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Nature Communications|September 1, 2018
Loss-of-function mutations in ATP6AP1 and ATP6AP2 in granular cell tumorsFresia Pareja, Alissa H Brandes, Thais Basili, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
Frontiers in Oncology|October 5, 2023
ctDNA-based detection of molecular residual disease in stage I-III non-small cell lung cancer patients treated with definitive radiotherapyEmily S Lebow, Narek Shaverdian, Jordan E Eichholz, et al.
HGG Advances|October 12, 2024
A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
Cancer Discovery|December 24, 2021
Cancer-Causative Mutations Occurring in Early EmbryogenesisFresia Pareja, Ryan N Ptashkin, David N Brown, et al.
NPJ Breast Cancer|August 21, 2019
Homologous recombination DNA repair defects in PALB2-associated breast cancersAnqi Li, Felipe C Geyer, Pedro Blecua, et al.
Nature Genetics|August 9, 2011
Germline mutations in RAD51D confer susceptibility to ovarian cancerChey Loveday, Clare Turnbull, Emma Ramsay, et al.
Nature|December 25, 2009
Complex landscapes of somatic rearrangement in human breast cancer genomesPhilip J Stephens, David J McBride, Meng-Lay Lin, et al.
NPJ Breast Cancer|November 23, 2019
Erratum: Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancersAnqi Li, Felipe C Geyer, Pedro Blecua, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 22, 2005
Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotypeSunil R Lakhani, Jorge S Reis-Filho, Laura Fulford, et al.
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