A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease

Copy Number ◽

Copy Number Variations ◽

Comparative Genomic ◽

Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH)

Research in Autism Spectrum Disorders ◽

10.1016/j.rasd.2015.12.012 ◽

2016 ◽

Vol 23 ◽

pp. 145-151 ◽

Cited By ~ 4

Author(s):

Eloisa S. Moreira ◽

Isabela M.W. Silva ◽

Naila Lourenço ◽

Danielle P. Moreira ◽

Cintia M. Ribeiro ◽

...

Keyword(s):

Autism Spectrum Disorder ◽

Copy Number ◽

Autism Spectrum ◽

Copy Number Variations ◽

Spectrum Disorder ◽

Comparative Genomic ◽

A Bayesian Analysis of Copy Number Variations in Array Comparative Genomic Hybridization Data

International Journal of Biomedical Data Mining ◽

10.4172/2090-4924.1000116 ◽

2015 ◽

Vol 04 (01) ◽

Author(s):

Xiaowei Wu ◽

Hongxiao Zhu

Keyword(s):

Bayesian Analysis ◽

Copy Number ◽

Copy Number Variations ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Comparative Genomic Hybridization Data ◽

Hybridization Data

Incidental Detection of Cancer Predisposition Gene Copy Number Variations by Array Comparative Genomic Hybridization

The Journal of Pediatrics ◽

10.1016/j.jpeds.2014.07.042 ◽

2014 ◽

Vol 165 (5) ◽

pp. 1057-1059.e4 ◽

Cited By ~ 5

Author(s):

J. Austin Hamm ◽

Fady M. Mikhail ◽

Dana Hollenbeck ◽

Meagan Farmer ◽

Nathaniel H. Robin

Keyword(s):

Copy Number ◽

Gene Copy Number ◽

Copy Number Variations ◽

Cancer Predisposition ◽

Gene Copy ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Cancer Predisposition Gene

Reply: Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

Human Reproduction ◽

10.1093/humrep/deq285 ◽

2010 ◽

Vol 25 (12) ◽

pp. 3160-3161

Author(s):

C. R. Quilter ◽

A. C. Karcanias ◽

M. R. Bagga ◽

S. Duncan ◽

A. Murray ◽

...

Keyword(s):

X Chromosome ◽

Premature Ovarian Failure ◽

Copy Number ◽

Copy Number Variations ◽

Ovarian Failure ◽

Comparative Genomic ◽

Targeted array comparative genomic hybridization – A new diagnostic tool for the detection of large copy number variations in nemaline myopathy-causing genes

Neuromuscular Disorders ◽

10.1016/j.nmd.2012.07.007 ◽

2013 ◽

Vol 23 (1) ◽

pp. 56-65 ◽

Cited By ~ 24

Author(s):

K. Kiiski ◽

L. Laari ◽

V.-L. Lehtokari ◽

M. Lunkka-Hytönen ◽

C. Angelini ◽

...

Keyword(s):

Diagnostic Tool ◽

Copy Number ◽

Nemaline Myopathy ◽

Copy Number Variations ◽

Comparative Genomic ◽

Detection of Copy Number Variations from Array Comparative Genomic Hybridization Data Using Linear-chain Conditional Random Field Models

Probabilistic Graphical Models for Genetics, Genomics, and Postgenomics ◽

10.1093/acprof:oso/9780198709022.003.0016 ◽

2014 ◽

pp. 409-428

Author(s):

Xiaolin Yin ◽

Jing Li

Keyword(s):

Random Field ◽

Copy Number ◽

Conditional Random Field ◽

Linear Chain ◽

Copy Number Variations ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Hybridization Data

Array Comparative Genomic Hybridization Profiling Analysis Reveals Deoxyribonucleic Acid Copy Number Variations Associated with Premature Ovarian Failure

The Journal of Clinical Endocrinology & Metabolism ◽

10.1210/jc.2009-0186 ◽

2009 ◽

Vol 94 (11) ◽

pp. 4540-4546 ◽

Cited By ~ 52

Author(s):

Azzedine Aboura ◽

Claire Dupas ◽

Gérard Tachdjian ◽

Marie-France Portnoï ◽

Nathalie Bourcigaux ◽

...

Keyword(s):

Premature Ovarian Failure ◽

Copy Number ◽

Deoxyribonucleic Acid ◽

Copy Number Variations ◽

Ovarian Failure ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Profiling Analysis

O15: Identification of large-scale human-specific copy number variations by array comparative genomic hybridization

European Journal of Medical Genetics ◽

10.1016/j.ejmg.2005.10.051 ◽

2005 ◽

Vol 48 (4) ◽

pp. 478-479

Author(s):

Violaine Goidts ◽

Lluis Armengol ◽

Werner Schempp ◽

Jeffrey Conroy ◽

Stefan Müller ◽

...

Keyword(s):

Copy Number ◽

Large Scale ◽

Copy Number Variations ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Human Specific

Widespread, focal copy number variations (CNV) and whole chromosome aneuploidies in Trypanosoma cruzi strains revealed by array comparative genomic hybridization

BMC Genomics ◽

10.1186/1471-2164-12-139 ◽

2011 ◽

Vol 12 (1) ◽

Cited By ~ 62

Author(s):

Todd A Minning ◽

D Brent Weatherly ◽

Stephane Flibotte ◽

Rick L Tarleton

Keyword(s):

Trypanosoma Cruzi ◽

Copy Number ◽

Copy Number Variations ◽

Comparative Genomic ◽

Genome-wide analysis of copy number variations in Chinese sheep using array comparative genomic hybridization

Small Ruminant Research ◽

10.1016/j.smallrumres.2015.04.014 ◽

2015 ◽

Vol 128 ◽

pp. 19-26 ◽

Cited By ~ 5

Author(s):

Cheng-Lin Hou ◽

Fan-Hua Meng ◽

Wei Wang ◽

Shen-Yuan Wang ◽

Yan-Ping Xing ◽

...

Keyword(s):

Copy Number ◽

Copy Number Variations ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Genome Wide Analysis ◽

Genome Wide