M. Pilar Trelles

865 total citations
15 papers, 530 citations indexed

About

M. Pilar Trelles is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, M. Pilar Trelles has authored 15 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Cognitive Neuroscience and 6 papers in Molecular Biology. Recurrent topics in M. Pilar Trelles's work include Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). M. Pilar Trelles is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). M. Pilar Trelles collaborates with scholars based in United States, France and Australia. M. Pilar Trelles's co-authors include Alexander Kolevzon, Audrey Thurm, Catalina Betancur, Joseph D. Buxbaum, Paige M. Siper, Miduturu Srinivas, Clio Rubiños, Vytas K. Verselis, Thaddeus A. Bargiello and Latha Soorya and has published in prestigious journals such as Journal of Biological Chemistry, Journal of the American Academy of Child & Adolescent Psychiatry and Journal of Autism and Developmental Disorders.

In The Last Decade

M. Pilar Trelles

13 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Pilar Trelles United States	9	237	221	197	88	58	15	530
William J. Cutter United Kingdom	12	305 1.3×	212 1.0×	276 1.4×	71 0.8×	86 1.5×	16	659
Eugenia Conti Italy	15	169 0.7×	206 0.9×	381 1.9×	126 1.4×	106 1.8×	32	714
Zhen Zheng China	12	131 0.6×	143 0.6×	259 1.3×	71 0.8×	161 2.8×	17	527
Corneliu Bodea United States	4	514 2.2×	284 1.3×	563 2.9×	77 0.9×	100 1.7×	5	809
D.M. Hougaard Denmark	4	148 0.6×	103 0.5×	229 1.2×	60 0.7×	67 1.2×	6	430
Daniel Moreno‐De‐Luca United States	9	413 1.7×	179 0.8×	389 2.0×	63 0.7×	106 1.8×	16	677
Joseph P. Pillion United States	15	122 0.5×	72 0.3×	172 0.9×	90 1.0×	79 1.4×	29	600
Lars Melgaard Denmark	6	153 0.6×	108 0.5×	224 1.1×	60 0.7×	67 1.2×	7	425
Linda Lopez United States	11	225 0.9×	174 0.8×	470 2.4×	157 1.8×	92 1.6×	16	709
Maria Gudbrandsen United Kingdom	11	74 0.3×	80 0.4×	179 0.9×	72 0.8×	83 1.4×	24	350

Countries citing papers authored by M. Pilar Trelles

Since Specialization

Citations

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

Fields of papers citing papers by M. Pilar Trelles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Pilar Trelles. 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 M. Pilar Trelles. The network helps show where M. Pilar Trelles may publish in the future.

Co-authorship network of co-authors of M. Pilar Trelles

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

All Works

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15 of 15 papers shown

Trelles, M. Pilar, Behrang Mahjani, Emma Wilkinson, et al.. (2025). A Family Peer Advocate Model to Address Disparities in Access to Care for Minority Autistic Children with Co-Occurring Attention-Deficit/Hyperactivity Disorder. Journal of Developmental and Physical Disabilities. 37(2). 217–238.

Levy, Tess, Paige M. Siper, Danielle Halpern, et al.. (2024). Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome. Journal of Neurodevelopmental Disorders. 16(1). 25–25. 2 indexed citations

Koene, Saskia, Dagmar Berghuis, Angela Morgan, et al.. (2023). Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of Medical Genetics. 61(4). 399–404. 4 indexed citations

Levy, Tess, Bari Britvan, Jordana Weissman, et al.. (2022). Assessing the utility of electronic measures as a proxy for cognitive ability. Autism Research. 15(6). 988–995.

Guillory, Sylvia, Emma Wilkinson, Jordana Weissman, et al.. (2021). Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study. Journal of Neurodevelopmental Disorders. 13(1). 58–58. 8 indexed citations

Foss‐Feig, Jennifer H., Yitzchak Frank, Danielle Halpern, et al.. (2021). A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome. Molecular Autism. 12(1). 62–62. 12 indexed citations

Siper, Paige M., Sylvia Guillory, Teresa Tavassoli, et al.. (2021). Visual Evoked Potential Abnormalities in Phelan-McDermid Syndrome. Journal of the American Academy of Child & Adolescent Psychiatry. 61(4). 565–574.e1. 8 indexed citations

Trelles, M. Pilar, Tess Levy, Paige M. Siper, et al.. (2021). Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms. Molecular Autism. 12(1). 61–61. 26 indexed citations

Trelles, M. Pilar, et al.. (2020). Psychiatric illness and regression in individuals with Phelan-McDermid syndrome. Journal of Neurodevelopmental Disorders. 12(1). 7–7. 57 indexed citations

10.

Rubeis, Silvia De, Paige M. Siper, Allison Durkin, et al.. (2018). Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations. Molecular Autism. 9(1). 31–31. 138 indexed citations

11.

Jamison, Jesslyn, Paige M. Siper, M. Pilar Trelles, et al.. (2017). Examining the Efficacy of a Family Peer Advocate Model for Black and Hispanic Caregivers of Children with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 47(5). 1314–1322. 69 indexed citations

12.

Andelfinger, Grégor, et al.. (2017). Congenital Heart Disease and Neurodevelopment: Clinical Manifestations, Genetics, Mechanisms, and Implications. Canadian Journal of Cardiology. 33(12). 1543–1555. 61 indexed citations

13.

Soorya, Latha, et al.. (2017). Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome. The Clinical Neuropsychologist. 32(7). 1226–1255. 55 indexed citations

14.

Rubiños, Clio, et al.. (2012). Triarylmethanes, a New Class of Cx50 Inhibitors. Frontiers in Pharmacology. 3. 106–106. 15 indexed citations

15.

Verselis, Vytas K., M. Pilar Trelles, Clio Rubiños, Thaddeus A. Bargiello, & Miduturu Srinivas. (2008). Loop Gating of Connexin Hemichannels Involves Movement of Pore-lining Residues in the First Extracellular Loop Domain. Journal of Biological Chemistry. 284(7). 4484–4493. 75 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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