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S. Finer · SciRah

Researcher profile · Semantic Scholar

S. Finer

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S. Finer — researcher profile on SciRah

h-index: 16
Works: 79
Citations: 1,990

Most-cited papers

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Ken Suzuki, K. Hatzikotoulas, L. Southam, H. Taylor +360 more
2024Nature540 citations Open access
Semantic Scholar
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Wei Zhou, M. Kanai, Kuan-Han H. Wu, Humaira Rasheed +148 more
2022Cell Genomics388 citations Open access
Semantic Scholar
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
M. Adams, F. Streit, Xiangrui Meng, S. Awasthi +374 more
2025Cell247 citations Open access
Semantic Scholar
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Xiangrui Meng, Georgina Navoly, O. Giannakopoulou, D. Levey +74 more
2024Nature Genetics167 citations Open access
Semantic Scholar
A second update on mapping the human genetic architecture of COVID-19
Masahiro Shea J. Mattia Christine Benjamin M. Mark Andrea G Kanai Andrews Cordioli Stevens Neale Daly Ganna Pa, Masahiro Shea J. Mattia Christine Benjamin M. Mark Andrea Kanai Andrews Cordioli Stevens Neale Daly Ganna, Masahiro Kanai, S. Andrews +496 more
2022Nature108 citations Open access
Semantic Scholar
Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals
Qin-Qin Huang, N. Sallah, D. Dunca, B. Trivedi +14 more
2022Nature Communications56 citations Open access
Semantic Scholar
Genetic basis of early onset and progression of type 2 diabetes in South Asians
S. Hodgson, A. Williamson, M. Bigossi, D. Stow +10 more
2024Nature Medicine54 citations Open access
Semantic Scholar
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Albert Henry, Xiaodong Mo, C. Finan, M. Chaffin +177 more
2025Nature Genetics48 citations Open access
Semantic Scholar
Ethnic differences in early onset multimorbidity and associations with health service use, long-term prescribing, years of life lost, and mortality: A cross-sectional study using clustering in the UK Clinical Practice Research Datalink
Fabiola Eto, Miriam Samuel, R. Henkin, Meera Mahesh +9 more
2023PLoS Medicine42 citations Open access
Semantic Scholar
CYP2C19 Genotype Prevalence and Association With Recurrent Myocardial Infarction in British–South Asians Treated With Clopidogrel
E. Magavern, Benjamin Jacobs, H. Warren, G. Finocchiaro +4 more
2023JACC: Advances37 citations Open access
Semantic Scholar
Influence of autozygosity on common disease risk across the phenotypic spectrum
D. Malawsky, E. V. van Walree, B. Jacobs, T. Heng +17 more
2023medRxiv31 citations Open access
Semantic Scholar
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
B. Jacobs, D. Stow, S. Hodgson, J. Zollner +13 more
2024Nature Communications24 citations Open access
Semantic Scholar
Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72
Noori Chai, Michael S. Haney, Julien Couthouis, D. Morgens +7 more
2019bioRxiv22 citations Open access
Semantic Scholar
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Aeron M. Small, Ta-Yu Yang, Shinsuke Itoh, S. Thériault +97 more
2025Nature Genetics17 citations Open access
Semantic Scholar
Initial findings from the DecodeME genome-wide association study of myalgic encephalomyelitis/chronic fatigue syndrome
T. Boutin, A. Bretherick, J. Dibble, E. Ewaoluwagbemiga +39 more
2025medRxiv17 citations Open access
Semantic Scholar
What does social prescribing look like in practice? A qualitative case study informed by practice theory.
Sara Calderón-Larrañaga, Trisha Greenhalgh, S. Finer, Megan Clinch
2024Social Science & Medicine (1967)16 citations Open access
Semantic Scholar
Unravelling the potential of social prescribing in individual-level type 2 diabetes prevention: a mixed-methods realist evaluation
Sara Calderón-Larrañaga, T. Greenhalgh, Megan Clinch, J. Robson +3 more
2023BMC Medicine16 citations Open access
Semantic Scholar
Artificial Intelligence for Multiple Long-term conditions (AIM): A consensus statement from the NIHR AIM consortia
H. Dambha-Miller, A. Farmer, K. Nirantharakumar, Thomas Jackson +10 more
202316 citations Open access
Semantic Scholar
Prevalence of multimorbidity in survivors of 28 cancer sites: an English nationwide cross-sectional study.
Tahania Ahmad, Abu Zm Dayem Ullah, C. Chelala, D. Gopal +5 more
2024American Journal of Cancer Research13 citations Open access
Semantic Scholar
Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistanis and Bangladeshis
Qin-Qin Huang, N. Sallah, D. Dunca, B. Trivedi +14 more
2021medRxiv12 citations Open access
Semantic Scholar
Undiagnosed G6PD deficiency in Black and Asian individuals is prevalent and contributes to health inequalities in type 2 diabetes diagnosis and complications
Susan Martin, Miriam Samuel, D. Stow, Alys M. Ridsdale +8 more
2025Diabetes Care11 citations
Semantic Scholar
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries
A. Huerta-Chagoya, Joohyun Kim, R. Mandla, Ying-Chang Lu +254 more
2025medRxiv9 citations
Semantic Scholar
Trends in weight gain recorded in English primary care before and during the Coronavirus-19 pandemic: An observational cohort study using the OpenSAFELY platform
Miriam Samuel, Robin Y. Park, S. Eastwood, Fabiola Eto +14 more
2023medRxiv9 citations Open access
Semantic Scholar
Rare variant contribution to cholestatic liver disease in a South Asian population in the United Kingdom
J. Zollner, S. Finer, K. Linton, S. Akhtar +65 more
2022medRxiv9 citations Open access
Semantic Scholar
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Samantha L. White, Maizy S. Brasher, J. Pattee, Wei Zhou +81 more
2026Nature Genetics8 citations Open access
Semantic Scholar
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity
Hye In Kim, C. DeBoever, K. Walter, G. Kalantzis +47 more
2025medRxiv8 citations Open access
Semantic Scholar
Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting.
M. Fejzo, Xin-Ran Wang, Qing Tan, J. Zollner +96 more
2026Nature Genetics6 citations Open access
Semantic Scholar
Advancing the communication of genetic risk for cardiometabolic diseases: a critical interpretive synthesis
Jing Hui Law, Naji Sultan, S. Finer, Nina Fudge
2023BMC Medicine6 citations Open access
Semantic Scholar
Characterisation of type 2 diabetes subgroups and their association with ethnicity and clinical outcomes: a UK real-world data study using the East London Database
R. Mathur, Sally A. Hull, S. Hodgson, S. Finer
2021medRxiv6 citations Open access
Semantic Scholar
Ethnic differences in early onset multimorbidity and associations with health service use, long-term prescribing, years of life lost, and mortality: an observational study using person-level clustering in the UK Clinical Practice Research Datalink
F. Eto, M. Samuel, R. Henkin, M. Mahesh +9 more
2023medRxiv5 citations Open access
Semantic Scholar
Data-driven prioritization of high-risk individuals for weight loss interventions
K. Demircan, J. Carrasco-Zanini, A. Williamson, C. Beuchel +11 more
2026Nature Medicine4 citations Open access
Semantic Scholar
Genetics of Cholesterol and Coronary Disease Risk across Six Global Ancestries
S. Urbut, Qiu-Li Chen, Y. Sui, A. Misra +10 more
2025NEJM Evidence4 citations Open access
Semantic Scholar
Evidence of ethnic variations in the relationships between routinely recorded clinical factors and T2D: a systematic review and meta-analysis
Binur Orazumbekova, Tooba Hamdani, S. Hodgson, Miriam Samuel +5 more
2025International Journal of Obesity4 citations
Semantic Scholar
Multi-ancestry GWAS of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity
M. Fejzo, Xin-Ran Wang, J. Zollner, N. Pujol-Gualdo +25 more
2024medRxiv4 citations Open access
Semantic Scholar
Investigating misclassification of type 1 diabetes in a population-based cohort of British Pakistanis and Bangladeshis using polygenic risk scores
Ti-Ming Liu, A. Sankareswaran, Gordon Paterson, D. P. Fraser +12 more
2023Scientific Reports4 citations Open access
Semantic Scholar
Multi-ancestry GWAS of major depression aids locus discovery, fine-mapping, gene prioritisation, and causal inference
Xiangrui Meng, Georgina Navoly, O. Giannakopoulou, D. Levey +70 more
2022bioRxiv4 citations Open access
Semantic Scholar
Group clinics for young adults living with diabetes in an ethnically diverse, socioeconomically deprived population: mixed-methods evaluation
C. Papoutsi, D. Hargreaves, A. Hagell, N. Hounsome +6 more
2022Health and Social Care Delivery Research4 citations Open access
Semantic Scholar
The genetic architecture of fibromyalgia across 2.5 million individuals
I. Kerrebijn, G. Bjornsdottir, K. Arbabi, L. Urpa +49 more
2026Nature Medicine3 citations Open access
Semantic Scholar
Nanoparticle-enriched mass spectrometry proteomics in British South Asians identifies links between genetic variants, plasma protein levels and disease risk
M. Pietzner, A. Williamson, K. Hunt, M. Koprulu +6 more
2026Nature Genetics3 citations Open access
Semantic Scholar
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Caroline Brito Nunes, V. Rukins, A. H. Cissé, F. White +75 more
2025Nature Communications3 citations Open access
Semantic Scholar
Nanoparticle enriched mass spectrometry proteomics in British South Asians identifies novel variant-protein-disease mechanisms
M. Pietzner, A. Williamson, K. Hunt, M. Koprulu +7 more
2025medRxiv3 citations Open access
Semantic Scholar
Understanding the potential contribution of polygenic risk scores to the prediction of gestational and type 2 diabetes in women from British Pakistani and Bangladeshi groups: a cohort study in Genes and Health
J. Zollner, D. V. van Heel, Binur Orazumbekova, S. Hodgson +69 more
2025medRxiv3 citations Open access
Semantic Scholar
Weight trends among adults with diabetes or hypertension during the COVID-19 pandemic: an observational study using OpenSAFELY
Miriam Samuel, Robin Y. Park, S. Eastwood, Fabiola Eto +14 more
2024The British journal of general practice : the journal of the Royal College of General Practitioners3 citations Open access
Semantic Scholar
O10 Acne polygenic risk score derived from genome-wide association metaregression enables prediction of severity
X. Du-Harpur, Jessye Maxwell, Brittany L. Mitchell, L. Pardo +46 more
2025British Journal of Dermatology2 citations
Semantic Scholar
Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity
T. Heng, K. Walter, Qin-Qin Huang, J. Karjalainen +7 more
2025American Journal of Human Genetics2 citations Open access
Semantic Scholar
Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Samantha L. White, Maizy S. Brasher, J. Pattee, Wei Zhou +79 more
2025medRxiv2 citations Open access
Semantic Scholar
Perceived risk of type 2 diabetes: Using linked genomic, clinical and questionnaire data to understand the potential use of genetic risk tools in British South Asians
Jing Hui Law, D. Stow, S. Hodgson, D. V. van Heel +3 more
2024medRxiv2 citations Open access
Semantic Scholar
The contribution of apolipoprotein E genetic variation to dementia risk in British South Asians
B. Jacobs, A. Chandra, I. Foote, Faiza Durrani +11 more
2026Brain Communications1 citations Open access
Semantic Scholar
Equity and impact of social prescribing in type 2 diabetes prevention: cross-sectional and cohort study using national primary care data.
Sara Calderón-Larrañaga, Bernardo Meza-Torres, S. de Lusignan, R. Mathur +2 more
2026The British journal of general practice : the journal of the Royal College of General Practitioners1 citations Open access
Semantic Scholar
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration
D. Palmer, Barney Hill, S. Hodgson, Maarja Jõeloo +49 more
2026medRxiv1 citations Open access
Semantic Scholar

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