Guillermo Antiñolo

6.6k total citations
179 papers, 3.3k citations indexed

About

Guillermo Antiñolo is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Guillermo Antiñolo has authored 179 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 65 papers in Surgery and 37 papers in Genetics. Recurrent topics in Guillermo Antiñolo's work include Congenital gastrointestinal and neural anomalies (40 papers), Retinal Development and Disorders (40 papers) and Congenital Anomalies and Fetal Surgery (27 papers). Guillermo Antiñolo is often cited by papers focused on Congenital gastrointestinal and neural anomalies (40 papers), Retinal Development and Disorders (40 papers) and Congenital Anomalies and Fetal Surgery (27 papers). Guillermo Antiñolo collaborates with scholars based in Spain, United States and United Kingdom. Guillermo Antiñolo's co-authors include Salud Borrego, Raquel M. Fernández, Manuel López-Alonso, Macarena Ruiz‐Ferrer, Isabel Barragán, Irene Marcos, Charis Eng, María González‐del Pozo, Agustı́n Ruiz and Ana Torroglosa and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Guillermo Antiñolo

170 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guillermo Antiñolo Spain 30 2.0k 913 792 537 261 179 3.3k
Salud Borrego Spain 28 1.8k 0.9× 1.1k 1.2× 738 0.9× 331 0.6× 181 0.7× 135 3.0k
Arnold Munnich France 25 1.9k 1.0× 410 0.4× 724 0.9× 860 1.6× 254 1.0× 54 3.2k
Marco Seri Italy 38 2.3k 1.2× 1.1k 1.2× 1.4k 1.7× 92 0.2× 463 1.8× 193 5.3k
M. Leppert United States 40 2.8k 1.4× 658 0.7× 1.4k 1.7× 561 1.0× 646 2.5× 169 6.1k
Ludwine Messiaen United States 39 2.2k 1.1× 375 0.4× 932 1.2× 180 0.3× 150 0.6× 145 5.0k
Gwenaëlle Collod‐Béroud France 21 1.7k 0.9× 317 0.3× 1.6k 2.0× 114 0.2× 220 0.8× 38 3.6k
Meena Upadhyaya United Kingdom 44 2.5k 1.3× 569 0.6× 837 1.1× 60 0.1× 571 2.2× 166 6.7k
Heinrich Schrewe Germany 28 1.5k 0.8× 265 0.3× 373 0.5× 217 0.4× 124 0.5× 46 2.2k
Sylvie Odent France 36 2.7k 1.4× 333 0.4× 1.5k 1.9× 153 0.3× 230 0.9× 152 3.8k
Stavit A. Shalev Israel 29 1.8k 0.9× 114 0.1× 709 0.9× 310 0.6× 211 0.8× 88 2.6k

Countries citing papers authored by Guillermo Antiñolo

Since Specialization
Citations

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

Fields of papers citing papers by Guillermo Antiñolo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guillermo Antiñolo

This figure shows the co-authorship network connecting the top 25 collaborators of Guillermo Antiñolo. A scholar is included among the top collaborators of Guillermo Antiñolo 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 Guillermo Antiñolo. Guillermo Antiñolo 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.
Pozo, María González‐del, et al.. (2025). New genetic diagnoses for inherited retinal dystrophies by integrating splicing tools into NGS pipelines. npj Genomic Medicine. 10(1). 52–52.
2.
Antiñolo, Guillermo, et al.. (2025). Impact of continuous glucose monitoring on pregnancy outcomes in women with pregestational diabetes. Acta Diabetologica. 62(8). 1205–1212.
3.
Tous, Cristina, Pedro Seoane, Raquel M. Fernández, et al.. (2024). Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease. Biomolecules. 14(2). 164–164. 2 indexed citations
4.
Tous, Cristina, et al.. (2024). Delving into the Role of lncRNAs in Papillary Thyroid Cancer: Upregulation of LINC00887 Promotes Cell Proliferation, Growth and Invasion. International Journal of Molecular Sciences. 25(3). 1587–1587. 5 indexed citations
5.
García‐Díaz, Lutgardo, et al.. (2024). A Detailed Exploration of the Ex Utero Intrapartum Treatment Procedure with Center-Specific Advancements. SHILAP Revista de lepidopterología. 13(1). 76–86. 1 indexed citations
6.
García‐Díaz, Lutgardo, et al.. (2023). Maternal and obstetric outcomes after Ex-Utero Intrapartum Treatment (EXIT): a single center experience. BMC Pregnancy and Childbirth. 23(1). 831–831. 4 indexed citations
7.
García‐Díaz, Lutgardo, et al.. (2022). Mode of delivery, perinatal outcome and neurodevelopment in uncomplicated monochorionic diamniotic twins: a single-center retrospective cohort study. BMC Pregnancy and Childbirth. 22(1). 89–89. 8 indexed citations
8.
García‐Díaz, Lutgardo, et al.. (2021). Diagnóstico prenatal de atresia de yeyuno con ecografía 3D con reconstrucción en superficie (HDlive): reporte de caso y revisión de la literatura. SHILAP Revista de lepidopterología. 72(2). 202–209. 1 indexed citations
9.
García‐Díaz, Lutgardo, et al.. (2020). Ex-Utero Intrapartum Treatment (EXIT): indications and outcome in fetal cervical and oropharyngeal masses. BMC Pregnancy and Childbirth. 20(1). 598–598. 15 indexed citations
10.
Pozo, María González‐del, et al.. (2020). Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants. Journal of Translational Medicine. 18(1). 73–73. 25 indexed citations
11.
García‐Díaz, Lutgardo, et al.. (2020). Maternal effects induced by oral digoxin during treatment of fetal tachyarrhythmia: Case series and literature review. European Journal of Obstetrics & Gynecology and Reproductive Biology. 256. 354–357. 6 indexed citations
12.
Torroglosa, Ana, et al.. (2019). Epigenetic Mechanisms in Hirschsprung Disease. International Journal of Molecular Sciences. 20(13). 3123–3123. 26 indexed citations
13.
Pozo, María González‐del, et al.. (2018). Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencing. Scientific Reports. 8(1). 13312–13312. 20 indexed citations
15.
Torroglosa, Ana, Maria M. Alves, Roberto Fernández, et al.. (2016). Epigenetics in ENS development and Hirschsprung disease. Developmental Biology. 417(2). 209–216. 34 indexed citations
16.
García‐Alonso, Luz, Jorge Jiménez, José Carbonell‐Caballero, et al.. (2014). The role of the interactome in the maintenance of deleterious variability in human populations. Molecular Systems Biology. 10(9). 752–752. 23 indexed citations
17.
Antiñolo, Guillermo, et al.. (2010). Utilidad del diagnóstico genético preimplantatorio en enfermedades raras y otras enfermedades genéticas: [Conferencia]. 49–52. 1 indexed citations
18.
Audo, Isabelle, José‐Alain Sahel, Saddek Mohand‐Saïd, et al.. (2010). EYS is a major gene for rod-cone dystrophies in France. Human Mutation. 31(5). E1406–E1435. 84 indexed citations
20.
Royo, José Luís, Agustı́n Ruiz, Salud Borrego, et al.. (2001). Fluorescence Resonance Energy Transfer Analysis of CCR2-V64I and SDF1-3′A Polymorphisms: Prevalence in Southern Spain HIV Type 1 + Cohort and Noninfected Population. AIDS Research and Human Retroviruses. 17(8). 663–666. 9 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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