Sarah Lindsay

27.0k total citations
19 papers, 1.2k citations indexed

About

Sarah Lindsay is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sarah Lindsay has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Sarah Lindsay's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Rare Diseases (4 papers). Sarah Lindsay is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Rare Diseases (4 papers). Sarah Lindsay collaborates with scholars based in United Kingdom, United States and Canada. Sarah Lindsay's co-authors include Matthew E. Hurles, Raheleh Rahbari, Robert J. Hardwick, Andrew D. Morris, Arthur Wüster, Anna F. Dominiczak, David J. Porteous, Michael R. Stratton, Blair H. Smith and Ludmil B. Alexandrov and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Genetics.

In The Last Decade

Sarah Lindsay

18 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah Lindsay United Kingdom 12 707 613 230 225 109 19 1.2k
Catarina D. Campbell United States 13 561 0.8× 534 0.9× 220 1.0× 111 0.5× 34 0.3× 20 1.2k
Peter M. Kroisel Austria 16 658 0.9× 935 1.5× 65 0.3× 172 0.8× 148 1.4× 38 1.5k
Asaf Hellman Israel 12 683 1.0× 1.7k 2.7× 269 1.2× 83 0.4× 170 1.6× 18 1.9k
Donncha S. Dunican United Kingdom 17 388 0.5× 1.6k 2.7× 193 0.8× 148 0.7× 106 1.0× 21 1.8k
Matthieu Gérard France 22 542 0.8× 1.7k 2.7× 92 0.4× 122 0.5× 48 0.4× 35 1.9k
Irina Stancheva United Kingdom 23 626 0.9× 1.8k 2.9× 306 1.3× 115 0.5× 103 0.9× 28 2.0k
David J. Katz United States 12 924 1.3× 1.7k 2.8× 87 0.4× 113 0.5× 410 3.8× 20 1.9k
Irene Hernando-Herraez United Kingdom 12 345 0.5× 1.2k 2.0× 110 0.5× 84 0.4× 75 0.7× 13 1.4k
Kelly Thomas United States 15 962 1.4× 790 1.3× 87 0.4× 61 0.3× 79 0.7× 22 1.6k

Countries citing papers authored by Sarah Lindsay

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Lindsay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Lindsay

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

All Works

19 of 19 papers shown
1.
Bian, Wenxin, Jing Wang, Matthias Hoben, et al.. (2025). Exploring Safety Concerns in Assisted Living Communities: A Qualitative Comparison of Resident, Family, and Staff Perspectives. Journal of the American Medical Directors Association. 26(12). 105910–105910.
2.
Lindsay, Sarah, et al.. (2023). Elastomeric Porous Poly(glycerol sebacate) Methacrylate (PGSm) Microspheres as 3D Scaffolds for Chondrocyte Culture and Cartilage Tissue Engineering. International Journal of Molecular Sciences. 24(13). 10445–10445. 1 indexed citations
3.
Radford, Elizabeth J., Malin H. L. Andersson, James Stephenson, et al.. (2023). Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation. Nature Communications. 14(1). 7702–7702. 24 indexed citations
4.
Hartnett, Janice, et al.. (2022). Quality-Improvement Initiative for Expedited Partner Therapy Provision in an Obstetrics and Gynecology Office. Obstetrics and Gynecology. 140(2). 305–310. 1 indexed citations
5.
Massey, Andrew, et al.. (2021). Bubble concept for sporting tournaments during the COVID-19 pandemic: Football Club World Cup. BMJ Open Sport & Exercise Medicine. 7(2). e001126–e001126. 10 indexed citations
6.
Gardner, Eugene J., Alejandro Sifrim, Sarah Lindsay, et al.. (2021). Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders. The American Journal of Human Genetics. 108(11). 2186–2194. 11 indexed citations
7.
Lindsay, Sarah, Raheleh Rahbari, Joanna Kaplanis, Thomas Keane, & Matthew E. Hurles. (2019). Similarities and differences in patterns of germline mutation between mice and humans. Nature Communications. 10(1). 4053–4053. 78 indexed citations
8.
Beal, Marc A., Matthew J. Meier, Andrew Williams, et al.. (2019). Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspring. Communications Biology. 2(1). 228–228. 26 indexed citations
9.
Carvalho, Claudia M.B., Rolph Pfundt, Daniel A. King, et al.. (2015). Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements. The American Journal of Human Genetics. 96(4). 555–564. 42 indexed citations
10.
Rahbari, Raheleh, Arthur Wüster, Sarah Lindsay, et al.. (2015). Timing, rates and spectra of human germline mutation. Nature Genetics. 48(2). 126–133. 381 indexed citations
11.
Lindsay, Sarah, et al.. (2015). The genome-wide effects of ionizing radiation on mutation induction in the mammalian germline. Nature Communications. 6(1). 100 indexed citations
12.
MacArthur, Jacqueline A. L., Timothy D. Spector, Sarah Lindsay, et al.. (2014). The Rate of Nonallelic Homologous Recombination in Males Is Highly Variable, Correlated between Monozygotic Twins and Independent of Age. PLoS Genetics. 10(3). e1004195–e1004195. 23 indexed citations
13.
Wheeler, Eleanor, Ni Huang, Elena G. Bochukova, et al.. (2013). Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. Nature Genetics. 45(5). 513–517. 219 indexed citations
14.
Liu, Pengfei, Klaudia Walter, Karin Writzl, et al.. (2012). Multiple de novo copy number variations in two subjects with developmental problems and multiple congenital anomalies. BMC Proceedings. 6(S6). 1 indexed citations
15.
Conrad, Donald F., Christine Bird, Benjamin P. Blackburne, et al.. (2010). Mutation spectrum revealed by breakpoint sequencing of human germline CNVs. Nature Genetics. 42(5). 385–391. 169 indexed citations
16.
Lindsay, Sarah, Mehrdad Khajavi, James R. Lupski, & Matthew E. Hurles. (2006). A Chromosomal Rearrangement Hotspot Can Be Identified from Population Genetic Variation and Is Coincident with a Hotspot for Allelic Recombination. The American Journal of Human Genetics. 79(5). 890–902. 72 indexed citations
17.
Gribble, Susan, Dimitrios Rafail Kalaitzopoulos, D. C. Burford, et al.. (2006). Ultra-high resolution array painting facilitates breakpoint sequencing. Journal of Medical Genetics. 44(1). 51–58. 23 indexed citations
18.
Lindsay, Sarah. (2005). Shotgun haplotyping: a novel method for surveying allelic sequence variation. Nucleic Acids Research. 33(18). e152–e152. 5 indexed citations
19.
Murray, Joseph A., et al.. (1991). GENETIC AND PHYSICAL MAPPING AROUND THE RETINITIS-PIGMENTOSA (RP2) LOCUS IN XP11.23. UCL Discovery (University College London). 1 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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