Thomas Liehr

Thomas Liehr

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Thomas Liehr

Thomas Liehr

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Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka.

Int J Mol Sci 2020 Jul 1;21(13). Epub 2020 Jul 1.

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, D-07747 Jena, Germany.

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http://dx.doi.org/10.3390/ijms21134716DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369978PMC
July 2020

Landscape of snake' sex chromosomes evolution spanning 85 MYR reveals ancestry of sequences despite distinct evolutionary trajectories.

Sci Rep 2020 Jul 27;10(1):12499. Epub 2020 Jul 27.

Coordenação de Biodiversidade, Laboratory of Animal Genetics, Instituto Nacional de Pesquisas da Amazônia, Av. André Araújo 2936, Petrópolis, Manaus, AM, 69067-375, Brazil.

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http://dx.doi.org/10.1038/s41598-020-69349-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385105PMC
July 2020

Gene clusters related to metamorphosis in Solea senegalensis are highly conserved.

Comp Biochem Physiol Part D Genomics Proteomics 2020 Jun 29;35:100706. Epub 2020 Jun 29.

Area de Genética, Facultad de Ciencias del Mar y Ambientales, Universidad de Cádiz, Puerto Real 11510, Cádiz, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.cbd.2020.100706DOI Listing
June 2020

Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability.

J Histochem Cytochem 2020 Apr 28;68(4):239-251. Epub 2020 Feb 28.

Institute of Human Genetics, Jena University Hospital, Friedrich-Schiller University Jena, Jena, Germany.

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http://dx.doi.org/10.1369/0022155420910113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132824PMC
April 2020

Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus (Crustacea: Decapoda: Palaemonidae).

Int J Mol Sci 2020 Apr 9;21(7). Epub 2020 Apr 9.

Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP C.P. 676, Brazil.

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http://dx.doi.org/10.3390/ijms21072599DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178241PMC
April 2020

First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations.

Sci Rep 2020 Apr 14;10(1):6306. Epub 2020 Apr 14.

Department of Human Genetics, University Medicine Greifswald, and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany.

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http://dx.doi.org/10.1038/s41598-020-63337-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156631PMC
April 2020

Molecular cytogenetic pilot study on pleomorphic adenomas of salivary glands.

Oncol Lett 2020 Feb 10;19(2):1125-1130. Epub 2019 Dec 10.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, D-07747 Jena, Germany.

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http://dx.doi.org/10.3892/ol.2019.11198DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955655PMC
February 2020

Algorithm for the diagnosis of patients with neurodevelopmental disorders and suspicion of a genetic syndrome.

Arch Argent Pediatr 2020 Feb;118(1):52-55

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.

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http://dx.doi.org/10.5546/aap.2020.eng.52DOI Listing
February 2020

Chromosome Microdissection on Semi-Archived Material.

Cytometry A 2019 12 18;95(12):1285-1288. Epub 2019 Sep 18.

Jena University Hospital, Institute of Human Genetics, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1002/cyto.a.23896DOI Listing
December 2019

Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review.

Front Genet 2019 11;10:1131. Epub 2019 Nov 11.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.3389/fgene.2019.01131DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859531PMC
November 2019

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

Front Genet 2019 14;10:1165. Epub 2019 Nov 14.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.3389/fgene.2019.01165DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868022PMC
November 2019

(Cyto)genomic and epigenetic characterization of BICR 10 cell line and three new established primary human head and neck squamous cell carcinoma cultures.

Genes Genomics 2019 10 18;41(10):1207-1221. Epub 2019 Jul 18.

Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, Polo Ciências da Saúde, 3000-354, Coimbra, Portugal.

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http://dx.doi.org/10.1007/s13258-019-00850-6DOI Listing
October 2019

Evolution of the Proto Sex-Chromosome in .

Int J Mol Sci 2019 Oct 15;20(20). Epub 2019 Oct 15.

Área de Genética, Facultad de Ciencias del Mar y Ambientales, INMAR, Universidad de Cádiz, 11510 Cádiz, Spain.

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http://dx.doi.org/10.3390/ijms20205111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829477PMC
October 2019

DNA Copy Number Variations as Markers of Mutagenic Impact.

Int J Mol Sci 2019 Sep 24;20(19). Epub 2019 Sep 24.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, D-07747 Jena, Germany.

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http://dx.doi.org/10.3390/ijms20194723DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801639PMC
September 2019

Extensive Chromosomal Reorganization in Fishes (Cichlidae, Cichlinae) Fits the Complex Evolutionary Diversification of the Genus.

Int J Mol Sci 2019 Aug 21;20(17). Epub 2019 Aug 21.

Departamento de Biologia Celular e Genética, Centro de Biociências, Universidade Federal do Rio Grande do Norte, Natal 59078-970, RN, Brazil.

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http://dx.doi.org/10.3390/ijms20174077DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747227PMC
August 2019

Deciphering the Origin and Evolution of the XXY System in Two Closely-Related Species (Oplegnathidae and Centrarchiformes).

Int J Mol Sci 2019 Jul 22;20(14). Epub 2019 Jul 22.

Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos SP 13565-905, Brazil.

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http://dx.doi.org/10.3390/ijms20143571DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678977PMC
July 2019

Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH).

Methods Mol Biol 2019 ;1885:129-137

Jena University Hospital, Institute of Human Genetics, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1007/978-1-4939-8889-1_9DOI Listing
June 2019

Genome and Phylogenetic Analysis of Genes Involved in the Immune System of - Potential Applications in Aquaculture.

Front Genet 2019 11;10:529. Epub 2019 Jun 11.

Área de Genética, Facultad de Ciencias del Mar y Ambientales, Universidad de Cádiz, Cádiz, Spain.

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http://dx.doi.org/10.3389/fgene.2019.00529DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579814PMC
June 2019

Detection and Correlation of Single and Concomitant , and Alterations in Gliomas.

Int J Mol Sci 2019 May 30;20(11). Epub 2019 May 30.

Laboratório de Cultura de Tecidos e Citogenética, SAMAM, Instituto Evandro Chagas, Ananindeua, PA 67030-000, Brazil.

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http://dx.doi.org/10.3390/ijms20112658DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600458PMC
May 2019

Chromothripsis Detectable in Small Supernumerary Marker Chromosomes (sSMC) Using Fluorescence In Situ Hybridization (FISH).

Authors:
Thomas Liehr

Methods Mol Biol 2018 ;1769:79-84

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1007/978-1-4939-7780-2_6DOI Listing
February 2019

From Human Cytogenetics to Human Chromosomics.

Authors:
Thomas Liehr

Int J Mol Sci 2019 Feb 14;20(4). Epub 2019 Feb 14.

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, D-07747 Jena, Germany.

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http://dx.doi.org/10.3390/ijms20040826DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413437PMC
February 2019

Characterization of RB1 Deletions in Interphase and Metaphase by Molecular Cytogenetics Exemplified in Chronic Lymphatic Leukemia.

Authors:
Thomas Liehr

Methods Mol Biol 2018 ;1726:1-6

Jena University Hospital, Institute of Human Genetics, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1007/978-1-4939-7565-5_1DOI Listing
January 2019

Complex karyotype including ring chromosome 11 in a patient with acute myeloid leukemia: case report.

Sao Paulo Med J 2018 Jul-Aug;136(4):361-367. Epub 2017 Aug 21.

Biologist and Professor, Universidade do Estado do Rio de Janeiro (UERJ), and Researcher, Research Coordination, Instituto Nacional de Câncer (INCA), Rio de Janeiro (RJ), Brazil.

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http://dx.doi.org/10.1590/1516-3180.2016.0252150217DOI Listing
December 2018

A preliminary integrated genetic map distinguishes every chromosome pair and locates essential genes related to abiotic adaptation of Crassostrea angulata/gigas.

BMC Genet 2018 11 15;19(1):104. Epub 2018 Nov 15.

Area de Genética. Facultad de Ciencias del Mar y Ambientales, Universidad de Cádiz. Polígono Río San Pedro, 11510 Puerto Real, Cádiz, Spain.

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http://dx.doi.org/10.1186/s12863-018-0689-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238303PMC
November 2018

Reorganization of chromosomal interactions in the 2q37-deletion syndrome.

EMBO J 2018 08 19;37(15). Epub 2018 Jun 19.

Experimental and Clinical Research Center (ECRC), a joint cooperation between the Charité Medical Faculty and the Max Delbrück Center for Molecular Medicine (MDC), Berlin, Germany.

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http://dx.doi.org/10.15252/embj.201696257DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068439PMC
August 2018

De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome.

Clin Dysmorphol 2018 Jul;27(3):97-100

Department of Pediatric Neurology, Clinic for Pediatrics, Braunschweig.

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http://dx.doi.org/10.1097/MCD.0000000000000224DOI Listing
July 2018

Assessing Skewed X-Chromosome Inactivation.

Curr Protoc Hum Genet 2018 Jul 10:e66. Epub 2018 Jul 10.

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.

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http://dx.doi.org/10.1002/cphg.66DOI Listing
July 2018

Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndrome.

Hematol Transfus Cell Ther 2019 Jan-Mar;41(1):84-87. Epub 2018 Jul 6.

Hospital Universitário Oswaldo Cruz, Recife, PE, Brazil; Faculdade de Ciências Médicas da Universidade de Pernambuco (FCM UPE), Recife, PE, Brazil. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S25311379183009
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http://dx.doi.org/10.1016/j.htct.2018.05.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371640PMC
July 2018

Small Supernumerary Marker Chromosome May Provide Information on Dosage-insensitive Pericentric Regions in Human.

Curr Genomics 2018 Apr;19(3):192-199

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747Jena, Germany.

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http://dx.doi.org/10.2174/1389202918666170717163830DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850507PMC
April 2018

Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis.

J Oral Sci 2018 Mar 26;60(1):70-81. Epub 2018 Feb 26.

Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra.

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http://dx.doi.org/10.2334/josnusd.16-0811DOI Listing
March 2018

Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44).

Mol Cytogenet 2018 13;11:22. Epub 2018 Mar 13.

1Molecular Biology and Biotechnology Department, Human Genetics Division, Chromosomes Laboratory, Atomic Energy Commission of Syria, P.O. Box 6091, Damascus, Syria.

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http://dx.doi.org/10.1186/s13039-018-0370-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851247PMC
March 2018

Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.

Cancer Genet 2018 02 19;221:25-30. Epub 2017 Dec 19.

Cytogenetics Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Post-Graduate Program in Oncology, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Internal Medicine post-graduation program of Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil. Electronic address:

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http://dx.doi.org/10.1016/j.cancergen.2017.12.002DOI Listing
February 2018

Molecular Cytogenetic Characterization Identified the Murine B-Cell Lymphoma Cell Line A-20 as a Model for Sporadic Burkitt's Lymphoma.

J Histochem Cytochem 2017 11 13;65(11):669-677. Epub 2017 Sep 13.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1369/0022155417731319DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665108PMC
November 2017

New Insights into Phasmatodea Chromosomes.

Genes (Basel) 2017 Nov 17;8(11). Epub 2017 Nov 17.

Novosibirsk State University, 630090 Novosibirsk, Russia.

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http://dx.doi.org/10.3390/genes8110327DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704240PMC
November 2017

Spatial organization of fibroblast and spermatocyte nuclei with different B-chromosome content in Korean field mouse, Apodemus peninsulae (Rodentia, Muridae).

Genome 2017 Oct 21;60(10):815-824. Epub 2017 Jul 21.

a Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, 630090 Novosibirsk, Russia.

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http://dx.doi.org/10.1139/gen-2017-0029DOI Listing
October 2017

Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy.

J Pediatr Genet 2017 Sep 7;6(3):165-168. Epub 2017 Mar 7.

Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.

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http://dx.doi.org/10.1055/s-0037-1599195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548530PMC
September 2017

A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome.

Mol Cytogenet 2017 11;10:35. Epub 2017 Sep 11.

Cytogenetic Laboratory, Bone Marrow Transplantation Center, National Cancer Institute (INCA), Praça Cruz Vermelha no. 23, 6° andar. Centro, CEP, Rio de Janeiro, RJ 20230-130 Brazil.

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http://dx.doi.org/10.1186/s13039-017-0335-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5594429PMC
September 2017

Analysis of the histone cluster in Senegalese sole (Solea senegalensis): evidence for a divergent evolution of two canonical histone clusters.

Genome 2017 May 10;60(5):441-453. Epub 2016 Dec 10.

a Área de Genética, Facultad de Ciencias del Mar y Ambientales, Universidad de Cádiz, 11510 Cádiz, Spain.

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http://dx.doi.org/10.1139/gen-2016-0143DOI Listing
May 2017

Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report.

J Med Case Rep 2017 Apr 7;11(1):94. Epub 2017 Apr 7.

Molecular Biology and Biotechnology Department, Human Genetics Div., Atomic Energy Commission of Syria, P.O. Box 6091, Damascus, Syria.

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http://dx.doi.org/10.1186/s13256-017-1251-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383952PMC
April 2017

Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia.

J Pediatr Hematol Oncol 2017 03;39(2):e85-e91

*Pediatric Oncohematology Center, Hospital Oswaldo Cruz/Post Graduation Program, Faculty of Medical Sciences †Biologic Sciences Institute, Pernambuco University, Recife/PE ‡Cytogenetics Department, Bone Marrow Unit, National Cancer Institute, Rio de Janeiro/RJ, Brazil §Institute of Human Genetics, Jena University Hospital, Jena, Germany.

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http://dx.doi.org/10.1097/MPH.0000000000000720DOI Listing
March 2017

Noninvasive Prenatal Testing - When Is It Advantageous to Apply.

Biomed Hub 2017 Jan-Apr;2(1):1-11. Epub 2017 Mar 4.

Institute of Human Genetics, Friedrich Schiller University, Jena, Germany.

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http://dx.doi.org/10.1159/000458432DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945944PMC
March 2017

Unusual Duplication in the Pericentromeric Region of Chromosome 9 in a Patient with Phenotypic Alterations.

Cytogenet Genome Res 2016 7;150(2):100-105. Epub 2017 Jan 7.

Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1159/000453574DOI Listing
February 2017

"Classical cytogenetics" is not equal to "banding cytogenetics".

Authors:
Thomas Liehr

Mol Cytogenet 2017 16;10. Epub 2017 Feb 16.

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Kollegiengasse 10, D-07743 Jena, Germany.

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https://molecularcytogenetics.biomedcentral.com/articles/10.
Publisher Site
http://dx.doi.org/10.1186/s13039-017-0305-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314467PMC
February 2017

Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports.

BMC Res Notes 2017 Jan 18;10(1):52. Epub 2017 Jan 18.

Laboratório de Marcadores Circulantes, Departamento de Patologia e Laboratórios, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

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http://dx.doi.org/10.1186/s13104-016-2369-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241924PMC
January 2017

Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities.

Int J Mol Cell Med 2017 17;6(1):61-65. Epub 2017 Jan 17.

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568194PMC
January 2017