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Somatic mosaicism for copy number variation in differentiated human tissues

Human mutation, 2008-09, Vol.29 (9), p.1118-1124

2008

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Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer

Nature genetics, 2014-06, Vol.46 (6), p.624-628

2014

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Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation

Frontiers in medicine, 2023, Vol.10, p.1172565-1172565

2023

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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

American journal of human genetics, 2008-03, Vol.82 (3), p.763-771

2008

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Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation

American journal of medical genetics. Part A, 2010-10, Vol.152A (10), p.2595-2598

2010

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Human cytomegalovirus tegument protein pp65 is detected in all intra- and extra-axial brain tumours independent of the tumour type or grade

PloS one, 2014-09, Vol.9 (9), p.e108861-e108861

2014

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Efficient IgG-Mediated Suppression of Primary Antibody Responses in Fcγ Receptor-Deficient Mice

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (5), p.2244-2249

1999

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Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer

JCO precision oncology, 2023-01, Vol.7, p.e2300039

2023

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Enhanced susceptibility to low-dose collagen-induced arthritis in CR1/2-deficient female mice--possible role of estrogen on CR1 expression

The FASEB journal, 2009-08, Vol.23 (8), p.2450-2458

2009

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Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression

European journal of human genetics : EJHG, 2010-05, Vol.18 (5), p.560-568

2010

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Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma

International journal of cancer, 2010-03, Vol.126 (6), p.1390-1402

2010

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Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array

Genes chromosomes & cancer, 2009-10, Vol.48 (10), p.897-907

2009

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Distal 22q11.2 microduplication encompassing the BCR gene

American journal of medical genetics. Part A, 2008-12, Vol.146A (23), p.3075-3081

2008

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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency

BioMed research international, 2015-01, Vol.2015, p.862039-12

2015

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Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

Neuro-oncology (Charlottesville, Va.), 2009-12, Vol.11 (6), p.803-818

2009

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The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden

Journal of translational medicine, 2023-05, Vol.21 (1), p.342-342, Article 342

2023

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A segmental maximum a posteriori approach to genome-wide copy number profiling

Bioinformatics, 2008-03, Vol.24 (6), p.751-758

2008

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A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene

American journal of medical genetics. Part A, 2007-09, Vol.143A (18), p.2178-2184

2007

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Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis

Endocrine-related cancer, 2010-09, Vol.17 (3), p.561-579

2010

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Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma

Cancers, 2023-03, Vol.15 (7), p.1972

2023

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The potential of liquid biopsy for detection of the KIAA1549-BRAF fusion in circulating tumor DNA from children with pilocytic astrocytoma

Neuro-oncology advances, 2024-01, Vol.6 (1), p.vdae008-vdae008

2024

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A role for complement in feedback enhancement of antibody responses by IgG3

The Journal of experimental medicine, 2003-05, Vol.197 (9), p.1183-1190

2003

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Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling

Journal of neuro-oncology, 2012-03, Vol.107 (1), p.37-49

2012

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Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2

Human mutation, 2005-12, Vol.26 (6), p.540-549

2005

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Somatic mosaicism for copy number variation in differentiated human tissues

Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer

Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation

Human cytomegalovirus tegument protein pp65 is detected in all intra- and extra-axial brain tumours independent of the tumour type or grade

Efficient IgG-Mediated Suppression of Primary Antibody Responses in Fcγ Receptor-Deficient Mice

Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer

Spatially resolved clonal copy number alterations in benign and malignant tissue

Enhanced susceptibility to low-dose collagen-induced arthritis in CR1/2-deficient female mice--possible role of estrogen on CR1 expression

Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression

Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma

Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array

Distal 22q11.2 microduplication encompassing the BCR gene

Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency

Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden

A segmental maximum a posteriori approach to genome-wide copy number profiling

A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene

Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis

Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma

The potential of liquid biopsy for detection of the KIAA1549-BRAF fusion in circulating tumor DNA from children with pilocytic astrocytoma

A role for complement in feedback enhancement of antibody responses by IgG3

Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2

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