Jacobsen, I. S., Tümer, Z., Tommerup, N.
, Børglum, A., Horsbøl, H.
& Mors, O. (2005).
T(4;12) translocation an a patient with bipolar affective disorder. Abstract from T(4;12) translocation an a patient with bipolar affective disorder.
Kamm, C., Healey, D. G., Quinn, N. P., Wüllner, U., Müller, J. C., Schols, L., Geser, F., Burk, K.
, Børglum, A., Pellecchia, M. T., Tolosa, E., del Sorbo, F., Nilsson, C., Bandmann, O., Sharma, M., Mayer, P., Gasteiger, M., Haworth, A., Ozawa, T. ... Gasser, T. (2005).
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. Brain,
128, 1855-1860.
Buttenschøn, H. N., Als, T. D., Daoud, A. E., Foldager, L., Wang, AG.
, Børglum, A., Kruse, TA., Lauritsen, MB.
& Mors, O. (2005).
The glutamate decarboxylase gene 1 as a potential candidate gene for autism.. Abstract from XIIIthWorld Congress on Psychiatric Genetics, The Westin Copley Place, Boston.
Mogensen, J., Perrot, A., Andersen, P. S., Havndrup, O., Klausen, I. C., Christiansen, M.
, Bross, P., Egeblad, H., Bundgaard, H., Osterziel, K. J., Haltern, G., Lapp, H., Reinecke, P.
, Gregersen, N. & Børglum, A. D. (2004).
Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.
Journal of Medical Genetics,
41(1), e10.
Alderton, G. K., Joenje, H., Varon, R.
, Børglum, A., Jeggo, P. A. & O'Driscoll, M. (2004).
Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.
Human Molecular Genetics,
13(24), 3127-38.
https://doi.org/10.1093/hmg/ddh335Jørgensen, T. H.
, Buttenschøn, H. N., Wang, A. G.
, Als, T. D., Børglum, A. & Ewald, H. (2004).
The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers.
Hum. Genet.,
115(1), 19-28.
Børglum, A., Kirov, G., Craddock, N.
, Mors, O., Muir, W., Murray, V., McKee, I., Collier, D. A.
, Ewald, H., Owen, M. J., Blackwood, D. & Kruse, T. A. (2003).
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
117B(1), 18-22.
Severinsen, J., Binderup, H.
, Mors, O., Wang, A. G., Vang, M., Murray, V., Muir, W., Mckee, I., Kruse, T. A., Blackwood, D. HR., Ewald, H.
& Børglum, A. (2002).
Association study of candidate genes for susceptibility to schizophrenia and bipolar disorder on chromosome 22Q13. Abstract from X World Congress on Psychiatric Genetics, 2002, Bruxelles, Belgium.
Del-Favero, J., Gestel, S. V.
, Børglum, A., Muir, W.
, Ewald, H., Mors, O., Ivezic, S., Oruc, L., Adolfsson, R., Blackwood, D., Kruse, T., Mendlewicz, J., Schalling, M. & Van Broeckhoven, C. (2002).
European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
European Journal of Human Genetics,
10(4), 276-80.
https://doi.org/10.1038/sj.ejhg.5200803Hansen, 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/s00439-002-0837-9Lauritsen, 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.
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.
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., 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.
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.
