Postdoctoral Fellows and Visiting Scholars

Bruna is a postdoctoral scholar in Cardiovascular Medicine. She completed her Doctor of Medicine in 2018 from Ruprecht Karl Universitat Heidelberg. She is a cardiologist Department of Cardiology, Pneumology and Angiology, Heidelberg University Hospital, Germany.

Mikael is a visiting scholar from The Swedish School of Sport and Health Sciences, Stockholm, Sweden, where he holds a position as assistant professor in the department of Professors P-O. Ã…strand and B. Ekblom. He received his Master’s degree in physiology (2006) and his PhD in Medical Science – physiology (2011) from Karolinska Institutet in Sweden. He did his thesis on the physiology of ultra-endurance athletes (Adventure Racers). His research evolves in the area of endurance performance, exercise induced cardiac fatigue and circulatory adaptations. At the Ashley lab he is involved in the projects “extreme physiology” and “the Athlete Genome”.

Dr. Hector Rodrigo Mendez is a Medical Geneticist from Argentina. Rodrigo completed a residency program in Medical Genetics at Centro Nacional de Genetica Medica – ANLIS (Buenos Aires, Argentina) and a Master’s program in Medical Molecular Biology at Buenos Aires University.
Rodrigo continued his scientific career at a German Genomic Start-up, working as a human geneticist and providing his experience in rare disorders, genomic data (WGS/WES/gene panels) analysis, variant interpretation, and its integration with a deep focus on genotype-phenotype correlation.
Rodrigo’s areas of expertise are rare disorders, NGS technology, Whole Genome Sequencing analysis, and ACMG interpretation guidelines, and his research aims are:
– Collection and analysis of clinical data through deep-learning phenotyping approaches.
– Multi-omic data integration to elucidate complex and rare genetic disorders.
– International collaborations to break down barriers to research participation amongst those who have been under-represented.

Jack is an Australian physician (MD, PhD) currently working as a Post-Doctoral Research Fellow at Stanford University. He is supervised by Professor Euan Ashley and is an active member of the Ashley Lab.

Jack’s fellowship concerns the diagnosis and risk prediction of cardiovascular disease. Jack employs a variety of statistical methods to assess new diagnostic technologies, such as smart phones and smart wearables, and my work also extends to computational cardiac genetics. The data sources he utilizes to conduct my research are numerous, but include large datasets such as the UK Biobank, as well as publicly available dataset (meta-analysis and meta-research). He also has previously used large electronic health records (>250 million EHRs).

Aside from his own research prioritizes (above), Jack also work on studies conducted collaboratively within the Ashley Lab, the Division of Cardiovascular Medicine. These studies broadly include digital health randomized controlled trials (RCTs) and meta-research (including statistical methods such as meta-analysis, meta-regression etc).

Jack previously completed a DPhil (PhD) in clinical epidemiology at the University of Oxford as a Clarendon Scholar. The title of his DPhil thesis was: “Biostatistical and meta-research approaches to assess diagnostic tests”. Jack’s published research is available at the google scholar page ( and some of his code is publicly available at his GitHub (

Beyond academic institutions, Jack consults to the World Health Organization (WHO); including on WHO guidelines, where he is currently the methodological chair for a WHO guideline concerning the early(ier) detection of disease in adults. Jack also work as an associate editor at one of the BMJ sub-journals: BMJ EBM. During my DPhil Jack worked clinically at Oxford University Hospitals (John Radcliffe Hospital) and intend to return to clinical practice as a Physician-Scientist at Stanford upon the completion of my research Fellowship.

You can follow Jack on twitter ( where you will find him tweeting about statistics, surfing, cardiology, medicine, epidemiology, health policy, and, occasionally, politics.

Theresia is a Visiting Scholar in the Division of Cardiovascular Medicine. She obtained her MSc in Biochemistry/Molecular Biology at the University of Alaska Fairbanks, USA (2013), and her PhD in Basic Metabolic Research at the University of Copenhagen, Denmark (2018). Her overall research interest is to investigate how common genetic variation contributes to cardiometabolic disease and how lifestyle factors interact with a genetic predisposition to common disease traits. In the Hansen lab at the University of Copenhagen, she applied diverse statistical genetic analysis methods in European cohort studies to uncover genetic underpinnings of adiposity and metabolic disease-related traits, and to understand their complex relationship with lifestyle at the molecular level. She received funding from the Novo Nordisk Foundation and the Stanford Bio-X program to carry out a three year project at Stanford as part of the Knowles lab and the Ashley lab. During her three years, she focuses on combining a computational and experimental framework to identify novel genetic variants that are causally related to cardiometabolic disease, and to investigate their relationship to lifestyle factors. At the Ashley lab she is involved in the ELITE project that is seeking to discover genetic determinants of physical fitness in the world’s most elite endurance athletes. Her vision is to provide insights that will pave the way for personalized prevention and treatment, and for new drug targets.

Samiya is a postdoctoral scholar in the Ashley Lab, Stanford University School of Medicine. She obtained her Ph.D. (in 2019) at The Australian National University, Australia. She studied Electrical and Computer Science Engineering and is specialized in wearable technology and wireless body-centric networks. During her Ph.D., she performed extensive experimental analysis to optimize wireless communication performance between wearable sensors, with cross-layer techniques and predictive analytics, to build autonomous human-centered networks. In the Ashley Lab, she is working towards developing artificial intelligence based wearable system for monitoring cardiac arrhythmia. She is also researching on various machine learning and deep learning based prediction with wearable data analysis for healthcare applications that include physical activity recognition, sleep prediction, monitoring sleep disorders associated with cardiovascular health. Outside of work, she likes traveling, hiking, watching movies, and trying new recipes.

Aditya joined the Ashley Lab as a postdoctoral scholar in January 2021. He did his PhD in molecular medicine (2020) at PGIMER, India. His thesis was on knocking down the tumorigenic BCR-ABL1 transcript using CRISPR in CML. His current research interests are in developing “super AAVs” for the effective transduction of cardiomyocytes. He is also working on the functional mapping of mutations on protein 3D structures. Outside the lab, Aditya likes traveling, hiking, and going camping in the mountains.

Qianru joined the Ashley lab as a postdoctoral scholar in the summer of 2019. Qianru obtained her Master’s degree (2014) and Ph.D. (2018) in Mechanical Engineering from MIT, where she innovates microfluidic technologies to measure biophysical properties of bacteria for applications in sustainable energy and synthetic biology. In her Ph.D. thesis project, she developed a novel microfluidic process to rapidly identify and sort electricity-producing bacteria for use in microbial fuel cells and bioremediation. Her microfluidic system noninvasively classified bacteria according to their cell surface polarizability, an inherent electrical property of microorganisms, which was found to be an indicator of cell extracellular electron transfer. Currently, she is interested in applying microfluidics-enabled phenotyping of single cardiomyocytes to efforts in understanding the pathogenesis of hypertrophic cardiomyopathy. Outside the lab, Qianru is a badminton player, and a big fan of comedy shows and detective films.

Laurens van de Wiel is Dutch scientist from Berghem, The Netherlands. Laurens spent his undergrad in Software Development (BSc, Avans Hogeschool ‘s-Hertogenbosch) and Computing Science (MSc, Radboud University Nijmegen). Laurens continued his career at a start-up, where he created large-scale, real-time analytical software. Laurens continued on his academic trajectory at the Radboudumc in Nijmegen, where he started his PhD in bioinformatics. During his PhD, Laurens integrated genetic data with protein 3D structures and protein domains. He utilized the skills he obtained before setting out on his academic trajectory; building large-scale, robust, reliable software. Exemplified by the MetaDome Web server ( During his PhD, he developed novel methodologies for the interpretation of genetic variants of unknown clinical significance and, by integrating structural and evolutionary biology with genomics, Laurens identified 36 novel disease-gene associations for developmental disorders. These discoveries enabled diagnosis for over 500 families worldwide. Laurens’ areas of expertise are (bioinformatic) software development, data integration of genetic variation with other omics.

Rachel grew up in Colorado and attended the University of Colorado in Boulder to study Molecular, Cellular, and Developmental Biology. She then attended the University of Wisconsin, Madison for her graduate work where she received her PhD (2020) in Molecular and Environmental Toxicology. In graduate school, Rachel studied the aryl hydrocarbon receptor, a protein responsible for the metabolism and toxicity of many environmental pollutants. She used genome engineering methods to generate mouse models of the Ah receptor in an effort to better understand the role of this receptor in hepatovasclar development and immune regulation. Along the way, Rachel observed significant phenotypic consequences of mice harboring genetic variation in the Ah receptor, causing her to develop an interest in genotype-phenotype relationships. In joining the Ashley lab, Rachel hoped to better understand the phenotypic consequences of genetic variation on the single cell level. She also hopes to use genome engineering methods to better understand the mechanism and biology of familial heart disease. When not in the lab, she enjoys running, playing ultimate frisbee, and camping.

Sunil is a postdoctoral scholar in Ashley lab. Sunil received his Ph.D. in Molecular and Cellular Pharmacology from University of Miami Miller School of Medicine (2019), where he studied the role of phosphorylation of regulatory light chains (RLCs) in rescuing hypertrophic cardiomyopathy. In the Ashley lab, Sunil is working on troponin T common variant directed allele-specific silencing to normalize pathological cardiomyopathy in larger population. As such, he is involved in patient-derived iPSC-CM disease modeling, long read DNA/RNA sequencing, shRNA/ASO design etc. Outside of lab, Sunil enjoys Netflix thrillers, trying new cuisines and exploring the wilderness.

Yuta is a postdoctoral research fellow in Ashley lab. He graduated and received DVM from Tokyo University of Agriculture and Technology in 2013. At veterinary school, he investigated the valvular disease of dogs. After graduation, he focused on the inherited cardiac diseases, and conducted research on CALM gene mutation-related arrhythmias (Calmodulinopathy) using iPS cell model in Kyoto University where he obtained a PhD in 2017. His current research interests are pathophysiological mechanism and gene therapy approach for inherited cardiac diseases. Outside the lab, he enjoys watching baseball games, reading books, playing video games, and California life.