[HTML][HTML] An overview of the BIOASQ large-scale biomedical semantic indexing and question answering competition
Background This article provides an overview of the first BioASQ challenge, a competition on
large-scale biomedical semantic indexing and question answering (QA), which took place …
large-scale biomedical semantic indexing and question answering (QA), which took place …
Conserved non-coding elements: developmental gene regulation meets genome organization
D Polychronopoulos, JWD King, AJ Nash… - Nucleic acids …, 2017 - academic.oup.com
Comparative genomics has revealed a class of non-protein-coding genomic sequences that
display an extraordinary degree of conservation between two or more organisms, regularly …
display an extraordinary degree of conservation between two or more organisms, regularly …
A key role for Ctf4 in coupling the MCM2‐7 helicase to DNA polymerase α within the eukaryotic replisome
A Gambus, F Van Deursen, D Polychronopoulos… - The EMBO …, 2009 - embopress.org
The eukaryotic replisome is a crucial determinant of genome stability, but its structure is still
poorly understood. We found previously that many regulatory proteins assemble around the …
poorly understood. We found previously that many regulatory proteins assemble around the …
[HTML][HTML] Knowledge graph-based recommendation framework identifies drivers of resistance in EGFR mutant non-small cell lung cancer
A Gogleva, D Polychronopoulos, M Pfeifer… - Nature …, 2022 - nature.com
Resistance to EGFR inhibitors (EGFRi) presents a major obstacle in treating non-small cell
lung cancer (NSCLC). One of the most exciting new ways to find potential resistance markers …
lung cancer (NSCLC). One of the most exciting new ways to find potential resistance markers …
[PDF][PDF] Pathogenic huntingtin repeat expansions in patients with frontotemporal dementia and amyotrophic lateral sclerosis
…, C Patch, D Perez-Gil, D Polychronopoulos… - Neuron, 2021 - cell.com
We examined the role of repeat expansions in the pathogenesis of frontotemporal dementia
(FTD) and amyotrophic lateral sclerosis (ALS) by analyzing whole-genome sequence data …
(FTD) and amyotrophic lateral sclerosis (ALS) by analyzing whole-genome sequence data …
[HTML][HTML] Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective …
…, A Rueda, D Polychronopoulos… - The Lancet …, 2022 - thelancet.com
Background Repeat expansion disorders affect about 1 in 3000 individuals and are clinically
heterogeneous diseases caused by expansions of short tandem DNA repeats. Genetic …
heterogeneous diseases caused by expansions of short tandem DNA repeats. Genetic …
Cardiac Investigations in Sudden Unexpected Death in DEPDC5‐Related Epilepsy
…, SA Watters, D Halai, D Polychronopoulos… - Annals of …, 2022 - Wiley Online Library
Objective Germline loss‐of‐function mutations in DEPDC5, and in its binding partners (NPRL2/3)
of the mammalian target of rapamycin (mTOR) repressor GATOR1 complex, cause …
of the mammalian target of rapamycin (mTOR) repressor GATOR1 complex, cause …
Guided self-scheduling: A practical scheduling scheme for parallel supercomputers
CD Polychronopoulos, DJ Kuck - Ieee transactions on …, 1987 - ieeexplore.ieee.org
This paper proposes guided self-scheduling, a new approach for scheduling arbitrarily
nested parallel program loops on shared memory multiprocessor systems. Utilizing loop …
nested parallel program loops on shared memory multiprocessor systems. Utilizing loop …
[HTML][HTML] Migrant entrepreneurship support in Europe: a PRISMA systematic literature review
D Polychronopoulos, A Nguyen-Duc - F1000Research, 2023 - ncbi.nlm.nih.gov
Background This systematic literature review (SLR) analyzes migrant entrepreneurship
support in Europe through three research questions (RQs) to understand 1) migrant …
support in Europe through three research questions (RQs) to understand 1) migrant …
[HTML][HTML] Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
…, C Patch, D Perez-Gil, D Polychronopoulos… - Genetics in …, 2022 - Elsevier
Purpose Biallelic variants in UCHL1 have been associated with a progressive early-onset
neurodegenerative disorder, autosomal recessive spastic paraplegia type 79. In this study, we …
neurodegenerative disorder, autosomal recessive spastic paraplegia type 79. In this study, we …