Silvestre Oltra

1.9k total citations
69 papers, 1.1k citations indexed

About

Silvestre Oltra is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Silvestre Oltra has authored 69 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 36 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Silvestre Oltra's work include Genomic variations and chromosomal abnormalities (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Epigenetics and DNA Methylation (11 papers). Silvestre Oltra is often cited by papers focused on Genomic variations and chromosomal abnormalities (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Epigenetics and DNA Methylation (11 papers). Silvestre Oltra collaborates with scholars based in Spain, Germany and Czechia. Silvestre Oltra's co-authors include Francisco Martı́nez, Carmen Orellana, Sandra Monfort, Mónica Rosello, Sonia Mayo, Victoria Castel, Elena Grau, Adela Cañete, Alfonso Caro‐Llopis and Magdalena Beneyto and has published in prestigious journals such as Journal of Clinical Oncology, Scientific Reports and European Journal of Cancer.

In The Last Decade

Silvestre Oltra

66 papers receiving 1.1k citations

Peers

Countries citing papers authored by Silvestre Oltra

Since Specialization

Citations

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

Fields of papers citing papers by Silvestre Oltra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvestre Oltra

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

#	Work	Indexed citations
1	Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study 2025 ·Amyloid ·(unknown), Alfonso Caro‐Llopis, (unknown), Mónica Rosello, Silvestre Oltra, Laia Pedrola, Sandra Monfort, (unknown), Francisco Martı́nez, Carmen Orellana	0
2	Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel PIGA Variant Not Associated with a Skewed X-Inactivation Pattern 2024 ·Genes ·(unknown), Lourdes Cordón, Amparo Sempere, Laia Pedrola, (unknown), Silvestre Oltra, Sandra Monfort, Alfonso Caro‐Llopis, (unknown), (unknown), Mónica Rosello, Carmen Orellana, Francisco Martı́nez	0
3	Genome-wide DNA methylation profiling in anorexia nervosa discordant identical twins 2022 ·Translational Psychiatry ·(unknown), David Hervás, (unknown), (unknown), Francisco J. Vaz Leal, (unknown), Luis Beato‐Fernández, Silvestre Oltra, Juan Sandoval, Luis Rojo‐Moreno	10
4	Germline Predisposition to Pediatric Cancer, from Next Generation Sequencing to Medical Care 2021 ·Cancers ·(unknown), Silvestre Oltra, Yania Yáñez, (unknown), (unknown), Vanessa Segura, (unknown), Julia Balaguer, (unknown), (unknown), José María Fernández, (unknown), Bárbara Torres, Mara Andrés, M Tasso, Victoria Castel, Jaime Font de Mora, Adela Cañete	10
5	Prevalence of pathogenic copy number variants among children conceived by donor oocyte 2021 ·Scientific Reports ·Sandra Monfort, Carmen Orellana, Silvestre Oltra, Mónica Rosello, Alfonso Caro‐Llopis, Francisco Martı́nez	2
6	Retinoblastoma and mosaic 13q deletion: a case report 2021 ·International Journal of Retina and Vitreous ·(unknown), Silvestre Oltra, Julia Balaguer, Honorio Barranco, Yania Yáñez, Vanessa Segura, (unknown), (unknown), (unknown), Victoria Castel, Adela Cañete	2
7	Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing 2020 ·Pediatric Research ·Mónica Rosello, Alfonso Caro‐Llopis, Carmen Orellana, Silvestre Oltra, (unknown), (unknown), Sandra Monfort, Laia Pedrola, Francisco Martı́nez, Miguel Tomás Vila	26
8	Li–Fraumeni syndrome heterogeneity 2019 ·Clinical & Translational Oncology ·(unknown), Yania Yáñez, Vanessa Segura, (unknown), Bárbara Torres, Julia Balaguer, Silvestre Oltra, Victoria Castel, Adela Cañete	22
9	A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome 2015 ·American Journal of Medical Genetics Part A ·Eglė Preikšaitienė, Alfonso Caro‐Llopis, (unknown), Silvestre Oltra, Carmen Orellana, (unknown), Mónica Rosello, Jūratė Kasnauskienė, Sandra Monfort, Vaidutis Kučinskas, Sonia Mayo, Francisco Martı́nez	7
10	In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients 2015 ·BioMed Research International ·Sonia Mayo, Sandra Monfort, Mónica Rosello, Silvestre Oltra, Carmen Orellana, Francisco Martı́nez	3
11	Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients 2012 ·Annals of Hematology ·Irene Luna, Esperanza Such, José Cervera, Eva Barragán, Antonio Jiménez‐Velasco, (unknown), Mariam Ibáñez, Inés Gómez‐Seguí, Maria López‐Pavía, Marta Llop, Óscar Fuster, Silvestre Oltra, Federico Moscardó, David Martínez‐Cuadrón, (unknown), (unknown), Pau Montesinos, Guillermo Martı́n, Pascual Bolufer, Miguel Á. Sanz	6
12	De novo Interstitial Triplication of <i>MECP2</i> in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation 2011 ·Cytogenetic and Genome Research ·Sonia Mayo, Sandra Monfort, Mónica Rosello, Carmen Orellana, Silvestre Oltra, Judith Armstrong, Vicenç Català, Francisco Martı́nez	19
13	Aberrant methylation of tumor suppressor genes in patients with refractory anemia with ring sideroblasts 2010 ·Leukemia Research ·Ana Valencia, José Cervera, Esperanza Such, Mariam Ibáñez, Inés Gómez‐Seguí, Irene Luna, Leonor Senent, Silvestre Oltra, Miguel Á. Sanz, Guillermo Sanz	7
14	Rare chromosomal complement of trisomy 21 in a boy conceived by IVF and cryopreservation 2009 ·Reproductive BioMedicine Online ·(unknown), Mónica Rosello, Francisco Martı́nez, (unknown), Sandra Monfort, Silvestre Oltra, (unknown), Carmen Orellana	2
15	Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion 2009 ·Cytogenetic and Genome Research ·Mónica Rosello, Sandra Monfort, Carmen Orellana, (unknown), (unknown), Silvestre Oltra, Francisco Martı́nez	11
16	Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families of Eastern Spain 2007 ·Breast Cancer Research and Treatment ·(unknown), (unknown), (unknown), Silvestre Oltra, Eva Barragán, Eladio A. Velasco, Isabel Chirivella González, (unknown), Carmen Guillén‐Ponce, Eduardo Martínez de Dueñas, (unknown)	5
17	Robust, Easy, and Dose-Sensitive Methylation Test for the Diagnosis of Prader–Willi and Angelman Syndromes 2006 ·Genetic Testing ·Francisco Martı́nez, Ana M. León, Sandra Monfort, Silvestre Oltra, Mónica Rosello, Carmen Orellana	8
18	A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation 2006 ·European Journal of Human Genetics ·Isabel Martínez‐Garay, Miguel Tomás Vila, Silvestre Oltra, Juliane Ramser, María Dolores Moltó, Félix Prieto, Alfons Meindl, Kerstin Kutsche, Francisco Martı́nez	28
19	Recombinant X chromosome in a prenatal diagnosis 2006 ·Cytogenetic and Genome Research ·Carmen Orellana, Lourdes Badı́a, Francisco Martı́nez, Silvestre Oltra, Sandra Monfort, Mónica Rosello, José Cervera, (unknown), F. Prieto	3
20	Mutation screening of USH3 gene (clarin‐1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability 2004 ·Clinical Genetics ·Elena Aller, Teresa Jaijo, Silvestre Oltra, Jorge L. Alió del Barrio, Francisco Galán, Carmén Nájera, Magdalena Beneyto, (unknown)	25

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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