PubRank

Lisa J Martin

Author PubWeight™ 116.27‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mammographic density and the risk and detection of breast cancer. N Engl J Med 2007 14.32
2 Breast tissue composition and susceptibility to breast cancer. J Natl Cancer Inst 2010 3.39
3 A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nat Genet 2002 3.19
4 Mammographic density and breast cancer risk: current understanding and future prospects. Breast Cancer Res 2011 2.86
5 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. Nat Genet 2010 2.47
6 Body size, mammographic density, and breast cancer risk. Cancer Epidemiol Biomarkers Prev 2006 2.44
7 Hypoplastic left heart syndrome is heritable. J Am Coll Cardiol 2007 2.24
8 Bicuspid aortic valve is heritable. J Am Coll Cardiol 2004 2.18
9 Mammographic density as a surrogate marker for the effects of hormone therapy on risk of breast cancer. Cancer Epidemiol Biomarkers Prev 2006 1.91
10 Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve. J Am Coll Cardiol 2009 1.88
11 Coordinate interaction between IL-13 and epithelial differentiation cluster genes in eosinophilic esophagitis. J Immunol 2010 1.85
12 MicroRNA signature in patients with eosinophilic esophagitis, reversibility with glucocorticoids, and assessment as disease biomarkers. J Allergy Clin Immunol 2012 1.79
13 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. Nat Genet 2011 1.77
14 Variants of thymic stromal lymphopoietin and its receptor associate with eosinophilic esophagitis. J Allergy Clin Immunol 2010 1.74
15 Risk factors for aortic valve disease in bicuspid aortic valve: a family-based study. Am J Med Genet A 2011 1.55
16 Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation. Heart Rhythm 2012 1.51
17 Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip. BMC Genet 2007 1.47
18 Variable expression of neurofibromatosis 1 in monozygotic twins. Am J Med Genet A 2011 1.45
19 Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mamm Genome 2012 1.43
20 High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders. J Allergy Clin Immunol 2013 1.35
21 Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring) 2007 1.32
22 Mammographic density: a heritable risk factor for breast cancer. Methods Mol Biol 2009 1.24
23 Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships. Genet Med 2012 1.20
24 Genetic contributions to social impulsivity and aggressiveness in vervet monkeys. Biol Psychiatry 2004 1.19
25 Mammographic density: a hormonally responsive risk factor for breast cancer. J Br Menopause Soc 2006 1.13
26 Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. PLoS One 2011 1.10
27 Association of FTO gene variants with adiposity in African-American adolescents. Obesity (Silver Spring) 2010 1.09
28 Differences in candidate gene association between European ancestry and African American asthmatic children. PLoS One 2011 1.09
29 Comparison of measures of marker informativeness for ancestry and admixture mapping. BMC Genomics 2011 1.07
30 Mammographic density. Breast Cancer Res 2009 1.05
31 Genetic determinants of obesity-related lipid traits. J Lipid Res 2004 1.04
32 Interactions between noncontiguous haplotypes in the adiponectin gene ACDC are associated with plasma adiponectin. Diabetes 2006 1.04
33 Mammographic density, response to hormones, and breast cancer risk. J Clin Oncol 2011 1.04
34 Mammographic breast density and breast cancer: evidence of a shared genetic basis. Cancer Res 2012 1.03
35 Barriers to and motivations for physician referral of patients to cancer genetics clinics. J Genet Couns 2011 1.02
36 Pediatric plexiform neurofibromas: impact on morbidity and mortality in neurofibromatosis type 1. J Pediatr 2011 1.02
37 Population structure analysis using rare and common functional variants. BMC Proc 2011 1.02
38 Maternal low-protein diet or hypercholesterolemia reduces circulating essential amino acids and leads to intrauterine growth restriction. Diabetes 2008 1.00
39 Impaired immune function in children with Fanconi anaemia. Br J Haematol 2011 0.97
40 Race and unequal burden of perioperative pain and opioid related adverse effects in children. Pediatrics 2012 0.96
41 The role of mitochondrial genome in essential hypertension in a Chinese Han population. Eur J Hum Genet 2009 0.95
42 Differences in measured mammographic density in the menstrual cycle. Cancer Epidemiol Biomarkers Prev 2009 0.93
43 Adolescent sex differences in adiponectin are conditional on pubertal development and adiposity. Obes Res 2005 0.93
44 Value of an Additional Review for Eosinophil Quantification in Esophageal Biopsies. J Pediatr Gastroenterol Nutr 2015 0.93
45 Effect of population stratification analysis on false-positive rates for common and rare variants. BMC Proc 2011 0.92
46 Genetics of monoamine metabolites in baboons: overlapping sets of genes influence levels of 5-hydroxyindolacetic acid, 3-hydroxy-4-methoxyphenylglycol, and homovanillic acid. Biol Psychiatry 2004 0.91
47 Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses. BMC Proc 2009 0.91
48 Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc 2007 0.89
49 Characterization of congenital anomalies in individuals with choanal atresia. Arch Otolaryngol Head Neck Surg 2009 0.89
50 Mammographic features associated with interval breast cancers in screening programs. Breast Cancer Res 2014 0.89
51 Limited RNA editing in exons of mouse liver and adipose. Genetics 2013 0.88
52 The genes influencing adiponectin levels also influence risk factors for metabolic syndrome and type 2 diabetes. Hum Biol 2007 0.88
53 Identification of a novel percent mammographic density locus at 12q24. Hum Mol Genet 2012 0.88
54 Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. Atherosclerosis 2004 0.87
55 Accuracy of haplotype estimation in a region of low linkage disequilibrium. BMC Genet 2005 0.87
56 Genetics of pain perception, COMT and postoperative pain management in children. Pharmacogenomics 2014 0.86
57 Application of genetic/genomic approaches to allergic disorders. J Allergy Clin Immunol 2010 0.86
58 Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13. Genet Epidemiol 2003 0.86
59 Stability of adolescent body mass index during three years of follow-up. J Pediatr 2007 0.85
60 Human milk adiponectin is associated with infant growth in two independent cohorts. Breastfeed Med 2009 0.85
61 Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing. Fam Cancer 2010 0.85
62 Human milk adiponectin affects infant weight trajectory during the second year of life. J Pediatr Gastroenterol Nutr 2012 0.84
63 Risk factors for breast cancer in postmenopausal Caucasian and Chinese-Canadian women. Breast Cancer Res 2010 0.84
64 Genetic variation in small proline rich protein 2B as a predictor for asthma among children with eczema. Ann Allergy Asthma Immunol 2012 0.83
65 A genome-wide linkage study of mammographic density, a risk factor for breast cancer. Breast Cancer Res 2011 0.83
66 Intergenerational genomic DNA methylation patterns in mouse hybrid strains. Genome Biol 2014 0.82
67 Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol. Am J Med Genet A 2009 0.82
68 Comparison of false-discovery rate for genome-wide and fine mapping regions. BMC Proc 2007 0.81
69 Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. Hum Genomics 2013 0.80
70 Disruption of the aortic elastic lamina and medial calcification share genetic determinants in mice. Circ Cardiovasc Genet 2009 0.80
71 The genetics of obesity in Mexican Americans: the evidence from genome scanning efforts in the San Antonio family heart study. Hum Biol 2003 0.80
72 Genetics and outcomes after traumatic brain injury (TBI): what do we know about pediatric TBI? J Pediatr Rehabil Med 2012 0.79
73 Food, beverage, and macronutrient intakes in postmenopausal Caucasian and Chinese-Canadian women. Nutr Cancer 2011 0.79
74 Response to Pomozi et al's research commentary. Circ Res 2013 0.79
75 Evaluation of growth in patients with isolated cleft lip and/or cleft palate. Pediatrics 2010 0.79
76 Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromes. J Pediatr Gastroenterol Nutr 2014 0.79
77 IGF receptor gene variants in normal adolescents: effect on stature. Eur J Endocrinol 2012 0.79
78 HDL cholesterol in females in the Framingham Heart Study is linked to a region of chromosome 2q. BMC Genet 2003 0.78
79 Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes. Springerplus 2012 0.78
80 A locus on chromosome 10 influences C-reactive protein levels in two independent populations. Hum Genet 2007 0.78
81 Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach. BMC Proc 2011 0.78
82 Adiponectin receptor 1 variants associated with lower insulin resistance in African Americans. Obesity (Silver Spring) 2007 0.77
83 Family- and population-based designs identify different rare causal variants. BMC Proc 2011 0.77
84 Codeine-related adverse drug reactions in children following tonsillectomy: a prospective study. Laryngoscope 2013 0.77
85 Complex story of the genetic origins of pediatric heart disease. Circulation 2010 0.77
86 Fractures in children with neurofibromatosis type 1 from two NF clinics. Am J Med Genet A 2013 0.77
87 Personalized medicine, availability, and group disparity: an inquiry into how physicians perceive and rate the elements and barriers of personalized medicine. Public Health Genomics 2014 0.76
88 Influence of Catechol-O-methyltransferase on Executive Functioning Longitudinally After Early Childhood Traumatic Brain Injury: Preliminary Findings. J Head Trauma Rehabil 2016 0.76
89 Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis. BMC Genet 2012 0.75
90 Genetic risk signatures of opioid-induced respiratory depression following pediatric tonsillectomy. Pharmacogenomics 2014 0.75
91 Mammographic density and breast cancer: a comparison of related and unrelated controls in the Breast Cancer Family Registry. Breast Cancer Res 2013 0.75
92 Lifetime physical activity in postmenopausal Caucasian and Chinese-Canadian women. Eur J Cancer Prev 2014 0.75
93 Linkage analysis for complex diseases using variance component analysis: SOLAR. Methods Mol Med 2006 0.75
94 Catechol-O-Methyltransferase Genotypes and Parenting Influence on Long-Term Executive Functioning After Moderate to Severe Early Childhood Traumatic Brain Injury: An Exploratory Study. J Head Trauma Rehabil 2017 0.75
95 The impact of supervision training on genetic counselor supervisory identity development. J Genet Couns 2014 0.75