PubRank

Peter Holmans

Author PubWeight™ 114.64‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A survey of genetic human cortical gene expression. Nat Genet 2007 12.04
2 Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008 10.52
3 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 7.44
4 Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet 2010 5.78
5 Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet 2009 4.52
6 Genetic control of human brain transcript expression in Alzheimer disease. Am J Hum Genet 2009 3.35
7 Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010 3.13
8 Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Hum Mol Genet 2007 2.73
9 Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry 2012 2.48
10 Effects of differential genotyping error rate on the type I error probability of case-control studies. Hum Hered 2006 2.21
11 Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Am J Psychiatry 2012 2.20
12 A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. Am J Hum Genet 2005 2.04
13 Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proc Natl Acad Sci U S A 2004 1.95
14 Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 2005 1.93
15 Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010 1.86
16 Full genome screen for Alzheimer disease: stage II analysis. Am J Med Genet 2002 1.77
17 Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Hum Mol Genet 2010 1.72
18 Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. Br J Psychiatry 2013 1.70
19 Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum Mol Genet 2012 1.68
20 Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration. J Neurosci 2007 1.66
21 Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Arch Gen Psychiatry 2005 1.48
22 Conservation of regional gene expression in mouse and human brain. PLoS Genet 2007 1.47
23 Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16. Am J Psychiatry 2007 1.46
24 Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers. Am J Psychiatry 2007 1.43
25 Genetics of recurrent early-onset depression (GenRED): design and preliminary clinical characteristics of a repository sample for genetic linkage studies. Am J Med Genet B Neuropsychiatr Genet 2003 1.26
26 Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Med 2004 1.26
27 Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proc Natl Acad Sci U S A 2006 1.25
28 Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study. Genet Epidemiol 2011 1.22
29 Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis. PLoS Med 2012 1.19
30 Streamlined analysis of pooled genotype data in SNP-based association studies. Genet Epidemiol 2005 1.18
31 Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. Am J Med Genet B Neuropsychiatr Genet 2013 1.11
32 High loading of polygenic risk for ADHD in children with comorbid aggression. Am J Psychiatry 2013 1.10
33 Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophr Bull 2014 1.10
34 Genetic risk sum score comprised of common polygenic variation is associated with body mass index. Hum Genet 2010 1.10
35 Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurol 2013 1.09
36 Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study. Neurosci Lett 2004 1.09
37 The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees. BMC Genet 2005 1.08
38 Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Hum Mol Genet 2007 1.03
39 Genetic differences between five European populations. Hum Hered 2010 0.98
40 Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Ann Neurol 2006 0.97
41 Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. Eur J Hum Genet 2012 0.95
42 Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. Am J Med Genet B Neuropsychiatr Genet 2005 0.92
43 Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3. Biol Psychiatry 2008 0.91
44 Analyses of single marker and pairwise effects of candidate loci for rheumatoid arthritis using logistic regression and random forests. BMC Proc 2007 0.90
45 Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. Br J Psychiatry 2011 0.90
46 Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Hum Mutat 2005 0.90
47 An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction. Biol Psychiatry 2011 0.89
48 A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Hum Mol Genet 2012 0.89
49 Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15. Genet Epidemiol 2007 0.86
50 A comparison of four clustering methods for brain expression microarray data. BMC Bioinformatics 2008 0.85
51 Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. PLoS One 2012 0.84
52 Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. Am J Med Genet B Neuropsychiatr Genet 2004 0.82
53 Comparison of methods for combining case-control and family-based association studies. Hum Hered 2009 0.80
54 ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. PLoS One 2011 0.80
55 Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? Am J Med Genet B Neuropsychiatr Genet 2008 0.77
56 Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression. Am J Med Genet B Neuropsychiatr Genet 2007 0.76