PubRank

Thomas F Wienker

Author PubWeight™ 82.46‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
2 Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy. Am J Hum Genet 2001 4.50
3 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nat Genet 2009 3.58
4 Genome-wide association study of alcohol dependence. Arch Gen Psychiatry 2009 3.08
5 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet 2009 2.93
6 Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 2011 2.71
7 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. Nat Genet 2010 2.56
8 SNP-based analysis of genetic substructure in the German population. Hum Hered 2006 2.21
9 Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet 2012 2.15
10 Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet 2008 1.80
11 Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study. J Assoc Res Otolaryngol 2008 1.73
12 VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation. Thromb Haemost 2005 1.55
13 The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. Hum Mol Genet 2007 1.52
14 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
15 Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. Biol Psychiatry 2010 1.39
16 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
17 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
18 Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet 2010 1.26
19 Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE. Bioinformatics 2006 1.21
20 How to model a complex trait. 2. Analysis with two disease loci. Hum Hered 2003 1.16
21 Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol. Hepatology 2007 1.15
22 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
23 Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis. J Invest Dermatol 2006 1.07
24 The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis. Hum Genet 2006 1.05
25 The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q. Am J Hum Genet 2007 1.04
26 Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancy. Hepatology 2007 0.99
27 Integrated sequence analysis pipeline provides one-stop solution for identifying disease-causing mutations. Hum Mutat 2014 0.96
28 Familial aggregation of alopecia areata. J Am Acad Dermatol 2006 0.96
29 The human pseudoautosomal regions: a review for genetic epidemiologists. Eur J Hum Genet 2008 0.96
30 The opioid peptides enkephalin and beta-endorphin in alcohol dependence. Biol Psychiatry 2008 0.95
31 Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating. Proc Natl Acad Sci U S A 2012 0.94
32 A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. J Hypertens 2009 0.94
33 Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered 2010 0.93
34 Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene. J Am Soc Nephrol 2002 0.93
35 IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci 2009 0.93
36 Linkage analysis of alcohol dependence using MOD scores. BMC Genet 2005 0.92
37 Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes. Cerebrovasc Dis 2008 0.92
38 Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin. Am J Med Genet A 2009 0.92
39 Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cells. Blood 2007 0.92
40 Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts. J Invest Dermatol 2005 0.90
41 Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthma. J Allergy Clin Immunol 2004 0.90
42 Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24. Am J Hum Genet 2005 0.90
43 How to model a complex trait. 1. General considerations and suggestions. Hum Hered 2003 0.89
44 VEGF gene haplotypes are associated with sarcoidosis. Chest 2009 0.89
45 A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2). Hum Hered 2009 0.87
46 Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemia. Eur J Hum Genet 2004 0.87
47 Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease. J Invest Dermatol 2007 0.86
48 A common origin of the 4143insA ADAMTS13 mutation. Thromb Haemost 2006 0.86
49 Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder. Int J Neuropsychopharmacol 2005 0.85
50 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
51 Geostatistical inference of main Y-STR-haplotype groups in Europe. Forensic Sci Int Genet 2011 0.82
52 Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation. J Clin Microbiol 2006 0.82
53 Spatial assessment of Argentinean genetic admixture with geographical information systems. Forensic Sci Int Genet 2010 0.82
54 NDST1 missense mutations in autosomal recessive intellectual disability. Am J Med Genet A 2014 0.81
55 Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13. Eur J Hum Genet 2007 0.81
56 Quantitative trait loci contributing to physiological and behavioural ethanol responses after acute and chronic treatment. Int J Neuropsychopharmacol 2009 0.80
57 Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci 2012 0.79
58 High levels of brain-type creatine kinase activity in human platelets and leukocytes: a genetic anomaly with autosomal dominant inheritance. Blood Cells Mol Dis 2011 0.78
59 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
60 gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians. Blood Coagul Fibrinolysis 2005 0.78
61 A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability. Eur J Hum Genet 2015 0.76
62 Analysis of quantitative trait loci in mice suggests a role of Enoph1 in stress reactivity. J Neurochem 2013 0.76
63 No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach. Hum Genet 2003 0.76
64 A recoding scheme for X-linked and pseudoautosomal loci to be used with computer programs for autosomal LOD-score analysis. Hum Hered 2004 0.75
65 No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1. Am J Med Genet 2002 0.75
66 A newly recognized autosomal recessive syndrome affecting neurologic function and vision. Am J Med Genet A 2013 0.75
67 Familial aggregation of pure tone hearing thresholds in an aging European population. Otol Neurotol 2013 0.75