| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2018PLoSO..1308828H |
| P356 | DOI | 10.1371/JOURNAL.PONE.0208828 |
| P932 | PMC publication ID | 6287820 |
| P698 | PubMed publication ID | 30532134 |
| P50 | author | David M Hougaard | Q87889187 |
| Michael Christiansen | Q90373085 | ||
| Jimmi Nielsen | Q96099113 | ||
| Alfonso B. Demur | Q117264934 | ||
| Thomas Werge | Q29122092 | ||
| Merete Nordentoft | Q30456284 | ||
| Jorgen K. Kanters | Q50884207 | ||
| Marie Bækvad-Hansen | Q55762199 | ||
| Jonas Bybjerg-Grauholm | Q57640435 | ||
| Christian Hagen | Q58309994 | ||
| Thomas D. Als | Q60446908 | ||
| James L. Kennedy | Q73266726 | ||
| Vanessa F. Gonçalves | Q87614338 | ||
| Preben Bo Mortensen | Q39051287 | ||
| Ole Mors | Q41638422 | ||
| Paula Louise Hedley | Q42173385 | ||
| Anders D. Børglum | Q46997890 | ||
| P2093 | author name string | Christine S Hansen | |
| P2860 | cites work | Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency | Q24308632 |
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| Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation | Q37156232 | ||
| Modification by KCNE1 variants of the hERG potassium channel response to premature stimulation and to pharmacological inhibition | Q37411148 | ||
| Ethnic origin and increased risk for schizophrenia in immigrants to countries of recent and longstanding immigration | Q37682286 | ||
| Mitochondrial DNA (mtDNA) and schizophrenia | Q37803459 | ||
| Monogenic Mitochondrial Disorders | Q37995644 | ||
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| A cybrid cell model for the assessment of the link between mitochondrial deficits and sporadic Parkinson's disease | Q38915128 | ||
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| MtDNA meta-analysis reveals both phenotype specificity and allele heterogeneity: a model for differential association | Q42320268 | ||
| The power to detect disease associations with mitochondrial DNA haplogroups | Q43259568 | ||
| Geographic distribution of multiple sclerosis: An update with special reference to Europe and the Mediterranean region | Q43477891 | ||
| Full spectrum of psychiatric disorders related to foreign migration: a Danish population-based cohort study | Q44840172 | ||
| Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study | Q45008584 | ||
| Crohn's disease and ulcerative colitis. Occurrence, course and prognosis during the first year of disease in a European population-based inception cohort | Q45830165 | ||
| A matrilineal genetic legacy from the last glacial maximum confers susceptibility to schizophrenia in Han Chinese | Q47215069 | ||
| Analysis of European mitochondrial haplogroups with Alzheimer disease risk | Q47246890 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ggplot2 | Q326489 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | schizophrenia | Q41112 |
| P304 | page(s) | e0208828 | |
| P577 | publication date | 2018-12-10 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease | |
| P478 | volume | 13 |
| Q90288509 | Novel Complex Interactions between Mitochondrial and Nuclear DNA in Schizophrenia and Bipolar Disorder | cites work | P2860 |
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