Publications by Jutta Wirth

2017

Landgraf, C., Wilhelm, K., Wirth, J., Weiss, M. Kipper, S. 2017. Affairs happen—to whom? A study on extrapair paternity in common nightingales. 
Curr Zool
 2017 zox024. doi: 10.1093/cz/zox024

2003-2013

Subject Molecular biology

Wirth, J. 2013
Aus Zellen kultivierte Hamburger? In-vitro-Fleisch und Zellkultur für die Gesundheit.
BIOforum 1WILEY-VCH Verlag GmbH & Co. KGaA, GIT VERLAG, 26–28.

Wirth, J. 2013
Hartnäckige kleine Schädlinge in der Diagnose: kein russisches Roulette.
MTA Dialog 3, 217-221.

Wirth, J. 2013
Quelle des ewigen Lebens, wie Zellen die Uhr zurückdrehen.
MTA Dialog 1, 16-22.


Subject: Human genetics

Maass, P.G., Wirth, J., Aydin, A., Rump, A., Stricker, S., Tinschert, S., Otero, M., Tsuchimochi, K., Goldring, M.B., Luft, F.C., Bähring, S.A. 2010
cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;11.2) and leads to Brachydactyly Type E.
Hum Mol Genet: 19(5):848-60

Ehling, D., Kennerknecht, I., Junge, A., Prager, B., Exeler, R., Lemcke, B., Horst, J., Schmitt-John, T.,  Bartsch, O., Wirth, J.  2004
Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies.
Am J Med Genet: 15;131(3):265-72.

Glaeser, B., Shirnershan, K., Bink, K., Wirth, J., Kehrer-Sawatzki, H., Bartz, U., Zoll, B., Bohlander, S.K.
Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations.
Am J Med Genet 30;126(3):229-36.

Hertz, J.M,, Sivertsen, B., Silahtaroglu, A., Bugge, M., Kalscheuer, V., Weber, A., Wirth, J., Ropers, H.H., Tommerup, N., Tumer, Z. 2004
Early onset, non-progressive, mild cerebellar ataxia co-segregating with a familial balanced translocation t(8;20)(p22;q13).
J Med Genet; 41(3):e25.

2001-2002
Subject: Human cancer

Barbi, G., Rossier, E., Vossbeck, S., Hummler, H., Lang, D., Flock, F., Terinde, R., Wirth, J., Vogel, W., Kehrer-Sawatzki, H. 2002 
Constitutional de novo interstitial deletion of 8 Mb on chromosome 22q12.1-12.3 encompassing the neurofibromatosis type 2 (NF2) locus in a dysmorphic girl with severe malformations.
J Med Genet; 39(2):E6.

Stankiewicz, P., Brozek, I., Helias-Rodzewicz, Z., Wierzba, J., Pilch, J., Bocian, E., Balcerska, A., Wozniak, A., Kardas, I., Wirth, J. Mazurczak, T., Limon, J. 2001
Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.
Am J Med Genet; 101(3) 226-39.

Subject: Animal Behaviour

Naguib M, Hammerschmidt K, Wirth J. 2001
Microgeographic variation, habitat effects and individual signature cues in calls of chiffchaffs Phylloscopus collybita canarensis.
Ethology; 107 (4): 341-355.

Subject: Human Cancer

Nothwang, H.G., Kim, H.G., Aoki, J., Geisterfer, M., Kubart, S., Wegner, R.D., van Moers, A., Ashworth, L.K., Haaf, T., Bell, J., Arai, H., Tommerup, N., Ropers, H.H., Wirth, J. 2001
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain.
Hum Mol Genet; 10(8):797-806.

Borck, G., Wirth, J., Hardt, T., Tonnies, H., Brondum-Nielsen, K., Bugge, M., Tommerup, N., Nothwang, H.G., Ropers, H.H., Haaf, T. 2001
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome.
J Med Genet; 38(2):117-21.

Zhu, G., Gillessen-Kaesbach, G., Wirth, J., Passarge, E., Bartsch, O. 2001
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2).
Am J Med Genet; 98(4):317-9.

Subject: Epigenetics, Imprinting

Wirth, J., Back, E., Huttenhofer, A., Nothwang, H.G., Lich, C., Gross, S., Menzel, C., Schinzel, A., Kioschis, P., Tommerup, N., Ropers, H.H., Horsthemke, B., Buiting, K. 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15.
Hum Mol Genet; 10(3):201-10.

Nothwang, H.G., Schroer, A., van der Maarel, S., Kubart, S., Schneider, S., Riesselmann, L., Menzel, C., Hinzmann, B., Vogt, D., Rosenthal, A., Fryns, J., Tommerup, N., Haaf, T., Ropers, H.H., Wirth, J. 2000
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.
Cytogenet Cell Genet; 90(1-2):126-33.