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Anna C. Need

Department of Brain Sciences
H指数:54
被引数:1.5万

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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
2022-02-1728
OAAI
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis
2021-12-0117
OAAI
Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics

通过大规模认知gis和转录组学识别促智药物靶标

2021-05-2513
OAAI
A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage
2021-04-2687
OAAI
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

VWA1的祖先10 bp重复扩增导致隐性遗传性运动神经病

BRAIN
IF11.7
2021-01-1827
OAAI
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways

认知,教育和精神分裂症的多效性荟萃分析区分早期神经发育和成人突触通路的作用

2019-08-0169
OAAI
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (vol 9, 2098, 2018)

对300,486个体的研究确定了影响一般认知功能的148独立遗传位点 (第9卷,2098,2018)

2019-05-0110
OAAI
A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative
2019-01-0162
OAAI
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

269,867个体的全基因组关联荟萃分析确定了与智力的新遗传和功能联系

2018-06-25739
OAAI
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder
2018-05-0256
OAAI
Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

大规模认知ghis荟萃分析揭示了组织特异性神经表达和潜在的促智药物靶点

2017-11-0185
OAAI
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium (vol 22, pg 336, 2017)
2017-09-1224
OAAI
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium
2017-01-17166
OAAI
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
2017-01-0113
OAAI