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NEK8 Links the ATR-Regulated Replication Stress Response and S Phase CDK Activity to Renal Ciliopathies

Molecular cell, 2013-08, Vol.51 (4), p.423-439

2013

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Nek8 Regulates the Expression and Localization of Polycystin-1 and Polycystin-2

Journal of the American Society of Nephrology, 2008-03, Vol.19 (3), p.469-476

2008

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ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

Nature communications, 2015-01, Vol.6 (1), p.6023-6023, Article 6023

2015

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An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes

Frontiers in oncology, 2022-08, Vol.12, p.942741-942741

2022

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Development and evaluation of INT2GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome

Frontiers in oncology, 2024-01, Vol.13, p.1284690-1284690

2024

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Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia

Cytoskeleton (Hoboken, N.J.), 2010-02, Vol.67 (2), p.112-119

2010

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Loss of the Ciliary Kinase Nek8 Causes Left-Right Asymmetry Defects

Journal of the American Society of Nephrology, 2013-01, Vol.24 (1), p.100-112

2013

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Deriving tumor purity from cancer next generation sequencing data: applications for quantitative ERBB2 (HER2) copy number analysis and germline inference of BRCA1 and BRCA2 mutations

Modern pathology, 2022-10, Vol.35 (10), p.1458-1467

2022

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Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data

Data in brief, 2021-12, Vol.39, p.107653-107653, Article 107653

2021

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An optimized protocol for evaluating pathogenicity of VHL germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variants

MethodsX, 2022-01, Vol.9, p.101761-101761, Article 101761

2022

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Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse

Genome Research, 2006-03, Vol.16 (3), p.436-440

2006

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Contamination Assessment for Cancer Next-Generation Sequencing: Method Development and Clinical Implementation

Archives of pathology & laboratory medicine (1976), 2022-02, Vol.146 (2), p.227

2022

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Contamination Assessment for Cancer Next-Generation Sequencing

Archives of pathology & laboratory medicine (1976), 2022-01, Vol.146 (2), p.227-232

2022

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A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Neural development, 2011-01, Vol.6 (1), p.3-3

2011

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Targeted Informatics for Optimal Detection, Characterization, and Quantification of FLT3 Internal Tandem Duplications Across Multiple Next-Generation Sequencing Platforms

The Journal of molecular diagnostics : JMD, 2020-09, Vol.22 (9), p.1162-1178

2020

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Validation of targeted next‐generation sequencing of cell‐free DNA from archival cerebrospinal fluid specimens for the detection of somatic variants in cancer involving the leptomeninges: Cytopathologic and radiographic correlation

Cancer cytopathology, 2024-04, Vol.132 (4), p.214-223

2024

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Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic results

European journal of medical genetics, 2021-12, Vol.64 (12), p.104359, Article 104359

2021

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Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210

The New England journal of medicine, 2010-01, Vol.362 (3), p.206-216

2010

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ViroPanel: Hybrid Capture and Massively Parallel Sequencing for Simultaneous Detection and Profiling of Oncogenic Virus Infection and Tumor Genome

The Journal of molecular diagnostics : JMD, 2020-04, Vol.22 (4), p.476-487

2020

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Advancing Precision Oncology in Hereditary Paraganglioma-Pheochromocytoma Syndromes: Integrated Interpretation and Data Sharing of the Germline and Tumor Genomes

Cancers, 2024-02, Vol.16 (5), p.947

2024

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Novel Pathogenic Germline Variant of the Adenomatous Polyposis Coli (APC) Gene, p.S2627Gfs12 Identified in a Mild Phenotype of APC-Associated Polyposis: A Case Report

The American journal of case reports, 2020-12, Vol.21, p.e927293-e927293

2020

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Defects in ciliary localization of Nek8 is associated with cystogenesis

Pediatric nephrology (Berlin, West), 2008-03, Vol.23 (3), p.377-387

2008

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Abstract 3417: Detection and analysis of oncovirus integration sites in FFPE-derived human tumor samples using hybrid capture and massively parallel sequencing

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.3417-3417

2018

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Development and evaluation of INT 2 GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome

Frontiers in oncology, 2023, Vol.13, p.1284690

2023

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NEK8 Links the ATR-Regulated Replication Stress Response and S Phase CDK Activity to Renal Ciliopathies

Nek8 Regulates the Expression and Localization of Polycystin-1 and Polycystin-2

ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes

Development and evaluation of INT2GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome

Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia

Loss of the Ciliary Kinase Nek8 Causes Left-Right Asymmetry Defects

Deriving tumor purity from cancer next generation sequencing data: applications for quantitative ERBB2 (HER2) copy number analysis and germline inference of BRCA1 and BRCA2 mutations

Assessment of genomic alterations in non-syndromic von Hippel-Lindau: Insight from integrating somatic and germline next generation sequencing genomic data

An optimized protocol for evaluating pathogenicity of VHL germline variants in patients suspected with von Hippel-Lindau syndrome: Using somatic genome to inform the role of germline variants

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse

Contamination Assessment for Cancer Next-Generation Sequencing: Method Development and Clinical Implementation

Contamination Assessment for Cancer Next-Generation Sequencing

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Targeted Informatics for Optimal Detection, Characterization, and Quantification of FLT3 Internal Tandem Duplications Across Multiple Next-Generation Sequencing Platforms

Validation of targeted next‐generation sequencing of cell‐free DNA from archival cerebrospinal fluid specimens for the detection of somatic variants in cancer involving the leptomeninges: Cytopathologic and radiographic correlation

Pathogenicity of VHL variants in families with non-syndromic von Hippel-Lindau phenotypes: An integrated evaluation of germline and somatic genomic results

Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210

ViroPanel: Hybrid Capture and Massively Parallel Sequencing for Simultaneous Detection and Profiling of Oncogenic Virus Infection and Tumor Genome

Advancing Precision Oncology in Hereditary Paraganglioma-Pheochromocytoma Syndromes: Integrated Interpretation and Data Sharing of the Germline and Tumor Genomes

Novel Pathogenic Germline Variant of the Adenomatous Polyposis Coli (APC) Gene, p.S2627Gfs12 Identified in a Mild Phenotype of APC-Associated Polyposis: A Case Report

Germline Sequencing Improves Tumor-Only Sequencing Interpretation in a Precision Genomic Study of Patients With Pediatric Solid Tumor

Defects in ciliary localization of Nek8 is associated with cystogenesis

Abstract 3417: Detection and analysis of oncovirus integration sites in FFPE-derived human tumor samples using hybrid capture and massively parallel sequencing

Development and evaluation of INT 2 GRATE: a platform for comprehensive assessment of the role of germline variants informed by tumor signature profile in Lynch syndrome

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