基本信息
浏览量:47
职业迁徙
个人简介
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
研究兴趣
论文共 43 篇作者统计合作学者相似作者
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Frontiers in oncology (2023): 1150629-1150629
Caine Lucas Grandt,Lara Kim Brackmann,Ronja Foraita,Heike Schwarz,Willempje Hummel-Bartenschlager,Thomas Hankeln,Christiane Kraemer,Sebastian Zahnreich,Philipp Drees,Johanna Mirsch,Claudia Spix,Maria Blettner,Heinz Schmidberger,Harald Binder,Moritz Hess,Danuta Galetzka,Federico Marini,Alicia Poplawski,Manuela Marron
Molecular medicineno. 1 (2023)
Grandt Caine Lucas,Brackmann Lara Kim,Poplawski Alicia,Schwarz Heike,Hummel-Bartenschlager Willempje,Hankeln Thomas,Kraemer Christiane,Marini Federico,Zahnreich Sebastian,Schmitt Iris,Drees Philipp,Mirsch Johanna,Grabow Desiree,Schmidberger Heinz,Binder Harald,Hess Moritz,Galetzka Danuta,Marron Manuela
Caine Lucas Grandt,Lara Kim Brackmann,Ronja Foraita,Heike Schwarz, Willempje Hummel Bartenschlager,Thomas Hankeln,Christiane Kraemer,Sebastian Zahnreich,Philipp Drees,Johanna Mirsch,Claudia Spix,Maria Blettner,Heinz Schmidberger,Harald Binder,Moritz Hess,Danuta Galetzka,Federico Marini,Alicia Poplawski,Manuela Marron
Research Square (Research Square) (2022)
PubMed (2022): 117-143
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,Hakim Echchannaoui
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,Peter Kaatsch,Alicia Poplawski,Moritz Hess,Harald Binder,Thomas Hankeln,Maria Blettner,Heinz Schmidberger
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作者统计
#Papers: 43
#Citation: 753
H-Index: 13
G-Index: 27
Sociability: 5
Diversity: 3
Activity: 20
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