Artificial intelligence for modelling infectious disease epidemics
Kraemer MUG. et al, (2025), Nature, 638, 623 - 635
Ethical issues in Nipah virus control and research: addressing a neglected disease
Johnson T. et al, (2024), Journal of Medical Ethics, 50, 612 - 617
'Something that helped the whole picture': Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service.
McInnes-Dean H. et al, (2024), Prenatal diagnosis, 44, 465 - 479
Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues
Sahan K. et al, (2024), Journal of Medical Ethics
A Large Language Model Approach to Educational Survey Feedback Analysis
Parker MJ. et al, (2024), International Journal of Artificial Intelligence in Education
Assembling a global health image: Ethical and pragmatic tensions through the lenses of photographers.
Alenichev A. et al, (2024), PLOS global public health, 4
Ethics and Tropical Diseases: Some Global Considerations
Jamrozik E. et al, (2024), Manson's Tropical Diseases, 64 - 69
Introduction: Research Ethics and Health Policy in Epidemics and Pandemics
Parker M. et al, (2024), Public Health Ethics Analysis, 1 - 22
The challenges and potential solutions of achieving meaningful consent amongst research participants in northern Thailand: a qualitative study.
Greer RC. et al, (2023), BMC medical ethics, 24
“The Nobodies”: unidentified dead bodies—a global health crisis requiring urgent attention
Suwalowska H. et al, (2023), The Lancet Global Health
Beyond translations, perspectives for researchers to consider to enhance comprehension during consent processes for health research in sub-saharan Africa: a scoping review.
Busisiwe N. et al, (2023), BMC medical ethics, 24
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland
Wright CF. et al, (2023), New England Journal of Medicine
Navigating uncertainties of death: Minimally Invasive Autopsy Technology in global health
Suwalowska H. et al, (2023), Global Public Health, 18
Healthcare resource allocation decisions and non-emergency treatments in the aftermath of Covid-19 pandemic. How should children with chronic illness feature in prioritisation processes?
Lignou S. et al, (2023), Wellcome open research, 8
Invisibility in global health: A case for disturbing bioethical frameworks.
Alenichev A. et al, (2023), Wellcome open research, 8
Equitable Design and Use of Digital Surveillance Technologies During COVID-19: Norms and Concerns
Pratt B. et al, (2022), Journal of Empirical Research on Human Research Ethics, 17, 573 - 586
Science in the time of COVID-19: Reflections on the UK Events Research Programme.
Marteau TM. et al, (2022), Nature communications, 13
Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service
Hill M. et al, (2022), NIHR Open Research, 2, 10 - 10
Initiation of an Emulsion Microinfusion: Flow Direction Influences Delivery Onset Rate
Tsao AC. et al, (2022), European Journal of Pharmaceutical Sciences, 172
Work-Up and Outcome of Hepatic Resection for Peri-Hilar Cholangiocarcinoma (PH-CCA) without Staging Laparoscopy
Jegatheeswaran S. et al, (2022), Cancers, 14
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies
Schröter J. et al, (2022), European Journal of Human Genetics, 30, 298 - 306
Further delineation of phenotypic spectrum of SCN2A-related disorder
Richardson R. et al, (2022), American Journal of Medical Genetics, Part A, 188, 867 - 877
A network of empirical ethics teams embedded in research programmes across multiple sites: opportunities and challenges in contributing to COVID-19 research and responses.
Ngwenya N. et al, (2022), Wellcome open research, 7
Transepithelial nasal potential difference in patients with, and at risk of acute respiratory distress syndrome
Mac Sweeney R. et al, (2021), Thorax, 76, 1099 - 1107
Expanding the phenotype of SETD5-related disorder and presenting a novel association with bone fragility
Anderson E. et al, (2021), Clinical Genetics, 100, 352 - 354
Heterozygous variants in SPTBN1 cause intellectual disability and autism
Rosenfeld JA. et al, (2021), American Journal of Medical Genetics, Part A, 185, 2037 - 2045
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants
Jacobs EZ. et al, (2021), Clinical Genetics, 99, 259 - 268
A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis
Aagaard Nolting L. et al, (2020), Clinical Genetics, 97, 927 - 932
Setting up an Office Allergy Practice: Current Recommendations for Sterility and Supervision
Parker MJ., (2020), Current Otorhinolaryngology Reports, 8, 170 - 174
Delineation of phenotypes and genotypes related to cohesin structural protein RAD21
Krab LC. et al, (2020), Human Genetics, 139, 575 - 592
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum
Yates TM. et al, (2020), Human Mutation, 41, 1042 - 1050
De Novo Variants in SPOP Cause Two Clinically Distinct Neurodevelopmental Disorders
Nabais Sá MJ. et al, (2020), American Journal of Human Genetics, 106, 405 - 411
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders
Barbosa S. et al, (2020), American Journal of Human Genetics, 106, 338 - 355
Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA–protein interaction
Williamson KA. et al, (2020), Genetics in Medicine, 22, 598 - 609
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis
Weiss K. et al, (2020), Genetics in Medicine, 22, 389 - 397
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
Mak CCY. et al, (2020), Brain, 143, 55 - 68
Dual diagnosis causing severe phenotype in a patient with Angelman syndrome
Kanani F. et al, (2019), Clinical Dysmorphology, 28, 158 - 161
PROCalcitonin-based algorithm for antibiotic use in Acute Pancreatitis (PROCAP): study protocol for a randomised controlled trial.
Siriwardena AK. et al, (2019), Trials, 20
Clinical report follow up: Type 1 Collagenopathy presenting with a Russell–Silver phenotype
Kanani F. et al, (2019), American Journal of Medical Genetics, Part A, 179, 139 - 140
Survival following rectal cancer surgery: does the age matter?
Al-Abed Y. et al, (2019), Acta Chirurgica Belgica, 119, 282 - 288
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect
Metz KA. et al, (2018), Annals of Neurology, 84, 766 - 780
Strengthening ethical community engagement in contemporary Malawi
Nyirenda D. et al, (2018), Wellcome Open Research, 3, 115 - 115
Genomics for paediatricians: Promises and pitfalls
Hammond CL. et al, (2018), Archives of Disease in Childhood, 103, 895 - 900
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications
Wolfe K. et al, (2018), American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 177, 397 - 405
Need to improve awareness and treatment compliance in high-risk patients for diabetic complications in Nepal
Sapkota RP. et al, (2018), BMJ Open Diabetes Research and Care, 6