque's work include Muscle Physiology and Disorders (6 papers), Cardiomyopathy and Myosin Studies (5 papers) and Ion channel regulation and function (2 papers). H. Luque is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Cardiomyopathy and Myosin Studies (5 papers) and Ion channel regulation and function (2 papers). H. Luque collaborates with scholars based in Finland, France and Hungary. H. Luque's co-authors include Bjarne Udd, Peter Hackman, J. Sarparanta, Anna Vihola, Per Harald Jonson, Juha Kere, Sara Lehtinen, Gabrielle Åhlberg, Mark Screen and Anni Evilä and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

H. Luque

10 papers receiving 264 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H. Luque Finland	6	231	129	55	50	39	11	265
Satu Sandell Finland	10	232 1.0×	114 0.9×	56 1.0×	89 1.8×	41 1.1×	21	313
Sara Lehtinen Finland	4	130 0.6×	54 0.4×	43 0.8×	27 0.5×	15 0.4×	6	158
Mridul Johari Finland	9	133 0.6×	63 0.5×	39 0.7×	54 1.1×	18 0.5×	28	194
A. Maerkens Germany	5	202 0.9×	83 0.6×	33 0.6×	69 1.4×	62 1.6×	8	275
Rosanna Trovato Italy	6	146 0.6×	43 0.3×	33 0.6×	79 1.6×	22 0.6×	20	201
S.M. Dorosz Australia	4	342 1.5×	324 2.5×	107 1.9×	95 1.9×	102 2.6×	6	421
Xavière Lornage France	10	186 0.8×	105 0.8×	40 0.7×	54 1.1×	28 0.7×	19	243
S. White Australia	5	311 1.3×	289 2.2×	108 2.0×	73 1.5×	93 2.4×	5	374
James P. Orengo United States	8	348 1.5×	45 0.3×	27 0.5×	195 3.9×	20 0.5×	14	416
L. Demay France	13	596 2.6×	301 2.3×	42 0.8×	58 1.2×	78 2.0×	18	661

Countries citing papers authored by H. Luque

Since Specialization

Citations

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

Fields of papers citing papers by H. Luque

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Luque

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

All Works

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11 of 11 papers shown

Sarparanta, J., Per Harald Jonson, Jens Reimann, et al.. (2023). Extension of the DNAJB2a isoform in a dominant neuromyopathy family. Human Molecular Genetics. 32(21). 3029–3039. 4 indexed citations

Johari, Mridul, Marco Savarese, Anna Vihola, et al.. (2020). NEW GENES IN NEUROMUSCULAR DISEASES. Neuromuscular Disorders. 30. S46–S46. 1 indexed citations

Vihola, Anna, H. Luque, Marco Savarese, et al.. (2017). Diagnostic anoctamin‐5 protein defect in patients with ANO5‐mutated muscular dystrophy. Neuropathology and Applied Neurobiology. 44(5). 441–448. 16 indexed citations

Charton, Karine, J. Sarparanta, Anna Vihola, et al.. (2015). CAPN3-mediated processing of C-terminal titin replaced by pathological cleavage in titinopathy. Human Molecular Genetics. 24(13). 3718–3731. 36 indexed citations

Jonson, Per Harald, Anni Evilä, Tanya Stojkovic, et al.. (2015). A novel mutation in DNAJB6 causes LGMD1D in two French families. Neuromuscular Disorders. 25. S236–S236.

Jonson, Per Harald, J. Sarparanta, H. Luque, & Bjarne Udd. (2012). G.P.38 The LGMD1D gene DNAJB6: Its role in sarcomeric protein maintenance and aggregation. Neuromuscular Disorders. 22(9-10). 830–831. 1 indexed citations

Hackman, Peter, J. Sarparanta, Sara Lehtinen, et al.. (2012). Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1. Annals of Neurology. 73(4). 500–509. 103 indexed citations

Muelas, Nuria, Peter Hackman, H. Luque, et al.. (2011). Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients. Clinical Genetics. 81(5). 491–494. 16 indexed citations

Hackman, Peter, Satu Sandell, J. Sarparanta, et al.. (2011). Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus. Neuromuscular Disorders. 21(5). 338–344. 16 indexed citations

10.

Sarparanta, J., Per Harald Jonson, H. Luque, & Bjarne Udd. (2011). P2.26 LGMD1D mutations impair the antiaggregation activity of DNAJB6. Neuromuscular Disorders. 21(9-10). 668–668. 1 indexed citations

11.

Muelas, Nuria, Peter Hackman, H. Luque, et al.. (2010). MYH7 gene tail mutation causing myopathic profiles beyond Laing distal myopathy. Neurology. 75(8). 732–741. 71 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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