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Alison H. Trainer

Observed names: A H Trainer, A Trainer, A. Trainer, Alison H Trainer, Alison Trainer, Trainer, Alison H, Trainer, Alison H.
Observed institutions: University of Modena and Reggio Emilia, The Royal Melbourne Hospital, Memorial Sloan Kettering Cancer Center, The University of Melbourne, Walter and Eliza Hall Institute of Medical Research, QIMR Berghofer Medical Research Institute, Royal Hospital for Children, Peter MacCallum Cancer Centre, Wellington Hospital, Monash Medical Centre, Complejo Hospitalario Universitario de Santiago, Prince of Wales Hospital, Victorian Clinical Genetics Services, Centre for Biomedical Network Research on Rare Diseases, Royal Hospital for Sick Children, Fundación Pública Galega de Medicina Xenómica, Instituto de Investigación Sanitaria de Santiago, Servicio Gallego de Salud, University of Glasgow
OpenAlex ID: A5111848353
Cancer Risks Associated With GermlinePALB2Pathogenic Variants: An International Study of 524 Families
2019 · Xin Yang, Goska Leslie, et al. · Journal of Clinical Oncology · 435
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Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk
2012 · Nick Orr, Alina Lemnrau, et al. · Nature Genetics · 105
A Role for Common Genomic Variants in the Assessment of Familial Breast Cancer
2012 · Sarah Sawyer, Gillian Mitchell, et al. · Journal of Clinical Oncology · 85
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
2020 · Iris Kramer, Maartje J. Hooning, et al. · The American Journal of Human Genetics · 65
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Homologous recombination DNA repair defects in PALB2-associated breast cancers
2019 · Anqi Li, Felipe C. Geyer, et al. · npj Breast Cancer · 56
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Chromosome 22q11 microdeletions in tetralogy of Fallot.
1996 · A H Trainer, N Morrison, et al. · Archives of Disease in Childhood · 53
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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness
2019 · Vivek L. Patel, Evan L. Busch, et al. · Cancer Research · 52
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Rare variants in XRCC2 as breast cancer susceptibility alleles: Table 1
2012 · Florentine S Hilbers, Juul T Wijnen, et al. · Journal of Medical Genetics · 46
Breast and Prostate Cancer Risks for MaleBRCA1andBRCA2Pathogenic Variant Carriers Using Polygenic Risk Scores
2021 · Daniel R Barnes, Valentina Silvestri, et al. · JNCI Journal of the National Cancer Institute · 45
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COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
2013 · COMPLEXO, Melissa C Southey, et al. · Breast Cancer Research · 40
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Reduced heart rate variability following repair of tetralogy of Fallot
1999 · K A McLeod, W S Hillis, et al. · Heart · 38
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Multi-omic analysis of SDHB-deficient pheochromocytomas and paragangliomas identifies metastasis and treatment-related molecular profiles
2025 · Aidan Flynn, Andrew D. Pattison, et al. · Nature Communications · 33
Parity and lactation induce T-cell-mediated breast cancer protection
2025 · Balaji Virassamy, Franco Caramia, et al. · Nature · 26
The impact of coding germline variants on contralateral breast cancer risk and survival
2023 · Anna Morra, Nasim Mavaddat, et al. · The American Journal of Human Genetics · 26
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Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum
2024 · Cristina Fortuno, Bing-Jian Feng, et al. · JCO Precision Oncology · 25
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Mendelian randomisation study of smoking exposure in relation to breast cancer risk
2021 · Hanla A. Park, Sonja Neumeyer, et al. · British Journal of Cancer · 22
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Tumour morphology predicts PALB2 germline mutation status
2013 · kConFab9, Z L Teo, et al. · British Journal of Cancer · 22
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FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women
2023 · Gisella Figlioli, Amandine Billaud, et al. · European Journal of Human Genetics · 15
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
2022 · Christopher Hakkaart, John F. Pearson, et al. · Communications Biology · 14
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The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia
2013 · Zhi L. Teo, Sarah D. Sawyer, et al. · Familial Cancer · 13
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
2022 · Hakkaart, Christopher, Pearson, John F., et al. · Research at the University of Copenhagen (University of Copenhagen) · 4
De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasia
2003 · S Joss, A Howatson, et al. · Clinical Genetics · 4
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
2021 · Juliette Coignard, Michael Lush, et al. · Nature Communications
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Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers
2019 · Anqi Li, Felipe C. Geyer, et al. · npj Breast Cancer
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Familial cylindromatosis, Brooke-Spiegler syndrome and multiple famililal trichoepithiliomas: Tumour mapping of 26 patients with CYLD mutations suggest androgen stimulation may play a role in tumourigenesis
2008 · Neil Rajan, J. Langtry, et al. · Newcastle University ePrints (Newcastle Univesity)
Works count: 27
Citation count: 1,224
H-index: 17
I10-index: 20
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