标题
Rare variants inTMEM132Din a case-control sample for panic disorder
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Volume 159B, Issue 8, Pages 896-907
出版商
Wiley
发表日期
2012-08-22
DOI
10.1002/ajmg.b.32096
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。- Replication and meta-analysis of TMEM132D gene variants in panic disorder
- (2012) A Erhardt et al. Translational Psychiatry
- vipR: variant identification in pooled DNA using R
- (2011) A. Altmann et al. BIOINFORMATICS
- SHRiMP2: Sensitive yet Practical Short Read Mapping
- (2011) Matei David et al. BIOINFORMATICS
- Mapping Rare and Common Causal Alleles for Complex Human Diseases
- (2011) Soumya Raychaudhuri CELL
- dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions
- (2011) Xiaoming Liu et al. HUMAN MUTATION
- Genome-Wide Association Study of the Child Behavior Checklist Dysregulation Profile
- (2011) Eric Mick et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
- (2011) Gosia Trynka et al. NATURE GENETICS
- TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
- (2011) Erica E Davis et al. NATURE GENETICS
- Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
- (2011) Manuel A Rivas et al. NATURE GENETICS
- The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression
- (2011) Martin A. Kohli et al. NEURON
- Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder
- (2011) René A. W. Frank et al. PLoS One
- Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population
- (2011) Lotte N. Moens et al. PLoS One
- Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer
- (2010) Jun Mitsui et al. JOURNAL OF HUMAN GENETICS
- TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
- (2010) A Erhardt et al. MOLECULAR PSYCHIATRY
- Understanding mechanisms underlying human gene expression variation with RNA sequencing
- (2010) Joseph K. Pickrell et al. NATURE
- Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
- (2010) Christopher T Johansen et al. NATURE GENETICS
- High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
- (2010) Sarah E Calvo et al. NATURE GENETICS
- Statistical analysis strategies for association studies involving rare variants
- (2010) Vikas Bansal et al. NATURE REVIEWS GENETICS
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- Missing heritability and strategies for finding the underlying causes of complex disease
- (2010) Evan E. Eichler et al. NATURE REVIEWS GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Reduced Expression of IFIH1 Is Protective for Type 1 Diabetes
- (2010) Kate Downes et al. PLoS One
- Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies
- (2010) A. Eyre-Walker PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Rare Variants Create Synthetic Genome-Wide Associations
- (2010) Samuel P. Dickson et al. PLOS BIOLOGY
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Common vs. rare allele hypotheses for complex diseases
- (2009) Nicholas J Schork et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Deep sequencing to reveal new variants in pooled DNA samples
- (2009) Astrid A. Out et al. HUMAN MUTATION
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Human genetic variation and its contribution to complex traits
- (2009) Kelly A. Frazer et al. NATURE REVIEWS GENETICS
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
- (2009) S. Nejentsev et al. SCIENCE
- Genome-wide association studies: potential next steps on a genetic journey
- (2008) M. I. McCarthy et al. HUMAN MOLECULAR GENETICS
- Personal genomes: The case of the missing heritability
- (2008) Brendan Maher NATURE
- Common and rare variants in multifactorial susceptibility to common diseases
- (2008) Walter Bodmer et al. NATURE GENETICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started