Nuala Sykes

5.1k total citations
8 papers, 621 citations indexed

About

Nuala Sykes is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Nuala Sykes has authored 8 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Cognitive Neuroscience and 3 papers in Molecular Biology. Recurrent topics in Nuala Sykes's work include Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Nuala Sykes is often cited by papers focused on Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Nuala Sykes collaborates with scholars based in United Kingdom, Italy and Australia. Nuala Sykes's co-authors include Anthony P. Monaco, Janine A. Lamb, Sonja C. Vernes, Simon E. Fisher, Fiona McKenzie, Cecilia Lai, Anthony Bailey, Faraneh Vargha‐Khadem, Robert L. Smith and Elena Bonora and has published in prestigious journals such as The American Journal of Human Genetics, Movement Disorders and European Journal of Human Genetics.

In The Last Decade

Nuala Sykes

8 papers receiving 600 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nuala Sykes United Kingdom	7	366	265	257	129	52	8	621
A. Gulhan Ercan‐Sencicek United States	11	432 1.2×	271 1.0×	434 1.7×	45 0.3×	84 1.6×	22	832
Alexis Rea United States	6	321 0.9×	279 1.1×	218 0.8×	38 0.3×	73 1.4×	7	619
Seth Dobrin United States	8	441 1.2×	239 0.9×	372 1.4×	32 0.2×	89 1.7×	15	789
Angela Caruso Italy	15	176 0.5×	279 1.1×	201 0.8×	42 0.3×	74 1.4×	28	624
Pelagia Deriziotis Netherlands	10	750 2.0×	400 1.5×	919 3.6×	56 0.4×	107 2.1×	12	1.4k
Kay MacDermot United Kingdom	9	260 0.7×	77 0.3×	206 0.8×	137 1.1×	18 0.3×	13	621
Julia V. Perederiy United States	8	505 1.4×	499 1.9×	441 1.7×	113 0.9×	172 3.3×	8	1.0k
Tiffany Vu United States	8	469 1.3×	191 0.7×	341 1.3×	70 0.5×	35 0.7×	9	691
Laura Addis United Kingdom	11	262 0.7×	195 0.7×	150 0.6×	213 1.7×	55 1.1×	15	613
Claire S. Leblond France	14	475 1.3×	478 1.8×	352 1.4×	21 0.2×	125 2.4×	18	892

Countries citing papers authored by Nuala Sykes

Since Specialization

Citations

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

Fields of papers citing papers by Nuala Sykes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nuala Sykes

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

All Works

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8 of 8 papers shown

Holt, Richard, Nuala Sykes, Inês C. Conceição, et al.. (2012). CNVs leading to fusion transcripts in individuals with autism spectrum disorder. European Journal of Human Genetics. 20(11). 1141–1147. 28 indexed citations

Sykes, Nuala, Claudio Toma, Emanuela V. Volpi, et al.. (2009). Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European Journal of Human Genetics. 17(10). 1347–1353. 54 indexed citations

Sousa, Inês, Taane G. Clark, Claudio Toma, et al.. (2008). MET and autism susceptibility: family and case–control studies. European Journal of Human Genetics. 17(6). 749–758. 64 indexed citations

Sykes, Nuala & Janine A. Lamb. (2007). Autism: the quest for the genes. Expert Reviews in Molecular Medicine. 9(24). 1–15. 37 indexed citations

Bacchelli, Elena, Francesco Blasi, Simona Carone, et al.. (2006). A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus. American Journal of Medical Genetics Part A. 767–768. 1 indexed citations

MacDermot, Kay, Elena Bonora, Nuala Sykes, et al.. (2005). Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits. The American Journal of Human Genetics. 76(6). 1074–1080. 291 indexed citations

Barnby, Gabrielle, Nuala Sykes, Andrew P. Morris, et al.. (2005). Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT. The American Journal of Human Genetics. 76(6). 950–966. 140 indexed citations

Fabbrini, Giovanni, Francesco Brancati, Laura Vacca, et al.. (2004). A novel family with an unusual early‐onset generalized dystonia. Movement Disorders. 20(1). 81–86. 6 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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