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PΨFinder: a practical tool for the identification and visualization of novel pseudogenes in DNA sequencing data

BMC bioinformatics, 2022-02, Vol.23 (1), p.59-59, Article 59

2022

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PB1806: ULTRA‐SENSITIVE MINIMAL RESIDUAL DISEASE (MRD) MONITORING FOR LEUKEMIA PATIENTS USING SUPERRCA MUTATION ASSAYS WITH FLOW CYTOMETER READOUT

HemaSphere, 2023-08, Vol.7 (S3), p.e249690d-n/a

2023

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Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population

Oncology reports, 2016-11, Vol.36 (5), p.2823-2835

2016

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The value of genome-wide analysis in craniosynostosis

Frontiers in genetics, 2024-01, Vol.14, p.1322462-1322462

2024

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Combinatory analysis of immune cell subsets and tumor-specific genetic variants predict clinical response to PD-1 blockade in patients with non-small cell lung cancer

Frontiers in oncology, 2023-02, Vol.12, p.1073457-1073457

2023

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P331: WGS/WES as unique diagnostic tool for the genetic screening of patients with craniosynostosis

Genetics in Medicine Open, 2023, Vol.1 (1), p.100359, Article 100359

2023

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Immune checkpoint blockade and biomarkers of clinical response in non–small cell lung cancer

Scandinavian journal of immunology, 2020-12, Vol.92 (6), p.e12980-n/a

2020

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Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families

BMC medicine, 2008-04, Vol.6 (1), p.10-10, Article 10

2008

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PÎ¨Finder: a practical tool for the identification and visualization of novel pseudogenes in DNA sequencing data

BMC bioinformatics, 2022-02, Vol.23 (1)

2022

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Combinatory analysis of immune cell subsets and tumor-specific genetic variants can predict clinical response to PD-1 blockade for non-small cell lung cancer patients

The Journal of immunology (1950), 2023-05, Vol.210 (1_Supplement), p.159-159.17

2023

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Parallel sequencing used in detection of mosaic mutations: Comparison with four diagnostic DNA screening techniques

Human mutation, 2009-06, Vol.30 (6), p.1012-1020

2009

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Abstract 3473: Comprehensive genetic screening in hereditary colorectal cancer

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.3473-3473

2019

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Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Genetics in medicine, 2019-08, Vol.21 (8), p.1868-1873

2019

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The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis

European journal of medical genetics, 2022-05, Vol.65 (5), p.104476-104476, Article 104476

2022

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Identification of known and novel familial cancer genes in Swedish colorectal cancer families

International journal of cancer, 2021-08, Vol.149 (3), p.627-634

2021

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NGS targeted screening of 100 Scandinavian patients with coronal synostosis

American journal of medical genetics. Part A, 2020-02, Vol.182 (2), p.348-356

2020

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Merged testing for colorectal cancer syndromes and re‐evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort

Genes chromosomes & cancer, 2022-10, Vol.61 (10), p.585-591

2022

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Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

Familial cancer, 2017-04, Vol.16 (2), p.195-203

2017

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GREM1 and POLE variants in hereditary colorectal cancer syndromes

Genes chromosomes & cancer, 2016-01, Vol.55 (1), p.95-106

2016

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Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis

Oncogene, 2011-12, Vol.30 (50), p.4977-4989

2011

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GREM 1 and POLE variants in hereditary colorectal cancer syndromes

Genes chromosomes & cancer, 2016-01, Vol.55 (1), p.95-106

2016

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Diagnostic accuracy of different caries risk assessment methods. A systematic review

Journal of dentistry, 2015-12, Vol.43 (12), p.1385-1393

2015

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Threshold values affect predictive accuracy of caries risk assessment

Acta odontologica Scandinavica, 2019-05, Vol.77 (4), p.315-327

2019

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A novel classification system for assessment of approximal caries lesion progression in bitewing radiographs

Dento-maxillo-facial radiology, 2016-01, Vol.45 (5), p.20160039-20160039

2016

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The major factors that influence endodontic retreatment decisions

Swedish dental journal, 2003, Vol.27 (1), p.23

2003

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PΨFinder: a practical tool for the identification and visualization of novel pseudogenes in DNA sequencing data

PB1806: ULTRA‐SENSITIVE MINIMAL RESIDUAL DISEASE (MRD) MONITORING FOR LEUKEMIA PATIENTS USING SUPERRCA MUTATION ASSAYS WITH FLOW CYTOMETER READOUT

Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population

The value of genome-wide analysis in craniosynostosis

Combinatory analysis of immune cell subsets and tumor-specific genetic variants predict clinical response to PD-1 blockade in patients with non-small cell lung cancer

P331: WGS/WES as unique diagnostic tool for the genetic screening of patients with craniosynostosis

Immune checkpoint blockade and biomarkers of clinical response in non–small cell lung cancer

Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families

PÎ¨Finder: a practical tool for the identification and visualization of novel pseudogenes in DNA sequencing data

Combinatory analysis of immune cell subsets and tumor-specific genetic variants can predict clinical response to PD-1 blockade for non-small cell lung cancer patients

Parallel sequencing used in detection of mosaic mutations: Comparison with four diagnostic DNA screening techniques

Abstract 3473: Comprehensive genetic screening in hereditary colorectal cancer

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis

Identification of known and novel familial cancer genes in Swedish colorectal cancer families

NGS targeted screening of 100 Scandinavian patients with coronal synostosis

Merged testing for colorectal cancer syndromes and re‐evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort

Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

GREM1 and POLE variants in hereditary colorectal cancer syndromes

Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis

GREM 1 and POLE variants in hereditary colorectal cancer syndromes

Diagnostic accuracy of different caries risk assessment methods. A systematic review

Threshold values affect predictive accuracy of caries risk assessment

A novel classification system for assessment of approximal caries lesion progression in bitewing radiographs

The major factors that influence endodontic retreatment decisions

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