Published in Neurogenetics on December 24, 2013
Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics (2009) 190.94
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res (2010) 97.51
dbSNP: the NCBI database of genetic variation. Nucleic Acids Res (2001) 76.97
A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet (2011) 59.36
Histone H3K27ac separates active from poised enhancers and predicts developmental state. Proc Natl Acad Sci U S A (2010) 15.13
A vertebrate globin expressed in the brain. Nature (2000) 5.34
Neuroglobin is up-regulated by and protects neurons from hypoxic-ischemic injury. Proc Natl Acad Sci U S A (2001) 3.12
ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative. Neurology (1997) 3.04
A systems level analysis of transcriptional changes in Alzheimer's disease and normal aging. J Neurosci (2008) 2.97
Cytoglobin: a novel globin type ubiquitously expressed in vertebrate tissues. Mol Biol Evol (2002) 2.53
Neuroglobin protects the brain from experimental stroke in vivo. Proc Natl Acad Sci U S A (2003) 2.42
Neuroglobin-overexpressing transgenic mice are resistant to cerebral and myocardial ischemia. Proc Natl Acad Sci U S A (2006) 2.05
Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs. Forensic Sci Int Genet (2007) 2.03
How does the eye breathe? Evidence for neuroglobin-mediated oxygen supply in the mammalian retina. J Biol Chem (2002) 1.85
Human neuroglobin, a hexacoordinate hemoglobin that reversibly binds oxygen. J Biol Chem (2001) 1.75
Neuroglobin protects nerve cells from apoptosis by inhibiting the intrinsic pathway of cell death. Apoptosis (2010) 1.33
Validation of endogenous controls for quantitative gene expression analysis: application on brain cortices of human chronic alcoholics. Brain Res (2006) 1.29
A globin in the nucleus! J Biol Chem (2003) 1.23
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells. Hum Mol Genet (1995) 1.23
Evidence for parent of origin effect in late-onset Alzheimer disease. Am J Med Genet (2002) 1.20
Neuroglobin protects PC12 cells against oxidative stress. Brain Res (2007) 1.18
Reference genes identified in SH-SY5Y cells using custom-made gene arrays with validation by quantitative polymerase chain reaction. Anal Biochem (2004) 1.15
Molecular cloning of seal myoglobin mRNA. Nucleic Acids Res (1982) 1.14
Neuroglobin expression in ischemic stroke. Stroke (2010) 1.09
Neuroglobin protects PC12 cells against beta-amyloid-induced cell injury. Neurobiol Aging (2007) 1.08
Hypoxia/ischemia and the regulation of neuroglobin and cytoglobin expression. IUBMB Life (2005) 1.07
Multiple protective activities of neuroglobin in cultured neuronal cells exposed to hypoxia re-oxygenation injury. J Neurochem (2009) 1.06
Neuroglobin mRNA expression after transient global brain ischemia and prolonged hypoxia in cell culture. Brain Res (2006) 1.01
Neuroglobin overexpression in cultured human neuronal cells protects against hydrogen peroxide insult via activating phosphoinositide-3 kinase and opening the mitochondrial K(ATP) channel. Antioxid Redox Signal (2010) 0.98
Gene expression reveals overlap between normal aging and Alzheimer's disease genes. Neurobiol Aging (2010) 0.97
Effects of short-term hypoxia on neuroglobin levels and localization in mouse brain tissues. Neuropathol Appl Neurobiol (2005) 0.96
A role for human neuroglobin in apoptosis. IUBMB Life (2010) 0.95
Regulation of myoglobin expression. J Exp Biol (2010) 0.95
Alzheimer's risk variants in the clusterin gene are associated with alternative splicing. Transl Psychiatry (2011) 0.94
Neuroglobin genetic polymorphisms and their relationship to functional outcomes after traumatic brain injury. J Neurotrauma (2010) 0.93
Neuroglobin and Alzheimer's dementia: genetic association and gene expression changes. Neurobiol Aging (2008) 0.91
Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms. Am J Med Genet B Neuropsychiatr Genet (2005) 0.89
Effect of aging on neuroglobin expression in rodent brain. Neurobiol Aging (2005) 0.89
Association between Ngb polymorphisms and ischemic stroke in the Southern Chinese Han population. BMC Med Genet (2008) 0.88
Functional and sequence analysis of human neuroglobin gene promoter region. Biochim Biophys Acta (2011) 0.86
Antihypoxic effects of neuroglobin in hypoxia-preconditioned mice and SH-SY5Y cells. Neurosignals (2009) 0.83
Neuroglobin protein is upregulated in Alzheimer's disease. J Alzheimers Dis (2013) 0.80
Crystalline human myoglobin from heart-muscle and urine. Arch Biochem (1947) 0.77
Population-based norms for the Mini-Mental State Examination by age and educational level. JAMA (1993) 12.83
Alpha-2 macroglobulin is genetically associated with Alzheimer disease. Nat Genet (1998) 7.26
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat Genet (1996) 3.13
Long-term treatment of girls with ornithine transcarbamylase deficiency. N Engl J Med (1996) 3.05
ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative. Neurology (1997) 3.04
Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nat Genet (1993) 2.27
Use of proxies to measure health and functional status in epidemiologic studies of community-dwelling women aged 65 years and older. Am J Epidemiol (1996) 1.67
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum Mol Genet (1997) 1.57
Reliability and validity of NINCDS-ADRDA criteria for Alzheimer's disease. The National Institute of Mental Health Genetics Initiative. Arch Neurol (1994) 1.35
A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM. Genomics (1993) 1.26
Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14. Am J Hum Genet (1993) 1.23
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells. Hum Mol Genet (1995) 1.23
Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes. Hum Mutat (1994) 1.19
Normal phenotype with paternal uniparental isodisomy for chromosome 21. Am J Hum Genet (1993) 1.15
Paternal nondisjunction in trisomy 21: excess of male patients. Hum Mol Genet (1993) 1.15
Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: the NIMH Alzheimer Disease Genetics Initiative. Am J Med Genet (2000) 1.13
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. Am J Hum Genet (1994) 1.09
Predicting performance on the Mini-Mental State Examination. Use of age- and education-specific equations. J Am Geriatr Soc (1987) 1.06
Development and validation of a Structured Telephone Interview for Dementia Assessment (STIDA): the NIMH Genetics Initiative. J Geriatr Psychiatry Neurol (1997) 0.99
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism. Eur J Hum Genet (1999) 0.97
Alzheimer's risk variants in the clusterin gene are associated with alternative splicing. Transl Psychiatry (2011) 0.94
Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations. J Neurol Neurosurg Psychiatry (1998) 0.94
Dementia: case ascertainment in a community survey. J Gerontol (1991) 0.93
The antisaccade task in a sample of 2,006 young men. I. Normal population characteristics. Exp Brain Res (2002) 0.93
beta2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort. Mol Psychiatry (2007) 0.90
Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients. Transl Psychiatry (2013) 0.90
The epidemiology of delirium in the community: the Eastern Baltimore Mental Health Survey. Int Psychogeriatr (1991) 0.90
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans. Hum Mol Genet (1998) 0.89
Apolipoprotein E and presenilin-1 genotypes in Huntington's disease. J Neurol (1999) 0.87
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter. Am J Med Genet (1997) 0.86
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype. Am J Med Genet (2000) 0.84
GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: a genetic association study. Am J Med Genet (2001) 0.84
The antisaccade task in a sample of 2,006 young males. II. Effects of task parameters. Exp Brain Res (2002) 0.83
Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder. Psychiatr Genet (1999) 0.80
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome. Am J Med Genet (2000) 0.79
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region. Hum Genet (1997) 0.79
Schizophrenia-related RGS4 gene variations specifically disrupt prefrontal control of saccadic eye movements. Psychol Med (2011) 0.78
Association between the GABA(A) receptor alpha5 subunit gene locus (GABRA5) and bipolar affective disorder. Am J Med Genet (1998) 0.78
Active eye fixation performance in 940 young men: effects of IQ, schizotypy, anxiety and depression. Exp Brain Res (2003) 0.78
Apolipoprotein E polymorphism in the Greek population. Clin Genet (1997) 0.78
A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p. Genomics (1993) 0.77
Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset. Neuropsychobiology (2001) 0.77
Intelligence and medial temporal lobe function in older adults: a functional MR imaging-based investigation. AJNR Am J Neuroradiol (2009) 0.76
Effects of direction on saccadic performance in relation to lateral preferences. Exp Brain Res (2003) 0.76
Serotonin transporter gene variants and prediction of stress-induced risk for psychological distress. Genes Brain Behav (2011) 0.76
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Mol Psychiatry (2017) 0.75
Adolescents with closed head injuries. A report of initial cognitive deficits. Am J Dis Child (1988) 0.75
Genomic structure, expression pattern, and chromosomal localization of the human calsenilin gene: no association between an exonic polymorphism and Alzheimer's disease. Neurosci Lett (2000) 0.75
Tetrasomy 18p de novo: parental origin and different mechanisms of formation. Eur J Hum Genet (1996) 0.75
Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci. Hum Mol Genet (1993) 0.75
Three novel mutations in the gap junction beta 1 (GJB1) gene coding region identified in Charcot-Marie-Tooth patients of Greek origin: T55I, R164Q, V120E. Mutation in brief no 236. Online. Hum Mutat (1999) 0.75