Susan Lindsay

10.9k total citations
108 papers, 4.2k citations indexed

About

Susan Lindsay is a scholar working on Molecular Biology, Genetics and Developmental Neuroscience. According to data from OpenAlex, Susan Lindsay has authored 108 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 26 papers in Genetics and 10 papers in Developmental Neuroscience. Recurrent topics in Susan Lindsay's work include Congenital heart defects research (12 papers), Epigenetics and DNA Methylation (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Susan Lindsay is often cited by papers focused on Congenital heart defects research (12 papers), Epigenetics and DNA Methylation (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Susan Lindsay collaborates with scholars based in United Kingdom, United States and France. Susan Lindsay's co-authors include Adrian Bird, Gavin J. Clowry, David I. Wilson, Nadhim Bayatti, T Strachan, Majlinda Lako, Steven Lisgo, I.L. Chaikoff, John Burn and Lesley M. Forrester and has published in prestigious journals such as Nature, Science and Nature Genetics.

In The Last Decade

Susan Lindsay

108 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susan Lindsay United Kingdom 37 2.7k 1.3k 503 463 393 108 4.2k
E. Bryan Crenshaw United States 32 4.0k 1.5× 1.3k 1.0× 667 1.3× 544 1.2× 435 1.1× 51 5.9k
Tessa Homfray United Kingdom 25 3.3k 1.3× 1.1k 0.9× 474 0.9× 787 1.7× 616 1.6× 69 5.8k
D. Wénzel Germany 19 2.9k 1.1× 439 0.4× 430 0.9× 867 1.9× 614 1.6× 59 4.8k
Siew‐Lan Ang United States 37 4.4k 1.7× 988 0.8× 906 1.8× 640 1.4× 383 1.0× 48 6.2k
M. Albert Basson United Kingdom 34 3.2k 1.2× 758 0.6× 514 1.0× 276 0.6× 176 0.4× 73 4.6k
Anthony T. Yachnis United States 46 2.4k 0.9× 934 0.7× 375 0.7× 1.0k 2.3× 315 0.8× 143 6.4k
James Ellis Canada 44 5.1k 1.9× 1.9k 1.5× 995 2.0× 697 1.5× 214 0.5× 123 7.1k
Carol-Anne Martin United Kingdom 5 3.5k 1.3× 523 0.4× 298 0.6× 747 1.6× 614 1.6× 7 5.2k
Yukio Saijoh Japan 39 5.7k 2.2× 2.0k 1.6× 741 1.5× 281 0.6× 127 0.3× 77 6.8k
Atsushi Yoshiki Japan 35 2.2k 0.8× 839 0.7× 188 0.4× 987 2.1× 322 0.8× 108 4.2k

Countries citing papers authored by Susan Lindsay

Since Specialization
Citations

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

Fields of papers citing papers by Susan Lindsay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Lindsay

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

All Works

20 of 20 papers shown
1.
Fletcher, Emily V., Ranad Shaheen, Michael S. Nahorski, et al.. (2021). Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly. Journal of Medical Genetics. 59(4). 358–365. 2 indexed citations
2.
3.
Chavali, Pavithra L., Lovorka Stojic, Luke W. Meredith, et al.. (2017). Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replication. Science. 357(6346). 83–88. 117 indexed citations
4.
5.
Lindsay, Susan, et al.. (2013). The Early Fetal Development of Human Neocortical GABAergic Interneurons. Cerebral Cortex. 25(3). 631–645. 65 indexed citations
6.
Thomas, Mervyn G., Moira Crosier, Susan Lindsay, et al.. (2012). Retinal Changes In Idiopathic Infantile Nystagmus Associated With FRMD7 Mutations. Investigative Ophthalmology & Visual Science. 53(14). 520–520. 1 indexed citations
7.
Bayatti, Nadhim, Christopher E. Shaw, J A Eyre, et al.. (2008). Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development. European Journal of Neuroscience. 28(8). 1449–1456. 59 indexed citations
8.
Burton, Nick, Bill Hill, Duncan Davidson, et al.. (2005). JAtlasView: a Java atlas-viewer for browsing biomedical 3D images and atlases. BMC Bioinformatics. 6(1). 47–47. 13 indexed citations
9.
Lisgo, Steven, T Strachan, Duncan Davidson, et al.. (1999). Mapping gene expression domains and neuronal cell differentiation during human embryonic forebrain development. The American Journal of Human Genetics. 2 indexed citations
10.
Hanley, Neil A., Steve Ball, Mark Clement-Jones, et al.. (1999). Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination. Mechanisms of Development. 87(1-2). 175–180. 134 indexed citations
11.
Huber, Reid, Richard Mazzarella, Ellson Chen, et al.. (1998). Glypican 3 and glypican 4 are juxtaposed in Xq26.1. Gene. 225(1-2). 9–16. 12 indexed citations
12.
Ross, Alison, Víctor L. Ruiz‐Pérez, Yiming Wang, et al.. (1998). A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis. Nature Genetics. 20(4). 358–361. 204 indexed citations
13.
Lindsay, Susan, Mark Ireland, Jill Clayton‐Smith, et al.. (1997). Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.. Journal of Medical Genetics. 34(6). 480–483. 58 indexed citations
14.
Rankin, Julia, Kenneth Smith, Emmanuel Huguet, et al.. (1997). A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas. Oncogene. 14(10). 1249–1253. 75 indexed citations
15.
Sertedaki, Amalia & Susan Lindsay. (1996). CAC – the neglected repeat. BioEssays. 18(3). 237–242. 5 indexed citations
16.
Thiselton, Dawn L., Smaragda Kamakari, Michel P. Coleman, et al.. (1993). Dinucleotide repeat polymorphism at the DXS556 locus. Human Molecular Genetics. 2(5). 613–613. 3 indexed citations
17.
Lindsay, Susan, C.F. Inglehearn, Ann Curtis, & Shomi S. Bhattacharya. (1992). Molecular genetics of inherited retinal degenerations. Current Opinion in Genetics & Development. 2(3). 459–466. 11 indexed citations
18.
Lindsay, Susan, et al.. (1965). Medullary carcinoma of the thyroid gland.. PubMed. 80(6). 575–82. 23 indexed citations
19.
Nichols, C. W., Susan Lindsay, Douglas Chapman, & I.L. Chaikoff. (1960). Prolonged Δ 4 -Cholestenone Feeding in Birds. Circulation Research. 8(1). 16–28. 2 indexed citations
20.
Lindsay, Susan, et al.. (1960). Levels of Eosinophils, Platelets, Leukocytes and 17-Hydroxycorticosteroids During Normal Menstrual Cycle.. Experimental Biology and Medicine. 104(1). 145–147. 17 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

Breakdown of academic impact, for papers by E. Bryan Crenshaw Breakdown of academic impact, for papers by Tessa Homfray Breakdown of academic impact, for papers by D. Wénzel Breakdown of academic impact, for papers by Siew‐Lan Ang Breakdown of academic impact, for papers by M. Albert Basson Breakdown of academic impact, for papers by Anthony T. Yachnis Breakdown of academic impact, for papers by James Ellis Breakdown of academic impact, for papers by Carol-Anne Martin Breakdown of academic impact, for papers by Yukio Saijoh Breakdown of academic impact, for papers by Atsushi Yoshiki
Rankless by CCL
2026