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。Increased BDNF Promoter Methylation in the Wernicke Area of Suicide Subjects
Simona Keller et al.
ARCHIVES OF GENERAL PSYCHIATRY (2010)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Brain Derived Neurotrophic Factor (BDNF) Genetic Polymorphism (Val66Met) in Suicide: A Study of 512 Cases
F. Zarrilli et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
An international comparability study on quantification of total methyl cytosine content
Inchul Yang et al.
ANALYTICAL BIOCHEMISTRY (2009)
Copy Number Variation in Human Health, Disease, and Evolution
Feng Zhang et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)
Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
Audrey Guilmatre et al.
ARCHIVES OF GENERAL PSYCHIATRY (2009)
Microarray-Based Genomic DNA Profiling Technologies in Clinical Molecular Diagnostics
Yiping Shen et al.
CLINICAL CHEMISTRY (2009)
Three Novel CFTR Polymorphic Repeats Improve Segregation Analysis for Cystic Fibrosis
Ausilia Elce et al.
CLINICAL CHEMISTRY (2009)
Copy number variants, diseases and gene expression
Charlotte N. Henrichsen et al.
HUMAN MOLECULAR GENETICS (2009)
Genetic Modifiers of Liver Disease in Cystic Fibrosis
Jaclyn R. Bartlett et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2009)
Genomic imprinting disorders in humans: a mini-review
Merlin G. Butler
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2009)
Mapping and sequencing of structural variation from eight human genomes (Reprinted from Nature, vol 453, pg 56-64, 2008)
Jeffrey M. Kidd et al.
NATURE GENETICS (2009)
Copy number variation at 1q21.1 associated with neuroblastoma
Sharon J. Diskin et al.
NATURE (2009)
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
Marwan Shinawi et al.
NATURE GENETICS (2009)
Causes and consequences of microRNA dysregulation in cancer
Carlo M. Croce
NATURE REVIEWS GENETICS (2009)
Structural Chromosomal Variations in Neurological Diseases
Bernadette Kalman et al.
NEUROLOGIST (2009)
Genome-wide high throughput analysis of DNA methylation in eukaryotes
Kyle R. Pomraning et al.
METHODS (2009)
Common variants in polygenic schizophrenia
Joseph T. Glessner et al.
GENOME BIOLOGY (2009)
A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions
A. Cecile J. W. Janssens et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy
V. Sanna et al.
HAEMOPHILIA (2008)
Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies
Arthur S. Lee et al.
HUMAN MOLECULAR GENETICS (2008)
The impact of microRNAs on protein output
Daehyun Baek et al.
NATURE (2008)
Widespread changes in protein synthesis induced by microRNAs
Matthias Selbach et al.
NATURE (2008)
A skin microRNA promotes differentiation by repressing 'stemness'
Rui Yi et al.
NATURE (2008)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson et al.
NATURE (2008)
Genotype, haplotype and copy-number variation in worldwide human populations
Mattias Jakobsson et al.
NATURE (2008)
LNA-mediated microRNA silencing in non-human primates
Joacim Elmen et al.
NATURE (2008)
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease
Sheila A. Fisher et al.
NATURE GENETICS (2008)
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy et al.
NATURE REVIEWS GENETICS (2008)
Loss of microRNA cluster miR-29a/b-1 in sporadic Alzheimer's disease correlates with increased BACE1/β-secretase expression
Sebastien S. Hebert et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Circulating microRNAs as stable blood-based markers for cancer detection
Patrick S. Mitchell et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Mapping and sequencing of structural variation from eight human genomes
Jeffrey M. Kidd et al.
NATURE (2008)
A microRNA feedback circuit in midbrain dopamine neurons
Jongpil Kim et al.
SCIENCE (2007)
Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability
Jacques S. Beckmann et al.
NATURE REVIEWS GENETICS (2007)
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
Simon N. Stacey et al.
NATURE GENETICS (2007)
Challenges and standards in integrating surveys of structural variation
Stephen W. Scherer 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)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton et al.
NATURE (2007)
A common allele on chromosome 9 associated with coronary heart disease
Ruth McPherson et al.
SCIENCE (2007)
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
Julius Gudmundsson et al.
NATURE GENETICS (2007)
Haemophilia A: molecular insights
Giuseppe Castaldo et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2007)
Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy
Gerd Meyer zu Horste et al.
ANNALS OF NEUROLOGY (2007)
Genome-wide association studies provide new insights into type 2 diabetes aetiology
Timothy M. Frayling
NATURE REVIEWS GENETICS (2007)
Accurate and reliable high-throughput detection of copy number variation in the human genome
Heike Fiegler 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)
Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder
Hamid Mostafavi Abdolmaleky et al.
HUMAN MOLECULAR GENETICS (2006)
Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation
Raman P. Nagarajan et al.
EPIGENETICS (2006)
A brain-specific microRNA regulates dendritic spine development
GM Schratt et al.
NATURE (2006)
Copy number variants and pharmacogenomics
K Ouahchi et al.
PHARMACOGENOMICS (2006)
Silencing of microRNAs in vivo with 'antagomirs'
J Krützfeldt et al.
NATURE (2005)
Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis
Y Zhao et al.
NATURE (2005)
Stem cell division is regulated by the microRNA pathway
SD Hatfield et al.
NATURE (2005)
Distribution of human β-defensin polymorphisms in various control and cystic fibrosis populations
A Vankeerberghen et al.
GENOMICS (2005)
Frequency of new copy number variation in humans
GJB van Ommen
NATURE GENETICS (2005)
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
E Gonzalez et al.
SCIENCE (2005)
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
C Tufarelli et al.
NATURE GENETICS (2003)
The power and the promise of DNA methylation markers
PW Laird
NATURE REVIEWS CANCER (2003)
Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A)
MW Sereda et al.
NATURE MEDICINE (2003)
Haemophilia B: From molecular diagnosis to gene therapy
G Castaldo et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2003)
Finding genes that underlie complex traits
AM Glazier et al.
SCIENCE (2002)
Recent segmental duplications in the human genome
JA Bailey et al.
SCIENCE (2002)
Genotype-phenotype correlation in cystic fibrosis: The role of modifier genes
F Salvatore et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans
BJ Reinhart et al.
NATURE (2000)
Aberrant CpG-island methylation has non-random and tumour-type-specific patterns
JF Costello et al.
NATURE GENETICS (2000)
分享论文
