| human | Q5 |
| P496 | ORCID iD | 0000-0002-1843-9842 |
| P1153 | Scopus author ID | 8931613700 |
| P69 | educated at | Queen Mary University of London | Q195668 |
| P108 | employer | University of Cambridge | Q35794 |
| Queen Mary University of London | Q195668 | ||
| King's College London | Q245247 | ||
| P734 | family name | Newhouse | Q16878036 |
| Newhouse | Q16878036 | ||
| Newhouse | Q16878036 | ||
| P735 | given name | Stephen | Q4927100 |
| Stephen | Q4927100 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q37054037 | A Pathway Based Classification Method for Analyzing Gene Expression for Alzheimer's Disease Diagnosis |
| Q54246649 | A genome-wide association study for extremely high intelligence. |
| Q39140766 | Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease |
| Q50646784 | Alzheimer's disease biomarker discovery using SOMAscan multiplexed protein technology. |
| Q34543157 | An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis |
| Q42499208 | An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline. |
| Q57481517 | Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder |
| Q48615424 | Assessment of ZnT3 and PSD95 protein levels in Lewy body dementias and Alzheimer's disease: association with cognitive impairment. |
| Q24630508 | Blood pressure loci identified with a gene-centric array |
| Q27345159 | Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets |
| Q38152257 | Candidate blood proteome markers of Alzheimer's disease onset and progression: a systematic review and replication study |
| Q35671414 | Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study |
| Q35746977 | Circulating Proteomic Signatures of Chronological Age. |
| Q35783787 | Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium |
| Q21143760 | Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies |
| Q92197348 | Differential gene expression analysis in blood of first episode psychosis patients |
| Q56353844 | Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies |
| Q24657931 | Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip |
| Q35181532 | Genes and hypertension |
| Q38730776 | Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study |
| Q28654771 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization |
| Q28655720 | Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis |
| Q37705236 | Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study |
| Q28554877 | Genome-Wide Association of Heroin Dependence in Han Chinese |
| Q24643127 | Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia |
| Q96646267 | Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways |
| Q37200992 | Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations |
| Q37223293 | Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis |
| Q56970816 | Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study |
| Q54975927 | Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci. |
| Q30419436 | Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci |
| Q30425020 | Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci |
| Q35015795 | Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension |
| Q39043511 | Linking Genetics of Brain Changes to Alzheimer's Disease: Sparse Whole Genome Association Scan of Regional MRI Volumes in the ADNI and AddNeuroMed Cohorts |
| Q34458862 | Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height |
| Q56457854 | Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height |
| Q39634019 | Mitochondrial dysfunction and immune activation are detectable in early Alzheimer's disease blood |
| Q47750917 | Multi-polygenic score approach to trait prediction |
| Q46631793 | No Evidence to Suggest that the Use of Acetylcholinesterase Inhibitors Confounds the Results of Two Blood-Based Biomarker Studies in Alzheimer's Disease |
| Q48807243 | No differences in hippocampal volume between carriers and non-carriers of the ApoE ε4 and ε2 alleles in young healthy adolescents. |
| Q40350674 | Pharmacogenetics of antidepressant response: A polygenic approach |
| Q50648690 | Pharmacogenetics of pemetrexed combination therapy in lung cancer: pathway analysis reveals novel toxicity associations. |
| Q34427001 | Plasma based markers of [11C] PiB-PET brain amyloid burden |
| Q58782266 | Polygenic risk score analyses of symptoms and treatment response in an antipsychotic-naive first episode of psychosis cohort |
| Q33426861 | Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion |
| Q59544267 | Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis |
| Q31002427 | Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray |
| Q28473781 | SLC2A9 is a high-capacity urate transporter in humans |
| Q57900177 | Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients |
| Q33475633 | Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array |
| Q36466470 | The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder |
| Q33773036 | Trajectories of dementia-related cognitive decline in a large mental health records derived patient cohort |
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