Bettina Meiser

12.6k total citations
246 papers, 7.3k citations indexed

About

Bettina Meiser is a scholar working on Genetics, Sociology and Political Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bettina Meiser has authored 246 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 173 papers in Genetics, 65 papers in Sociology and Political Science and 61 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bettina Meiser's work include BRCA gene mutations in cancer (164 papers), Family Support in Illness (55 papers) and Prenatal Screening and Diagnostics (32 papers). Bettina Meiser is often cited by papers focused on BRCA gene mutations in cancer (164 papers), Family Support in Illness (55 papers) and Prenatal Screening and Diagnostics (32 papers). Bettina Meiser collaborates with scholars based in Australia, United States and United Kingdom. Bettina Meiser's co-authors include Kathy Tucker, Phyllis Butow, Michael Friedländer, Nadine A. Kasparian, Kristine Barlow‐Stewart, Elizabeth Lobb, Belinda Thewes, Jane Halliday, Michelle Peate and Alexandra Barratt and has published in prestigious journals such as The Lancet, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Bettina Meiser

245 papers receiving 7.1k citations

Peers

Countries citing papers authored by Bettina Meiser

Since Specialization

Citations

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

Fields of papers citing papers by Bettina Meiser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bettina Meiser

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Population-based BRCA1/2 testing programmes are highly acceptable in the Jewish community: results of the JeneScreen Study 2022 ·Journal of Medical Genetics ·Jane Tiller, (unknown), Rajneesh Kaur, Simone M. Rowley, Yi-An Ko, (unknown), Agnes Bankier, Bettina Meiser, Kristine Barlow‐Stewart, Leslie Burnett, Chris Jacobs, Paul A. James, Alison H. Trainer, (unknown), Ian Campbell, Lesley Andrews, Martin B. Delatycki	5
2	Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting 2022 ·European Journal of Human Genetics ·Megan Best, Phyllis Butow, (unknown), Chris Jacobs, Nicci Bartley, (unknown), Christine E. Napier, Mandy L. Ballinger, David M. Thomas, Barbara B. Biesecker, Kathy Tucker, Ilona Juraskova, Bettina Meiser, Timothy E. Schlub, Ainsley J. Newson	5
3	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
4	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
5	Evaluation of two population screening programmes for BRCA1/2 founder mutations in the Australian Jewish community: a protocol paper 2021 ·BMJ Open ·(unknown), Jane Tiller, Bettina Meiser, Kristine Barlow‐Stewart, Simone M. Rowley, Yi-An Ko, (unknown), Ian Campbell, Rajneesh Kaur, Agnes Bankier, Leslie Burnett, Chris Jacobs, Paul A. James, Alison H. Trainer, (unknown), Martin B. Delatycki, Lesley Andrews	2
6	Psychological predictors of advanced cancer patients’ preferences for return of results from comprehensive tumor genomic profiling 2021 ·American Journal of Medical Genetics Part A ·Bettina Meiser, Phyllis Butow, (unknown), Christine E. Napier, Timothy E. Schlub, Nicci Bartley, Ilona Juraskova, Mandy L. Ballinger, David M. Thomas, Kathy Tucker, David Goldstein, Barbara B. Biesecker, Megan Best, (unknown)	1
7	Family communication about genomic sequencing: A qualitative study with cancer patients and relatives 2020 ·Patient Education and Counseling ·Amelia K. Smit, Nicci Bartley, Megan Best, Christine E. Napier, Phyllis Butow, Ainsley J. Newson, Kathy Tucker, Mandy L. Ballinger, David M. Thomas, Chris Jacobs, Bettina Meiser, David Goldstein, (unknown), Ilona Juraskova	10
8	Advanced cancer patient preferences for receiving molecular profiling results 2020 ·Psycho-Oncology ·Megan Best, Phyllis Butow, Chris Jacobs, Ilona Juraskova, (unknown), Bettina Meiser, David Goldstein, Mandy L. Ballinger, Nicci Bartley, Christine E. Napier, (unknown), David M. Thomas, Kathy Tucker, Timothy E. Schlub, Ainsley J. Newson, (unknown)	7
9	Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder 2020 ·Journal of Affective Disorders ·(unknown), Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Janice M. Fullerton, Kristine Barlow‐Stewart, Peter R. Schofield, Claudio Toma, Holly L. Peay, Philip B. Mitchell	16
10	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
11	Patient perspectives on molecular tumor profiling: “Why wouldn’t you?” 2019 ·BMC Cancer ·(unknown), Megan Best, Nicci Bartley, Chris Jacobs, Ilona Juraskova, David Goldstein, Ainsley J. Newson, (unknown), Bettina Meiser, Mandy L. Ballinger, Christine E. Napier, David M. Thomas, Barbara B. Biesecker, Phyllis Butow	26
12	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
13	IMPLICATIONS OF THE USE OF GENETIC TESTS IN PSYCHIATRY, WITH A FOCUS ON MAJOR DEPRESSIVE DISORDER: A REVIEW 2012 ·Depression and Anxiety ·Alex Wilde, Philip B. Mitchell, Bettina Meiser, Peter R. Schofield	12
14	The nature and structure of psychological distress in people at high risk for melanoma: a factor analytic study 2011 ·Psycho-Oncology ·Nadine A. Kasparian, Ursula M. Sansom‐Daly, Roderick P. McDonald, Bettina Meiser, Phyllis Butow, Graham J. Mann	7
15	Attitudes to Genetic Testing in Families with Multiple Cases of Bipolar Disorder 2008 ·Genetic Testing ·Bettina Meiser, Nadine A. Kasparian, Philip B. Mitchell, Kimberly A. Strong, Judy M. Simpson, (unknown), Shab Mireskandari, Peter R. Schofield	43
16	Attitudes Toward Genetic Testing for Cancer Risk after Genetic Counseling and Decision Support: A Qualitative Comparison between Hereditary Cancer Types 2007 ·Genetic Testing ·Claire E. Wakefield, Nadine A. Kasparian, Bettina Meiser, Judi Homewood, Judy Kirk, Kathy Tucker	9
17	Evaluation of a support workshop for partners of breast cancer patients: a pilot study 2006 ·UNSWorks (UNSW Sydney) ·Shab Mireskandari, Bettina Meiser, Belinda Thewes	3
18	An evaluation of support groups for young women with early breast cancer 2005 ·Cancer Forum ·David Cairns, Bettina Meiser, Hilary Gunn, Belinda Thewes	1
19	Psychological Impact of Genetic Testing for Breast Cancer Susceptibility in Women of Ashkenazi Jewish Background: A Prospective Study 2004 ·Genetic Testing ·Lesley Andrews, Bettina Meiser, Carmel Apicella, Kathy Tucker	40
20	Non-English-speaking persons' perceptions of mental illness and associated information needs: an exploratory study of the Arabic-, Greek- and Italian-speaking communities in New South Wales 1996 ·Health Promotion Journal of Australia ·(unknown), Bettina Meiser	6

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.

Explore authors with similar magnitude of impact