Published in Hum Hered on January 01, 2002
A powerful strategy to account for multiple testing in the context of haplotype analysis. Am J Hum Genet (2004) 2.07
A comprehensive literature review of haplotyping software and methods for use with unrelated individuals. Hum Genomics (2005) 1.84
Haplotype and missing data inference in nuclear families. Genome Res (2004) 1.69
Entropy-based SNP selection for genetic association studies. Hum Genet (2003) 1.36
The impact of using related individuals for haplotype reconstruction in population studies. Genetics (2005) 1.31
A survey of current software for haplotype phase inference. Hum Genomics (2004) 0.94
Efficacy assessment of SNP sets for genome-wide disease association studies. Nucleic Acids Res (2007) 0.90
A new method for haplotype inference including full-sib information. Genetics (2007) 0.78
A novel tool for individual haplotype inference using mixed data. J Biomed Sci (2009) 0.75
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nat Genet (2009) 3.58
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet (2009) 2.93
Genome association studies of complex diseases by case-control designs. Am J Hum Genet (2003) 2.74
Maximum-likelihood estimation of haplotype frequencies in nuclear families. Genet Epidemiol (2004) 2.59
Complete mitochondrial genome sequence of a Middle Pleistocene cave bear reconstructed from ultrashort DNA fragments. Proc Natl Acad Sci U S A (2013) 2.45
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet (2012) 2.15
A powerful strategy to account for multiple testing in the context of haplotype analysis. Am J Hum Genet (2004) 2.07
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. Am J Hum Genet (2002) 1.99
Direct multiplex sequencing (DMPS)--a novel method for targeted high-throughput sequencing of ancient and highly degraded DNA. Genome Res (2009) 1.69
Withering away--25,000 years of genetic decline preceded cave bear extinction. Mol Biol Evol (2010) 1.35
Haplotype interaction analysis of unlinked regions. Genet Epidemiol (2005) 1.27
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. Genomics (2003) 1.22
Discovery of lost diversity of paternal horse lineages using ancient DNA. Nat Commun (2011) 1.20
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25. Birth Defects Res A Clin Mol Teratol (2010) 0.98
Association of DNA polymorphisms in the synaptic vesicular amine transporter gene (SLC18A2) with alcohol and nicotine dependence. Neuropsychopharmacology (2005) 0.97
Is FKBP5 a genetic marker of affective psychosis? A case control study and analysis of disease related traits. BMC Psychiatry (2006) 0.96
Detection of parent-of-origin effects in nuclear families using haplotype analysis. Hum Hered (2006) 0.95
Influence of climate warming on arctic mammals? New insights from ancient DNA studies of the collared lemming Dicrostonyx torquatus. PLoS One (2010) 0.93
High resolution T association tests of complex diseases based on family data. Ann Hum Genet (2005) 0.93
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci (2009) 0.93
Association of the interleukin-1 receptor antagonist gene with asthma. Am J Respir Crit Care Med (2004) 0.92
Impact of missing genotype data on Monte-Carlo simulation based haplotype analysis. Hum Hered (2005) 0.90
TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate. J Hum Genet (2008) 0.90
Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients. Eur J Oral Sci (2010) 0.89
A rapid medical screening process improves emergency department patient flow during surge associated with novel H1N1 influenza virus. Ann Emerg Med (2010) 0.88
Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central Europe. Cleft Palate Craniofac J (2008) 0.88
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample. Am J Med Genet A (2013) 0.88
Identification of probable genotyping errors by consideration of haplotypes. Eur J Hum Genet (2006) 0.87
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen. Birth Defects Res A Clin Mol Teratol (2014) 0.87
Impact of genotyping errors on type I error rate of the haplotype-sharing transmission/disequilibrium test (HS-TDT). Am J Hum Genet (2004) 0.86
ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies. BMC Psychiatry (2005) 0.86
Inferential testing for linkage with GENEHUNTER-MODSCORE: the impact of the pedigree structure on the null distribution of multipoint MOD scores. Genet Epidemiol (2008) 0.86
On the asymptotic equivalence of allelic and trend statistic under Hardy-Weinberg equilibrium. Ann Hum Genet (2008) 0.86
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Hum Genet (2014) 0.85
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. Am J Med Genet A (2009) 0.85
Family-based study of markers at the 5'-flanking region of the human dopamine transporter gene reveals potential association with schizophrenic psychoses. Eur Arch Psychiatry Clin Neurosci (2006) 0.84
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate. Birth Defects Res A Clin Mol Teratol (2012) 0.83
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci (2009) 0.83
Simultaneous quantification of alpha-tocopherol and four major carotenoids in botanical materials by normal phase liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry. J Chromatogr A (2005) 0.81
Correlation between polymerization shrinkage and marginal fit of temporary crowns. Dent Mater (2008) 0.81
Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia. Schizophr Res (2003) 0.81
Nanoscale spinel LiFeTiO4 for intercalation pseudocapacitive Li(+) storage. Phys Chem Chem Phys (2014) 0.81
Sibship T2 association tests of complex diseases for tightly linked markers. Hum Genomics (2005) 0.80
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway. Birth Defects Res A Clin Mol Teratol (2014) 0.79
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci (2012) 0.79
Intercalation-driven reversible control of magnetism in bulk ferromagnets. Adv Mater (2014) 0.79
Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population. Birth Defects Res A Clin Mol Teratol (2013) 0.78
The DRD2 TaqIA polymorphism and demand of dopaminergic medication in Parkinson's disease. Mov Disord (2008) 0.78
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent. Int J Pediatr Otorhinolaryngol (2009) 0.78
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients. Int J Pediatr Otorhinolaryngol (2010) 0.78
Introducing a new recruitment approach to sample collection for genetic association studies in opioid dependence. Eur Psychiatry (2003) 0.78
Separation of amino acids, peptides and corresponding Amadori compounds on a silica column at elevated temperature. J Chromatogr A (2007) 0.77
Association study of 5'-UTR polymorphisms of the human dopamine transporter gene with manic depression. Bipolar Disord (2006) 0.77
Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis. Pharmacogenetics (2002) 0.77
Comment on "The impact of genotyping error on haplotype reconstruction and frequency estimation". Eur J Hum Genet (2003) 0.76
Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia. Eur J Gastroenterol Hepatol (2016) 0.76
Motor complications in patients form the German Competence Network on Parkinson's disease and the DRD3 Ser9Gly polymorphism. Mov Disord (2009) 0.75
The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach. BMC Psychiatry (2010) 0.75
A family-based association study in Central Europeans: no evidence for the cystathionine beta-synthase c.844ins68 gene variant as a risk factor for non-syndromic cleft lip and palate. Am J Med Genet A (2007) 0.75
Structures of CsEuBr3 and its degradation product Cs2EuBr5.10H2O. Acta Crystallogr B (2007) 0.75
[No association of 141C-ins/del polymorphism in the D2 dopamine receptor gene in schizophrenia]. Psychiatr Prax (2003) 0.75
Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families. Int J Cancer (2002) 0.75
Design and construction of multicrystal analyser detectors using Rowland circles: application to MAD26 at ALBA. J Synchrotron Radiat (2011) 0.75
Variation in the calpain-10 gene is not associated with gestational diabetes mellitus. Scand J Clin Lab Invest (2013) 0.75
Lactic acid quantitation in hand dishwashing liquid using an HILIC-UV methodology. J Sep Sci (2010) 0.75