Sonia Mayo

1.3k total citations
32 papers, 814 citations indexed

About

Sonia Mayo is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sonia Mayo has authored 32 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Sonia Mayo's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Sonia Mayo is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomics and Rare Diseases (4 papers). Sonia Mayo collaborates with scholars based in Spain, United States and United Kingdom. Sonia Mayo's co-authors include Francisco Martı́nez, Mónica Rosello, Lola Peñarrubia, Carmen Orellana, Susana Rodríguez‐Navarro, Nuria Andrés‐Colás, Silvestre Oltra, Sandra Monfort, Sergi Puig and Dennis J. Thiele and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The Plant Journal and International Journal of Molecular Sciences.

In The Last Decade

Sonia Mayo

31 papers receiving 788 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sonia Mayo Spain	14	341	305	292	94	72	32	814
Abdul Hameed Pakistan	12	346 1.0×	66 0.2×	146 0.5×	16 0.2×	39 0.5×	21	620
Aris Polyzos United States	12	772 2.3×	134 0.4×	110 0.4×	69 0.7×	11 0.2×	25	1.1k
Sheila Ernest Canada	12	213 0.6×	30 0.1×	200 0.7×	39 0.4×	22 0.3×	17	706
Diane Carette France	19	754 2.2×	33 0.1×	120 0.4×	51 0.5×	22 0.3×	31	1.1k
Igor Kondrychyn Singapore	15	483 1.4×	41 0.1×	124 0.4×	65 0.7×	13 0.2×	23	779
N.L.A. Cacheiro United States	21	895 2.6×	355 1.2×	626 2.1×	105 1.1×	19 0.3×	39	1.4k
Catherine Pairault France	16	542 1.6×	31 0.1×	232 0.8×	79 0.8×	29 0.4×	29	1.1k
Rajikala Suganthan Norway	14	1.1k 3.2×	64 0.2×	146 0.5×	113 1.2×	18 0.3×	22	1.3k
Ying Luo China	10	393 1.2×	37 0.1×	266 0.9×	19 0.2×	19 0.3×	26	713
Mary C. Francis United Kingdom	6	462 1.4×	64 0.2×	113 0.4×	86 0.9×	9 0.1×	9	922

Countries citing papers authored by Sonia Mayo

Since Specialization

Citations

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

Fields of papers citing papers by Sonia Mayo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Mayo

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ghosh, Ritwik, Souvik Dubey, Dipayan Roy, Sonia Mayo, & Julián Benito‐León. (2024). Congenital myasthenia syndrome with demyelinating sensorimotor neuropathy responsive to salbutamol monotherapy: a novel clinical phenotype of CHRNE mutation. Neurological Sciences. 45(7). 3555–3558.

Mayo, Sonia, et al.. (2022). Noninvasive prenatal testing: How far can we reach detecting fetal copy number variations. European Journal of Obstetrics & Gynecology and Reproductive Biology. 272. 150–155. 4 indexed citations

Arteche‐López, Ana, M Gómez-Cano, Juan Francisco Quesada‐Espinosa, et al.. (2022). Expanding the Phenotypic Spectrum of Alazami Syndrome: Two Unrelated Spanish Families. Neuropediatrics. 54(1). 31–36. 1 indexed citations

Zahir, Farah, Tracy Tucker, Sonia Mayo, et al.. (2016). Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes. American Journal of Medical Genetics Part A. 170(11). 2916–2926. 12 indexed citations

Caro‐Llopis, Alfonso, Mónica Rosello, Carmen Orellana, et al.. (2016). De novo mutations in genes of mediator complex causing syndromic intellectual disability: mediatorpathy or transcriptomopathy?. Pediatric Research. 80(6). 809–815. 30 indexed citations

Fieremans, Nathalie, Hilde Van Esch, Maureen Holvoet, et al.. (2016). Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern. Human Mutation. 37(8). 804–811. 65 indexed citations

Preikšaitienė, Eglė, Alfonso Caro‐Llopis, Silvestre Oltra, et al.. (2015). A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome. American Journal of Medical Genetics Part A. 167(6). 1342–1348. 7 indexed citations

Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2015). In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients. BioMed Research International. 2015. 1–8. 3 indexed citations

Martı́nez, Francisco, Purificación Marín Reina, Antonio Pérez Aytés, et al.. (2015). Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes. Pediatric Research. 78(5). 533–539. 28 indexed citations

10.

Perea‐García, Ana, Amparo Andrés-Bordería, Sonia Mayo, et al.. (2015). Modulation of copper deficiency responses by diurnal and circadian rhythms inArabidopsis thaliana. Journal of Experimental Botany. 67(1). 391–403. 30 indexed citations

11.

Galán, Francisco, et al.. (2014). Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX,r(9)(p24q34), and a de novo Interstitial 9p Deletion. Cytogenetic and Genome Research. 144(4). 275–279. 20 indexed citations

12.

Rosello, Mónica, Francisco Martı́nez, Sandra Monfort, et al.. (2014). Phenotype profiling of patients with intellectual disability and copy number variations. European Journal of Paediatric Neurology. 18(5). 558–566. 19 indexed citations

13.

López-Carrasco, Amparo, Sandra Monfort, Mónica Rosello, et al.. (2013). Localización cromosómica de duplicaciones submicroscópicas en pacientes con trastornos del neurodesarrollo para identificar casos con alto riesgo de recurrencia familiar. Medicina Clínica. 142(12). 531–537. 3 indexed citations

14.

Andrés‐Colás, Nuria, Ana Perea‐García, Sonia Mayo, et al.. (2013). Comparison of global responses to mild deficiency and excess copper levels in Arabidopsis seedlings. Metallomics. 5(9). 1234–1234. 23 indexed citations

15.

López-Carrasco, Amparo, Silvestre Oltra, Sandra Monfort, et al.. (2012). Mutation screening of AURKB and SYCP3 in patients with reproductive problems. Molecular Human Reproduction. 19(2). 102–108. 13 indexed citations

16.

Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2011). De novo Interstitial Triplication of <i>MECP2</i> in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation. Cytogenetic and Genome Research. 135(2). 93–101. 19 indexed citations

17.

Monfort, Sandra, Silvestre Oltra, Mónica Rosello, et al.. (2011). Partial Duplication of 18q Including a Distal Critical Region for Edwards Syndrome in a Patient with Normal Phenotype and Oligoasthenospermia: Case Report. Cytogenetic and Genome Research. 133(1). 78–83. 7 indexed citations

18.

Martı́nez, Francisco, Sandra Monfort, Mónica Rosello, et al.. (2010). Enrichment of ultraconserved elements among genomic imbalances causing mental delay and congenital anomalies. BMC Medical Genomics. 3(1). 54–54. 14 indexed citations

19.

Mayo, Sonia, et al.. (2008). Clinical laboratory automated urinalysis: comparison among automated microscopy, flow cytometry, two test strips analyzers, and manual microscopic examination of the urine sediments. Journal of Clinical Laboratory Analysis. 22(4). 262–270. 57 indexed citations

20.

Andrés‐Colás, Nuria, Vicente Sancenón, Susana Rodríguez‐Navarro, et al.. (2005). The Arabidopsis heavy metal P‐type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots. The Plant Journal. 45(2). 225–236. 249 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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