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Age- and sex-specific effects of stress on parvalbumin interneurons in preclinical models: Relevance to sex differences in clinical neuropsychiatric and neurodevelopmental disorders

Neuroscience and biobehavioral reviews, 2021-12, Vol.131, p.1228-1242

2021

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PD-1 regulates KLRG1 + group 2 innate lymphoid cells

The Journal of experimental medicine, 2017-06, Vol.214 (6), p.1663-1678

2017

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RE: Heterozygous BRCA1/BRCA2 and mismatch repair gene pathogenic variants in children and adolescents with cancer

JNCI : Journal of the National Cancer Institute, 2023-02, Vol.115 (2), p.224-225

2023

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Prepubertal ovariectomy confers resilience to stress-induced anxiety in adult female mice

Psychoneuroendocrinology, 2023-02, Vol.148, p.105997-105997, Article 105997

2023

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Fanconi Anaemia, Childhood Cancer and the BRCA Genes

Genes, 2021-09, Vol.12 (10), p.1520

2021

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BRCA1 and BRCA2 pathogenic variant carriers and endometrial cancer risk: A cohort study

European journal of cancer (1990), 2020-09, Vol.136, p.169-175

2020

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Decolonising knowledge co-production: examining the role of positionality and partnerships to support Indigenous-led bush product enterprises in northern Australia

Sustainability science, 2022-03, Vol.17 (2), p.333-350

2022

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Breast cancer after ovarian cancer in BRCA1 and BRCA2 pathogenic variant heterozygotes: Lower rates for 5 years post chemotherapy

Genetics in medicine, 2024-09, Vol.26 (9), p.101172, Article 101172

2024

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Germline FH Mutations Presenting With Pheochromocytoma

The journal of clinical endocrinology and metabolism, 2014-10, Vol.99 (10), p.E2046-E2050

2014

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Concern regarding classification of germline TP53 variants as likely pathogenic

Human mutation, 2019-06, Vol.40 (6), p.828-831

2019

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30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes

European journal of human genetics : EJHG, 2022-04, Vol.30 (4), p.413-419

2022

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Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161

Familial cancer, 2023-07, Vol.22 (3), p.341-344

2023

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Germline SDHB Mutations and Familial Renal Cell Carcinoma

JNCI : Journal of the National Cancer Institute, 2008-09, Vol.100 (17), p.1260-1262

2008

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Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies

JAMA oncology, 2017-12, Vol.3 (12), p.1702

2017

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Is Reflex Germline BRCA1/2 Testing Necessary in Women Diagnosed with Non-Mucinous High-Grade Epithelial Ovarian Cancer Aged 80 Years or Older?

Cancers, 2023-01, Vol.15 (3), p.730

2023

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Pathology update to the Manchester Scoring System based on testing in over 4000 families

Journal of medical genetics, 2017-10, Vol.54 (10), p.674

2017

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High detection rate from genetic testing in BRCA-negative women with familial epithelial ovarian cancer

Genetics in medicine, 2022-12, Vol.24 (12), p.2578-2586

2022

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Assessment of mismatch repair deficiency in ovarian cancer

Journal of medical genetics, 2021-10, Vol.58 (10), p.687

2021

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New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer

Familial cancer, 2021, Vol.20 (1), p.1-7

2021

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Specialist oncological surgery for removal of the ovaries and fallopian tubes in BRCA1 and BRCA2 pathogenic variant carriers may reduce primary peritoneal cancer risk to very low levels

International journal of cancer, 2021-03, Vol.148 (5), p.1155-1163

2021

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Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC)

Journal of medical genetics, 2023-01, Vol.60 (1), p.41

2023

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Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell Carcinoma

Cancer discovery, 2015-07, Vol.5 (7), p.723-729

2015

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Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers

Journal of medical genetics, 2022-04, Vol.59 (4), p.328

2022

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Challenging the believed proportion of ovarian cancer attributable to BRCA2 versus BRCA1 pathogenic variants

European journal of cancer (1990), 2020-01, Vol.124, p.88-90

2020

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Age- and sex-specific effects of stress on parvalbumin interneurons in preclinical models: Relevance to sex differences in clinical neuropsychiatric and neurodevelopmental disorders

PD-1 regulates KLRG1 + group 2 innate lymphoid cells

RE: Heterozygous BRCA1/BRCA2 and mismatch repair gene pathogenic variants in children and adolescents with cancer

Prepubertal ovariectomy confers resilience to stress-induced anxiety in adult female mice

Fanconi Anaemia, Childhood Cancer and the BRCA Genes

BRCA1 and BRCA2 pathogenic variant carriers and endometrial cancer risk: A cohort study

Decolonising knowledge co-production: examining the role of positionality and partnerships to support Indigenous-led bush product enterprises in northern Australia

Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB , SDHC and SDHD

Breast cancer after ovarian cancer in BRCA1 and BRCA2 pathogenic variant heterozygotes: Lower rates for 5 years post chemotherapy

Germline FH Mutations Presenting With Pheochromocytoma

Concern regarding classification of germline TP53 variants as likely pathogenic

30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes

Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161

Germline SDHB Mutations and Familial Renal Cell Carcinoma

Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies

Is Reflex Germline BRCA1/2 Testing Necessary in Women Diagnosed with Non-Mucinous High-Grade Epithelial Ovarian Cancer Aged 80 Years or Older?

Pathology update to the Manchester Scoring System based on testing in over 4000 families

High detection rate from genetic testing in BRCA-negative women with familial epithelial ovarian cancer

Assessment of mismatch repair deficiency in ovarian cancer

New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer

Specialist oncological surgery for removal of the ovaries and fallopian tubes in BRCA1 and BRCA2 pathogenic variant carriers may reduce primary peritoneal cancer risk to very low levels

Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC)

Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell Carcinoma

Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers

Challenging the believed proportion of ovarian cancer attributable to BRCA2 versus BRCA1 pathogenic variants

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