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Hansen, J. J., Bross, P., Westergaard, M., Nielsen, M. N., Eiberg, H., Børglum, A., Mogensen, J., Kristiansen, K., Bolund, L. & Gregersen, N. (2002). Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter. Human Genetics, 112(1), 71-7. https://doi.org/10.1007/s00439-002-0837-9

Lauritsen, M. B., Børglum, A., Betancur, C., Philippe, A., Kruse, T. A., Leboyer, M. & Ewald, H. (2002). Investigation of two variants in the DOPA decarboxylase gene in patients with autism. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 114(4), 466-70. https://doi.org/10.1002/ajmg.10379

Nyegaard, M., Børglum, A. D., Bruun, T. G., Collier, D. A., Russ, C., Mors, O., Ewald, H. & Kruse, T. A. (2002). Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder. Molecular Psychiatry, 7(7), 745-54. https://doi.org/10.1038/sj.mp.4001049

Jørgensen, T. H., Børglum, A., Mors, O., Wang, A. G., Pinaud, M., Zacharov, T. F., Dahl, H. A., Vang, M., Kruse, T. A. & Ewald, H. (2002). Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 114, 245-252.

Børglum, A. D., Balslev, T., Haagerup, A., Birkebaek, N., Binderup, H., Kruse, T. A. & Hertz, J. M. (2001). A new locus for Seckel syndrome on chromosome 18p11.31-q11.2. European Journal of Human Genetics, 9(10), 753-7. https://doi.org/10.1038/sj.ejhg.5200701

Mogensen, J., Andersen, P. S., Steffensen, U., Christiansen, M., Egeblad, H., Gregersen, N. & Børglum, A. D. (2001). Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy. Journal of Medical Genetics, 38(3), 193-8.

Børglum, A. D., Hampson, M., Kjeldsen, T. E., Muir, W., Murray, V., Ewald, H., Mors, O., Blackwood, D. & Kruse, T. A. (2001). Dopa decarboxylase genotypes may influence age at onset of schizophrenia. Molecular Psychiatry, 6(6), 712-7. https://doi.org/10.1038/sj.mp.4000902

Andersen, P. S., Havndrup, O., Bundgaard, H., Moolman-Smook, J. C., Larsen, L. A., Mogensen, J., Brink, P. A., Børglum, A. D., Corfield, V. A., Kjeldsen, K., Vuust, J. & Christiansen, M. (2001). Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations. Journal of Medical Genetics, 38(12), E43.

Mogensen, J., Kruse, T. A. & Børglum, A. D. (1999). Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping. Cytogenetic and Genome Research, 84(1-2), 35-6.

Børglum, A. D., Bruun, T. G., Kjeldsen, T. E., Ewald, H., Mors, O., Kirov, G., Russ, C., Freeman, B., Collier, D. A. & Kruse, T. A. (1999). Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder. Molecular Psychiatry, 4(6), 545-51.

Mogensen, J., Kruse, T. A. & Børglum, A. D. (1998). Assignment of the human skeletal muscle alpha-actin gene (ACTA1) to chromosome 1q42.13-->q42.2 by radiation hybrid mapping. Cytogenetic and Genome Research, 83(3-4), 224-5.

Mogensen, J., Kruse, T. A. & Børglum, A. D. (1997). Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping. Cytogenetic and Genome Research, 79(3-4), 272-3.

Børglum, A., Nyegaard, M., Kvistgaard, AB., Mullaart, E., Uitterlinden, AG., Vijg, J. & Kruse, T. A. (1997). Mapping of 34 minisatellite loci resolved by two-dimensional DNA typing. Cytogenetic and Genome Research, 79(3-4), 248-56. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=9605866&query_hl=1&itool=pubmed_docsum

Børglum, A. D., Flint, T., Hansen, L. L. & Kruse, T. A. (1997). Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis. Human Genetics, 99(1), 80-2.

Børglum, A. D., Flint, T., Tommerup, N., Fleckner, J., Justesen, J. & Kruse, T. A. (1996). Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32. Cytogenetic and Genome Research, 73(1-2), 99-103.

Hertz, M. J., Børglum, A., Brandt, C. A. & Bisgård, C. (1995). Hereditaer motorisk sensorisk neuropati (Charcot-Marie-Tooths sygdom). Molekyloergenetiske aspekter. Ugeskrift for Læger, 157(25), 3613-8.

Børglum, A. D., Flint, T., Madsen, P. S., Celis, J. E. & Kruse, T. A. (1995). Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21. Human Genetics, 96(5), 592-6.

Børglum, A. D., Mullaart, E., Kvistgaard, A. B., Uitterlinden, A. G., Vijg, J. & Kruse, T. A. (1995). Two-dimensional DNA typing as a genetic marker system in humans. Cytogenetic and Genome Research, 71(3), 260-5.

Mullaart, E., Verwest, A. M., Børglum, A. D., Uitterlinden, A. G., te Meerman, G. J., Kruse, T. A. & Vijg, J. (1995). Two-dimensional DNA typing of human pedigrees: spot pattern characterization and segregation. Genomics, 29(3), 641-6.

Hertz, J. M., Børglum, A. D., Brandt, C. A., Flint, T. & Bisgaard, C. (1994). Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication. Clinical Genetics, 46(4), 291-4.

Børglum, A. D., Byskov, A., Ragno, P., Roldan, A. L., Tripputi, P., Cassani, G., Danø, K., Blasi, F., Bolund, L. & Kruse, T. A. (1992). Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2. American Journal of Human Genetics, 50(3), 492-7.

Børglum, A. D., Byskov, A., Roldan, A. L. & Kruse, T. A. (1992). Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR). Human Genetics, 89(5), 584.

Børglum, A. D., Byskov, A., Cubellis, M. V. & Kruse, T. A. (1991). An EcoRI polymorphism for the PLAUR gene. Nucleic Acids Research, 19(23), 6661.

Displaying results 401 to 423 out of 423

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Revised 15.03.2021

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Susanne Schousboe Sjøgaard