Niels Tommerup

Search results

• 2011

  A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA)

  Klitten, L. L., Møller, R. S., Nikanorova, M., Silahtaroglu, A., Hjalgrim, H. & Tommerup, N., Dec 2011, In: Epilepsia-lehti. 52, 12, p. e190-3

  Research output: Contribution to journal › Journal article › Research › peer-review
  29 Citations (Scopus)

• A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1

  Buonincontri, R., Bache, I., Silahtaroglu, A., Elbro, C., Nielsen, A-M. V., Ullmann, R., Arkesteijn, G. & Tommerup, N., 1 Jan 2011, In: Behavior Genetics. 41, 1, p. 125-33 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  17 Citations (Scopus)

• Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

  Rehman, S. U., Baig, S. M., Eiberg, H., Rehman, S. U., Ahmad, I., Malik, N. A., Tommerup, N. & Hansen, L., 2011, In: Neurogenetics. 12, 3, p. 247-51 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  5 Citations (Scopus)

• Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation

  Nielsen, M. G., Lind-Thomsen, A., Mang, Y., Bak, M., Møller, M., Ullmann, R., Kristoffersson, U., Kalscheuer, V. M., Henriksen, K. F., Bugge, M., Tümer, Z. & Tommerup, N., Jul 2011, In: European Journal of Medical Genetics. 54, 4, p. e383-8

  Research output: Contribution to journal › Journal article › Research › peer-review
  7 Citations (Scopus)

• Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

  Hansen, C. H., Kjaergaard, S., Bak, M., Hansen, C., Elschich, Z., Anderson, C. M., Henriksen, K. F., Hjalgrim, H., Kirchhoff, M., Bijlsma, E., Nielsen, M., den Hollander, N., Ruivenkamp, C., Isidor, B., Le Caignec, C., Zannolli, R., Mucciolo, M., Renieri, A., Mari, F., Anderlid, B-M. & 4 others, Andrieux, J., Dieux, A., Tommerup, N. & Bache, I., 2011, In: Clinical Genetics. 82, 3, p. 248-55 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  117 Citations (Scopus)

• Cost-effective multiplexing before capture allows screening of 25 000 clinically relevant SNPs in childhood acute lymphoblastic leukemia

  Wesolowska, A., Gautier, L., Weinhold, N., Audouze, K. M. L., Brunak, S., Sicheritz-Ponten, T., Gupta, R., Dalgaard, M. D., Nielsen, B. F., Leffers, H., Borst, L., Helt, L. R., Nersting, J., Schmiegelow, K., Bak, M. & Tommerup, N., 1 Jun 2011, In: Leukemia. 25, 6, p. 1001-1006 6 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  19 Citations (Scopus)

• Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsy

  Klitten, L. L., Møller, R. S., Ravn, K., Hjalgrim, H. & Tommerup, N., 1 Jan 2011, In: European Journal of Human Genetics. 19, 1, p. 1-2 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  7 Citations (Scopus)

• Genome-wide detection of chromosomal rearrangements, indels, and mutations in circular chromosomes by short read sequencing

  Skovgaard, O., Bak, M., Løbner-Olesen, A. & Tommerup, N., 2011, In: Genome Research. 21, 8, p. 1388-1393 6 p.

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

  Open Access

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  72 Citations (Scopus)

  86 Downloads (Pure)

• High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations

  Kariminejad, R., Lind-Thomsen, A., Tümer, Z., Erdogan, F., Ropers, H. H., Tommerup, N., Ullmann, R. & Møller, R. S., Dec 2011, In: Human Mutation. 32, 12, p. 1427-35 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  22 Citations (Scopus)

• Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects

  Cingöz, S., Bache, I., Bjerglund, L., Ropers, H-H., Tommerup, N., Jensen, H., Brøndum-Nielsen, K. & Tümer, Z., 1 Jan 2011, In: American Journal of Medical Genetics. Part A. 155A, 1, p. 203-6 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  7 Citations (Scopus)

• Jarid1b targets genes regulating development and is involved in neural differentiation

  Schmitz, S. U., Albert, M., Malatesta, M., Morey Ramonell, L., Johansen, J. V., Bak, M., Tommerup, N., Abarrategui Garcia, I. & Helin, K., 2011, In: E M B O Journal. 30, 22, p. 4586-600 15 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  161 Citations (Scopus)

• The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders

  Bech, S., Nørremølle, A., Winge, K., Hasholt, L., Tommerup, N., Svenstrup, K., Nielsen, J. E. & Hjermind, L. E., 1 Jun 2011, In: Parkinsonism & Related Disorders. 17, 5, p. 398-9 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  4 Citations (Scopus)
• 2010

  A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation

  Kleine-Kohlbrecher, D., Christensen, J., Vandamme, J., Abarrategui, I., Bak, M., Tommerup, N., Shi, X., Gozani, O., Rappsilber, J., Salcini, A. E. & Helin, K., 23 Apr 2010, In: Molecular Cell. 38, 2, p. 165-78 13 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  176 Citations (Scopus)

• A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

  Anjum, I., Eiberg, H., Baig, S. M., Tommerup, N. & Hansen, L., Mar 2010, In: Molecular Vision. 16, p. 549-55 6 p.

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

  26 Citations (Scopus)

• Ancient human genome sequence of an extinct Palaeo-Eskimo

  Rasmussen, M., Li, Y., Lindgreen, S., Pedersen, J. S., Albrechtsen, A., Moltke, I., Metspalu, M., Metspalu, E., Kivisild, T., Gupta, R., Bertalan, M., Nielsen, K., Gilbert, T., Wang, Y., Raghavan, M., Campos, P., Kamp, H. L. M., Wilson, A. S., Gledhill, A., Tridico, S. & 32 others, Bunce, M., Lorenzen, E., Binladen, J. K. M. A., Guo, X., Zhao, J., Zhang, X., Zhang, H., Li, Z., Chen, M., Orlando, L. A. A., Kristiansen, K., Bak, M., Tommerup, N., Bendixen, C., Pierre, T. L., Grønnow, B., Meldgaard, M., Andreasen, C., Fedorova, S. A., Osipova, L. P., Higham, T. F. G., Ramsey, C. B., Hansen, T. V. O., Nielsen, F. C., Crawford, M. H., Brunak, S., Sicheritz-Pontén, T., Villems, R., Nielsen, R., Krogh, A., Wang, J. & Willerslev, E., 11 Feb 2010, In: Nature. 463, 7282, p. 757-762 6 p.

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

  Open Access

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  606 Citations (Scopus)

  50 Downloads (Pure)

• Autoimmune diseases in women with Turner's syndrome

  Jørgensen, K. T., Rostgaard, K., Bache, I., Biggar, R. J., Nielsen, N. M., Tommerup, N. & Frisch, M., 2010, In: Arthritis & Rheumatism. 62, 3, p. 658-66 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  146 Citations (Scopus)

• Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

  Farooq, M., Baig, S., Tommerup, N. & Kjaer, K. W., 2010, In: American Journal of Medical Genetics. Part A. 152A, 2, p. 495-7 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  18 Citations (Scopus)

• Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features

  Sehested, L. T., Møller, R. S., Bache, I., Andersen, N. B., Ullmann, R., Tommerup, N. & Tümer, Z., 1 Dec 2010, In: American Journal of Medical Genetics. Part A. 152A, 12, p. 3115-9 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  33 Citations (Scopus)

• 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, L. A., 2010, In: Molecular Systems Biology. 6, p. 381

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

  Open Access
  79 Citations (Scopus)

• Genome-wide analysis of CDX2 binding in intestinal epithelial cells (Caco-2)

  Boyd, M., Hansen, M., Jensen, T. G. K., Perearnau, A., Olsen, A. K., Bram, L. L., Bak, M., Tommerup, N., Olsen, J. & Troelsen, J. T., Aug 2010, In: Journal of Biological Chemistry. 285, 33, p. 25115-25 10 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  64 Citations (Scopus)

• Haploinsufficiency of TAB2 causes congenital heart defects in humans

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

  Research output: Contribution to journal › Journal article › Research › peer-review
  84 Citations (Scopus)

• JARID2 regulates binding of the Polycomb repressive complex 2 to target genes in ES cells

  Pasini, D., Cloos, P. A. C., Walfridsson, J., Olsson, L., Bukowski, J-P., Johansen, J. V., Bak, M., Tommerup, N., Rappsilber, J. & Helin, K., 2010, In: Nature. 464, 7286, p. 306-10 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  466 Citations (Scopus)

• Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

  Farooq, M., Troelsen, J. T., Boyd, M., Eiberg, H., Hansen, L., Hussain, M. S., Rehman, S. U., Azhar, A., Ali, A., Bakhtiar, S. M., Tommerup, N., Baig, S. M. & Kjaer, K. W., Jun 2010, In: European Journal of Human Genetics. 18, 6, p. 733-6 3 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  43 Citations (Scopus)

• Single-molecule denaturation mapping of DNA in nanofluidic channels

  Reisner, W., Larsen, N. B., Silahtaroglu, A., Kristensen, A., Tommerup, N., Tegenfeldt, J. O. & Flyvbjerg, H., 2010, In: Proceedings of the National Academy of Science of the United States of America. 107, 30, p. 13294-9 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  188 Citations (Scopus)
• 2009

  9q Subtelomeric deletion syndrome with diaphragmatic hernia

  Klitten, L. L., Tommerup, N., Hjalgrim, H. & Møller, R. S., 2009, In: American Journal of Medical Genetics. Part A. 149A, 5, p. 1086-8 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  1 Citation (Scopus)

• A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation

  Kalscheuer, V. M., Musante, L., Fang, C., Hoffmann, K., Fuchs, C., Carta, E., Deas, E., Venkateswarlu, K., Menzel, C., Ullmann, R., Tommerup, N., Dalprà, L., Tzschach, A., Selicorni, A., Lüscher, B., Ropers, H-H., Harvey, K. & Harvey, R. J., 2009, In: Human Mutation. 30, 1, p. 61-8 7 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  115 Citations (Scopus)

• A novel subtype of distal symphalangism affecting only the 4th finger

  Kjaer, K. W., Tiner, M., Cingoz, S., Karatosun, V., Tommerup, N., Mundlos, S. & Gunal, I., 2009, In: American Journal of Medical Genetics. Part A. 149A, 7, p. 1571-3 2 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  7 Citations (Scopus)

• 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, Z., Møllgård, K., Barbi, G., Rossier, E., Bendsen, E., Møller, R. S., Ullmann, R., He, J., Papadopoulos, N., Tommerup, N. & Larsen, L. A., 2009, In: European Journal of Human Genetics.

  Research output: Contribution to journal › Journal article › Research › peer-review
  20 Citations (Scopus)

• Compound heterozygous ASPM mutations in Pakistani MCPH families

  Muhammad, F., Mahmood Baig, S., Hansen, L., Sajid Hussain, M., Anjum Inayat, I., Aslam, M., Anver Qureshi, J., Toilat, M., Kirst, E., Wajid, M., Nürnberg, P., Eiberg, H., Tommerup, N. & Kjaer, K. W., 2009, In: American Journal of Medical Genetics. Part A. 149A, 5, p. 926-30 4 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  32 Citations (Scopus)

• Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2

  Dathe, K., Kjaer, K. W., Brehm, A., Meinecke, P., Nürnberg, P., Neto, J. C., Brunoni, D., Tommerup, N., Ott, C. E., Klopocki, E., Seemann, P. & Mundlos, S., 2009, In: American Journal of Human Genetics. 84, 4, p. 483-92 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  132 Citations (Scopus)

• 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, L. A., Lage, K., Maroun, L. L., Kjaer, I., Niemann, C. U., Andersen, M., Knudsen, M. A., Møllgård, K. & Tommerup, N., 2009, In: Experimental & Molecular Medicine. 41, 2, p. 77-85 8 p.

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

  18 Citations (Scopus)

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

  Brudzewsky, D., Pedersen, A. E., Claesson, M. H., Gad, M., Kristensen, N. N., Lage, K., Jensen, T., Tommerup, N., Larsen, L. A., Knudsen, S. & Tümer, Z., 2009, In: Scandinavian Journal of Immunology. 69, 5, p. 437-46 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  5 Citations (Scopus)

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

  Hilhorst-Hofstee, Y., Tümer, Z., Born, P., Knijnenburg, J., Hansson, K., Yatawara, V., Steensberg, J., Ullmann, R., Arkesteijn, G., Tommerup, N. & Larsen, L. A., 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
  4 Citations (Scopus)

• Sequence assembly

  Scheibye-Alsing, K., Hoffmann, S., Frankel, A. M., Jensen, P., Stadler, P. F., Mang, Y., Tommerup, N., Gilchrist, M. J., Hillig, A-B. N., Cirera Salicio, S., Jørgensen, C. B., Fredholm, M. & Gorodkin, J., 2009, In: Computational Biology and Chemistry. 33, 2, p. 121-136 16 p.

  Research output: Contribution to journal › Review › Research › peer-review
  42 Citations (Scopus)
• 2008

  A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.

  Gilling, M., Lauritsen, M. B., Møller, M., Henriksen, K. F., Vicente, A., Oliveira, G., Cintin, C., Eiberg, H., Andersen, P. S., Mors, O., Rosenberg, T., Brøndum-Nielsen, K., Cotterill, R. M. J., Lundsteen, C., Ropers, H-H., Ullmann, R., Bache, I., Tümer, Z. & Tommerup, N., 2008, In: European Journal of Human Genetics. 16, 3, p. 312-9 7 p.

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

  Open Access

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  14 Citations (Scopus)

  1963 Downloads (Pure)

• A Cryptic Unbalanced Translocation Resulting in del 13q and dup 15q

  Teszas, A., Møller, R. S., Kellermayer, R., Czako, M., Kjær, K. W., Ullmann, R., Melegh, B., Tommerup, N. & Kosztolanyi, G., 2008, In: American Journal of Medical Genetics. Part A. 146A, 19, p. 2570-2573 3 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  2 Citations (Scopus)

• A novel mutation in IRF6 resulting in VWS-PPS spectrum disorder with renal aplasia

  Medeiros, F. D., Hansen, L., Mawlad, E., Eiberg, H., Asklund, C., Tommerup, N. & Jakobsen, L. P., 2008, In: American Journal of Medical Genetics. Part A. 146A, 12, p. 1605-1608 3 p.

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

  11 Citations (Scopus)

• A systematic chromosomal approach for detection of novel candidate dyslexia loci and genes

  Buonincontri, R., Bache, I., Grigorenko, E. L. & Tommerup, N., 2008, In: Cellular Oncology. 30, 3, p. 250 1 p.

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

• Balanced translocation in a patient with severe myoclonic epilepsy of infancy disrupts the sodium channel gene SCN1A

  Møller, R. S., Schneider, L. M., Hansen, C. P., Bugge, M., Ullmann, R., Tommerup, N. & Tumer, Z., 2008, In: Epilepsia. 49, 6, p. 1091-1094 3 p.

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

  Open Access
  10 Citations (Scopus)

• Comparative genomics beyond sequence-based alignments: RNA structures in the ENCODE regions

  Þórarinsson, E., Yao, Z., Wiklund, E. D., Bramsen, J. B., Hansen, C., Kjems, J., Tommerup, N., Ruzzo, W. L. & Gorodkin, J., 2008, In: Genome Research. 18, 2, p. 242-251 10 p.

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

  78 Citations (Scopus)

• 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, N., Ullmann, R., Tümer, Z. & Larsen, L. A., 2008, In: European Journal of Medical Genetics. 51, 1, p. 81-6 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  20 Citations (Scopus)

• 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, L., Tommerup, N., Tumer, Z. & Larsen, L. A., 2008, In: DNA and Cell Biology. 27, 5, p. 251-U16

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

  11 Citations (Scopus)

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

  Erdogan, F., Larsen, L. A., Zhang, L., Tümer, Z., Tommerup, N., Chen, W., Jacobsen, J. R., Schubert, M., Jurkatis, J., Tzschach, A., Ropers, H-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
  114 Citations (Scopus)

• Investigation of 4q-deletion in two unrelated patients using array CGH

  Kaalund, S. S., Møller, R. S., Teszas, A., Miranda, M., Kosztolanyi, G., Ullmann, R., Tommerup, N. & Tumer, Z., 2008, In: American Journal of Medical Genetics. Part A. 146A, 18, p. 2431-2434 3 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  16 Citations (Scopus)

• MicroRNA expression in the adult mouse central nervous system.

  Bak, M., Silahtaroglu, A., Møller, M., Christensen, M., Rath, M. F., Skryabin, B., Tommerup, N. & Kauppinen, S., 2008, In: RNA: A publication of the RNA Society. 14, 3, p. 432-44 12 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  423 Citations (Scopus)

• Mowat-Wilson syndrome: an underdiagnosed syndrome?

  Engenheiro, E., Møller, R. S., Pinto, M., Soares, G., Nikanorova, M., Carreira, I. M., Ullmann, R., Tommerup, N. & Tumer, Z., 2008, In: Clinical Genetics. 73, 6, p. 579-584 5 p.

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

  20 Citations (Scopus)

• Multiple hypomethylation of maternally imprinted genes

  Tumer, Z., Temple, K., Mackay, D. J., Boonen, S. E., Olsen, B. S., Mortensen, H. B., Porksen, S., Bondrum-Nielsen, K., Tommerup, N., Hahnemann, J. M. & Boonen, S. E., 2008, In: Cellular Oncology. 30, 3, p. 275-275

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

• Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly

  Møller, R. S., Kubart, S., Hoeltzenbein, M., Heye, B., Vogel, I., Hansen, C. P., Menzel, C., Ullmann, R., Tommerup, N., Ropers, H. H., Tumer, Z. & Kalscheuer, V. M., 2008, In: American Journal of Human Genetics. 82, 5, p. 1165-1170 5 p.

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

  130 Citations (Scopus)
• 2007

  A human phenome-interactome network of protein complexes implicated in genetic disorders

  Lage, K., Karlberg, E. O., Størling, Z. M., Olason, P. I., Pedersen, A. G., Rigina, O., Hinsby, A. M., Tümer, Z., Pociot, F., Tommerup, N., Moreau, Y. & Brunak, S., 2007, In: Nature Biotechnology. 25, 3, p. 309-16 7 p.

  Research output: Contribution to journal › Journal article › Research › peer-review
  761 Citations (Scopus)

• Autoimmune diseases in a Danish cohort of 4,866 carriers of constitutional structural chromosomal rearrangements

  Bache, I., Nielsen, N. M., Rostgaard, K., Tommerup, N. & Frisch, M., 2007, In: Arthritis and Rheumatism. 56, 7, p. 2402-2409 7 p.

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

  9 Citations (Scopus)