Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding

por Karadeniz, Nilüfer, Mrasek, Kristin, Weise, Anja
Publicado 2008

The hierarchically organized splitting of chromosomal bands for all human chromosomes

por Kosyakova, Nadezda, Weise, Anja, Mrasek, Kristin, Claussen, Uwe, Liehr, Thomas, Nelle, Heike
Publicado 2009

Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unravelling the full complexity of multi-factorial multidrug resistance

por Kadioglu, Onat, Cao, Jingming, Kosyakova, Nadezda, Mrasek, Kristin, Liehr, Thomas, Efferth, Thomas
Publicado 2016

Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines

por Lopez Corrales, Nestor Luis, Mrasek, Kristin, Voigt, Martin, Liehr, Thomas, Kosyakova, Nadezda
Publicado 2012

Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon

por Manvelyan, Marina, Hunstig, Friederike, Mrasek, Kristin, Bhatt, Samarth, Pellestor, Franck, Weise, Anja, Liehr, Thomas
Publicado 2008

First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease

por Filipović, Jelena, Joksić, Gordana, Vujić, Dragana, Joksić, Ivana, Mrasek, Kristin, Weise, Anja, Liehr, Thomas
Publicado 2016

Identification of potential novel drug resistance mechanisms by genomic and transcriptomic profiling of colon cancer cells with p53 deletion

por Kadioglu, Onat, Saeed, Mohamed, Mahmoud, Nuha, Azawi, Shaymaa, Mrasek, Kristin, Liehr, Thomas, Efferth, Thomas
Publicado 2021

Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them

por Liehr, Thomas, Mrasek, Kristin, Kosyakova, Nadezda, Ogilvie, Caroline Mackie, Vermeesch, Joris, Trifonov, Vladimir, Rubtsov, Nikolai
Publicado 2008

Common Fragile Sites: Genomic Hotspots of DNA Damage and Carcinogenesis

por Ma, Ke, Qiu, Li, Mrasek, Kristin, Zhang, Jun, Liehr, Thomas, Quintana, Luciana Gonçalves, Li, Zheng
Publicado 2012

Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the Literature

por Liehr, Thomas, Weise, Anja, Mrasek, Kristin, Ziegler, Monika, Padutsch, Niklas, Wilhelm, Kathleen, Al-Rikabi, Ahmed
Publicado 2019

Chromosome distribution in human sperm – a 3D multicolor banding-study

por Manvelyan, Marina, Hunstig, Friederike, Bhatt, Samarth, Mrasek, Kristin, Pellestor, Franck, Weise, Anja, Simonyan, Isabella, Aroutiounian, Rouben, Liehr, Thomas
Publicado 2008

Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report

por Aktas, Dilek, Weise, Anja, Utine, Eda, Alehan, Dursun, Mrasek, Kristin, von Eggeling, Ferdinand, Thieme, Heike, Tuncbilek, Ergul, Liehr, Thomas
Publicado 2009

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

por Liehr, Thomas, Karamysheva, Tatyana, Merkas, Martina, Brecevic, Lukrecija, Hamid, Ahmed B., Ewers, Elisabeth, Mrasek, Kristin, Kosyakova, Nadezda, Weise, Anja
Publicado 2010

Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family

por Wafa, Abdulsamad, Ali, Belal, Moassass, Faten, Kheder, Maged, Aljapawe, Abdulmunim, Al‐Halabi, Bassel, Mrasek, Kristin, Liehr, Thomas, Al‐Achkar, Walid
Publicado 2022

Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues

por Mkrtchyan, Hasmik, Gross, Madeleine, Hinreiner, Sophie, Polytiko, Anna, Manvelyan, Marina, Mrasek, Kristin, Kosyakova, Nadezda, Ewers, Elisabeth, Nelle, Heike, Liehr, Thomas, Volleth, Marianne, Weise, Anja
Publicado 2010

Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair

por Aktas, Dilek, Utine, Eda G, Mrasek, Kristin, Weise, Anja, von Eggeling, Ferdinand, Yalaz, Kalbiye, Posorski, Nicole, Akarsu, Nurten, Alikasifoglu, Mehmet, Liehr, Thomas, Tuncbilek, Ergul
Publicado 2010

Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report

por Mulatinho, Milene Vianna, de Carvalho Serao, Cassio Luiz, Scalco, Fernanda, Hardekopf, David, Pekova, Sona, Mrasek, Kristin, Liehr, Thomas, Weise, Anja, Rao, Nagesh, Llerena, Juan Clinton
Publicado 2012

Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens

por Fan, Xiaobo, Supiwong, Weerayuth, Weise, Anja, Mrasek, Kristin, Kosyakova, Nadezda, Tanomtong, Alongkoad, Pinthong, Krit, Trifonov, Vladimir A., Cioffi, Marcelo de Bello, Grothmann, Pierre, Liehr, Thomas, Oliveira, Edivaldo H.C.de
Publicado 2015

The Human Genome Puzzle – the Role of Copy Number Variation in Somatic Mosaicism

por Mkrtchyan, Hasmik, Gross, Madeleine, Hinreiner, Sophie, Polytiko, Anna, Manvelyan, Marina, Mrasek, Kristin, Kosyakova, Nadezda, Ewers, Elisabeth, Nelle, Heike, Liehr, Thomas, Bhatt, Samarth, Thoma, Karen, Gebhart, Erich, Wilhelm, Sylvia, Fahsold, Raimund, Volleth, Marianne, Weise, Anja
Publicado 2010

Parental origin of deletions and duplications – about the necessity to check for cryptic inversions

por Liehr, Thomas, Schreyer, Isolde, Kuechler, Alma, Manolakos, Emmanouil, Singer, Sylke, Dufke, Andreas, Wilhelm, Kathleen, Jančušková, Tereza, Čmejla, Radek, Othman, Moneeb A. K., Al-Rikabi, Ahmed H., Mrasek, Kristin, Ziegler, Monika, Kankel, Stefanie, Kreskowski, Katharina, Weise, Anja
Publicado 2018