Published in PLoS Genet on June 24, 2010
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet (2011) 5.01
From patients to partners: participant-centric initiatives in biomedical research. Nat Rev Genet (2012) 3.44
Crowdsourced health research studies: an important emerging complement to clinical trials in the public health research ecosystem. J Med Internet Res (2012) 2.01
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. Nat Genet (2013) 1.85
The missense of smell: functional variability in the human odorant receptor repertoire. Nat Neurosci (2013) 1.79
A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell (2013) 1.75
Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia. PLoS Genet (2013) 1.68
Efficient replication of over 180 genetic associations with self-reported medical data. PLoS One (2011) 1.65
Genetic variation in the odorant receptor OR2J3 is associated with the ability to detect the "grassy" smelling odor, cis-3-hexen-1-ol. Chem Senses (2012) 1.63
Direct-to-consumer genomics reinvents itself. Nat Biotechnol (2012) 1.63
Direct-to-consumer personalized genomic testing. Hum Mol Genet (2011) 1.61
The genetic ancestry of African Americans, Latinos, and European Americans across the United States. Am J Hum Genet (2014) 1.61
Sensitivity of genome-wide-association signals to phenotyping strategy: the PROP-TAS2R38 taste association as a benchmark. PLoS One (2011) 1.56
Public knowledge of and attitudes toward genetics and genetic testing. Genet Test Mol Biomarkers (2013) 1.52
Novel associations for hypothyroidism include known autoimmune risk loci. PLoS One (2012) 1.50
Population structure, migration, and diversifying selection in the Netherlands. Eur J Hum Genet (2013) 1.47
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. Nat Genet (2016) 1.47
Adapting standards: ethical oversight of participant-led health research. PLoS Med (2013) 1.43
Tales the double helix tells. Investig Genet (2010) 1.39
Research conducted using data obtained through online communities: ethical implications of methodological limitations. PLoS Med (2012) 1.35
eMERGEing progress in genomics-the first seven years. Front Genet (2014) 1.30
Personalized investigation. Nat Med (2010) 1.29
Evidence for archaic adaptive introgression in humans. Nat Rev Genet (2015) 1.28
Consent and internet-enabled human genomics. PLoS Genet (2010) 1.28
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. Age (Dordr) (2011) 1.26
Genetic variants associated with breast size also influence breast cancer risk. BMC Med Genet (2012) 1.26
Replicability and robustness of genome-wide-association studies for behavioral traits. Psychol Sci (2014) 1.18
Dispositional optimism. Trends Cogn Sci (2014) 1.17
PCSK6 is associated with handedness in individuals with dyslexia. Hum Mol Genet (2010) 1.14
A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Nat Commun (2016) 1.13
Human pigmentation genes under environmental selection. Genome Biol (2012) 1.11
Saturation of the human phenome. Curr Genomics (2010) 1.09
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. PLoS One (2012) 1.07
Exposome informatics: considerations for the design of future biomedical research information systems. J Am Med Inform Assoc (2013) 1.07
Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies. Ann N Y Acad Sci (2013) 1.05
Translational bioinformatics: linking the molecular world to the clinical world. Clin Pharmacol Ther (2012) 1.05
Excretion and perception of a characteristic odor in urine after asparagus ingestion: a psychophysical and genetic study. Chem Senses (2010) 1.04
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. Nat Commun (2016) 1.04
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Am J Hum Genet (2011) 1.01
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma. J Invest Dermatol (2016) 1.01
Exploring signatures of positive selection in pigmentation candidate genes in populations of East Asian ancestry. BMC Evol Biol (2013) 0.99
Do polymorphisms in chemosensory genes matter for human ingestive behavior? Food Qual Prefer (2013) 0.97
An olfactory demography of a diverse metropolitan population. BMC Neurosci (2012) 0.96
Genetics of taste and smell: poisons and pleasures. Prog Mol Biol Transl Sci (2010) 0.95
Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans. Hum Genet (2012) 0.95
openSNP--a crowdsourced web resource for personal genomics. PLoS One (2014) 0.95
2010 translational bioinformatics year in review. J Am Med Inform Assoc (2011) 0.94
Left brain, right brain: facts and fantasies. PLoS Biol (2014) 0.94
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. Hum Mol Genet (2016) 0.94
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS Genet (2013) 0.94
Physical and neurobehavioral determinants of reproductive onset and success. Nat Genet (2016) 0.94
The gustatory and olfactory systems during infancy: implications for development of feeding behaviors in the high-risk neonate. Clin Perinatol (2011) 0.93
Just the facts, please. Nat Biotechnol (2013) 0.93
A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots. J Invest Dermatol (2015) 0.93
Unravelling the human genome-phenome relationship using phenome-wide association studies. Nat Rev Genet (2016) 0.92
Computationally translating molecular discoveries into tools for medicine: translational bioinformatics articles now featured in JAMIA. J Am Med Inform Assoc (2011) 0.92
Customers or research participants? Guidance for research practices in commercialization of personal genomics. Genet Med (2012) 0.91
Genetic analysis of chemosensory traits in human twins. Chem Senses (2012) 0.91
A genome-wide association study of brain lesion distribution in multiple sclerosis. Brain (2013) 0.90
Escape from crossover interference increases with maternal age. Nat Commun (2015) 0.90
The genetic relationship between handedness and neurodevelopmental disorders. Trends Mol Med (2013) 0.89
Exome sequencing of only seven Qataris identifies potentially deleterious variants in the Qatari population. PLoS One (2012) 0.89
Rare coding variants and X-linked loci associated with age at menarche. Nat Commun (2015) 0.87
Why it is hard to find genes associated with social science traits: theoretical and empirical considerations. Am J Public Health (2013) 0.87
Reading and language disorders: the importance of both quantity and quality. Genes (Basel) (2014) 0.86
Nucleic acid detection with CRISPR-Cas13a/C2c2. Science (2017) 0.85
A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults. Biol Psychiatry (2015) 0.85
A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia. Nat Commun (2015) 0.85
Systems biology of asthma and allergic diseases: a multiscale approach. J Allergy Clin Immunol (2014) 0.84
Genetic self knowledge and the future of epidemiologic confounding. Am J Hum Genet (2010) 0.84
Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease. Public Health Genomics (2014) 0.84
A genome-wide study on the perception of the odorants androstenone and galaxolide. Chem Senses (2012) 0.83
Surveillance of Acute Respiratory Infections Using Community-Submitted Symptoms and Specimens for Molecular Diagnostic Testing. PLoS Curr (2015) 0.83
Genetic contributions to intergroup responses: a cautionary perspective. Front Hum Neurosci (2012) 0.82
Phenotype prediction from genome-wide association studies: application to smoking behaviors. BMC Syst Biol (2012) 0.81
A Functional Interleukin-18 Haplotype Predicts Depression and Anxiety through Increased Threat-Related Amygdala Reactivity in Women but Not Men. Neuropsychopharmacology (2016) 0.80
Convergent effects of mouse Pet-1 deletion and human PET-1 variation on amygdala fear and threat processing. Exp Neurol (2013) 0.80
Mammalian odorant receptors: functional evolution and variation. Curr Opin Neurobiol (2015) 0.80
Effectiveness of a web-based protocol for the screening and phenotyping of individuals with Tourette syndrome for genetic studies. Am J Med Genet B Neuropsychiatr Genet (2012) 0.80
Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralization. J Neurosci (2015) 0.79
Neurogenethics: An emerging discipline at the intersection of ethics, neuroscience, and genomics. Appl Transl Genom (2015) 0.79
Basal forebrain moderates the magnitude of task-dependent amygdala functional connectivity. Soc Cogn Affect Neurosci (2014) 0.79
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. Hum Mol Genet (2015) 0.79
Genetic basis of olfactory cognition: extremely high level of DNA sequence polymorphism in promoter regions of the human olfactory receptor genes revealed using the 1000 Genomes Project dataset. Front Psychol (2014) 0.79
Disentangling public participation in science and biomedicine. Genome Med (2014) 0.78
Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data. J Data Mining Genomics Proteomics (2013) 0.78
Allelic frequencies of 20 visible phenotype variants in the korean population. Genomics Inform (2013) 0.78
Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes. Hum Mol Genet (2015) 0.78
Estimating the Ages of Selection Signals from Different Epochs in Human History. Mol Biol Evol (2015) 0.77
Olfactory receptor genes cooperate with protocadherin genes in human extreme obesity. Genes Nutr (2015) 0.77
Evolutionary triangulation: informing genetic association studies with evolutionary evidence. BioData Min (2016) 0.77
Case-control association mapping by proxy using family history of disease. Nat Genet (2017) 0.76
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Genes (Basel) (2015) 0.76
Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma. Nat Commun (2016) 0.76
Genetically predicted milk consumption and bone health, ischemic heart disease and type 2 diabetes: a Mendelian randomization study. Eur J Clin Nutr (2017) 0.76
Sniffing out significant "Pee values": genome wide association study of asparagus anosmia. BMJ (2016) 0.75
Clinical and Genetic Factors Associated with Cutaneous Squamous Cell Carcinoma in Kidney and Heart Transplant Recipients. Transplant Direct (2015) 0.75
Genetic ancestry inference using support vector machines, and the active emergence of a unique American population. Eur J Hum Genet (2012) 0.75
Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries. Elife (2017) 0.75
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Hum Mol Genet (2017) 0.75
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature (2007) 144.95
Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet (2006) 115.71
A haplotype map of the human genome. Nature (2005) 105.70
Statistical significance for genomewide studies. Proc Natl Acad Sci U S A (2003) 88.64
Genomic control for association studies. Biometrics (1999) 64.39
Global variation in copy number in the human genome. Nature (2006) 57.50
Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet (2005) 25.34
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet (2007) 24.68
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet (1999) 22.84
A note on exact tests of Hardy-Weinberg equilibrium. Am J Hum Genet (2005) 18.98
Imputation-based analysis of association studies: candidate regions and quantitative traits. PLoS Genet (2007) 15.55
A human genome diversity cell line panel. Science (2002) 14.11
Why most discovered true associations are inflated. Epidemiology (2008) 11.22
Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet (2007) 8.79
Practical issues in imputation-based association mapping. PLoS Genet (2008) 6.76
The fine-scale and complex architecture of human copy-number variation. Am J Hum Genet (2008) 5.08
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet (1995) 4.97
A classification of hand preference by association analysis. Br J Psychol (1970) 4.68
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. PLoS Genet (2008) 4.57
Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis. Mech Dev (2001) 3.52
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry (2007) 3.49
Two newly identified genetic determinants of pigmentation in Europeans. Nat Genet (2008) 3.31
Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet (2009) 3.18
ACTN3 genotype is associated with human elite athletic performance. Am J Hum Genet (2003) 3.12
The human olfactory receptor gene family. Proc Natl Acad Sci U S A (2004) 2.74
SNEEZING IN RESPONSE TO LIGHT. Neurology (1964) 2.50
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. Am J Hum Genet (2006) 2.14
Molecular genetics of human pigmentation diversity. Hum Mol Genet (2009) 2.03
A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness. Hum Mol Genet (2007) 1.96
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Am J Hum Genet (2007) 1.82
Ectodermal dysplasias associated with clefting: significance of scalp dermatitis. J Am Acad Dermatol (1992) 1.63
S100A11, S100A10, annexin I, desmosomal proteins, small proline-rich proteins, plasminogen activator inhibitor-2, and involucrin are components of the cornified envelope of cultured human epidermal keratinocytes. J Biol Chem (1997) 1.63
A polymorphism of the ability to smell urinary metabolites of asparagus. Br Med J (1981) 1.58
Autosomal dominant transmission of the "photic sneeze reflex". N Engl J Med (1984) 1.28
Trichohyalin mechanically strengthens the hair follicle: multiple cross-bridging roles in the inner root shealth. J Biol Chem (2003) 1.25
Mouse coat color mutations: from fancy mice to functional genomics. Dev Dyn (2006) 1.22
Isolation and characterization of human repetin, a member of the fused gene family of the epidermal differentiation complex. J Invest Dermatol (2005) 1.17
Identification of Basonuclin2, a DNA-binding zinc-finger protein expressed in germ tissues and skin keratinocytes. Genomics (2004) 1.17
Trichohyalin, an intermediate filament-associated protein of the hair follicle. J Cell Biol (1986) 1.16
Phenotypic effects of genetic variability in human clock genes on circadian and sleep parameters. J Genet (2008) 1.15
Food idiosyncrasies: beetroot and asparagus. Drug Metab Dispos (2001) 1.14
Basonuclins 1 and 2, whose genes share a common origin, are proteins with widely different properties and functions. Proc Natl Acad Sci U S A (2006) 1.11
Abnormal development of the locus coeruleus in Ear2(Nr2f6)-deficient mice impairs the functionality of the forebrain clock and affects nociception. Genes Dev (2005) 1.10
Active inhibition of plasma cell development in resting B cells by microphthalmia-associated transcription factor. J Exp Med (2004) 1.10
Mapping of three translocation breakpoints associated with orofacial clefting within 6p24 and identification of new transcripts within the region. Cytogenet Genome Res (2004) 1.06
Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice. J Neurosci Res (2010) 1.06
Heterodimeric interactions between chicken ovalbumin upstream promoter-transcription factor family members ARP1 and ear2. J Biol Chem (1999) 0.95
Human hair shape is programmed from the bulb. Br J Dermatol (2005) 0.93
Odorous urine following asparagus ingestion in man. Experientia (1987) 0.89
On light-induced sneezing. Eye (Lond) (2009) 0.85
Paper chromatography of human hair follicles and hair extracts. Br J Dermatol (1960) 0.84
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Efficiency and power in genetic association studies. Nat Genet (2005) 25.56
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
High-throughput droplet digital PCR system for absolute quantitation of DNA copy number. Anal Chem (2011) 10.11
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Nat Genet (2007) 8.74
Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature (2009) 8.12
De novo mutations in histone-modifying genes in congenital heart disease. Nature (2013) 5.15
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet (2011) 5.01
Whole population, genome-wide mapping of hidden relatedness. Genome Res (2008) 4.72
Caenorhabditis elegans mutant allele identification by whole-genome sequencing. Nat Methods (2008) 4.71
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry (2011) 4.29
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. PLoS Genet (2012) 4.27
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. Nat Genet (2009) 4.11
Pervasive hitchhiking at coding and regulatory sites in humans. PLoS Genet (2009) 4.02
Optimal two-stage genotyping designs for genome-wide association scans. Genet Epidemiol (2006) 3.41
A structural EM algorithm for phylogenetic inference. J Comput Biol (2002) 2.67
Pesticide resistance via transposition-mediated adaptive gene truncation in Drosophila. Science (2005) 2.56
Integrative eQTL-based analyses reveal the biology of breast cancer risk loci. Cell (2013) 2.56
Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. Am J Hum Genet (2010) 2.54
Comparing platforms for C. elegans mutant identification using high-throughput whole-genome sequencing. PLoS One (2008) 2.24
Overlapping pools for high-throughput targeted resequencing. Genome Res (2009) 2.11
Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia. Nat Genet (2006) 2.07
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. PLoS Genet (2009) 2.02
Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles. Gastroenterology (2011) 2.01
Length distributions of identity by descent reveal fine-scale demographic history. Am J Hum Genet (2012) 1.91
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. Nat Genet (2013) 1.85
The genetic prehistory of southern Africa. Nat Commun (2012) 1.78
Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia. PLoS Genet (2013) 1.68
Efficient replication of over 180 genetic associations with self-reported medical data. PLoS One (2011) 1.65
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arterioscler Thromb Vasc Biol (2008) 1.63
DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Am J Hum Genet (2011) 1.62
Cryptic distant relatives are common in both isolated and cosmopolitan genetic samples. PLoS One (2012) 1.55
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. PLoS Genet (2012) 1.52
High rate of recent transposable element-induced adaptation in Drosophila melanogaster. PLoS Biol (2008) 1.52
Regularities of context-dependent codon bias in eukaryotic genes. Nucleic Acids Res (2002) 1.50
The architecture of long-range haplotypes shared within and across populations. Mol Biol Evol (2011) 1.50
Novel associations for hypothyroidism include known autoimmune risk loci. PLoS One (2012) 1.50
Ultrafast genome-wide scan for SNP-SNP interactions in common complex disease. Genome Res (2012) 1.45
High-resolution analysis of copy number alterations and associated expression changes in ovarian tumors. BMC Med Genomics (2009) 1.33
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiol Aging (2014) 1.32
Droplet Digital™ PCR quantitation of HER2 expression in FFPE breast cancer samples. Methods (2012) 1.26
Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing. PeerJ (2013) 1.26
Genetic variants associated with breast size also influence breast cancer risk. BMC Med Genet (2012) 1.26
The ethics of characterizing difference: guiding principles on using racial categories in human genetics. Genome Biol (2008) 1.26
A long-term three dimensional liver co-culture system for improved prediction of clinically relevant drug-induced hepatotoxicity. Toxicol Appl Pharmacol (2013) 1.25
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Nat Commun (2013) 1.25
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs. Pharmacogenet Genomics (2012) 1.21
Dazl functions in maintenance of pluripotency and genetic and epigenetic programs of differentiation in mouse primordial germ cells in vivo and in vitro. PLoS One (2009) 1.19
The Groucho ortholog UNC-37 interacts with the short Groucho-like protein LSY-22 to control developmental decisions in C. elegans. Development (2010) 1.18
Similar levels of X-linked and autosomal nucleotide variation in African and non-African populations of Drosophila melanogaster. BMC Evol Biol (2007) 1.15
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet (2012) 1.14
eBLOCKs: enumerating conserved protein blocks to achieve maximal sensitivity and specificity. Nucleic Acids Res (2005) 1.14
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae. Proc Natl Acad Sci U S A (2009) 1.13
A branch-and-bound algorithm for the inference of ancestral amino-acid sequences when the replacement rate varies among sites: Application to the evolution of five gene families. Bioinformatics (2002) 1.11
A spatially explicit nanomechanical model of the half-sarcomere: myofilament compliance affects Ca(2+)-activation. Ann Biomed Eng (2004) 1.08
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Genome Biol (2012) 1.08
North African Jewish and non-Jewish populations form distinctive, orthogonal clusters. Proc Natl Acad Sci U S A (2012) 1.05
Allelic selection of amplicons in glioblastoma revealed by combining somatic and germline analysis. PLoS Genet (2010) 1.02
Race and ethnicity in genetic research. Am J Med Genet A (2007) 1.01
GeneHub-GEPIS: digital expression profiling for normal and cancer tissues based on an integrated gene database. Nucleic Acids Res (2007) 1.00
Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum Mol Genet (2010) 0.98
HLA type inference via haplotypes identical by descent. J Comput Biol (2011) 0.98
A pragmatic consideration of ethical issues relating to personal genomics. Am J Bioeth (2009) 0.95
The variance of identity-by-descent sharing in the Wright-Fisher model. Genetics (2012) 0.95
Calling amplified haplotypes in next generation tumor sequence data. Genome Res (2011) 0.95
Detecting identity by descent and homozygosity mapping in whole-exome sequencing data. PLoS One (2012) 0.95
Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin Embedded Tumors with Droplet Digital PCR. Transl Med (Sunnyvale) (2012) 0.93
A recent adaptive transposable element insertion near highly conserved developmental loci in Drosophila melanogaster. Mol Biol Evol (2009) 0.92
Power to detect selective allelic amplification in genome-wide scans of tumor data. Bioinformatics (2009) 0.91
Inference of historical migration rates via haplotype sharing. Bioinformatics (2013) 0.87
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. J Invest Dermatol (2013) 0.85
Inference of modules associated to eQTLs. Nucleic Acids Res (2012) 0.85
Inferring the strength of selection in Drosophila under complex demographic models. Mol Biol Evol (2008) 0.85
MutaGeneSys: estimating individual disease susceptibility based on genome-wide SNP array data. Bioinformatics (2007) 0.84
Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers. Pharmacogenet Genomics (2007) 0.84
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information. Eur J Hum Genet (2009) 0.83
Coverage tradeoffs and power estimation in the design of whole-genome sequencing experiments for detecting association. Bioinformatics (2011) 0.81
Variants in exons and in transcription factors affect gene expression in trans. Genome Biol (2013) 0.80
MetaSeq: privacy preserving meta-analysis of sequencing-based association studies. Pac Symp Biocomput (2013) 0.79
A hidden Markov model for copy number variant prediction from whole genome resequencing data. BMC Bioinformatics (2011) 0.79
Trick or treat: the effect of placebo on the power of pharmacogenetic association studies. Hum Genomics (2005) 0.78
Erratum: Detection and interpretation of shared genetic influences on 42 human traits. Nat Genet (2016) 0.77
Computational problems in perfect phylogeny haplotyping: typing without calling the allele. IEEE/ACM Trans Comput Biol Bioinform (2008) 0.77
Correction: Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding. PLoS Genet (2016) 0.75
On the applicability of a haplotype map to un-assayed populations. Hum Genet (2003) 0.75
Typing without calling the allele: a strategy for inferring SNP haplotypes. Eur J Hum Genet (2005) 0.75
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun (2015) 0.75
Longitudinal study shows increasing obesity and hyperglycemia in micronesia. Obesity (Silver Spring) (2013) 0.75