Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9
Rhode, J, Hagenau, L, Beimdiek, J, Ullmann, R, Hossain, F, Tzvetkova, A, Jensen, L R, Kuss, A W
Published in Stem cell research (01.12.2023)
Published in Stem cell research (01.12.2023)
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Journal Article
GMCT : A Monte Carlo simulation package for macromolecular receptors
Ullmann, R. Thomas, Ullmann, G. Matthias
Published in Journal of computational chemistry (30.03.2012)
Published in Journal of computational chemistry (30.03.2012)
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Journal Article
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
Kirov, George, Gumus, Dilihan, Chen, Wei, Norton, Nadine, Georgieva, Lyudmila, Sari, Murat, O’Donovan, Michael C, Erdogan, Fikret, Owen, Michael J, Ropers, Hans-Hilger, Ullmann, Reinhard
Published in Human molecular genetics (01.02.2008)
Published in Human molecular genetics (01.02.2008)
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Journal Article
Genome-wide copy number variation analysis in attention-deficit hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree
Lesch, K-P, Selch, S, Renner, T J, Jacob, C, Nguyen, T T, Hahn, T, Romanos, M, Walitza, S, Shoichet, S, Dempfle, A, Heine, M, Boreatti-Hümmer, A, Romanos, J, Gross-Lesch, S, Zerlaut, H, Wultsch, T, Heinzel, S, Fassnacht, M, Fallgatter, A, Allolio, B, Schäfer, H, Warnke, A, Reif, A, Ropers, H-H, Ullmann, R
Published in Molecular psychiatry (01.05.2011)
Published in Molecular psychiatry (01.05.2011)
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Journal Article
Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP
ROPERS, Fabienne, DERIVERY, Emmanuel, VARON, Raymonda, RAJAB, Anna, HAO HU, GARSHASBI, Masoud, KARBASIYAN, Mohsen, HEROLD, Martin, NÜRNBERG, Gudrun, ULLMANN, Reinhard, GAUTREAU, Alexis, SPERLING, Karl
Published in Human molecular genetics (01.07.2011)
Published in Human molecular genetics (01.07.2011)
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Journal Article
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
Published in Journal of medical genetics (01.11.2008)
Published in Journal of medical genetics (01.11.2008)
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Journal Article
Industrial best practice: cases of study by automotive chip- makers
Abbati, L. Degli, Ullmann, R., Paganini, G., Coppetta, M., Zaia, L., Huard, V., Montfort, O., Cantoro, R., Insinga, G., Venini, F., Calao, P., Bernardi, P.
Published in 2021 IEEE International Symposium on Defect and Fault Tolerance in VLSI and Nanotechnology Systems (DFT) (06.10.2021)
Published in 2021 IEEE International Symposium on Defect and Fault Tolerance in VLSI and Nanotechnology Systems (DFT) (06.10.2021)
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Conference Proceeding
Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis
Thorwarth, A, Mueller, I, Biebermann, H, Ropers, H. H, Grueters, A, Krude, H, Ullmann, R
Published in The journal of clinical endocrinology and metabolism (01.07.2010)
Published in The journal of clinical endocrinology and metabolism (01.07.2010)
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Journal Article
Simulation of the Electron Transfer between the Tetraheme Subunit and the Special Pair of the Photosynthetic Reaction Center Using a Microstate Description
Becker, Torsten, Ullmann, R. Thomas, Ullmann, G. Matthias
Published in The journal of physical chemistry. B (22.03.2007)
Published in The journal of physical chemistry. B (22.03.2007)
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Journal Article
Acute high-dose X-radiation-induced genomic changes in A549 cells
Muradyan, A, Gilbertz, K, Stabentheiner, S, Klause, S, Madle, H, Meineke, V, Ullmann, R, Scherthan, H
Published in Radiation research (01.06.2011)
Published in Radiation research (01.06.2011)
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Journal Article
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation
Erdogan, F., Chen, W., Kirchhoff, M., Kalscheuer, V.M., Hultschig, C., Müller, I., Schulz, R., Menzel, C., Bryndorf, T., Ropers, H.-H., Ullmann, R.
Published in Cytogenetic and genome research (01.11.2006)
Published in Cytogenetic and genome research (01.11.2006)
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Journal Article
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney
Wieser, R., Fritz, B., Ullmann, R., Müller, I., Galhuber, M., Storlazzi, C.T., Ramaswamy, A., Christiansen, H., Shimizu, N., Rehder, H.
Published in Human mutation (01.08.2005)
Published in Human mutation (01.08.2005)
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Journal Article
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4
Steichen-Gersdorf, E, Gaßner, I, Superti-Furga, A, Ullmann, R, Stricker, S, Klopocki, E, Mundlos, S
Published in Clinical genetics (01.12.2008)
Published in Clinical genetics (01.12.2008)
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Journal Article