PubRank

R M Cantor

Author PubWeight™ 60.05‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus. J Clin Invest 1997 2.57
2 Rapid-sequence intubation of the pediatric patient. Pediatric Emergency Medicine Committee of the American College of Emergency Physicians. Ann Emerg Med 1996 2.40
3 PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosus. J Clin Invest 1999 2.14
4 Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Mol Psychiatry 2005 1.87
5 Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry 2011 1.65
6 Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus. Genes Immun 2006 1.54
7 Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse. Nat Genet 1998 1.51
8 A prospective analysis of intramuscular meperidine, promethazine, and chlorpromazine in pediatric emergency department patients. Ann Emerg Med 1991 1.42
9 Expanding the range of ZNF804A variants conferring risk of psychosis. Mol Psychiatry 2010 1.41
10 Association between serum amyloid A proteins and coronary artery disease: evidence from two distinct arteriosclerotic processes. Circulation 1997 1.34
11 Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD). Mol Psychiatry 2000 1.30
12 The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. Am J Hum Genet 1983 1.22
13 Septic shock and respiratory failure in community-acquired pneumonia have different TNF polymorphism associations. Am J Respir Crit Care Med 2001 1.21
14 Family-based association analysis implicates IL-4 in susceptibility to Kawasaki disease. Genes Immun 2005 1.21
15 A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. Am J Hum Genet 1999 1.20
16 The apoAI-CIII-AIV gene cluster. Atherosclerosis 2001 1.20
17 Paternal age and autism are associated in a family-based sample. Mol Psychiatry 2007 1.18
18 Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders. Am J Hum Genet 1986 1.18
19 Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p. Hypertension 2001 1.16
20 Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation. Am J Med Genet 1998 1.14
21 Cytogenetic abnormalities in uterine myomas are associated with myoma size. Mol Hum Reprod 1998 1.06
22 Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes. J Clin Invest 1997 1.05
23 Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder. Mol Psychiatry 2006 1.05
24 Increased frequency of alleles associated with elevated tumor necrosis factor-alpha levels in children with Kawasaki disease. Pediatr Res 2001 1.00
25 GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Mol Psychiatry 2010 1.00
26 High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. Mol Psychiatry 2009 0.97
27 Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13. Mol Psychiatry 2006 0.93
28 Multilocus genetic determinants of LDL particle size in coronary artery disease families. Am J Hum Genet 1996 0.93
29 Trapeziometacarpal joint arthrodesis: a functional evaluation. J Hand Surg Am 1992 0.92
30 Allowing for sex differences increases power in a GWAS of multiplex Autism families. Mol Psychiatry 2010 0.92
31 Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype. Am J Hum Genet 1998 0.91
32 Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia. J Lipid Res 1999 0.90
33 Identification of a murine locus conveying susceptibility to cadmium-induced forelimb malformations. Genomics 2000 0.89
34 Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia. Hum Mol Genet 2000 0.89
35 Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods. Am J Hum Genet 1985 0.84
36 New genetic variants in the apoA-I and apoC-III genes and familial combined hyperlipidemia. J Lipid Res 2001 0.82
37 QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders. Mol Psychiatry 2011 0.82
38 Seasonal variation of serotonin turnover in human cerebrospinal fluid, depressive symptoms and the role of the 5-HTTLPR. Transl Psychiatry 2013 0.82
39 PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population. Am J Hum Genet 1997 0.82
40 Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A. Int J Obes Relat Metab Disord 2000 0.81
41 Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q. Arterioscler Thromb Vasc Biol 1999 0.80
42 Quantitative trait loci mapping of serum IgE in an isolated Hutterite population. Genet Epidemiol 2001 0.80
43 Plasma cocaine and tetracaine levels following application of topical anesthesia in children. Ann Emerg Med 1992 0.80
44 The genetic basis of systemic lupus erythematosus. Proc Assoc Am Physicians 1998 0.80
45 Serum C3 but not plasma acylation-stimulating protein is elevated in Finnish patients with familial combined hyperlipidemia. Arterioscler Thromb Vasc Biol 2001 0.80
46 Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia. J Lipid Res 2000 0.79
47 Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. II. Sandhoff disease gene frequencies in American Jewish and non-Jewish populations. Am J Hum Genet 1987 0.79
48 A genetic analysis of taste threshold for phenylthiocarbamide. Acta Genet Med Gemellol (Roma) 1981 0.79
49 Education and testing strategy for large-scale cystic fibrosis carrier screening. J Genet Couns 1994 0.78
50 Identification of two single nucleotide polymorphisms in exon 8 of PAX2. Mol Genet Metab 1999 0.78
51 Central anticholinergic syndrome due to Jimson weed physostigmine: therapy revisited? J Toxicol Clin Toxicol 1998 0.77
52 Intramuscular meperidine, promethazine, and chlorpromazine: analysis of use and complications in 487 pediatric emergency department patients. Ann Emerg Med 1989 0.76
53 Power and validity of methods to identify variability genes. Genet Epidemiol 1991 0.76
54 Comparison of intramuscular meperidine and promethazine with and without chlorpromazine: a randomized, prospective, double-blind trial. Ann Emerg Med 1993 0.76
55 Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus. Trans Am Ophthalmol Soc 1993 0.75
56 Analysis of the covariance structure of digital ridge counts in the offspring of monozygotic twins. Genetics 1983 0.75
57 Two newly identified SNPs in the APO AI-CIII intergenic region are strongly associated with familial combined hyperlipidaemia. Eur J Clin Invest 2001 0.75
58 Factors influencing the identification of major genes in a complex disease genome scan. Genet Epidemiol 1997 0.75
59 HLA haplotype sharing and proband genotype in IDDM. Genet Epidemiol Suppl 1986 0.75
60 Productive osseous changes about the wrist in rheumatoid arthritis. Skeletal Radiol 1987 0.75
61 The impact of a didactic session on the success of feline endotracheal intubation by paramedics. Pediatr Emerg Care 1989 0.75
62 A multivariate genetic analysis of ridge count data from the offspring of monozygotic twins. Acta Genet Med Gemellol (Roma) 1983 0.75
63 Goldschlager allergy in a gold allergic patient. Vet Hum Toxicol 1999 0.75
64 The lecithin/sphingomyelin ratio in a high-risk obstetric population. Obstet Gynecol 1976 0.75