Related references
Note: Only part of the references are listed.Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
John A. Todd et al.
NATURE GENETICS (2007)
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
Miles Parkes et al.
NATURE GENETICS (2007)
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
David J. Hunter et al.
NATURE GENETICS (2007)
A common allele on chromosome 9 associated with coronary heart disease
Ruth McPherson et al.
SCIENCE (2007)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation
Pawel Stankiewicz et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2007)
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
Laura J. Scott et al.
SCIENCE (2007)
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
Richa Saxena et al.
SCIENCE (2007)
Variation in FTO contributes to childhood obesity and severe adult obesity
Christian Dina et al.
NATURE GENETICS (2007)
High-resolution profiling of histone methylations in the human genome
Artern Barski et al.
CELL (2007)
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Timothy M. Frayling et al.
SCIENCE (2007)
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
Meredith Yeager et al.
NATURE GENETICS (2007)
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
Julius Gudmundsson et al.
NATURE GENETICS (2007)
Strong association of de novo copy number mutations with autism
Jonathan Sebat et al.
SCIENCE (2007)
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4
Cecile Libioulle et al.
PLOS GENETICS (2007)
Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases
Xinyan Lu et al.
PLOS ONE (2007)
A genome-wide association study identifies novel risk loci for type 2 diabetes
Robert Sladek et al.
NATURE (2007)
Microarray genetic screening: a prenatal roadblock for life?
Evelyne Shuster
LANCET (2007)
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
Jochen Hampe et al.
NATURE GENETICS (2007)
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Eleftheria Zeggini et al.
SCIENCE (2007)
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
Daisuke Komura et al.
GENOME RESEARCH (2006)
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
Richard H. Duerr et al.
SCIENCE (2006)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration
Zhenglin Yang et al.
SCIENCE (2006)
HTRA1 promoter polymorphism in wet age-related macular degeneration
Andrew DeWan et al.
SCIENCE (2006)
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
M-L Jacquemont et al.
JOURNAL OF MEDICAL GENETICS (2006)
Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: A new approach for newborn screening follow-up
Phyllis Gardner et al.
PEDIATRICS (2006)
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping
Daniel A. Peiffer et al.
GENOME RESEARCH (2006)
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
Andrew J. Sharp et al.
NATURE GENETICS (2006)
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome
Devin P. Locke et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Highly parallel genomic assays
Jian-Bing Fan et al.
NATURE REVIEWS GENETICS (2006)
Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing
Roman K. Thomas et al.
NATURE MEDICINE (2006)
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive-clinical cases
Usa G. Shaffer et al.
JOURNAL OF PEDIATRICS (2006)
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region
Deborah J. Smyth et al.
NATURE GENETICS (2006)
A common genetic variant is associated with adult and childhood obesity
A Herbert et al.
SCIENCE (2006)
Comparative genomic hybridization and prenatal diagnosis
Ignatia B. Van den Veyver et al.
CURRENT OPINION IN OBSTETRICS & GYNECOLOGY (2006)
Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis
S Yzer et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Pyrosequencing: History, biochemistry and future
A Ahmadian et al.
CLINICA CHIMICA ACTA (2006)
BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)
B Ylstra et al.
NUCLEIC ACIDS RESEARCH (2006)
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
JAS Vorstman et al.
MOLECULAR PSYCHIATRY (2006)
Emerging technologies in DNA sequencing
ML Metzker
GENOME RESEARCH (2005)
Genomic disorders: Molecular mechanisms for rearrangements and conveyed phenotypes
JR Lupski et al.
PLOS GENETICS (2005)
Segmental duplications and copy-number variation in the human genome
AJ Sharp et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Genome-wide association studies for common diseases and complex traits
JN Hirschhorn et al.
NATURE REVIEWS GENETICS (2005)
Highly multiplexed molecular inversion probe genotyping: Over 10,000 targeted SNPs genotyped in a single tube assay
P Hardenbol et al.
GENOME RESEARCH (2005)
Large-scale genotyping of complex DNA
GC Kennedy et al.
NATURE BIOTECHNOLOGY (2003)
Multiplexed genotyping with sequence-tagged molecular inversion probes
P Hardenbol et al.
NATURE BIOTECHNOLOGY (2003)
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene
K Jaakson et al.
HUMAN MUTATION (2003)
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
JD Rioux et al.
NATURE GENETICS (2001)
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
JP Hugot et al.
NATURE (2001)