Published in Am J Med Genet B Neuropsychiatr Genet on July 05, 2006
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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene. PLoS Genet (2010) 4.29
Personalized epigenomic signatures that are stable over time and covary with body mass index. Sci Transl Med (2010) 3.81
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet (2010) 3.63
Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies. Int J Epidemiol (2012) 3.62
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network. Cell (2013) 3.26
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios. Am J Hum Genet (2005) 3.03
Results of a high-resolution genome screen of 437 Alzheimer's disease families. Hum Mol Genet (2003) 3.00
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Arch Neurol (2010) 2.91
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. JAMA (2013) 2.58
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Behavioral risk exposure and host genetics of susceptibility to HIV-1 infection. J Infect Dis (2005) 1.89
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign. Am J Hum Genet (2003) 1.81
Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations. Genet Med (2007) 1.75
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology (2006) 1.71
Role of activating FcγR gene polymorphisms in Kawasaki disease susceptibility and intravenous immunoglobulin response. Circ Cardiovasc Genet (2012) 1.65
Interaction between FEZ1 and DISC1 in regulation of neuronal development and risk for schizophrenia. Neuron (2011) 1.57
Host immunogenetics and control of human herpesvirus-8 infection. J Infect Dis (2006) 1.52
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Multiple hits for the association of uterine fibroids on human chromosome 1q43. PLoS One (2013) 1.50
Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees. Biol Psychiatry (2003) 1.49
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genet Epidemiol (2011) 1.47
Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms. BMC Genet (2005) 1.44
Association between apolipoprotein E genotype and Alzheimer disease in African American subjects. Arch Neurol (2002) 1.37
Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Am J Psychiatry (2003) 1.36
A comprehensive genetic association study of Alzheimer disease in African Americans. Arch Neurol (2011) 1.33
Gene-environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop. Genet Epidemiol (2011) 1.33
Impact of schizophrenia candidate genes on schizotypy and cognitive endophenotypes at the population level. Biol Psychiatry (2007) 1.32
DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth. Int J Epidemiol (2012) 1.30
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia. Am J Hum Genet (2009) 1.27
Simple biologically informed inflammatory index of two serum cytokines predicts 10 year all-cause mortality in older adults. J Gerontol A Biol Sci Med Sci (2013) 1.25
Effect of COMT Val158Met polymorphism on the Continuous Performance Test, Identical Pairs Version: tuning rather than improving performance. Am J Psychiatry (2005) 1.23
Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men. Biol Psychiatry (2004) 1.23
Heritability estimates of endophenotypes of long and health life: the Long Life Family Study. J Gerontol A Biol Sci Med Sci (2010) 1.22
Associations between total serum IgE levels and the 6 potentially functional variants within the genes IL4, IL13, and IL4RA in German children: the German Multicenter Atopy Study. J Allergy Clin Immunol (2003) 1.20
Evidence for parent of origin effect in late-onset Alzheimer disease. Am J Med Genet (2002) 1.20
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): recruitment and assessment methods. Schizophr Res (2006) 1.19
IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health Study. Hum Genet (2007) 1.18
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet (2007) 1.16
Genetic variation in base excision repair genes and the prevalence of advanced colorectal adenoma. Cancer Res (2007) 1.15
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients. Am J Psychiatry (2010) 1.15
Genetic dissection methods: designs used for tests of gene-environment interaction. Curr Opin Genet Dev (2004) 1.14
The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network. J Autism Dev Disord (2012) 1.14
Factorial composition of self-rated schizotypal traits among young males undergoing military training. Schizophr Bull (2004) 1.07
Genetic variation in the nucleotide excision repair pathway and colorectal cancer risk. Cancer Epidemiol Biomarkers Prev (2006) 1.07
Comparison of measures of marker informativeness for ancestry and admixture mapping. BMC Genomics (2011) 1.07
African-American community attitudes and perceptions toward schizophrenia and medical research: an exploratory study. J Natl Med Assoc (2006) 1.06
Epigenetic epidemiology: promises for public health research. Environ Mol Mutagen (2014) 1.06
Interaction of body mass index and framingham risk score in predicting incident coronary disease in families. Circulation (2005) 1.05
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses. Am J Med Genet B Neuropsychiatr Genet (2005) 1.05
Exploring biologically relevant pathways in frailty. J Gerontol A Biol Sci Med Sci (2011) 1.05
Effect of schizotypy on cognitive performance and its tuning by COMT val158 met genotype variations in a large population of young men. Biol Psychiatry (2006) 1.05
Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism. Proc Natl Acad Sci U S A (2011) 1.03
Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls. Neurogenetics (2010) 1.02
Variants in mannose-binding lectin and tumour necrosis factor alpha affect survival in cystic fibrosis. J Med Genet (2006) 1.02
Familiality of novel factorial dimensions of schizophrenia. Arch Gen Psychiatry (2009) 1.02
Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin. Hum Mol Genet (2003) 1.01
SynaptomeDB: an ontology-based knowledgebase for synaptic genes. Bioinformatics (2012) 0.99
The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate. Cleft Palate Craniofac J (2011) 0.96
Mismatch repair polymorphisms and the risk of colorectal cancer. Int J Cancer (2007) 0.95
Variation in IL10 and other genes involved in the immune response and in oxidation and prostate cancer recurrence. Cancer Epidemiol Biomarkers Prev (2012) 0.94
Vaccines for otitis media: proposals for overcoming obstacles to progress. Vaccine (2005) 0.94
Infant siblings and the investigation of autism risk factors. J Neurodev Disord (2012) 0.94
HLA antigens, alleles and haplotypes among the Yup'ik Alaska natives: report of the ASHI Minority Workshops, Part II. Hum Immunol (2002) 0.93
Associations between specific serum IgE response and 6 variants within the genes IL4, IL13, and IL4RA in German children: the German Multicenter Atopy Study. J Allergy Clin Immunol (2004) 0.93
HLA alleles and haplotypes among the Lakota Sioux: report of the ASHI minority workshops, part III. Hum Immunol (2004) 0.91
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses. BMC Proc (2009) 0.91
Phenotypic and genetic characterization of patients with features of "nonclassic" forms of cystic fibrosis. J Pediatr (2005) 0.91
Neuroglobin and Alzheimer's dementia: genetic association and gene expression changes. Neurobiol Aging (2008) 0.91
A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed. Vaccine (2012) 0.90
Concordance rates and modifiable risk factors for lower urinary tract symptoms in twins. Epidemiology (2006) 0.90
Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis. Eur J Hum Genet (2010) 0.89
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs. PLoS One (2010) 0.89
Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms. Am J Med Genet B Neuropsychiatr Genet (2005) 0.89
Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. Eur J Hum Genet (2010) 0.89
Polymorphic variants in alpha-methylacyl-CoA racemase and prostate cancer. Prostate (2007) 0.89
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. Circ Res (2011) 0.89
Influence of control selection in genome-wide association studies: the example of diabetes in the Framingham Heart Study. BMC Proc (2009) 0.88
COMT Val158Met moderation of stress-induced psychosis. Psychol Med (2007) 0.88
Variants in the alpha-Methylacyl-CoA racemase gene and the association with advanced distal colorectal adenoma. Cancer Epidemiol Biomarkers Prev (2007) 0.88
Detection of SNP-SNP interactions in trios of parents with schizophrenic children. Genet Epidemiol (2010) 0.88
The robustness of generalized estimating equations for association tests in extended family data. Hum Hered (2012) 0.88
Family-based SNP association study on 8q24 in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet (2008) 0.88
A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH Genetic Initiative. Am J Med Genet B Neuropsychiatr Genet (2008) 0.87
Salivary Actinomyces naeslundii genospecies 2 and Lactobacillus casei levels predict pregnancy outcomes. J Periodontol (2005) 0.87