PubRank

Tim Becker

Author PubWeight™ 71.02‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males. Hum Genet 2007 2.36
2 INTERSNP: genome-wide interaction analysis guided by a priori information. Bioinformatics 2009 2.02
3 Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet 2008 1.80
4 Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression. Biol Psychiatry 2005 1.61
5 Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum Mol Genet 2012 1.48
6 No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample. Psychiatr Genet 2007 1.42
7 Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. Am J Hum Genet 2005 1.35
8 CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD. PLoS One 2009 1.34
9 The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder. Biol Psychiatry 2005 1.31
10 Replication of LCE3C-LCE3B CNV as a risk factor for psoriasis and analysis of interaction with other genetic risk factors. J Invest Dermatol 2009 1.26
11 Genetic association analysis with FAMHAP: a major program update. Bioinformatics 2008 1.26
12 Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet 2010 1.26
13 The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am J Hum Genet 2003 1.26
14 Family-based association analysis with tightly linked markers. Hum Hered 2003 1.24
15 Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes. Am J Psychiatry 2005 1.21
16 Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet 2012 1.14
17 The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiol Dis 2011 1.12
18 The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis. Hum Genet 2006 1.05
19 DNA sequence variants of the FKBP5 gene are associated with unipolar depression. Int J Neuropsychopharmacol 2010 1.04
20 Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children. Am J Med Genet B Neuropsychiatr Genet 2005 1.01
21 High-throughput miRNA and mRNA sequencing of paired colorectal normal, tumor and metastasis tissues and bioinformatic modeling of miRNA-1 therapeutic applications. PLoS One 2013 1.00
22 A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation. Hum Mol Genet 2009 0.98
23 Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. Schizophr Res 2009 0.97
24 The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Hum Mol Genet 2009 0.97
25 Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci. Hum Mol Genet 2011 0.95
26 Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered 2010 0.93
27 Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. Eur J Hum Genet 2011 0.92
28 Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance. J Invest Dermatol 2012 0.91
29 Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat Genet 2004 0.90
30 Association of BRD2 polymorphisms with photoparoxysmal response. Neurosci Lett 2006 0.90
31 The use of human sweat gland-derived stem cells for enhancing vascularization during dermal regeneration. J Invest Dermatol 2012 0.89
32 Genetic variants in CTLA4 are strongly associated with alopecia areata. J Invest Dermatol 2011 0.89
33 Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals. Hum Brain Mapp 2009 0.88
34 No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biol Psychiatry 2005 0.88
35 A novel validation algorithm allows for automated cell tracking and the extraction of biologically meaningful parameters. PLoS One 2011 0.87
36 Unipolar depression and hippocampal volume: impact of DNA sequence variants of the glucocorticoid receptor gene. Am J Med Genet B Neuropsychiatr Genet 2008 0.86
37 A common origin of the 4143insA ADAMTS13 mutation. Thromb Haemost 2006 0.86
38 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
39 Haplotype-based systematic association studies of ATP1A2 in migraine with aura. Am J Med Genet B Neuropsychiatr Genet 2006 0.85
40 Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease. Neurosci Lett 2007 0.85
41 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
42 Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex. Am J Med Genet A 2006 0.84
43 Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression. Eur J Hum Genet 2012 0.84
44 Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample. Psychiatr Genet 2007 0.83
45 Testing association in the presence of linkage using the GRE and multiple markers. Genet Epidemiol 2008 0.83
46 Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6. Hum Genet 2010 0.83
47 Integrated genome-wide pathway association analysis with INTERSNP. Hum Hered 2012 0.83
48 An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion. BMC Med Genet 2011 0.83
49 No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder. Psychiatr Genet 2007 0.81
50 GENESTAT: an information portal for design and analysis of genetic association studies. Eur J Hum Genet 2008 0.81
51 Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation. Eur J Hum Genet 2011 0.81
52 Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. Neurosci Lett 2006 0.80
53 Genetic modifiers in cystic fibrosis. N Engl J Med 2006 0.80
54 Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsy. Neurogenetics 2003 0.80
55 CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestine. Eur J Hum Genet 2012 0.79
56 Quick, "imputation-free" meta-analysis with proxy-SNPs. BMC Bioinformatics 2012 0.79
57 Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss. Arch Dermatol Res 2013 0.78
58 No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder. Psychiatr Genet 2005 0.78
59 No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. Psychiatr Genet 2006 0.78
60 Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2006 0.78
61 A one-degree-of-freedom test for supra-multiplicativity of SNP effects. PLoS One 2013 0.77
62 No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia. Psychiatr Genet 2007 0.77
63 Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss. J Dermatol Sci 2013 0.77
64 Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder. Psychiatr Genet 2008 0.77
65 Photonic crystal slabs for surface contrast enhancement in microscopy of transparent objects. Opt Express 2012 0.76
66 A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2010 0.76
67 Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss. Arch Dermatol Res 2012 0.76
68 Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identified. Exp Dermatol 2012 0.76
69 No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
70 No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
71 Comment on "The impact of genotyping error on haplotype reconstruction and frequency estimation". Eur J Hum Genet 2003 0.76
72 No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach. Hum Genet 2003 0.76
73 No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample. Psychiatr Genet 2007 0.75
74 Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics. J Psychiatr Res 2012 0.75
75 Rare variant testing of imputed data: an analysis pipeline typified. Hum Hered 2014 0.75
76 Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia. Psychiatr Genet 2010 0.75
77 Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors. Fam Cancer 2012 0.75
78 Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study. Acta Derm Venereol 2017 0.75