Suzanne Rix

1.5k total citations
4 papers, 621 citations indexed

About

Suzanne Rix is a scholar working on Genetics, Molecular Biology and Urology. According to data from OpenAlex, Suzanne Rix has authored 4 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Urology. Recurrent topics in Suzanne Rix's work include Genetic and Kidney Cyst Diseases (4 papers), Urological Disorders and Treatments (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Suzanne Rix is often cited by papers focused on Genetic and Kidney Cyst Diseases (4 papers), Urological Disorders and Treatments (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Suzanne Rix collaborates with scholars based in United Kingdom, United States and France. Suzanne Rix's co-authors include Philip L. Beales, Peter Scambler, Norann A. Zaghloul, Eyal Banin, Wafaa Eyaid, Carmen C. Leitch, Majid Alfadhel, Erica E. Davis, Anna Dı́az-Font and Nicholas Katsanis and has published in prestigious journals such as Nature Genetics, The Journal of Comparative Neurology and Human Molecular Genetics.

In The Last Decade

Suzanne Rix

4 papers receiving 613 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Suzanne Rix United Kingdom	4	538	499	91	63	39	4	621
Anna Dı́az-Font Spain	10	398 0.7×	443 0.9×	127 1.4×	45 0.7×	28 0.7×	12	622
Simon A. Ramsbottom United Kingdom	13	209 0.4×	360 0.7×	82 0.9×	45 0.7×	33 0.8×	16	432
Juliana Helou United States	5	314 0.6×	329 0.7×	35 0.4×	76 1.2×	29 0.7×	5	399
Cynthia J. Hommerding United States	7	685 1.3×	587 1.2×	66 0.7×	102 1.6×	28 0.7×	7	741
Hannah Verdin Belgium	14	268 0.5×	317 0.6×	26 0.3×	29 0.5×	20 0.5×	29	467
Alessandro Zullo Italy	7	321 0.6×	324 0.6×	55 0.6×	37 0.6×	20 0.5×	10	426
Fernanda Sarquis Jehee Brazil	13	521 1.0×	393 0.8×	70 0.8×	72 1.1×	52 1.3×	26	691
Magdalena Cárdenas-Rodríguez Uruguay	8	273 0.5×	284 0.6×	54 0.6×	24 0.4×	17 0.4×	12	364
Geneviève Pierquin Belgium	10	173 0.3×	188 0.4×	59 0.6×	59 0.9×	31 0.8×	24	318
Naiara Akizu United States	11	229 0.4×	380 0.8×	44 0.5×	50 0.8×	19 0.5×	19	484

Countries citing papers authored by Suzanne Rix

Since Specialization

Citations

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

Fields of papers citing papers by Suzanne Rix

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Rix

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

All Works

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4 of 4 papers shown

1.

Rix, Suzanne, Amélie Calmont, Peter Scambler, & Philip L. Beales. (2011). An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia. Human Molecular Genetics. 20(7). 1306–1314. 70 indexed citations

2.

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

3.

Leitch, Carmen C., Norann A. Zaghloul, Erica E. Davis, et al.. (2008). Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nature Genetics. 40(4). 443–448. 292 indexed citations

4.

Beales, Philip L., Jonathan L. Tobin, Chiara Bacchelli, et al.. (2007). IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy. Nature Genetics. 39(6). 727–729. 227 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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