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TraceMontage: A method for merging multiple independent neuronal traces

Journal of neuroscience methods, 2020-02, Vol.332, p.108560-108560, Article 108560

2020

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Clinical implications of the genetics of sporadic colorectal cancer

ANZ journal of surgery, 2019-10, Vol.89 (10), p.1224-1229

2019

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Post-explant profiling of subcellular-scale carbon fiber intracortical electrodes and surrounding neurons enables modeling of recorded electrophysiology

Journal of neural engineering, 2023-03, Vol.20 (2), p.26019

2023

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

Breast cancer research and treatment, 2021-09, Vol.189 (2), p.363-375

2021

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nGauge: Integrated and Extensible Neuron Morphology Analysis in Python

Neuroinformatics (Totowa, N.J.), 2022-07, Vol.20 (3), p.755-764

2022

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Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach

Human mutation, 2022-12, Vol.43 (12), p.1921-1944

2022

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Phosphohistone H3 outperforms Ki67 as a marker of outcome for breast cancer patients

Histopathology, 2015-10, Vol.67 (4), p.538-547

2015

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Weber C Ankle Fractures: A Retrospective Audit of Screw Number, Size, Complications, and Retrieval Rates

The Journal of foot and ankle surgery, 2015-05, Vol.54 (3), p.454-457

2015

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RNAscope compatibility with image analysis platforms for the quantification of tissue-based colorectal cancer biomarkers in archival formalin-fixed paraffin-embedded tissue

Acta histochemica, 2021-09, Vol.123 (6), p.151765-151765, Article 151765

2021

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Optimized Neuron Tracing Using Post Hoc Reanalysis

2023 IEEE 20th International Symposium on Biomedical Imaging (ISBI), 2023, p.1-5

2023

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Evaluation of a 5-Tier Scheme Proposed for Classification of Sequence Variants Using Bioinformatic and Splicing Assay Data: Inter-Reviewer Variability and Promotion of Minimum Reporting Guidelines

Human mutation, 2013-10, Vol.34 (10), p.1424-1431

2013

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Unsupervised Neural Tracing In Densely Labeled Multispectral Brainbow Images

2021 IEEE 18th International Symposium on Biomedical Imaging (ISBI), 2021, p.1122-1126

2021

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Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity

Human mutation, 2010-06, Vol.31 (6), p.E1484-E1505

2010

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Toward understanding the molecular basis of ovarian cancer

Human mutation, 2009-12, Vol.30 (12), p.v-v

Walker, Logan C.

2009

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Teaching Python for Data Science: Collaborative development of a modular & interactive curriculum

Journal of Open Source Education, 2021-01, Vol.4 (46), p.138

2021

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Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary

Human mutation, 2011-06, Vol.32 (6), p.678-687

2011

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Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition

Human genetics, 2015-03, Vol.134 (3), p.269-278

2015

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P061: ATM and PALB2 variant curation guidelines progress update: ClinGen Hereditary Breast, Ovarian, and Pancreatic Cancer Variant Curation Expert Panel

Genetics in Medicine Open, 2023, Vol.1 (1), p.100080, Article 100080

2023

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

Breast cancer research and treatment, 2012-08, Vol.134 (3), p.1005-1011

2012

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P076: The ClinGen ENIGMA BRCA1/2 expert panel: A dynamic framework for evidence-based recommendations to improve classification criteria for variants in BRCA1/2

Genetics in Medicine Open, 2023, Vol.1 (1), p.100095, Article 100095

2023

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pCAP-based peptide substrates: The new tool in the box of tyrosine phosphatase assays

Methods (San Diego, Calif.), 2014-01, Vol.65 (2), p.165-174

2014

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Familial Mutations of the Transcription Factor RUNX1 (AML1, CBFA2) Predispose to Acute Myeloid Leukemia

Leukemia & lymphoma, 2004-01, Vol.45 (1), p.1-10

2004

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Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers

Breast cancer research and treatment, 2008-11, Vol.112 (2), p.229-236

2008

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Comparison Of A Real-time Hydration Device With Weight Loss And Saliva Osmolality Following Exercise: 51

Medicine and science in sports and exercise, 2021-08, Vol.53 (8S), p.16-17

2021

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Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z‐scores improves detection and reliability

Genetic epidemiology, 2021-04, Vol.45 (3), p.237-248

2021

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TraceMontage: A method for merging multiple independent neuronal traces

Clinical implications of the genetics of sporadic colorectal cancer

Post-explant profiling of subcellular-scale carbon fiber intracortical electrodes and surrounding neurons enables modeling of recorded electrophysiology

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

nGauge: Integrated and Extensible Neuron Morphology Analysis in Python

Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach

Phosphohistone H3 outperforms Ki67 as a marker of outcome for breast cancer patients

Weber C Ankle Fractures: A Retrospective Audit of Screw Number, Size, Complications, and Retrieval Rates

RNAscope compatibility with image analysis platforms for the quantification of tissue-based colorectal cancer biomarkers in archival formalin-fixed paraffin-embedded tissue

Optimized Neuron Tracing Using Post Hoc Reanalysis

Evaluation of a 5-Tier Scheme Proposed for Classification of Sequence Variants Using Bioinformatic and Splicing Assay Data: Inter-Reviewer Variability and Promotion of Minimum Reporting Guidelines

Unsupervised Neural Tracing In Densely Labeled Multispectral Brainbow Images

Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity

Toward understanding the molecular basis of ovarian cancer

Teaching Python for Data Science: Collaborative development of a modular & interactive curriculum

Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary

Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition

P061: ATM and PALB2 variant curation guidelines progress update: ClinGen Hereditary Breast, Ovarian, and Pancreatic Cancer Variant Curation Expert Panel

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

P076: The ClinGen ENIGMA BRCA1/2 expert panel: A dynamic framework for evidence-based recommendations to improve classification criteria for variants in BRCA1/2

pCAP-based peptide substrates: The new tool in the box of tyrosine phosphatase assays

Familial Mutations of the Transcription Factor RUNX1 (AML1, CBFA2) Predispose to Acute Myeloid Leukemia

Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers

Comparison Of A Real-time Hydration Device With Weight Loss And Saliva Osmolality Following Exercise: 51

Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z‐scores improves detection and reliability

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