# Hugh Watkins

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hugh-watkins/

## Facts

| Field | Value |
| --- | --- |
| Citations | 119,268 |
| Field | Cardiomyopathy and Myosin Studies |
| h-index | 145 |
| i10-index | 430 |
| Last Known Institution | Centre for Human Genetics |
| OpenAlex ID | https://openalex.org/A5033758288 |
| ORCID iD | https://orcid.org/0000-0002-5287-9016 |
| Works | 852 |

## Researcher papers

- [Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk](https://scholariq.org/papers/genetic-variants-in-novel-pathways-influence-blood-pressure-and-cardiovascular/)
- [Left Ventricular Non-Compaction](https://scholariq.org/papers/left-ventricular-non-compaction/)
- [Current State of Knowledge on Aetiology, Diagnosis, Management, and Therapy of Peripartum Cardiomyopathy: A Position Statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy](https://scholariq.org/papers/current-state-of-knowledge-on-aetiology-diagnosis-management-and-therapy-of-2/)
- [Mendelian randomization of blood lipids for coronary heart disease](https://scholariq.org/papers/mendelian-randomization-of-blood-lipids-for-coronary-heart-disease/)
- [Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants](https://scholariq.org/papers/discovery-and-systematic-characterization-of-risk-variants-and-genes-for/)
- [Whole-genome sequencing of patients with rare diseases in a national health system](https://scholariq.org/papers/whole-genome-sequencing-of-patients-with-rare-diseases-in-a-national-health/)
- [Factors influencing success of clinical genome sequencing across a broad spectrum of disorders](https://scholariq.org/papers/factors-influencing-success-of-clinical-genome-sequencing-across-a-broad/)
- [Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity](https://scholariq.org/papers/common-genetic-variants-and-modifiable-risk-factors-underpin-hypertrophic/)
- [Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM Registry](https://scholariq.org/papers/distinct-subgroups-in-hypertrophic-cardiomyopathy-in-the-nhlbi-hcm-registry/)
- [Germline selection shapes human mitochondrial DNA diversity](https://scholariq.org/papers/germline-selection-shapes-human-mitochondrial-dna-diversity/)
- [Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension](https://scholariq.org/papers/phenotypic-characterization-of-i-eif2ak4-i-mutation-carriers-in-a-large-cohort/)

## Researcher topics

- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Cardiovascular Function and Risk Factors](https://scholariq.org/topics/cardiovascular-function-and-risk-factors/)
- [Cardiovascular Effects of Exercise](https://scholariq.org/topics/cardiovascular-effects-of-exercise/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Researcher university

- [Centre for Human Genetics](https://scholariq.org/institutions/centre-for-human-genetics/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.