A Curtis

764 total citations
7 papers, 201 citations indexed

About

A Curtis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, A Curtis has authored 7 papers receiving a total of 201 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in A Curtis's work include Hereditary Neurological Disorders (2 papers), Protein Kinase Regulation and GTPase Signaling (1 paper) and Signaling Pathways in Disease (1 paper). A Curtis is often cited by papers focused on Hereditary Neurological Disorders (2 papers), Protein Kinase Regulation and GTPase Signaling (1 paper) and Signaling Pathways in Disease (1 paper). A Curtis collaborates with scholars based in United Kingdom and Sweden. A Curtis's co-authors include V. Spencer, Frances Elmslie, R M Gardiner, John Burn, Smaragda Kamakari, Susan Lindsay, Georgia Chenevix‐Trench, Judith Goodship, L. D. Allan and Julie R. Korenberg and has published in prestigious journals such as Nucleic Acids Research, Neurology and Genomics.

In The Last Decade

A Curtis

7 papers receiving 192 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Curtis United Kingdom	6	137	77	62	30	30	7	201
Emmanuelle Lagrue France	8	110 0.8×	64 0.8×	79 1.3×	41 1.4×	12 0.4×	20	229
Susi Strozzi Switzerland	7	68 0.5×	30 0.4×	30 0.5×	24 0.8×	11 0.4×	11	180
Nadine M. Aziz United States	7	95 0.7×	35 0.5×	97 1.6×	25 0.8×	15 0.5×	7	301
Rosa Pasquariello Italy	11	95 0.7×	50 0.6×	39 0.6×	53 1.8×	21 0.7×	43	257
Emi Shirahata Japan	7	59 0.4×	84 1.1×	35 0.6×	5 0.2×	10 0.3×	11	172
Ulvi Vaher Estonia	9	106 0.8×	55 0.7×	141 2.3×	15 0.5×	24 0.8×	15	303
Julien Van‐Gils France	8	72 0.5×	19 0.2×	70 1.1×	19 0.6×	10 0.3×	19	155
Karen J. Loechner United States	11	127 0.9×	107 1.4×	43 0.7×	46 1.5×	9 0.3×	21	266
Daniel Amsallem France	10	173 1.3×	25 0.3×	222 3.6×	81 2.7×	13 0.4×	21	335
Domenico Serino Italy	9	61 0.4×	35 0.5×	57 0.9×	30 1.0×	8 0.3×	22	192

Countries citing papers authored by A Curtis

Since Specialization

Citations

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

Fields of papers citing papers by A Curtis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Curtis

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

All Works

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7 of 7 papers shown

1.

Shaw, Pamela J., Janine Tomkins, Janet Y. Slade, et al.. (1998). Kennedy's disease: Unusual molecular pathologic and clinical features. Neurology. 51(1). 252–255. 31 indexed citations

2.

Connolly, Sheelah, et al.. (1996). Co‐dominant Inheritance of Hyperekplexia and Spastic Paraparesis. Developmental Medicine & Child Neurology. 38(8). 739–743. 10 indexed citations

3.

Elmslie, Frances, et al.. (1996). Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.. Journal of Medical Genetics. 33(5). 435–436. 65 indexed citations

4.

Curtis, A, Susan Lindsay, Eileen Boye, et al.. (1993). X chromosome linkage studies in familial Rett syndrome. Human Genetics. 90(5). 551–5. 38 indexed citations

5.

Wilson, Laura, A Curtis, Julie R. Korenberg, et al.. (1993). A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.. PubMed. 53(6). 1262–8. 37 indexed citations

6.

Porteous, Mary, A Curtis, Susan Lindsay, et al.. (1992). The gene for aarskog syndrome is located between DXS255 and DXS566 (Xp11.2–Xq13). Genomics. 14(2). 298–301. 19 indexed citations

7.

Curtis, A, et al.. (1991). A new Xmnl polymorphism for the DMD probe PERT 87–8. Nucleic Acids Research. 19(3). 680–680. 1 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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