Mary‐Anne Young

3.0k total citations
78 papers, 1.7k citations indexed

About

Mary‐Anne Young is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Sociology and Political Science. According to data from OpenAlex, Mary‐Anne Young has authored 78 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 20 papers in Pediatrics, Perinatology and Child Health and 15 papers in Sociology and Political Science. Recurrent topics in Mary‐Anne Young's work include BRCA gene mutations in cancer (63 papers), Genomics and Rare Diseases (14 papers) and Family Support in Illness (14 papers). Mary‐Anne Young is often cited by papers focused on BRCA gene mutations in cancer (63 papers), Genomics and Rare Diseases (14 papers) and Family Support in Illness (14 papers). Mary‐Anne Young collaborates with scholars based in Australia, United States and United Kingdom. Mary‐Anne Young's co-authors include Bettina Meiser, Paul A. James, Tatiane Yanes, Kathy Tucker, Clara Gaff, Gillian Mitchell, Laura Forrest, Elizabeth Lobb, Phyllis Butow and Mandy L. Ballinger and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and JNCI Journal of the National Cancer Institute.

In The Last Decade

Mary‐Anne Young

76 papers receiving 1.6k citations

Peers

Countries citing papers authored by Mary‐Anne Young

Since Specialization

Citations

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

Fields of papers citing papers by Mary‐Anne Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary‐Anne Young. 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 Mary‐Anne Young. The network helps show where Mary‐Anne Young may publish in the future.

Co-authorship network of co-authors of Mary‐Anne Young

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Navigating genomic testing: Evaluation of an e-learning module with general practitioners 2024 ·Focus on Health Professional Education A Multi-Professional Journal ·Bronwyn Terrill, (unknown), (unknown), Mary‐Anne Young	1
2	Publics’ knowledge of, attitude to and motivation towards health-related genomics: a scoping review 2024 ·European Journal of Human Genetics ·(unknown), (unknown), Stephanie Best, Mary‐Anne Young, Bronwyn Terrill	3
3	Genetic counsellors: facilitating the integration of genomics into health care 2024 ·The Medical Journal of Australia ·Tatiane Yanes, Eliza Courtney, Mary‐Anne Young, (unknown), Aideen McInerney‐Leo, Jodie Ingles	3
4	Development and evaluation of a novel educational program for providers on the use of polygenic risk scores 2023 ·Genetics in Medicine ·Tatiane Yanes, (unknown), Mary‐Anne Young, (unknown), Amanda Willis, (unknown), Bronwyn Terrill, Simone McInerny, Laura Forrest, (unknown), Rachel Williams, (unknown), Paul A. James	4
5	Pharmacogenomic testing: perception of clinical utility, enablers and barriers to adoption in Australian hospitals 2022 ·Internal Medicine Journal ·(unknown), Bronwyn Terrill, Jan‐Willem C. Alffenaar, Asad E. Patanwala, Sarah Kummerfeld, Richard O. Day, Mary‐Anne Young, Sophie L. Stocker	18
6	Knowledge, views and expectations for cancer polygenic risk testing in clinical practice: A cross‐sectional survey of health professionals 2021 ·Clinical Genetics ·Amelia K. Smit, (unknown), David Espinoza, (unknown), Mary‐Anne Young, Kate Dunlop, Jane Tiller, Ainsley J. Newson, Bettina Meiser, Anne Ε. Cust, Tatiane Yanes	24
7	Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology 2021 ·Journal of Community Genetics ·(unknown), (unknown), Amanda Willis, Mary‐Anne Young, Bronwyn Terrill	6
8	My Research Results: a program to facilitate return of clinically actionable genomic research findings 2021 ·European Journal of Human Genetics ·Amanda Willis, Bronwyn Terrill, (unknown), Alison McEwen, Mandy L. Ballinger, Mary‐Anne Young	7
9	Breast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior 2021 ·Genetics in Medicine ·Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Mary‐Anne Young, Philip B. Mitchell, (unknown), Simone McInerny, (unknown), Kristine Barlow‐Stewart, Yoland Antill, Lucinda Salmon, (unknown), Brigid Betz‐Stablein, Paul A. James	15
10	Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study 2021 ·Genetic Testing and Molecular Biomarkers ·(unknown), Laura Forrest, (unknown), (unknown), Lisa Devereux, Paul A. James, Ian Campbell, Alison H. Trainer, Mary‐Anne Young	2
11	Women’s responses and understanding of polygenic breast cancer risk information 2020 ·Familial Cancer ·Tatiane Yanes, Rajneesh Kaur, Bettina Meiser, (unknown), Simone McInerny, Kristine Barlow‐Stewart, Yoland Antill, Lucinda Salmon, (unknown), Paul A. James, Mary‐Anne Young	15
12	Uptake of polygenic risk information among women at increased risk of breast cancer 2019 ·Clinical Genetics ·Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, (unknown), Simone McInerny, (unknown), Kristine Barlow‐Stewart, Yoland Antill, Lucinda Salmon, (unknown), Mary‐Anne Young, Paul A. James	19
13	Polygenic breast cancer risk: A prospective study of uptake and outcomes among high-risk women 2018 ·Twin Research and Human Genetics ·Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, (unknown), Mary‐Anne Young, Kristine Barlow‐Stewart, Thomas John, (unknown), Yoland Antill, (unknown), Tony Roscioli, Jane Halliday, Phillip M. Mitchell, Paul A. James	1
14	Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review 2018 ·Clinical Genetics ·Brittany C. McGill, Claire E. Wakefield, Janine Vetsch, Kristine Barlow‐Stewart, Nadine A. Kasparian, Andrea Farkas Patenaude, Mary‐Anne Young, Richard J. Cohn, Kathy Tucker	27
15	Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership 2017 ·Journal of Community Genetics ·Laura Forrest, Gillian Mitchell, (unknown), Lara Petelin, Kate Richardson, Lyon Mascarenhas, Mary‐Anne Young	5
16	Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study 2017 ·BMC Cancer ·Tatiane Yanes, Bettina Meiser, Mary‐Anne Young, Rajneesh Kaur, Gillian Mitchell, Kristine Barlow‐Stewart, Tony Roscioli, Jane Halliday, Paul A. James	10
17	Relation of HLA class I and II supertypes with spontaneous clearance of hepatitis C virus 2013 ·Genes and Immunity ·Mark H. Kuniholm, Kathryn Anastos, Andrea Kovács, (unknown), Darlene Marti, Alessandro Sette, Ruth M. Greenblatt, Marion G. Peters, Mardge H. Cohen, Howard Minkoff, Stephen J. Gange, Chloe L. Thio, Mary‐Anne Young, Xiaonan Xue, Mary Carrington, Howard D. Strickler	6
18	The attitudes of people with sarcoma and their family towards genomics and incidental information arising from genetic research 2013 ·Minerva Access (University of Melbourne) ·(unknown), Mary‐Anne Young, Amy S. Herlihy, Gillian Mitchell, David M. Thomas, Mandy L. Ballinger, Kathy Tucker, Craig Lewis, Susan J. Neuhaus, Jane Halliday	11
19	Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer 2007 ·Familial Cancer ·Maurice B. Loughrey, Paul Waring, Angela Tan, (unknown), (unknown), Victoria Beshay, Mary‐Anne Young, Grant A. McArthur, Alex Boussioutas, Alexander Dobrovic	131
20	Risk-reducing surgery in women with familial susceptibility for breast and/or ovarian cancer 2006 ·European Journal of Cancer ·Yoland Antill, John Reynolds, Mary‐Anne Young, Judy Kirk, Kathy Tucker, (unknown), Shirley Wong, Tracy Dudding, Juliana Di Iulio, Kelly‐Anne Phillips	34

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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