Kristine Barlow-Stewart

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 16

Top Topics

Cervical Cancer Screening

Decision Making

Top Venues

European journal of human genetics : EJHG

Journal of genetic counseling

BMC medical ethics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG 32 (7) (2024)
Cassandra Muller, Lyndon Gallacher, Louise Keogh, Aideen M McInerney-Leo, Tiffany F Boughtwood, Penny Gleeson, Kristine Barlow-Stewart, Martin B Delatycki, Ingrid Winship, Kristen J Nowak, Margaret Otlowski, Paul A Lacaze, Jane M Tiller
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. European journal of human genetics : EJHG (2024)
Jacintha Luermans, Jane Fleming, Rosie O'Shea, Kristine Barlow-Stewart, Emma Elizabeth Palmer, Melanie Leffler
"We are not a typical family anymore": Exploring the experiences and support needs of fathers of children with Fragile X syndrome in Australia. American journal of medical genetics. Part A (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Stephanie White, Tamara Mossfield, Jane Fleming, Kristine Barlow-Stewart, Sondhya Ghedia, Rebecca Dickson, Fiona Richards, Yvonne Bombard, Veronica Wiley
Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready? European journal of human genetics : EJHG (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Correction: Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Jane M Tiller, Andrew Bakshi, Grace Dowling, Louise Keogh, Aideen M McInerney-Leo, Kristine Barlow-Stewart, Tiffany F Boughtwood, Penny Gleeson, Martin B Delatycki, Ingrid Winship, Margaret Otlowski, Paul A Lacaze
Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing. European journal of human genetics : EJHG (2023)
Jessica M Gereis, Kate Hetherington, Lauren Ha, Eden G Robertson, David S Ziegler, Kristine Barlow-Stewart, Katherine M Tucker, Jonathan Michael Marron, Claire E Wakefield
Parents' understanding of genome and exome sequencing for pediatric health conditions: a systematic review. European journal of human genetics : EJHG 30 (11) (2022)
Georgina M Schlub, Ashley Crook, Kristine Barlow-Stewart, Jane Fleming, Judy Kirk, Kathy Tucker, Sian Greening
Helping young children understand inherited cancer predisposition syndromes using bibliotherapy. Journal of genetic counseling 30 (4) (2021)
Hamizah Sa'at, Yew Kong Lee, Sook-Yee Yoon, Siu Wan Wong, Yin-Ling Woo, Kristine Barlow-Stewart, Nur Aishah Mohd Taib
The needs of Southeast Asian BRCA mutation carriers considering risk-reducing salpingo-oophorectomy: a qualitative study. Familial cancer (2021)
Kristine Barlow-Stewart, Kayley Bardsley, Elle Elan, Jane Fleming, Yemima D Berman, Ron Fleischer, Krista Recsei, Daniel Goldberg, John Tucker, Leslie Burnett
Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community. Journal of community genetics (2021)
Natalia Meggiolaro, Kristine Barlow-Stewart, Kate Dunlop, Ainsley J Newson, Jane Fleming
Disclosure to genetic relatives without consent - Australian genetic professionals' awareness of the health privacy law. BMC medical ethics 21 (1) (2020)
Sarah Josephi-Taylor, Kristine Barlow-Stewart, Arthavan Selvanathan, Tony Roscioli, Alan Bittles, Bettina Meiser, Lisa Worgan, Sulekha Rajagopalan, Alison Colley, Edwin P Kirk
User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia. Journal of genetic counseling 28 (2) (2018)
Veronica F Quinn, Bettina Meiser, Katherine Tucker, Kathy M Tucker, Kaaren J Watts, Belinda Rahman, Michelle Peate, Christobel M Saunders, Elizabeth Geelhoed, Margaret Gleeson, Kristine Barlow-Stewart, Michael Field, Marion Harris, Yoland C Antill, Linda Cicciarelli, Karen Crowe, Michael T Bowen, Gillian Mitchell
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)