Lars Allan Larsen

Lars Allan Larsen

Professor

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    1 - 50 out of 83Page size: 50
    1. 1997
    2. Published

      High-throughput analysis of Fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis

      Larsen, Lars Allan, Grønskov, K., Nørgaard-Pedersen, B., Brøndum-Nielsen, K., Hasholt, Lis Frydenreich & Vuunst, J., 1997, In: Human Genetics. 100, p. 564-568

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. 1998
    4. Published

      Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome

      Kanters, Jørgen K., Larsen, Lars Allan, Orholm, M., Agner, E., Andersen, P. S., Vuust, J. & Christiansen, M., 1 Jan 1998, In: Journal of Cardiovascular Electrophysiology. 9, 6, p. 620-624 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. 2001
    6. Published

      Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome

      Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Svendsen, I. H., Jacobsen, J. R., Vuust, J., Wetrell, G., Tranebjærg, Lisbeth & Christiansen, M., 2001, In: Clinical Chemistry. 47, 8, p. 1390-1395

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

      Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Svendsen, I. H., Jacobsen, J. R., Vuust, J., Wettrell, G., Tranebjærg, Lisbeth, Bathen, J. & Christiansen, M., 6 Aug 2001, In: Clinical Chemistry. 47, 8, p. 1390-1395 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. 2003
    9. Published

      Capillary electrophoresis-based single stand dna conformation analysis in high-throughput mutation screening

      Andersen, P. S., Jespersgaard, C., Vuust, J., Christiansen, M. & Larsen, Lars Allan, 2003, In: Human Mutation. Vol. 21, p. 455-65

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. Published

      High-througput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

      Andersen, P. S., Jespersgaard, C., Vuust, J., Christiansen, M. & Larsen, Lars Allan, 2003, In: Human Mutation. Vol. 21, p. 116-122

      Research output: Contribution to journal › Journal article › Research › peer-review

    11. Published

      Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations

      Havndrup, O., Bundgaard, H., Andersen, P. S., Larsen, Lars Allan, Vuust, J., Kjeldsen, K. & Christiansen, M., 2003, In: Cardiovascular Research. Vol. 57, p. 298-301

      Research output: Contribution to journal › Journal article › Research › peer-review

    12. Published

      The Hedgehog signaling pathway - implications for drug targets in cancer and neurodegenerative disorders

      Bak, M., Hansen, C., Tommerup, Niels & Larsen, Lars Allan, 2003, In: Pharmacogenomics. Vol. 4, p. 411-429

      Research output: Contribution to journal › Journal article › Research › peer-review

    13. 2004
    14. Published

      Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

      Boonen, S. E., Stahl, D., Kreiborg, Sven, Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels, Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 132A, p. 324-328

      Research output: Contribution to journal › Journal article › Research › peer-review

    15. Published

      Does KCNE5 play a role in long QT syndrome?

      Hofman-Bang, J., Jespersen, Thomas, Grunnet, Morten, Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Kjeldsen, K. & Christiansen, M., 2004, In: Clinica Chimica Acta. 345, 1-2, p. 49-53 4 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    16. Published

      GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment

      Grønskov, K., Larsen, Lars Allan, Rendtorff, N. D., Parving, A., Nørgaard-Pedersen, B. & Brøndum-Nielsen, K., 2004, In: Genet Test. Vol. 8, p. 181-184

      Research output: Contribution to journal › Journal article › Research › peer-review

    17. Published

      Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

      Andersen, P. S., Havndrup, O., Bundgaard, H., Larsen, Lars Allan, Vuust, J., Pedersen, A. K., Kjeldsen, K. & Christiansen, M., 2004, In: European Journal of Human Genetics. Vol. 12, p. 673-677

      Research output: Contribution to journal › Journal article › Research › peer-review

    18. Published

      High Throughput Mutation Screening

      Andersen, P. S. & Larsen, Lars Allan, 2004, Molecular Analysis and Genome Discovery. New York: IEEE Computer Society Press, p. chap. 5

      Research output: Chapter in Book/Report/Conference proceeding › Report chapter › Research

    19. Published

      Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome family

      Henriksen, A. M., Tümer, Asuman Zeynep, Tommerup, Niels, Tranebjærg, Lisbeth & Larsen, Lars Allan, 2004, In: Genetic Testing. 8, 4, p. 404-6 2 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    20. Published

      T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome

      Kanters, J. K., Fanoe, S., Larsen, Lars Allan, Bloch-Thomsen, P. E., Toft, E. & Christansen, M., 2004, In: Heart Rhythm. Vol. 1, p. 285-292

      Research output: Contribution to journal › Journal article › Research › peer-review

    21. 2005
    22. Published

      Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

      Boonen, S. E., Stahl, D., Kreiborg, S., Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels & Brøndum-Nielsen, K., 2005, In: American Journal of Medical Genetics. Part A. Vol. 132, p. 324-328

      Research output: Contribution to journal › Journal article › Research › peer-review

    23. Published

      High Throughput Single-Strand Conformation Polymorphism Analysis on a Microfabricated Capillary Array Electrophoresis Dervice

      Tian, H., Emrich, C. A., Scherer, J., Mathies, R. A., Andersen, P. S., Larsen, Lars Allan & Christiansen, M., 2005, In: Electrophoresis. Vol. 26, p. 1834-1842

      Research output: Contribution to journal › Journal article › Research › peer-review

    24. Published

      Mutations in the HERG ion channel: A novel link between long QT syndrome and sudden death syndrome

      Christiansen, M., Tønder, N., Larsen, Lars Allan, Andersen, P. S., Simonsen, H. B., Øyen, N., Kanters, J. K., Jacobsen, J. R., Fosdal, I., Wettrell, G. & Kjeldsen, K., 2005, In: American Journal of Cardiology. Vol. 95, p. 433-434

      Research output: Contribution to journal › Journal article › Research › peer-review

    25. Published

      Mutations in the genes KCND2 and KCND3 encoding the ion-channels Kv 4.2. and Kv 4.3, conducting the cardiac fast transient outward current ( ITo,f), are not a frequent cause of Long QT syndrome

      Frank-Hansen, R., Larsen, Lars Allan, Andersen, P. S., Jespersgård, C. & Christiansen, M., 2005, In: Clinica Chimica Acta. Vol. 351, p. 95-100

      Research output: Contribution to journal › Journal article › Research › peer-review

    26. Published

      One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region

      Hougs, L., Havndrup, O., Bundgård, Henning, Køber, Lars Valeur, Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. 13, 2, p. 161-5 4 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    27. Published

      One-third of Danish hyperytrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

      Hougs, L., Havndrup, O., Bundgaard, H., Køber, L., Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. Vol. 13, p. 161-165

      Research output: Contribution to journal › Journal article › Research › peer-review

    28. Published

      Potassium Must Be Considered in Congenital Long QT Syndrome

      Christiansen, M., Kjeldsen, K., Wettrell, G., Larsen, Lars Allan, Lundkvist, L., Andersen, P. S., Tran, C. T., Kanters, J. K. & Vuust, J., 2005, In: Cardiology. Vol. 5, p. 54-58

      Research output: Contribution to journal › Journal article › Research › peer-review

    29. Published

      The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome

      Tümer, Asuman Zeynep, Henriksen, A. M., Bache, Iben, Larsen, Lars Allan, Brixen, K., Illum, N., Rasmussen, K. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 135A, p. 339-341

      Research output: Contribution to journal › Journal article › Research › peer-review

    30. 2006
    31. Published

      Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease

      Baekvad-Hansen, M., Tümer, Asuman Zeynep, Delicado, A., Erdogan, F., Tommerup, Niels & Larsen, Lars Allan, 2006, In: American Journal of Medical Genetics. Part A. 140A, 5, p. 427-433 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    32. Published

      Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNA.

      Bak, M., Conley, L., Hedegaard, J., Larsen, Lars Allan, Sørensen, P., Bendixen, C. & Tommerup, Niels, 2006, In: Analytical Biochemistry. 358, 1, p. 111-9 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    33. Published

      Hedgehog signaling in small-cell lung cancer: Frequent in vivo but a rare event in vitro

      Vestergaard, J., Pedersen, M. W., Pedersen, N., Ensinger, C., Tümer, Asuman Zeynep, Tommerup, Niels, Poulsen, H. S. & Larsen, Lars Allan, 2006, In: Lung Cancer. 52, 3, p. 281-290 9 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    34. Published

      Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics

      Jespersgaard, C., Larsen, Lars Allan, Baba, S., Kukita, Y., Tahira, T., Christiansen, M., Vuust, J., Hayashi, K. & Andersen, P. S., 2006, In: Electrophoresis. 27, 19, p. 3816-3822 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    35. Published

      Screening for fragilt X-syndrom. Internationale erfaringer

      Vuust, J., Larsen, Lars Allan, Gronskov, K., Norgaard-Pedersen, B. & Brondum-Nielsen, K., 2006, In: Ugeskrift for læger. 168, 43, p. 3704-3709 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    36. Published

      Screening of 99 Danish patients with congenital heart disease for GATA4 mutations

      Zhang, L., Tümer, Asuman Zeynep, Jacobsen, J. R., Andersen, P. S., Tommerup, Niels & Larsen, Lars Allan, 2006, In: Genetic Testing. 10, 4, p. 277-80 3 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    37. 2007
    38. Published

      A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome

      Dahl, C., Grønskov, K., Larsen, Lars Allan, Guldberg, P. & Brøndum-Nielsen, K., 2007, In: Clinical Chemistry. 53, 4, p. 790-793 3 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    39. Published

      Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.

      Nielsen, N. H., Winkel, B. G., Kanters, Jørgen K., Schmitt, Nicole, Hofman-Bang, J., Jensen, H. S., Bentzen, Bo Hjorth, Sigurd, B., Larsen, Lars Allan, Andersen, P. S., Kjeldsen, K., Grunnet, Morten, Christiansen, M., Olesen, Søren-Peter & Haunsø, Stig, 2007, In: Biochemical and Biophysical Research Communications. 354, 3, p. 776-82 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    40. Published

      Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2

      Jakobsen, L. P., Ullmann, R., Christensen, S. B., Jensen, K. E., Molsted, K., Henriksen, K. F., Hansen, C., Knudsen, M. A. F., Larsen, Lars Allan, Tommerup, Niels & Tümer, Asuman Zeynep, 2007, In: Journal of Medical Genetics. 44, 6, p. 381-386 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    41. Published

      Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detection

      Larsen, Lars Allan, Jespersgaard, C. & Andersen, P. S., 2007, In: Nature Protocols (Print Edition). 2, 6, p. 1458-1466 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    42. Published

      YKL-40 protein expression in the early developing human musculoskeletal system

      Johansen, J. S., Høyer, P. E., Larsen, Lars Allan, Price, P. A. & Møllgård, Kjeld, 2007, In: Journal of Histochemistry & Cytochemistry. 55, 12, p. 1213-1228 15 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    43. 2008
    44. Published

      Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

      Andersen, P. S., Havndrup, O., Hougs, L., Sørensen, K. M., Jensen, M., Larsen, Lars Allan, Hedley, P., Bie Thomsen, A. R., Moolman-Smook, J., Christiansen, M. & Bundgård, Henning, 2008, In: Human Mutation. 30, 3, p. 363-370 7 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    45. Published

      Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephaly

      Erdogan, F., Belloso, J. M., Gabau, E., Ajbro, K. D., Guitart, M., Ropers, H. H., Tommerup, Niels, Ullmann, R., Tümer, Asuman Zeynep & Larsen, Lars Allan, 2008, In: European Journal of Medical Genetics. 51, 1, p. 81-6 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    46. Published

      GLI1 is involved in cell cycle regulation and proliferation of NT2 embryonal carcinoma stem cells

      Vestergaard, J., Lind-Thomsen, A., Pedersen, M. W., Jarmer, H. O., Bak, M., Hasholt, Lis Frydenreich, Tommerup, Niels, Tümer, Asuman Zeynep & Larsen, Lars Allan, 2008, In: DNA and Cell Biology. 27, 5, p. 251-U16

      Research output: Contribution to journal › Journal article › Research › peer-review

    47. Published

      High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease

      Erdogan, F., Larsen, Lars Allan, Zhang, L., Tümer, Asuman Zeynep, Tommerup, Niels, Chen, W., Jacobsen, J. R., Schubert, M., Jurkatis, J., Tzschach, A., Ropers, H. & Ullmann, R., 2008, In: Journal of Medical Genetics. 45, 11, p. 704-709 5 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    48. Published

      Mapping of 5q35 chromosomal rearrangements within a genomically unstable region

      Buysse, K., Crepel, A., Menten, B., Pattyn, F., Antonacci, F., Veltman, J. A., Larsen, Lars Allan, Tümer, Asuman Zeynep, de Klein, A., van de Laar, I., Devriendt, K., Mortier, G. & Speleman, F., 2008, In: Journal of Medical Genetics. 45, 10, p. 672-678 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    49. Published

      Multiplex Ligation-Dependent Probe Amplification Technique for Copy Number Analysis on Small Amounts of DNA Material

      Sørensen, K., Andersen, P., Larsen, Lars Allan, Schwartz, M., Schouten, J. & Nygren, A., 2008, In: Analytical Chemistry. 80, p. 9363-9368 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    50. 2009
    51. Published

      Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development

      Zhang, L., Tümer, Asuman Zeynep, Møllgård, Kjeld, Barbi, G., Rossier, E., Bendsen, E., Møller, R. S., Ullmann, R., He, J., Papadopoulos, N., Tommerup, Niels & Larsen, Lars Allan, 2009, In: European Journal of Human Genetics.

      Research output: Contribution to journal › Journal article › Research › peer-review

    52. Published

      Expression analyses of human cleft palate tissue suggest a role for osteopontin and immune related factors in palatal development

      Jakobsen, L. P., Borup, R., Vestergaard, J., Larsen, Lars Allan, Lage, K., Maroun, L. L., Kjær, Inger, Niemann, C. U., Andersen, M., Knudsen, M. A., Møllgård, Kjeld & Tommerup, Niels, 2009, In: Experimental & Molecular Medicine. 41, 2, p. 77-85 8 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    53. Published

      Genome-wide gene expression profiling of SCID mice with T-cell-mediated Colitis

      Brudzewsky, D., Pedersen, Anders Elm, Claesson, Mogens Helweg, Gad, M., Kristensen, N. N., Lage, K., Jensen, T., Tommerup, Niels, Larsen, Lars Allan, Knudsen, S. & Tümer, Asuman Zeynep, 2009, In: Scandinavian Journal of Immunology. 69, 5, p. 437-46 9 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    54. Published

      Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24

      Hilhorst-Hofstee, Y., Tümer, Asuman Zeynep, Born, P., Knijnenburg, J., Hansson, K., Yatawara, V., Steensberg, J., Ullmann, R., Arkesteijn, G., Tommerup, Niels & Larsen, Lars Allan, 2009, In: American Journal of Medical Genetics. Part A. 149A, 8, p. 1830-3 3 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    55. Published

      The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation

      Clement, C. A., Kristensen, S. G., Møllgård, Kjeld, Pazour, G. J., Yoder, B. K., Larsen, Lars Allan & Christensen, Søren Tvorup, 2009, In: Journal of Cell Science. 122, Pt 17, p. 3070-82 12 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    56. Published

      Using Nucleofection of siRNA Constructs for Knockdown of Primary Cilia in P19.CL6 Cancer Stem Cell Differentiation into Cardiomyocytes

      Clement, C. A., Larsen, Lars Allan & Christensen, Søren Tvorup, 2009, Methods in Cell Biology. Sloboda, R. D. (ed.). Academic Press, Vol. 94. p. 181-197

      Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research

    57. 2010
    58. Published

      Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples

      Sørensen, K. M., Agergaard, P., Olesen, C., Andersen, P. S., Larsen, Lars Allan, Ostergaard, J. R., Schouten, J. P. & Christiansen, M., 2010, In: Journal of Molecular Diagnostics. 12, 2, p. 147-51 4 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    59. Published

      Dissecting spatio-temporal protein networks driving human heart development and related disorders

      Hansen, K. L., Møllgård, K., Greenway, S., Wakimoto, H., Gorham, J. M., Workman, C. T., Bendsen, E., Hansen, N. T., Rigina, O., Roque, F. S., Wiese, C., Christoffels, V. M., Roberts, A. E., Smoot, L. B., Pu, W. T., Donahoe, P. K., Tommerup, N., Brunak, S., Seidman, C. E., Seidman, J. G. & 1 others, Larsen, Lars Allan, 2010, In: Molecular Systems Biology. 6, p. 381

      Research output: Contribution to journal › Journal article › Research › peer-review

    60. Published

      Haploinsufficiency of TAB2 causes congenital heart defects in humans

      Thienpont, B., Zhang, L., Postma, A. V., Breckpot, J., Tranchevent, L., Van Loo, P., Møllgård, Kjeld, Tommerup, Niels, Bache, Iben, Tümer, Asuman Zeynep, van Engelen, K., Menten, B., Mortier, G., Waggoner, D., Gewillig, M., Moreau, Y., Devriendt, K. & Larsen, Lars Allan, 2010, In: American Journal of Human Genetics. 86, 6, p. 839-49 10 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    61. Published

      Recombinant Adeno-Associated Virus-Mediated microRNA Delivery into the Postnatal Mouse Brain Reveals a Role for miR-134 in Dendritogenesis in Vivo

      Christensen, M., Larsen, Lars Allan, Kauppinen, S. & Schratt, G., 2010, In: Frontiers in Neural Circuits. 3, p. 16

      Research output: Contribution to journal › Journal article › Research › peer-review

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