Michael O. Woods

8.3k total citations
37 papers, 1.3k citations indexed

About

Michael O. Woods is a scholar working on Pathology and Forensic Medicine, Genetics and Oncology. According to data from OpenAlex, Michael O. Woods has authored 37 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pathology and Forensic Medicine, 20 papers in Genetics and 14 papers in Oncology. Recurrent topics in Michael O. Woods's work include Genetic factors in colorectal cancer (20 papers), Colorectal Cancer Screening and Detection (13 papers) and Colorectal Cancer Treatments and Studies (7 papers). Michael O. Woods is often cited by papers focused on Genetic factors in colorectal cancer (20 papers), Colorectal Cancer Screening and Detection (13 papers) and Colorectal Cancer Treatments and Studies (7 papers). Michael O. Woods collaborates with scholars based in Canada, United States and Australia. Michael O. Woods's co-authors include Patrick S. Parfrey, Jane S. Green, William S. Davidson, H. Banfield Younghusband, Roger C. Green, Nicholas Katsanis, Stephen J. Ansley, Philip L. Beales, Terry‐Lynn Young and Donna Hefferton and has published in prestigious journals such as Nature Genetics, PLoS ONE and JNCI Journal of the National Cancer Institute.

In The Last Decade

Michael O. Woods

37 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael O. Woods Canada 20 557 535 525 418 265 37 1.3k
Kristina Lagerstedt‐Robinson Sweden 24 445 0.8× 589 1.1× 777 1.5× 617 1.5× 401 1.5× 74 1.8k
Yuya Kobayashi United States 9 1.1k 1.9× 552 1.0× 342 0.7× 208 0.5× 428 1.6× 17 1.5k
Tina Pesaran United States 16 1.2k 2.2× 827 1.5× 379 0.7× 327 0.8× 567 2.1× 43 1.9k
S.A. Whitmore Australia 18 255 0.5× 536 1.0× 418 0.8× 167 0.4× 73 0.3× 26 1.3k
Louise Flanagan Ireland 10 205 0.4× 282 0.5× 246 0.5× 319 0.8× 158 0.6× 13 762
Aytekin Akyol Türkiye 14 154 0.3× 464 0.9× 181 0.3× 313 0.7× 151 0.6× 40 964
Kelly Gonzalez United States 13 423 0.8× 413 0.8× 110 0.2× 267 0.6× 248 0.9× 18 943
Camille Charbonnier France 12 239 0.4× 371 0.7× 81 0.2× 294 0.7× 190 0.7× 23 902
Kristiina Avela Finland 17 402 0.7× 633 1.2× 113 0.2× 118 0.3× 132 0.5× 34 1.1k
Chiara Baldo Italy 15 228 0.4× 371 0.7× 133 0.3× 322 0.8× 62 0.2× 31 947

Countries citing papers authored by Michael O. Woods

Since Specialization
Citations

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

Fields of papers citing papers by Michael O. Woods

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael O. Woods. 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 Michael O. Woods. The network helps show where Michael O. Woods may publish in the future.

Co-authorship network of co-authors of Michael O. Woods

This figure shows the co-authorship network connecting the top 25 collaborators of Michael O. Woods. A scholar is included among the top collaborators of Michael O. Woods 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 Michael O. Woods. Michael O. Woods 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.
Etchegary, Holly, Katherine E. Watkins, Michael O. Woods, et al.. (2022). Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model. PLoS ONE. 17(12). e0279317–e0279317. 3 indexed citations
2.
Lu, Yujia, Yu Zhao, Jenny Chang‐Claude, et al.. (2022). Genetic Predictors for Fecal Propionate and Butyrate-Producing Microbiome Pathway Are Not Associated with Colorectal Cancer Risk: A Mendelian Randomization Analysis. Cancer Epidemiology Biomarkers & Prevention. 32(2). 281–286. 3 indexed citations
3.
Green, Jane S., Somayyeh Fahiminiya, Jacek Majewski, et al.. (2020). A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features. Scientific Reports. 10(1). 10827–10827. 14 indexed citations
4.
Hu, Ting, et al.. (2018). Ensemble learning for detecting gene-gene interactions in colorectal cancer. PeerJ. 6. e5854–e5854. 19 indexed citations
5.
Green, Jane S., et al.. (2018). Impact of colonoscopic screening in Familial Colorectal Cancer Type X. Molecular Genetics & Genomic Medicine. 6(6). 1021–1030. 7 indexed citations
6.
Green, Jane S., et al.. (2017). Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland. Familial Cancer. 17(2). 205–208. 2 indexed citations
7.
Zhai, Guangju, Jiayi Zhou, Michael O. Woods, et al.. (2015). Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability. European Journal of Human Genetics. 24(7). 1063–1070. 19 indexed citations
8.
Zhu, Yun, Peter Wang, Sevtap Savas, et al.. (2014). Influence of pre-diagnostic cigarette smoking on colorectal cancer survival: overall and by tumour molecular phenotype. British Journal of Cancer. 110(5). 1359–1366. 40 indexed citations
9.
Rothenmund, Heidi, Harminder Singh, Bernard Candas, et al.. (2013). Hereditary Colorectal Cancer Registries in Canada: Report from the Colorectal Cancer Association of Canada Consensus Meeting; Montreal, Quebec; October 28, 2011. Current Oncology. 20(5). 273–278. 5 indexed citations
10.
Zhu, Yun, Hao Wu, Peter Wang, et al.. (2013). Dietary patterns and colorectal cancer recurrence and survival: a cohort study. BMJ Open. 3(2). e002270–e002270. 58 indexed citations
11.
Green, Roger C., et al.. (2012). Inherited deleterious variants inGALNT12are associated with CRC susceptibility. Human Mutation. 33(7). 1056–1058. 40 indexed citations
12.
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
13.
Fernandez, Bridget A., George A Fox, Rick Bhatia, et al.. (2012). A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features. Respiratory Research. 13(1). 64–64. 65 indexed citations
14.
Lindor, Noralane M., Kari G. Rabe, Gloria M. Petersen, et al.. (2009). Parent of origin effects on age at colorectal cancer diagnosis. International Journal of Cancer. 127(2). 361–366. 5 indexed citations
15.
Stuckless, Susan, et al.. (2006). The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome. Familial Cancer. 6(1). 1–12. 21 indexed citations
16.
Woods, Michael O., Susan Stuckless, Jane S. Green, et al.. (2005). High Frequency of Hereditary Colorectal Cancer in Newfoundland Likely Involves Novel Susceptibility Genes. Clinical Cancer Research. 11(19). 6853–6861. 45 indexed citations
17.
Beales, Philip L., Nicholas Katsanis, Richard A. Lewis, et al.. (2001). Genetic and Mutational Analyses of a Large Multiethnic Bardet-Biedl Cohort Reveal a Minor Involvement of BBS6 and Delineate the Critical Intervals of Other Loci. The American Journal of Human Genetics. 68(3). 606–616. 57 indexed citations
18.
Katsanis, Nicholas, Philip L. Beales, Michael O. Woods, et al.. (2000). Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome. Nature Genetics. 26(1). 67–70. 224 indexed citations
19.
Young, Terry‐Lynn, Lynette S. Penney, Michael O. Woods, et al.. (1999). A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31. The American Journal of Human Genetics. 64(3). 900–904. 90 indexed citations
20.
Young, Terry‐Lynn, Michael O. Woods, Patrick S. Parfrey, et al.. (1999). A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I (BBS1) Interval to 1 cM. The American Journal of Human Genetics. 65(6). 1680–1687. 36 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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