PubRank

Stacey S Cherny

Author PubWeight™ 122.71‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2001 53.16
2 Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet 2002 5.20
3 Diabetes prevalence and therapeutic target achievement in the United States, 1999 to 2006. Am J Med 2009 4.53
4 Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proc Natl Acad Sci U S A 2004 3.73
5 Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases. Genet Epidemiol 2011 2.78
6 Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets. Hum Genet 2011 1.93
7 Genetic and environmental contributions to general cognitive ability through the first 16 years of life. Dev Psychol 2004 1.68
8 Use of multivariate linkage analysis for dissection of a complex cognitive trait. Am J Hum Genet 2003 1.62
9 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Proc Natl Acad Sci U S A 2009 1.56
10 Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. Am J Hum Genet 2012 1.49
11 Optimal selection strategies for QTL mapping using pooled DNA samples. Eur J Hum Genet 2002 1.45
12 Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening. Am J Hum Genet 2011 1.26
13 The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Ann Hum Genet 2006 1.26
14 Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset. BMC Res Notes 2011 1.24
15 A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma. J Natl Cancer Inst 2009 1.21
16 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. Hum Mol Genet 2010 1.17
17 Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese. Eur J Endocrinol 2010 1.17
18 Impaired intellect and memory: a missing link between genetic risk and schizophrenia? Arch Gen Psychiatry 2010 1.15
19 Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships. Hum Mol Genet 2004 1.14
20 Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins. Twin Res Hum Genet 2007 1.12
21 Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophr Bull 2014 1.10
22 A knowledge-based weighting framework to boost the power of genome-wide association studies. PLoS One 2010 1.08
23 Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. Hum Mol Genet 2011 1.07
24 Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genet Epidemiol 2008 1.06
25 Utility of the trnH-psbA intergenic spacer region and its combinations as plant DNA barcodes: a meta-analysis. PLoS One 2012 1.05
26 Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. PLoS One 2012 1.03
27 ELF1 is associated with systemic lupus erythematosus in Asian populations. Hum Mol Genet 2010 0.99
28 Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. J Clin Invest 2013 0.98
29 Significant linkage to migraine with aura on chromosome 11q24. Hum Mol Genet 2003 0.96
30 Using glycosylated hemoglobin to define the metabolic syndrome in United States adults. Diabetes Care 2010 0.96
31 RET and NRG1 interplay in Hirschsprung disease. Hum Genet 2013 0.94
32 A genome-wide scan for loci influencing adolescent cannabis dependence symptoms: evidence for linkage on chromosomes 3 and 9. Drug Alcohol Depend 2006 0.94
33 Gamma-glutamyl transferase level predicts the development of hypertension in Hong Kong Chinese. Clin Chim Acta 2011 0.94
34 A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits. PLoS One 2012 0.94
35 Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans. J Clin Invest 2011 0.93
36 Mapping of a Hirschsprung's disease locus in 3p21. Eur J Hum Genet 2008 0.93
37 Genome-wide copy number variation study in anorectal malformations. Hum Mol Genet 2012 0.91
38 Heritability of hallucinations in adolescent twins. Psychiatry Res 2012 0.90
39 Genome-wide copy number analysis uncovers a new HSCR gene: NRG3. PLoS Genet 2012 0.90
40 Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. J Hepatol 2013 0.90
41 Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population. PLoS One 2010 0.89
42 Elevated plasma level of soluble F11 receptor/junctional adhesion molecule-A (F11R/JAM-A) in hypertension. Am J Hypertens 2009 0.89
43 RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients. PLoS One 2011 0.88
44 Association of a polymorphism in the lipin 1 gene with systolic blood pressure in men. Am J Hypertens 2008 0.87
45 Mutations in the NRG1 gene are associated with Hirschsprung disease. Hum Genet 2011 0.86
46 Novel sib pair selection strategy increases power in quantitative association analysis. Behav Genet 2009 0.86
47 Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data. Hum Mutat 2011 0.86
48 Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene. Eur J Endocrinol 2011 0.85
49 Mutational analysis of SHH and GLI3 in anorectal malformations. Birth Defects Res A Clin Mol Teratol 2008 0.85
50 Fine mapping of the NRG1 Hirschsprung's disease locus. PLoS One 2011 0.85
51 Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese. Am J Hypertens 2011 0.82
52 A genetic variant in the gene encoding adrenomedullin predicts the development of dysglycemia over 6.4 years in Chinese. Clin Chim Acta 2010 0.82
53 Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians. Hum Mol Genet 2013 0.81
54 Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population. Am J Med Genet B Neuropsychiatr Genet 2010 0.81
55 Targeted next-generation sequencing on Hirschsprung disease: a pilot study exploits DNA pooling. Ann Hum Genet 2014 0.80
56 Gene network analysis of candidate loci for human anorectal malformations. PLoS One 2013 0.78
57 A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis. Am J Med Genet B Neuropsychiatr Genet 2008 0.77
58 Role of genetic variants in the gene encoding lipocalin-2 in the development of elevated blood pressure. Clin Exp Hypertens 2011 0.77
59 Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia. PLoS One 2013 0.75
60 No NRG1 V266L in Chinese patients with schizophrenia. Psychiatr Genet 2011 0.75
61 A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men. Thromb Haemost 2010 0.75