Published in Am J Hum Genet on March 23, 2005
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
A haplotype map of the human genome. Nature (2005) 105.70
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet (2007) 14.99
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet (2007) 12.62
Pathway-based approaches for analysis of genomewide association studies. Am J Hum Genet (2007) 12.27
Proportionally more deleterious genetic variation in European than in African populations. Nature (2008) 6.61
Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am J Hum Genet (2009) 5.65
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet (2009) 5.14
Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience (2015) 5.06
Web-based, participant-driven studies yield novel genetic associations for common traits. PLoS Genet (2010) 5.02
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet (2011) 5.01
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration. Nat Genet (2006) 4.51
Genomewide association for schizophrenia in the CATIE study: results of stage 1. Mol Psychiatry (2008) 4.14
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet (2010) 3.93
Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Mol Psychiatry (2008) 3.85
Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans. Kidney Int (2009) 3.58
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. Proc Natl Acad Sci U S A (2007) 3.50
The relationship of DNA methylation with age, gender and genotype in twins and healthy controls. PLoS One (2009) 3.41
The role of geography in human adaptation. PLoS Genet (2009) 3.41
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet Neurol (2007) 2.99
Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD. Nephrol Dial Transplant (2009) 2.88
Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Lancet Oncol (2011) 2.85
Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women. PLoS Genet (2008) 2.85
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Nat Genet (2010) 2.81
Tracking footprints of artificial selection in the dog genome. Proc Natl Acad Sci U S A (2010) 2.53
An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28. J Cereb Blood Flow Metab (2011) 2.52
A high-density screen for linkage in multiple sclerosis. Am J Hum Genet (2005) 2.50
Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs. J Appl Physiol (1985) (2010) 2.43
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. Nat Genet (2010) 2.34
Genome-wide association scan for five major dimensions of personality. Mol Psychiatry (2008) 2.29
The strength of selection on ultraconserved elements in the human genome. Am J Hum Genet (2007) 2.21
Polymorphisms of the IL12B and IL23R genes are associated with psoriasis. J Invest Dermatol (2008) 2.20
Genetic basis for adverse events after smallpox vaccination. J Infect Dis (2008) 2.09
The genome response to artificial selection: a case study in dairy cattle. PLoS One (2009) 2.08
Independent susceptibility markers for atrial fibrillation on chromosome 4q25. Circulation (2010) 1.90
Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication. Circ Cardiovasc Genet (2008) 1.89
Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. Genome Res (2010) 1.87
Detecting false-positive signals in exome sequencing. Hum Mutat (2012) 1.87
Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet (2010) 1.86
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genet Med (2015) 1.84
A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity. Clin Pharmacol Ther (2013) 1.80
Unlocking the vault: next-generation museum population genomics. Mol Ecol (2013) 1.77
Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies. Genet Epidemiol (2009) 1.76
Gemcitabine and arabinosylcytosin pharmacogenomics: genome-wide association and drug response biomarkers. PLoS One (2009) 1.75
Extracellular superoxide dismutase haplotypes are associated with acute lung injury and mortality. Am J Respir Crit Care Med (2008) 1.73
Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study. Circ Cardiovasc Genet (2009) 1.71
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study. PLoS Genet (2008) 1.67
Linkage disequilibrium in related breeding lines of chickens. Genetics (2007) 1.66
A whole genome Bayesian scan for adaptive genetic divergence in West African cattle. BMC Genomics (2009) 1.65
Associations between CYP2B6 polymorphisms and pharmacokinetics after a single dose of nevirapine or efavirenz in African americans. J Infect Dis (2009) 1.63
optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants. Bioinformatics (2012) 1.62
Commercially available outbred mice for genome-wide association studies. PLoS Genet (2010) 1.58
IGF-I and IGFBP-3 polymorphisms in relation to circulating levels among African American and Caucasian women. Cancer Epidemiol Biomarkers Prev (2009) 1.58
Association of genetic ancestry with preterm delivery and related traits among African American mothers. Am J Obstet Gynecol (2009) 1.56
Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping. BMC Genet (2008) 1.53
Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Gut (2013) 1.51
Insights into the genetic history of French cattle from dense SNP data on 47 worldwide breeds. PLoS One (2010) 1.51
Exact tests of Hardy-Weinberg equilibrium and homogeneity of disequilibrium across strata. Am J Hum Genet (2006) 1.50
Novel associations for hypothyroidism include known autoimmune risk loci. PLoS One (2012) 1.50
A high density linkage map of the bovine genome. BMC Genet (2009) 1.49
Association study of GSK3 gene polymorphisms with schizophrenia and clozapine response. Psychopharmacology (Berl) (2008) 1.46
Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin. Hum Genet (2007) 1.45
Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. Mol Psychiatry (2009) 1.44
Distributions of Hardy-Weinberg equilibrium test statistics. Genetics (2008) 1.43
Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative. Genet Epidemiol (2012) 1.42
A time transect of exomes from a Native American population before and after European contact. Nat Commun (2016) 1.41
Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response. Mol Psychiatry (2008) 1.38
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet (2010) 1.37
The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study. PLoS Med (2011) 1.36
POPULATION GENETICS. Genomic evidence for the Pleistocene and recent population history of Native Americans. Science (2015) 1.33
Genetic variation predicting cisplatin cytotoxicity associated with overall survival in lung cancer patients receiving platinum-based chemotherapy. Clin Cancer Res (2011) 1.32
Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes (2010) 1.30
Signatures of diversifying selection in European pig breeds. PLoS Genet (2013) 1.30
Genotoxic effects in swimmers exposed to disinfection by-products in indoor swimming pools. Environ Health Perspect (2010) 1.29
Progesterone receptor polymorphisms and clinical response to 17-alpha-hydroxyprogesterone caproate. Am J Obstet Gynecol (2011) 1.28
Genetic variants associated with breast size also influence breast cancer risk. BMC Med Genet (2012) 1.26
Distribution and clinical correlates of viral and host genotypes in Chinese patients with chronic hepatitis C virus infection. J Gastroenterol Hepatol (2014) 1.23
Variant association tools for quality control and analysis of large-scale sequence and genotyping array data. Am J Hum Genet (2014) 1.21
Association of FKBP5 polymorphisms with suicidal events in the Treatment of Resistant Depression in Adolescents (TORDIA) study. Am J Psychiatry (2009) 1.21
C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene. J Infect Dis (2011) 1.21
Maternal cigarette smoking, metabolic gene polymorphisms, and preterm delivery: new insights on GxE interactions and pathogenic pathways. Hum Genet (2008) 1.20
Traffic-related air pollution, oxidative stress genes, and asthma (ECHRS). Environ Health Perspect (2009) 1.18
Bayesian methods for examining Hardy-Weinberg equilibrium. Biometrics (2009) 1.17
Phenotypic and genetic variation in leptin as determinants of weight regain. Int J Obes (Lond) (2010) 1.14
Ethnicity-specific pharmacogenetics: the case of warfarin in African Americans. Pharmacogenomics J (2013) 1.14
Influence of CYP2B6 polymorphisms on the persistence of plasma nevirapine concentrations following a single intra-partum dose for the prevention of mother to child transmission in HIV-infected Thai women. J Antimicrob Chemother (2009) 1.14
Identification of single nucleotide polymorphisms in the p21 (CDKN1A) gene and correlations with longevity in the Italian population. Aging (Albany NY) (2009) 1.13
A test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in cases. Am J Hum Genet (2008) 1.12
Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10. J Appl Toxicol (2010) 1.11
The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans. Hum Genet (2009) 1.11
Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1. Genome Med (2013) 1.11
Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. Genomics (2008) 1.10
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. PLoS Genet (2011) 1.10
Loss of function of transient receptor potential vanilloid 1 (TRPV1) genetic variant is associated with lower risk of active childhood asthma. J Biol Chem (2010) 1.08
Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry. Prostate (2009) 1.08
WIDDE: a Web-Interfaced next generation database for genetic diversity exploration, with a first application in cattle. BMC Genomics (2015) 1.07
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. Am J Hum Genet (2008) 1.07
A model-based approach for identifying signatures of ancient balancing selection in genetic data. PLoS Genet (2014) 1.07
Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility. Blood (2009) 1.06
The International HapMap Project. Nature (2003) 73.65
MENDELIAN PROPORTIONS IN A MIXED POPULATION. Science (1908) 60.99
Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics (1992) 21.26
Methods for genotyping single nucleotide polymorphisms. Annu Rev Genomics Hum Genet (2001) 5.79
Using haplotype blocks to map human complex trait loci. Trends Genet (2003) 4.61
A disequilibrium coefficient approach to Hardy-Weinberg testing. Biometrics (1989) 4.04
Genotyping for human whole-genome scans: past, present, and future. Adv Genet (2001) 3.80
Eighty years ago: the beginnings of population genetics. Genetics (1988) 3.22
Tests for establishing compatibility of an observed genotype distribution with Hardy-Weinberg equilibrium in the case of a biallelic locus. Biometrics (2004) 2.74
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
An integrated map of genetic variation from 1,092 human genomes. Nature (2012) 59.82
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet (2008) 15.94
A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet (2006) 12.45
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Family-based association tests for genomewide association scans. Am J Hum Genet (2007) 10.67
Microarray-based genomic selection for high-throughput resequencing. Nat Methods (2007) 9.62
Haplotype inference in random population samples. Am J Hum Genet (2002) 8.07
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies. Nat Genet (2004) 5.78
Synaptic, transcriptional and chromatin genes disrupted in autism. Nature (2014) 5.30
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet (2008) 5.28
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature (2005) 4.92
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet (2014) 4.13
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat Genet (2012) 4.13
Genomic alterations in cultured human embryonic stem cells. Nat Genet (2005) 3.89
Genetic loci influencing kidney function and chronic kidney disease. Nat Genet (2010) 3.75
Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal. Am J Hum Genet (2005) 3.62
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet (2011) 3.46
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet (2011) 3.40
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet (2013) 3.25
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat Genet (2011) 3.18
Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet (2013) 2.92
FTO genotype is associated with phenotypic variability of body mass index. Nature (2012) 2.77
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. Am J Hum Genet (2003) 2.51
Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arrays. Genome Res (2004) 2.47
Microdeletions of 3q29 confer high risk for schizophrenia. Am J Hum Genet (2010) 2.38
Meta-analysis of genome scans of age-related macular degeneration. Hum Mol Genet (2005) 2.34
Global gene expression analysis reveals evidence for decreased lipid biosynthesis and increased innate immunity in uninvolved psoriatic skin. J Invest Dermatol (2009) 2.06
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus. Hum Mol Genet (2003) 1.87
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. Am J Hum Genet (2009) 1.87
A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. Genome Res (2013) 1.72
Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics (2004) 1.72
A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One (2012) 1.72
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology (2006) 1.71
Haplotype and missing data inference in nuclear families. Genome Res (2004) 1.69
Amelioration of Sardinian beta0 thalassemia by genetic modifiers. Blood (2009) 1.62
Microarray-based resequencing of multiple Bacillus anthracis isolates. Genome Biol (2004) 1.61
Assessment of the psoriatic transcriptome in a large sample: additional regulated genes and comparisons with in vitro models. J Invest Dermatol (2010) 1.61
Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. Genome Biol (2008) 1.61
Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.60
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa. Am J Hum Genet (2009) 1.52
Population bottlenecks as a potential major shaping force of human genome architecture. PLoS Genet (2007) 1.47
An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome. J Mol Diagn (2006) 1.40
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nat Genet (2013) 1.39
SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics (2010) 1.36
Aberrant gating of photic input to the suprachiasmatic circadian pacemaker of mice lacking the VPAC2 receptor. J Neurosci (2004) 1.30
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Hum Mol Genet (2013) 1.23
Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies. Am J Hum Genet (2007) 1.23
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. Am J Epidemiol (2011) 1.19
Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies. Hum Mutat (2011) 1.17
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males. Am J Med Genet A (2010) 1.16
Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis. Hum Mol Genet (2008) 1.12
Autosomal recessive causes likely in early-onset Alzheimer disease. Arch Neurol (2011) 1.08
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease. Circ Res (2017) 1.06
Targeted sequencing of the human X chromosome exome. Genomics (2011) 1.06
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. PLoS One (2011) 1.05
Analysis of long non-coding RNAs highlights tissue-specific expression patterns and epigenetic profiles in normal and psoriatic skin. Genome Biol (2015) 1.03
On the probability that a novel variant is a disease-causing mutation. Genome Res (2005) 1.02
What is a suitable dissolution method for drug nanoparticles? Pharm Res (2008) 1.01
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biol (2014) 0.98
Pharmacokinetic parameter prediction from drug structure using artificial neural networks. Int J Pharm (2004) 0.95
QPLOT: a quality assessment tool for next generation sequencing data. Biomed Res Int (2013) 0.95
Regression-based sib pair linkage analysis for binary traits. Hum Hered (2003) 0.95
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLoS One (2010) 0.93
Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci. Arthritis Rheum (2013) 0.93
Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease. J Pediatr Gastroenterol Nutr (2014) 0.92
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase. Hum Mol Genet (2009) 0.92
The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry. PLoS One (2011) 0.91
Mometasone furoate degradation and metabolism in human biological fluids and tissues. Biopharm Drug Dispos (2003) 0.90
Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse. G3 (Bethesda) (2012) 0.88
Population genetics identifies challenges in analyzing rare variants. Genet Epidemiol (2015) 0.87
Population demographic history can cause the appearance of recombination hotspots. Am J Hum Genet (2012) 0.87
Empirical evaluation of oligonucleotide probe selection for DNA microarrays. PLoS One (2010) 0.84
Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder. Hum Mol Genet (2012) 0.83
Genistein cooperates with the histone deacetylase inhibitor vorinostat to induce cell death in prostate cancer cells. BMC Cancer (2012) 0.82
Microarray oligonucleotide probe designer (MOPeD): A web service. Open Access Bioinformatics (2010) 0.81
Simultaneous neutron scattering and Raman scattering. Appl Spectrosc (2009) 0.80
Variation in the lymphotoxin-alpha/tumor necrosis factor locus modifies risk of erythema nodosum in sarcoidosis. J Invest Dermatol (2009) 0.80
A model of binding on DNA microarrays: understanding the combined effect of probe synthesis failure, cross-hybridization, DNA fragmentation and other experimental details of affymetrix arrays. BMC Genomics (2012) 0.79
Paraoxonase-1 polymorphisms in Alzheimer's disease, Parkinson's disease, and AD-PD spectrum diseases. Neurobiol Aging (2010) 0.79
Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. Eur J Hum Genet (2012) 0.79
Association study of serotonin pathway genes in attempted suicide. Am J Med Genet B Neuropsychiatr Genet (2011) 0.79
Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture. Inflamm Bowel Dis (2012) 0.79
Multiple pharmacokinetic parameter prediction for a series of cephalosporins. J Pharm Sci (2003) 0.76
Enhanced genetic maps from family-based disease studies: population-specific comparisons. BMC Med Genet (2011) 0.76
Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression. Am J Med Genet B Neuropsychiatr Genet (2007) 0.76
A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic Galactosemia. JIMD Rep (2015) 0.75
A comprehensive search for recombinogenic motifs in the human genome. PLoS One (2013) 0.75
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet (2016) 0.75
Integrating Next-Generation Genomic Sequencing and Mass Spectrometry to Estimate Allele-Specific Protein Abundance in Human Brain. J Proteome Res (2017) 0.75
Dissolution kinetic behavior of drug nanoparticles and their conformity to the diffusion model. Langmuir (2008) 0.75
Focused-ion-beam milling: a novel approach to probing the interior of particles used for inhalation aerosols. Pharm Res (2007) 0.75
Selective descriptor pruning for QSAR/QSPR studies using artificial neural networks. J Comput Chem (2003) 0.75