Sarah Rickard

638 total citations
7 papers, 385 citations indexed

About

Sarah Rickard is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Sarah Rickard has authored 7 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Surgery. Recurrent topics in Sarah Rickard's work include Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (2 papers) and Genomics and Rare Diseases (1 paper). Sarah Rickard is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (2 papers) and Genomics and Rare Diseases (1 paper). Sarah Rickard collaborates with scholars based in United Kingdom, Netherlands and United States. Sarah Rickard's co-authors include Shinji Saitoh, Robert D. Nicholls, Jessica L. Buxton, Bärbel Dittrich, Bernhard Zabel, Karin Buiting, Bernd Korn, Poustka Annemarie, Bernhard Horsthemke and Andreas Winterpacht and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Sarah Rickard

7 papers receiving 366 citations

Peers

Sarah Rickard

MB

GENET

PPCH

SS

CN

Alisha Wilkens United States

Teresa Palladino Italy

Jiale Xiang China

Barbara Günther Austria

Judith Löffler Austria

Rikkert L. Snoeckx Belgium

Payman Jamali Iran

Joy Samanich United States

Nikolay A. Barashkov Russia

Rita Teek Estonia

Alisha Wilkens United States

Sarah Rickard

239 ×0.8

MB

255 ×1.0

GENET

104 ×0.9

PPCH

61 ×0.9

SS

26 ×0.8

CN

Citations per year, relative to Sarah Rickard Sarah Rickard (= 1×) peers Alisha Wilkens

Countries citing papers authored by Sarah Rickard

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Rickard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Rickard

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Rickard, Sarah, et al.. (2024). Nurses' Perceptions of Caring at Work. JONA The Journal of Nursing Administration. 54(3). 154–159. 1 indexed citations

2.

Hitchins, Megan P., Sarah Rickard, Fatima Dhalla, et al.. (2005). Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS (Am J Med Genet 125A: 167–172). American Journal of Medical Genetics Part A. 135A(3). 346–346. 1 indexed citations

3.

Hitchins, Megan P., Sarah Rickard, Fatima Dhalla, et al.. (2003). Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS. American Journal of Medical Genetics Part A. 125A(2). 167–172. 39 indexed citations

4.

Rickard, Sarah & Louise C. Wilson. (2003). Analysis of GNAS1 and Overlapping Transcripts Identifies the Parental Origin of Mutations in Patients with Sporadic Albright Hereditary Osteodystrophy and Reveals a Model System in Which to Observe the Effects of Splicing Mutations on Translated and Untranslated Messenger RNA. The American Journal of Human Genetics. 72(4). 961–974. 27 indexed citations

5.

Rickard, Sarah, William van’t Hoff, Angela Barnicoat, et al.. (2001). Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1 : molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM. Human Genetics. 108(5). 398–403. 45 indexed citations

6.

Houseman, Mark, Lucy Ellis, Alistair T. Pagnamenta, et al.. (2001). Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss. Journal of Medical Genetics. 38(1). 20–25. 75 indexed citations

7.

Dittrich, Bärbel, Karin Buiting, Bernd Korn, et al.. (1996). Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nature Genetics. 14(2). 163–170. 197 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.

Explore authors with similar magnitude of impact