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Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease

  • Javier Simón-Sánchez ,

    Contributed equally to this work with: Javier Simón-Sánchez, Laura L. Kilarski

    Affiliation Section of Medical Genomics, Department of Clinical Genetics, VU University Medical Centre, Amsterdam, The Netherlands

  • Laura L. Kilarski ,

    Contributed equally to this work with: Javier Simón-Sánchez, Laura L. Kilarski

    Affiliations MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom, Department of Psychological Medicine & Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom

  • Michael A. Nalls,

    Affiliation Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, United States of America

  • Maria Martinez,

    Affiliations Inserm, UMR 1043, Toulouse, France, Paul Sabatier University, Toulouse, France

  • Claudia Schulte,

    Affiliation Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, and DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany

  • Peter Holmans,

    Affiliations MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom, Department of Psychological Medicine & Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom

  • International Parkinson's Disease Genomics Consortium ,

    a Membership of the International Parkinson's Disease Genomics Consortium is provided in the Acknowledgments.

  • Wellcome Trust Case Control Consortium ,

    b Membership of the Wellcome Trust Case Control Consortium is provided in supporting information.

    Affiliation MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom

  • Thomas Gasser,

    Affiliation Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, and DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany

  • John Hardy,

    Affiliation Department of Molecular Neuroscience, UCL Institute of Neurology, London, United Kingdom

  • Andrew B. Singleton,

    Affiliation Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, United States of America

  • Nicholas W. Wood,

    Affiliation Department of Molecular Neuroscience, UCL Institute of Neurology, London, United Kingdom

  • Alexis Brice,

    Affiliations Université Pierre et Marie Curie-Paris6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Paris, France, Inserm, U975, Paris, France, Cnrs, UMR 7225, Paris, France

  • Peter Heutink,

    Affiliation Section of Medical Genomics, Department of Clinical Genetics, VU University Medical Centre, Amsterdam, The Netherlands

  • Nigel Williams ,

    williamsnm@cf.ac.uk (NW); morrishr@cf.ac.uk (HRM)

    Affiliations MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom, Department of Psychological Medicine & Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom

  •  [ ... ],
  • Huw R. Morris

    williamsnm@cf.ac.uk (NW); morrishr@cf.ac.uk (HRM)

    Affiliations MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom, Department of Psychological Medicine & Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom

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Abstract

Parkinson's disease (PD) occurs in both familial and sporadic forms, and both monogenic and complex genetic factors have been identified. Early onset PD (EOPD) is particularly associated with autosomal recessive (AR) mutations, and three genes, PARK2, PARK7 and PINK1, have been found to carry mutations leading to AR disease. Since mutations in these genes account for less than 10% of EOPD patients, we hypothesized that further recessive genetic factors are involved in this disorder, which may appear in extended runs of homozygosity.

We carried out genome wide SNP genotyping to look for extended runs of homozygosity (ROHs) in 1,445 EOPD cases and 6,987 controls. Logistic regression analyses showed an increased level of genomic homozygosity in EOPD cases compared to controls. These differences are larger for ROH of 9 Mb and above, where there is a more than three-fold increase in the proportion of cases carrying a ROH. These differences are not explained by occult recessive mutations at existing loci. Controlling for genome wide homozygosity in logistic regression analyses increased the differences between cases and controls, indicating that in EOPD cases ROHs do not simply relate to genome wide measures of inbreeding. Homozygosity at a locus on chromosome19p13.3 was identified as being more common in EOPD cases as compared to controls. Sequencing analysis of genes and predicted transcripts within this locus failed to identify a novel mutation causing EOPD in our cohort.

There is an increased rate of genome wide homozygosity in EOPD, as measured by an increase in ROHs. These ROHs are a signature of inbreeding and do not necessarily harbour disease-causing genetic variants. Although there might be other regions of interest apart from chromosome 19p13.3, we lack the power to detect them with this analysis.

Introduction

Parkinson's disease (PD) is an age-related neurodegenerative condition which causes a progressive L-DOPA responsive hypokinetic movement disorder related to nigro-striatal dopaminergic cell loss [1]. There is heterogeneity in the extent of non-motor symptoms and the presence of dystonia and L-DOPA related treatment complications. Autosomal dominant, recessive, common and rare variant genetic factors have been identified as being relevant to the development of PD [2][7]. The identification of these factors has informed clinical diagnosis, the study of disease heterogeneity, neuropathology and the understanding of the underlying pathogenic mechanisms. Furthermore, knowledge of genetic factors contributing to PD might enable the development of predictive testing and personalised treatments in the future. Age is the most certain risk factor for PD with the majority of patients developing disease after the age of 65 [8]. However, 3.6% of patients develop early-onset PD (EOPD) before the age of 45 and 1% develop their disease before the age of 40 [9]. Presumably, these outlying cases relate to the effects of exceptional genetic and/or environmental risk factors. Segregation analysis in PD indicates that there is an up to eight-fold increased risk of developing PD in siblings of patients with EOPD, supporting the effect of autosomal recessive genes [10], [11].

PARK2 (parkin), PARK7 (DJ-1) and PINK1 (PARK6) have been identified as loci/genes that contain mutations causing an autosomal recessive form of the disease, based on mutation discovery in consanguineous families following homozygosity mapping and positional cloning [12][14]. Recently mutations in ATP13A2, PLA2G6, FBXO7 and SPG11 which cause a similar syndrome, pallido-pyramidal early onset parkinsonism, have also been identified using homozygosity mapping [15]. Pathogenic mutations in EOPD genes are not confined to familial or consanguineous patients. Screening of outbred EOPD patients has identified compound heterozygous and further homozygous mutations [16], [17]. Overall, 5% of EOPD cases have mutations in known autosomal recessive genes, with approximately half being homozygous and half being compound heterozygous [18].

Genome wide single nucleotide polymorphism (SNP) chips have been used to identify common risk alleles for typical sporadic PD [3][7]. However, they also provide the opportunity to identify homozygous runs in the genome [19], [20], shown to be abundant in ostensibly outbred populations [21]. This suggests that large-scale homozygosity mapping might be used to identify new genes in apparently outbred individuals with autosomal recessive disease, and to estimate the burden of recessive loci in a particular disease population [22]. We hypothesise that there are further autosomal recessive risk factors for EOPD and have performed genome wide homozygosity analysis, to determine the presence and extent of excess homozygosity in patients with early onset disease.

Methods

Participants and genotyping

DNA samples in this study were analysed as part of genome-wide association studies (GWAS) included in the International PD Genomics Consortium (IPDGC) meta-analysis published in the Lancet in February 2011 [23]. The authors are members of the consortium and consortium members are co-authors of this paper. The study represents a re-analysis of a part of the GWAS meta-analysis data (relating to early onset PD) and additional Cardiff EOPD samples were genotyped and included in this study, generated and analysed by our centre. Approval for this was given by the UK Research Ethics Committee Approval (REC for Wales 09/MRE09/35). Part of the data was generated by the Wellcome Trust Case Control Consortium 2 (WTCCC2). The authors have the permission and approval of both IPDCG and WTCCC2 to carry out this work and both IPDGC and WTCCC2 have approved this manuscript for submission for publication.

DNA samples from PD patients meeting Queen Square Brain Bank criteria with an age at onset (AAO) at or below 50 years (n = 1557 – France 466, Netherlands 286, Germany 239, USA 280, UK 286) (table 1) were collected and genotyped with Illumina HumanHap 550, Human660W-Quad, or Human1M-Duo beadchips (www.illumina.com), and had undergone some prior quality control procedures (QC). Following two rounds of QC aiming to unify the datasets (see supporting information S1 for details), consensus genotypic information for 412,212 unique SNPs was available for 1,445 EOPD cases and 6,987 controls (1958 British Birth Cohort (n = 1225, http://www.b58cgene.sgul.ac.uk), the British Blood Donor Service (n = 2510), US-American NINDS spousal and population controls (n = 750), the Rotterdam Study (n = 1559), and German controls from the KORA study and POPGEN project (n = 943)) (table S1). Detailed sample information is available elsewhere [3], [5][7].

The mean AAO for EOPD cases was 41.36 years (n = 1427, range: 7–50, standard deviation (SD): 7.24), with 940 individuals AAO≤45 years and 581 individuals AAO≤40 years (see Figure S1 for histogram of AAO distribution). Average chronological age of EOPD cases was 59.54 as of 2010 (range: 27–95, SD: 9.59, n = 853), and the average chronological age of controls was 53.95 (range: 21–101, SD: 8.67, n = 6973). 37.1% of cases and 52.4% of controls were female.

Runs of homozygosity

Initial identification of ROHs was performed using PLINK v1.07 [24]. A window of 50 SNPs was defined as homozygous if it contained at most 1 heterozygous genotype and 1 missing genotype. Such windows were moved across the genome, and a SNP was counted as part of a ROH if >5% of windows spanning it were homozygous. These are the values suggested in PLINK, designed to minimize the probability of a window being called homozygous by chance, while ensuring that SNPs on the edge of a true ROH will be assigned to that ROH. Each ROH had to contain on average at least 1 SNP per 50 kb. The minimum length of the ROH was set at 1 Mb and sequentially increased by 1 Mb up to 10 Mb.

Plotting these ROHs as custom tracks in UCSC genome browser (http://genome.ucsc.edu/) showed that the majority of 1–2 Mb ROHs, occur in clusters containing hundreds to thousands of samples and are, most likely, identical by state (IBS) instead of identical by descent (IBD). A SNP locus or region of loci is said to be IBD if the homozygous alleles have originated from the same ancestor, while IBS refers to loci/regions that are merely homozygous by chance. In an attempt to remove homozygous runs that occurred at a high frequency in the sample population and that might bias our downstream analyses, we identified all regions at which at least 1% of all individuals (both cases and controls) harboured a ROH of 2 Mb or more in length. Within most of these regions, the mean length of overlapping common ROHs tended to be largely uniform. However some rare ROHs (<1% frequency in the study population) that were considerably longer and thus more likely to be IBD appeared to span some of these regions independently of the common ROHs. Those whose length deviated more than 3 SD from the mean length of the ROHs in that region, were retained in the analysis (figure S2 illustrates which ROHs would remain in the analysis following this approach in an example of one such region). This filtering approach was repeated for ROHs with a minimum length of 3, 4, and 5 Mb. At 6 Mb and above, no more regions with a ROH frequency >1% were identified.

Statistical analyses

Basic homozygosity burden analysis.

The proportion of individuals with at least one ROH of a given minimum length and the total number of ROHs per individual (rate) were calculated for both all ROH and rare ROH. Means were compared between cases and controls using simple one-tailed T-tests, and empirical p values were generated by permuting case/control status (100 million permutations, resulting in accuracy up to 1×10−8).

Homozygosity burden analysis using logistic regression models.

In order to estimate the magnitude of risk associated with elevated levels of genome wide homozygosity, and to allow the inclusion of potentially confounding variables, analyses were further refined with a series of logistic regression models. Thus, the proportion of samples with ROHs above a given length and the total number of ROHs per individual were modelled separately as independent variables with case-control status as the dependent variable. Chronological age as of 2010 (when available) and the two first components (C1 and C2) of the multidimensional scaling matrix (MDS) (which captures about 90% of genetic variation in Caucasian populations - see supporting information S1) were included as covariates. To remove the possibility of chance occurrences of homozygosity affecting our statistical calculations, genome-wide rates of homozygosity (f coefficients) outside of linkage disequilibrium were calculated using PLINK v.1.07, in a linkage disequilibrium trimmed dataset (supporting information S1). This statistic summarizes the proportion of genotypes in our trimmed dataset that deviated from the expected number of homozygous genotypes in each population under assumptions of Hardy-Weinberg equilibrium. A more negative f would suggest a high level of heterozygosity in a sample; a more positive f estimate would suggest elevated rates of homozygosity beyond what is expected under normal assumptions. This statistic was then applied as a covariate to our logistic regression models. Logistic models were executed using R v.2.11.1 [25].

Exclusion of known PARK loci.

In order to test whether the excess of homozygosity detected might be due to carriers of homozygous mutations in the most prominent PARK genes, both the one-tailed t-tests and the logistic regression models were repeated after excluding those samples with ROHs overlapping the genomic position of any of these genes. For this purpose, the start and end positions of RefSeq genes for ATP13A2, FA2H, FBXO7, LRRK2, PARK2, PARK7, PINK1, PDXK, PLA2G6, SNCA, and SPG11, were downloaded from the UCSC table browser (build NCBI36/hg18). If more than one transcript was present, the longest available transcript was used as a reference. A total of 47 cases and 184 controls harboured ROHs>2 Mb in length overlapping with at least one of these genes.

Homozygosity Mapping.

Two approaches were used to find genomic regions in which extended homozygosity differed between cases and controls. First, we used PLINK v1.07 to define pools of overlapping ROHs. Each pool contained at least two different ROHs that did not have to match allelically. This approach identified 1,820 unique pools containing two or more ROHs. The genomic region spanned by all the runs in a certain pool was used to define 1,604 unique consensus regions spanning at least 2 consecutive SNPs. The number of times each of these consensus regions was completely overlapped by ROHs in cases and controls was counted and p values calculated based on 100,000 permutations. Multiple test corrections were applied based on the number of consensus regions tested.

In a second approach (gene-based) trying to identify genomic regions differentially overlapped by ROHs in cases versus controls in our cohort, a list containing the genomic coordinates of 19,058 genes and predicted transcripts in the human genome (NCBI B36 assembly) was downloaded from the PLINK resources website (http://pngu.mgh.harvard.edu/~purcell/plink/res.shtml). Using PLINK v1.07, the number of times a given gene was overlapped by ROHs in cases and controls was counted and p values were calculated based on 100,000 permutations. P values were multiple test-corrected based on the number of genes and predicted transcripts in our list.

Results

A total of 216,660 homozygous runs ranging in size from 1 to ∼71.6 Mb (mean length: 1.4 Mb) and containing 50 to 9,743 contiguous homozygous SNPs, were identified. The exact number of ROHs identified at any given size threshold in cases and controls can be found in table S2. Every case and control had at least one ROH measuring more than 1 Mb (table S3 a). The mean number of ROH (greater than 1 Mb) per person was 25.5 (25.22 in cases, and 25.79 in controls, ratio: 0.98, p = 1, table S3 b). We therefore focused on ROH of at least 2 Mb length in subsequent analyses, of which there were 19,025 in our dataset.

Basic homozygosity burden analysis

Around 88% of cases and 90% of controls harboured ROHs of at least 2 Mb length (ratio: 0.98, p = 0.97). However, at 3 Mb minimum length, a small but significant increase in the proportion of cases with ROHs versus controls became apparent (42.6% vs. 39.4%, ratio: 1.08, p = 0.01). The biggest difference in the proportion of samples with an ROH of a given minimum size was seen at 9 Mb (4.4% vs. 1.4%, ratio: 3.17, p<1×10−8) (table S3 a). At a minimum length of 2 Mb, the average number (rate) of ROHs in cases was 2.24 and 2.26 in controls (ratio: 0.99, p = 0.65). At a minimum length of 3 Mb, the rate in cases and controls dropped to 0.65 and 0.52, respectively, indicating a highly significant excess of homozygosity in cases (ratio: 1.25, p = 2.30×10−6). Again, the biggest difference was seen at a threshold of 9 Mb, with a rate of 0.08 in cases, and 0.02 in controls (ratio: 3.48, p<1×10−8) (table S3 b). This initial analysis showed a clear excess of homozygosity by all metrics tested in cases as compared to controls.

Analysis was repeated following filtering for rare ROHs. The number of rare ROHs is shown in table S2 b). When taking only rare ROHs into consideration, the case-specific excess of the number of homozygous runs per person (rate) became more pronounced, reaching statistical significance at a size threshold of 2 Mb (0.91 vs. 0.82, ratio: 1.10, p = 0.01) and remained strongly significant throughout (table 2 a, figure 1). The proportion of individuals with at least one rare ROH of a given length dropped overall, and the difference between cases and controls became significant at 4 Mb (0.12 vs. 0.08, ratio: 1.45, p = 6.50×10−6) (table 2 b, figure 2). As expected, there was no increased burden in cases when the analysis was performed using exclusively common ROHs with a frequency >1% (data not shown).

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Figure 1. Number of rare ROHs at different size thresholds in EOPD and control groups.

In this bar plot the average number of rare ROHs per person (rate) in either EOPD (red) or control (blue) groups is shown for different minimum size thresholds. The black line represents the ratio of average rate in cases vs. average rate in controls. Differences were statistically significant from a threshold of 2 Mb (0.91 vs. 0.82, ratio: 1.09, p = 0.01) and remained strongly significant throughout, peaking at 9 Mb (0.04 vs. 0.01, ratio: 3.17, p<1.00×10−8.

https://doi.org/10.1371/journal.pone.0028787.g001

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Figure 2. Proportion of cases and controls with rare ROH of a given minimum size.

This bar plot displays the proportion of individuals presenting with at least one ROH of a given size threshold in EOPD (red) and control groups (blue). The ratio of the case/control proportions is represented by the black line. The difference between ROH-positive proportions in cases and controls became statistically significant at 4 Mb (0.12 vs. 0.08, ratio: 1.45, p = 4.30×10−6), and remained highly significant throughout higher size thresholds.

https://doi.org/10.1371/journal.pone.0028787.g002

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Table 2. Proportion and Rate of rare ROHs in EOPD cases and controls.

https://doi.org/10.1371/journal.pone.0028787.t002

Homozygosity burden analysis using logistic regression models

Logistic models both without (Model 1) and with covariates (f coefficient, age, MDS factors) (Models 2–4) suggest a highly significant association between the presence of one or more particularly longer ROHs (proportion) and disease phenotype (Tables S4a, S5a), as well as the rate of ROHs and phenotype (tables S4 b, S5 b). Including the genome-wide rate of homozygosity outside of LD (i.e. f) as a covariate decreased the average log10(p) by 2.1 units (Model 2). In other words, controlling for background genome wide homozygosity increased the detection of differences in ROHs between cases and controls. Taking into account chronological age increased the average log10(p) by 3.9, suggesting that the marginally older age of our cases had a confounding effect (Model 3). Accounting for potential population stratification had an impact on the significance of our findings, also increasing the average log10(p) by 3.86, (Model 4, table 3). The measure of rate is more attenuated through incorporation of all covariates than the measure of proportion. However, rate as well as proportion measures still remained significantly associated with case status from a minimum ROH length of 3 Mb onwards.

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Table 3. Logistic models for proportion and rate of rare ROHs.

https://doi.org/10.1371/journal.pone.0028787.t003

Investigating the source of excess homozygosity in EOPD

Given that the most striking differences were apparent at ROHs of 8–9 Mb in length, we further investigated the role of individuals with ROHs of >8 Mb (71 cases and 110 controls). Removing these individuals from the analysis led to a complete loss of significant differences in both the proportion of samples with ROHs (table S6 a) and the rate of ROHs per person (table S6 b). While a degree of significance was lost due to the exclusion of rare long ROHs of 8 Mb and above, these individuals also carried an excess of shorter ROHs. Differences in proportion (table S7 a) and rate (table S7 b) were still significant after restricting analysis to only ROHs below 8 Mb in length. We observed that those 71 cases that had at least one ROH>8 Mb had a higher frequency of runs between 2–7 Mb than the remaining 1,374 cases (3.78 vs 2.07, ratio: 1.83, p<1×10−8; figure S3). The average AAO of these 71 cases was 40.73 years (range: 13–50, SD: 8.23, n = 70), and not significantly different from the rest of cases (AAO: 41.25, SD: 7.21, range: 7–50, n = 1351) as assessed by two-sample two-tailed t-test assuming equal variances (p = 0.56). There was a 10-fold increase of the mean f coefficient when comparing samples with or without 8 Mb ROHs (0.014 versus 0.001, respectively, p = 1.16×10−16). The distribution of cases with 8 Mb ROH across the different populations under study was as follows: 25.35% France, 25.35% Germany, 23.94% Netherlands, 15.49% USA and 9.86% UK. This did not differ significantly from the distribution of cases without 8 Mb ROH, apart from the observation that German cases were more likely to have 8 Mb ROH than any other (Fisher's exact test p value = 0.01). 7 of the 71 individuals (9.86%) carried a ROH of >2 Mb across PARK2 (parkin), ATP13A2, FBXO7 or PLAS2G6, which was a significantly higher percentage of carriers than that found in cases without long ROH (2.91%, p = 0.01).

Homozygosity Mapping

The first homozygosity mapping approach involved testing consensus regions where two or more ROHs overlapped at a minimum of 2 SNPs for association with disease phenotype. In the present dataset there were 1,604 consensus regions overlapped by rare ROHs of at least 2 Mb length. One consensus region, located on chromosome 19p13.3, remained significantly associated with EOPD after correction for multiple testing (uncorrected p value = 4.00×10−5, corrected p = 5.79×10−3, Consensus #1 in table 4). 6 cases and no controls carried a ROH spanning this region. These cases were originally from Germany (3 cases) and the UK, France and USA (1 case each). The mean AAO in these cases was 39 (range = 29–49) and not significantly different from other cases as shown by a two tailed t-test (p = 0.54). Interestingly all six cases belonged to the group of cases with at least one ROH above 8 Mb length, although the longest ROH for a given person was not necessarily overlapping consensus region #1 (mean length of ROH = 7.5 Mb; range = 2.9–16.3 Mb).

This consensus region spans ∼184 kb in chromosome 19p13.3 and contains 12 genes and predicted transcripts, namely: CLPP, ALKBH7, PSPN, GTF2F1, KHSRP, MIR3940, SLC25A41, SLC25A23, CRB3, DENND1C, TUBB4 and TNFSF9 (figure S4). The presence of deletions and duplications in this region was excluded by visual examination of the genotyping intensity data (data not shown). There was no extended shared haplotype among cases with homozygosity in the 19p13.3 region. Sanger sequencing of all exons and exon-intron boundaries of genes and predicted transcripts contained in this genomic region failed to find any associated variants. Another 118 consensus regions were nominally associated with EOPD (p<0.05). However, none of them passed correction for multiple testing. A list of the top 10 associated regions can be found in table 4.

In the second approach of homozygosity mapping, all genes and predicted transcripts according to NCBI B36 assembly were used as the unit of analysis. Of the 19,058 genes queried, a total of 17,182 were spanned by at least one ROH. Eleven genes across a 174 kb stretch on chromosome 19 were intersected by significantly more ROHs in the cases compared to controls, a finding that remained significant following multiple test correction (p = 0.01) and was mostly overlapping with the region identified by the consensus approach described above.

Nominal significance was also achieved for an additional 1,816 genes; however these did not withstand genome wide correction. Given that a single ROH will typically span multiple genes, then in the context of this experiment each locus is not truly independent and therefore the genome wide correction for ∼19,000 independent tests is highly conservative. This is emphasised by post hoc analysis which revealed that, as expected, a large proportion of the associated genes were spanned by the same set of ROHs and it was possible to assign all 1,827 genes to 300 independent groups containing 1 – 66 genes each (table 5 shows the top 10 regions with uncorrected p values≤0.01; figure S5 shows the three most significantly associated gene groups on chromosome 19p13.3).

Exclusion of known PARK loci

All samples with ROHs of above 2 Mb overlapping any of the 12 known parkinsonism and pallido-pyramidal syndrome genes were removed. After removal, both the basic burden analysis and logistic regressions models produced similar results as those described above (tables S8, S9, S10, and S11). These results indicate that excess of homozygosity outside the known parkinsonism and pallido-pyramidal syndrome genes represent a risk for EOPD in our population and that further recessive genes are yet to be identified. Performing the gene-based homozygosity mapping explained before in the aforementioned genes, resulted in the association displayed in table S12. To note, only PARK2 (parkin) was statistically more often overlapped by ROHs in cases versus controls after multiple test correction (p = 0.04), further supporting the idea that novel genetic factors are underlying the excess of homozygosity detected in our cases. Additionally, any evidence of association of ROH across PARK2 (parkin) disappeared when 2 cases with known mutations in the gene were excluded from the analysis (p = 0.31, p corrected = 0.86).

Discussion

In this work, we have demonstrated an increased rate of genomic homozygosity based on an increased proportion of EOPD patients with long homozygous sequences as compared to controls. In addition, two different homozygosity mapping approaches identified a region in chromosome 19p13.3 in which cases carried significantly more ROHs than controls.

This study was based on a very large series of patients with EOPD. The excess number of ROHs in cases becomes apparent at a threshold of 3 Mb for all homozygous tracts and at 2 Mb when considering only rare homozygous tracts. The effects became most pronounced at a threshold of 9 Mb where there is a 3.5 fold increase in the proportion of EOPD cases with a homozygous track as compared to controls.

Possible confounding effects in this work include ethnic/regional and age differences between cases and controls and the retention of cases with mutations in known genes. Because differences in homozygosity measures among Caucasian populations have been reported previously [21], [26], C1 and C2 components of the population MDS matrix were included as co-factors in our analyses. This approach attenuated statistically significant differences in the rate of ROH (p = 0.01), but did not affect the highly significant differences in proportions.

Age factors were addressed by ensuring approximate matching in the ages of cases as compared to controls (average year of birth 1950 vs. 1956, respectively) and by carrying out regression analyses including chronological age as a covariate. Besides, inbreeding coefficients (f) calculated on a LD-pruned version of our dataset were included as covariates in our models to correct for autozygosity differences across different generations in outbred individuals [27]. The effect of this coefficient merits particular comment. Including the f as a covariate increased case-control differences suggesting that the excess of homozygous runs in cases does not relate to genome wide homozygosity, but rather to an excess of a small number of longer runs of homozygosity, likely to be homozygous by descent and to contain pathogenic mutations. In controls, the proportion and rate of homozygous runs relates more directly to the effect of background genome wide homozygosity.

Furthermore, the effect of occult homozygous mutations in genes previously associated with EOPD or other related disorders was excluded by repeating the analysis without those samples with ROHs overlapping known loci for PD, pallido-pyramidal and parkinsonism dystonia genes. Of note, gene-based homozygosity analysis in these genes revealed that only ROHs overlapping PARK2 (parkin) were associated with EOPD after correcting for multiple tests. Removal of the samples involved in this association did not remove the association described after our basic burden and logistic regression analyses. These results strongly suggest the role of other unknown genetic factors playing an important role in the risk for recessive EOPD.

In other disorders, similar analyses aimed at showing an increased homozygous burden in cases have resulted in mixed results. One study reported an increased homozygous burden in patients with colorectal cancer [28] but this finding was not replicated [29]. In a study of ROH in bipolar disorder, no increased burden was seen [30]. Lencz and colleagues [31] demonstrated the presence of 9 ROHs significantly overrepresented in a cohort of 178 patients with schizophrenia as compared to 144 healthy controls. Hildebrandt and colleagues [22] demonstrated the feasibility of homozygosity mapping using SNP microarrays by investigating ROH in individuals from families with varying degrees of consanguinity and two different paediatric autosomal recessive kidney diseases, and 93% of known mutations were identified in ROH of sizes as small as 2 Mb. In the realm of neurological disorders, one study investigated homozygous runs in ostensibly outbred individuals with late onset AD and identified a trend to excess homozygosity in AD, as well as one consensus region spanning 7 genes, which was significantly more common in cases as compared to controls [32], however this finding was not replicated in a more recent study [33].

Finally, using two different homozygosity mapping approaches one region on the short arm of chromosome 19 was found to be associated with EOPD after correcting for multiple testing. Six different cases from four different countries contained rare ROHs overlapping in a ∼184 kb stretch in this chromosome 19. Twelve genes were contained within the region. Of particular interest is PSPN, which encodes persephin, a neurotrophic factor shown to promote survival of ventral midbrain dopaminergic neurons in vitro [34]. Visual examination of the genotyping intensity data of the samples involved in this association failed to find any structural variant overlapping with this genomic region (data not shown). Also, exome sequencing of these samples failed to find any variant to be associated with EOPD in our population (data not shown). These results might suggest that a non-coding variant or a more complex structural alteration is leading to disease in these patients. Sequence capture of the entire region may help understanding the etiology of EOPD in these cases.

We succeeded in showing an excess of homozygosity (in terms of ROHs) in EOPD cases versus controls. To note, these ROHs are not necessarily harbouring disease-causing variants. However, a small proportion of them might carry recessive alleles associated with EOPD. Although we succeeded in identifying one candidate region using homozygosity mapping in our cohort, this related to a small number of cases and a new Mendelian gene was not identified. There are a number of possible factors which may explain our results: i) a larger population is needed to detect new genes for EOPD in unrelated cases, ii) there may be common pathogenic mutations in shorter ROHs in inbred individuals which are difficult to detect through conventional mapping, iii) there may be a large number of recessive genes for EOPD which are highly penetrant but individually uncommon, or iv) the effect is explained by a burden of multiple low penetrance homozygous alleles in cases.

Further work in which ROH are analysed with whole exome data will be needed to resolve these issues. The identification of autosomal recessive genes for EOPD to date has been based on the identification of specific consanguineous families. Novel genetic technologies will allow us to determine new Mendelian genetic factors, without traditional linkage and positional cloning. The present work indicates our current knowledge of the genetic aetiology of EOPD is incomplete and that given sufficient sample size it should be possible to clone new autosomal recessive genes for EOPD following the investigation of apparently outbred unrelated patients.

Supporting Information

Figure S1.

Distribution of AAO in the case population under study.

https://doi.org/10.1371/journal.pone.0028787.s002

(TIF)

Figure S2.

Histogram depicting frequency of ROH of given lengths in a region containing common ROH. According to our filtering approach, only the ROH in red would remain in the analysis on the basis of their length exceeding 3× SD+Mean. In this example: 3592.39 kb+3098.77 kb = 6691.16 kb

https://doi.org/10.1371/journal.pone.0028787.s003

(TIF)

Figure S3.

Frequency of ROHs in cases with and without a ROH of >8 Mb length. 71 cases were found to harbour at least one ROH of at least 8Mb length. Comparing these individuals against the remainder of cases (n = 1374) shows a small but significant rise in the number of ROH in those 71 cases, at various ROH lengths.

https://doi.org/10.1371/journal.pone.0028787.s004

(TIF)

Figure S4.

Consensus associated region in chromosome 19p13.3. ROHs in cases are shown in red. Consensus region to all ROHs in the region is shown in blue. No ROHs in controls spanned this region. RefSeq genes and transcripts in region are shown in blue.

https://doi.org/10.1371/journal.pone.0028787.s005

(TIFF)

Figure S5.

Three most significantly associated gene groups on chromosome 19. Genes spanned by ROHs in cases significantly more often than by ROHs in controls are shown in red. The three associated gene groups are shown in black. Blue bars denote case ROH, and brown bars denote control ROH. White arrows signify that a ROH continues beyond the borders of the image. The scale bar is 1Mb long.

https://doi.org/10.1371/journal.pone.0028787.s006

(TIFF)

Table S1.

Number of samples excluded during QC. a) Number of samples excluded during QC (1). b) Number of samples excluded during QC (2)

https://doi.org/10.1371/journal.pone.0028787.s007

(DOC)

Table S3.

Burden analysis. a) Proportion of samples with ROH of a given minimum size. b) Rate of ROH of a given minimum size

https://doi.org/10.1371/journal.pone.0028787.s009

(DOC)

Table S4.

Logistic models. a) Logistic models with proportion of samples with at least one ROH of a given minimum size as independent variable, and phenotype as dependent variable. b) Logistic models with rate of ROH of a given minimum size as independent variable, and phenotype as dependent variable. (Covariates - Model 1: unadjusted; Model 2: f; Model 3: f, age; Model 4: f, age, MDS)

https://doi.org/10.1371/journal.pone.0028787.s010

(DOC)

Table S5.

Logistic models. a) Logistic models with proportion of samples with at least one rare ROH of a given minimum size as independent variable, and phenotype as dependent variable. b) Logistic models with rate of rare ROH of a given minimum size as independent variable, and phenotype as dependent variable. (Covariates - Model 1: unadjusted; Model 2: f; Model 3: f, age; Model 4: f, age, MDS)

https://doi.org/10.1371/journal.pone.0028787.s011

(DOC)

Table S6.

Burden analysis following the exclusion of samples with ROH>8 Mb in size. a) Proportion of samples with ROH of a given minimum size. b) Rate of ROH of a given minimum size.

https://doi.org/10.1371/journal.pone.0028787.s012

(DOC)

Table S7.

Burden analysis following the exclusion of ROH>8 Mb in size. a) Proportion of samples with ROH of a given minimum size. b) Rate of ROH of a given minimum size.

https://doi.org/10.1371/journal.pone.0028787.s013

(DOC)

Table S8.

Burden analysis following the exclusion of samples with all ROH>2 Mb size across known PARK loci. a) Proportion of samples with all ROH of a given minimum size. b) Rate of all ROH of a given minimum size.

https://doi.org/10.1371/journal.pone.0028787.s014

(DOC)

Table S9.

Burden analysis following the exclusion of samples with rare ROH>2 Mb size across known PARK loci. a) Proportion of samples with rare ROH of a given minimum size. b) Rate of rare ROH of a given minimum size.

https://doi.org/10.1371/journal.pone.0028787.s015

(DOC)

Table S10.

Logistic models following the exclusion of samples with all ROH>2 Mb across known PARK loci. a) Logistic models with proportion of samples with at least one ROH of a given minimum size as independent variable, and phenotype as dependent variable. b) Logistic models with rate of all ROH of a given minimum size as independent variable, and phenotype as dependent variable. (Covariates - Model 1: unadjusted; Model 2: f; Model 3: f, age; Model 4: f, age, MDS)

https://doi.org/10.1371/journal.pone.0028787.s016

(DOC)

Table S11.

Logistic models following the exclusion of samples with rare ROH>2 Mb across known PARK loci. a) Logistic models with proportion of samples with at least one rare ROH of a given minimum size as independent variable, and phenotype as dependent variable. b) Logistic models with rate of rare ROH of a given minimum size as independent variable, and phenotype as dependent variable. (Covariates - Model 1: unadjusted; Model 2: f; Model 3: f, age; Model 4: f, age, MDS)

https://doi.org/10.1371/journal.pone.0028787.s017

(DOC)

Table S12.

Gene-based homozygosity mapping results of the most prominent PARK genes. P = uncorrected p value. P* = p value corrected for multiple testing using 100,000 case/control status permutations

https://doi.org/10.1371/journal.pone.0028787.s018

(DOC)

Acknowledgments

This study was undertaken on behalf of the International Parkinson's Disease Genomics Consortium (members are listed below). We used genome-wide association data generated by the Wellcome Trust Case-Control Consortium 2 (WTCCC2) from UK patients with Parkinson's disease and UK control individuals from the 1958 Birth Cohort and National Blood Service. This study utilized the high-performance computational capabilities of the Biowulf Linux cluster at the National Institutes of Health, Bethesda, Md. (http://biowulf.nih.gov).We also want to thank the Hersenstichting Nederland (http://www.hersenstichting.nl), the Neuroscience Campus Amsterdam and the Prinses Beatrix Fonds (http://www.prinsesbeatrixfonds.nl) for sponsoring this work.

International Parkinson Disease Genomics Consortium Members

Javier Simón-Sánchez (Department of Clinical Genetics, Section of Medical Genomics, VU University Medical Centre, Amsterdam, The Netherlands), Laura L. Kilarski (MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK), Michael A. Nalls (Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA), María Martinez (INSERM UMR 1043, CPTP; and Paul Sabatier University, Toulouse, France), Claudia Schulte (Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research), Peter Holmans (Department of Psychological Medicine & Neurology, Cardiff University School of Medicine, Cardiff, UK), Sampath Arepalli (Laboratory of Neurogenetics, National Institute on Aging), Roger A Barker (Department of Neurology, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK), Yoav Ben-Shlomo (Department of Social Medicine, Bristol University, UK), Henk W Berendse (Department of Neurology, VU University Medical Center, Amsterdam, The Netherlands), Daniela Berg (Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research), Kailash Bhatia (Department of Motor Neuroscience, UCL Institute of Neurology), Rob M A de Bie (Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands), Alessandro Biffi (Center for Human Genetic Research and Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; and Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA), Bastiaan R. Bloem (Department of Neurology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands), Zoltan Bochdanovits (Department of Clinical Genetics, Section of Medical Genomics, VU University Medical Centre), Michael Bonin (Department of Medical Genetics, Institute of Human Genetics, University of Tübingen, Tübingen, Germany), Jose M Bras (Department of Molecular Neuroscience, UCL Institute of Neurology), Kathrin Brockmann (Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research), Janet Brooks (Laboratory of Neurogenetics, National Institute on Aging), David J Burn (Newcastle University Clinical Ageing Research Unit, Campus for Ageing and Vitality, Newcastle upon Tyne, UK), Gavin Charlesworth (Department of Molecular Neuroscience, UCL Institute of Neurology), Honglei Chen (Epidemiology Branch, National Institute of Environmental Health Sciences, National Institutes of Health, NC, USA), Patrick F Chinnery (Neurology M4104, The Medical School, Framlington Place, Newcastle upon Tyne, UK), Sean Chong (Laboratory of Neurogenetics, National Institute on Aging), Carl E Clarke (School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK; and Department of Neurology, City Hospital, Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK), Mark R Cookson (Laboratory of Neurogenetics, National Institute on Aging), Jean Christophe Corvol (INSERM, UMR_S975; Université Pierre et Marie Curie-Paris; CNRS; and INSERM CIC-9503, Hôpital Pitié-Salpêtrière, Paris, France), Philippe Damier (CHU Nantes, CIC0004, Service de Neurologie, Nantes, France), Panos Deloukas (Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK), Günther Deuschl (Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Christian-Albrechts-Universität Kiel, Kiel, Germany), David T Dexter (Parkinson's Disease Research Group, Faculty of Medicine, Imperial College London, London, UK), Karin D van Dijk (Department of Neurology, VU University Medical Center, Amsterdam, The Netherlands), Allissa Dillman (Laboratory of Neurogenetics, National Institute on Aging), Frank Durif (Service de Neurologie, Hôpital Gabriel Montpied, Clermont-Ferrand, France), Alexandra Dürr (INSERM, UMR_S975; Université Pierre et Marie Curie-Paris; CNRS; and AP-HP, Pitié-Salpêtrière Hospital), Sarah Edkins (Wellcome Trust Sanger Institute), Jonathan R Evans (Cambridge Centre for Brain Repair, Cambridge, UK), Thomas Foltynie (UCL Institute of Neurology), Jianjun Gao (Epidemiology Branch, National Institute of Environmental Health Sciences), Michelle Gardner (Department of Molecular Neuroscience, UCL Institute of Neurology), J Raphael Gibbs (Laboratory of Neurogenetics, National Institute on Aging; and Department of Molecular Neuroscience, UCL Institute of Neurology), Alison Goate (Department of Psychiatry, Department of Neurology, Washington University School of Medicine, MI, USA), Emma Gray (Wellcome Trust Sanger Institute), Rita Guerreiro (Department of Molecular Neuroscience, UCL Institute of Neurology), Dena G Hernandez (Laboratory of Neurogenetics, National Institute on Aging; and Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK), Jacobus J van Hilten (Department of Neurology, Leiden University Medical Center, Leiden, Netherlands), Albert Hofman (Department of Epidemiology, Erasmus University Medical Center, Rotterdam, Netherlands), Albert Hollenbeck (AARP, Washington DC, USA), Janice Holton (Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology), Xuemei Huang (Departments of Neurology, Radiology, Neurosurgery, Pharmacology, Kinesiology, and Bioengineering, Pennsylvania State University– Milton S Hershey Medical Center, Hershey, PA, USA), Heiko Huber (Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research), Gavin Hudson (Neurology M4104, The Medical School, Newcastle upon Tyne, UK), Sarah E Hunt (Wellcome Trust Sanger Institute), Thomas Illig (Institute of Epidemiology, Helmholtz Zentrum Mnchen, German Research Centre for Environmental Health, Neuherberg, Germany), Jean-Charles Lambert (INSERM U744, Lille, France; and Institut Pasteur de Lille, Université de Lille Nord, Lille, France), Cordelia Langford (Cambridge Centre for Brain Repair), Andrew Lees (Queen Square Brain Bank for Neurological Disorders), Suzanne Lesage (INSERM, UMR_S975 [ formerly UMR_S679], Paris, France; Université Pierre et Marie Curie-Paris, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, Paris, France; and CNRS, Paris, France), Peter Lichtner (Institute of Human Genetics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany), Patricia Limousin (Institute of Neurology, Sobell Department, Unit of Functional Neurosurgery, London, UK), Grisel Lopez (Section on Molecular Neurogenetics, Medical Genetics Branch, NHGRI, National Institutes of Health), Delia Lorenz (Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein), Alisdair McNeill (Department of Clinical Neurosciences, UCL Institute of Neurology), Catriona Moorby (School of Clinical and Experimental Medicine, University of Birmingham), Matthew Moore (Laboratory of Neurogenetics, National Institute on Aging), Karen E Morrison (School of Clinical and Experimental Medicine, University of Birmingham; and Neurosciences Department, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK), Ese Mudanohwo (Neurogenetics Unit, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery), Sean S O'Sullivan (Queen Square Brain Bank for Neurological Disorders), Justin Pearson (MRC Centre for Neuropsychiatric Genetics and Genomics), Michael J Owen (MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK), Joel S Perlmutter (Department of Neurology, Radiology, and Neurobiology at Washington University, St Louis), Pierre Pollak (Service de Neurologie, CHU de Grenoble, Grenoble, France), Bart Post (Department of Neurology, Radboud University Nijmegen Medical Centre), Simon Potter (Wellcome Trust Sanger Institute), Bernard Ravina (Translational Neurology, Biogen Idec, MA, USA), Tamas Revesz (Queen Square Brain Bank for Neurological Disorders), Olaf Riess (Department of Medical Genetics, Institute of Human Genetics, University of Tübingen), Fernando Rivadeneira (Departments of Epidemiology and Internal Medicine, Erasmus University Medical Center), Patrizia Rizzu (Department of Clinical Genetics, Section of Medical Genomics, VU University Medical Centre), Mohamad Saad (INSERM UMR 1043, CPTP, Toulouse, France; and Paul Sabatier University, Toulouse, France), Stephen Sawcer (University of Cambridge, Department of Clinical Neurosciences, Addenbrooke's hospital, Cambridge, UK), Anthony Schapira (Department of Clinical Neurosciences, UCL Institute of Neurology), Hans Scheffer (Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands), Manu Sharma (Departmentfor Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, and DZNE, German Center for Neurodegenerative Diseases, Tübingen, Germany), Karen Shaw (Queen Square Brain Bank for Neurological Disorders), Una-Marie Sheerin (Department of Molecular Neuroscience, UCL Institute of Neurology), Ira Shoulson (Department of Neurology, University of Rochester, Rochester, NY, USA), Ellen Sidransky (Section on Molecular Neurogenetics, Medical Genetics Branch, NHGRI), Chris C A Spencer (Wellcome Trust Centre for Human Genetics, Oxford, UK), Amy Strange (Wellcome Trust Centre for Human Genetics), Carlie M Tanner (Clinical Research Department, The Parkinson's Institute and Clinical Center, Sunnyvale, CA, USA), Avazeh Tashakkori-Ghanbaria (Wellcome Trust Sanger Institute), François Tison (Service de Neurologie, Hôpital Haut-Lévêque, Pessac, France), André G Uitterlinden (Departments of Epidemiology and Internal Medicine, Erasmus University Medical Center), Daan Velseboer (Department of Neurology, Academic Medical Center), Marie Vidailhet (INSERM, UMR_S975, Université Pierre et Marie Curie-Paris, CNRS, UMR 7225), Bart van de Warrenburg (Department of Neurology, Radboud University Nijmegen Medical Centre), Mirdhu Wickremaratchi (Department of Neurology, Cardiff University, Cardiff , UK), Caroline H Williams-Gray (Department of Neurology, Addenbrooke's Hospital), Sophie Winder-Rhodes (Cambridge Centre for Brain Repair, University of Cambridge), Wellcome Trust Case-Control Consortium 2, Diana Zelenika (Centre National de Génotypage, Institut Génomique, Commissariat à l'Energie Atomique, Evry, France), Thomas Gasser (Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, and DZNE, German Center for Neurodegenerative Diseases), John Hardy (Department of Molecular Neuroscience, UCL Institute of Neurology), Andrew B Singleton (Laboratory of Neurogenetics, National Institute on Aging), Nicholas W Wood (UCL Genetics Institute; and Department of Molecular Neuroscience, UCL Institute of Neurology), Alexis Brice (INSERM, UMR_S975, Université Pierre et Marie Curie-Paris, CNRS, UMR 7225, AP-HP, Pitié-Salpêtrière Hospital), Peter Heutink (Department of Clinical Genetics, Section of Medical Genomics, VU University Medical Centre), Nigel Williams (MRC Centre for Neuropsychiatric Genetics and Genomics), Huw R Morris (MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff , UK).

Author Contributions

Conceived and designed the experiments: HRM NMW LLK JS-S CS. Performed the experiments: JS-S LLK. Analyzed the data: LLK JS-S. Contributed reagents/materials/analysis tools: CS. Wrote the paper: LLK JS-S HRM NMW. Contributed samples: TG JH ABS NWW AB PH NMW HRM WTCCC2. Critically reviewed manuscript: MAN MM PAH JH AB NMW HRM JS-S LLK.

References

  1. 1. Lees AJ, Hardy J, Revesz T (2007) Parkinson's disease. Lancet 373: 2055–2066.
  2. 2. Hardy J (2010) Genetic Analysis of Pathways to Parkinson's Disease. Neuron 68: 201–206.
  3. 3. Simón-Sánchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, et al. (2009) Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 41: 1308–1312.
  4. 4. Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, et al. (2009) Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 41: 1303–1307.
  5. 5. Spencer CC, Plagnol V, Strange A, et al. UK Parkinson's Disease Consortium, Wellcome Trust Case Control Consortium 2 (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet 20: 345–353.
  6. 6. Saad M, Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, et al. (2011) Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Hum Mol Genet 20: 615–627.
  7. 7. Simón-Sánchez J, van Hilten JJ, van de Warrenburg B, Post B, Berendse HW, et al. (2011) Genome-wide association study confirms Extant PD risk loci among the Dutch. Eur J Hum Genet.
  8. 8. Van Den Eeden SK, Tanner CM, Bernstein AL, Fross RD, Leimpeter A, et al. (2003) Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity. Am J Epidemiol 157: 1015–1022.
  9. 9. Wickremaratchi MM, Perera D, O'Loghlen C, Sastry D, Morgan E, et al. (2009) Prevalence and age of onset of Parkinson's disease in Cardiff: a community based cross sectional study and meta-analysis. J Neurol Neurosurg Psychiatry 80: 805–807.
  10. 10. Thacker EL, Ascherio A (2008) Familial Aggregation of Parkinson's Disease: A Meta-Analysis. Mov Disord 23: 1174–1183.
  11. 11. Marder K, Levy G, Louis ED, Mejia-Santana H, Cote L, et al. (2003) Familial aggregation of early- and late-onset Parkinson's disease. Ann. Neurol 54: 507–513.
  12. 12. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, et al. (1998) Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392: 605–608.
  13. 13. Valente EM, Abou-Sleiman PM, Caputo V, Muqit MMK, Harvey K, et al. (2004) Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304: 1158–1160.
  14. 14. Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, et al. (2003) Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 256–259.
  15. 15. Paisán-Ruiz C, Guevara R, Federoff M, Hanagasi H, Sina F, et al. (2010) Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord 25: 1791–1800.
  16. 16. Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, et al. (2000) Association between early-onset Parkinson's disease and mutations in the parkin gene. N Engl J Med 342: 1560–1567.
  17. 17. Brooks J, Ding J, Simon-Sanchez J, Paisan-Ruiz C, Singleton AB, et al. (2009) Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control. J Med Genet 46: 375–381.
  18. 18. Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C (2010) Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. Hum Mutat 31: 763–780.
  19. 19. Simon-Sanchez J, Scholz S, Fung H-C, Matarin M, Hernandez D, et al. (2007) Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. Hum Mol Genet 16: 1–14.
  20. 20. Gibbs JR, Singleton AB (2006) Application of Genome-wide Single Nucleotide Polymorphism Typing: Simple Association and beyond. PLoS Genet 2(10): e150.
  21. 21. McQuillan R, Leutenegger A-L, Abdel-Rahman R, Franklin CS, Pericic M, et al. (2008) Runs of homozygosity in European populations. Am J Hum Genet 83: 359–372.
  22. 22. Hildebrandt F, Heeringa SF, Rüschendorf F, Attanasio M, Nürnberg G, et al. (2009) A systematic approach to mapping recessive disease genes in individuals from outbred populations. PLoS Genet 5(1): e1000353.
  23. 23. Nalls MA, Plagnol V, Hernandez DG, Sharma M, et al. International Parkinson Disease Genomics Consortium (2011) Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet 377: 641–649.
  24. 24. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, et al. (2007) PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses. Am J Hum Genet 81: 559–575.
  25. 25. R Development Core Team (2009) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0, http://www.R-project.org.
  26. 26. Nothnagel M, Lu TT, Kayser M, Krawczak M (2010) Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans. Hum Mol Genet 19: 2927–2935.
  27. 27. Nalls MA, Simon-Sanchez J, Gibbs JR, Paisan-Ruiz C, Bras JT, et al. (2009) Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics. PLoS Genet 5(3): e1000415.
  28. 28. Bacolod MD, Schemmann GS, Wang S, Shattock R, Giardina , et al. (2008) The signatures of autozygosity among patients with colorectal cancer. Cancer Research 68: 2610–2621.
  29. 29. Spain SL, Cazier J-B, Houlston R, Carvajal-Carmona L, Tomlinson I (2009) Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom. Cancer Research 69: 7422–7429.
  30. 30. Vine AE, McQuillin A, Bass NJ, Pereira A, Kandaswamy R, et al. (2009) No evidence for excess runs of homozygosity in bipolar disorder. Psychiatric Genetics 19: 165–170.
  31. 31. Lencz T, Lambert C, DeRosse P, Burdick KE, Morgan TV, et al. (2007) Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. PCNS 104: 19942–19947.
  32. 32. Nalls MA, Guerreiro RJ, Simon-Sanchez J, Bras JT, Traynor BJ, et al. (2009) Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease. Neurogenetics 10: 183–190.
  33. 33. Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, et al. (2011) No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet 156: 764–771.
  34. 34. Milbrandt J, de Sauvage FJ, Fahrner TJ, Baloh RH, Leitner ML, et al. (1998) Persephin, a Novel Neurotrophic Factor Related to GDNF and Neurturin. Neuron 2: 245–253.