Genome-Wide Copy Number Variation in Sporadic Amyotrophic Lateral Sclerosis in the Turkish Population: Deletion of EPHA3 Is a Possible Protective Factor

The genetic variability and commonality of neurodevelopmental disease

(2012) Bradley P. Coe et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

(2012) Philippe Corcia et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Analysis of molecular cytogenetic alterations in uterine leiomyosarcoma by array-based comparative genomic hybridization

(2012) Mohammad Raish et al.   JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

(2012) Annelies Van Hoecke et al.   NATURE MEDICINE

SMN1 gene duplications are associated with sporadic ALS

(2012) H. M. Blauw et al.   NEUROLOGY

ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population

(2012) Suna Lahut et al.   PLoS One

Frequent loss of HLA alleles associated with copy number-neutral 6pLOH in acquired aplastic anemia

(2011) T. Katagiri et al.   BLOOD

Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma

(2011) S. Miller et al.   NEURO-ONCOLOGY

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

(2010) Alessandra Ferlini et al.   BMC Medical Genetics

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

(2010) Hylke M. Blauw et al.   HUMAN MOLECULAR GENETICS

Genomic copy number variations in three Southeast Asian populations

(2010) Chee-Seng Ku et al.   HUMAN MUTATION

Integrating common and rare genetic variation in diverse human populations

(2010)   NATURE

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

(2009) T. H. Shaikh et al.   GENOME RESEARCH

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

(2009) Michael A van Es et al.   NATURE GENETICS

The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci

(2009) Louise V. Wain et al.   PLoS One

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

(2009) J. E. Landers et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians

(2009) Hajime Matsuzaki et al.   GENOME BIOLOGY

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations

(2008) S. Cronin et al.   HUMAN MOLECULAR GENETICS

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

(2008) Hylke M Blauw et al.   LANCET NEUROLOGY