Tuesday, May 05, 2026

 

The boy on the balcony who never came outside



A childhood observation in a small Turkish town became the quiet origin of Dr. Dilek Colak's neuroscience career




Genomic Press

Dilek Colak, PhD, Weill Cornell Medicine, Cornell University, USA. 

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Dilek Colak, PhD, Weill Cornell Medicine, Cornell University, USA.

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Credit: Dilek Colak






NEW YORK, New York, USA, 5 May 2026 — There was a boy on a balcony in Sakarya. Dr. Dilek Colak, who now runs a laboratory at Weill Cornell Medicine that peers into human brain organoids the size of a lentil, grew up across the street from him. The boy had a mental illness. He watched the other children play. He did not come down. Decades later, in a Genomic Psychiatry Interview published today, Dr. Colak names that single childhood observation as the quiet seed of everything that followed.

“Though I have forgotten the faces of most of my childhood friends,” she says, “I never forgot the boy who was always apart from us. That early, quiet observation of his isolation stayed with me, ultimately grounding my scientific interest in the brain and drawing me toward a career in neuroscience.”

From Hazelnut Harvests to Human Brain Organoids

Dr. Colak was born in Sakarya, a city on the Black Sea side of northern Turkiye. She grew up until high school in a small town surrounded by farm animals and the smell of hazelnuts at harvest. The curiosity that began there carried her, eventually, to the Max Planck Institute for Neuroscience and the Helmholtz Center Stem Cell Institute in Munich, where she completed doctoral work under Dr. Magdalena Götz on the cellular logic of brain development. In 2009 she crossed the Atlantic for a postdoctoral position in the laboratory of Dr. Samie Jaffrey at Weill Cornell Medicine.

The move felt impulsive. She worried that she was following the city rather than the science. She was wrong about that, and the error has defined her life. “I was excited to shift my focus to molecular neuroscience in the Jaffrey lab, I worried that my choice was driven more by a desire to live in New York than by a fair evaluation of all my options,” she recalls. “However, it proved transformative; not only did the Jaffrey lab provide the training for my seminal discoveries and the foundation for my own laboratory, but I also met my husband and started my family here.”

Inside the Jaffrey lab, Dr. Colak uncovered an RNA-directed silencing mechanism implicated in Fragile X Syndrome. The finding reframed her ambitions. A laboratory bench could not, by itself, turn a molecular insight into a treatment. She launched her own group in 2015. She is now Associate Professor at the Feil Family Brain and Mind Research Institute and at the Gale and Ira Drukier Institute for Children’s Health, a dual appointment that places her at the interface of molecular neuroscience and pediatric medicine.

What Scientific Excellence Leaves Out

Dr. Colak’s current work focuses on how non-neuronal astrocytes and RNA degradation pathways regulate brain function and behavior, with autism and schizophrenia as the conditions she most wants to understand. Her group combines genetically engineered mouse models with human stem cell-derived brain organoids. The goal is to define what she calls the molecular signatures of these disorders, to see how breakdowns in local protein synthesis and cell-to-cell communication might surface, eventually, as the behaviors that send patients and families to clinics.

Ask her what she enjoys most about running a laboratory and she answers without hedging. “What I enjoy most is the opportunity to question long-standing dogmas and to investigate neglected areas of research.” The interview suggests she means it. Pressed on what the scientific community should examine about itself, she offers a sharp critique of how merit is currently tallied.

“Scientific excellence is often measured through a narrow lens that overvalues high-impact journals and quantitative ‘basic science,’ often at the expense of locally relevant research and clinical expertise,” she argues. “True transformation requires moving beyond these reductive metrics toward holistic frameworks that prioritize qualitative expert judgment and the diverse societal impacts of global research.”

It is not a fashionable position inside institutions that still rank themselves by impact factor. It is worth noting that a scientist whose own training ran through Max Planck, Helmholtz, and Weill Cornell is making it.

A Private Fear, Plainly Named

Dr. Colak identifies as her greatest achievement the crossing of systemic barriers and a lack of resources in order to pursue higher education, finding the opportunities abroad that built both the science and the family. Her heroes are trailblazer women. The living person she most admires is Malala Yousafzai. Her favorite occupations are traveling, running, and skiing. She lives in Tenafly, New Jersey.

Asked about her greatest fear, she does not reach for the abstract. “I harbor a quiet, persistent fear of an unfinished story,” she says, “of not being there to witness my children’s transition into adulthood.” It is the sort of sentence that sits differently on the page when you remember that her laboratory is built around children’s brains.

Her motto is likewise plain. Appreciate what you have while you work on what you want. She would live, given the choice, in a Mediterranean town. She treasures non-digital childhood photographs, her college-era jeans, and the first drawings and videos of her daughters. She is, in her own description, determined and energetic, working to be less of a perfectionist so that time goes further.

Somewhere inside all of that, the boy on the balcony is still watching.

Dr. Dilek Colak’s Genomic Press interview is part of a larger series called Innovators and Ideas that highlights the people behind today’s most influential scientific breakthroughs. Each interview in the series offers a blend of cutting-edge research and personal reflections, providing readers with a comprehensive view of the scientists shaping the future. By combining a focus on professional achievements with personal insights, this interview style invites a richer narrative that both engages and educates readers. This format provides an ideal starting point for profiles that explore the scientist’s impact on the field, while also touching on broader human themes. More information on the research leaders and rising stars featured in our Innovators and Ideas – Genomic Press Interview series can be found on our interview website: https://interviews.genomicpress.com/.

The Genomic Press Interview in Genomic Psychiatry titled “Dilek Colak: How do glial cells achieve multiple functions, and how do they contribute to neurodevelopmental and neuropsychiatric diseases?,” is freely available via Open Access, starting on 5 May 2026 in Genomic Psychiatry at the following hyperlink: https://doi.org/10.61373/gp026k.0030.

About Genomic Psychiatry: Genomic Psychiatry: Advancing Science from Genes to Society (ISSN: 2997-2388, online and 2997-254X, print) represents a paradigm shift in genetics journals by interweaving advances in genomics and genetics with progress in all other areas of contemporary psychiatry. Genomic Psychiatry publishes peer-reviewed medical research articles of the highest quality from any area within the continuum that goes from genes and molecules to neuroscience, clinical psychiatry, and public health.

Visit the Genomic Press Virtual Library: https://issues.genomicpress.com/bookcase/gtvov/

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Dilek Colak: How do glial cells achieve multiple functions, and how do they contribute to neurodevelopmental and neuropsychiatric diseases? 

Dilek Colak: How do glial cells achieve multiple functions, and how do they contribute to neurodevelopmental and neuropsychiatric diseases?

Credit

Dilek Colak

 

Brain Health emergency: Microplastic burden in the human brain now linked to stroke and dementia, with apheresis emerging as the first plausible removal pathway



New Brain Health Perspective from Genomic Press converges measurement, mechanism, and intervention as the field moves from alarm to action





Genomic Press

A human brain composited against a landscape of plastic waste. 

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A human brain composited against a landscape of plastic waste. The brain accumulates microplastic concentrations seven to thirty times higher than liver or kidney, with the heaviest burdens documented in donors with dementia.

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Credit: Composite image created by Julio Licinio from two photographs licensed via Depositphotos.





NEW YORK, 5 May 2026 — In a Perspective published today in the inaugural issue of Brain Health (https://doi.org/10.61373/bh026p.0006), an international team of investigators argues that the human microplastic burden has crossed the threshold from environmental concern to brain health emergency. The article appears alongside the launch of Brain Health, a new peer-reviewed journal from Genomic Press dedicated to the science of lifelong brain resilience.

The Perspective synthesizes evidence across three domains that until recently sat in separate scientific silos. Decedent human brain tissue, sampled from a 2016 to 2024 cohort and analyzed by Nihart and colleagues at the University of New Mexico, carries microplastic concentrations seven to thirty times higher than matched samples of liver or kidney. The cumulative tissue burden rose by approximately fifty percent across that eight-year window. Donors with diagnosed dementia carried the heaviest loads. Polyethylene predominated, presenting largely as nanoscale, shard-like fragments.

The cardiovascular evidence is now equally striking. Marfella and colleagues, working with patients undergoing carotid endarterectomy, identified microplastics and nanoplastics inside atheromatous plaque. Patients whose plaque tested positive for these particles experienced a roughly fourfold increase in the composite risk of myocardial infarction, stroke, or death over thirty-four weeks of follow-up. As the new Perspective notes, this is a brain finding as much as a cardiac one, because stroke is a brain outcome.

How do these particles reach the brain in the first place? Animal data are now closing that gap. Polystyrene nanoparticles administered orally to mice were shown by Kopatz and colleagues to cross the blood-brain barrier within two hours of exposure, with the biomolecular corona acquired in transit functioning as the passport for entry. Larger particles do not cross. Nanoscale particles do.

“We are looking at an organ where the highest measured concentrations of microplastics meet the most consequential clinical endpoints in medicine,” says Dr. Julio Licinio, lead author of the Perspective and Publisher and CEO of Genomic Press. “Cognition, mood, stroke, dementia. Treating this as a peripheral environmental concern, when the relevant peripheral organs carry less of the contaminant than the central one, has become difficult to defend.”

The Perspective also foregrounds a delivery vehicle that operates at population scale: ultra-processed food. Group 4 of the NOVA classification, ultra-processed foods now supply more than half of caloric intake in the United States. They are also high-throughput vectors for microplastic exposure, through packaging migration during heating and storage, mechanical wear during industrial processing, and downstream contamination. Independent of microplastic content, ultra-processed food consumption has been linked in large prospective cohorts to depression, anxiety, cognitive decline, stroke, and dementia. A meta-analysis of 385,541 participants found a fifty-three percent increase in the odds of common mental disorder symptoms in those with the highest ultra-processed food intake. UK Biobank data link the same dietary pattern to increased dementia risk. The REGARDS cohort showed that a ten percent rise in relative ultra-processed food intake was associated with a sixteen percent increase in cognitive impairment risk and an eight percent increase in stroke risk, holding independently of adherence to Mediterranean, DASH, or MIND dietary patterns.

“The boundary between physical and mental health has always been more administrative than biological,” notes Dr. Nicholas Fabiano of the University of Ottawa Department of Psychiatry, a co-author on the Perspective. “Microplastics do not respect that boundary. The same particles that lodge in atheroma also reach the brain. The same dietary exposures that raise cardiovascular risk also raise risk for depression and dementia. We are looking at one problem with many clinical faces.”

The Perspective treats removal as the next frontier rather than a distant aspiration. Bornstein and colleagues, working at the University Hospital Carl Gustav Carus in Dresden, recently reported that therapeutic apheresis can extract material consistent with microplastic particles from human plasma. The mechanism is biologically plausible. The clinical infrastructure already exists in tertiary centers worldwide. On present evidence, apheresis is the most promising candidate intervention the field has produced.

“We were initially surprised by what we observed,” says Dr. Stefan R. Bornstein of Technische Universität Dresden and King’s College London, senior co-author. “Apheresis is an established clinical modality. The fact that it appears to engage these particles in vivo opens a path that did not exist a year ago. The work now is to validate the signal against measurement standards the broader scientific community can agree on, and to develop scalable alternatives matched to polymer specificity, tissue compartment, and patient population.”

“What the field still lacks is the measurement infrastructure that would let us rank polymers by harm and confirm that interventions are working,” adds Dr. Charlotte Steenblock, also of Technische Universität Dresden and a co-author. “Without validated, reproducible, polymer-specific quantification, no removal strategy can be confirmed in the strict sense. That is not a weakness of the apheresis approach. It is a feature of a field operating ahead of its own analytical tools.”

The authors note that the science of brain health, at the level of national funding priority, is now moving toward subtraction with the same seriousness it has long given to addition. In April 2026, ARPA-H, the agency built on the model that produced GPS, the early Internet, and the foundational work behind mRNA vaccines, launched STOMP: Systematic Targeting Of MicroPlastics. The program is organized around the same three priorities the new Perspective identifies: develop measurements that can characterize nanoscale particles in complex biological tissue, illuminate the mechanisms by which microplastics traffic through organs and cause harm, and translate that knowledge into clinical removal.

Vulnerable populations sit at the center of the policy question. Microplastics have been localized within the intracellular compartment of human placenta, implying fetal exposure during the most consequential window of neurodevelopment. Children, with developing blood-brain barriers and higher per-kilogram intake than adults, carry a lifetime burden trajectory that today’s adult cohorts cannot predict. Patients with established cerebrovascular disease, in whom the Marfella signal becomes most clinically relevant, are already in clinics today. So are patients with neurodegenerative disease, in whom the Nihart finding of disproportionately high brain burden raises a question that will not go away: are these particles passenger, accelerator, or contributor?

In the absence of a validated clinical removal modality, the Perspective notes, population-scale exposure reduction is currently achievable only by reducing ultra-processed food consumption. That is not a trivial intervention. It is, however, the one lever the field has at present that operates at the scale of the problem.

The peer-reviewed Perspective, “The human microplastic burden and brain health: from measurement to pathophysiology and removal,” appears online on 5 May 2026 in Brain Health, in the journal’s inaugural issue, and is freely accessible at https://doi.org/10.61373/bh026p.0006.

About Brain Health

Brain Health is a high-quality, peer-reviewed medical research journal published by Genomic Press, New York, dedicated to the science of lifelong brain resilience and longevity. The journal’s scope spans molecular and cellular neuroscience, neuroimaging, electrophysiology, computational modeling, clinical trials, epidemiology, digital health, behavioral intervention science, psychology, normative data, and the social sciences and humanities, organized around the question of how human brains remain resilient, recover when injured, and stay functional across the longest possible arc of a life.

The human microplastic burden and brain health: From measurement to pathophysiology and removal 

The human microplastic burden and brain health: From measurement to pathophysiology and removal

Credit

Julio Licinio

 

New ‘Ecclesiastical’ Moth named after Pope Leo XIV







Pensoft Publishers

Pyralis papaleonei sp. nov., holotype 

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Pyralis papaleonei sp. nov., holotype.

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Credit: Peter Huemer





Distinguished by its striking colors and a name that carries the weight of a high ecclesiastical office, a new species of moth has been discovered in the rugged terrain of Greece. When researchers from the Tyrolean State Museum, the Finnish Museum of Natural History and the Bavarian State Collection of Zoology identified this unique insect in the White Mountains of Crete, they chose a name that reflects both its noble appearance and a message of environmental hope: Pyralis papaleonei – derived from “Papa Leone” (Pope Leo).

The discovery, published in the open-access journal Nota Lepidopterologica on 28 April 2026, highlights that even among such conspicuous European moths, overlooked species remain to be discovered. The new species is currently only known from the White Mountains (Lefka Ori) in the western part of Crete, where it appears to be an endemic treasure of the island.

Striking purple forewings

The so-called Pope Leo Moth has a wingspan of around two centimeters, placing it among the medium-sized representatives of its group. Its most distinctive features are its purple forewings with an orange-golden patch and prominent white bands. The moths were recorded at artificial light sources and appear to be mainly active in June. So far, little is known about the biology and lifestyle of the new species. It was distinguished from related species based on classical morphological characteristics – such as wing pattern, coloration, and genital morphology – as well as genetic fingerprinting. Molecular analyses revealed a divergence of around six percent from its closest relative, clearly indicating that it represents a distinct species.

A tradition of remarkable species names

Butterflies and moths are often named after physical characteristics, geographic origins, or in honor of distinguished individuals. Within the genus Pyralis, however, a particular tradition can be observed: as early as 1775, Austrian naturalists Michael Denis and Ignaz Schiffermüller described the first species of the group as Pyralis regalis (“royal”), inspired by its splendid coloration. This was followed by sonorous names such as Pyralis princeps and Pyralis cardinalis, also referring to the remarkable beauty of these moths.

All these species belong to the diverse superfamily Pyraloidea, which comprises around 16,000 described species worldwide and represents one of the largest groups among micro-moths.

Taxonomy as the “first profession” of humankind

The naming of living organisms also has a cultural-historical dimension: in the Old Testament (Genesis 2), Adam is firstly tasked with naming all animals. In this sense, taxonomy – the science of classifying, naming, and organising organisms – can be regarded as one of humanity’s earliest endeavors.

For study leader Peter Huemer of the Tyrolean State Museum Ferdinandeum, naming a species is therefore more than a formal scientific act: it also serves as a symbolic appeal to the head of the Catholic Church, Pope Leo XIV, to highlight humanity’s central responsibility in safeguarding creation. This is particularly fitting as butterflies and moths are regarded in Christianity as symbols of resurrection, transformation (metamorphosis), and the immortal soul.

Only a fraction of global biodiversity documented

Peter Huemer, former head of the Natural Science Collections at the Tyrolean State Museums and now a volunteer researcher, explains:

“We are facing a global biodiversity crisis, yet only a fraction of the world’s species has been scientifically documented. Effective conservation of biodiversity requires that species are first recognised, described, and named.”

Around 700 new moth species are described each year, primarily in the tropics. However, fundamental research in Europe is far from complete: in the Alps alone, approximately 200 previously unknown species have been identified in recent decades.

With their internationally significant scientific collections, the Tyrolean State Museums make an important contribution to this work. The discovery of the Pope Leo Moth, Pyralis papaleonei, highlights how much remains to be discovered even in well-studied regions of Europe—and underscores the urgent need to protect sensitive habitats.


Specimen of Pyralis regalis.

Specimens of Pyralis papaleonei.

Type-locality of Pyralis papaleonei sp. Nov. (Greece, Crete, Omalos plateau).

Credit

Peter Huemer