Lindsay Brown

2.3k total citations
35 papers, 1.0k citations indexed

About

Lindsay Brown is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lindsay Brown has authored 35 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lindsay Brown's work include Genomic variations and chromosomal abnormalities (6 papers), DNA Repair Mechanisms (4 papers) and BRCA gene mutations in cancer (3 papers). Lindsay Brown is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), DNA Repair Mechanisms (4 papers) and BRCA gene mutations in cancer (3 papers). Lindsay Brown collaborates with scholars based in Canada, United Kingdom and United States. Lindsay Brown's co-authors include David G. Huntsman, Virginia Murray, Julien Penders, Jolyon M. Medlock, C. Blake Gilks, Melinda A. Miller, Robin Parker, Chris Van Hoof, Paul T. Spellman and Ie−Ming Shih and has published in prestigious journals such as Nature, New England Journal of Medicine and JNCI Journal of the National Cancer Institute.

In The Last Decade

Lindsay Brown

34 papers receiving 995 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lindsay Brown Canada 20 443 224 213 159 103 35 1.0k
Yoshiki Kudo Japan 28 707 1.6× 227 1.0× 172 0.8× 214 1.3× 180 1.7× 96 2.5k
Bernd Frank Germany 24 748 1.7× 277 1.2× 228 1.1× 210 1.3× 96 0.9× 48 1.5k
Kristina Allen‐Brady United States 22 440 1.0× 93 0.4× 622 2.9× 122 0.8× 52 0.5× 80 1.4k
David Connor Australia 24 609 1.4× 90 0.4× 49 0.2× 78 0.5× 155 1.5× 72 1.8k
Francesca M. Spagnoli United Kingdom 24 1.1k 2.5× 210 0.9× 267 1.3× 228 1.4× 55 0.5× 54 2.0k
Sascha Tierling Germany 24 1.2k 2.6× 152 0.7× 516 2.4× 217 1.4× 72 0.7× 56 2.0k
Jennifer Yen United States 13 396 0.9× 136 0.6× 144 0.7× 149 0.9× 140 1.4× 34 996
Margaret A. Smith United States 17 451 1.0× 192 0.9× 220 1.0× 30 0.2× 101 1.0× 43 1.5k
Andrew van Hasselt Hong Kong 21 415 0.9× 319 1.4× 78 0.4× 143 0.9× 139 1.3× 41 1.3k
Sarah Collins United States 21 635 1.4× 67 0.3× 189 0.9× 105 0.7× 194 1.9× 58 1.4k

Countries citing papers authored by Lindsay Brown

Since Specialization
Citations

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

Fields of papers citing papers by Lindsay Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lindsay Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Lindsay Brown. A scholar is included among the top collaborators of Lindsay Brown 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 Lindsay Brown. Lindsay Brown 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.
Loeff, Ina Schim van der, Angela L. Duker, Gillian Rice, et al.. (2025). Mutations in RNU4ATAC Are Associated With Chilblain‐Like Lesions and Enhanced Type I Interferon Signalling. European Journal of Immunology. 55(5). e202451518–e202451518.
2.
O’Neill, Kieran, Lindsay Brown, Kamilla Schlade‐Bartusiak, et al.. (2021). An approach to rapid characterization of DMD copy number variants for prenatal risk assessment. American Journal of Medical Genetics Part A. 185(8). 2541–2545. 7 indexed citations
3.
Jacquinet, Adeline, Lindsay Brown, Pengfei Liu, et al.. (2017). Expanding the FANCO/RAD51C associated phenotype: Cleft lip and palate and lobar holoprosencephaly, two rare findings in Fanconi anemia. European Journal of Medical Genetics. 61(5). 257–261. 9 indexed citations
4.
Thibodeau, My Linh, Michelle Steinraths, Lindsay Brown, et al.. (2017). Genomic and Cytogenetic Characterization of a Balanced Translocation Disrupting <b><i>NUP98</i></b>. Cytogenetic and Genome Research. 152(3). 117–121. 2 indexed citations
5.
Tucker, Tracy, Michelle Steinraths, Tanya N. Nelson, et al.. (2015). Incidental finding of paternal UPD15 in a child with a deletion of 11q21–q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features. Clinical Dysmorphology. 25(2). 77–81. 1 indexed citations
6.
McCarthy, Cormac, Lindsay Brown, Patricia A. Jones, et al.. (2013). Use of a care bundle in the emergency department for acute exacerbations of chronic obstructive pulmonary disease: a feasibility study. International Journal of COPD. 8. 605–605. 30 indexed citations
7.
Brown, Lindsay, Jolyon M. Medlock, & Virginia Murray. (2013). Impact of drought on vector-borne diseases – how does one manage the risk?. Public Health. 128(1). 29–37. 63 indexed citations
8.
Tucker, Tracy, Kamilla Schlade‐Bartusiak, Patrice Eydoux, Tanya N. Nelson, & Lindsay Brown. (2012). Uniparental disomy: can SNP array data be used for diagnosis?. Genetics in Medicine. 14(8). 753–756. 24 indexed citations
9.
Schlade‐Bartusiak, Kamilla, Lindsay Brown, Brenda Lomax, et al.. (2012). BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1). American Journal of Medical Genetics Part A. 158A(9). 2322–2327. 19 indexed citations
10.
Falconer, Ester, Elizabeth A. Chavez, Steven S.S. Poon, et al.. (2009). Identification of sister chromatids by DNA template strand sequences. Nature. 463(7277). 93–97. 71 indexed citations
11.
Brown, Lindsay, Samuel Leung, Tarek A. Bismar, et al.. (2009). Co-amplification of CCND1 and EMSY is associated with an adverse outcome in ER-positive tamoxifen-treated breast cancers. Breast Cancer Research and Treatment. 121(2). 347–354. 34 indexed citations
12.
Grundlehner, Bernard, Lindsay Brown, Julien Penders, & B. Gyselinckx. (2009). The Design and Analysis of a Real-Time, Continuous Arousal Monitor. 115. 156–161. 23 indexed citations
13.
Brown, Lindsay & David G. Huntsman. (2007). Fluorescent in situ hybridization on tissue microarrays: challenges and solutions. Journal of Molecular Histology. 38(2). 151–157. 39 indexed citations
14.
Savage, Kay, Samuel Leung, Shawn Todd, et al.. (2007). Distribution and significance of caveolin 2 expression in normal breast and invasive breast cancer: an immunofluorescence and immunohistochemical analysis. Breast Cancer Research and Treatment. 110(2). 245–256. 65 indexed citations
15.
Lee, Cheng‐Han, David G. Huntsman, Maggie C.U. Cheang, et al.. (2005). Assessment of Her-1, Her-2, and Her-3 Expression and Her-2 Amplification in Advanced Stage Ovarian Carcinoma. International Journal of Gynecological Pathology. 24(2). 147–152. 58 indexed citations
16.
Prentice, Leah, Ashleen Shadeo, Valia S. Lestou, et al.. (2005). NRG1 gene rearrangements in clinical breast cancer: identification of an adjacent novel amplicon associated with poor prognosis. Oncogene. 24(49). 7281–7289. 52 indexed citations
17.
Raouf, Afshin, et al.. (2005). Genomic Instability of Human Mammary Epithelial Cells Overexpressing a Truncated Form of EMSY. JNCI Journal of the National Cancer Institute. 97(17). 1302–1306. 32 indexed citations
18.
Bamforth, Fiona, Lindsay Brown, Janine Senz, & David G. Huntsman. (2003). Mechanisms of monozygotic (MZ) twinning: A possible role for the cell adhesion molecule, E‐cadherin. American Journal of Medical Genetics Part A. 120A(1). 59–62. 9 indexed citations
19.
Pharoah, Paul D.P., Carla Oliveíra, José Carlos Machado, et al.. (2002). CDH1 c‐160a promotor polymorphism is not associated with risk of stomach cancer. International Journal of Cancer. 101(2). 196–197. 53 indexed citations
20.
Dowd, N., et al.. (1999). Iontophoretic Vincristine in the Treatment of Postherpetic Neuralgia. Journal of Pain and Symptom Management. 17(3). 175–180. 12 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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