@article{UBHD-68323689,
  author={Behnecke, Anne and Hinderhofer, Katrin and Jauch, Anna and Janssen, Johannes W. G. and Moog, Ute},
  title={Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13)},
  year={2012},
  pages={494-498},
  language={eng},
  issn={1399-0004},
  volume={82},
  number={5},
  note={Received 8 July 2011, revised and accepted for publication 26 September 2011, first published: 28 September 2011 ; Gesehen am 31.10.2018},
  journal={Clinical genetics},
  doi={10.1111/j.1399-0004.2011.01792.x},
}
@article{UBHD-68639744,
  author={Blake, Jonathon and Riddell, Andrew and Theiß, Susanne and Gonzalez, Alexis Perez and Haase, Bettina and Jauch, Anna and Janssen, Johannes W. G. and Ibberson, David and Pavlinic, Dinko and Moog, Ute and Benes, Vladimir and Runz, Heiko},
  title={Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation},
  year={2014},
  language={eng},
  issn={1932-6203},
  volume={9(2014},
  note={Gesehen am 23.09.2020},
  journal={PLOS ONE},
  doi={10.1371/journal.pone.0090894},
}
@article{UBHD-68666390,
  author={Bochtler, Tilmann and St{\"o}lzel, Friedrich and Heilig, Christoph E. and Kunz, Christina and Mohr, Brigitte and Jauch, Anna and Janssen, Johannes W. G. and Kramer, Michael and Benner, Axel and Bornh{\"a}user, Martin and Ho, Anthony Dick and Ehninger, Gerhard and Schaich, Markus and Kr{\"a}mer, Alwin},
  title={Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemia},
  year={2013},
  pages={3898-3905},
  language={eng},
  issn={1527-7755},
  volume={31},
  number={31},
  note={Gesehen am 27.11.2020},
  journal={Journal of clinical oncology},
  doi={10.1200/JCO.2013.50.7921},
}
@article{UBHD-67289375,
  author={Braunger, J{\"u}rgen and Bartram, Claus R. and Janssen, Johannes W. G.},
  title={Intracellular signaling of the Ufo/Axl receptor tyrosine kinase is mediated mainly by a multisubstrate docking-site},
  year={1997},
  pages={2619-2631},
  language={eng},
  issn={0950-9232},
  volume={14},
  journal={Oncogene},
}
@article{UBHD-68699542,
  author={Cristian, Flavia-Bianca and K{\"o}ppel, Alexandra and Janssen, Johannes W. G. and Utikal, Jochen and Rappold, Gudrun and Berkel, Simone},
  title={Generation of two hiPSC lines from a patient with autism spectrum disorder harboring a 120 kb deletion in SHANK2 and two control lines from each parent},
  year={2020},
  pages={5 S.},
  language={eng},
  issn={1876-7753},
  volume={49(2020) Artikel-Nummer 102004},
  number={5 Seiten},
  note={Gesehen am 16.02.2021},
  journal={Stem cell research},
  doi={10.1016/j.scr.2020.102004},
}
@article{UBHD-67879207,
  author={Dikow, Nicola and Maas, Bianca and Karch, Stephanie and Granzow, Martin and Janssen, Johannes W. G. and Jauch, Anna and Hinderhofer, Katrin and Sutter, Christian and Schubert-Bast, Susanne and Moog, Ute},
  title={3p25.3 Microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior},
  year={2014},
  pages={3061-3068},
  language={eng},
  issn={1552-4833},
  volume={164},
  number={12},
  note={Gesehen am 30.09.2015},
  journal={American journal of medical genetics},
  doi={10.1002/ajmg.a.36761},
}
@article{UBHD-68673938,
  author={Dikow, Nicola and Maas, Bianca and Gaspar, Harald and Kreiss‐Nachtsheim, Martina and Engels, Hartmut and Kuechler, Alma and Garbes, Lutz and Netzer, Christian and Neuhann, Teresa M. and Koehler, Udo and Casteels, Kristina and Devriendt, Koen and Janssen, Johannes W. G. and Jauch, Anna and Hinderhofer, Katrin and Moog, Ute},
  title={The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1},
  subtitle={is it really a reversed sotos syndrome?},
  year={2013},
  pages={2158-2166},
  language={eng},
  issn={1552-4833},
  volume={161},
  number={9},
  note={Gesehen am 16.12.2020},
  journal={American journal of medical genetics},
  doi={10.1002/ajmg.a.36046},
}
@article{UBHD-68638067,
  author={Evers, Christina and Jungwirth, Maria Sophia and Morgenthaler, J. and Hinderhofer, Katrin and Maas, B. and Janssen, Johannes W. G. and Jauch, Anna and Hehr, Ute and Steinbeisser, Herbert and Moog, Ute},
  title={Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1},
  subtitle={further insights into a genetic paradox},
  year={2014},
  pages={347-353},
  language={eng},
  issn={1399-0004},
  volume={85},
  number={4},
  note={First published: 24 April 2013 ; Gesehen am 16.09.2020},
  journal={Clinical genetics},
  doi={10.1111/cge.12171},
}
@article{UBHD-68618391,
  author={Evers, Christina and Mitter, Diana and Strobl‐Wildemann, Gertrud and Haug, Ulrich and Hackmann, Karl and Maas, Bianca and Janssen, Johannes W. G. and Jauch, Anna and Hinderhofer, Katrin and Moog, Ute},
  title={Duplication Xp11.22-p14 in females},
  subtitle={does X-inactivation help in assessing their significance?},
  year={2015},
  pages={553-562},
  language={eng},
  issn={1552-4833},
  volume={167},
  number={3},
  note={Gesehen am 20.07.2020},
  journal={American journal of medical genetics},
  doi={10.1002/ajmg.a.36897},
}
@article{UBHD-67879731,
  author={Evers, Christina and Maas, Bianca and Koch, Karin and Jauch, Anna and Janssen, Johannes W. G. and Sutter, Christian and Hinderhofer, Katrin and Moog, Ute},
  title={Mosaic deletion of EXOC6B},
  subtitle={further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability},
  year={2014},
  pages={3088-3094},
  language={eng},
  issn={1552-4833},
  volume={164},
  number={12},
  note={Gesehen am 01.10.2015},
  journal={American journal of medical genetics},
  doi={10.1002/ajmg.a.36770},
}
@article{UBHD-68913159,
  author={Evers, Christina and Heidemann, Ph and Dunstheimer, D and Schulze, E and Haag, C and Janssen, Johannes W. G. and Fischer, C and Jauch, Anna and Moog, Ute},
  title={Pseudoautosomal inheritance of Léri-Weill syndrome},
  subtitle={what does it mean?},
  year={2011},
  pages={489-494},
  language={eng},
  issn={1399-0004},
  volume={79},
  number={5},
  note={Gesehen am 02.05.2022},
  journal={Clinical genetics},
  doi={10.1111/j.1399-0004.2010.01488.x},
}
@article{UBHD-68333454,
  author={Evers, Christina and Janssen, Johannes W. G. and Jauch, Anna and Moog, Ute},
  title={A small terminal deletion 11q in a boy without Jacobsen syndrome},
  subtitle={narrowing the critical region for the 11q Jacobsen syndrome phenotype},
  year={2012},
  pages={680-684},
  language={eng},
  issn={1552-4833},
  volume={158A},
  number={3},
  note={Gesehen am 28.11.2018},
  journal={American journal of medical genetics},
  doi={10.1002/ajmg.a.34433},
}
@article{UBHD-68312037,
  author={H{\"a}mmerling, Susanne Hedwig and Behnisch, Wolfgang and Doerks, Tobias and Korbel, Jan Oliver and Bork, Peer and Moog, Ute and Hentze, Sabine and Janssen, Johannes W. G. and Jauch, Anna and Bartram, Claus R. and Koch, Karin and Bandapalli, Obul Reddy and Kulozik, Andreas},
  title={A 15q24 microdeletion in transient myeloproliferative Disease (TMD) and acute megakaryoblastic leukaemia (AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/AMKL},
  year={2012},
  pages={180-187},
  language={eng},
  issn={1365-2141},
  volume={157},
  number={2},
  note={Gesehen am 05.10.2018},
  journal={British journal of haematology},
  doi={10.1111/j.1365-2141.2012.09028.x},
}
@article{UBHD-69157848,
  author={Hansen-Hagge, Thomas E. and Janssen, Johannes W. G. and Hameister, Horst and Papa, Feroz R. and Zechner, Ulrich and Seriu, Taku and Jauch, Anna and Becke, Daniela and Hochstrasser, Mark and Bartram, Claus R.},
  title={An evolutionarily conserved gene on human chromosome 5q33-q34,UBH1, encodes a novel deubiquitinating enzyme},
  year={1998},
  pages={411-418},
  language={eng},
  issn={1089-8646},
  volume={49},
  number={3},
  note={Elektronische Reproduktion der Druck-Ausgabe 25. Mai 2002 ; Gesehen am 04.01.2024},
  journal={Genomics},
  doi={10.1006/geno.1998.5275},
}
@article{UBHD-69064194,
  author={Heilig, Christoph E. and L{\"o}ffler, Harald and Mahlknecht, Ulrich Rudolph and Janssen, Johannes W. G. and Ho, Anthony Dick and Jauch, Anna and Kr{\"a}mer, Alwin},
  title={Chromosomal instability correlates with poor outcome in patients with myelodysplastic syndromes irrespectively of the cytogenetic risk group},
  year={2010},
  pages={895-902},
  language={eng},
  issn={1582-4934},
  volume={14},
  number={4 vom: Apr.},
  note={First published: 10 May 2010 ; Gesehen am 11.04.2023},
  journal={Journal of cellular and molecular medicine},
  doi={10.1111/j.1582-4934.2009.00905.x},
}
@article{UBHD-68198761,
  author={Heller, Anette and Bauer, Sonja and Grekova, Svitlana and Janssen, Johannes W. G. and Bauer, Nathalie and Herr, Ingrid and Giese, Thomas and Gaida, Matthias and Hackert, Thilo and Fritz, Stefan and Giese, Nathalia},
  title={Establishment and characterization of a novel cell line, asan-paca, derived from human adenocarcinoma arising in intraductal papillary mucinous neoplasm of the pancreas},
  year={2016},
  pages={1452-1460},
  language={eng},
  issn={1536-4828},
  volume={45},
  number={10},
  note={Gesehen am 06.12.2017},
  journal={Pancreas},
  doi={10.1097/MPA.0000000000000673},
}
@article{UBHD-67289350,
  author={Janssen, Johannes W. G. and Jauch, Anna and Bartram, Claus R.},
  title={Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32)},
  year={2000},
  pages={2691-2698},
  language={eng},
  issn={0006-4971},
  volume={95},
  journal={Blood},
}
@book{UBHD-65107711,
  author={Janssen, Johannes W. G.},
  title={Funktionelle Charakterisierung von Onkogenen des Menschen nach Isolation mittels DNA Transfektion},
  year={2000},
  pages={Getr. Z{\"a}hlung},
  language={ger},
  note={Enth{\"a}lt Zeitschriftenaufs{\"a}tze},
  school={Heidelberg., Univ., Habil.-Schr., 2000},
  library={UB [Signatur: 2000 U 383]},
}
@article{UBHD-69159058,
  author={Janssen, Johannes W. G. and Schleithoff, Lothar and Bartram, Claus R. and Schulz, Ansgar Stephan},
  title={An oncogenic fusion product of the phosphatidylinositol 3-kinase p85β subunit and HUMORF8, a putative deubiquitinating enzyme},
  year={1998},
  pages={1767-1772},
  language={eng},
  issn={1476-5594},
  volume={16},
  number={13},
  note={Gesehen am 08.01.2024},
  journal={Oncogene},
  doi={10.1038/sj.onc.1201695},
}
@article{UBHD-67290002,
  author={Janssen, Johannes W. G. and Bartram, Claus R.},
  title={Pre-pre-B acute lymphoblastic leukemia},
  subtitle={high frequency of alternatively spliced ALL1-AF4 transcripts and absence of minimal residual disease during complete remission},
  year={1994},
  pages={3835-3842},
  language={eng},
  issn={0006-4971},
  volume={84},
  journal={Blood},
}
@article{UBHD-68586284,
  author={Kaiser, Ann-Sophie and Maas, Bianca and Wolff, Anna and Sutter, Christian and Janssen, Johannes W. G. and Hinderhofer, Katrin and Moog, Ute},
  title={Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia},
  year={2015},
  pages={704-707},
  language={eng},
  issn={1476-5438},
  volume={23},
  number={5},
  note={Published online 13 August 2014 ; Gesehen am 16.06.2020},
  journal={European journal of human genetics},
  doi={10.1038/ejhg.2014.163},
}
@article{UBHD-68947818,
  author={Keller, Sascha and Ridinger, Johannes and Rupp, Anne-Kathleen and Janssen, Johannes W. G. and Altevogt, Peter},
  title={Body fluid derived exosomes as a novel template for clinical diagnostics},
  year={2011},
  pages={1-9},
  language={eng},
  issn={1479-5876},
  volume={9},
  number={Artikel-ID 86},
  note={Gesehen am 28.07.2022},
  journal={Journal of translational medicine},
  doi={10.1186/1479-5876-9-86},
}
@article{UBHD-68327755,
  author={Kuçi, Zyrafete and Jauch, Anna and Janssen, Johannes W. G. and Greil, Johann},
  title={Mesenchymal stromal cells from pooled mononuclear cells of multiple bone marrow donors as rescue therapy in pediatric severe steroid-refractory graft-versus-host disease},
  subtitle={a multicenter survey},
  year={2016},
  pages={985-994},
  language={eng},
  issn={1592-8721},
  volume={101},
  number={8},
  note={Pre-published: May 12, 2016 ; Gesehen am 13.11.2018},
  journal={Haematologica},
  doi={10.3324/haematol.2015.140368},
}
@article{UBHD-67289356,
  author={Nakao, Makoto and Janssen, Johannes W. G. and Bartram, Claus R.},
  title={Rapid and reliable quantification of minimal residual disease in acute lymphoblastic leukemia using rearranged immunoglobulin and T-cell receptor loci by LightCycler technology},
  year={2000},
  pages={3281-3289},
  language={eng},
  issn={0008-5472},
  volume={60},
  journal={Cancer research},
}
@article{UBHD-69135150,
  author={Ramdohr, Florian and Fabarius, Alice and Maier, Bettina and Bretschneider, Daniela and Jauch, Anna and Monecke, Astrid and Metzeler, Klaus H. and Janssen, Johannes W. G. and Schlenk, Richard Friedrich and Kayser, Sabine},
  title={Atypical presentation of patients with chronic myeloid leukemia in chronic phase},
  subtitle={case report},
  year={2022},
  pages={1-7},
  language={eng},
  issn={2234-943X},
  volume={12(2022) vom: Aug.},
  number={Artikel-ID 960914},
  note={Gesehen am 30.10.2023},
  journal={Frontiers in oncology},
  doi={10.3389/fonc.2022.960914},
}
@article{UBHD-69159049,
  author={Rieder, Harald and Bonwetsch, Christine and Janssen, L. A. J. and Maurer, J. and Janssen, Johannes W. G. and Schwartz, Stefan and Ludwig, Wolf-Dieter and Gassmann, Winfried and Bartram, Claus R. and Thiel, Eckhard and L{\"o}ffler, Helmut and G{\"o}kbuget, Nicola and Hoelzer, Dieter and Fonatsch, Christa},
  title={High rate of chromosome abnormalities detected by fluorescence in situ hybridization using BCR and ABL probes in adult acute lymphoblastic leukemia},
  year={1998},
  pages={1473-1481},
  language={eng},
  issn={1476-5551},
  volume={12},
  number={9},
  note={Gesehen am 08.01.2024},
  journal={Leukemia},
  doi={10.1038/sj.leu.2401127},
}
@article{UBHD-67289370,
  author={Schaaf, Christian P. and Bartram, Claus R. and Janssen, Johannes W. G.},
  title={Novel interaction partners of the TPR/MET tyrosine kinase},
  year={2005},
  pages={267-269},
  language={eng},
  issn={0892-6638},
  volume={19},
  journal={The FASEB journal},
}
@article{UBHD-69159429,
  author={Schlieben, Sigrid and Janssen, Johannes W. G. and Bartram, Claus R.},
  title={Incidence and clinical outcome of children with BCR/ABL-positive acute lymphoblastic leukemia (ALL). A prospective RT-PCR study based on 673 patients enrolled in the German pediatric multicenter therapy trials ALL-BFM-90 and CoALL-05-92},
  year={1996},
  pages={957-963},
  language={eng},
  issn={0887-6924},
  volume={10},
  number={6},
  journal={Leukemia},
}
@article{UBHD-68666689,
  author={Sumer, Simon and Hoffmann, Sandra and Laue, Svenja and Campbell, Birgit and R{\"a}decke, Kristin and Frajs, Viktoria and Clauss, Sebastian and K{\"a}{\"a}b, Stefan and Janssen, Johannes W. G. and Jauch, Anna and Laugwitz, Karl-Ludwig and Dorn, Tatjana and Moretti, Alessandra and Rappold, Gudrun},
  title={Precise correction of heterozygous SHOX2 mutations in hiPSCs derived from patients with atrial fibrillation via genome editing and sib selection},
  year={2020},
  pages={999-1013},
  language={eng},
  issn={2213-6711},
  volume={15},
  number={4},
  note={Gesehen am 30.11.2020},
  journal={Stem cell reports},
  doi={10.1016/j.stemcr.2020.08.015},
}
@article{UBHD-69050895,
  author={Zhong, Rujia and Schimanski, Theresa and Zhang, Feng and Lan, Huan and Hohn, Alyssa and Xu, Qiang and Huang, Mengying and Liao, Zhenxing and Qiao, Lin and Yang, Zhen and Li, Yingrui and Zhao, Zhihan and Li, Xin and Rose, Lena and Albers, Sebastian and Maywald, Lasse and M{\"u}ller, Jonas and Dinkel, Hendrik and Saguner, Ardan and Janssen, Johannes W. G. and Swamy, Narasimha and Xi, Yannick and Lang, Siegfried and Kleinsorge, Mandy and Duru, Firat and Zhou, Xiao-Bo and Diecke, Sebastian and Cyganek, Lukas and Akın, Ibrahim and El-Battrawy, Ibrahim},
  title={A preclinical study on brugada syndrome with a CACNB2 variant using human cardiomyocytes from induced pluripotent stem cells},
  year={2022},
  pages={1-17},
  language={eng},
  issn={1422-0067 and 1661-6596},
  volume={23},
  note={Gesehen am 13.03.2023},
  journal={International journal of molecular sciences},
  doi={10.3390/ijms23158313},
}