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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

Human molecular genetics, 2009-04, Vol.18 (8), p.1497-1503

2009

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Access-Site Complications in Mechanical Thrombectomy for Acute Ischemic Stroke: A Review of Prospective Trials

American journal of neuroradiology : AJNR, 2020-03, Vol.41 (3), p.477-481

2020

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Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation

Psychological medicine, 2018-07, Vol.48 (10), p.1608-1615

2018

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Genomic microarrays in the spotlight

Trends in genetics, 2004-02, Vol.20 (2), p.87-94

2004

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High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization

Clinical cancer research, 2008-02, Vol.14 (4), p.1015-1024

2008

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CACNA1C risk variant affects reward responsiveness in healthy individuals

Translational psychiatry, 2014-10, Vol.4 (10), p.e461-e461

2014

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Replication study implicates COMT val158met polymorphism as a modulator of probabilistic reward learning

Genes, brain and behavior, 2015-07, Vol.14 (6), p.486-492

2015

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Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH

Journal of medical genetics, 2006-01, Vol.43 (1), p.28-38

2006

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Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Molecular psychiatry, 2017-10, Vol.22 (10), p.1509-1509

2017

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Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)

Human mutation, 2008, Vol.29 (1), p.74-82

2008

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MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Translational psychiatry, 2017-01, Vol.7 (1), p.e1012-e1012

2017

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Molecular psychiatry, 2018-01, Vol.23 (1), p.162-163

2018

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Molecular psychiatry, 2017-10, Vol.22 (10), p.1509-1509

2017

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Copy-number polymorphisms: mining the tip of an iceberg

Trends in genetics, 2005-06, Vol.21 (6), p.315-317

2005

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Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-04, Vol.153B (3), p.766-774

2010

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Improving hyperspectral image segmentation by applying inverse noise weighting and outlier removal for optimal scale selection

ISPRS journal of photogrammetry and remote sensing, 2021-01, Vol.171, p.348-366

2021

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Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus

BMC genomics, 2007-01, Vol.8 (1), p.16-16, Article 16

2007

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Nonengraftment donor lymphocyte infusions for refractory acute myeloid leukemia

Blood cancer journal (New York), 2015-12, Vol.5 (12), p.e371-e371

2015

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Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection

Journal of molecular medicine (Berlin, Germany), 2003-07, Vol.81 (7), p.443-451

2003

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Elevated P3b latency variability in carriers of ZNF804A risk allele for psychosis

NeuroImage (Orlando, Fla.), 2015-08, Vol.116, p.207-213

2015

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Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH

Genomics (San Diego, Calif.), 2006-08, Vol.88 (2), p.152-162

2006

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Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array‐CGH

International journal of cancer, 2006-03, Vol.118 (5), p.1159-1164

2006

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Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme

Genes chromosomes & cancer, 2005-10, Vol.44 (2), p.161-169

2005

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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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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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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

Access-Site Complications in Mechanical Thrombectomy for Acute Ischemic Stroke: A Review of Prospective Trials

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation

Genomic microarrays in the spotlight

High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization

CACNA1C risk variant affects reward responsiveness in healthy individuals

Replication study implicates COMT val158met polymorphism as a modulator of probabilistic reward learning

Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

Copy-number polymorphisms: mining the tip of an iceberg

Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis

Improving hyperspectral image segmentation by applying inverse noise weighting and outlier removal for optimal scale selection

Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus

Nonengraftment donor lymphocyte infusions for refractory acute myeloid leukemia

Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection

Elevated P3b latency variability in carriers of ZNF804A risk allele for psychosis

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH

Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array‐CGH

Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme

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

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

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