Javier Sánchez

481 total citations
23 papers, 349 citations indexed

About

Javier Sánchez is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Javier Sánchez has authored 23 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Hematology. Recurrent topics in Javier Sánchez's work include Genomic variations and chromosomal abnormalities (8 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Javier Sánchez is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Javier Sánchez collaborates with scholars based in Spain, Argentina and Chile. Javier Sánchez's co-authors include Rafael Durán, Ricardo Moreno‐Otero, Carmelo García‐Monzón, Guillermo Antiñolo, Salud Borrego, Emilio de Juan, Rafael Fernández, Olga Rubio, Alberto Benguría and Roberto de Marco and has published in prestigious journals such as SHILAP Revista de lepidopterología, Hepatology and Journal of Medical Genetics.

In The Last Decade

Javier Sánchez

22 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Javier Sánchez Spain 10 172 104 67 62 62 23 349
Tin Louie United States 7 105 0.6× 99 1.0× 65 1.0× 88 1.4× 74 1.2× 11 417
Selahattin Tekeş Türkiye 12 104 0.6× 146 1.4× 15 0.2× 83 1.3× 54 0.9× 33 364
Roberto Perniola Italy 14 49 0.3× 153 1.5× 17 0.3× 49 0.8× 18 0.3× 22 454
V. Sabato Italy 8 110 0.6× 43 0.4× 269 4.0× 32 0.5× 12 0.2× 13 504
G. Servais Belgium 12 115 0.7× 51 0.5× 20 0.3× 25 0.4× 6 0.1× 19 389
E.S. Curtoni Italy 10 37 0.2× 60 0.6× 73 1.1× 29 0.5× 7 0.1× 21 339
H Schulze Germany 7 95 0.6× 199 1.9× 14 0.2× 165 2.7× 10 0.2× 18 355
Wilma Carvalho Neves Forte Brazil 11 35 0.2× 27 0.3× 20 0.3× 58 0.9× 14 0.2× 47 333
DJ Phillips Australia 9 210 1.2× 40 0.4× 10 0.1× 19 0.3× 7 0.1× 9 323
Pravat Kumar Thatoi India 5 63 0.4× 15 0.1× 26 0.4× 84 1.4× 10 0.2× 16 368

Countries citing papers authored by Javier Sánchez

Since Specialization
Citations

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

Fields of papers citing papers by Javier Sánchez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Javier Sánchez

This figure shows the co-authorship network connecting the top 25 collaborators of Javier Sánchez. A scholar is included among the top collaborators of Javier Sánchez 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 Sánchez. Javier Sánchez 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.
García‐Díaz, Lutgardo, et al.. (2017). Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy. Case Reports in Obstetrics and Gynecology. 2017(1). 1471704–1471704. 3 indexed citations
2.
Hmadcha, Abdelkrim, Yolanda Aguilera, Javier Sánchez, et al.. (2016). Derivation of HVR1, HVR2 and HVR3 human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis (PGD) for monogenic disorder. Stem Cell Research. 16(3). 635–639. 1 indexed citations
3.
Burillo‐Sanz, Sergio, et al.. (2016). RUNX1 amplification in AML with myelodysplasia‐related changes and ring 21 chromosomes. Hematological Oncology. 35(4). 894–899. 5 indexed citations
4.
Fernández, Raquel M., Javier Sánchez, Lutgardo García‐Díaz, et al.. (2016). Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations. American Journal of Medical Genetics Part A. 170(5). 1268–1273. 9 indexed citations
5.
Sánchez, Javier, et al.. (2014). An Active Isodicentric X Chromosome in a Case of Refractory Anaemia with Ring Sideroblasts Associated with Marked Thrombocytosis. SHILAP Revista de lepidopterología. 2014. 1–3. 3 indexed citations
6.
Sánchez, Javier, et al.. (2014). Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13. SHILAP Revista de lepidopterología. 2014. 1–4. 2 indexed citations
7.
Rubio, Olga, Javier Sánchez, & Rafael Fernández. (2013). Life-sustaining treatment limitation criteria upon admission to the intensive care unit: Results of a Spanish national multicenter survey. Medicina Intensiva (English Edition). 37(5). 333–338. 3 indexed citations
8.
Calderón‐Cabrera, Cristina, Isabel Montero, Rosario M. Morales, et al.. (2013). Differential cytogenetic profile in advanced chronic myeloid leukemia with sequential lymphoblastic and myeloblastic blast crisis. Leukemia Research Reports. 2(2). 79–81. 3 indexed citations
9.
Rubio, Olga, Javier Sánchez, & Rafael Fernández. (2012). Criterios para limitar los tratamientos de soporte vital al ingreso en unidad de cuidados intensivos: resultados de una encuesta multicéntrica nacional. Medicina Intensiva. 37(5). 333–338. 13 indexed citations
10.
Cabello, Beatriz Muñoz, Salud Borrego, Irene Marcos, et al.. (2010). Somatic mosaicism for Y120X mutation in the MECP2 gene causes atypical Rett syndrome in a male. Brain and Development. 33(7). 608–611. 18 indexed citations
11.
Cervera, José, Pau Montesinos, José‐Ángel Hernández‐Rivas, et al.. (2009). Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy. Haematologica. 95(3). 424–431. 50 indexed citations
12.
Gutiérrez, Juan M., et al.. (2001). Prenatal diagnosis of 13q– syndrome in a fetus with holoprosencephaly and thumb agenesis. Ultrasound in Obstetrics and Gynecology. 17(2). 166–168. 17 indexed citations
13.
Sánchez, Javier, et al.. (1999). [Dissociated cholestasis in patients with HIV-1 infection, Prevalence and diagnostic value of liver biopsy].. PubMed. 199(2). 81–3.
14.
Ruiz, Agustı́n, et al.. (1997). PCR Mutagenesis-Based Method for Generation of Positive Controls for SSCP Analysis. BioTechniques. 23(4). 704–708. 4 indexed citations
15.
Marco, Roberto de, Alberto Benguría, Javier Sánchez, & Emilio de Juan. (1996). Effects of the space environment on Drosophila melanogaster development. Implications of the IML-2 experiment. Journal of Biotechnology. 47(2-3). 179–189. 18 indexed citations
16.
Antiñolo, Guillermo, et al.. (1996). Reverse mutation in fragile X syndrome.. PubMed. 58(1). 237–9. 10 indexed citations
17.
Borrego, Salud, et al.. (1994). Molecular and clinical analyses of cystic fibrosis in the South of Spain. Clinical Genetics. 46(4). 287–290. 5 indexed citations
18.
Tlsty, Thea D., Piotr Jonczyk, Anne White, et al.. (1993). Loss of Chromosomal Integrity in Neoplasia. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 645–654. 11 indexed citations
19.
Sánchez, Javier, et al.. (1993). Hepatitis C virus antibodies and liver disease in patients with porphyria cutanea tarda. Hepatology. 17(4). 551–557. 116 indexed citations
20.
Goldschmidt, Ernst, et al.. (1992). Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound.. Journal of Medical Genetics. 29(6). 434–436. 12 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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