Alison Ross

5.7k total citations
10 papers, 1.6k citations indexed

About

Alison Ross is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Alison Ross has authored 10 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Alison Ross's work include Genetic Syndromes and Imprinting (7 papers), Genetic and Kidney Cyst Diseases (6 papers) and Genomics and Rare Diseases (2 papers). Alison Ross is often cited by papers focused on Genetic Syndromes and Imprinting (7 papers), Genetic and Kidney Cyst Diseases (6 papers) and Genomics and Rare Diseases (2 papers). Alison Ross collaborates with scholars based in United Kingdom, Canada and United States. Alison Ross's co-authors include Philip L. Beales, Nicholas Katsanis, José L. Badano, Stephen J. Ansley, Michel R. Leroux, Bethan E. Hoskins, Jun Chul Kim, Carmen C. Leitch, Josephine Hill and Richard A. Lewis and has published in prestigious journals such as Nature, Nature Genetics and The Journal of Comparative Neurology.

In The Last Decade

Alison Ross

10 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alison Ross United Kingdom	7	1.1k	1.1k	274	211	106	10	1.6k
Mandy J. Croyle United States	11	538 0.5×	608 0.5×	105 0.4×	90 0.4×	54 0.5×	21	758
Phil Beales United Kingdom	6	748 0.7×	916 0.8×	212 0.8×	57 0.3×	70 0.7×	8	1.1k
Dragana Josifova United Kingdom	14	748 0.7×	611 0.5×	162 0.6×	54 0.3×	50 0.5×	27	1.1k
Anne Puech United States	15	604 0.5×	351 0.3×	109 0.4×	39 0.2×	17 0.2×	25	851
Emilie Legué United States	10	524 0.5×	392 0.4×	147 0.5×	46 0.2×	67 0.6×	13	654
Michelle L. Brinkmeier United States	21	916 0.8×	488 0.4×	65 0.2×	130 0.6×	10 0.1×	44	1.5k
Sarah S. Washington United States	6	402 0.4×	332 0.3×	121 0.4×	538 2.5×	32 0.3×	7	1.0k
Rhodora Gacayan United States	8	575 0.5×	281 0.3×	76 0.3×	94 0.4×	23 0.2×	8	850
Isabelle Maystadt Belgium	14	514 0.4×	516 0.5×	86 0.3×	51 0.2×	55 0.5×	32	946
Rachel Schot Netherlands	16	355 0.3×	260 0.2×	107 0.4×	78 0.4×	33 0.3×	35	686

Countries citing papers authored by Alison Ross

Since Specialization

Citations

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

Fields of papers citing papers by Alison Ross

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Ross

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

All Works

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10 of 10 papers shown

Yu, Jing, Ana Lisa Taylor Tavares, Woolf T. Walker, et al.. (2023). Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project. Journal of Medical Genetics. 60(12). 1235–1244. 4 indexed citations

Poole, Rebecca, Alison Cozens, Nicola Foulds, et al.. (2023). Expanding the neurodevelopmental phenotype associated with HK1 de novo heterozygous missense variants. European Journal of Medical Genetics. 66(3). 104696–104696. 1 indexed citations

Ansari, Morad, Hemant Bengani, Graeme R. Grimes, et al.. (2018). BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange–like syndrome. Nature Genetics. 50(3). 329–332. 89 indexed citations

May‐Simera, Helen, Alison Ross, Suzanne Rix, et al.. (2009). Patterns of expression of Bardet‐Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions. The Journal of Comparative Neurology. 514(2). 174–188. 32 indexed citations

Kim, Jun Chul, José L. Badano, Muneer A. Esmail, et al.. (2004). The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nature Genetics. 36(5). 462–470. 329 indexed citations

Fan, Yanli, Jane S. Green, Alison Ross, et al.. (2004). Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet?Biedl syndrome 1 critical interval. Human Genetics. 116(1-2). 62–71. 3 indexed citations

Fan, Yanli, Muneer A. Esmail, Stephen J. Ansley, et al.. (2004). Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome. Nature Genetics. 36(9). 989–993. 253 indexed citations

Ansley, Stephen J., José L. Badano, Oliver E. Blacque, et al.. (2003). Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome. Nature. 425(6958). 628–633. 495 indexed citations

Beales, Philip L., José L. Badano, Alison Ross, et al.. (2003). Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome. The American Journal of Human Genetics. 72(5). 1187–1199. 182 indexed citations

10.

Ross, Alison, Víctor L. Ruiz‐Pérez, Yiming Wang, et al.. (1998). A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis. Nature Genetics. 20(4). 358–361. 204 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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