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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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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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Genomic microarrays in the spotlight

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

2004

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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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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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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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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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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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Telomerase activity is a biomarker for high grade malignant peripheral nerve sheath tumors in neurofibromatosis type 1 individuals

Genes chromosomes & cancer, 2008-03, Vol.47 (3), p.238-246

2008

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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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Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray

Genes chromosomes & cancer, 2005-08, Vol.43 (4), p.329-338

2005

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High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas

Human genetics, 2005-11, Vol.118 (1), p.35-44

2005

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High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas

Genes chromosomes & cancer, 2005-03, Vol.42 (3), p.228-237

2005

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Genomic microarrays in the spotlight

Drug discovery today, 2004-12, Vol.9 (24), p.45-52

2004

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High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH

International journal of oncology, 2003-03, Vol.22 (3), p.615

2003

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Experimental approaches for identifying schizophrenia risk genes

Current topics in behavioral neurosciences, 2010, Vol.4, p.587

2010

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Does chromosome 22 have anything to do with sex determination: Further studies on a 46,XX,22q11.2 del male

American journal of medical genetics. Part A, 2003-11, Vol.123A (1), p.64-67

2003

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

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

2006

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Microarray-based comparative genomic hybridization in neurofibromatoses and digeorge syndrome

Mantripragada, Kiran K

2005

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

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

Genomic microarrays in the spotlight

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

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

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

Copy-number polymorphisms: mining the tip of an iceberg

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

Telomerase activity is a biomarker for high grade malignant peripheral nerve sheath tumors in neurofibromatosis type 1 individuals

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

Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray

High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas

High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas

Genomic microarrays in the spotlight

High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH

Experimental approaches for identifying schizophrenia risk genes

Does chromosome 22 have anything to do with sex determination: Further studies on a 46,XX,22q11.2 del male

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

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

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

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

Microarray-based comparative genomic hybridization in neurofibromatoses and digeorge syndrome

A full-coverage, high-resolution human chromosome 22 genomic microarrayfor clinical and research applications

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