Nuala H. Simpson

1.1k total citations
12 papers, 471 citations indexed

About

Nuala H. Simpson is a scholar working on Genetics, Cognitive Neuroscience and Developmental and Educational Psychology. According to data from OpenAlex, Nuala H. Simpson has authored 12 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Cognitive Neuroscience and 4 papers in Developmental and Educational Psychology. Recurrent topics in Nuala H. Simpson's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (3 papers). Nuala H. Simpson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (3 papers). Nuala H. Simpson collaborates with scholars based in United Kingdom, Netherlands and Australia. Nuala H. Simpson's co-authors include Dianne F. Newbury, Simon E. Fisher, Anthony P. Monaco, Elizabeth R Hennessy, Clyde Francks, Gina Conti‐Ramsden, Patrick Bolton, Anne O’Hare, Silvia Paracchini and Gillian Baird and has published in prestigious journals such as PLoS ONE, Scientific Reports and Developmental Medicine & Child Neurology.

In The Last Decade

Nuala H. Simpson

12 papers receiving 467 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nuala H. Simpson United Kingdom	11	279	192	158	152	31	12	471
William M. Brandler United Kingdom	8	232 0.8×	138 0.7×	102 0.6×	303 2.0×	15 0.5×	8	494
Tom S. Scerri United Kingdom	4	280 1.0×	350 1.8×	107 0.7×	147 1.0×	44 1.4×	4	492
Caroline Phillips United Kingdom	13	81 0.3×	223 1.2×	142 0.9×	118 0.8×	16 0.5×	16	632
Marilee A. Martens United States	13	93 0.3×	91 0.5×	90 0.6×	125 0.8×	42 1.4×	19	616
Sophia Docherty United Kingdom	13	197 0.7×	57 0.3×	176 1.1×	76 0.5×	45 1.5×	14	453
Anna Järvinen‐Pasley United Kingdom	10	79 0.3×	186 1.0×	67 0.4×	318 2.1×	47 1.5×	10	594
Natalie R. Powers United States	11	154 0.6×	173 0.9×	263 1.7×	73 0.5×	28 0.9×	18	492
Elizabeth R Hennessy Netherlands	5	141 0.5×	92 0.5×	66 0.4×	94 0.6×	11 0.4×	5	231
Ana Tryfon Canada	11	87 0.3×	98 0.5×	40 0.3×	333 2.2×	35 1.1×	13	375

Countries citing papers authored by Nuala H. Simpson

Since Specialization

Citations

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

Fields of papers citing papers by Nuala H. Simpson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nuala H. Simpson. 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 Nuala H. Simpson. The network helps show where Nuala H. Simpson may publish in the future.

Co-authorship network of co-authors of Nuala H. Simpson

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

All Works

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12 of 12 papers shown

Parker, Adam James, Zoe Woodhead, David P. Carey, et al.. (2022). Inconsistent language lateralisation – Testing the dissociable language laterality hypothesis using behaviour and lateralised cerebral blood flow. Cortex. 154. 105–134. 17 indexed citations

Mountford, Hayley S., Dorothy Bishop, Paul A. Thompson, Nuala H. Simpson, & Dianne F. Newbury. (2020). Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(2). 256–266. 6 indexed citations

Hoischen, Alexander, Joris A. Veltman, Nuala H. Simpson, et al.. (2017). Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment. Scientific Reports. 7(1). 46105–46105. 62 indexed citations

Pettigrew, Kerry A., Kristina Moll, Kate Northstone, et al.. (2015). Lack of replication for the myosin‐18B association with mathematical ability in independent cohorts. Genes Brain & Behavior. 14(4). 369–376. 15 indexed citations

Pettigrew, Kerry A., Emily Reeves, Marianna E. Hayiou‐Thomas, et al.. (2015). Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment. PLoS ONE. 10(8). e0134997–e0134997. 32 indexed citations

Simpson, Nuala H., Fabiola Ceroni, Laura Covill, et al.. (2015). Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics. 23(10). 1370–1377. 35 indexed citations

Nudel, Ron, Nuala H. Simpson, Gillian Baird, et al.. (2014). Associations of HLA alleles with specific language impairment. Journal of Neurodevelopmental Disorders. 6(1). 1–1. 88 indexed citations

Ceroni, Fabiola, Nuala H. Simpson, Clyde Francks, et al.. (2014). Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. European Journal of Human Genetics. 22(10). 1165–1171. 18 indexed citations

Nudel, Ron, Nuala H. Simpson, Anne O’Hare, et al.. (2014). Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment. Genes Brain & Behavior. 13(4). 418–429. 63 indexed citations

10.

Gialluisi, Alessandro, Dianne F. Newbury, Richard K. Olson, et al.. (2014). Genome‐wide screening for DNA variants associated with reading and language traits. Genes Brain & Behavior. 13(7). 686–701. 77 indexed citations

11.

Ceroni, Fabiola, Nuala H. Simpson, Dianne F. Newbury, et al.. (2014). A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma. Autism Research. 7(2). 254–263. 31 indexed citations

12.

Simpson, Nuala H., Laura Addis, William M. Brandler, et al.. (2013). Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine & Child Neurology. 56(4). 346–353. 27 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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