Andrée MacMillan

1.4k total citations
7 papers, 147 citations indexed

About

Andrée MacMillan is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Andrée MacMillan has authored 7 papers receiving a total of 147 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Genetics. Recurrent topics in Andrée MacMillan's work include Genetic factors in colorectal cancer (3 papers), DNA Repair Mechanisms (2 papers) and Cancer Genomics and Diagnostics (2 papers). Andrée MacMillan is often cited by papers focused on Genetic factors in colorectal cancer (3 papers), DNA Repair Mechanisms (2 papers) and Cancer Genomics and Diagnostics (2 papers). Andrée MacMillan collaborates with scholars based in Canada, Germany and United States. Andrée MacMillan's co-authors include Elke Holinski‐Feder, Holly Etchegary, Peter Reilich, Sabine Krause, Jens Reimann, Douglass M. Turnbull, Gráinne S. Gorman, Rita Horváth, Nicolai Schramm and Gregor Witte and has published in prestigious journals such as Journal of Neurology, Cancer Medicine and BMC Medical Genetics.

In The Last Decade

Andrée MacMillan

7 papers receiving 144 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrée MacMillan Canada 7 69 55 47 44 21 7 147
Antonia Henne Germany 4 119 1.7× 25 0.5× 17 0.4× 29 0.7× 7 0.3× 6 195
Friedrich Stock Germany 6 134 1.9× 17 0.3× 65 1.4× 25 0.6× 8 0.4× 8 207
Naomi Meeks United States 8 86 1.2× 18 0.3× 50 1.1× 11 0.3× 5 0.2× 16 169
Emanuela Ponzi Italy 7 87 1.3× 13 0.2× 93 2.0× 16 0.4× 6 0.3× 14 182
Joe Catanese United States 2 152 2.2× 17 0.3× 29 0.6× 37 0.8× 5 0.2× 2 201
Özkan Özdemir Türkiye 7 100 1.4× 13 0.2× 47 1.0× 11 0.3× 5 0.2× 22 173
Mariya Kozenko Canada 6 99 1.4× 10 0.2× 58 1.2× 27 0.6× 2 0.1× 8 159
Ghunwa Nakouzi United States 8 103 1.5× 32 0.6× 56 1.2× 22 0.5× 2 0.1× 15 180
Bryan Sayson Canada 7 70 1.0× 8 0.1× 48 1.0× 35 0.8× 2 0.1× 8 160
Maurizia Orlandi Italy 6 277 4.0× 27 0.5× 17 0.4× 15 0.3× 15 0.7× 7 342

Countries citing papers authored by Andrée MacMillan

Since Specialization
Citations

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

Fields of papers citing papers by Andrée MacMillan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrée MacMillan

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

All Works

7 of 7 papers shown
1.
MacMillan, Andrée, et al.. (2020). Group plus “mini” individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction. Hereditary Cancer in Clinical Practice. 18(1). 3–3. 17 indexed citations
2.
Dawson, Lesa, Kerri Smith, Andrée MacMillan, et al.. (2019). A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect. Molecular Genetics & Genomic Medicine. 8(2). e1070–e1070. 7 indexed citations
3.
Dicks, Elizabeth, et al.. (2019). Universal tumor screening for Lynch syndrome: Perceptions of Canadian pathologists and genetic counselors of barriers and facilitators. Cancer Medicine. 8(7). 3614–3622. 6 indexed citations
4.
Dicks, Elizabeth, et al.. (2018). Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors. Journal of Community Genetics. 10(3). 335–344. 10 indexed citations
5.
Fernandez, Bridget A., Jane S. Green, Ford Bursey, et al.. (2012). Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype. BMC Medical Genetics. 13(1). 111–111. 13 indexed citations
6.
Reilich, Peter, Rita Horváth, Sabine Krause, et al.. (2011). The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene. Journal of Neurology. 258(11). 1987–1997. 71 indexed citations
7.
Finnis, Merran, Marie Mangelsdorf, Elke Holinski‐Feder, et al.. (2005). XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene. BMC Medical Genetics. 6(1). 16–16. 23 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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