Search Results - "Slavin TP"

The impact of VUS reclassification on reproductive decision making.

Authors: Peyser, Alexandra Onel, Kenan Hershlag, Avner

Source: PLoS ONE. 5/27/2025, Vol. 20 Issue 5, p1-8. 8p.

Erratum: Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.

Authors: Slavin TP Maxwell KN Lilyquist J et al.

Source: NPJ breast cancer [NPJ Breast Cancer] 2017 Nov 07; Vol. 3, pp. 44. Date of Electronic Publication: 2017 Nov 07 (Print Publication: 2017).

Publication Type: Journal Article; Published Erratum

Journal Info: Publisher: Breast Cancer Research Foundation Country of Publication: United States NLM ID: 101674891 Publication Model: eCollection Cited Medium: Print ISSN: 2374-4677 (Print) Linking ISSN: 23744677 NLM ISO Abbreviation: NPJ Breast Cancer Subsets: PubMed not MEDLINE

Active surveillance selection and 3-year durability in intermediate-risk prostate cancer following genomic testing.

Authors: Lenz L Clegg W Iliev D et al.

Source: Prostate cancer and prostatic diseases [Prostate Cancer Prostatic Dis] 2025 Jun; Vol. 28 (2), pp. 427-434. Date of Electronic Publication: 2024 Sep 05.

Publication Type: Journal Article; Observational Study

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9815755 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5608 (Electronic) Linking ISSN: 13657852 NLM ISO Abbreviation: Prostate Cancer Prostatic Dis Subsets: MEDLINE

High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer.

Authors: Schwartz, Mathias Ibadioune, Sabrina Delhomelle, Hélène et al.

Source: Clinical Epigenetics. 6/3/2025, Vol. 17 Issue 1, p1-6. 6p.

Aging and the global cancer burden: A population-based cohort study and predictive modelling analysis using the global cancer database.

Authors: Pustake, Manas Ganiyani, Mohammad Arfat Joshi, Swarada et al.

Source: Journal of Cancer Research & Therapeutics. Jan-Mar2026, Vol. 22 Issue 1, p36-45. 10p.

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Germline mutations and age at onset of lung adenocarcinoma.

Authors: Reckamp KL Behrendt CE Slavin TP et al.

Source: Cancer [Cancer] 2021 Aug 01; Vol. 127 (15), pp. 2801-2806. Date of Electronic Publication: 2021 Apr 15.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 0374236 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0142 (Electronic) Linking ISSN: 0008543X NLM ISO Abbreviation: Cancer Subsets: MEDLINE

Breast cancer risks associated with missense variants in breast cancer susceptibility genes.

Authors: Dorling, Leila Carvalho, Sara Allen, Jamie et al.

Source: Genome Medicine. 5/18/2022, Vol. 14 Issue 1, p1-17. 17p.

Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

Authors: Danishevich, Anastasiia Fedorova, Daria Bodunova, Natalia et al.

Source: Hereditary Cancer in Clinical Practice. 2/17/2025, Vol. 23 Issue 1, p1-13. 13p.

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BRCA1/2 Reversion Mutations in Japanese Patients with Metastatic Breast Cancer Progressing on Olaparib: OLIVE (WJOG15321B).

Authors: Sakai H Kusumoto-Matsuo R Hosonaga M et al.

Source: Breast cancer (Tokyo, Japan) [Breast Cancer] 2026 May; Vol. 33 (3), pp. 790-797. Date of Electronic Publication: 2026 Apr 10.

Publication Type: Journal Article; Multicenter Study; Observational Study

Journal Info: Publisher: Maruzen Co Country of Publication: Japan NLM ID: 100888201 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1880-4233 (Electronic) Linking ISSN: 13406868 NLM ISO Abbreviation: Breast Cancer Subsets: MEDLINE

Quality assurance within the context of genome diagnostics (a german perspective).

Authors: Florian, Kraft Benet-Pagès, Anna Berner, Daniel et al.

Source: Medizinische Genetik. Jun2023, Vol. 35 Issue 2, p91-104. 14p.

Age-specific familial risks in cancer as clues to germline genetic and environmental causes: focus on colorectal, endometrial, prostate, kidney, breast and lung cancers.

Authors: Hemminki, Kari Försti, Asta Hemminki, Otto et al.

Source: Hereditary Cancer in Clinical Practice. 2/21/2025, Vol. 23 Issue 1, p1-9. 9p.

Cosegregation analysis following an excellent response to olaparib in a pancreatic cancer patient carrier of BRCA2:c.7892 T > C variant enables its reclassification from VUS to pathogenic.

Authors: Strojnik K Blatnik A Krajc M et al.

Source: BJC reports [BJC Rep] 2026 Feb 16; Vol. 4 (1), pp. 5. Date of Electronic Publication: 2026 Feb 16.

Publication Type: Journal Article

Journal Info: Publisher: Nature Portfolio Country of Publication: England NLM ID: 9918752188106676 Publication Model: Electronic Cited Medium: Internet ISSN: 2731-9377 (Electronic) Linking ISSN: 27319377 NLM ISO Abbreviation: BJC Rep Subsets: PubMed not MEDLINE

Validation of a clinical breast cancer risk assessment tool combining a polygenic score for all ancestries with traditional risk factors.

Authors: Mabey B Hughes E Kucera M et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Jul; Vol. 26 (7), pp. 101128. Date of Electronic Publication: 2024 Jun 03.

Publication Type: Journal Article; Validation Study; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Genotype-phenotype correlations in PMS2 -associated constitutional mismatch repair deficiency: a systematic literature review.

Authors: Munteanu, Cătălin Vasile Lighezan, Diana Luisa Capcelea, Alexandru et al.

Source: Oncology Reviews. 2025, p1-14. 14p.

Mosaicism in genetic tumour syndromes.

Authors: Boros M.Sc., Matej Bourdeaut, Franck Fleischmann, Lara S. et al.

Source: Medizinische Genetik. Nov2025, Vol. 37 Issue 4, p279-293. 15p.

Bridging Technology and Pretest Genetic Services: Quantitative Study of Chatbot Interaction Patterns, User Characteristics, and Genetic Testing Decisions.

Authors: Yi, Yang Kaiser-Jackson, Lauren Bather, Jemar R et al.

Source: Journal of Medical Internet Research. 2025, Vol. 27, p1-25. 25p.

Paediatric Paraganglioma with Variant of Unknown Significance on Genetic Testing.

Authors: Ong, Jia Ling Pinto, Diluka Rajeev, Reshma et al.

Source: Case Reports in Oncology. 2025, Vol. 18 Issue 1, p255-261. 7p.

A novel electrochemical immunosensor for the ultrasensitive detection of vascular endothelial growth factor based on MB@Cu-MOFs/MWCNTs composite.

Authors: Liu, Junjie Wu, Shengxi Zhang, Lu et al.

Source: Microchimica Acta. Jan2025, Vol. 192 Issue 1, p1-13. 13p.