Marc Clausen

830 total citations
19 papers, 244 citations indexed

About

Marc Clausen is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Economics and Econometrics. According to data from OpenAlex, Marc Clausen has authored 19 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 5 papers in Public Health, Environmental and Occupational Health and 5 papers in Economics and Econometrics. Recurrent topics in Marc Clausen's work include Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (9 papers) and Health Systems, Economic Evaluations, Quality of Life (5 papers). Marc Clausen is often cited by papers focused on Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (9 papers) and Health Systems, Economic Evaluations, Quality of Life (5 papers). Marc Clausen collaborates with scholars based in Canada, United States and Australia. Marc Clausen's co-authors include Yvonne Bombard, Ann Kurth, Chloe Mighton, Kasmintan A. Schrader, Jordan Lerner‐Ellis, Salma Shickh, Luc Janss, ASM Shihavuddin, Stig Uggerhøj Andersen and Anders Bjorholm Dahl and has published in prestigious journals such as SHILAP Revista de lepidopterología, Frontiers in Plant Science and Journal of Medical Genetics.

In The Last Decade

Marc Clausen

17 papers receiving 242 citations

Peers

Countries citing papers authored by Marc Clausen

Since Specialization

Citations

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

Fields of papers citing papers by Marc Clausen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Clausen

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Parents’ attitudes towards research involving genome sequencing of their healthy children: a qualitative study 2023 ·European Journal of Human Genetics ·(unknown), Chloe Mighton, Marc Clausen, (unknown), Selina Casalino, Theresa Kim, Christine Kowal, Catherine S. Birken, Jonathon L. Maguire, Yvonne Bombard	1
2	P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review 2023 ·SHILAP Revista de lepidopterología ·Salma Shickh, Chloe Mighton, Marc Clausen, (unknown), (unknown), (unknown), Emma Reble, Tracy Graham, Seema Panchal, Andrea Eisen, Christine Elser, Kasmintan A. Schrader, Nancy N. Baxter, Andreas Laupacis, Jordan Lerner‐Ellis, Raymond H. Kim, Yvonne Bombard	0
3	Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol 2023 ·BMJ Open ·(unknown), Ling Lee, Fiona Lynch, Melissa Martyn, Elly Lynch, Ivan Macciocca, Lisette Curnow, (unknown), Sebastian Lunke, Belinda Chong, Justine E. Marum, Martin B. Delatycki, Lilian Downie, Ilias Goranitis, Danya F. Vears, Stephanie Best, Marc Clausen, Yvonne Bombard, Zornitza Stark, Clara Gaff	7
4	How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey 2023 ·Genetics in Medicine ·Chloe Mighton, Marc Clausen, Salma Shickh, Nancy N. Baxter, Adena Scheer, (unknown), (unknown), Raymond H. Kim, Emily Glogowski, Kasmintan A. Schrader, Dean A. Regier, Jordan Lerner‐Ellis, Ahmed M. Bayoumi, Kevin E. Thorpe, Yvonne Bombard	2
5	P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population 2023 ·SHILAP Revista de lepidopterología ·Emma Reble, (unknown), (unknown), Marc Clausen, Salma Shickh, Chloe Mighton, José‐Mario Capo‐Chichi, (unknown), Abdul Noor, Raymond H. Kim, Jordan Lerner‐Ellis, Yvonne Bombard	0
6	“Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing 2022 ·Genetics in Medicine ·Salma Shickh, Chloe Mighton, Marc Clausen, (unknown), (unknown), (unknown), (unknown), Emma Reble, (unknown), (unknown), Jordan Lerner‐Ellis, Nancy N. Baxter, Andreas Laupacis, Yvonne Bombard	2
7	Patient-facing digital tools for delivering genetic services: a systematic review 2022 ·Journal of Medical Genetics ·(unknown), Salma Shickh, (unknown), Stephanie Luca, Marc Clausen, (unknown), (unknown), (unknown), Robin Z. Hayeems, Yvonne Bombard	27
8	Widening the lens of actionability: A qualitative study of primary care providers’ views and experiences of managing secondary genomic findings 2021 ·European Journal of Human Genetics ·(unknown), June Carroll, Meredith Vanstone, Marc Clausen, (unknown), Emma Reble, Chloe Mighton, Salma Shickh, Melyssa Aronson, Andrea Eisen, Christine Elser, Jordan Lerner‐Ellis, Raymond H. Kim, Yvonne Bombard	7
9	Patient and public preferences for being recontacted with updated genomic results: a mixed methods study 2021 ·Human Genetics ·Chloe Mighton, Marc Clausen, (unknown), (unknown), Salma Shickh, Nancy N. Baxter, Adena Scheer, Emily Glogowski, Kasmintan A. Schrader, Kevin E. Thorpe, Raymond H. Kim, Jordan Lerner‐Ellis, Dean A. Regier, Ahmed M. Bayoumi, Yvonne Bombard	7
10	Challenges and practical solutions for managing secondary genomic findings in primary care 2021 ·European Journal of Medical Genetics ·(unknown), June Carroll, Meredith Vanstone, Marc Clausen, (unknown), Emma Reble, Chloe Mighton, Salma Shickh, Melyssa Aronson, Andrea Eisen, Christine Elser, Jordan Lerner‐Ellis, Raymond H. Kim, Yvonne Bombard	4
11	Health-care practitioners’ preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment 2020 ·Genetics in Medicine ·Shan Jiang, Aslam H. Anis, (unknown), (unknown), Kasmintan A. Schrader, (unknown), Christine M. Armour, Marc Clausen, Yvonne Bombard, Dean A. Regier	11
12	Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders’ perspectives 2020 ·CMAJ Open ·Marc Clausen, Chloe Mighton, (unknown), (unknown), Wei Fang Dai, Rebecca E. Mercer, Jaclyn Beca, Wanrudee Isaranuwatchai, Kelvin Chan, Yvonne Bombard	7
13	Greenotyper: Image-Based Plant Phenotyping Using Distributed Computing and Deep Learning 2020 ·Frontiers in Plant Science ·(unknown), Marc Clausen, (unknown), ASM Shihavuddin, Anders Bjorholm Dahl, Luc Janss, Stig Uggerhøj Andersen	32
14	Quality of life drives patients’ preferences for secondary findings from genomic sequencing 2020 ·European Journal of Human Genetics ·(unknown), Chloe Mighton, Lindsay Carlsson, Marc Clausen, Selina Casalino, Salma Shickh, (unknown), (unknown), Seema Panchal, Kara Semotiuk, (unknown), Christine Elser, Andrea Eisen, Raymond H. Kim, Jordan Lerner‐Ellis, June Carroll, Emily Glogowski, Kasmintan A. Schrader, (unknown)	17
15	Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings 2020 ·Human Genetics ·Emma Reble, (unknown), (unknown), Sam Khalouei, Marc Clausen, (unknown), Salma Shickh, Chloe Mighton, Iris Cohn, Kasmintan A. Schrader, Raymond H. Kim, Jordan Lerner‐Ellis, Yvonne Bombard	11
16	Primary care provider perspectives on using genomic sequencing in the care of healthy children 2019 ·European Journal of Human Genetics ·(unknown), Chloe Mighton, Marc Clausen, Selina Casalino, Theresa Kim, Christine Kowal, Catherine S. Birken, Jonathon L. Maguire, Yvonne Bombard	7
17	The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results 2018 ·European Journal of Human Genetics ·Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan A. Schrader, Michael F. Evans, Adena Scheer, Nancy N. Baxter, Jada G. Hamilton, Jordan Lerner‐Ellis, Kenneth Offit, Mark E. Robson, Andreas Laupacis	36
18	Computerized Counseling Reduces HIV-1 Viral Load and Sexual Transmission Risk 2014 ·JAIDS Journal of Acquired Immune Deficiency Syndromes ·Ann Kurth, Freya Spielberg, Charles M. Cleland, Barrot H. Lambdin, David R. Bangsberg, Pamela Frick, (unknown), Marc Clausen, Robert G. Norman, David Lockhart, Jane M. Simoni, King K. Holmes	49
19	CARE+ user study: usability and attitudes towards a tablet pc computer counseling tool for HIV+ men and women. 2006 ·PubMed ·Meredith M. Skeels, Ann Kurth, Marc Clausen, (unknown), (unknown)	17

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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