Brenda McInnes

592 total citations
8 papers, 242 citations indexed

About

Brenda McInnes is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Reproductive Medicine. According to data from OpenAlex, Brenda McInnes has authored 8 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 2 papers in Public Health, Environmental and Occupational Health and 2 papers in Reproductive Medicine. Recurrent topics in Brenda McInnes's work include Genomics and Rare Diseases (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and BRCA gene mutations in cancer (2 papers). Brenda McInnes is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and BRCA gene mutations in cancer (2 papers). Brenda McInnes collaborates with scholars based in Canada, United States and United Kingdom. Brenda McInnes's co-authors include Alfred Rademaker, Renée H. Martin, Rubén Martín‐Arenas, Calvin Greene, Leona Barclay, François P. Bernier, A. Micheil Innes, Deborah A. Marshall, Karen V. MacDonald and Kym M. Boycott and has published in prestigious journals such as Human Reproduction, Genetics in Medicine and American Journal of Medical Genetics Part C Seminars in Medical Genetics.

In The Last Decade

Brenda McInnes

8 papers receiving 238 citations

Peers

Brenda McInnes

GENET

RM

PPCH

PHEOH

MB

Soumaya Mougou Tunisia

J. Lespinasse France

Capucine Hyon France

Rubén Martín‐Arenas Spain

Theresa Naluai-Cecchini United States

Pere Mir Spain

Ludmila Voložonoka Latvia

Alvin S.T. Lim Singapore

Judith Gianotten Netherlands

Géraldine Joly‐Hélas France

Soumaya Mougou Tunisia

Brenda McInnes

121 ×0.7

GENET

93 ×1.0

RM

61 ×0.8

PPCH

114 ×1.6

PHEOH

87 ×1.9

MB

Citations per year, relative to Brenda McInnes Brenda McInnes (= 1×) peers Soumaya Mougou

Countries citing papers authored by Brenda McInnes

Since Specialization

Citations

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

Fields of papers citing papers by Brenda McInnes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brenda McInnes

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

All Works

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8 of 8 papers shown

1.

Michaels-Igbokwe, Christine, Brenda McInnes, Karen V. MacDonald, et al.. (2020). (Un)standardized testing: the diagnostic odyssey of children with rare genetic disorders in Alberta, Canada. Genetics in Medicine. 23(2). 272–279. 21 indexed citations

2.

Marshall, Deborah A., Karen V. MacDonald, Sebastian Heidenreich, et al.. (2019). The value of diagnostic testing for parents of children with rare genetic diseases. Genetics in Medicine. 21(12). 2798–2806. 40 indexed citations

3.

Innes, A. Micheil, Brenda McInnes, & David A. Dyment. (2018). Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(4). 387–397. 10 indexed citations

4.

Sawyer, Sarah L., Frank Dicke, Adam Kirton, et al.. (2013). Longer Term Survival of a Child With Autosomal Recessive Cutis Laxa Due to a Mutation in FBLN4. American Journal of Medical Genetics Part A. 161(5). 1148–1153. 18 indexed citations

5.

Shetty, Shashirekha, Kym M. Boycott, Jillian S. Parboosingh, et al.. (2007). Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis. Clinical Dysmorphology. 16(4). 253–256. 4 indexed citations

6.

Martin, Renée H., Brenda McInnes, & Alfred Rademaker. (1999). Analysis of aneuploidy for chromosomes 13, 21, X and Y by multicolour fluorescence in situ hybridisation (FISH) in a 47,XYY male. Zygote. 7(2). 131–134. 24 indexed citations

7.

McInnes, Brenda, Alfred Rademaker, & Rubén Martín‐Arenas. (1998). Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human spermatozoa using multicolour fluorescence in-situ hybridization. Human Reproduction. 13(9). 2489–2494. 55 indexed citations

8.

McInnes, Brenda, et al.. (1998). Abnormalities for chromosomes 13 and 21 detected in spermatozoa from infertile men. Human Reproduction. 13(10). 2787–2790. 70 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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