Zeynep Tümer
Clinical Professor
- 2021
- Published
Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders
Nøstvik, M., Kateta, S. M., Schönewolf-Greulich, B., Afenjar, A., Barth, M., Boschann, F., Doummar, D., Haack, T. B., Keren, B., Livshits, L. A., Mei, D., Park, J., Pisano, T., Prouteau, C., Umair, M., Waqas, A., Ziegler, A., Guerrini, R., Møller, R. S. & Tümer, Asuman Zeynep, 2021, In: Clinical Genetics. 100, 5, p. 628-633Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deciphering the premature mortality in PIGA-CDG – An untold story
Bayat, A., Kløvgaard, M., Johannesen, K. M., Stefan Barakat, T., Kievit, A., Montomoli, M., Parrini, E., Pietrafusa, N., Schelhaas, J., van Slegtenhorst, M., Miya, K., Guerrini, R., Tranebjærg, Lisbeth, Tümer, Asuman Zeynep, Rubboli, Guido & Møller, R. S., 2021, In: Epilepsy Research. 170, 106530.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Elevated expression of SLC6A4 encoding the serotonin transporter (SERT) in gilles de la tourette syndrome
Hildonen, M., Levy, A. M., Dahl, C., Bjerregaard, V. A., Møller, L. B., Guldberg, P., Debes, Nanette M Monique Mol & Tümer, Asuman Zeynep, 2021, In: Genes. 12, 1, p. 1-10 10 p., 86.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ewas of monozygotic twins implicate a role of mtor pathway in pathogenesis of tic spectrum disorder
Hildonen, M., Levy, A. M., Hansen, C. S., Bybjerg-Grauholm, J., Skytthe, A., Debes, Nanette M Monique Mol, Tan, Q. & Tümer, Asuman Zeynep, 2021, In: Genes. 12, 10, 1510.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Oliver McFarlane syndrome: two new cases and a review of the literature
Lisbjerg, K., Andersen, M. K. G., Bertelsen, M., Brost, A. G., Buchvald, F. F., Jensen, R. B., Bisgaard, A. M., Rosenberg, T., Tümer, Asuman Zeynep & Kessel, Line, 2021, In: Ophthalmic Genetics. 42, 4, p. 464-473Research output: Contribution to journal › Journal article › Research › peer-review
- 2020
- Published
upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohorts
Hjortshøj, T. D., Sørensen, A. R., Yusibova, M., Hansen, Bo Mølholm, Dunø, M., Balslev-Harder, M., Grønskov, K., van Hagen, J. M., Polstra, A. M., Eggermann, T., Finken, M. J. J. & Tümer, Asuman Zeynep, Jun 2020, In: Clinical Genetics. 97, 6, p. 902-907Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Delineation of phenotypes and genotypes related to cohesin structural protein RAD21
Krab, L. C., Marcos-Alcalde, I., Assaf, M., Balasubramanian, M., Andersen, J. B., Bisgaard, A. M., Fitzpatrick, D. R., Gudmundsson, S., Huisman, S. A., Kalayci, T., Maas, S. M., Martinez, F., McKee, S., Menke, L. A., Mulder, P. A., Murch, O. D., Parker, M., Pie, J., Ramos, F. J., Rieubland, C. & 6 others, , May 2020, In: Human Genetics. 139, p. 575-592Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A Missense Mutation in RAB28 in a Family with Cone-Rod Dystrophy and Postaxial Polydactyly Prevents Localization of RAB28 to the Primary Cilium
Jespersgaard, C., Hey, A. B., Ilginis, T., Hjortshøj, T. D., Fang, M., Bertelsen, M., Bech, N., Jensen, H., Larsen, L. J., Tümer, Asuman Zeynep, Rosenberg, T., Brøndum-Nielsen, K., Møller, L. B. & Grønskov, K., Feb 2020, In: Investigative Ophthalmology & Visual Science. 61, 2, 10 p., 2761939.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Bi-Allelic Pathogenic Variations in MERTK Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa
Jespersgaard, C., Bertelsen, M., Arif, F., Gellert-Kristensen, H. G., Fang, M., Jensen, H., Rosenberg, T., Tümer, Asuman Zeynep, Møller, L. B., Brøndum-Nielsen, K. & Grønskov, K., 2020, In: Genes. 11, 12, 10 p., 1517.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Chromothripsis and DNA Repair Disorders
Nazaryan-Petersen, L., Bjerregaard, Victoria Alexandra, Nielsen, Finn Cilius, Tommerup, Niels & Tümer, Asuman Zeynep, 2020, In: Journal of Clinical Medicine. 9, 3, 9 p., 613.Research output: Contribution to journal › Review › Research › peer-review
ID: 7071
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2602
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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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1859
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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