Germline copy number variants are not associated with globally acquired copy number changes in familial breast tumours

por Walker, Logan C., Krause, Lutz, Spurdle, Amanda B., Waddell, Nic
Publicado 2012

The Role of Constitutional Copy Number Variants in Breast Cancer

por Walker, Logan C., Wiggins, George A.R., Pearson, John F.
Publicado 2015

Genome-Wide Gene Expression Analyses of BRCA1- and BRCA2-Associated Breast and Ovarian Tumours

por Wiggins, George A. R., Walker, Logan C., Pearson, John F.
Publicado 2020

Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with BRCA1 and BRCA2 Mutation Status in Familial Breast Cancer Patients

por Walker, Logan C., Thompson, Bryony A., Waddell, Nic, Investigators, kConFab, Grimmond, Sean M., Spurdle, Amanda B.
Publicado 2010

Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2 transcripts

por Whiley, Phillip J, Pettigrew, Christopher A, Brewster, Brooke L, Walker, Logan C, Spurdle, Amanda B, Brown, Melissa A
Publicado 2010

Dual-Color Fluorescence In Situ Hybridization Reveals an Association of Chromosome 8q22 but Not 8p21 Imbalance with High Grade Invasive Breast Carcinoma

por Walker, Logan C., McDonald, Margaret, Wells, J. Elisabeth, Harris, Gavin C., Robinson, Bridget A., Morris, Christine M.
Publicado 2013

Investigation of Experimental Factors That Underlie BRCA1/2 mRNA Isoform Expression Variation: Recommendations for Utilizing Targeted RNA Sequencing to Evaluate Potential Spliceoge...

por Lattimore, Vanessa L., Pearson, John F., Currie, Margaret J., Spurdle, Amanda B., Robinson, Bridget A., Walker, Logan C.
Publicado 2018

Assessment of intra-tumoural colorectal cancer prognostic biomarkers using RNA in situ hybridisation

por Morley-Bunker, Arthur, Pearson, John, Currie, Margaret J., Morrin, Helen, Whitehead, Martin R., Eglinton, Tim, Walker, Logan C.
Publicado 2019

Variable expression quantitative trait loci analysis of breast cancer risk variants

por Wiggins, George A. R., Black, Michael A., Dunbier, Anita, Merriman, Tony R., Pearson, John F., Walker, Logan C.
Publicado 2021

Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry

por Walker, Logan C., Pearson, John F., Wiggins, George A. R., Giles, Graham G., Hopper, John L., Southey, Melissa C.
Publicado 2017

Increased gene expression variability in BRCA1-associated and basal-like breast tumours

por Wiggins, George A. R., Black, Michael A., Dunbier, Anita, Morley-Bunker, Arthur E., Pearson, John F., Walker, Logan C.
Publicado 2021

Nanopore sequencing of full-length BRCA1 mRNA transcripts reveals co-occurrence of known exon skipping events

por de Jong, Lucy C., Cree, Simone, Lattimore, Vanessa, Wiggins, George A. R., Spurdle, Amanda B., Miller, Allison, Kennedy, Martin A., Walker, Logan C.
Publicado 2017

Cytomegalovirus and Epstein-Barr Virus in Breast Cancer

por Richardson, Ann K., Currie, Margaret J., Robinson, Bridget A., Morrin, Helen, Phung, Yen, Pearson, John F., Anderson, Trevor P., Potter, John D., Walker, Logan C.
Publicado 2015

Quantifying BRCA1 and BRCA2 mRNA Isoform Expression Levels in Single Cells

por Lattimore, Vanessa L., Pearson, John F., Morley-Bunker, Arthur E., Investigators, kConFab, Spurdle, Amanda B., Robinson, Bridget A., Currie, Margaret J., Walker, Logan C.
Publicado 2019

BRCA1 and BRCA2 Missense Variants of High and Low Clinical Significance Influence Lymphoblastoid Cell Line Post-Irradiation Gene Expression

por Waddell, Nic, Ten Haaf, Anette, Marsh, Anna, Johnson, Julie, Walker, Logan C., Investigators, kConFab, Gongora, Milena, Brown, Melissa, Grover, Piyush, Girolami, Mark, Grimmond, Sean, Chenevix-Trench, Georgia, Spurdle, Amanda B.
Publicado 2008

Targeted RNA‐seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes

por Brandão, Rita D., Mensaert, Klaas, López‐Perolio, Irene, Tserpelis, Demis, Xenakis, Markos, Lattimore, Vanessa, Walker, Logan C., Kvist, Anders, Vega, Ana, Gutiérrez‐Enríquez, Sara, Díez, Orland, de la Hoya, Miguel, Spurdle, Amanda B., De Meyer, Tim, Blok, Marinus J.
Publicado 2019

Differential Expression of BARD1 Isoforms in Melanoma

por McDougall, Lorissa I., Powell, Ryan M., Ratajska, Magdalena, Lynch-Sutherland, Chi F., Hossain, Sultana Mehbuba, Wiggins, George A. R., Harazin-Lechowska, Agnieszka, Cybulska-Stopa, Bożena, Motwani, Jyoti, Macaulay, Erin C., Reid, Glen, Walker, Logan C., Ryś, Janusz, Eccles, Michael R.
Publicado 2021

APPLICATION OF THE ACMG/AMP FRAMEWORK TO CAPTURE EVIDENCE RELEVANT TO PREDICTED AND OBSERVED IMPACT ON SPLICING: RECOMMENDATIONS FROM THE CLINGEN SVI SPLICING SUBGROUP

por Walker, Logan C., de la Hoya, Miguel, Wiggins, George A.R., Lindy, Amanda, Vincent, Lisa M., Parsons, Michael T, Canson, Daffodil M, Bis-Brewer, Dana, Cass, Ashley, Tchourbanov, Alexander, Zimmermann, Heather, Byrne, Alicia B, Pesaran, Tina, Karam, Rachid, Harrison, Steven, Spurdle, Amanda B
Publicado 2023

Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification

por Walker, Logan C., Lattimore, Vanessa Lilian, Kvist, Anders, Kleiblova, Petra, Zemankova, Petra, de Jong, Lucy, Wiggins, George A. R., Hakkaart, Christopher, Cree, Simone L., Behar, Raquel, Houdayer, Claude, Investigators, kConFab, Parsons, Michael T., Kennedy, Martin A., Spurdle, Amanda B., de la Hoya, Miguel
Publicado 2019

Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants

por Leman, Raphaël, Tubeuf, Hélène, Raad, Sabine, Tournier, Isabelle, Derambure, Céline, Lanos, Raphaël, Gaildrat, Pascaline, Castelain, Gaia, Hauchard, Julie, Killian, Audrey, Baert-Desurmont, Stéphanie, Legros, Angelina, Goardon, Nicolas, Quesnelle, Céline, Ricou, Agathe, Castera, Laurent, Vaur, Dominique, Le Gac, Gérald, Ka, Chandran, Fichou, Yann, Bonnet-Dorion, Françoise, Sevenet, Nicolas, Guillaud-Bataille, Marine, Boutry-Kryza, Nadia, Schultz, Inès, Caux-Moncoutier, Virginie, Rossing, Maria, Walker, Logan C., Spurdle, Amanda B., Houdayer, Claude, Martins, Alexandra, Krieger, Sophie
Publicado 2020