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36 items matching your search terms.
Advanced cancer patient preferences for receiving molecular profiling results
Best, M.; Butow, P.; Jacobs, C.; Juraskova, I.; Savard, J.; Meiser, B.; Goldstein, D.; Ballinger, M.; Bartley, N.; Napier, C.; Davies, G.; Thomas, D.; Tucker, K.; Schlub, T.; Newson, A. J.; PiGeOn Project, .
PSYCHO-ONCOLOGY 29 (10) :1533-1539, 2020 10.1002/pon.5446
Cancer patients' views and understanding of genome sequencing: a qualitative study
Bartley, N.; Best, M.; Jacobs, C.; Juraskova, I.; Newson, A. J.; Savard, J.; Meiser, B.; Ballinger, M. L.; Thomas, D. M.; Biesecker, B.; Butow, P.
JOURNAL OF MEDICAL GENETICS 57 (10) :671-676, 2020 10.1136/jmedgenet-2019-106410
Advanced cancer patient wnowledge of and attitudes towards tumor molecular profiling
Davies, G.; Butow, P.; Napier, C. E.; Bartley, N.; Juraskova, I.; Meiser, B.; Ballinger, M. L.; Thomas, D. M.; Schlub, T. E.; Best, M. C.; members of the PiGeOn, Project.
Translational Oncology 13 (9) :100799, 2020 10.1016/j.tranon.2020.100799
Assessment of the value of tumor variation profiling perceived by patients with cancer
Butow, P.; Davies, G.; Napier, C. E.; Schlub, T.; Best, M. C.; Bartley, N.; Juraskova, I.; Meiser, B.; Ballinger, M. L.; Biesecker, B.; Goldstein, D.; Thomas, D. M.; PiGeOn, Project
JAMA Network Open 3 (5) :e204721, 2020 10.1001/jamanetworkopen.2020.4721
Frequency of pathogenic germline variants in cancer-susceptibility genes in patients with osteosarcoma
Mirabello, L.; Zhu, B.; Koster, R.; Karlins, E.; Dean, M.; Yeager, M.; Gianferante, M.; Spector, L. G.; Morton, L. M.; Karyadi, D.; Robison, L. L.; Armstrong, G. T.; Bhatia, S.; Song, L.; Pankratz, N.; Pinheiro, M.; Gastier-Foster, J. M.; Gorlick, R.; de Toledo, S. R. C.; Petrilli, A. S.; Patino-Garcia, A.; Lecanda, F.; Gutierrez-Jimeno, M.; Serra, M.; Hattinger, C.; Picci, P.; Scotlandi, K.; Flanagan, A. M.; Tirabosco, R.; Amary, M. F.; Kurucu, N.; Ilhan, I. E.; Ballinger, M. L.; Thomas, D. M.; Barkauskas, D. A.; Mejia-Baltodano, G.; Valverde, P.; Hicks, B. D.; Zhu, B.; Wang, M.; Hutchinson, A. A.; Tucker, M.; Sampson, J.; Landi, M. T.; Freedman, N. D.; Gapstur, S.; Carter, B.; Hoover, R. N.; Chanock, S. J.; Savage, S. A.
JAMA Oncology 6 (5) :724-734, 2020 10.1001/jamaoncol.2020.0197
Who should access germline genome sequencing? A mixed methods study of patient views
Best, M. C.; Butow, P.; Jacobs, C.; Savard, J.; Biesecker, B.; Ballinger, M. L.; Bartley, N.; Davies, G.; Napier, C. E.; Smit, A. K.; Thomas, D. M.; Newson, A. J.; Members of the PiGeOn Project, .
CLINICAL GENETICS 97 (2) :329-337, 2020 10.1111/cge.13664
Penetrance of different cancer types in families with Li-Fraumeni syndrome: A validation study using multicenter cohort.
Shin, S. J.; Dodd-Eaton, E. B.; Peng, G.; Bojadzieva, J.; Chen, J.; Amos, C. I.; Frone, M. N.; Khincha, P. P.; Mai, P. L.; Savage, S. A.; Ballinger, M. L.; Thomas, D. M.; Yuan, Y.; Strong, L. C.; Wang, W.
CANCER RESEARCH 80 (2) :354-360, 2020 10.1158/0008-5472.CAN-19-0728
Patient perspectives on molecular tumor profiling: "Why wouldn't you?"
Best, M. C.; Bartley, N.; Jacobs, C.; Juraskova, I.; Goldstein, D.; Newson, A. J.; Savard, J.; Meiser, B.; Ballinger, M.; Napier, C.; Thomas, D.; Biesecker, B.; Butow, P.
BMC Cancer 19 (1) :753, 2019 10.1186/s12885-019-5920-x
A quantitative model to predict pathogenicity of missense variants in the TP53 gene
Fortuno, C.; Cipponi, A.; Ballinger, M. L.; Tavtigian, S. V.; Olivier, M.; Ruparel, V.; Haupt, Y.; Haupt, S.; Study, I. S. K.; Tucker, K.; Spurdle, A. B.; Thomas, D. M.; James, P. A.
HUMAN MUTATION 40 (6) :788-800, 2019 10.1002/humu.23739
Therapeutic implications of germline genetic findings in cancer
Thavaneswaran, S.; Rath, E.; Tucker, K.; Joshua, A. M.; Hess, D.; Pinese, M.; Ballinger, M. L.; Thomas, D. M.
Nature Reviews Clinical Oncology 16 (6) :386-396, 2019 10.1038/s41571-019-0179-3
OpenAccess publication Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts
Jones, R. M.; Melton, P. E.; Pinese, M.; Rea, A. J.; Ingley, E.; Ballinger, M. L.; Wood, D. J.; Thomas, D. M.; Moses, E. K.
BMC Medical Genetics 20 (1) :69, 2019 10.1186/s12881-019-0808-9
Diagnosis of fusion genes using targeted RNA sequencing
Heyer, E. E.; Deveson, I. W.; Wooi, D.; Selinger, C. I.; Lyons, R. J.; Hayes, V. M.; O'Toole, S. A.; Ballinger, M. L.; Gill, D.; Thomas, D. M.; Mercer, T. R.; Blackburn, J.
Nature Communications 10 (1) :1388, 2019 10.1038/s41467-019-09374-9
Translating genomic risk into an early detection strategy for sarcoma
Ballinger, M. L.; Pinese, M.; Thomas, D. M.
GENES CHROMOSOMES & CANCER 58 :130-136, 2019 10.1002/gcc.22697
Cancer Molecular Screening and Therapeutics (MoST): a framework for multiple, parallel signal-seeking studies of targeted therapies for rare and neglected cancers
Thavaneswaran, S.; Sebastian, L.; Ballinger, M.; Best, M.; Hess, D.; Lee, C. K.; Sjoquist, K. M.; Hague, W. E.; Butow, P. N.; Simes, R. J.; Thomas, D.
MEDICAL JOURNAL OF AUSTRALIA 209 (8) :354-355, 2018
Development and pilot testing of a decision aid for genomic research participants notified of clinically actionable research findings for cancer risk
Willis, A. M.; Smith, S. K.; Meiser, B.; Ballinger, M. L.; Thomas, D. M.; Tattersall, M.; Young, M. A.
Journal of Genetic Counseling 27 (5) :1055-1066, 2018 10.1007/s10897-018-0223-y