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Pregnancy After Kidney Transplantation and its Impact on Graft Function: Some Answers but Several Questions Still Remain

Transplantation, 2022-06, Vol.106 (6), p.1109-1110

Claes, Kathleen J.

2022

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Comparison of microsatellite instability detection by immunohistochemistry and molecular techniques in colorectal and endometrial cancer

Scientific reports, 2021-06, Vol.11 (1), p.12880-12880, Article 12880

2021

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The psychological impact of genetic testing in childhood cancer: A systematic review

Psycho-oncology (Chichester, England), 2024-01, Vol.33 (1), p.e6279-n/a

2024

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Budget Impact of Disease-Modifying Treatments and a CRISPR Gene-Edited Therapy for Sickle Cell Disease

Clinical drug investigation, 2024-08, Vol.44 (8), p.611-627

2024

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Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay

Oncology reports, 2017-03, Vol.37 (3), p.1379-1386

2017

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EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer

European journal of human genetics : EJHG, 2024-05, Vol.32 (5), p.479-488

2024

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The Case | Asymmetric kidney cysts in a patient with negative family history

Kidney international, 2024-08, Vol.106 (2), p.323-324

2024

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Decoding NF1 Intragenic Copy-Number Variations

American journal of human genetics, 2015-08, Vol.97 (2), p.238-249

2015

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SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

Genome biology, 2014-06, Vol.15 (6), p.R80-R80, Article R80

2014

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Long term response on Regorafenib in non-V600E BRAF mutated colon cancer: a case report

BMC cancer, 2019-06, Vol.19 (1), p.567-567, Article 567

2019

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Zebrafish Avatars: Toward Functional Precision Medicine in Low-Grade Serous Ovarian Cancer

Cancers, 2024-05, Vol.16 (10), p.1812

2024

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Missing heritability in Bloom syndrome: First report of a deep intronic variant leading to pseudo‐exon activation in the BLM gene

Clinical genetics, 2021-02, Vol.99 (2), p.292-297

2021

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Bone mineral density, bone turnover markers, and incident fractures in de novo kidney transplant recipients

Kidney international, 2019-06, Vol.95 (6), p.1461-1470

2019

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Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies

Clinical journal of the American Society of Nephrology, 2023-07, Vol.18 (7), p.881-891

2023

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Accurate detection and quantification of epigenetic and genetic second hits in BRCA1 and BRCA2-associated hereditary breast and ovarian cancer reveals multiple co-acting second hits

Cancer letters, 2018-07, Vol.425, p.125-133

2018

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Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

Human genetics, 2018-07, Vol.137 (6-7), p.511-520

2018

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Timing of blood sampling for butyrylcholinesterase phenotyping in patients with prolonged neuromuscular block after mivacurium or suxamethonium

Acta anaesthesiologica Scandinavica, 2021-02, Vol.65 (2), p.182-187

2021

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Zebrafish as an in vivo screening tool to establish PARP inhibitor efficacy

DNA repair, 2021-01, Vol.97, p.103023-103023, Article 103023

2021

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Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation

Breast cancer research : BCR, 2016-05, Vol.18 (1), p.52-52, Article 52

2016

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Identification of potentially actionable genetic variants in epithelial ovarian cancer: a retrospective cohort study

NPJ precision oncology, 2024-03, Vol.8 (1), p.71-71, Article 71

2024

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Atypical Hemolytic Uremic Syndrome Occurring After Receipt of mRNA-1273 COVID-19 Vaccine Booster: A Case Report

American journal of kidney diseases, 2023-03, Vol.81 (3), p.364-367

2023

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Methodological Quality Assessment of Budget Impact Analyses for Orphan Drugs: A Systematic Review

Frontiers in pharmacology, 2021-04, Vol.12, p.630949-630949

2021

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The Zebrafish as an Emerging Model to Study DNA Damage in Aging, Cancer and Other Diseases

Frontiers in cell and developmental biology, 2019-01, Vol.6, p.178-178

2019

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Dealing with pseudogenes in molecular diagnostics in the next-generation sequencing era

Methods in molecular biology (Clifton, N.J.), 2014-01, Vol.1167, p.303

2014

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p-Cresol and Cardiovascular Risk in Mild-to-Moderate Kidney Disease

Clinical journal of the American Society of Nephrology, 2010-07, Vol.5 (7), p.1182-1189

2010

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Pregnancy After Kidney Transplantation and its Impact on Graft Function: Some Answers but Several Questions Still Remain

Comparison of microsatellite instability detection by immunohistochemistry and molecular techniques in colorectal and endometrial cancer

The psychological impact of genetic testing in childhood cancer: A systematic review

Budget Impact of Disease-Modifying Treatments and a CRISPR Gene-Edited Therapy for Sickle Cell Disease

Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay

EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer

The Case | Asymmetric kidney cysts in a patient with negative family history

Decoding NF1 Intragenic Copy-Number Variations

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

Long term response on Regorafenib in non-V600E BRAF mutated colon cancer: a case report

Zebrafish Avatars: Toward Functional Precision Medicine in Low-Grade Serous Ovarian Cancer

Missing heritability in Bloom syndrome: First report of a deep intronic variant leading to pseudo‐exon activation in the BLM gene

Bone mineral density, bone turnover markers, and incident fractures in de novo kidney transplant recipients

Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies

Accurate detection and quantification of epigenetic and genetic second hits in BRCA1 and BRCA2-associated hereditary breast and ovarian cancer reveals multiple co-acting second hits

Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

Timing of blood sampling for butyrylcholinesterase phenotyping in patients with prolonged neuromuscular block after mivacurium or suxamethonium

Zebrafish as an in vivo screening tool to establish PARP inhibitor efficacy

Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation

Identification of potentially actionable genetic variants in epithelial ovarian cancer: a retrospective cohort study

Atypical Hemolytic Uremic Syndrome Occurring After Receipt of mRNA-1273 COVID-19 Vaccine Booster: A Case Report

Methodological Quality Assessment of Budget Impact Analyses for Orphan Drugs: A Systematic Review

The Zebrafish as an Emerging Model to Study DNA Damage in Aging, Cancer and Other Diseases

Dealing with pseudogenes in molecular diagnostics in the next-generation sequencing era

p-Cresol and Cardiovascular Risk in Mild-to-Moderate Kidney Disease

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