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Epigenetic therapy in combination with a multi-epitope cancer vaccine targeting shared tumor antigens for high-risk myelodysplastic syndrome - a phase I clinical trial

Cancer Immunology, Immunotherapy, 2022-02, Vol.71 (2), p.433-444

2022

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Atypical presentation of γ/δ mycosis fungoides with an unusual phenotype and SOCS1 mutation

Open life sciences, 2024-07, Vol.19 (1), p.20220925-14

2024

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Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors

Frontiers in oncology, 2023, Vol.13, p.1147591-1147591

2023

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Human genetic deficiencies reveal the roles of complement in the inflammatory network: Lessons from nature

Proceedings of the National Academy of Sciences - PNAS, 2009-09, Vol.106 (37), p.15861-15866

2009

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Test of an Improved DNA and RNA Purification Protocol—Importance of Proteinase K and Co-Purified Small RNAs

Separations, 2022-11, Vol.9 (11), p.324

2022

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Inactivating BTK mutations in large B‐cell lymphoma in a real‐world cohort: Strong correlation with BCL2 translocation

EJHaem, 2022-08, Vol.3 (3), p.936-939

2022

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Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy

American journal of kidney diseases, 2013-11, Vol.62 (5), p.978-983

2013

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P1148: MULTI‐SITE PRE‐THERAPEUTIC BIOPSIES REVEALS GENETIC HETEROGENEITY IN PATIENTS WITH NEWLY DIAGNOSED DIFFUSE LARGE B‐CELL LYMPHOMA

HemaSphere, 2023-08, Vol.7 (S3), p.e1611122-n/a

2023

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C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations

Clinical Immunology, 2007-07, Vol.124 (1), p.33-40

2007

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Next generation sequencing in routine diagnostics of mature non‐Hodgkin 's B‐cell lymphomas

European journal of haematology, 2023-10, Vol.111 (4), p.583-591

2023

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Anti-glomerular basement membrane glomerulonephritis and thrombotic microangiopathy in first degree relatives: a case report

BMC nephrology, 2012-07, Vol.13 (1), p.64-64, Article 64

2012

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Next generation sequencing in routine diagnostics of mature non-Hodgkin's B-cell lymphomas

European journal of haematology, 2023-10, Vol.111 (4), p.583-591

2023

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Test of the FlashFREEZE unit in tissue samples freezing for biobanking purposes

Cell and tissue banking, 2023-06, Vol.24 (2), p.435-447

2023

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Mutational landscape in Waldenström macroglobulinemia evaluated using a next-generation sequencing lymphoma panel in routine clinical practice

Leukemia & lymphoma, 2024-06, Vol.65 (6), p.758-767

2024

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Multi-site pre-therapeutic biopsies demonstrate genetic heterogeneity in patients with newly diagnosed diffuse large B-cell lymphoma

Leukemia & lymphoma, 2023-06, Vol.ahead-of-print (ahead-of-print), p.1-9

2023

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Paired comparison of the analytical performance between the Oncomine™ Comprehensive Assay v3 and whole-exome sequencing of ovarian cancer tissue

Molecular biology reports, 2024-12, Vol.51 (1), p.820, Article 820

2024

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High-Grade B-Cell Lymphomas with MYC and BCL2 Translocations Lack Tumor-Associated Macrophages and PD-L1 Expression: A Possible Noninflamed Subgroup

Blood, 2020-11, Vol.136 (Supplement 1), p.28-29

2020

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Therapeutic Cancer Vaccination Targeting Shared Tumor Associated Antigens in Combination with Azacitidine for High Risk Myelodysplastic Syndrome - a Phase I Clinical Trial

Blood, 2020-11, Vol.136 (Supplement 1), p.23-24

2020

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The value of next‐generation sequencing in routine diagnostics and management of patients with cytopenia

International journal of laboratory hematology, 2022-06, Vol.44 (3), p.531-537

2022

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Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis

Molecular diagnosis & therapy, 2021-03, Vol.25 (2), p.251-266

2021

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Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency

Clinical immunology (Orlando, Fla.), 2015-10, Vol.160 (2), p.315-318

2015

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Primary immunodeficiency: complex genetic disorders?

Clinical chemistry (Baltimore, Md.), 2007-02, Vol.53 (2), p.159-160

2007

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Complement plays a central role in Candida albicans‐induced cytokine production by human PBMCs

European journal of immunology, 2012-04, Vol.42 (4), p.993-1004

2012

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Bone Involvement as a Primary Rare Manifestation of Waldenstrom Macroglobulinemia: A Case Report and Prevalence in a Nationwide Population-Based Cohort Study

Journal of hematology, 2022-12, Vol.11 (6), p.233-239

2022

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Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency

Journal of autoimmunity, 2015-08, Vol.62 (Jun 25), p.39-44

2015

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Epigenetic therapy in combination with a multi-epitope cancer vaccine targeting shared tumor antigens for high-risk myelodysplastic syndrome - a phase I clinical trial

Atypical presentation of γ/δ mycosis fungoides with an unusual phenotype and SOCS1 mutation

Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors

Human genetic deficiencies reveal the roles of complement in the inflammatory network: Lessons from nature

Test of an Improved DNA and RNA Purification Protocol—Importance of Proteinase K and Co-Purified Small RNAs

Inactivating BTK mutations in large B‐cell lymphoma in a real‐world cohort: Strong correlation with BCL2 translocation

Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy

P1148: MULTI‐SITE PRE‐THERAPEUTIC BIOPSIES REVEALS GENETIC HETEROGENEITY IN PATIENTS WITH NEWLY DIAGNOSED DIFFUSE LARGE B‐CELL LYMPHOMA

C1q deficiency in an Inuit family: Identification of a new class of C1q disease-causing mutations

Next generation sequencing in routine diagnostics of mature non‐Hodgkin 's B‐cell lymphomas

Anti-glomerular basement membrane glomerulonephritis and thrombotic microangiopathy in first degree relatives: a case report

Next generation sequencing in routine diagnostics of mature non-Hodgkin's B-cell lymphomas

Test of the FlashFREEZE unit in tissue samples freezing for biobanking purposes

Mutational landscape in Waldenström macroglobulinemia evaluated using a next-generation sequencing lymphoma panel in routine clinical practice

Multi-site pre-therapeutic biopsies demonstrate genetic heterogeneity in patients with newly diagnosed diffuse large B-cell lymphoma

Paired comparison of the analytical performance between the Oncomine™ Comprehensive Assay v3 and whole-exome sequencing of ovarian cancer tissue

High-Grade B-Cell Lymphomas with MYC and BCL2 Translocations Lack Tumor-Associated Macrophages and PD-L1 Expression: A Possible Noninflamed Subgroup

Therapeutic Cancer Vaccination Targeting Shared Tumor Associated Antigens in Combination with Azacitidine for High Risk Myelodysplastic Syndrome - a Phase I Clinical Trial

The value of next‐generation sequencing in routine diagnostics and management of patients with cytopenia

Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis

Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency

Primary immunodeficiency: complex genetic disorders?

Complement plays a central role in Candida albicans‐induced cytokine production by human PBMCs

Bone Involvement as a Primary Rare Manifestation of Waldenstrom Macroglobulinemia: A Case Report and Prevalence in a Nationwide Population-Based Cohort Study

Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency

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