Current team members: 15
Current nationalities: 9
I studied biotechnology at Jagiellonian University in Krakow, Poland, where I was trained to be the experimentalist I am today, with a deep appreciation for the art of methodology used in life sciences. My journey in academia has always been marked by a common underlying theme: pursuing a fundamental biological question, while developing innovative technologies to address it.
As a master student, I got interested in signal transduction, which led me to join the lab of Ivan Dikic in Frankfurt, where I explored the role of ubiquitin in DNA damage repair. During that period, together with my colleagues, I demonstrated that novel ubiquin-binding domains (UBDs) present in the Y-family DNA polymerases are required for replication of damaged DNA in a process called translesion synthesis (TLS) (Bienko et al., Science 2005). I then went on to study the function of monoubiquitylation of such proteins, and discovered a complex network of monoubiquitylation and ubiquitin-binding events playing a central regulatory role in DNA translesion synthesis (Bienko et al., Mol Cell 2010).
In order to broaden my horizons and expand my expertise, I then switched research field and joined the Systems Biology lab of Alexander van Oudenaarden lab at MIT for my postdoctoral training. The prestigious Human Frontier Science Program recognized my aspiration to change field by awarding me with a postdoctoral fellowship. In Alexander’s lab we developed a powerful pipeline for high-definition DNA FISH (HD-FISH) combined with single-molecule RNA FISH (Bienko et al., Nature Methods 2013), which my group is now actively using to characterize various exciting aspects of RNA and DNA biology in single cells. In 2013, I moved with Alexander’s Lab to the Hubrecht Institute in the Netherlands, were I became enthusiastic about single-cell sequencing technologies and started developing novel approaches for integrated sequencing and microscopy in single cells. In 2015, I became an Assistant Professor at Karolinska Institutet and one of 16 Research Fellows at the Science for Life Laboratory, where I lead a team aiming at developing a comprehensive conceptual framework that explains how the key molecule of life is organized in the 3D confinement of the cell’s nucleus and how this arrangement shapes cells identity.
I was born in Cuneo, Italy, but if this were a political manifesto, I would prefer to be called a citizen of the future United States of Europe. In 2003, I received an M.D. from the University of Pavia, Italy where I attended the prestigious Collegio Ghislieri for excellence in higher education. From 2004 until 2007, I attended the School of Specialization in Medical Oncology at the University of Turin and Cuneo Santa Croce Hospital, Italy where I became familiar with the complexity and challenges of treating cancer patients. Being fascinated by mechanisms of disease and biotechnologies, after finishing my medical training I became a PhD student in Ivan Dikic’s Lab at Goethe University in Frankfurt, Germany and University of Pavia, Italy where I worked on DNA repair regulatory mechanisms by ubiquitin, and gained a lot of expertise in molecular biology and protein biochemistry methods. Looking for the next challenge, in 2011 I moved to Boston to join Alexander van Oudenaarden’s Lab at MIT where I learnt to value multidisciplinarity and quantitative science as the keywords that will shape biology and medicine in the next decade, and became passionate about molecular methods development. It was during this fantastic period that, together with Magda, I developed the HD-FISH and FuseFISH methods that are described here. In 2013, I joined Alexander van Oudenaarden’s Lab at the Hubrecht Institute, Netherlands where I conceived several methods and technology improvements that lie at the core of research in my lab. In 2015, I became an Assistant Professor at Karolinska Institutet and joined SciLifeLab to start an exciting new journey through science and technology.
Have you ever come across this sentence: “If the 20th century was the century of physics, the 21st century will be the century of biology”? Well…I decided to see how and why this might be the case.
I defended my PhD thesis in Physics in 2007 at the Politecnico di Torino (Italy); since then I have worked at the Universite’ Pierre et Marie Curie in Paris, at the University of Southern California in Los Angeles, and at the Institute for Quantum Computing in Waterloo. My area of research has focused on quantum physics, information theory, and network science; my major contributions to these fields have been the development of new algorithms for the solution of hard computational problems, and of new techniques for the study of complex systems and big data.
In 2014 I felt the need to start a new career adventure and, excited by the big data revolution, I looked for an environment where my analytic and computational skills could be useful in approaching new fascinating problems. Biology, an old passion of mine, presented itself as the perfect arena where I could help tackling scientific and clinically relevant questions whose answers hide in the increasing flood of data coming from new sequencing and microscopy technologies.
From January 2015 I work in the Bienko and Crosetto labs, where not only I take care of their computational infrastructure but, most importantly, I participate in the delicate process of shaping questions, experiments and data-analysis pipelines according to the tools and techniques that the two groups use and develop.
I am from Zhangshu, a small town located in southeast of China. In 2006, I got my bachelor degree in Biological Engineering in Chang’an University located in Xi’an.I pursued master education in Biological Physics at Kungliga Tekniska Högskolan in Stockholm, Sweden. In September 2007, I joined Lene Oddershede‘s Optical Tweezers group at Niels Bohr Institute, University of Copenhagen for my master thesis for a year. Then I joined Jerker Widengren‘s group in Stockholm for my PhD focusing on both technical development and application of single molecule sensitive fluorescence spectroscopy and super-resolution STED microscopy for biochemical and biomedical studies. After defending my PhD thesis in June 2014, I continued in his lab for two years as a researcher. In September 2016, I went to the industry and worked at Vanadis Diagnostics (a company of PerkinElmer) in Stockholm as a Principal Optical Design Engineer, developing fully automated fluorescence imaging system. Since September 2017, I came back to academia and joined Magda’s lab as a researcher. I enjoy taking challenges in science and technology.
I grew up in Neede, a small village in the east of the Netherlands. Although my childhood dream was to become a Medical Doctor, I quickly realized that I preferred science to medicine when I started medical school. I switched fields and enrolled in a MSc program in Biomedical Sciences at Utrecht University, specifying in Cancer Genomics & Developmental Biology. As part of this program, I spent a year in New York City for a research internship at Mount Sinai School of Medicine. Early 2011, right after receiving my MSc degree, I joined the group of Wouter de Laat at the Hubrecht Institute in Utrecht for my PhD studies. During the five years in the de Laat lab, I had a wonderful time studying the 3D architecture of the genome applying techniques such as 4C and Hi-C. Together with my colleagues, I followed the changes in genome conformation during differentiation of pluripotent stem cells to more differentiated cell types, as well as during reprogramming to induced pluripotency. Furthermore, we developed novel methods to study 3D chromatin organization. In the beginning of 2016 my PhD contract finished and I joined Cergentis (a spin-off company of de Laat lab) as a product developer, to gain a bit of experience in a small biotech company. At night, I completed the (final) chapters of my PhD thesis, which I defended in June 2016 at Utrecht University. In the fall of 2016, I moved to Stockholm to join Nicola’s group at Karolinska Institutet and SciLifeLab as a postdoctoral scientist.
I was born between 80s and 90s in a small city called Mollet del Vallès, located at 10 km from the nice city of Barcelona. Some years later I obtained Bachelor’s degree in Biology, specialized in Microbiology and Sanitary Biology, from the Autonomous University of Barcelona. During those nice years I was enrolled at the Microbiology Department studying a potential role of Mycobacterium species in creating antifungal compounds. Afterwards, I obtained a Master’s degree in Immunology from the University of Barcelona, and had a great opportunity to work in the prestigious association of Banc de sang i teixits de Catalunya (Blood and tissues bank of Catalonia), where I was conducting a collaborative work in order to develop quick and cost-effective techniques for HLA genotyping, based on multiplex PCR. I then started my PhD in Miguel Angel Peinado’s group at the Institute for Predictive and Personalized Medicine against Cancer (IMPPC). My PhD project was focused on deciphering epigenetic changes occurring in the colorectal cancer formation and expansion, mainly DNA methylation, histone modifications as well as chromatin conformational changes. I also worked on leukemia or pre-leukemic malignancies, such as MDS or AML, focusing on the complex epigenetic effects behind the administration of azacitidine or deoxy-azacitidine.
Recently, I joined Magda’s group as a Postdoc at the SciLifeLab Institute. My current projects in the lab include development of new techniques that allow us to get a better picture on how chromosome organization modulates genome expression. Personally, I am interested in applying these new techniques to study how genome organization is affected in various disease models, for example in cancer.
I earned a M.Sc. degree in engineering physics from Lund University, Faculty of Engineering in 2008 with a major in mathematics. After that, I moved to Uppsala and joined the Centre for Image Analysis where I studied under supervision from Gunilla Borgefors, Cris L. Luengo Hendriks and Anders Brun until I defended my thesis in December 2014. I’m now applying methods from physics, mathematics, machine learning and image analysis to reveal the inner structure of the nucleus. At the same time learning a great deal about cell biology. The Swedish Society for Medical Research funds me until 2017.
I was born in Shandong province, which is located in the northeast of China. In 2009, I received my M.D. from Shandong University, and in the same year, I was admitted to Ph.D study in the same University without entrance examination because of high scores achieved during University study. In 2010, I got support from the China Scholarship Council (CSC) for study abroad. Then at the beginning of 2011, I came to Karolinska Institutet and joined Magnus Björkholm’s group, starting Ph.D research about molecular alterations and clonal evolution in acute myeloid leukemia. At the end of 2014, I finished my Ph.D study, and joined BiCroLab following my great interest in tumor heterogeneity research and their developed fantastic methods.
I was born in Larisa, Greece and at 2012 I obtained my degree in Molecular Biology and Genetics from Democritus University of Thrace. At 2013, I moved to Stockholm since I was admitted to the Master’s Program in Biomedicine of Karolinska Institute from which I graduated at 2015. During this time, I had the opportunity to perform my rotations at Hong’s Qian lab in the Center of Hematology and Regenerative medicine (HERM), where I studied the multilineage differentiation capacity of the bone marrow Mesenchymal Stem Cells in myeloproliferative neoplasm mice, as well as the Leukotriene Receptors expression on the Leukemic Stem Cells in CML. It was during my master thesis that I joined Magda’s team, where we employed single cell and single molecule methods in an effort to characterize the expression and localisation of the FMR1 gene in Fragile X Spectrum Disorders. Fascinated by the enigma of the nuclear architecture, I am now starting my PhD, hoping to contribute to deciphering the design principles of genome organization and its interplay with gene expression.
I was born near Verona, Italy and I obtained my B.Sc. (2012) and M.Sc. (2014) in Biotechnology at the University of Trento. There, I developed a passion for bioimaging and computational biology during two internships: first (2012) at Arosio’s Molecular Imaging Lab, where I analyzed images of HIV-infected cells, and then (2014) at Demichelis’ Computational Oncology Lab, where I gained experience in developing computational tools and on tumor heterogeneity and cancer progression. In 2013 I participated to the iGEM competition as a member of the UniTN-Trento team, engineering E. coli to control the fruit ripening process, and in 2014 I received a Summer Fellowship Grant from the Giovanni-Armenise Harvard Foundation to spend two months at Quackenbush’s Computational Biology and Functional Genomic Lab at the Dana-Farber Cancer Institute (Boston, MA), where I contributed to the development of a gene network visualization interface. After obtaining my M.Sc., I spent 6 more months at Demichelis’ Lab to study the association between prostate cancer genome lesions and Gleason Score. In september 2015, I joined Magda’s team at Science for Life Laboratory / Karolinska Institutet to uncover the nuclear 3D architecture principles and how this influences gene expression.
I come from Poland, where I graduated from Biotechnology at the West Pomeranian University of Technology. During my master program, I did an Erasmus summer internship in the lab of Professors Eva Klein and George Klein at Department of Microbiology, Tumor and Cell Biology at Karolinska Institutet, pursuing my interest in tumor biology. After my graduation, I was given the opportunity to join their group for a research project, where I tried to elucidate the effects of interferons on malignant hematopoietic cells. During that time, I observed that cells differ in their responses to various treatments even though they come from the same population, triggering my curiosity for cell-to-cell variability. To combine this with my interest in technologies that push biology forward, in January 2015 I joined the group of Magda Bienko at the Laboratory for Quantitative Biology of the Nucleus at Science for Life Laboratory / Karolinska Institutet, to study the interplay between gene expression and genome organization. Since that time, I have been involved in many rummy projects with the aim to develop new methods for better understanding of the nuclear architecture.
I was born in Maanshan, a small city along Yangtze River in southeast part of China. I obtained my bachelor degree in Engineering of Food technology in 2014 in China and graduated from Toxicology master programme in Karolinska Institutet June, 2016. I did my master thesis on investigating new protein interacting partner of caspase-2 in non-apoptotic process in Professor Boris Zhivotovsky’s lab in the Unit of Toxicology, Institute of Environmental Medicine, KI from November 2015 to May 2016. Because of my interest in genetic research, I joined the group of Magda Bienko for summer project right after I graduated from master programme, to understand the genome structure and organization in the nucleus.
I am from Tehran, Iran and in 2010 I moved to Uppsala in Sweden for a M.Sc. program in genomics and bioinformatics. My thesis focused on “Integration polymorphism of Canine Endogenous Retroviruses” in the lab of Göran Andersson at IMBIM, Uppsala University.
To figure out which branch of molecular biology I was most interested in, I joined Mats Nilsson’s group, who focuses on developing novel technology for nucleic acid analysis. There, I got introduced to the fascinating field of circularizable oligonucleotide probes, so-called padlock probes.
Having experienced a lab with strong technology development spirit, soon I realised this is the path I would like to further continue my journey in science. This motivated me to join the Crosetto Lab at Karolinska Institutet and SciLifelab for my Ph.D. studies, where I am currently developing genome-wide methods to map DNA double-strand breaks (DSBs) in cancer and other diseases, as well as other exciting technologies.
In my early studies I was thrilled by the fact that such small molecule could encode and command complex organisms and it had settled my interest’s foundation in studying chromatin. The genetic engineering’s recent achievements made me start a bachelor in Biotechnology at Aveiro University, in Portugal. Along the bachelor, Nanotechnology had caught my attention and inspired me to pursue a BSc thesis in drug development which was functionalized to a magnetic nanoparticle to combat tumours by light activation. The BSc thesis had spark my enthusiasm to keep learning nanotechnologies applied to biological systems. To complement my biological background, I started the master in Bioengineering and Nanosystems at Technical University of Lisbon with a deeper focus in physics, informatics, electronics and other engineering fields. It was granted the opportunity to develop my MSc thesis in Cees Dekker lab group at the Kavli Institute in TU Delft, the Netherlands. The project aimed to define the condensin model to compact DNA by using magnetic-tweezers, a single-molecule technique. In BiCroLab, I am relating specific genome events with diseases and learn about the genome organization.
I was born in Perugia, Italy in 1991. I studied at University of Perugia where I received a Batchelor Degree as a Medical Laboratory Technologist in November 2013. During this period I worked at the University Hospital with a focus on disease diagnostic. In October 2015 I obtained a MSc Degree in Medical Biotechnology. For my thesis I worked at the Department of Surgery and Biomedical Sciences, Section of Gastroenterology. In January 2016 I joined the group of Nicola Crosetto for a traineeship within the Erasmus + programme following my interest in the development of new molecular methods for understanding disease processes.