L. Jackson

发表

The challenges of the expanded availability of genomic information: an agenda-setting paper

M. Wjst, I. Budin-Ljøsne, B. Peterlin, 2017, Journal of Community Genetics.

Can I get a retweet please? Health research recruitment and the Twittersphere.

H. Skirton, L. Jackson, A. O'Connor, 2014, Journal of advanced nursing.

Advancing the Power of Economic Evidence to Inform Investments in Children, Youth, and Families

Youth Board on Children, Families., L. Jackson, 2016 .

The Clinical Utility of Compounded Bioidentical Hormone Therapy

D. Mattison, L. Jackson, R. Parker, 2020 .

Impact of presymptomatic genetic testing on young adults: a systematic review

H. Skirton, C. Hennessy, L. Jackson, 2015, European Journal of Human Genetics.

Acute Coronary Syndrome Screening and Diagnostic Practice Variation

B. Patterson, J. Carlson, T. Strout, 2017, Academic emergency medicine : official journal of the Society for Academic Emergency Medicine.

A systematic review of interventions to provide genetics education for primary care

H. Skirton, M. Paneque, L. Jackson, 2016, BMC Family Practice.

Non‐invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers

L. Chitty, H. Skirton, L. Jackson, 2015, Prenatal diagnosis.

GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology

Samuel E. Jones, R. Mägi, C. Lindgren, 2018, American journal of human genetics.

Health care for young adults undergoing predictive genetic testing for cardiomyopathies

T. Homfray, H. Skirton, S. Prasad, 2017 .

Hospital admission and emergency care attendance risk for SARS-CoV-2 delta (B.1.617.2) compared with alpha (B.1.1.7) variants of concern: a cohort study

Joshua B. Singer, Darren L. Smith, Shane A. McCarthy, 2021, The Lancet Infectious Diseases.

The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages

M. Macek, H. Skirton, M. Cornel, 2018, Genetics in Medicine.

Guidance for patients considering direct-to-consumer genetic testing and health professionals involved in their care: development of a practical decision tool.

H. Skirton, L. Jackson, L. Goldsmith, 2014, Family practice.

Direct-to-consumer genomic testing: systematic review of the literature on user perspectives

Heather Skirton, Leigh Jackson, H. Skirton, 2012, European Journal of Human Genetics.

Incidental findings in genetic research and clinical diagnostic tests: A systematic review

H. Skirton, L. Jackson, A. O'Connor, 2012, American journal of medical genetics. Part A.

European Society of Human Genetics (2018). Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. European Journal of Human Genetics .

N. Hawkins, A. Clarke, H. Kayserili, 2018 .

Quality in genetic counselling for presymptomatic testing — clinical guidelines for practice across the range of genetic conditions

H. Skirton, A. Tibben, L. Jackson, 2012, European Journal of Human Genetics.

Incidental Findings in Genetic Research and Genetic Testing

L. Jackson, Leigh Jackson, 2014 .

Genomic medicine: what are the challenges for the National Health Service?

H. Skirton, L. Jackson, A. O'Connor, 2012, Personalized medicine.

Points to consider for laboratories reporting results from diagnostic genomic sequencing

B. Knoppers, A. Clarke, K. Sénécal, 2017, European Journal of Human Genetics.

Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature

H. Skirton, L. Jackson, A. O'Connor, 2013, Journal of Community Genetics.

Compounded Topical Pain Creams

L. Jackson, D. Schwinn, Leigh Jackson, 2020 .

Assessing the analytical validity of SNP-chips for detecting very rare pathogenic variants: implications for direct-to-consumer genetic testing

Caroline F Wright, Leigh Jackson, J. Tyrrell, 2019, bioRxiv.

Very rare pathogenic genetic variants detected by SNP-chips are usually false positives: implications for direct-to-consumer genetic testing

Caroline F. Wright, Leigh Jackson, Andrew T. Hattersley, 2019 .

Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study

H. Skirton, C. Hennessy, L. Jackson, 2017, European Journal of Human Genetics.

Evidence for penetrance in patients without a family history of disease: a systematic review

L. Jackson, Heather Turner, Leigh Jackson, 2020, European Journal of Human Genetics.

Recontacting patients in clinical genetics services European Society of Human Genetics

N. Hawkins, A. Clarke, H. Kayserili, 2018 .

Implications of secondary findings for clinical contexts

Kazuto Kato, L. Leitsalu, L. Milani, 2020, Secondary Findings in Genomic Research.

A Comparative Safety Analysis of Medicines Based on the UK Pharmacovigilance and General Practice Prescribing Data in England

M. Weedon, L. Jackson, K. Mokbel, 2022, In Vivo.

The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages

M. Macek, H. Skirton, M. Cornel, 2018, Genetics in Medicine.

Implementing genetic education in primary care: the Gen-Equip programme

A. Kent, M. Macek, H. Skirton, 2017, Journal of Community Genetics.

Management of Incidental Findings from Genetic Tests: Perspectives of Ethics Committee Members

H. Skirton, L. Jackson, A. O'Connor, 2015 .

Impact of fetal or child loss on parents' perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions.

H. Skirton, L. Jackson, A. O'Connor, 2016, Midwifery.

Informed consent for blood tests in people with a learning disability.

H. Skirton, L. Jackson, L. Goldsmith, 2013, Journal of advanced nursing.

Offering prenatal diagnostic tests: European guidelines for clinical practice

L. Chitty, H. Skirton, L. Jackson, 2014, European Journal of Human Genetics.

Offering prenatal diagnostic tests: European guidelines for clinical practice

L. Chitty, H. Skirton, L. Jackson, 2013, European Journal of Human Genetics.

Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations

H. Skirton, L. Jackson, A. O'Connor, 2012, Clinical genetics.

Development of a Secure Website to Facilitate Information Sharing in Families at High Risk of Bowel Cancer—The Familyweb Study

Ray B. Jones, H. Skirton, Selina Goodman, 2021, Cancers.

Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents

H. Skirton, C. Hennessy, L. Jackson, 2018, European Journal of Human Genetics.

Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature

H. Skirton, L. Jackson, A. O'Connor, 2013, Journal of Community Genetics.

Are health professionals ready for direct-to-consumer genetic and genomic testing?

H. Skirton, L. Jackson, A. O'Connor, 2013, Personalized medicine.

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

N. Hawkins, A. Clarke, H. Kayserili, 2018, European Journal of Human Genetics.

Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study

H. Skirton, C. Hennessy, L. Jackson, 2017, European Journal of Human Genetics.

Genetic counselling as a route to enhanced autonomy: using a sequential mixed methods research approach to develop a theory regarding presymptomatic genetic testing for young adults at risk of inherited cancer syndromes

H. Skirton, C. Hennessy, L. Jackson, 2021, Journal of Community Genetics.

Implementing genetic education in primary care: the Gen-Equip programme

A. Kent, H. Skirton, M. Cornel, 2017, Journal of Community Genetics.