| The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions N Rahmioglu, S Mortlock, M Ghiasi, PL Møller, L Stefansdottir, ... Nature genetics 55 (3), 423-436, 2023 | 92 | 2023 |
| Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly G Holley, D Beyter, H Ingimundardottir, PL Møller, S Kristmundsdottir, ... Genome Biology 22 (1), 28, 2021 | 53 | 2021 |
| Genetic risk of coronary artery disease, features of atherosclerosis, and coronary plaque burden MK Christiansen, L Nissen, S Winther, PL Møller, L Frost, JK Johansen, ... Journal of the American Heart Association 9 (3), e014795, 2020 | 26 | 2020 |
| Sortilin as a biomarker for cardiovascular disease revisited PL Møller, PD Rohde, S Winther, P Breining, L Nissen, A Nykjaer, ... Frontiers in cardiovascular medicine 8, 652584, 2021 | 22 | 2021 |
| Systematic evaluation of signal-to-noise ratio in variant detection from single cell genome multiple displacement amplification and exome sequencing AT Simonsen, MC Hansen, E Kjeldsen, PL Møller, JJ Hindkjær, ... BMC genomics 19, 1-9, 2018 | 15 | 2018 |
| Sex differences in clinical characteristics of migraine and its burden: a population‐based study MA Chalmer, LJA Kogelman, I Callesen, CG Christensen, TR Techlo, ... European Journal of Neurology 30 (6), 1774-1784, 2023 | 13 | 2023 |
| Polygenic risk score–enhanced risk stratification of coronary artery disease in patients with stable chest pain MK Christiansen, S Winther, L Nissen, BJ Vilhjalmsson, L Frost, ... Circulation: Genomic and Precision Medicine 14 (3), e003298, 2021 | 13 | 2021 |
| Familial analysis reveals rare risk variants for migraine in regulatory regions TR Techlo, AH Rasmussen, PL Møller, M Bøttcher, S Winther, ... neurogenetics 21, 149-157, 2020 | 13 | 2020 |
| Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer’s disease G Monti, M Kjolby, AMG Jensen, M Allen, J Reiche, PL Møller, ... Acta neuropathologica communications 9, 1-18, 2021 | 11 | 2021 |
| Sortilin regulates blood–brain barrier integrity AE Toth, HC Helms, A Harazin, KB Johnsen, C Goldeman, A Burkhart, ... The FEBS Journal 289 (4), 1062-1079, 2022 | 10 | 2022 |
| Benchmarking small variant detection with ONT reveals high performance in challenging regions PL Møller, G Holley, D Beyter, M Nyegaard, BV Halldórsson bioRxiv, 2020.10. 22.350009, 2020 | 7 | 2020 |
| DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals K Banasik, PL Møller, TR Techlo, PC Holm, GB Walters, A Ingason, ... BMC genomic data 24 (1), 30, 2023 | 4 | 2023 |
| Diagnostic yield of genetic testing in young patients with atrioventricular block of unknown cause J Resdal Dyssekilde, TC Frederiksen, MK Christiansen, ... Journal of the American Heart Association 11 (9), e025643, 2022 | 4 | 2022 |
| Danish study of Non-Invasive Testing in Coronary Artery Disease 3 (Dan-NICAD 3): study design of a controlled study on optimal diagnostic strategy S Winther, LD Rasmussen, J Westra, SRK Abdulzahra, JN Dahl, ... Open Heart 10 (2), e002328, 2023 | 3 | 2023 |
| Reappraisal of sex differences in migraine MA Chalmer, I Callesen, LJA Kogelman, CG Christensen, TR Techlo, ... | 2 | 2022 |
| Unraveling clonal heterogeneity at the stem cell level in myelodysplastic syndrome: In pursuit of cell subsets driving disease progression AT Simonsen, M Bill, CA Rosenberg, MH Hansen, PL Møller, E Kjeldsen, ... Leukemia research 92, 106350, 2020 | 2 | 2020 |
| Integrating detection of copy neutral chromosomal losses in a clinical setting in leukemia and lymphoma by means of allelic imbalance and read depth ratio comparison MC Hansen, O Cédile, M Ludvigsen, E Kjeldsen, PL Møller, N Abildgaard, ... BioRxiv, 590752, 2019 | 1 | 2019 |
| Protocol: Danish study of Non-Invasive Testing in Coronary Artery Disease 3 (Dan-NICAD 3): study design of a controlled study on optimal diagnostic strategy S Winther, LD Rasmussen, J Westra, SRK Abdulzahra, JN Dahl, ... Open Heart 10 (2), 2023 | | 2023 |
| Rare risk variants associate with epigenetic dysregulation in migraine TR Techlo, MA Chalmer, PL Møller, LJA Kogelman, IA Olofsson, ... medRxiv, 2021.12. 20.21268001, 2021 | | 2021 |
| PF528 INTEGRATING DETECTION OF COPY NEUTRAL CHROMOSOMAL LOSSES IN A CLINICAL SETTING IN LEUKEMIA AND LYMPHOMA BY MEANS OF ALLELIC IMBALANCE AND READ DEPTH RATIO COMPARISON MC Hansen, O Cédile, M Ludvigsen, E Kjeldsen, PL Møller, N Abildgaard, ... HemaSphere 3, 216-217, 2019 | | 2019 |
