| Year |
Citation |
Score |
| 2023 |
de Knegt VE, Hedley PL, Hedermann G, Wilstrup C, Bækvad-Hansen M, Thagaard IN, Hjalgrim H, Kanters J, Melbye M, Hougaard DM, Hviid A, Krebs L, Breindahl M, Lausten-Thomsen U, Christiansen M. The impact of the COVID-19 lockdown on birthweight among singleton term birth in Denmark. Plos One. 18: e0283909. PMID 37079534 DOI: 10.1371/journal.pone.0283909 |
0.474 |
|
| 2023 |
de Knegt VE, Hedley PL, Eltvedt AK, Placing S, Wøjdemann K, Shalmi AC, Rode L, Kanters JK, Sundberg K, Tabor A, Lausten-Thomsen U, Christiansen M. First-Trimester Maternal Serum Adiponectin/Leptin Ratio in Pre-Eclampsia and Fetal Growth. Life (Basel, Switzerland). 13. PMID 36676079 DOI: 10.3390/life13010130 |
0.503 |
|
| 2021 |
Krøll J, Jensen HK, Jespersen C, Kanters JK, Hansen MS, Christiansen M, Westergaard LM, Fosbøl EL, Rørth R, Torp-Pedersen C, Køber L, Bundgaard H, Tfelt-Hansen J, Weeke PE. Severity of congenital long QT syndrome disease manifestation and risk of depression, anxiety, and mortality: a nationwide study. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. PMID 34652436 DOI: 10.1093/europace/euab252 |
0.485 |
|
| 2021 |
de Knegt VE, Hedley PL, Kanters JK, Thagaard IN, Krebs L, Christiansen M, Lausten-Thomsen U. The Role of Leptin in Fetal Growth during Pre-Eclampsia. International Journal of Molecular Sciences. 22. PMID 33925454 DOI: 10.3390/ijms22094569 |
0.475 |
|
| 2020 |
Hagen CM, Elson JL, Hedley PL, Aidt FH, Havndrup O, Jensen MK, Kanters JK, Atherton JJ, McGaughran J, Bundgaard H, Christiansen M. Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathy. Mitochondrial Dna. Part a, Dna Mapping, Sequencing, and Analysis. 1-7. PMID 32602800 DOI: 10.1080/24701394.2020.1782897 |
0.496 |
|
| 2019 |
Weeke PE, Kellemann JS, Jespersen CB, Theilade J, Kanters JK, Hansen MS, Christiansen M, Marstrand P, Gislason GH, Torp-Pedersen C, Bundgaard H, Jensen HK, Tfelt-Hansen J. Long-term proarrhythmic pharmacotherapy among patients with congenital long QT syndrome and risk of arrhythmia and mortality. European Heart Journal. PMID 31079148 DOI: 10.1093/Eurheartj/Ehz228 |
0.554 |
|
| 2019 |
Hadji-Turdeghal K, Andreasen L, Hagen CM, Ahlberg G, Ghouse J, Bækvad-Hansen M, Bybjerg-Grauholm J, Hougaard DM, Hedley P, Haunsø S, Svendsen JH, Kanters JK, Jepps TA, Skov MW, Christiansen M, et al. Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. Cardiovascular Research. PMID 31049583 DOI: 10.1093/Cvr/Cvz106 |
0.517 |
|
| 2018 |
Bybjerg-Grauholm J, Hagen CM, Gonçalves VF, Bækvad-Hansen M, Hansen CS, Hedley PL, Kanters JK, Nielsen J, Theisen M, Mors O, Kennedy J, Als TD, Demur AB, Nordentoft M, Børglum A, ... ... Christiansen M, et al. Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes. Plos One. 13: e0208829. PMID 30543675 DOI: 10.1371/Journal.Pone.0208829 |
0.52 |
|
| 2018 |
Hagen CM, Gonçalves VF, Hedley PL, Bybjerg-Grauholm J, Bækvad-Hansen M, Hansen CS, Kanters JK, Nielsen J, Mors O, Demur AB, Als TD, Nordentoft M, Børglum A, Mortensen PB, Kennedy J, ... ... Christiansen M, et al. Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease. Plos One. 13: e0208828. PMID 30532134 DOI: 10.1371/Journal.Pone.0208828 |
0.512 |
|
| 2017 |
Hasholt L, Ballegaard M, Bundgaard H, Christiansen M, Law I, Lund AM, Norremolle A, Krogh Rasmussen A, Ravn K, Tumer Z, Wibrand F, Feldt-Rasmussen U. The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease. Scandinavian Journal of Clinical and Laboratory Investigation. 1-5. PMID 29037082 DOI: 10.1080/00365513.2017.1390782 |
0.308 |
|
| 2017 |
Dembic M, Hedley PL, Torp-Pedersen C, Køber L, Christiansen M. Pregnancy-associated plasma protein-A (PAPP-A) and the proform of the eosinophil major basic protein (ProMBP) are associated with increased risk of death in heart failure patients. Scandinavian Journal of Clinical and Laboratory Investigation. 77: 352-357. PMID 28537443 DOI: 10.1080/00365513.2017.1325926 |
0.314 |
|
| 2017 |
Hyltén-Cavallius L, Iepsen EW, Christiansen M, Graff C, Linneberg A, Pedersen O, Holst JJ, Hansen T, Torekov SS, Kanters JK. Glucose ingestion causes cardiac repolarization disturbances in type 1 Long QT syndrome patients and healthy subjects. Heart Rhythm. PMID 28400316 DOI: 10.1016/J.Hrthm.2017.04.018 |
0.575 |
|
| 2017 |
Hyltén-Cavallius L, Iepsen EW, Wewer Albrechtsen NJ, Svendstrup M, Lubberding AF, Hartmann B, Jespersen T, Linneberg A, Christiansen M, Vestergaard H, Pedersen O, Holst JJ, Kanters JK, Hansen T, Torekov SS. Patients With Long-QT Syndrome Caused by Impaired hERG-Encoded Kv11.1 Potassium Channel Have Exaggerated Endocrine Pancreatic and Incretin Function Associated With Reactive Hypoglycemia. Circulation. 135: 1705-1719. PMID 28235848 DOI: 10.1161/Circulationaha.116.024279 |
0.551 |
|
| 2017 |
Christiansen M, Bybjerg-Grauholm J, Hagen C, Gonçalves V, Bækvad-Hansen M, Hansen C, Hedley P, Kanters J, Nielsen J, Theisen M, Mors O, Kennedy J, Werge T, Nordentoft M, Børglum A, et al. 5. Mitochondrial DNA Haplogroups are Associated with Psychiatric Disease: A Nation-Wide Study of 74,763 Danes Biological Psychiatry. 81. DOI: 10.1016/J.Biopsych.2017.02.016 |
0.507 |
|
| 2015 |
Kanters JK, Olesen MS, Christiansen M. KCNE1 G38S polymorphism is not the cause of long QT syndrome. Journal of Electrocardiology. PMID 26781364 DOI: 10.1016/J.Jelectrocard.2015.12.005 |
0.547 |
|
| 2015 |
Granström S, Godiksen MT, Christiansen M, Pipper CB, Martinussen T, Møgelvang R, Søgaard P, Willesen JL, Koch J. Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study. Journal of Veterinary Cardiology : the Official Journal of the European Society of Veterinary Cardiology. 17: S268-81. PMID 26776585 DOI: 10.1016/J.Jvc.2015.10.005 |
0.333 |
|
| 2015 |
Kanters JK, Skibsbye L, Hedley PL, Dembic M, Liang B, Hagen CM, Eschen O, Grunnet M, Christiansen M, Jespersen T. Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder family. Scandinavian Journal of Clinical and Laboratory Investigation. 1-11. PMID 26403377 DOI: 10.3109/00365513.2015.1091090 |
0.578 |
|
| 2015 |
Jensen MK, Havndrup O, Christiansen M, Andersen PS, Axelsson A, Køber L, Bundgaard H. Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathy. The International Journal of Cardiovascular Imaging. PMID 26231341 DOI: 10.1007/S10554-015-0723-X |
0.319 |
|
| 2015 |
Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jensen MK, Kanters JK, Pham TT, Bundgaard H, Christiansen M. Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy. Plos One. 10: e0124540. PMID 25923817 DOI: 10.1371/Journal.Pone.0124540 |
0.561 |
|
| 2015 |
Hong L, Andersen LJ, Graff C, Vedel-Larsen E, Wang F, Struijk JJ, Sogaard P, Hansen PR, Yang YZ, Christiansen M, Toft E, Kanters JK. T-wave morphology analysis of competitive athletes. Journal of Electrocardiology. 48: 35-42. PMID 25465868 DOI: 10.1016/J.Jelectrocard.2014.10.011 |
0.517 |
|
| 2014 |
Hedley PL, Carlsen AL, Christiansen KM, Kanters JK, Behr ER, Corfield VA, Christiansen M. MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome. Scandinavian Journal of Clinical and Laboratory Investigation. 74: 485-91. PMID 24809446 DOI: 10.3109/00365513.2014.905696 |
0.495 |
|
| 2014 |
Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, et al. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2. Bmc Medical Genetics. 15: 31. PMID 24606995 DOI: 10.1186/1471-2350-15-31 |
0.599 |
|
| 2014 |
Kanters JK, Yuan L, Hedley PL, Stoevring B, Jons C, Bloch Thomsen PE, Grunnet M, Christiansen M, Jespersen T. Flecainide provocation reveals concealed brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A. Circulation Journal : Official Journal of the Japanese Circulation Society. 78: 1136-43. PMID 24599044 DOI: 10.1253/Circj.Cj-13-1167 |
0.591 |
|
| 2014 |
Torekov SS, Iepsen E, Christiansen M, Linneberg A, Pedersen O, Holst JJ, Kanters JK, Hansen T. KCNQ1 long QT syndrome patients have hyperinsulinemia and symptomatic hypoglycemia. Diabetes. 63: 1315-25. PMID 24357532 DOI: 10.2337/Db13-1454 |
0.528 |
|
| 2013 |
Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M. MT-CYB mutations in hypertrophic cardiomyopathy. Molecular Genetics & Genomic Medicine. 1: 54-65. PMID 24498601 DOI: 10.1002/Mgg3.5 |
0.572 |
|
| 2013 |
Hedley PL, Durrheim GA, Hendricks F, Goosen A, Jespersgaard C, Støvring B, Pham TT, Christiansen M, Brink PA, Corfield VA. Long QT syndrome in South Africa: the results of comprehensive genetic screening. Cardiovascular Journal of Africa. 24: 231-7. PMID 24217263 DOI: 10.5830/Cvja-2013-032 |
0.36 |
|
| 2013 |
Hedley PL, Kanters JK, Dembic M, Jespersen T, Skibsbye L, Aidt FH, Eschen O, Graff C, Behr ER, Schlamowitz S, Corfield V, McKenna WJ, Christiansen M. The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote. Circulation. Cardiovascular Genetics. 6: 452-61. PMID 24021552 DOI: 10.1161/Circgenetics.113.000137 |
0.597 |
|
| 2013 |
Theilade J, Kanters J, Henriksen FL, Gilså-Hansen M, Svendsen JH, Eschen O, Toft E, Reimers JI, Tybjærg-Hansen A, Christiansen M, Jensen HK, Bundgaard H. Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome. Cardiology. 126: 131-7. PMID 23969902 DOI: 10.1159/000350825 |
0.558 |
|
| 2013 |
Hagen CM, Aidt FH, Hedley PL, Jensen MK, Havndrup O, Kanters JK, Moolman-Smook JC, Larsen SO, Bundgaard H, Christiansen M. Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population. Plos One. 8: e71904. PMID 23940792 DOI: 10.1371/Journal.Pone.0071904 |
0.542 |
|
| 2013 |
Wang F, Liu J, Hong L, Liang B, Graff C, Yang Y, Christiansen M, Olesen SP, Zhang L, Kanters JK. The phenotype characteristics of type 13 long QT syndrome with mutation in KCNJ5 (Kir3.4-G387R). Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1500-6. PMID 23872692 DOI: 10.1016/J.Hrthm.2013.07.022 |
0.585 |
|
| 2013 |
Aidt FH, Nielsen SM, Kanters J, Pesta D, Nielsen TT, Nørremølle A, Hasholt L, Christiansen M, Hagen CM. Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model. Plos Currents. 5. PMID 23568011 DOI: 10.1371/Currents.Hd.D8917B4862929772C5A2F2A34Ef1C201 |
0.508 |
|
| 2013 |
Godiksen MTN, Kinnear C, Ravnsborg T, Højrup P, Granström S, Laursen IA, Hedley PL, Moolman-Smook JC, McKenna WJ, Koch J, Christiansen M. Feline Hypertrophic Cardiomyopathy Associated with the p.A31P Mutation in cMyBP-C Is Caused by Production of Mutated cMyBP-C with Reduced Binding to Actin Open Journal of Veterinary Medicine. 3: 95-103. DOI: 10.4236/Ojvm.2013.32016 |
0.307 |
|
| 2012 |
Refsgaard L, Olesen MS, Møller DV, Christiansen M, Haunsø S, Svendsen JH, Christensen AH. Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy. Applied & Translational Genomics. 1: 44-46. PMID 27896052 DOI: 10.1016/J.Atg.2012.06.001 |
0.32 |
|
| 2012 |
Andersen PS, Hedley PL, Page SP, Syrris P, Moolman-Smook JC, McKenna WJ, Elliott PM, Christiansen M. A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity. Biochemistry Research International. 2012: 685108. PMID 22957257 DOI: 10.1155/2012/685108 |
0.347 |
|
| 2012 |
Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH. High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation. Circulation. Cardiovascular Genetics. 5: 450-9. PMID 22685113 DOI: 10.1161/Circgenetics.111.962597 |
0.37 |
|
| 2012 |
Gjerris AC, Tabor A, Loft A, Christiansen M, Pinborg A. First trimester prenatal screening among women pregnant after IVF/ICSI. Human Reproduction Update. 18: 350-9. PMID 22523111 DOI: 10.1093/Humupd/Dms010 |
0.302 |
|
| 2012 |
Page SP, Kounas S, Syrris P, Christiansen M, Frank-Hansen R, Andersen PS, Elliott PM, McKenna WJ. Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome. Circulation. Cardiovascular Genetics. 5: 156-66. PMID 22267749 DOI: 10.1161/Circgenetics.111.960831 |
0.349 |
|
| 2012 |
Saberniak J, Jacobsen MB, Edvardsen T, Balta S, Demirkol S, Cakar M, Karaman M, Ay SA, Arslan Z, Bjorgvinsdottir L, Arnar DO, Indridason OS, Heidarsdottir R, Skogstrand K, Torfason B, ... ... Christiansen M, et al. Front & Back Matter The Cardiology. 121. DOI: 10.1159/000337946 |
0.462 |
|
| 2011 |
Hedley PL, Haundrup O, Andersen PS, Aidt FH, Jensen M, Moolman-Smook JC, Bundgaard H, Christiansen M. The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study. Journal of Negative Results in Biomedicine. 10: 12. PMID 21967835 DOI: 10.1186/1477-5751-10-12 |
0.339 |
|
| 2011 |
Lakdawala NK, Thune JJ, Maron BJ, Cirino AL, Havndrup O, Bundgaard H, Christiansen M, Carlsen CM, Dorval JF, Kwong RY, Colan SD, Køber LV, Ho CY. Electrocardiographic features of sarcomere mutation carriers with and without clinically overt hypertrophic cardiomyopathy. The American Journal of Cardiology. 108: 1606-13. PMID 21943931 DOI: 10.1016/J.Amjcard.2011.07.019 |
0.355 |
|
| 2011 |
Godiksen MT, Granstrøm S, Koch J, Christiansen M. Hypertrophic cardiomyopathy in young Maine Coon cats caused by the p.A31P cMyBP-C mutation--the clinical significance of having the mutation. Acta Veterinaria Scandinavica. 53: 7. PMID 21306647 DOI: 10.1186/1751-0147-53-7 |
0.327 |
|
| 2011 |
Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. [Short QT syndrome as an inherited condition]. Ugeskrift For Laeger. 173: 420-4. PMID 21299935 |
0.522 |
|
| 2011 |
Olesen MS, Jespersen T, Nielsen JB, Liang B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø S, Schmitt N, Svendsen JH. Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation. Cardiovascular Research. 89: 786-93. PMID 21051419 DOI: 10.1093/Cvr/Cvq348 |
0.35 |
|
| 2010 |
Christiansen M, Hedley PL. Long QT testing: implications for complex diagnosis in personalized medicine. Personalized Medicine. 7: 125-127. PMID 29783314 DOI: 10.2217/Pme.10.6 |
0.385 |
|
| 2010 |
Bastiaenen R, Hedley PL, Christiansen M, Behr ER. Therapeutic hypothermia and ventricular fibrillation storm in early repolarization syndrome. Heart Rhythm. 7: 832-4. PMID 20206297 DOI: 10.1016/J.Hrthm.2010.02.037 |
0.303 |
|
| 2010 |
Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S. Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides. Biochemical and Biophysical Research Communications. 393: 751-6. PMID 20171168 DOI: 10.1016/J.Bbrc.2010.02.075 |
0.308 |
|
| 2010 |
Christiansen M, Pihl K, Hedley PL, Gjerris AC, Lind PØ, Larsen SO, Krebs L, Larsen T. ADAM 12 may be used to reduce the false positive rate of first trimester combined screening for Down syndrome. Prenatal Diagnosis. 30: 110-4. PMID 20013872 DOI: 10.1002/Pd.2405 |
0.329 |
|
| 2009 |
Møller DV, Pham TT, Gustafsson F, Hedley P, Ersbøll MK, Bundgaard H, Andersen CB, Torp-Pedersen C, Køber L, Christiansen M. The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy. European Journal of Heart Failure. 11: 1031-5. PMID 19875404 DOI: 10.1093/Eurjhf/Hfp134 |
0.31 |
|
| 2009 |
Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M. The genetic basis of long QT and short QT syndromes: a mutation update. Human Mutation. 30: 1486-511. PMID 19862833 DOI: 10.1002/Humu.21106 |
0.566 |
|
| 2009 |
Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M. The genetic basis of Brugada syndrome: a mutation update. Human Mutation. 30: 1256-66. PMID 19606473 DOI: 10.1002/Humu.21066 |
0.512 |
|
| 2009 |
Graff C, Andersen MP, Xue JQ, Hardahl TB, Kanters JK, Toft E, Christiansen M, Jensen HK, Struijk JJ. Identifying drug-induced repolarization abnormalities from distinct ECG patterns in congenital long QT syndrome: a study of sotalol effects on T-wave morphology. Drug Safety. 32: 599-611. PMID 19530746 DOI: 10.2165/00002018-200932070-00006 |
0.538 |
|
| 2009 |
Møller DV, Andersen PS, Hedley P, Ersbøll MK, Bundgaard H, Moolman-Smook J, Christiansen M, Køber L. The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy. European Journal of Human Genetics : Ejhg. 17: 1241-9. PMID 19293840 DOI: 10.1038/Ejhg.2009.34 |
0.367 |
|
| 2009 |
Tfelt-Hansen J, Jespersen T, Hofman-Bang J, Rasmussen HB, Cedergreen P, Skovby F, Abriel H, Svendsen JH, Olesen SP, Christiansen M, Haunso S. Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A. The Canadian Journal of Cardiology. 25: 156-60. PMID 19279983 DOI: 10.1016/S0828-282X(09)70043-1 |
0.37 |
|
| 2009 |
Andersen PS, Havndrup O, Hougs L, Sørensen KM, Jensen M, Larsen LA, Hedley P, Thomsen AR, Moolman-Smook J, Christiansen M, Bundgaard H. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives. Human Mutation. 30: 363-70. PMID 19035361 DOI: 10.1002/Humu.20862 |
0.354 |
|
| 2008 |
Delpón E, Cordeiro JM, Núñez L, Thomsen PE, Guerchicoff A, Pollevick GD, Wu Y, Kanters JK, Larsen CT, Hofman-Bang J, Burashnikov E, Christiansen M, Antzelevitch C. Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome. Circulation. Arrhythmia and Electrophysiology. 1: 209-18. PMID 19122847 DOI: 10.1161/Circep.107.748103 |
0.547 |
|
| 2008 |
Gjerris AC, Loft A, Pinborg A, Christiansen M, Tabor A. The effect of a 'vanishing twin' on biochemical and ultrasound first trimester screening markers for Down's syndrome in pregnancies conceived by assisted reproductive technology. Human Reproduction (Oxford, England). 24: 55-62. PMID 18835870 DOI: 10.1093/Humrep/Den362 |
0.305 |
|
| 2008 |
Kanters JK, Haarmark C, Vedel-Larsen E, Andersen MP, Graff C, Struijk JJ, Thomsen PE, Christiansen M, Jensen HK, Toft E. T(peak)T(end) interval in long QT syndrome. Journal of Electrocardiology. 41: 603-8. PMID 18822425 DOI: 10.1016/J.Jelectrocard.2008.07.024 |
0.519 |
|
| 2008 |
Hedley P, Christiansen M. Serum leptin in first-trimester Down syndrome pregnancies. Prenatal Diagnosis. 28: 475-7. PMID 18437707 DOI: 10.1002/Pd.1998 |
0.314 |
|
| 2008 |
Frank-Hansen R, Page SP, Syrris P, McKenna WJ, Christiansen M, Andersen PS. Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations. European Journal of Human Genetics : Ejhg. 16: 1062-9. PMID 18337725 DOI: 10.1038/Ejhg.2008.52 |
0.363 |
|
| 2008 |
Pihl K, Sørensen TL, Nørgaard-Pedersen B, Larsen SO, Nguyen TH, Krebs L, Larsen T, Christiansen M. First-trimester combined screening for Down syndrome: prediction of low birth weight, small for gestational age and pre-term delivery in a cohort of non-selected women. Prenatal Diagnosis. 28: 247-53. PMID 18302310 DOI: 10.1002/Pd.1946 |
0.32 |
|
| 2008 |
Consuegra-Sanchez L, Petrovic I, Cosin-Sales J, Holt DW, Christiansen M, Kaski JC. Prognostic value of circulating pregnancy-associated plasma protein-A (PAPP-A) and proform of eosinophil major basic protein (pro-MBP) levels in patients with chronic stable angina pectoris. Clinica Chimica Acta; International Journal of Clinical Chemistry. 391: 18-23. PMID 18267116 DOI: 10.1016/J.Cca.2008.01.012 |
0.313 |
|
| 2008 |
Graff C, Andersen M, Xue J, Hardahl T, Kanters J, Toft E, Christiansen M, Jensen H, Struijk J. T-wave morphology reveals greater effect of d,l-sotalol than QTc Journal of Electrocardiology. 41: 644. DOI: 10.1016/J.Jelectrocard.2008.08.027 |
0.436 |
|
| 2008 |
Haarmark C, Andersen MP, Graff C, Hardahl TB, Struijk J, Toft E, Christiansen M, Jensen HK, Kanters JK. T-wave morphology differences depending on genotype in long QT syndrome Journal of Interventional Cardiac Electrophysiology. 21. DOI: 10.1007/S10840-008-9220-7 |
0.542 |
|
| 2007 |
Christiansen M, Spencer K, Laigaard J, Cowans NJ, Larsen SO, Wewer UM. ADAM 12 as a second-trimester maternal serum marker in screening for Down syndrome. Prenatal Diagnosis. 27: 611-5. PMID 17465398 DOI: 10.1002/Pd.1750 |
0.307 |
|
| 2007 |
Nielsen NH, Winkel BG, Kanters JK, Schmitt N, Hofman-Bang J, Jensen HS, Bentzen BH, Sigurd B, Larsen LA, Andersen PS, Haunsø S, Kjeldsen K, Grunnet M, Christiansen M, Olesen SP. Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients Biochemical and Biophysical Research Communications. 354: 776-782. PMID 17266934 DOI: 10.1016/J.Bbrc.2007.01.048 |
0.572 |
|
| 2007 |
Christiansen M, Sørensen TL, Nørgaard-Pedersen B. Human placental lactogen is a first-trimester maternal serum marker of Down syndrome. Prenatal Diagnosis. 27: 1-5. PMID 17154235 DOI: 10.1002/Pd.1600 |
0.323 |
|
| 2007 |
Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsøe S, McKenna WJ, Christiansen M. High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia. Clinical Genetics. 69: 504-11. PMID 16712702 DOI: 10.1111/J.1399-0004.2006.00621.X |
0.61 |
|
| 2007 |
Graff C, Xue J, Andersen MP, Kanters JK, Hardahl TB, Toft E, Christiansen M, Struijk JJ. T-wave convexity measure outperforms notch criterion as diagnostic marker for the HERG genotype Journal of Electrocardiology. 40: S82-S83. DOI: 10.1016/J.Jelectrocard.2007.08.028 |
0.51 |
|
| 2007 |
Andersen MP, Xue J, Graff C, Hardahl TB, Christiansen M, Toft E, Kanters JK, Struijk JJ. Repeatability of T-wave morphology measurements: superiority of a principal component analysis–based lead Journal of Electrocardiology. 40: S81. DOI: 10.1016/J.Jelectrocard.2007.08.023 |
0.498 |
|
| 2007 |
Sørensen TL, Larsen SO, Jønsson L, Riis J, Nørgaard-Pedersen B, Christiansen M. OP25.14: First trimester maternal serum screening for Down syndrome in Denmark: performance, parameters and centralized quality control in 23 653 Pregnancies from 17 centers Ultrasound in Obstetrics and Gynecology. 30: 545-546. DOI: 10.1002/Uog.4687 |
0.308 |
|
| 2007 |
Pihl K, Soerensen TL, Nguyen TH, Krebs L, Noergaard-Pedersen B, Larsen T, Christiansen M. OP19.01: PAPP-A and β-hCG as markers of low birth weight and preterm delivery in a consecutive cohort of 1867 pregnancies undergoing combined first trimester screening for Down syndrome Ultrasound in Obstetrics and Gynecology. 30: 520-520. DOI: 10.1002/Uog.4602 |
0.302 |
|
| 2007 |
Christiansen M, Sørensen TL, Laigaard J, Nørgaard-Pedersen B. OC84: Biochemical normalization of ADAM 12-towards serum-only screening for Down syndrome in the first-trimester Ultrasound in Obstetrics and Gynecology. 30: 392-392. DOI: 10.1002/Uog.4190 |
0.315 |
|
| 2006 |
Nyberg MT, Stoevring B, Behr ER, Ravn LS, McKenna WJ, Christiansen M. The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome. Clinica Chimica Acta; International Journal of Clinical Chemistry. 375: 87-91. PMID 17010328 DOI: 10.1016/J.Cca.2006.06.020 |
0.336 |
|
| 2006 |
Struijk JJ, Kanters JK, Andersen MP, Hardahl T, Graff C, Christiansen M, Toft E. Classification of the long-QT syndrome based on discriminant analysis of T-wave morphology. Medical & Biological Engineering & Computing. 44: 543-9. PMID 16937190 DOI: 10.1007/S11517-006-0061-1 |
0.563 |
|
| 2006 |
Kanters JK, Graff C, Andersen MP, Hardahl T, Toft E, Christiansen M, Bloch Thomsen PE, Struijk JJ. Long QT syndrome genotyping by electrocardiography: fact, fiction, or something in between? Journal of Electrocardiology. 39: S119-22. PMID 16920146 DOI: 10.1016/J.Jelectrocard.2006.06.008 |
0.573 |
|
| 2006 |
Laigaard J, Cuckle H, Wewer UM, Christiansen M. Maternal serum ADAM12 levels in Down and Edwards' syndrome pregnancies at 9-12 weeks' gestation. Prenatal Diagnosis. 26: 689-91. PMID 16752438 DOI: 10.1002/Pd.1480 |
0.315 |
|
| 2006 |
Kanters JK, Thomsen PE, Christiansen M, Toft E. Neurocardiogenic syncope in long-QT syndrome is not necessarily benign. Clinical Research in Cardiology : Official Journal of the German Cardiac Society. 95: 349; author reply 35. PMID 16741593 DOI: 10.1007/S00392-006-0385-8 |
0.551 |
|
| 2006 |
Wøjdemann KR, Larsen SO, Rode L, Shalmi A, Sundberg K, Christiansen M, Tabor A. First trimester Down syndrome screening: distribution of markers and comparison of assays for quantification of pregnancy-associated plasma protein-A. Scandinavian Journal of Clinical and Laboratory Investigation. 66: 101-11. PMID 16537243 DOI: 10.1080/00365510500406902 |
0.322 |
|
| 2006 |
Kanters JK, Thomsen PEB, Christiansen M, Toft E. Neurocardiogenic syncopein long–QT syndromeis not necessarily benign Clinical Research in Cardiology. 95: 392-392. DOI: 10.1007/S00392-006-0416-5 |
0.468 |
|
| 2005 |
Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 2: 1238-49. PMID 16253915 DOI: 10.1016/J.Hrthm.2005.07.025 |
0.36 |
|
| 2005 |
Christiansen M, Nørgaard-Pedersen B. Inhibin A is a maternal serum marker for Down's syndrome early in the first trimester. Clinical Genetics. 68: 35-9. PMID 15952984 DOI: 10.1111/J.1399-0004.2005.00441.X |
0.327 |
|
| 2005 |
Wøjdemann KR, Shalmi AC, Christiansen M, Larsen SO, Sundberg K, Brocks V, Bang J, Nørgaard-Pedersen B, Tabor A. Improved first-trimester Down syndrome screening performance by lowering the false-positive rate: a prospective study of 9941 low-risk women. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 25: 227-33. PMID 15736185 DOI: 10.1002/Uog.1834 |
0.32 |
|
| 2005 |
Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K. Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome. The American Journal of Cardiology. 95: 433-4. PMID 15670565 DOI: 10.1016/J.Amjcard.2004.09.054 |
0.578 |
|
| 2005 |
Laigaard J, Christiansen M, Fröhlich C, Pedersen BN, Ottesen B, Wewer UM. The level of ADAM12-S in maternal serum is an early first-trimester marker of fetal trisomy 18. Prenatal Diagnosis. 25: 45-6. PMID 15662668 DOI: 10.1002/Pd.1029 |
0.306 |
|
| 2005 |
Frank-Hansen R, Larsen LA, Andersen P, Jespersgaard C, Christiansen M. Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome. Clinica Chimica Acta; International Journal of Clinical Chemistry. 351: 95-100. PMID 15563876 DOI: 10.1016/J.Cccn.2004.08.017 |
0.345 |
|
| 2005 |
Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS. One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region. European Journal of Human Genetics : Ejhg. 13: 161-5. PMID 15483641 DOI: 10.1038/Sj.Ejhg.5201310 |
0.355 |
|
| 2005 |
Christiansen M, Kjeldsen K, Wettrell G, Larsen LA, Lundkvist L, Andersen PS, Tran CT, Kanters JK, Vuust J. Potassium must be considered in congenital long QT syndrome Heartdrug. 5: 54-58. DOI: 10.1159/000083388 |
0.59 |
|
| 2005 |
Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS. Erratum: One-third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region European Journal of Human Genetics. 13: 694-694. DOI: 10.1038/Sj.Ejhg.5201385 |
0.315 |
|
| 2005 |
Kanters JK, Bloch Thomsen PE, Toft E, Christiansen M. Clinical characteristics in Long QT syndrome from the Danish Long QT registry Heart Rhythm. 2: S311. DOI: 10.1016/J.Hrthm.2005.02.979 |
0.352 |
|
| 2004 |
Kanters JK, Fanoe S, Larsen LA, Bloch Thomsen PE, Toft E, Christiansen M. T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 1: 285-92. PMID 15851171 DOI: 10.1016/J.Hrthm.2004.05.002 |
0.568 |
|
| 2004 |
Hofman-Bang J, Jespersen T, Grunnet M, Larsen LA, Andersen PS, Kanters JK, Kjeldsen K, Christiansen M. Does KCNE5 play a role in long QT syndrome? Clinica Chimica Acta; International Journal of Clinical Chemistry. 345: 49-53. PMID 15193977 DOI: 10.1016/J.Cccn.2004.02.033 |
0.585 |
|
| 2004 |
Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Pedersen AK, Kjeldsen K, Christiansen M. Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency. European Journal of Human Genetics : Ejhg. 12: 673-7. PMID 15114369 DOI: 10.1038/Sj.Ejhg.5201190 |
0.341 |
|
| 2004 |
Christiansen M, Larsen SO, Oxvig C, Qin QP, Wagner JM, Overgaard MT, Gleich GJ, Sottrup-Jensen L, Nørgaard-Pedersen B. Screening for Down's syndrome in early and late first and second trimester using six maternal serum markers. Clinical Genetics. 65: 11-6. PMID 15032969 DOI: 10.1111/J..2004.00177.X |
0.316 |
|
| 2004 |
Mogensen J, Perrot A, Andersen PS, Havndrup O, Klausen IC, Christiansen M, Bross P, Egeblad H, Bundgaard H, Osterziel KJ, Haltern G, Lapp H, Reinecke P, Gregersen N, Børglum AD. Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy. Journal of Medical Genetics. 41: e10. PMID 14729850 DOI: 10.1136/Jmg.2003.010447 |
0.365 |
|
| 2004 |
Christiansen M, Jaliashvili I. Total pregnancy-associated plasma protein A--a first trimester maternal serum marker for Down's syndrome: clinical and technical assessment of a poly-monoclonal enzyme immunoassay. Scandinavian Journal of Clinical and Laboratory Investigation. 63: 407-15. PMID 14594321 DOI: 10.1080/00365510310002248 |
0.333 |
|
| 2003 |
Toft E, Aarøe J, Jensen BT, Christiansen M, Fog L, Thomsen PE, Kanters JK. Long QT syndrome patients may faint due to neurocardiogenic syncope. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 5: 367-70. PMID 14753633 DOI: 10.1016/S1099-5129(03)00083-7 |
0.548 |
|
| 2003 |
Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA. Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening. Human Mutation. 21: 455-65. PMID 12673787 DOI: 10.1002/Humu.10169 |
0.323 |
|
| 2003 |
Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac β-myosin gene mutations Cardiovascular Research. 57: 347-357. PMID 12566107 DOI: 10.1016/S0008-6363(02)00711-3 |
0.352 |
|
| 2003 |
Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA. High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method. Human Mutation. 21: 116-22. PMID 12552558 DOI: 10.1002/Humu.10161 |
0.353 |
|
| 2003 |
W�jdemann K, Christiansen M, Shalmi AC, Sundberg K, Larsen SO, Tabor A. OC226: Combined screening for Down's syndrome in 221 twin pregnancies from the copenhagen first trimester study Ultrasound in Obstetrics and Gynecology. 22: 60-60. DOI: 10.1002/Uog.426 |
0.317 |
|
| 2003 |
Rode L, W�jdemann K, Larsen SO, Sundberg K, Shalmi AC, N�rgaard-Pedersen B, Christiansen M, Tabor A. OC057: Combined first and second trimester ultrasonic and serological screening for Down's syndrome?including an evaluation of ProMBP as a marker Ultrasound in Obstetrics and Gynecology. 22: 15-15. DOI: 10.1002/Uog.268 |
0.304 |
|
| 2002 |
Christiansen M, Høgdall EV, Larsen SO, Høgdall C. The variation of risk estimates through pregnancy in second trimester maternal serum screening for Down syndrome. Prenatal Diagnosis. 22: 385-7. PMID 12001192 DOI: 10.1002/Pd.297 |
0.315 |
|
| 2002 |
Qin Q, Christiansen M, Pettersson K. Point-of-Care Time-resolved Immunofluorometric Assay for Human Pregnancy-associated Plasma Protein A: Use in First-Trimester Screening for Down Syndrome Clinical Chemistry. 48: 473-483. DOI: 10.1093/Clinchem/48.3.473 |
0.31 |
|
| 2001 |
Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M. Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations Journal of Medical Genetics. 38. PMID 11748309 DOI: 10.1136/Jmg.38.12.E43 |
0.351 |
|
| 2001 |
Larsen LA, Christiansen M, Vuust J, Andersen PS. Recent developments in high-throughput mutation screening. Pharmacogenomics. 2: 387-99. PMID 11722288 DOI: 10.1517/14622416.2.4.387 |
0.315 |
|
| 2001 |
Larsen LA, Johnson M, Brown C, Christiansen M, Frank-Hansen R, Vuust J, Andersen PS. Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis. Human Mutation. 18: 451-7. PMID 11668638 DOI: 10.1002/Humu.1216 |
0.359 |
|
| 2001 |
Wøjdemann KR, Larsen SO, Shalmi A, Sundberg K, Christiansen M, Tabor A. First trimester screening for Down syndrome and assisted reproduction: no basis for concern. Prenatal Diagnosis. 21: 563-5. PMID 11494292 DOI: 10.1002/Pd.124 |
0.306 |
|
| 2001 |
Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age. The American Journal of Cardiology. 87: 1315-7. PMID 11377367 DOI: 10.1016/S0002-9149(01)01532-6 |
0.362 |
|
| 2001 |
Mogensen J, Andersen PS, Steffensen U, Christiansen M, Egeblad H, Gregersen N, Børglum AD. Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy Journal of Medical Genetics. 38: 193-198. PMID 11303515 DOI: 10.1136/Jmg.38.3.193 |
0.331 |
|
| 2001 |
Larsen LA, Andersen PS, Kanters J, Svendsen IH, Jacobsen JR, Vuust J, Wettrell G, Tranebjærg L, Bathen J, Christiansen M. Screening for Mutations and Polymorphisms in the Genes KCNH2 and KCNE2 Encoding the Cardiac HERG/MiRP1 Ion Channel: Implications for Acquired and Congenital Long Q-T Syndrome Clinical Chemistry. 47: 1390-1395. DOI: 10.1093/Clinchem/47.8.1390 |
0.587 |
|
| 2000 |
Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy. Scandinavian Cardiovascular Journal : Scj. 34: 558-63. PMID 11214007 DOI: 10.1080/140174300750064477 |
0.322 |
|
| 2000 |
Tyson J, Tranebjaerg L, McEntagart M, Larsen LA, Christiansen M, Whiteford ML, Bathen J, Aslaksen B, Sørland SJ, Lund O, Pembrey ME, Malcolm S, Bitner-Glindzicz M. Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen. Human Genetics. 107: 499-503. PMID 11140949 DOI: 10.1007/S004390000402 |
0.361 |
|
| 2000 |
Larsen LA, Christiansen M, Vuust J, Andersen PS. High throughput mutation screening by automated capillary electrophoresis. Combinatorial Chemistry & High Throughput Screening. 3: 393-409. PMID 11032956 DOI: 10.2174/1386207003331508 |
0.328 |
|
| 2000 |
Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M. Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2. Clinical Genetics. 57: 125-30. PMID 10735633 DOI: 10.1034/J.1399-0004.2000.570206.X |
0.588 |
|
| 1999 |
Christiansen M, Oxvig C, Wagner JM, Qin QP, Nguyen TH, Overgaard MT, Larsen SO, Sottrup-Jensen L, Gleich GJ, Norgaard-Pedersen B. The proform of eosinophil major basic protein: a new maternal serum marker for Down syndrome. Prenatal Diagnosis. 19: 905-10. PMID 10521813 DOI: 10.1002/(Sici)1097-0223(199910)19:10<905::Aid-Pd658>3.0.Co;2-Q |
0.316 |
|
| 1999 |
Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M. Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene. European Journal of Human Genetics : Ejhg. 7: 724-8. PMID 10482963 DOI: 10.1038/Sj.Ejhg.5200323 |
0.583 |
|
| 1999 |
Wald NJ, Watt HC, Norgaard-Pedersen B, Christiansen M. SP1 in pregnancies with Down syndrome in the first trimester of pregnancy. International Prenatal Screening Research Group. Prenatal Diagnosis. 19: 517-20. PMID 10416965 DOI: 10.1002/(Sici)1097-0223(199906)19:6<517::Aid-Pd591>3.0.Co;2-2 |
0.315 |
|
| 1999 |
Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M. Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain. Journal of Molecular and Cellular Cardiology. 31: 745-50. PMID 10329202 DOI: 10.1006/Jmcc.1998.0911 |
0.338 |
|
| 1999 |
Larsen LA, Christiansen M, Vuust J, Andersen PS. High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants. Human Mutation. 13: 318-27. PMID 10220146 DOI: 10.1002/(Sici)1098-1004(1999)13:4<318::Aid-Humu9>3.0.Co;2-F |
0.339 |
|
| 1999 |
Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M. A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome. Clinica Chimica Acta; International Journal of Clinical Chemistry. 280: 113-25. PMID 10090529 DOI: 10.1016/S0009-8981(98)00177-6 |
0.593 |
|
| 1998 |
Larsen SO, Christiansen M, Nørgaard-Pedersen B. Inclusion of serum marker measurements from a previous pregnancy improves Down syndrome screening performance. Prenatal Diagnosis. 18: 706-12. PMID 9706652 DOI: 10.1002/(Sici)1097-0223(199807)18:7<706::Aid-Pd338>3.0.Co;2-W |
0.329 |
|
| 1998 |
Kanters JK, Larsen LA, Orholm M, Agner E, Andersen PS, Vuust J, Christiansen M. Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome. Journal of Cardiovascular Electrophysiology. 9: 620-4. PMID 9654228 DOI: 10.1111/J.1540-8167.1998.Tb00944.X |
0.583 |
|
| 1998 |
Andersen PS, Larsen LA, Kanters JK, Havndrup O, Bundgaard H, Brandt NJ, Vuust J, Christiansen M. Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome. Molecular Diagnosis. 3: 105-111. DOI: 10.1016/S1084-8592(98)80058-1 |
0.571 |
|
| 1997 |
Qin QP, Christiansen M, Nguyen TH, Sørensen S, Larsen SO, Nørgaard-Pedersen B. Schwangerschaftsprotein 1 (SP1) as a maternal serum marker for Down syndrome in the first and second trimesters. Prenatal Diagnosis. 17: 101-8. PMID 9061756 DOI: 10.1002/(Sici)1097-0223(199702)17:2<101::Aid-Pd4>3.0.Co;2-H |
0.306 |
|
| 1997 |
Qin QP, Nguyen TH, Christiansen M, Larsen SO, Nørgaard-Pedersen B. Time-resolved immunofluorometric assay of pregnancy-associated plasma protein A in maternal serum screening for Down's syndrome in first trimester of pregnancy. Clinica Chimica Acta; International Journal of Clinical Chemistry. 254: 113-29. PMID 8896900 DOI: 10.1016/0009-8981(96)06378-4 |
0.337 |
|
| 1997 |
Qin Q, Christiansen M, Oxvig C, Pettersson K, Sottrup-Jensen L, Koch C, Nørgaard-Pedersen B. Double-monoclonal immunofluorometric assays for pregnancy-associated plasma protein A/proeosinophil major basic protein (PAPP-A/proMBP) complex in first-trimester maternal serum screening for Down syndrome Clinical Chemistry. 43: 2323-2332. DOI: 10.1093/Clinchem/43.12.2323 |
0.322 |
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