C. R. Boustred

3.5k total citations
15 papers, 635 citations indexed

About

C. R. Boustred is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, C. R. Boustred has authored 15 papers receiving a total of 635 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in C. R. Boustred's work include Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (5 papers) and Fetal and Pediatric Neurological Disorders (5 papers). C. R. Boustred is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (5 papers) and Fetal and Pediatric Neurological Disorders (5 papers). C. R. Boustred collaborates with scholars based in United Kingdom, Saudi Arabia and Norway. C. R. Boustred's co-authors include Lyn S. Chitty, Richard H. Scott, Natalie Trump, Nicholas Lench, Suzanne Drury, Kitty Lo, Vincent Plagnol, Fiona McKay, Sarah Mason and Hywel Williams and has published in prestigious journals such as Bioinformatics, Brain and The American Journal of Human Genetics.

In The Last Decade

C. R. Boustred

15 papers receiving 617 citations

Peers

C. R. Boustred

GENET

PPCH

PMH

SURGE

Ji Yoon Han South Korea

Linda M. Randolph United States

Linhuan Huang China

C. P. Schwarze Germany

Layla Shahmirzadi United States

Nidhi Shah United States

Dorota Dunin-Wąsowicz Poland

Christopher Chun Yu Mak Hong Kong

Caleb Bupp United States

Naama Orenstein Israel

Ji Yoon Han South Korea

C. R. Boustred

145 ×0.4

GENET

86 ×0.3

PPCH

139 ×0.9

103 ×1.3

PMH

18 ×0.2

SURGE

Citations per year, relative to C. R. Boustred C. R. Boustred (= 1×) peers Ji Yoon Han

Countries citing papers authored by C. R. Boustred

Since Specialization

Citations

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

Fields of papers citing papers by C. R. Boustred

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. R. Boustred. 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 C. R. Boustred. The network helps show where C. R. Boustred may publish in the future.

Co-authorship network of co-authors of C. R. Boustred

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

All Works

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15 of 15 papers shown

Deans, Zandra C., Christophe Roos, Farrah Khawaja, et al.. (2019). One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants. European Journal of Human Genetics. 28(2). 202–212. 13 indexed citations

Futema, Marta, Jackie A. Cooper, Marietta Charakida, et al.. (2017). Screening for familial hypercholesterolaemia in childhood: Avon Longitudinal Study of Parents and Children (ALSPAC). Atherosclerosis. 260. 47–55. 20 indexed citations

Ishida, Miho, Thomas Cullup, C. R. Boustred, et al.. (2017). A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly. Clinical Genetics. 93(4). 870–879. 22 indexed citations

Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations

Trump, Natalie, Amy McTague, Helen Brittain, et al.. (2016). Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Journal of Medical Genetics. 53(5). 310–317. 147 indexed citations

Drury, Suzanne, Sarah Mason, Fiona McKay, et al.. (2016). Implementing Non-Invasive Prenatal Diagnosis (NIPD) in a National Health Service Laboratory; From Dominant to Recessive Disorders. Advances in experimental medicine and biology. 924. 71–75. 32 indexed citations

Lo, Kitty, C. R. Boustred, Fiona McKay, et al.. (2016). Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities. Obstetrical & Gynecological Survey. 71(4). 211–213. 1 indexed citations

Futema, Marta, Meena Kumari, C. R. Boustred, Mika Kivimäki, & Steve E. Humphries. (2015). Would raising the total cholesterol diagnostic cut-off from 7.5 mmol/L to 9.3 mmol/L improve detection rate of patients with monogenic familial hypercholesterolaemia?. Atherosclerosis. 239(2). 295–298. 12 indexed citations

Drury, Suzanne, Hywel Williams, Natalie Trump, et al.. (2015). Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities. Prenatal Diagnosis. 35(10). 1010–1017. 129 indexed citations

10.

Lo, Kitty, C. R. Boustred, Fiona McKay, et al.. (2015). Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities. The American Journal of Human Genetics. 98(1). 34–44. 86 indexed citations

11.

Hill, Melissa, D. Wright, Rebecca Daley, et al.. (2014). Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol. BMC Pregnancy and Childbirth. 14(1). 229–229. 61 indexed citations

12.

Lo, Kitty, C. R. Boustred, Lyn S. Chitty, & Vincent Plagnol. (2014). RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy. Bioinformatics. 30(20). 2965–2967. 24 indexed citations

13.

Drury, Suzanne, C. R. Boustred, Mehmet Tekman, et al.. (2014). A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis—Further evidence of genotype–phenotype correlation. American Journal of Medical Genetics Part A. 164(7). 1777–1783. 21 indexed citations

14.

Alharbi, Khalid Khalaf, Tom G. Richardson, Imran Ali Khan, et al.. (2014). Influence of Adiposity-Related Genetic Markers in a Population of Saudi Arabians Where Other Variables Influencing Obesity May Be Reduced. Disease Markers. 2014. 1–6. 24 indexed citations

15.

Alsaadi, Muslim M., Tom R. Gaunt, C. R. Boustred, et al.. (2012). From a Single Whole Exome Read to Notions of Clinical Screening: Primary Ciliary Dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula. Annals of Human Genetics. 76(3). 211–220. 16 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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