| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ABL1 gene involvement within a complex three-way translocation (2;9;4) in perineurioma characterized by molecular cytogenetic methods
|
Duff, Deiter J.
|
|
2014
|
235-236 |
6 |
p. 263-267
5 p.
|
artikel
|
| 2 |
aCGH+SNP as a Promising Analytical Tool for the Detection of Chromosomal Abnormalities in Acute Leukemia
|
Chen, Chuanfei
|
|
2014
|
235-236 |
6 |
p. 285-
1 p.
|
artikel
|
| 3 |
A Comparison of Whole Genome Mate Pair Sequencing (MPseq) with Karyotype and FISH for Breakpoint Detection in Hematologic Cancers
|
Johnson, Sarah H.
|
|
2016
|
235-236 |
6 |
p. 290-
1 p.
|
artikel
|
| 4 |
Acquisition of a t(11;14)(q13;q32) in clonal evolution in a follicular lymphoma with a t(14;18)(q32;q21) and t(3;22)(q27;q11.2)
|
Koduru, Prasad R.
|
|
2015
|
235-236 |
6 |
p. 303-309
7 p.
|
artikel
|
| 5 |
Acute promyelocytic leukemia with a STAT5b-RARα fusion transcript defined by array-CGH, FISH, and RT-PCR
|
Chen, Haoyue
|
|
2012
|
235-236 |
6 |
p. 327-331
5 p.
|
artikel
|
| 6 |
A Maternally Inherited 133 kb Deletion of 14q32.2q32.31 Associated with a Paternal Uniparental Disomy 14 Phenotype
|
Vallee, Stephanie E.
|
|
2016
|
235-236 |
6 |
p. 301-
1 p.
|
artikel
|
| 7 |
A Mosaic Copy Number Gain of 5p15.3p13.3
|
Valle, Stephanie E.
|
|
2014
|
235-236 |
6 |
p. 286-287
2 p.
|
artikel
|
| 8 |
Amplified Allelic Imbalance – A Genetic Signature of Malignant Peripheral Nerve Sheath Tumors (MPNST)
|
Znoyko, Iya Y.
|
|
2015
|
235-236 |
6 |
p. 358-
1 p.
|
artikel
|
| 9 |
Analytical Validation of Chromosomal Microarray Analysis with Solid Tumor FFPE Specimens
|
Lefferts, Joel A.
|
|
2015
|
235-236 |
6 |
p. 360-361
2 p.
|
artikel
|
| 10 |
An Approach for Estimating Percent Aberrant and Absolute Copy Number per Event from SNP Arrays and NGS Technologies
|
Shams, Soheil
|
|
2016
|
235-236 |
6 |
p. 293-294
2 p.
|
artikel
|
| 11 |
Anchored Multiplex PCR Enables Comprehensive Profiling of Thyroid and Lung Cancer Mutations by Next Generation Sequencing
|
Haimes, Josh
|
|
2016
|
235-236 |
6 |
p. 288-
1 p.
|
artikel
|
| 12 |
Anchored Multiplex PCR Enables NGS-Based Detection of FLT3-ITDs
|
Bessette, Marc
|
|
2016
|
235-236 |
6 |
p. 285-
1 p.
|
artikel
|
| 13 |
An ider(17)(q10)t(15;17) with spliced long-type PML-RARA fusion transcripts in a case of acute promyelocytic leukemia
|
Hu, Xiaojing
|
|
2014
|
235-236 |
6 |
p. 253-257
5 p.
|
artikel
|
| 14 |
A Novel Mutation in Calreticulin (CALR) was Identified in a Patient of African American Origin with Thrombocytosis
|
Dash, D.P.
|
|
2015
|
235-236 |
6 |
p. 363-
1 p.
|
artikel
|
| 15 |
A novel PLAG1-RAD51L1 gene fusion resulting from a t(8;14)(q12;q24) in a case of lipoblastoma
|
Deen, Mazin
|
|
2013
|
235-236 |
6 |
p. 233-237
5 p.
|
artikel
|
| 16 |
A Novel 1p35.1p34.3 Microdeletion in a Baby Boy with Multiple Congenital Anomalies and Developmental Delay
|
Kantarci, Sibel
|
|
2014
|
235-236 |
6 |
p. 290-
1 p.
|
artikel
|
| 17 |
A Rare Variant Pediatric Ph+ Acute Lymphoblastic Leukemia with Five Copies of the BCR-ABL1 Fusion Characterized by FISH, Cytogenetics, and SNP Microarray
|
Carstens, Billie J.
|
|
2016
|
235-236 |
6 |
p. 285-286
2 p.
|
artikel
|
| 18 |
ARID1A and TERT promoter mutations in dedifferentiated meningioma
|
Abedalthagafi, Malak S.
|
|
2015
|
235-236 |
6 |
p. 345-350
6 p.
|
artikel
|
| 19 |
Array CGH and Conventional Karyotyping: The Description of Two Selected Cases
|
Barbato, Ingrid T.
|
|
2015
|
235-236 |
6 |
p. 362-363
2 p.
|
artikel
|
| 20 |
A study of adrenocortical tumors in children and adolescents by a comparative genomic hybridization technique
|
Mateo, Elvis Cueva
|
|
2011
|
235-236 |
6 |
p. 298-308
11 p.
|
artikel
|
| 21 |
ATRX driver mutation in a composite malignant pheochromocytoma
|
Comino-Méndez, Iñaki
|
|
2016
|
235-236 |
6 |
p. 272-277
6 p.
|
artikel
|
| 22 |
Beyond HER2: Evaluating the Status of Additional Clinically Relevant Biomarkers in HER2-Positive Breast Cancers
|
Haskell, Gloria T.
|
|
2016
|
235-236 |
6 |
p. 289-
1 p.
|
artikel
|
| 23 |
Bilateral Radial Ray Defects: An Atypical Presentation of 16p11.2 Microdeletion Syndrome
|
Vallee, Stephanie E.
|
|
2015
|
235-236 |
6 |
p. 365-
1 p.
|
artikel
|
| 24 |
Bone morphogenetic protein 4—a fascinating regulator of cancer cell behavior
|
Kallioniemi, Anne
|
|
2012
|
235-236 |
6 |
p. 267-277
11 p.
|
artikel
|
| 25 |
BRAF V600E mutations: a series of case reports in patients with non–small cell lung cancer
|
Goldman, Jamie M.
|
|
2015
|
235-236 |
6 |
p. 351-354
4 p.
|
artikel
|
| 26 |
Brigham and Women's Hospital's Experience Correlating Cytogenetic and Sequencing Panel Results for Management of Myeloid Disorders
|
McIntyre, Kelsey
|
|
2016
|
235-236 |
6 |
p. 291-
1 p.
|
artikel
|
| 27 |
Can SNP-Arrays Predict Specific Morphologic and Immunophenotypic Results in Myelodysplastic Syndromes?
|
McElhone, Scott W.
|
|
2016
|
235-236 |
6 |
p. 291-
1 p.
|
artikel
|
| 28 |
Challenges of Cell Free Fetal DNA Follow-Up Testing for Rare Chromosome Abnormalities: Lessons from Two Recent Cases
|
LeRoux, Jamie
|
|
2016
|
235-236 |
6 |
p. 298-
1 p.
|
artikel
|
| 29 |
Characterization of 17.94, a novel anaplastic Wilms' tumor cell line
|
Brown, Keith W.
|
|
2012
|
235-236 |
6 |
p. 319-326
8 p.
|
artikel
|
| 30 |
Characterization of a Novel Inverted Tandem Duplication by Mate Pair Sequencing (MPseq)
|
Baughn, Linda
|
|
2016
|
235-236 |
6 |
p. 296-297
2 p.
|
artikel
|
| 31 |
Characterization of a novel t(2;5;11) in a patient with concurrent AML and CLL: a case report and literature review
|
Zhang, Rui
|
|
2011
|
235-236 |
6 |
p. 328-333
6 p.
|
artikel
|
| 32 |
Chromosomal Microarray in the Era of Next Generation Sequencing: Still Going Strong and Making a Difference in Patient Care. Cases from Medical University of South Carolina
|
Znoyko, Iya
|
|
2016
|
235-236 |
6 |
p. 296-
1 p.
|
artikel
|
| 33 |
Chromothripsis-Like Pattern in Chromosome 17q12 Is Associated with HER2 Amplification in Breast Cancer
|
Lin, Kevin
|
|
2016
|
235-236 |
6 |
p. 290-291
2 p.
|
artikel
|
| 34 |
Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement
|
MacKinnon, Ruth N.
|
|
2013
|
235-236 |
6 |
p. 238-251
14 p.
|
artikel
|
| 35 |
Clinical genomics of renal epithelial tumors
|
Hagenkord, Jill M.
|
|
2011
|
235-236 |
6 |
p. 285-297
13 p.
|
artikel
|
| 36 |
Clinical Utility of Biocartis Idylla in Colorectal Cancer Patients' Tissue and Plasma
|
Patel, Khushali
|
|
2016
|
235-236 |
6 |
p. 293-
1 p.
|
artikel
|
| 37 |
Clinical Utility of DNA Arrays in Detecting Chromosomal Aberrations Associated with High-Risk Philadelphia-Like Acute Lymphoblastic Leukemia
|
Raca, Gordana
|
|
2014
|
235-236 |
6 |
p. 284-285
2 p.
|
artikel
|
| 38 |
Clinical Validation and Implementation of a Targeted Sequencing Panel for Predisposition to Inherited Cancer
|
Turner, Scott A.
|
|
2015
|
235-236 |
6 |
p. 362-
1 p.
|
artikel
|
| 39 |
Clinico- and Pathogenomic Analyses of a Single Institution Diffuse Large B-Cell Lymphoma Cohort
|
Guttapalli, Asha
|
|
2015
|
235-236 |
6 |
p. 357-358
2 p.
|
artikel
|
| 40 |
Clonal cytogenetic abnormalities in the plasma cell variant of Castleman disease
|
Reichard, Kaaren K.
|
|
2011
|
235-236 |
6 |
p. 323-327
5 p.
|
artikel
|
| 41 |
Combined characterization of a pituitary adenoma and a subcutaneous lipoma in a MEN1 patient with a whole gene deletion
|
Rusconi, Daniela
|
|
2011
|
235-236 |
6 |
p. 309-315
7 p.
|
artikel
|
| 42 |
Commentary regarding Schayek et al., entitled “The rate of recurrent BRCA1, BRCA2, and TP53 mutations in the general population, and unselected ovarian cancer cases, in Belo Horizonte, Brazil”
|
Sales Luiz Vianna, Fernanda
|
|
2016
|
235-236 |
6 |
p. 282-283
2 p.
|
artikel
|
| 43 |
Comparison of Three Commercially Available Platforms for Somatic Mutation Profiling in Solid Tumors
|
Grafodatskaya, Daria
|
|
2016
|
235-236 |
6 |
p. 287-
1 p.
|
artikel
|
| 44 |
Complex Syndactyly and Atypical Ectrodactyly in a Child with a Mosaic Karyotype Involving Trisomy 21 and Partial Duplication of Chromosome 21
|
Enchautegui-Colon, Yazmin
|
|
2015
|
235-236 |
6 |
p. 364-
1 p.
|
artikel
|
| 45 |
Comprehensive evaluation of the effectiveness of gene expression signatures to predict complete response to neoadjuvant chemoradiotherapy and guide surgical intervention in rectal cancer
|
Lopes-Ramos, Camila
|
|
2015
|
235-236 |
6 |
p. 319-326
8 p.
|
artikel
|
| 46 |
Congenital Heart Defects in Neonates: Determining the Incidence of Genetic Testing and Follow-up Consultation at UCLA
|
Kantarci, Sibel
|
|
2015
|
235-236 |
6 |
p. 359-
1 p.
|
artikel
|
| 47 |
Copy Number Detection in Exome Sequencing Compared to Chromosomal Microarray in a Clinical Setting
|
Rajagopalan, Ramakrishnan
|
|
2016
|
235-236 |
6 |
p. 300-
1 p.
|
artikel
|
| 48 |
Cover
|
|
|
2016
|
235-236 |
6 |
p. CO1-
1 p.
|
artikel
|
| 49 |
Cover 1
|
|
|
2014
|
235-236 |
6 |
p. OFC-
1 p.
|
artikel
|
| 50 |
Cover 1
|
|
|
2015
|
235-236 |
6 |
p. OFC-
1 p.
|
artikel
|
| 51 |
Cover 1
|
|
|
2012
|
235-236 |
6 |
p. OFC-
1 p.
|
artikel
|
| 52 |
Cover 1
|
|
|
2013
|
235-236 |
6 |
p. OFC-
1 p.
|
artikel
|
| 53 |
Cover 1
|
|
|
2011
|
235-236 |
6 |
p. OFC-
1 p.
|
artikel
|
| 54 |
Detection of Copy Number Variants by Next Generation Sequencing is Driven by Genomic DNA Integrity
|
Haimes, Josh D.
|
|
2016
|
235-236 |
6 |
p. 288-
1 p.
|
artikel
|
| 55 |
Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR
|
Babiarz, Joshua E.
|
|
2014
|
235-236 |
6 |
p. 287-
1 p.
|
artikel
|
| 56 |
Detection of Exon-Centric Copy Number Changes and Mutations with Customizable Target Enrichment
|
Jeong, Kyeong Soo
|
|
2016
|
235-236 |
6 |
p. 298-
1 p.
|
artikel
|
| 57 |
Detection of Genomic Imbalances Involved in Common Chromosomal Rearrangements of Acute Leukemia by Cytogenomic SNP Microarray Analysis
|
Yenamandra, A.
|
|
2014
|
235-236 |
6 |
p. 289-290
2 p.
|
artikel
|
| 58 |
Detection of TET2 abnormalities by fluorescence in situ hybridization in 41 patients with myelodysplastic syndrome
|
Dambruoso, Irene
|
|
2012
|
235-236 |
6 |
p. 285-294
10 p.
|
artikel
|
| 59 |
Development and Clinical Validation of Large Fusion Panel for Pediatric and Adult Cancers
|
Chang, Fengqi
|
|
2016
|
235-236 |
6 |
p. 286-
1 p.
|
artikel
|
| 60 |
Development of a Clinical Grade Interpretive Tool for Neoplastic Genomic Microarray Testing
|
Cao, Yang
|
|
2016
|
235-236 |
6 |
p. 285-
1 p.
|
artikel
|
| 61 |
DNA copy number aberrations associated with lymphovascular invasion in upper urinary tract urothelial carcinoma
|
Misumi, Taku
|
|
2012
|
235-236 |
6 |
p. 313-318
6 p.
|
artikel
|
| 62 |
Editorial Board
|
|
|
2016
|
235-236 |
6 |
p. CO2-
1 p.
|
artikel
|
| 63 |
Editorial Board
|
|
|
2014
|
235-236 |
6 |
p. IFC-
1 p.
|
artikel
|
| 64 |
Editorial Board
|
|
|
2015
|
235-236 |
6 |
p. A1-
1 p.
|
artikel
|
| 65 |
Editorial Board
|
|
|
2012
|
235-236 |
6 |
p. IFC-
1 p.
|
artikel
|
| 66 |
Editorial Board
|
|
|
2013
|
235-236 |
6 |
p. IFC-
1 p.
|
artikel
|
| 67 |
Editorial Board
|
|
|
2011
|
235-236 |
6 |
p. IFC-
1 p.
|
artikel
|
| 68 |
Effects of TSP-1 -696 C/T polymorphism on bladder cancer susceptibility and clinicopathologic features
|
Gu, Jinbao
|
|
2014
|
235-236 |
6 |
p. 247-252
6 p.
|
artikel
|
| 69 |
Enabling More Complete Genome Analysis Using 10x Linked-Reads
|
Jabara, Cassandra B.
|
|
2016
|
235-236 |
6 |
p. 297-
1 p.
|
artikel
|
| 70 |
Establishing a murine xenograft-model for long-term analysis of factors inducing chromosomal instability in myelodysplastic syndrome: Pitfalls and successes
|
Salari, Azam
|
|
2016
|
235-236 |
6 |
p. 258-266
9 p.
|
artikel
|
| 71 |
Evaluation of SNP Genomic Microarray Analysis as an Alternative to FISH Analysis of Pediatric Solid Tumors
|
Arnoldo, Anthony
|
|
2015
|
235-236 |
6 |
p. 361-362
2 p.
|
artikel
|
| 72 |
EWS/FLI-responsive GGAA microsatellites exhibit polymorphic differences between European and African populations
|
Beck, Robert
|
|
2012
|
235-236 |
6 |
p. 304-312
9 p.
|
artikel
|
| 73 |
Exploring and Mapping the Life Cycle of Precision Medicine Data
|
Quackenbush, John X.
|
|
2016
|
235-236 |
6 |
p. 293-
1 p.
|
artikel
|
| 74 |
Extraskeletal myxoid chondrosarcoma with a t(9;16)(q22;p11.2) resulting in a NR4A3-FUS fusion
|
Broehm, Cory J.
|
|
2014
|
235-236 |
6 |
p. 276-280
5 p.
|
artikel
|
| 75 |
Frequency of the ETV6-RUNX1, BCR-ABL1, TCF3-PBX1, and MLL-AFF1 fusion genes in Guatemalan pediatric acute lymphoblastic leukemia patients and their ethnic associations
|
Carranza, Claudia
|
|
2013
|
235-236 |
6 |
p. 227-232
6 p.
|
artikel
|
| 76 |
From chromosomal abnormalities to the identification of target genes in mouse models of breast cancer
|
Fabris, Victoria T.
|
|
2014
|
235-236 |
6 |
p. 233-246
14 p.
|
artikel
|
| 77 |
Genome-Wide Microarray Analysis Improves Routine Diagnosis of Hematological Malignancies
|
Shao, Lina
|
|
2014
|
235-236 |
6 |
p. 284-
1 p.
|
artikel
|
| 78 |
Genomic profile of a Li-Fraumeni-like syndrome patient with a 45,X/46,XX karyotype, presenting neither mutations in TP53 nor clinical stigmata of Turner syndrome
|
Basso, Tatiane R.
|
|
2015
|
235-236 |
6 |
p. 341-344
4 p.
|
artikel
|
| 79 |
Genomic Profiling of Plasmablastic Lymphoma Reveals Recurrent Copy Number Alterations and MYC Rearrangement as Common Genetic Abnormalities
|
Ji, Jianling
|
|
2016
|
235-236 |
6 |
p. 290-
1 p.
|
artikel
|
| 80 |
Getting to Know Your LCRs: Recognizing and Interpreting Atypical CNVs in Recurrent Syndromic Microdeletion/Duplication Regions Mediated by Alternative Low Copy Repeat Elements
|
Rowsey, Ross A.
|
|
2016
|
235-236 |
6 |
p. 300-
1 p.
|
artikel
|
| 81 |
HaloPlexHS Utilizes Molecular Barcodes to Improve Low Frequency Allele Detection
|
Zobeck, Katie L.
|
|
2016
|
235-236 |
6 |
p. 296-
1 p.
|
artikel
|
| 82 |
HER2 Assessment by MIP Microarray in a Breast Cancer Patient with Equivocal HER2 Status
|
Chen, Hui
|
|
2016
|
235-236 |
6 |
p. 286-287
2 p.
|
artikel
|
| 83 |
Historical note on the discovery of the Philadelphia chromosome
|
Gahrton, Gösta
|
|
2012
|
235-236 |
6 |
p. 338-339
2 p.
|
artikel
|
| 84 |
Hyperhaploid uterine mesenchymal tumors—a novel genetic subgroup?
|
Holzmann, Carsten
|
|
2016
|
235-236 |
6 |
p. 278-281
4 p.
|
artikel
|
| 85 |
Identification of a complex 17q rearrangement in a metanephric stromal tumor
|
Toutain, Jérôme
|
|
2011
|
235-236 |
6 |
p. 340-343
4 p.
|
artikel
|
| 86 |
Identification of a HMGA2-EFCAB6 gene rearrangement following next-generation sequencing in a patient with a t(12;22)(q14.3;q13.2) and JAK2V617F-positive myeloproliferative neoplasm
|
Martin, S. Eric
|
|
2012
|
235-236 |
6 |
p. 295-303
9 p.
|
artikel
|
| 87 |
Identification of Novel and Recurrent Copy Number Abnormalities (CNAs) in Pediatric High Grade B-Cell Lymphoma by Chromosomal Microarray
|
Hagiya, Ashley S.
|
|
2016
|
235-236 |
6 |
p. 287-288
2 p.
|
artikel
|
| 88 |
Impact of SNP CMA on Patient Management in 3338 Extensively Followed Individuals at the Greenwood Genetic Center
|
Chaubey, Alka
|
|
2016
|
235-236 |
6 |
p. 297-
1 p.
|
artikel
|
| 89 |
Implementation and Routine Clinical Use of the TruSight Myeloid Sequencing Panel in Patients with Myeloid Malignancies
|
Peterson, Jason D.
|
|
2015
|
235-236 |
6 |
p. 361-
1 p.
|
artikel
|
| 90 |
Implementation of Genomic Assays for Tumor Genome Profiling in a Clinical Laboratory Setting
|
Murray, Sarah S.
|
|
2016
|
235-236 |
6 |
p. 292-293
2 p.
|
artikel
|
| 91 |
Implementation of Genotyping Cell Free Nucleic Acid in Plasma Using Next Generation Sequencing Platforms in a Clinical Laboratory
|
Mehrotra, Meenakshi
|
|
2016
|
235-236 |
6 |
p. 291-292
2 p.
|
artikel
|
| 92 |
Increased LOH Resolution Achieved with the Addition of Comprehensive and Updated SNP Content on Agilent’s CGH +SNP Cancer and Postnatal Array Platform
|
Dutta, Anindita
|
|
2015
|
235-236 |
6 |
p. 364-
1 p.
|
artikel
|
| 93 |
Integrative Copy Number and Mutational Analysis Improves Glioma Diagnostics
|
Ramkissoon, Shakti H.
|
|
2014
|
235-236 |
6 |
p. 287-
1 p.
|
artikel
|
| 94 |
International Breakpoint Mapping Consortium (IBMC). Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization
|
Tommerup, Niels
|
|
2015
|
235-236 |
6 |
p. 359-360
2 p.
|
artikel
|
| 95 |
Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML
|
Dawson, Angelika J.
|
|
2011
|
235-236 |
6 |
p. 344-347
4 p.
|
artikel
|
| 96 |
Jumping translocations in bone marrow cells of pediatric patients with hematologic malignancies: a rare cytogenetic phenomenon
|
Lizcova, Libuse
|
|
2011
|
235-236 |
6 |
p. 348-349
2 p.
|
artikel
|
| 97 |
KRAS Amplification in a 73-Year-Old Man with Adenocarcinoma of Lung
|
Chen, Hui
|
|
2014
|
235-236 |
6 |
p. 288-
1 p.
|
artikel
|
| 98 |
Large Cryptic Derivative Chromosome 8 Detected by SNP Chromosomal Microarray
|
Jacques, Heather
|
|
2015
|
235-236 |
6 |
p. 365-
1 p.
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artikel
|
| 99 |
Lineage switch with t(6;11)(q27;q23) from T-cell lymphoblastic lymphoma to acute monoblastic leukemia at relapse
|
Higuchi, Yusuke
|
|
2016
|
235-236 |
6 |
p. 267-271
5 p.
|
artikel
|
| 100 |
Liquid Biopsy: Comparison of Mutation Detection Methods for Measurement of RET M918T Circulating Cell-Free DNA in Medullary Thyroid Cancer Patients
|
Evers, Caitlin
|
|
2016
|
235-236 |
6 |
p. 287-
1 p.
|
artikel
|
| 101 |
Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL
|
Utter, Rachel A.
|
|
2014
|
235-236 |
6 |
p. 286-
1 p.
|
artikel
|
| 102 |
Microdissecting the role of microRNAs in the pathogenesis of prostate cancer
|
Ayub, Shiekh Gazalla
|
|
2015
|
235-236 |
6 |
p. 289-302
14 p.
|
artikel
|
| 103 |
MicroRNAs as diagnostic markers for pancreatic ductal adenocarcinoma and its precursor, pancreatic intraepithelial neoplasm
|
Xue, Yue
|
|
2013
|
235-236 |
6 |
p. 217-221
5 p.
|
artikel
|
| 104 |
Molecular Characterization of Recurrent Partial Gene Duplications by Whole Genome Mate-Pair Sequencing (MPseq) to Improve the Accuracy of Chromosomal Microarray Reporting
|
Porath, Binu
|
|
2016
|
235-236 |
6 |
p. 299-300
2 p.
|
artikel
|
| 105 |
Molecular Characterization of WNT5B as a Candidate Gene for Developmental Delay Associated with 12p13.13 Microdeletions
|
Omorodion, Jacklyn
|
|
2014
|
235-236 |
6 |
p. 289-
1 p.
|
artikel
|
| 106 |
Molecular Cytogenetics Using Linked-Reads
|
Church, Deanna M.
|
|
2016
|
235-236 |
6 |
p. 297-
1 p.
|
artikel
|
| 107 |
Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2)
|
Kim, Seon Young
|
|
2014
|
235-236 |
6 |
p. 258-262
5 p.
|
artikel
|
| 108 |
Multiple Segmental Chromosomal Aberrations in Low-Risk Neuroblastoma are Associated with Metastatic Relapse
|
Mayfield, Jodi R.
|
|
2014
|
235-236 |
6 |
p. 288-
1 p.
|
artikel
|
| 109 |
My Cancer Genome
|
Micheel, Christine M.
|
|
2014
|
235-236 |
6 |
p. 289-
1 p.
|
artikel
|
| 110 |
Non-invasive Cell-free Tumor DNA-based Detection of Breast Cancer-related Copy Number Variations
|
Zimmermann, Bernhard G.
|
|
2014
|
235-236 |
6 |
p. 287-288
2 p.
|
artikel
|
| 111 |
Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients
|
Znoyko, Iya Y.
|
|
2014
|
235-236 |
6 |
p. 286-
1 p.
|
artikel
|
| 112 |
On the prevalence of the PAX8-PPARG fusion resulting from the chromosomal translocation t(2;3)(q13;p25) in adenomas of the thyroid
|
Klemke, Markus
|
|
2011
|
235-236 |
6 |
p. 334-339
6 p.
|
artikel
|
| 113 |
Petabyte-Scale Cancer Genomics in the Cloud
|
Davis-Dusenbery, Brandi N.
|
|
2015
|
235-236 |
6 |
p. 360-
1 p.
|
artikel
|
| 114 |
Postnatal Chromosomal Microarray Reveals a False Positive Trisomy 21 NIPS Result
|
Cao, Yang
|
|
2015
|
235-236 |
6 |
p. 357-
1 p.
|
artikel
|
| 115 |
12q amplification defines a subtype of extraskeletal osteosarcoma with good prognosis that is the soft tissue homologue of parosteal osteosarcoma
|
Kyriazoglou, Anastasios I.
|
|
2012
|
235-236 |
6 |
p. 332-336
5 p.
|
artikel
|
| 116 |
Rare Complete and Partial Monosomy 7 Mosaicism Detected in a Case with FTT and Borderline Motor Delay, Subsequently Diagnosed with Juvenile MDS: An Exposition of this Case and Other Interesting Mosaic Cancer Case Studies
|
Bickley, Vivienne M.
|
|
2014
|
235-236 |
6 |
p. 286-
1 p.
|
artikel
|
| 117 |
Rare Double-Hit with Two Translocations Involving IgH Both with BCL2 and BCL3 in a Monoclonal B-Cell Leukemia
|
Alpatov, Roman
|
|
2015
|
235-236 |
6 |
p. 362-
1 p.
|
artikel
|
| 118 |
RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations
|
Ahani, Ali
|
|
2011
|
235-236 |
6 |
p. 316-322
7 p.
|
artikel
|
| 119 |
Recurrent Genetic Alterations in Hepatitis C-Associated Hepatocellular Carcinoma Detected by Genomic Microarray and Their correlation with Histology and Clinical Outcome
|
Liu, Yajuan
|
|
2014
|
235-236 |
6 |
p. 285-
1 p.
|
artikel
|
| 120 |
Retrospective evaluation of the clinical and laboratory data from 300 patients of various hematological malignancies with chromosome 3 abnormalities
|
Liu, Dandan
|
|
2015
|
235-236 |
6 |
p. 333-340
8 p.
|
artikel
|
| 121 |
Role of CYP1A2 polymorphisms on lung cancer risk in a prospective study
|
Pavanello, Sofia
|
|
2012
|
235-236 |
6 |
p. 278-284
7 p.
|
artikel
|
| 122 |
Secondary Philadelphia chromosome and erythrophagocytosis in a relapsed acute myeloid leukemia after hematopoietic cell transplantation
|
Kelemen, Katalin
|
|
2014
|
235-236 |
6 |
p. 268-271
4 p.
|
artikel
|
| 123 |
Single nucleotide polymorphisms of the NF-κB and STAT3 signaling pathway genes predict lung cancer prognosis in a Chinese Han population
|
He, Fei
|
|
2015
|
235-236 |
6 |
p. 310-318
9 p.
|
artikel
|
| 124 |
Streamlining NGS Workflows Using Cancer Samples by the Application of Tthe DNA Integrity Number (DIN) from the Genomic DNA Screentape Assay
|
Borg, Solange
|
|
2015
|
235-236 |
6 |
p. 365-
1 p.
|
artikel
|
| 125 |
Summary of 262 Samples from 46 Patients Received for Preimplantation Genetic Screening by Array CGH: Hints at Early Stage Embryo Development
|
Smolarek, Teresa A.
|
|
2016
|
235-236 |
6 |
p. 300-
1 p.
|
artikel
|
| 126 |
Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization
|
Tommerup, Niels
|
|
2016
|
235-236 |
6 |
p. 301-
1 p.
|
artikel
|
| 127 |
Table of Contents
|
|
|
2016
|
235-236 |
6 |
p. A1-
1 p.
|
artikel
|
| 128 |
Table of Contents
|
|
|
2014
|
235-236 |
6 |
p. A1-
1 p.
|
artikel
|
| 129 |
Table of Contents
|
|
|
2015
|
235-236 |
6 |
p. A2-A3
nvt p.
|
artikel
|
| 130 |
Table of Contents
|
|
|
2013
|
235-236 |
6 |
p. A1-
1 p.
|
artikel
|
| 131 |
Table of Contents
|
|
|
2012
|
235-236 |
6 |
p. A1-A2
nvt p.
|
artikel
|
| 132 |
Table of Contents
|
|
|
2011
|
235-236 |
6 |
p. A1-A2
nvt p.
|
artikel
|
| 133 |
Terminal Gain of 12p13.33 and Terminal Loss of 9p24.3, Detected in a Child with Developmental Delay and Growth Issues and Due to a Maternal Unbalanced Rearrangement Between 12p and 9p
|
Haag, Mary M.
|
|
2015
|
235-236 |
6 |
p. 364-
1 p.
|
artikel
|
| 134 |
The Clinical Utility of a Combined Approach of CMA and NGS in Melanoma
|
Stokes, Jordan
|
|
2016
|
235-236 |
6 |
p. 295-
1 p.
|
artikel
|
| 135 |
The Constitutional Microarray Comparative Genomic Hybridization (aCGH) Experience at the Joana de Gusmão Children's Hospital
|
Ocampos, Maristela
|
|
2016
|
235-236 |
6 |
p. 299-
1 p.
|
artikel
|
| 136 |
The Cytogenomics of Pediatric T-Cell Acute Lymphoblastic Leukemia
|
Meredith, Matthew M.
|
|
2016
|
235-236 |
6 |
p. 292-
1 p.
|
artikel
|
| 137 |
The importance of codon context for understanding the Ig-like somatic hypermutation strand-biased patterns in TP53 mutations in breast cancer
|
Lindley, Robyn A.
|
|
2013
|
235-236 |
6 |
p. 222-226
5 p.
|
artikel
|
| 138 |
The lack of E318K MITF germline mutation in Latvian melanoma patients
|
Ozola, Aija
|
|
2015
|
235-236 |
6 |
p. 355-356
2 p.
|
artikel
|
| 139 |
The rate of recurrent BRCA1, BRCA2, and TP53 mutations in the general population, and unselected ovarian cancer cases, in Belo Horizonte, Brazil
|
Schayek, Hagit
|
|
2016
|
235-236 |
6 |
p. 283-284
2 p.
|
artikel
|
| 140 |
The Smallest Reported Distal 11q25 Deletion in Jacobsen Syndrome (JBS): Two Patients with Variable Phenotype
|
Zhang, Lei
|
|
2015
|
235-236 |
6 |
p. 360-
1 p.
|
artikel
|
| 141 |
Toward Standardized Reporting and Databasing of Polyploid Tumors
|
Hauenstein, Jennifer E.
|
|
2016
|
235-236 |
6 |
p. 289-
1 p.
|
artikel
|
| 142 |
Transcriptome Analysis (Rnaseq) Detects Gene Fusions and Point Mutations Associated with Ph-Like Acute Lymphoblastic Leukemia
|
Yap, Kai Lee
|
|
2015
|
235-236 |
6 |
p. 358-
1 p.
|
artikel
|
| 143 |
Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin
|
Xochelli, Aliki
|
|
2014
|
235-236 |
6 |
p. 281-283
3 p.
|
artikel
|
| 144 |
Trisomy 8 as the sole cytogenetic abnormality in an adult patient with acute lymphoblastic leukemia
|
Kourelis, Taxiarchis V.
|
|
2012
|
235-236 |
6 |
p. 337-338
2 p.
|
artikel
|
| 145 |
Tumor Culture for Chromosome Analysis: Children's Mercy Cytogenetics Laboratory 15-Year Database of Methods
|
Smith, Scott C.
|
|
2016
|
235-236 |
6 |
p. 294-
1 p.
|
artikel
|
| 146 |
Two DNA Tests Accurately Classify Gliomas into Five Molecular Groups with Prognostic and Predictive Significance
|
Yamada, Seiji
|
|
2016
|
235-236 |
6 |
p. 295-
1 p.
|
artikel
|
| 147 |
Unbalanced 11;18 translocation in an acute erythroid leukemia after radioactive iodine therapy
|
Trikalinos, Nikolaos A.
|
|
2013
|
235-236 |
6 |
p. 252-255
4 p.
|
artikel
|
| 148 |
Unusual ROS1 Translocation Pattern in a 61 Year-old Woman with Metastatic Adenocarcinoma of Lung
|
Chen, Hui
|
|
2015
|
235-236 |
6 |
p. 363-
1 p.
|
artikel
|
| 149 |
Use of a Next Generation Sequencing (NGS) Panel to Determine Related Donor Eligibility in a Case of Pediatric Myelodysplastic Syndrome (MDS)
|
Harb, Jason
|
|
2016
|
235-236 |
6 |
p. 288-289
2 p.
|
artikel
|
| 150 |
Utility of Genome-Wide Characterization of B-Cell Acute Lymphoblastic Leukemia Using SNP-Based Microarray
|
Monahan, Christine S.
|
|
2016
|
235-236 |
6 |
p. 292-
1 p.
|
artikel
|
| 151 |
Utility of Genomic Methylation Microarrays to Measure Spreading of X-Inactivation in Association with X;Autosome Translocations
|
McCready, Elizabeth
|
|
2016
|
235-236 |
6 |
p. 299-
1 p.
|
artikel
|
| 152 |
Utility of OncoScan Array Testing to Further Characterize Eleven Medulloblastoma Cases
|
Rustin, Jeannette G.
|
|
2016
|
235-236 |
6 |
p. 293-
1 p.
|
artikel
|
| 153 |
Utility of Whole Genome SNP Microarray and Targeted Somatic Mutations in Evaluation of Melanoma, Histologic Mimics of Melanoma, and Glioblastoma
|
Chaubey, Alka
|
|
2016
|
235-236 |
6 |
p. 286-
1 p.
|
artikel
|
| 154 |
Validation of Affymetrix Cytoscan HD: Children's Mercy Hospital Experience with Neoplastic Samples
|
Cooley, Linda D.
|
|
2014
|
235-236 |
6 |
p. 284-
1 p.
|
artikel
|
| 155 |
Validation of a Modified OncoScan Protocol for Use in a Clinical Laboratory
|
Paxton, Christian N.
|
|
2015
|
235-236 |
6 |
p. 361-
1 p.
|
artikel
|
| 156 |
Validation of a Multiplex Capillary Electrophoresis-Based Assay for Simultaneous Detection of the Common and Uncommon BCR-ABL1 Transcripts
|
Huang, Richard Sheng Poe
|
|
2016
|
235-236 |
6 |
p. 289-290
2 p.
|
artikel
|
| 157 |
What's Next in Cytogenetics: Molecular Characterization of De Novo Apparently Balanced Chromosomal Rearrangements to Assess Pathogenicity by Whole Genome Mate Pair Sequencing
|
Marcou, Cherisse A.
|
|
2016
|
235-236 |
6 |
p. 298-
1 p.
|
artikel
|
| 158 |
What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencing
|
Wilson, Melissa A.
|
|
2014
|
235-236 |
6 |
p. 272-275
4 p.
|
artikel
|
| 159 |
WHIM Syndrome Cured by Chromothripsis
|
Bryke, Christine R.
|
|
2015
|
235-236 |
6 |
p. 358-359
2 p.
|
artikel
|
| 160 |
Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinoma
|
Melo, Flavia M.
|
|
2016
|
235-236 |
6 |
p. 251-257
7 p.
|
artikel
|
| 161 |
Whole Exome Sequencing Elucidates Genomic Evolution of Extramedullary Acute Myeloid Leukemia (EM-AML) from Bone Marrow Acute Myeloid Leukemia (BM-AML)
|
Yap, Kai Lee
|
|
2016
|
235-236 |
6 |
p. 295-296
2 p.
|
artikel
|
| 162 |
Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules
|
Torres-Martín, Miguel
|
|
2015
|
235-236 |
6 |
p. 327-332
6 p.
|
artikel
|
| 163 |
Whole Genome Copy Number Analysis of Formalin Fixed Paraffin Embedded Samples Identifies Major Genomic Aberrations in Medulloblastoma
|
Robison, Nathan J.
|
|
2014
|
235-236 |
6 |
p. 290-
1 p.
|
artikel
|
| 164 |
Whole-Genome Mate-Pair Sequencing (MPseq) Improves Genomic Characterization of Patients with Hematologic Malignancies
|
Smoley, Stephanie A.
|
|
2016
|
235-236 |
6 |
p. 294-295
2 p.
|
artikel
|
| 165 |
Whole Genome SNP Array Improves Diagnosis and Therapy in Pediatric Brain Tumors
|
Shao, Lina
|
|
2016
|
235-236 |
6 |
p. 294-
1 p.
|
artikel
|
| 166 |
Y Chromosome Microdeletion Detection by Cytoscan HD Microarray Platform
|
Sederberg, Maria C.
|
|
2015
|
235-236 |
6 |
p. 359-
1 p.
|
artikel
|
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