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List of works by Thomas Liehr

A Family with an Inverted Tandem Duplication 5q22.1q23.2 ⬇️

scientific article published on October 6, 2012

A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement

scientific article published on 20 October 2015

A New Multicolor Fluorescence In Situ Hybridization Probe Set Directed Against Human Heterochromatin ⬇️

scientific article published on April 17, 2012

A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12) ⬇️

scientific article published on February 28, 2012

A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5 ⬇️

scientific article published on August 4, 2010

A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues ⬇️

scientific article published on 01 December 1996

A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes ⬇️

scientific article published on September 1, 2010

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

scientific article published on 01 August 1992

A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia ⬇️

scientific article published on May 17, 2012

Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1 ⬇️

scientific article published on 01 November 1997

An Insight into the Chromosomal Evolution of Lebiasinidae (Teleostei, Characiformes)

scientific article published on 28 March 2020

Assignment of the microvascular endothelial differentiation gene 1 (MDG1) to human chromosome band 14q24.2→q24.3 by fluorescence in situ hybridization ⬇️

scientific article published on January 1, 1997

Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3).

scientific article published in March 2007

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

scientific article

Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH‐technique ⬇️

scientific article published on 01 March 1998

Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics ⬇️

scientific article published on March 14, 2012

Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization ⬇️

scientific article published on September 10, 2010

Chromosomal Composition of Micronuclei in Human Leukocytes Exposed to Mitomycin C ⬇️

scientific article published on January 18, 2012

Chromosomal aberrations in spontaneously aborted products of conception from Ukraine

scientific article published on 7 January 2018

Chromosomal evolution in naked catfishes (Bagridae, Siluriformes): A comparative chromosome mapping study

scientific article published in 2014

Chromosome gain and loss in paraffin sections from malignant melanomas of the skin ⬇️

scientific article published on January 1, 1997

Chromosomes in a genome-wise order: evidence for metaphase architecture.

scientific article published on 27 April 2016

Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes ⬇️

scientific article published on December 29, 2012

Common Fragile Sites: Genomic Hotspots of DNA Damage and Carcinogenesis ⬇️

scientific article published on September 20, 2012

Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family

scientific article

Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS ⬇️

scientific article published on November 1, 2003

Complex chromosomal rearrangements: origin and meiotic behavior ⬇️

scientific article published on April 11, 2011

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

scientific article

Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors ⬇️

scientific article published on July 20, 2012

Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes ⬇️

scientific article published on June 30, 2011

Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

scientific article

Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family

scientific article published on 19 December 2019

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

scientific article published on 09 September 2020

DNA Copy Number Variations as Markers of Mutagenic Impact

scientific article published on 24 September 2019

DNA Damage in Moderate and Severe COVID-19 Cases: Relation to Demographic, Clinical, and Laboratory Parameters

scientific article published in 2024

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

scientific article published on 25 August 2016

De novo translocation involving two chromosomes in adult prolymphocytic leukemia—A rare case ⬇️

scientific article published on October 12, 2010

Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype ⬇️

scientific article published on May 29, 2012

Doxorubicin-Induced Translocation of mtDNA into the Nuclear Genome of Human Lymphocytes Detected Using a Molecular-Cytogenetic Approach

scientific article published on 17 October 2020

Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter ⬇️

scientific article published on 01 May 2003

Evolution of the Proto Sex-Chromosome in Solea senegalensis

scientific article published on 15 October 2019

Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines.

scientific article published in December 1999

First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding ⬇️

scientific article published on January 15, 2013

First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)

scientific article published on 17 December 2013

Giant Sex Chromosomes in Omophoita Species (Coleoptera, Chrysomelidae): Structural and Evolutionary Relationships Revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH)

scientific article published in 2023

Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report ⬇️

scientific article published on May 6, 2011

High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis)

High resolution karyotype of thai crab-eating macaque (Macaca fascicularis)

Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes)

scientific article published on 18 November 2020

How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set ⬇️

scientific article published on April 29, 2012

Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal ⬇️

scientific article published on May 15, 2003

Insertion of the 3′ ABL region into the long arm of chromosome 1 in a Philadelphia chromosome-negative chronic myeloid leukemia case ⬇️

scientific article published on September 23, 2010

Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae).

scientific article published on 22 November 2013

Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas ⬇️

scientific article published on 01 January 2003

Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier ⬇️

scientific article published on March 2, 2011

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

scientific article published on 09 April 2020

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

scientific article published on 01 July 2020

Molecular cytogenetic characterization of epithelioid hemangioendothelioma ⬇️

scientific article published on 01 December 2011

Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma ⬇️

scientific article published on February 16, 2011

Molecular diagnosis of PMP22 -associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations ⬇️

scientific article published on September 1, 1997

Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae)

scientific article published on 10 October 2020

New Eukaryotic Semaphorins with Close Homology to Semaphorins of DNA Viruses ⬇️

scientific article published on August 1, 1998

New cytogenetically visible copy number variant in region 8q21.2 ⬇️

scientific article published on January 5, 2011

Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos.

scientific article

Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisation ⬇️

scientific article published on 01 May 1998

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism

scientific article published on 01 January 2010

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

scientific article published on 9 March 2018

Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl ⬇️

scientific article published on October 4, 2010

Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13 ⬇️

scientific article published on 01 May 1998

Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature ⬇️

scientific article published on April 1, 2012

Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites

scientific article

Regional localization of Flic1, a calcyclin/S100A6-like gene, to rat Chromosome 7q22-31 by means of FISH ⬇️

scientific article published on January 1, 1998

Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH ⬇️

scientific article published on 01 July 1995

Revisiting the Karyotype Evolution of Neotropical Boid Snakes: A Puzzle Mediated by Chromosomal Fissions

scientific article published on 10 October 2020

Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles ⬇️

scientific article published on 5 June 2021

Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis ⬇️

scientific article published on 05 January 2011

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

scientific article published on June 11, 2012

Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia ⬇️

scientific article published on August 23, 2012

Small Supernumerary Marker Chromosomes and Uniparental Disomy Have a Story to Tell ⬇️

scientific article published on June 14, 2011

Small Supernumerary Marker Chromosomes in Human Infertility

scientific article

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes ⬇️

scientific article published on September 1, 2010

The Amazonian Red Side-Necked Turtle Rhinemys rufipes (Spix, 1824) (Testudines, Chelidae) Has a GSD Sex-Determining Mechanism with an Ancient XY Sex Microchromosome System

scientific article published on 12 September 2020

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

scientific article published on September 1, 2010

Trisomy 8 as the sole chromosomal aberration inmyelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations ⬇️

scientific article published on 01 October 2003

Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma ⬇️

scientific article published on December 1, 2011

Typical and partial cat eye syndrome: identification of the marker chromosome by FISH

scientific article published on August 1, 1992

Use of fluorescence in-situ hybridization (fish) for the estimation of the aberrant cell clone in leukemias with trisomy-8 or monosomy-7 detected by karyotyping ⬇️

scientific article published on 01 August 1993

Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species ⬇️

scientific article published on September 17, 2011

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