Javier Sanz

419 total citations
16 papers, 263 citations indexed

About

Javier Sanz is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Javier Sanz has authored 16 papers receiving a total of 263 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pulmonary and Respiratory Medicine, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Javier Sanz's work include Cystic Fibrosis Research Advances (10 papers), Neonatal Respiratory Health Research (6 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Javier Sanz is often cited by papers focused on Cystic Fibrosis Research Advances (10 papers), Neonatal Respiratory Health Research (6 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Javier Sanz collaborates with scholars based in Switzerland, United States and United Kingdom. Javier Sanz's co-authors include Sabina Gallati, Thomas von Känel, Manfred Ballmann, Nico Derichs, Bernhard Steiner, B. Tümmler, Antonia Zapf, André Schaller, Kaspar Truninger and Anabela S. Ramalho and has published in prestigious journals such as SHILAP Revista de lepidopterología, European Heart Journal and Clinical Chemistry.

In The Last Decade

Javier Sanz

13 papers receiving 256 citations

Peers

Countries citing papers authored by Javier Sanz

Since Specialization

Citations

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

Fields of papers citing papers by Javier Sanz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Javier Sanz

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Cystic fibrosis newborn screening in Switzerland – evaluation and scenarios for improvement after 11 years of follow-up 2024 ·Journal of Cystic Fibrosis ·Eva S.L. Pedersen, Carmen C.M. de Jong, (unknown), (unknown), Javier Sanz, (unknown), (unknown), (unknown), Nicolas Regamey, Claudia E. Kuehni, J Barben, (unknown)	0
2	Anaemia predicts iron homoeostasis dysregulation and modulates the response to empagliflozin in heart failure with reduced ejection fraction: the EMPATROPISM-FE trial 2024 ·European Heart Journal ·Christiane E. Angermann, Susanne Sehner, Louisa M.S. Gerhardt, Carlos G. Santos‐Gallego, Juan Antonio Requena-Ibáñez, Tanja Zeller, Christoph Maack, Javier Sanz, Stefan Frantz, Georg Ertl, Juan J. Badimón	6
3	“A Dangerous Black Box:” Idiopathic Hemophagocytic Lymphohistiocytosis in Adult Patients—A Case Report and Review of the Literature 2022 ·SHILAP Revista de lepidopterología ·(unknown), Javier Sanz, Alicia Rovó	0
4	Cutaneous squamous cell carcinoma in an autosomal‐recessive Adams–Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene 2022 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Javier Sanz, Mafalda Trippel, Sabina Gallati, Jochen Rößler	1
5	Characteristics and outcome of patients with solid tumour requiring admission to the intensive care unit. Usefulness of three severity score systems 2019 ·Medicina Clínica ·(unknown), (unknown), (unknown), (unknown), Diego Castaneda, (unknown), Javier Sanz, (unknown), (unknown), (unknown), Sara Alcántara Carmona, Marina Pérez Redondo, (unknown)	4
6	FRI0420 Association of supressor of cytokine signaling -3 (SOCS-3) expression with interleukin-23 receptor (IL-23R) single nucleotide polymorphisms (SNPS) in ankylosing spondylitis (AS) 2017 ·Annals of the Rheumatic Diseases ·M.A. Sánchez, Ricardo Villares, (unknown), José Luís López-Campos, (unknown), Javier Sanz, (unknown), Ana Royuela, Pilar Lucas, Mario Mellado, Juan Mulero	0
7	Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data 2010 ·Thorax ·Nico Derichs, Javier Sanz, Thomas von Känel, (unknown), Antonia Zapf, B. Tümmler, Sabina Gallati, Manfred Ballmann	105
8	The CFTR frameshift mutation 3905insT and its effect at transcript and protein level 2009 ·European Journal of Human Genetics ·Javier Sanz, Thomas von Känel, (unknown), Bernhard Steiner, André Schaller, Sabina Gallati	6
9	Ligation dependent allele specific quantification (LASQ) of CFTR cDNA on the LightCycler® using MLPA® hybridization probes 2008 ·Clinica Chimica Acta ·(unknown), Thomas von Känel, Javier Sanz, Sabina Gallati	1
10	Functional expression of connexin30 and connexin31 in the polarized human airway epithelium 2007 ·Differentiation ·Ludovic Wiszniewski, Javier Sanz, Isabelle Scerri, (unknown), Tecla Dudez, (unknown), Susanne Suter, Sabina Gallati, Marc Chanson	26
11	Detection of Exon Deletions within an Entire Gene (CFTR) by Relative Quantification on the LightCycler 2006 ·Clinical Chemistry ·(unknown), Franziska Joncourt, Javier Sanz, Thomas von Känel, Sabina Gallati	21
12	Rapid and reliable genotyping of polymorphic loci modifying correct splicing of CFTR pre-mRNA using mass spectrometry 2006 ·European Journal of Human Genetics ·André Schaller, Thomas von Känel, Benedikt Gehr, Javier Sanz, Sabina Gallati	1
13	Analysis of genomic CFTR DNA 2004 ·Journal of Cystic Fibrosis ·Claude Férec, Cédric Le Maréchal, M.‐P. Audrézet, Carlos M. Farinha, Margarida D. Amaral, Sabina Gallati, Javier Sanz, Bernhard Steiner, Nathalie Mouchel, Ann Harris, Martin Schwarz	7
14	Quantitative methods for the analysis of CFTR transcripts/splicing variants 2004 ·Journal of Cystic Fibrosis ·Margarida D. Amaral, Luka A. Clarke, Anabela S. Ramalho, Sebastian Beck, Fiona Broackes-Carter, Rebecca K. Rowntree, Nathalie Mouchel, S. Henry Williams, Ann Harris, Maria Tzetis, Bernhard Steiner, Javier Sanz, Sabina Gallati, (unknown), Batsheva Kerem, Timothy Hefferon, Garry R. Cutting, (unknown), (unknown)	11
15	The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutatedCFTR Alleles 2004 ·Human Mutation ·Bernhard Steiner, Kaspar Truninger, Javier Sanz, André Schaller, Sabina Gallati	38
16	Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts 2004 ·Journal of Cystic Fibrosis ·Anabela S. Ramalho, Sebastian Beck, Carlos M. Farinha, Luka A. Clarke, Ghanshyam D. Heda, Bernhard Steiner, Javier Sanz, Sabina Gallati, Margarida D. Amaral, Ann Harris, Maria Tzetis	36

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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