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You searched for: Author/Creator Allen, Jamie

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1. Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes. (8th January 2018)

2. Ensembl 2020. Issue Volume 48:Issue D1(2020) (6th November 2019)

3. Ensembl 2022. Issue Volume 50:Issue D1(2022) (17th November 2021)

5. Predicting the Likelihood of Carrying a BRCA1 or BRCA2 Mutation in Asian Patients With Breast Cancer. Issue 14 (10th May 2022)

6. Minigene‐based splicing analysis and ACMG/AMP‐based tentative classification of 56 ATM variants. Issue 1 (15th July 2022)

7. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Issue 5 (26th February 2016)

8. Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks. Issue 11 (4th August 2017)

9. Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia. Issue 2 (9th October 2017)

10. Inoculation with remnant prairie soils increased the growth of three native prairie legumes but not necessarily their associations with beneficial soil microbes. (23rd February 2020)