S. Larkins

508 total citations
12 papers, 258 citations indexed

About

S. Larkins is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, S. Larkins has authored 12 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in S. Larkins's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (3 papers). S. Larkins is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (3 papers). S. Larkins collaborates with scholars based in United Kingdom and United States. S. Larkins's co-authors include Peter Farndon, E. V. Davison, Celia Moss, Michael W. Stacey, Jason Gardosi, Jennifer Ball, Michael Griffith, N. R. Ling, Adam Gornall and Mike Griffiths and has published in prestigious journals such as British Journal of Cancer, Developmental Medicine & Child Neurology and Journal of Medical Genetics.

In The Last Decade

S. Larkins

12 papers receiving 230 citations

Peers

S. Larkins

GENET

PPCH

HEMAT

SURGE

Charlotte Jubert France

Catarina Lundin Sweden

Ching‐In Lau United Kingdom

Christine Kowalczyk‐Quintas Switzerland

Sylvia F. Pan United States

Mauri Keinänen Finland

Anisha Solanki United Kingdom

M P Font France

Alexander Platz Germany

H.F.L. Mark United States

Charlotte Jubert France

S. Larkins

103 ×0.9

106 ×0.9

GENET

22 ×0.3

PPCH

95 ×2.1

HEMAT

12 ×0.5

SURGE

Citations per year, relative to S. Larkins S. Larkins (= 1×) peers Charlotte Jubert

Countries citing papers authored by S. Larkins

Since Specialization

Citations

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

Fields of papers citing papers by S. Larkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Larkins

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

All Works

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12 of 12 papers shown

Tonks, Ann, Adam Gornall, S. Larkins, & Jason Gardosi. (2013). Trisomies 18 and 13: trends in prevalence and prenatal diagnosis – population based study. Prenatal Diagnosis. 33(8). 742–750. 23 indexed citations

Allen, Stephanie, S. Larkins, Susan Hamilton, et al.. (2011). Implementation and Experience of an Alternative QF-PCR and MLPA Diagnostic Strategy to Detect Chromosomal Abnormalities in Fetal and Neonatal Pathology Samples. Pediatric and Developmental Pathology. 14(6). 460–468. 10 indexed citations

Taibjee, Saleem, et al.. (2009). Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes. Clinical and Experimental Dermatology. 34(7). 823–829. 8 indexed citations

Allen, Stephanie, et al.. (2006). Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS. Prenatal Diagnosis. 26(12). 1160–1167. 15 indexed citations

Bown, Nick, Simon Cotterill, Paul Roberts, et al.. (2001). Cytogenetic abnormalities and clinical outcome in Wilms tumor: A study by the U.K. cancer cytogenetics group and the U.K. Children's Cancer Study Group†. Medical and Pediatric Oncology. 38(1). 11–21. 48 indexed citations

Larkins, S., et al.. (1999). Mild developmental delay due to ring chromosome 19 mosaicism. Developmental Medicine & Child Neurology. 41(1). 48–50. 1 indexed citations

Larkins, S., et al.. (1999). Mild developmental delay due to ring chromosome 19 mosaicism. Developmental Medicine & Child Neurology. 41(1). 48–50. 4 indexed citations

Jacob, Allison P., Mike Griffiths, S. Larkins, & J. A. Holmes. (1997). t(3;21) following peripheral blood stem cell transplantation in chronic phase chronic myeloid leukaemia. Bone Marrow Transplantation. 19(12). 1255–1258. 4 indexed citations

Moss, Celia, et al.. (1993). Epidermal mosaicism and Blaschko's lines.. Journal of Medical Genetics. 30(9). 752–755. 59 indexed citations

10.

Bunce, Christopher M., et al.. (1991). Defective erythropoiesis in primary myelofibrosis associated with a chromosome 11 abnormality. British Journal of Cancer. 64(1). 128–131. 4 indexed citations

11.

Lowe, J., Jennifer Ball, N. R. Ling, et al.. (1989). Two new IgA1-kappa plasma cell leukaemia cell lines (JJN-1 & JJN-2) which proliferate in response to B cell stimulatory factor 2.. PubMed. 75(1). 93–9. 51 indexed citations

12.

Griffiths, Mark, M. R. Creasy, Peter Farndon, et al.. (1988). Are double translocations double trouble?. Journal of Medical Genetics. 25(5). 326–331. 31 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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