Juan Pié

3.1k total citations
65 papers, 1.4k citations indexed

About

Juan Pié is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Juan Pié has authored 65 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 13 papers in Genetics. Recurrent topics in Juan Pié's work include Genomics and Chromatin Dynamics (24 papers), RNA Research and Splicing (18 papers) and Metabolism and Genetic Disorders (17 papers). Juan Pié is often cited by papers focused on Genomics and Chromatin Dynamics (24 papers), RNA Research and Splicing (18 papers) and Metabolism and Genetic Disorders (17 papers). Juan Pié collaborates with scholars based in Spain, Germany and United States. Juan Pié's co-authors include Feliciano J. Ramos, Beatriz Puisac, Núria Casals, María Arnedo, Fausto G. Hegardt, Antonio Musio, Joaquín J. García, Antonie D. Kline, Matthew A. Deardorff and Victoria Mok Siu and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Experimental Medicine.

In The Last Decade

Juan Pié

60 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Juan Pié Spain	21	1.0k	333	263	213	107	65	1.4k
Jürgen‐Christoph von Kleist-Retzow Germany	19	1.3k 1.3×	122 0.4×	388 1.5×	148 0.7×	44 0.4×	25	1.6k
Heleen te Brinke Netherlands	19	1.1k 1.1×	93 0.3×	328 1.2×	326 1.5×	18 0.2×	25	1.6k
Bryant P. Bullock United States	11	946 0.9×	183 0.5×	44 0.2×	153 0.7×	140 1.3×	13	1.9k
Cleanthe Spanaki Greece	22	534 0.5×	199 0.6×	153 0.6×	243 1.1×	9 0.1×	56	1.3k
Fresnida J. Ramos United States	14	1.4k 1.3×	163 0.5×	120 0.5×	638 3.0×	226 2.1×	16	2.2k
Olli Matilainen Finland	12	858 0.8×	61 0.2×	63 0.2×	358 1.7×	92 0.9×	17	1.4k
Hans‐Georg Sprenger Germany	14	973 0.9×	41 0.1×	172 0.7×	211 1.0×	60 0.6×	16	1.3k
Christoph Boehmer Germany	24	1.2k 1.2×	132 0.4×	34 0.1×	128 0.6×	38 0.4×	27	1.6k
Verónica Nin United States	17	645 0.6×	147 0.4×	27 0.1×	425 2.0×	98 0.9×	25	1.8k
Veronica Costa Italy	10	2.2k 2.1×	78 0.2×	504 1.9×	433 2.0×	20 0.2×	11	2.5k

Countries citing papers authored by Juan Pié

Since Specialization

Citations

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

Fields of papers citing papers by Juan Pié

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juan Pié

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

Arnedo, María, Beatriz Puisac, Ana Latorre, et al.. (2025). Ligand–Enzyme Interaction Modeling of Missense Variants Implicated in Mitochondrial HMG-CoA Synthase Deficiency. International Journal of Molecular Sciences. 26(17). 8266–8266.

Arnedo, María, Beatriz Puisac, Ana Latorre, et al.. (2024). Cornelia de Lange Spectrum. SHILAP Revista de lepidopterología. 100(5). 352–362. 2 indexed citations

Arnedo, María, Ana Latorre, Paulino Gómez‐Puertas, et al.. (2022). Molecular Basis of the Schuurs–Hoeijmakers Syndrome: What We Know about the Gene and the PACS-1 Protein and Novel Therapeutic Approaches. International Journal of Molecular Sciences. 23(17). 9649–9649. 10 indexed citations

Valenzuela, Irene, Ana Latorre, María Arnedo, et al.. (2022). A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome. Genes. 13(8). 1413–1413. 1 indexed citations

Latorre, Ana, Beatriz Puisac, María Arnedo, et al.. (2022). Endocrine Evaluation and Homeostatic Model Assessment in Patients with Cornelia de Lange Syndrome. Journal of Clinical Research in Pediatric Endocrinology. 16(2). 211–217. 2 indexed citations

Matute-Llorente, Ángel, Ana Latorre, Beatriz Puisac, et al.. (2021). Targeted Gene Sequencing, Bone Health, and Body Composition in Cornelia de Lange Syndrome. Applied Sciences. 11(2). 710–710. 5 indexed citations

Garcia, Patrícia Salomão, Ana Cuadrado, Antonio Gómez, et al.. (2021). Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome. Nature Communications. 12(1). 4551–4551. 25 indexed citations

Gold, Nina B., Dong Li, Anna Chassevent, et al.. (2020). Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder. Clinical Genetics. 98(6). 571–576. 10 indexed citations

Puisac, Beatriz, et al.. (2019). Cornelia de Lange syndrome: Ventricular size and function in six children without congenital heart defects. Medicina Clínica (English Edition). 154(2). 67–68. 1 indexed citations

10.

Arnedo, María, Ana Latorre, Paulino Gómez‐Puertas, et al.. (2019). More Than One HMG-CoA Lyase: The Classical Mitochondrial Enzyme Plus the Peroxisomal and the Cytosolic Ones. International Journal of Molecular Sciences. 20(24). 6124–6124. 19 indexed citations

11.

Puisac, Beatriz, Íñigo Marcos‐Alcalde, Bernd Schwahn, et al.. (2018). Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients. International Journal of Molecular Sciences. 19(4). 1010–1010. 23 indexed citations

12.

Puisac, Beatriz, Torkild Visnes, Christopher Bot, et al.. (2017). mRNA Quantification of NIPBL Isoforms A and B in Adult and Fetal Human Tissues, and a Potentially Pathological Variant Affecting Only Isoform A in Two Patients with Cornelia de Lange Syndrome. International Journal of Molecular Sciences. 18(3). 481–481. 3 indexed citations

13.

Puisac, Beatriz, et al.. (2017). Síndrome de Cornelia de Lange: incidencia de cardiopatía congénita en 149 pacientes. Medicina Clínica. 149(7). 300–302. 10 indexed citations

14.

Du, Likun, Torkild Visnes, Andrea Björkman, et al.. (2013). A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination. The Journal of Experimental Medicine. 210(12). 2503–2513. 29 indexed citations

15.

Arce, Carlos A., et al.. (2011). Regulation of plasma membrane Ca2+-ATPase activity by acetylated tubulin: Influence of the lipid environment. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818(3). 601–608. 7 indexed citations

16.

Rohatgi, Sarika, Dinah Clark, Antonie D. Kline, et al.. (2010). Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey. American Journal of Medical Genetics Part A. 152A(7). 1641–1653. 56 indexed citations

17.

Carrasco, Patricia, Sebastián Menao, Eduardo López‐Viñas, et al.. (2007). C-Terminal end and aminoacid Lys48 in HMG-CoA lyase are involved in substrate binding and enzyme activity. Molecular Genetics and Metabolism. 91(2). 120–127. 6 indexed citations

18.

Deardorff, Matthew A., Maninder Kaur, Dinah Yaeger, et al.. (2007). Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation. The American Journal of Human Genetics. 80(3). 485–494. 385 indexed citations

19.

García, Joaquín J., Rüssel J. Reiter, Juan Pié, et al.. (1999). Role of Pinoline and Melatonin in Stabilizing Hepatic Microsomal Membranes against Oxidative Stress. Journal of Bioenergetics and Biomembranes. 31(6). 609–616. 89 indexed citations

20.

Pié, Juan, Jorge Lloberas, Marie-Odile Rolland, et al.. (1998). Two Missense Point Mutations in Different Alleles in the 3-Hydroxy-3-methylglutaryl Coenzyme A Lyase Gene Produce 3-Hydroxy-3-methylglutaric Aciduria in a French Patient. Archives of Biochemistry and Biophysics. 358(2). 197–203. 11 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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