Publications

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Buttenschøn, H. N., Buch, H. N., Kristensen, A. S., Thomsen, JF., Mikkelsen, S., Bonde, JP., Kolsted, H., Kærlev, L., Kærgaard, A., Andersen, JH., Hansen, AM., Rugulies, R., Grynderup, M., Nygaard, KB., Boe, MH., Koefoed, P., Børglum, A., Erhardt, A., Woldby, D. & Mors, O. (2010). The norepinephrine transporter gene: a candidate gene for panic disorder. XVIIIth World Congress on Psychiatric Genetics. Book of abstracts., 292-293.

Buttenschøn, H. N., Buch, H. N., Kristensen, A. S., Thomsen, J. F., Mikkelsen, S., Bonde, J. P., Kolstad, H., Kærlev, L., Kærgaard, A., Andersen, J., Hansen, A. M., Rugulies, R. E., Grynderup, M., Nygaard, K. B., Boe, M. H., Koefoed, P., Børglum, A., Erhardt, A., Woldbye, D. & Mors, O. (2010). The norepinephrine transporter gene: a candidate gene for panic disorder. Poster session presented at Dansk Psykiatrisk Selskabs Årsmøde 2011, Nyborg, Denmark.

Gregersen, N., Børglum, A., Mors, O., Dahl, HA., Wang, AG., Nyegaard, M., Kruse, TA. & Als, TD. (2009). A genome-wide association search for panic disorder susceptibility genes in the isolated population of Faroe Islands. Poster session presented at A genome-wide association search for panic disorder susceptibility genes in the isolated population of Faroe Islands.

Buttenschøn, H., Lauritsen, M., Daoud, A., Hollegaard, M., Jørgensen, M., Tvedegaard, K., Hougaard, D., Børglum, A., Thorsen, P. & Mors, O. (2009). A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism. Journal of Neural Transmission, 116(3), 381-388. https://doi.org/10.1007/s00702-008-0142-4

Gregersen, N., Buttenschøn, H. N., Nygaard, M., Kristensen, A. S., Woldbye, D., Joensen, S., Kruse, T. A., Børglum, A., Mors, O., Dahl, H. & Hedemand, A. (2009). A PH sensitive sodium channel is a potential candidate gene for panic disorder. Poster session presented at World Congress of Psychiatric Genetics: Surfing the Wave of Discovery, San Diego, United States.

Bjarkam, C., Corydon, T., Olsen, I., Pallesen, J., Nyegaard, M., Fryland, T., Mors, O. & Børglum, A. (2009). Further immunohistochemical characterization of BRD1 a new susceptibility gene for schizophrenia and bipolar affective disorder. Brain Structure & Function, 214(1), 37-47. https://doi.org/10.1007/s00429-009-0219-3

Hollegaard, M., Grauholm, J., Børglum, A., Nyegaard, M., Nørgaard-Pedersen, B., Ørntoft, T., Mortensen, P. B., Wiuf, C., Mors, O., Didriksen, M., Thorsen, P. & Hougaard, D. M. (2009). Genome-wide scans using archived neonatal dried blood spot samples. B M C Genomics, 10, 297. https://doi.org/10.1186/1471-2164-10-297

Christensen, U., Møller-Larsen, S., Nyegaard, M., Haagerup, A., Hedemand, A., Brasch-Andersen, C., Kruse, T., Corydon, T. J., Deleuran, M. & Børglum, A. (2009). Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21. Human Genetics, 126(4), 549-557.

Demontis, D., Jensen, T. G. & Børglum, A. (2009). Studier af den genetiske variation giver gennembrud i forståelsen af en raekke hyppige sygdomme. Ugeskrift for Læger, 171(13), 1096.

Buttenschøn, H. N., Lauritsen, M. B., Daoud, A. E., Hollegaard, M. V., Jørgensen, M., Tvedegaard, K. C., Hougaard, D. M., Børglum, A., Thorsen, P. & Mors, O. (2008). A population based association study of GAD1 as a candidate gene for childhood autism. Poster session presented at The XV Wordl Congress of Psychiatric Genetics, New York, United States.

Deleuran, T., Olsen, I. M., Hansen, M. M., Zacharov, T. F., Børglum, A., Als, T. D. & Mors, O. (2008). A significant association study of bipolar affective disorder on chrosome 12q24. Abstract from World Congress on Psychiatric Genetics XV, New York, United States.

Møller-Larsen, S., Nyegaard, M., Haagerup, A., Vestbo, J., Kruse, T. & Børglum, A. (2008). Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders. Thorax, 63, 1064-9.

Nyegaard, M., Zacharov, T. F., Hedemand, A., Sørensen, K., Nordentoft, M., Nørgaard-Pedersen, B., Werge, T., Andersen, P., Hougaard, D. M., Pedersen, C. B., Mortensen, P. B., Mors, O. & Børglum, A. (2008). Association study between the five subunits of the NMDA receptor (GRIN1, GRIN2A, GRIN2B, GRIN2C and GRIN2D genes) and schizophrenia in a large DAnish sample. Poster session presented at XVIth World Congress on Psychiatric Genetics, Osaka, Japan.

Nyegaard, M., Quist, P., Groossens, D., Del-Favero, J., Kjeldsen, E., Pedersen, S., Zacharov, T. F., Mors, O. & Børglum, A. (2008). Genomic alterations on chromosome 3p21.1 and 17q21.31 in patients with schizophrenia and controls. Abstract from World Congress on Psychiatric Genetics XV, New York, United States.

Nexø, B. A., Vogel, U., Olsen, A., Nyegaard, M., Bukowy, Z., Rockenbauer, E., Zhang, X., Koca, C., Mains, M., Hansen, B., Hedemand, A., Kjeldgaard, A. H., Laska, M. J., Raaschou-Nielsen, O., Cold, S., Overvad, K., Tjønneland, A., Bolund, L. & Børglum, A. (2008). Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP. B M C Medical Genetics, 9(56), 1-12. https://doi.org/10.1186/1471-2350-9-56

Severinsen, J., Nyegaard, M., Bjarkam, C., Corydon, T. J., Olsen, I. M., Straarup, S., Nordentoft, M., Gurling, H. M., Mors, O. & Børglum, A. (2008). Support for BRD1 as a suspectibility gene for both schizophrenia and bipolar affective disorder. Abstract from World Congress on Psychiatric Genetics XV, New York, United States.

Corydon, T. J., Haagerup, A., Jensen, T. G., Binderup, H. G., Petersen, M. S., Kaltoft, K., Vestbo, J., Kruse, T. A. & Børglum, A. (2007). A functional CD86 polymorphism associated with asthma and related allergic disorders. J Med. Genet, 8(44), 509-15.

Teruel, B. M., Torralbas, M., Zacharov, T. F., Daoud, A. E., Gonzalez, L., Blanco, L., Ewald, H. L., Børglum, A., Kruse, T. & Mors, O. (2007). Linkage analyses in candidate regions for bipolar affective disorder in a large and complex pedigree from the Holguin region in Eastern Cuba. Revista Cubana de Genetica Comunitaria, 1(1), 37-43.

Børglum, A., Vernesi, C., Jensen, P. K. A., Madsen, B., Haagerup, A. & Barbujani, G. (2007). No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy. American Journal of Physical Anthropology, 132(2), 278-84. https://doi.org/10.1002/ajpa.20509

Mors, O. & Børglum, A. (2007). Psykiske lidelser – fra gen til klinik. Lægen i Midten, 3, 20-22.

Marcheco-Teruel, B., Flint, T. J., Wikman, F. P., Torralbas, M., González, L., Blanco, L., Tan, Q., Ewald, H., Orntoft, T., Kruse, T. A., Børglum, A. D. & Mors, O. (2006). A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 141B(8), 833-43. https://doi.org/10.1002/ajmg.b.30314

Marcheco-Teruel, B., Zacharov, T. F., Wikman, F., Torralbas, M., González, L., Blanco, L., Tan, Q., Ewald, H. L., Ørntoft, T. F., Kruse, T. A., Børglum, A. & Mors, O. (2006). A Genome-wide Scan for Bipolar Disorder in a Large and Complex Cuban Pedigree Confirm Previously Reported Linkage Findings and Reveals a New Susceptibility Locus at 5q21.3-22.3. In Am J Med Genet B Neuropsychiat Genet (pp. 750-750)

Børglum, A. (2006). Anmeldelse af ny lærebog i Medicinsk Genetik ved Søren Nørby og Peter K.A. Jensen (reds). Ugeskrift for Læger, 168(46), 4039-4039.

Severinsen, J., Als, T. D., Binderup, H., Kruse, T. A., Wang, A. G., Muir, W. J., Blackwood, D. H. R., Mors, O. & Børglum, A. (2006). Association analyses suggest GPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 141B, 524-533.

Als, T. D., Dahl, HA., Wikman, F., Zacharov, T. F., Wang, AG., Marcheco-Teruel, B., Ørntoft, T. F., Børglum, A., Vang, M., Kruse, TA. & Mors, O. (2006). Cryptic Relatedness among cases and controls in two isolated populations. In American Journal of Medical Genetics Part B-Neuropsychiatric Genetics (Vol. 141B, pp. 744-744)

Severinsen, J., Bjarkam, C., Kiær-Larsen, S., Olsen, I. M., Nielsen, M. M., Blechingberg, J., Nielsen, A. L., Holm, I. E., Foldager, L., Young, B. D., Muir, W. J., Blackwood, D. HR., Corydon, T. J., Mors, O. & Børglum, A. (2006). Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder. Molecular Psychiatry, 1126-1138. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16924267&itool=iconabstr&query_hl=1&itool=pubmed_docsum

Severinsen, J., Bjarkam, C., Kiær-Larsen, S., Olsen, I. M., Nielsen, M. M., Blechingberg, J., Nielsen, A. L., Holm, I. E., Foldager, L., Young, B. D., Muir, W. J., Blackwood, D. HR., Corydon, T. J., Mors, O. & Børglum, A. (2006). Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder.. Abstract from XlV World Congress on Psychiatric Genetics, Caliari, Italy.

Christensen, U., Haagerup, A., Binderup, H., Vestbo, J., Kruse, T. & Børglum, A. D. (2006). Family based association analysis of the IL2 and IL15 genes in allergic disorders. Eur J Hum Genet, 14, 227-235.

Nyegaard, M., Kjeldsen, E., Pedersen, S., Mors, O. & Børglum, A. (2006). Genomic Alterations in a Patient with Schizophrenia, Crohn's Disease and Polycystic Kidney Disease. In Am J Med Genet B Neuropsychiat Genet (pp. 755-755)

Als, T. D., TH, J., Børglum, A., Petersen, PA., Mors, O. & Wang, AG. (2006). Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands. Eur J Hum Genet, 14, 497-504.

Brasch-Andersen, C., Haagerup, A., Børglum, A. D., Vestbo, J. & Kruse, T. (2006). Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases. J Med. Genet, 43, e10.

Brasch-Andersen, C., Tan, Q., Børglum, A. D., Haagerup, A., Larsen, T. R., Vestbo, J. & Kruse, T. (2006). Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene. Thorax, 61, 874-79.

Vang, S., Corydon, T. J., Børglum, A., Scott, M. D., Frydman, J., Mogensen, J., Gregersen, N. & Bross, P. (2005). Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation. FEBS journal, 272(8), 2037-2049.

Vang, S., Corydon, T. J., Børglum, A. D., Scott, M. D., Frydman, J., Mogensen, J., Gregersen, N. & Bross, P. (2005). Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation. FEBS journal, 272(8), 2037-49. https://doi.org/10.1111/j.1742-4658.2005.04630.x

Severinsen, J., Als, T. D., Binderup, H., Wang, AG., Kruse, TA., Muir, WJ., Blackwood, DH., Mors, O. & Børglum, A. (2005). Association analysis suggesting GPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia. Abstract from XIII World Congress on Psychiatric Genetics 2005 Boston, USA.

Backlund, L., Rosvall, L., Mors, O., Kockum, I., Traskman-Bendz, L., Frisén, L., Børglum, A., Mortensen, P., Isacsson, G., Agren, H., Schalling, M. & Osby, U. (2005). Association between g72 haplotypes and bipolar disorder in a nordic sample. Abstract from Association between g72 haplotypes and bipolar disorder in a nordic sample.

Marcheco, T. B., Torralbas, M., Flint, T., El Daoud, A., Gonzalez, L., Blanco, L., Ewald, H., Børglum, A., Kruse, T. A. & Mors, O. (2005). Linkage analyses in candidate regions for bipolar affective disorder in a large and complex pedigree from the Holguin region in Eastern Cuba. Cuban J. Hum. Genet.

Mors, N. P. O. & Børglum, A. (2005). Status og perspektiver inden for psykiatrisk genomisk medicin. Ugeskrift for Læger, 167, 2191-2193.

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.

Børglum, A. (Ed.) (2005). Ugeskrift for Læger. In Mangler titel

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.

Haagerup, A., Børglum, A. D., Binderup, H. G. & Kruse, T. A. (2004). Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp. Allergy: European Journal of Allergy and Clinical Immunology, 59(1), 88-94.

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/ddh335

Jørgensen, 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.5200803

Displaying results 351 to 400 out of 423

Revised 15.03.2021

Susanne Schousboe Sjøgaard