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Chromosomal aberrations

Chromosome Inversions, Genomic Differentiation and Speciation in the African Malaria Mosquito Anopheles gambiae

Yoosook Lee, Travis C. Collier, [ ... ], Gregory C. Lanzaro

Classify Hyperdiploidy Status of Multiple Myeloma Patients Using Gene Expression Profiles

Yingxiang Li, Xujun Wang, [ ... ], Cheng Li

Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity

Robin G. Walters, Lachlan J. M. Coin, [ ... ], Alexandra I. F. Blakemore

The Properties of Genome Conformation and Spatial Gene Interaction and Regulation Networks of Normal and Malignant Human Cell Types

Zheng Wang, Renzhi Cao, [ ... ], Jianlin Cheng

A Novel and Major Quantitative Trait Locus for Fusarium Crown Rot Resistance in a Genotype of Wild Barley (Hordeum spontaneum L.)

Guangdeng Chen, Yaxi Liu, [ ... ], Chunji Liu

Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring

Valeria Capra, Samantha Mascelli, [ ... ], Elisa Tassano

Genomic EWS-FLI1 Fusion Sequences in Ewing Sarcoma Resemble Breakpoint Characteristics of Immature Lymphoid Malignancies

Manfred Berger, Uta Dirksen, [ ... ], Markus Metzler

Genetic Instability and Intratumoral Heterogeneity in Neuroblastoma with MYCN Amplification Plus 11q Deletion

Eva Villamón, Ana P. Berbegall, [ ... ], Rosa Noguera

Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

Nori Matsunami, Dexter Hadley, [ ... ], Hakon Hakonarson

A Pilot Study on Collective Effects of 22q13.31 Deletions on Gray Matter Concentration in Schizophrenia

Jingyu Liu, Alvaro Ulloa, [ ... ], Vince D. Calhoun

A Model-Based Clustering Method for Genomic Structural Variant Prediction and Genotyping Using Paired-End Sequencing Data

Matthew Hayes, Yoon Soo Pyon, Jing Li

Duplication of C7orf58, WNT16 and FAM3C in an Obese Female with a t(7;22)(q32.1;q11.2) Chromosomal Translocation and Clinical Features Resembling Coffin-Siris Syndrome

Jun Zhu, Jun Qiu, [ ... ], Farid F. Chehab

Deletion of Chromosomes 13q and 14q Is a Common Feature of Tumors with BRCA2 Mutations

Audrey Rouault, Guillaume Banneau, [ ... ], Michel Longy

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