| 37881831 | NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. | Alzheimers Dement | 2024 |
| 37162864 | hipFG: High-throughput harmonization and integration pipeline for functional genomics data. | | 2023 |
| 37947320 | hipFG: high-throughput harmonization and integration pipeline for functional genomics data. | | 2023 |
| 37461624 | Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. | medRxiv | 2023 |
| 35068457 | Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease. | Journal of Alzheimer's Disease | 2022 |
| 35379992 | New insights into the genetic etiology of Alzheimer's disease and related dementias. | Nat Genet | 2022 |
| 35047815 | FILER: a framework for harmonizing and querying large-scale functional genomics knowledge. | NAR Genomics and Bioinformatics | 2022 |
| 34873149 | Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci. | Transl Psychiatry | 2021 |
| 34804120 | Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project. | Frontiers in Genetics | 2021 |
| 32270138 | HIPPIE2: a method for fine-scale identification of physically interacting chromatin regions. | NAR Genomics and Bioinformatics | 2020 |
| 32330239 | SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants. | | 2020 |
| 30668832 | DASHR 2.0: integrated database of human small non-coding RNA genes and mature products. | | 2019 |
| 30351394 | VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project. | | 2019 |
| 30820047 | Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. | Nat Genet | 2019 |
| 29733404 | SPAR: small RNA-seq portal for analysis of sequencing experiments. | Nucleic Acids Research | 2018 |
| 30113658 | INFERNO: inferring the molecular mechanisms of noncoding genetic variants. | Nucleic Acids Research | 2018 |
| 28714976 | Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. | Nat Genet | 2017 |
| 26553799 | DASHR: database of small human noncoding RNAs. | Nucleic Acids Res | 2016 |
| 25778476 | A novel Alzheimer disease locus located near the gene encoding tau protein. | Mol Psychiatry | 2016 |
| 26092349 | Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. | Alzheimers Dement | 2016 |
| 26366463 | Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. | JAMA Neurol | 2015 |
| 25531812 | Rarity of the Alzheimer disease-protective APP A673T variant in the United States. | JAMA Neurol | 2015 |
| 25480377 | HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements. | | 2015 |
| 25470345 | Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology. | J Neuropathol Exp Neurol | 2015 |
| 25936935 | The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. | Alzheimers Dement | 2015 |
| 24922517 | Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. | PLoS One | 2014 |
| 25363760 | Synaptic, transcriptional and chromatin genes disrupted in autism. | Nature | 2014 |
| 24770881 | ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. | Acta Neuropathol | 2014 |
| 25199842 | Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. | JAMA Neurol | 2014 |
| 23571587 | Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. | JAMA | 2013 |
| 24162737 | Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. | Nat Genet | 2013 |
| 23943636 | DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experiments. | | 2013 |
| 24149843 | HAMR: high-throughput annotation of modified ribonucleotides. | RNA | 2013 |
| 23352160 | Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. | Neuron | 2013 |
| 22492627 | SAVoR: a server for sequencing annotation and visualization of RNA structures. | Nucleic Acids Research | 2012 |
| 22495311 | Patterns and rates of exonic de novo mutations in autism spectrum disorders. | Nature | 2012 |
| 22832108 | Global analysis of RNA secondary structure in two metazoans. | Cell Rep | 2012 |
| 20941385 | Genome-wide double-stranded RNA sequencing reveals the functional significance of base-paired RNAs in Arabidopsis. | PLoS Genetics | 2010 |
| 20041592 | Sleep behaviors and sleep quality in children with autism spectrum disorders. | Sleep | 2009 |
| 18028544 | Genome-wide expression profiling and bioinformatics analysis of diurnally regulated genes in the mouse prefrontal cortex. | Genome Biol | 2007 |
| 17096848 | Patterns of sequence conservation in presynaptic neural genes. | Genome Biol | 2006 |
| 12874602 | alpha 1d Adrenoceptor signaling is required for stimulus induced locomotor activity. | Molecular Psychiatry | 2003 |
| 12244319 | Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse. | Nat Genet | 2002 |
| 11389854 | A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle. | Molecular Cell | 2001 |
| 11145318 | An automated system for recording and analysis of sleep in mice. | Sleep | 2000 |