Zeynep Tümer
Clinical Professor
- 2015
- Published
Association Study of CHRNA7 Promoter Variants with Sensory and Sensorimotor Gating in Schizophrenia Patients and Healthy Controls: A Danish Case-Control Study
Bertelsen, B., Oranje, B., Melchior, L., Fagerlund, Birgitte, Werge, Thomas, Mikkelsen, Jens D., Tümer, Asuman Zeynep & Glenthøj, Birte Yding, Dec 2015, In: NeuroMolecular Medicine. 17, 4, p. 423-30 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deletion of 11q12.3-11q13.1 in a patient with intellectual disability and childhood facial features resembling Cornelia de Lange syndrome
Boyle, M. I., Jespersgaard, C., Nazaryan, L., Ravn, K., Brøndum-Nielsen, K., Bisgaard, A. & Tümer, Asuman Zeynep, 1 Nov 2015, In: Gene. 572, 1, p. 130-4 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation
Addis, L., Ahn, J. W., Dobson, R., Dixit, A., Ogilvie, C. M., Pinto, D., Vaags, A. K., Coon, H., Chaste, P., Wilson, S., Parr, J. R., Andrieux, J., Lenne, B., Tumer, Z., Leuzzi, V., Aubell, K., Koillinen, H., Curran, S., Marshall, C. R., Scherer, S. W. & 3 others, , Sep 2015, In: Human Mutation. 36, 9, p. 842-50 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Association study between CDH2 and Gilles de la Tourette syndrome in a Danish cohort
Nazaryan, L., Bertelsen, B., Padmanabhuni, S. S., Debes, N. M., LuCamp, L., Have, C. T. & Tümer, Asuman Zeynep, 30 Aug 2015, In: Psychiatry Research. 228, 3, p. 974-5 2 p.Research output: Contribution to journal › Letter › Research › peer-review
- Published
A mosaic small supernumerary marker chromosome 17 in a patient with Tourette syndrome, ADHD and intellectual disability: A case story and review of the literature
Cornelius, N., Bertelsen, B., Melchior, L., Nazaryan, L., Debes, N. M., Groth, C., Skov, L. & Tümer, Asuman Zeynep, 30 Jul 2015, In: Psychiatry Research. 228, 1, p. 179-81 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cornelia de Lange syndrome
Boyle, M. I., Jespersgaard, C., Brøndum-Nielsen, K., Bisgaard, A. & Tümer, Asuman Zeynep, Jul 2015, In: Clinical Genetics. 88, 1, p. 1-12 12 p., 12499.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity
De Rocker, N., Vergult, S., Koolen, D., Jacobs, E., Hoischen, A., Zeesman, S., Bang, B., Béna, F., Bockaert, N., Bongers, E. M., de Ravel, T., Devriendt, K., Giglio, S., Faivre, L., Joss, S., Maas, S., Marle, N., Novara, F., Nowaczyk, M. J. M., Peeters, H. & 16 others, , Jun 2015, In: Genetics In Medicine. 17, 6, p. 460-6 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Refinement of genotype-phenotype correlation in 18 patients carrying a 1q24q25 deletion
Chatron, N., Haddad, V., Andrieux, J., Désir, J., Boute, O., Dieux, A., Baumann, C., Drunat, S., Gérard, M., Bonnet, C., Leheup, B., Till, M., Rossi, M., Flori, E., Alembik, Y., Stewart, H., McParland, J., Bernardini, L., Castelluccio, P., Roos, L. & 11 others, , May 2015, In: American Journal of Medical Genetics. Part A. 167, 5, p. 1008-17 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder
Rajkumar, A. P., Christensen, J. H., Mattheisen, M., Jacobsen, I., Bache, Iben, Pallesen, J., Grove, J., Qvist, P., McQuillin, A., Gurling, H. M., Tümer, Asuman Zeynep, Mors, O. & Børglum, A. D., 1 Mar 2015, In: Bipolar Disorders (English Edition, Online). 17, 2, p. 205-211 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome
Sarri, C., Douzgou, S., Kontos, H., Anagnostopoulou, K., Tümer, Asuman Zeynep, Grigoriadou, M., Petersen, M. B., Kokotas, H., Merou, K., Pandelia, E., Giouroukou, E., Papanikolaou, K., Côté, G. B. & Gyftodimou, Y., 2015, In: Cytogenetic and Genome Research. 145, 1, p. 6-13 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 7071
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Dysfunction of the heteromeric KV7.3/KV7.5 potassium channel is associated with autism spectrum disorders
Research output: Contribution to journal › Journal article › Research › peer-review
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1863
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
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1136
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Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans
Research output: Contribution to journal › Journal article › Research › peer-review
Published