Genotype to phenotype—discovery and characterization of novel genomic disorders in a “genotype-first” era
出版年份 2009 全文链接
标题
Genotype to phenotype—discovery and characterization of novel genomic disorders in a “genotype-first” era
作者
关键词
-
出版物
GENETICS IN MEDICINE
Volume 11, Issue 12, Pages 836-842
出版商
Springer Nature
发表日期
2009-12-09
DOI
10.1097/gim.0b013e3181c175d2
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
- (2009) Andy Itsara et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Duplication hotspots, rare genomic disorders, and common disease
- (2009) Heather C Mefford et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- CNV and nervous system diseases – what’s new?
- (2009) W. Gu et al. CYTOGENETIC AND GENOME RESEARCH
- Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
- (2009) E.K. Bijlsma et al. European Journal of Medical Genetics
- Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects
- (2009) Gurdeep S Sagoo et al. GENETICS IN MEDICINE
- A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease
- (2009) H. C. Mefford et al. GENOME RESEARCH
- Characterization of six human disease-associated inversion polymorphisms
- (2009) Francesca Antonacci et al. HUMAN MOLECULAR GENETICS
- Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
- (2009) L. M. Dibbens et al. HUMAN MOLECULAR GENETICS
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
- (2009) B W M van Bon et al. JOURNAL OF MEDICAL GENETICS
- Targeted capture and massively parallel sequencing of 12 human exomes
- (2009) Sarah B. Ng et al. NATURE
- Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis
- (2009) Rafael de Cid et al. NATURE GENETICS
- 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
- (2009) Ingo Helbig et al. NATURE GENETICS
- De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
- (2009) Steven C Greenway et al. NATURE GENETICS
- Massively parallel exon capture and library-free resequencing across 16 genomes
- (2009) Emily H Turner et al. NATURE METHODS
- Association and Mutation Analyses of 16p11.2 Autism Candidate Genes
- (2009) Ravinesh A. Kumar et al. PLoS One
- Genomic disorders ten years on
- (2009) James R Lupski Genome Medicine
- A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia
- (2009) Anna C. Need et al. PLoS Genetics
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization
- (2008) Sarah A. Shoichet et al. Amyotrophic Lateral Sclerosis
- Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
- (2008) Susan L. Christian et al. BIOLOGICAL PSYCHIATRY
- Genetics of intellectual disability
- (2008) H Hilger Ropers CURRENT OPINION IN GENETICS & DEVELOPMENT
- A 15q13.3 microdeletion segregating with autism
- (2008) Alistair T Pagnamenta et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Private inherited microdeletion/microduplications: Implications in clinical practice
- (2008) Maria Antonietta Mencarelli et al. European Journal of Medical Genetics
- Novel microdeletion syndromes detected by chromosome microarrays
- (2008) Anne M. Slavotinek HUMAN GENETICS
- Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
- (2008) D T Miller et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
- (2008) F D Hannes et al. JOURNAL OF MEDICAL GENETICS
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Mapping and sequencing of structural variation from eight human genomes
- (2008) Jeffrey M. Kidd et al. NATURE
- Next-generation DNA sequencing
- (2008) Jay Shendure et al. NATURE BIOTECHNOLOGY
- Evolutionary toggling of the MAPT 17q21.31 inversion region
- (2008) Michael C Zody et al. NATURE GENETICS
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
- (2008) Andrew J Sharp et al. NATURE GENETICS
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- NDE1 and NDEL1: Multimerisation, alternate splicing and DISC1 interaction
- (2008) Nicholas J. Bradshaw et al. NEUROSCIENCE LETTERS
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease
- (2008) Ashleigh A Richards et al. PEDIATRIC RESEARCH
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
- (2008) T. Walsh et al. SCIENCE
- Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array
- (2007) Teresita Díaz de Ståhl et al. HUMAN MUTATION
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now