PubRank

Hilary Coon

Author PubWeight™ 132.06‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010 14.66
2 Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 2007 14.05
3 Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009 9.47
4 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
5 Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 2009 7.39
6 Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet 2003 6.63
7 Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 2014 5.30
8 Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 2003 4.48
9 A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 2010 3.42
10 Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet 2009 3.42
11 A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction. PLoS Genet 2008 3.25
12 Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet 2003 3.02
13 Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism. Am J Med Genet A 2006 3.01
14 A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children. Lancet 2002 2.69
15 Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet 2012 2.46
16 Twenty-year outcome for individuals with autism and average or near-average cognitive abilities. Autism Res 2009 2.06
17 Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes. Nicotine Tob Res 2009 1.84
18 Autism, regression, and the broader autism phenotype. Am J Med Genet 2002 1.80
19 Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network. J Autism Dev Disord 2004 1.79
20 Acute air pollution exposure and risk of suicide completion. Am J Epidemiol 2015 1.73
21 Neuropathy target esterase gene mutations cause motor neuron disease. Am J Hum Genet 2008 1.66
22 Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet 2003 1.50
23 A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet 2011 1.43
24 Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking. Nicotine Tob Res 2005 1.27
25 An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study. BMC Genet 2007 1.27
26 Fruit and vegetable consumption and LDL cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr 2004 1.23
27 Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. Am J Hypertens 2004 1.20
28 Sodium bicarbonate cotransporter polymorphisms are associated with baseline and 10-year follow-up blood pressures. Hypertension 2005 1.18
29 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
30 Confirmation of the association of the C4B null allelle in autism. Hum Immunol 2005 1.07
31 Psychiatric comorbidity and medication use in adults with autism spectrum disorder. J Autism Dev Disord 2014 1.03
32 Temporal lobe, autism, and macrocephaly. AJNR Am J Neuroradiol 2003 1.02
33 A genome scan for loci influencing anti-atherogenic serum bilirubin levels. Eur J Hum Genet 2002 0.99
34 Heterogeneous association between engrailed-2 and autism in the CPEA network. Am J Med Genet B Neuropsychiatr Genet 2008 0.97
35 Maternal prenatal weight gain and autism spectrum disorders. Pediatrics 2013 0.94
36 Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees. Hypertension 2003 0.93
37 The PHQ-9 as a brief assessment of lifetime major depression. Psychol Assess 2007 0.90
38 Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat. Kidney Int 2002 0.89
39 Multistudy fine mapping of chromosome 2q identifies XRCC5 as a chronic obstructive pulmonary disease susceptibility gene. Am J Respir Crit Care Med 2010 0.89
40 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
41 Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. Atherosclerosis 2004 0.87
42 Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study. J Autism Dev Disord 2013 0.87
43 Psychiatric symptoms in adults with phenylketonuria. Mol Genet Metab 2012 0.86
44 Familial aggregation and genome-wide linkage analysis of carotid artery plaque: the NHLBI family heart study. Hum Hered 2004 0.86
45 Comparative analysis of suicide, accidental, and undetermined cause of death classification. Suicide Life Threat Behav 2014 0.84
46 A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Autism Res 2010 0.82
47 Effect of neuronal nicotinic acetylcholine receptor genes (CHRN) on longitudinal cigarettes per day in adolescents and young adults. Nicotine Tob Res 2013 0.82
48 A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics. Mol Genet Metab 2012 0.82
49 Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Hum Genet 2004 0.82
50 Narrowing the broader autism phenotype: a study using the Communication Checklist-Adult Version (CC-A). Autism 2010 0.81
51 Use of a genealogical database demonstrates heritability of pulmonary fibrosis. Lung 2013 0.81
52 Autism spectrum disorder reclassified: a second look at the 1980s Utah/UCLA Autism Epidemiologic Study. J Autism Dev Disord 2013 0.80
53 Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. Eur J Hum Genet 2002 0.78
54 Model-fitting and linkage analysis of sodium-lithium countertransport. Eur J Hum Genet 2004 0.78
55 Meta-analysis of genome-wide linkage studies for quantitative lipid traits in African Americans. Hum Mol Genet 2005 0.78
56 Spatial relative risk patterns of autism spectrum disorders in Utah. J Autism Dev Disord 2015 0.77
57 Bakian et al. respond to "Assessing air pollution and suicide risk". Am J Epidemiol 2015 0.75
58 No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Autism Res 2011 0.75