基本信息
浏览量:47
职业迁徙
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Publications
Molecular karyotyping and gene expression analysis in childhood cancer patients. Galetzka D, Müller T, Dittrich M, Endres M, Kartal N, Sinizyn O, Rapp S, Zeller T, Müller C, Hankeln T, Scholz-Kreisel P, Chorzempa H, Mirsch J, Poplawski A, Rossmann H, Spix C, Haaf T, Prawitt D, Marron Manuela & Schmidberger Heinz.
J Mol Med (2020). doi.org/10.1007/s00109-020-01937-4
Homozygous variants in the gene SCAPER cause syndromic intellectual disability. Kahrizi K, Huber M, Galetzka D, Dewi S, Schröder J, Weis E, Kariminejad A, Fattahi Z, Ropers HH, Schweiger S, Najmabadi H, Winter J. Am J Med Genet A. 2019 Jul;179(7):1214-1225. doi: 10.1002/ajmg.a.61172. Epub 2019 May 9. PMID: 31069901
Abdalla E, Bartsch O, Galetzka D, Zechner U.: Novel clinical findings in the
first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1
Genes. Am J Med Genet A. 2017 Apr;173(4):1090-1093. two: 10.1002/ajmg.a.38107.
Schneider E, Dittrich M, Bäck J, Nanda I, Müller T, Seidmann L, Tralau T,
Galetzka D, El Hajj N, Haaf T.: CpG sites with continuously increasing or
decreasing methylation from early to late human fetal brain development. Gene.
2016 Oct 30;592(1):110-118. doi: 10.1016/j.gene.2016.07.058. Epub 2016 Jul 25.
PubMed PMID: 27468947
Molecular karyotyping and gene expression analysis in childhood cancer patients. Galetzka D, Müller T, Dittrich M, Endres M, Kartal N, Sinizyn O, Rapp S, Zeller T, Müller C, Hankeln T, Scholz-Kreisel P, Chorzempa H, Mirsch J, Poplawski A, Rossmann H, Spix C, Haaf T, Prawitt D, Marron Manuela & Schmidberger Heinz.
J Mol Med (2020). doi.org/10.1007/s00109-020-01937-4
Homozygous variants in the gene SCAPER cause syndromic intellectual disability. Kahrizi K, Huber M, Galetzka D, Dewi S, Schröder J, Weis E, Kariminejad A, Fattahi Z, Ropers HH, Schweiger S, Najmabadi H, Winter J. Am J Med Genet A. 2019 Jul;179(7):1214-1225. doi: 10.1002/ajmg.a.61172. Epub 2019 May 9. PMID: 31069901
Abdalla E, Bartsch O, Galetzka D, Zechner U.: Novel clinical findings in the
first Egyptian case of Sotos syndrome caused by complete deletion of the NSD1
Genes. Am J Med Genet A. 2017 Apr;173(4):1090-1093. two: 10.1002/ajmg.a.38107.
Schneider E, Dittrich M, Bäck J, Nanda I, Müller T, Seidmann L, Tralau T,
Galetzka D, El Hajj N, Haaf T.: CpG sites with continuously increasing or
decreasing methylation from early to late human fetal brain development. Gene.
2016 Oct 30;592(1):110-118. doi: 10.1016/j.gene.2016.07.058. Epub 2016 Jul 25.
PubMed PMID: 27468947
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Molecular medicine (Cambridge, Mass.)no. 1 (2023): 41-16
Danuta Galetzka,Julia Böck, Lukas Wagner,Marcus Dittrich,Olesja Sinizyn, Marco Ludwig,Heidi Rossmann,Claudia Spix,Markus Radsak,Peter Scholz-Kreisel,Johanna Mirsch,Matthias Linke,
user-5fe1a78c4c775e6ec07359f9(2022)
Kevin Jan Legscha,Edite Antunes Ferreira, Antonios Chamoun, Alexander Lang, Mohamed Hemaid Sayed Awwad, Gigi Nu Hoang Quy Ton,Danuta Galetzka,Borhane Guezguez,Michael Hundemer,Jean-Christophe Bourdon,Markus Munder,Matthias Theobald,
Manuela Marron,Lara Kim Brackmann,Heike Schwarz, Willempje Hummel-Bartenschlager,Sebastian Zahnreich,Danuta Galetzka,Iris Schmitt, Christian Grad,Philipp Drees,Johannes Hopf,Johanna Mirsch,Peter Scholz-Kreisel,
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