Elliot Sollis

6.9k total citations
9 papers, 240 citations indexed

About

Elliot Sollis is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Elliot Sollis has authored 9 papers receiving a total of 240 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Elliot Sollis's work include Genomics and Rare Diseases (4 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Elliot Sollis is often cited by papers focused on Genomics and Rare Diseases (4 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Elliot Sollis collaborates with scholars based in Netherlands, United Kingdom and Australia. Elliot Sollis's co-authors include Simon E. Fisher, Pelagia Derizioti, Arianna Vino, Sarah A. Graham, Kathryn N. North, Adrian Charles, Gianina Ravenscroft, Gareth Baynam, Nigel G. Laing and Sara B. Estruch and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Elliot Sollis

9 papers receiving 239 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elliot Sollis Netherlands	7	147	113	36	26	18	9	240
Paramita Chatterjee United States	9	183 1.2×	108 1.0×	27 0.8×	14 0.5×	8 0.4×	16	294
Aline Petrin United States	9	154 1.0×	229 2.0×	53 1.5×	27 1.0×	14 0.8×	12	310
Jamil Ahmad Pakistan	13	169 1.1×	133 1.2×	17 0.5×	27 1.0×	47 2.6×	25	407
Raffaella Stallone Italy	9	110 0.7×	147 1.3×	13 0.4×	20 0.8×	6 0.3×	16	312
Kerry Fagan Australia	8	125 0.9×	146 1.3×	29 0.8×	16 0.6×	9 0.5×	10	248
Katrin Männik Estonia	7	124 0.8×	163 1.4×	15 0.4×	41 1.6×	5 0.3×	9	222
Srirangan Sampath United States	8	165 1.1×	102 0.9×	11 0.3×	22 0.8×	4 0.2×	12	246
Vera Beyer Germany	9	181 1.2×	168 1.5×	12 0.3×	61 2.3×	15 0.8×	15	318
Amber Boys Australia	7	143 1.0×	154 1.4×	11 0.3×	41 1.6×	35 1.9×	10	281
Haruka Shinohara Japan	7	224 1.5×	69 0.6×	12 0.3×	31 1.2×	5 0.3×	10	310

Countries citing papers authored by Elliot Sollis

Since Specialization

Citations

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

Fields of papers citing papers by Elliot Sollis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elliot Sollis

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

All Works

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9 of 9 papers shown

Sollis, Elliot, Joery den Hoed, Sara B. Estruch, et al.. (2022). Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions. Human Molecular Genetics. 32(9). 1497–1510. 2 indexed citations

McMahon, Aoife, Elizabeth Lewis, Annalisa Buniello, et al.. (2021). Sequencing-based genome-wide association studies reporting standards. Cell Genomics. 1(1). 100005–100005. 10 indexed citations

MacArthur, Jacqueline A. L., Annalisa Buniello, Laura W. Harris, et al.. (2021). Workshop proceedings: GWAS summary statistics standards and sharing. Cell Genomics. 1(1). 100004–100004. 17 indexed citations

Sollis, Elliot, Annalisa Buniello, María Cerezo, et al.. (2019). User-focused development of the NHGRI-EBI Genome-Wide Association Studies Catalog. Faculty of 1000 Research Ltd. 8. 1 indexed citations

Hoed, Joery den, Elliot Sollis, Hanka Venselaar, et al.. (2018). Functional characterization of TBR1 variants in neurodevelopmental disorder. Scientific Reports. 8(1). 14279–14279. 22 indexed citations

Estruch, Sara B., Sarah A. Graham, Arianna Vino, et al.. (2018). Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders. Human Molecular Genetics. 27(7). 1212–1227. 43 indexed citations

Sollis, Elliot, Pelagia Derizioti, Hirotomo Saitsu, et al.. (2017). Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human Mutation. 38(11). 1542–1554. 30 indexed citations

Sollis, Elliot, Sarah A. Graham, Arianna Vino, et al.. (2015). Identification and functional characterization ofde novo FOXP1variants provides novel insights into the etiology of neurodevelopmental disorder. Human Molecular Genetics. 25(3). 546–557. 65 indexed citations

Ravenscroft, Gianina, Elliot Sollis, Adrian Charles, et al.. (2011). Fetal akinesia: review of the genetics of the neuromuscular causes: Table 1. Journal of Medical Genetics. 48(12). 793–801. 50 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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