Published in Fam Cancer on June 01, 2010
Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer. J Clin Oncol (2014) 1.91
Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition. JMIR Res Protoc (2014) 0.83
Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results. Patient Educ Couns (2013) 0.79
Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review. Front Oncol (2016) 0.78
Genetic counseling content: How does it impact health behavior? J Behav Med (2014) 0.77
Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up. J Clin Oncol (2016) 0.75
Mammographic density and the risk and detection of breast cancer. N Engl J Med (2007) 14.32
Breast tissue composition and susceptibility to breast cancer. J Natl Cancer Inst (2010) 3.39
A comprehensive linkage analysis for myocardial infarction and its related risk factors. Nat Genet (2002) 3.19
Mammographic density and breast cancer risk: current understanding and future prospects. Breast Cancer Res (2011) 2.86
Common variants at 5q22 associate with pediatric eosinophilic esophagitis. Nat Genet (2010) 2.47
Body size, mammographic density, and breast cancer risk. Cancer Epidemiol Biomarkers Prev (2006) 2.44
Propranolol induces regression of hemangioma cells through HIF-1α-mediated inhibition of VEGF-A. Ann Surg (2012) 2.35
Hypoplastic left heart syndrome is heritable. J Am Coll Cardiol (2007) 2.24
Bicuspid aortic valve is heritable. J Am Coll Cardiol (2004) 2.18
Mammographic density as a surrogate marker for the effects of hormone therapy on risk of breast cancer. Cancer Epidemiol Biomarkers Prev (2006) 1.91
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
Coordinate interaction between IL-13 and epithelial differentiation cluster genes in eosinophilic esophagitis. J Immunol (2010) 1.85
MicroRNA signature in patients with eosinophilic esophagitis, reversibility with glucocorticoids, and assessment as disease biomarkers. J Allergy Clin Immunol (2012) 1.79
Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. Nat Genet (2011) 1.77
Variants of thymic stromal lymphopoietin and its receptor associate with eosinophilic esophagitis. J Allergy Clin Immunol (2010) 1.74
Matrix metalloproteinase induction of Rac1b, a key effector of lung cancer progression. Sci Transl Med (2012) 1.67
Risk factors for aortic valve disease in bicuspid aortic valve: a family-based study. Am J Med Genet A (2011) 1.55
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation. Heart Rhythm (2012) 1.51
Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip. BMC Genet (2007) 1.47
Variable expression of neurofibromatosis 1 in monozygotic twins. Am J Med Genet A (2011) 1.45
Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mamm Genome (2012) 1.43
High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders. J Allergy Clin Immunol (2013) 1.35
Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring) (2007) 1.32
Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. Am J Hum Genet (2004) 1.32
Tumor cell-produced matrix metalloproteinase 9 (MMP-9) drives malignant progression and metastasis of basal-like triple negative breast cancer. Oncotarget (2014) 1.28
Mammographic density: a heritable risk factor for breast cancer. Methods Mol Biol (2009) 1.24
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
Genetic contributions to social impulsivity and aggressiveness in vervet monkeys. Biol Psychiatry (2004) 1.19
Mammographic density: a hormonally responsive risk factor for breast cancer. J Br Menopause Soc (2006) 1.13
Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. PLoS One (2011) 1.10
Differences in candidate gene association between European ancestry and African American asthmatic children. PLoS One (2011) 1.09
Association of FTO gene variants with adiposity in African-American adolescents. Obesity (Silver Spring) (2010) 1.09
Comparison of measures of marker informativeness for ancestry and admixture mapping. BMC Genomics (2011) 1.07
Screening for hazardous alcohol use and depressive symptomatology among HIV-infected patients in Nigeria: prevalence, predictors, and association with adherence. J Int Assoc Physicians AIDS Care (Chic) (2010) 1.05
Mammographic density. Breast Cancer Res (2009) 1.05
Genetic determinants of obesity-related lipid traits. J Lipid Res (2004) 1.04
Interactions between noncontiguous haplotypes in the adiponectin gene ACDC are associated with plasma adiponectin. Diabetes (2006) 1.04
Mammographic density, response to hormones, and breast cancer risk. J Clin Oncol (2011) 1.04
Mammographic breast density and breast cancer: evidence of a shared genetic basis. Cancer Res (2012) 1.03
Pediatric plexiform neurofibromas: impact on morbidity and mortality in neurofibromatosis type 1. J Pediatr (2011) 1.02
Barriers to and motivations for physician referral of patients to cancer genetics clinics. J Genet Couns (2011) 1.02
Population structure analysis using rare and common functional variants. BMC Proc (2011) 1.02
Optimizing the transduction efficiency of capsid-modified AAV6 serotype vectors in primary human hematopoietic stem cells in vitro and in a xenograft mouse model in vivo. Cytotherapy (2013) 1.01
Maternal low-protein diet or hypercholesterolemia reduces circulating essential amino acids and leads to intrauterine growth restriction. Diabetes (2008) 1.00
Impaired immune function in children with Fanconi anaemia. Br J Haematol (2011) 0.97
Race and unequal burden of perioperative pain and opioid related adverse effects in children. Pediatrics (2012) 0.96
The role of mitochondrial genome in essential hypertension in a Chinese Han population. Eur J Hum Genet (2009) 0.95
PRSS3/mesotrypsin is a therapeutic target for metastatic prostate cancer. Mol Cancer Res (2012) 0.93
Differences in measured mammographic density in the menstrual cycle. Cancer Epidemiol Biomarkers Prev (2009) 0.93
Adolescent sex differences in adiponectin are conditional on pubertal development and adiposity. Obes Res (2005) 0.93
Value of an Additional Review for Eosinophil Quantification in Esophageal Biopsies. J Pediatr Gastroenterol Nutr (2015) 0.93
Effect of population stratification analysis on false-positive rates for common and rare variants. BMC Proc (2011) 0.92
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses. BMC Proc (2009) 0.91
Vein wall remodeling after deep vein thrombosis: differential effects of low molecular weight heparin and doxycycline. Ann Vasc Surg (2010) 0.91
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
Aortopathy in the 7q11.23 microduplication syndrome. Am J Med Genet A (2014) 0.89
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc (2007) 0.89
Characterization of congenital anomalies in individuals with choanal atresia. Arch Otolaryngol Head Neck Surg (2009) 0.89
Mammographic features associated with interval breast cancers in screening programs. Breast Cancer Res (2014) 0.89
The genes influencing adiponectin levels also influence risk factors for metabolic syndrome and type 2 diabetes. Hum Biol (2007) 0.88
Identification of a novel percent mammographic density locus at 12q24. Hum Mol Genet (2012) 0.88
Limited RNA editing in exons of mouse liver and adipose. Genetics (2013) 0.88
Accuracy of haplotype estimation in a region of low linkage disequilibrium. BMC Genet (2005) 0.87
Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. Atherosclerosis (2004) 0.87
Genetics of pain perception, COMT and postoperative pain management in children. Pharmacogenomics (2014) 0.86
Application of genetic/genomic approaches to allergic disorders. J Allergy Clin Immunol (2010) 0.86
Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13. Genet Epidemiol (2003) 0.86
PEGylation extends circulation half-life while preserving in vitro and in vivo activity of tissue inhibitor of metalloproteinases-1 (TIMP-1). PLoS One (2012) 0.85
Human milk adiponectin is associated with infant growth in two independent cohorts. Breastfeed Med (2009) 0.85
Stability of adolescent body mass index during three years of follow-up. J Pediatr (2007) 0.85
Human milk adiponectin affects infant weight trajectory during the second year of life. J Pediatr Gastroenterol Nutr (2012) 0.84
Stromal-cell-derived factor (SDF) 1-alpha in combination with BMP-2 and TGF-β1 induces site-directed cell homing and osteogenic and chondrogenic differentiation for tissue engineering without the requirement for cell seeding. Cell Tissue Res (2012) 0.84
Risk factors for breast cancer in postmenopausal Caucasian and Chinese-Canadian women. Breast Cancer Res (2010) 0.84
Genetic variation in small proline rich protein 2B as a predictor for asthma among children with eczema. Ann Allergy Asthma Immunol (2012) 0.83
Peers and peer-based interventions in supporting reintegration and mental health among National Guard soldiers: a qualitative study. Mil Med (2012) 0.83
A genome-wide linkage study of mammographic density, a risk factor for breast cancer. Breast Cancer Res (2011) 0.83
Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol. Am J Med Genet A (2009) 0.82
Intergenerational genomic DNA methylation patterns in mouse hybrid strains. Genome Biol (2014) 0.82
Comparison of false-discovery rate for genome-wide and fine mapping regions. BMC Proc (2007) 0.81
The impact of psychiatric disorders on employment: results from a national survey (NESARC). Community Ment Health J (2012) 0.81
High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxia. Am J Med Genet A (2009) 0.80
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
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
Disruption of the aortic elastic lamina and medial calcification share genetic determinants in mice. Circ Cardiovasc Genet (2009) 0.80
Genetics and outcomes after traumatic brain injury (TBI): what do we know about pediatric TBI? J Pediatr Rehabil Med (2012) 0.79
Food, beverage, and macronutrient intakes in postmenopausal Caucasian and Chinese-Canadian women. Nutr Cancer (2011) 0.79
Evaluation of growth in patients with isolated cleft lip and/or cleft palate. Pediatrics (2010) 0.79
Response to Pomozi et al's research commentary. Circ Res (2013) 0.79
The role of different methods of nerve ablation in prevention of neuroma. Plast Reconstr Surg (2013) 0.79
Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromes. J Pediatr Gastroenterol Nutr (2014) 0.79
IGF receptor gene variants in normal adolescents: effect on stature. Eur J Endocrinol (2012) 0.79
Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes. Springerplus (2012) 0.78
Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach. BMC Proc (2011) 0.78
A locus on chromosome 10 influences C-reactive protein levels in two independent populations. Hum Genet (2007) 0.78
HDL cholesterol in females in the Framingham Heart Study is linked to a region of chromosome 2q. BMC Genet (2003) 0.78
Family- and population-based designs identify different rare causal variants. BMC Proc (2011) 0.77
Complex story of the genetic origins of pediatric heart disease. Circulation (2010) 0.77
Fractures in children with neurofibromatosis type 1 from two NF clinics. Am J Med Genet A (2013) 0.77
Codeine-related adverse drug reactions in children following tonsillectomy: a prospective study. Laryngoscope (2013) 0.77
Adiponectin receptor 1 variants associated with lower insulin resistance in African Americans. Obesity (Silver Spring) (2007) 0.77