| The genetic basis of long QT and short QT syndromes: a mutation update PL Hedley, P Jørgensen, S Schlamowitz, R Wangari, J Moolman‐Smook, ... Human mutation 30 (11), 1486-1511, 2009 | 424 | 2009 |
| Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death M Nyegaard, MT Overgaard, MT Søndergaard, M Vranas, ER Behr, ... The American Journal of Human Genetics 91 (4), 703-712, 2012 | 306 | 2012 |
| Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population PA Brink, L Crotti, V Corfield, A Goosen, G Durrheim, P Hedley, ... Circulation 112 (17), 2602-2610, 2005 | 181 | 2005 |
| The genetic basis of Brugada syndrome: a mutation update. PL Hedley, P Jørgensen, S Schlamowitz, J Moolman-Smook, JK Kanters, ... Hum Mutat 30 (9), 1256-1266, 2009 | 178 | 2009 |
| Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation MS Olesen, T Jespersen, JB Nielsen, B Liang, DV Møller, P Hedley, ... Cardiovascular research 89 (4), 786-793, 2011 | 117 | 2011 |
| Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives PS Andersen, O Havndrup, L Hougs, KM Sørensen, M Jensen, LA Larsen, ... Human mutation 30 (3), 363-370, 2009 | 115 | 2009 |
| High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation MS Olesen, L Yuan, B Liang, AG Holst, N Nielsen, JB Nielsen, PL Hedley, ... Circulation: Cardiovascular Genetics 5 (4), 450-459, 2012 | 114 | 2012 |
| Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome PJ Schwartz, E Vanoli, L Crotti, C Spazzolini, C Ferrandi, A Goosen, ... Journal of the American College of Cardiology 51 (9), 920-929, 2008 | 102 | 2008 |
| The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy DV Møller, PS Andersen, P Hedley, MK Ersbøll, H Bundgaard, ... European Journal of Human Genetics 17 (10), 1241-1249, 2009 | 90 | 2009 |
| Increased risk of preterm delivery and pre‐eclampsia in women with polycystic ovary syndrome and hyperandrogenaemia KV Naver, J Grinsted, SO Larsen, PL Hedley, FS Jørgensen, ... BJOG: An International Journal of Obstetrics & Gynaecology 121 (5), 575-581, 2014 | 72 | 2014 |
| Adipose expression of adipocytokines in women with polycystic ovary syndrome PF Svendsen, M Christiansen, PL Hedley, L Nilas, SB Pedersen, ... Fertility and sterility 98 (1), 235-241, 2012 | 69 | 2012 |
| Therapeutic hypothermia and ventricular fibrillation storm in early repolarization syndrome R Bastiaenen, PL Hedley, M Christiansen, ER Behr Heart rhythm 7 (6), 832-834, 2010 | 59 | 2010 |
| Relative atrial natriuretic peptide deficiency and inadequate renin and angiotensin II suppression in obese hypertensive men CL Asferg, SJ Nielsen, UB Andersen, A Linneberg, DV Møller, PL Hedley, ... Hypertension 62 (1), 147-153, 2013 | 45 | 2013 |
| Fc gamma receptor IIIB (FcγRIIIB) polymorphisms are associated with clinical malaria in Ghanaian children B Adu, D Dodoo, S Adukpo, PL Hedley, FKN Arthur, TA Gerds, SO Larsen, ... PLoS One 7 (9), e46197, 2012 | 42 | 2012 |
| The impact of fetal gender on first trimester nuchal translucency and maternal serum free β‐hCG and PAPP‐A MoM in normal and trisomy 21 pregnancies NJ Cowans, A Stamatopoulou, N Maiz, K Spencer, KH Nicolaides Prenatal Diagnosis: Published in Affiliation With the International Society …, 2009 | 41 | 2009 |
| Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population CM Hagen, FH Aidt, PL Hedley, MK Jensen, O Havndrup, JK Kanters, ... PloS one 8 (8), e71904, 2013 | 39 | 2013 |
| High‐efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi‐CE‐SSCP) mutation screening of SCN5A: a rapid genetic … J Hofman‐Bang, ER Behr, P Hedley, J Tfelt‐Hansen, JK Kanters, ... Clinical genetics 69 (6), 504-511, 2006 | 39 | 2006 |
| The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy DV Møller, TT Pham, F Gustafsson, P Hedley, MK Ersbøll, H Bundgaard, ... European journal of heart failure 11 (11), 1031-1035, 2009 | 33 | 2009 |
| A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity PS Andersen, PL Hedley, SP Page, P Syrris, JC Moolman-Smook, ... Biochemistry research international 2012, 2012 | 32 | 2012 |
| ADAM 12 may be used to reduce the false positive rate of first trimester combined screening for Down syndrome M Christiansen, K Pihl, PL Hedley, AC Gjerris, PØ Lind, SO Larsen, ... Prenatal Diagnosis: Published in Affiliation With the International Society …, 2010 | 27 | 2010 |
Michael ChristiansenStatens Serum InstitutBekræftet mail på ssi.dk
