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Repetitive Elements in Humans

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2072

Liehr, Thomas

2021

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Cytogenomics

Liehr, Thomas

1, 2021

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Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

Frontiers in genetics, 2021-06, Vol.12, p.682980-682980

Liehr, Thomas

2021

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Cytogenetics and Molecular Cytogenetics

Liehr, Thomas

First edition, 2023

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False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests?

Molecular cytogenetics, 2022-08, Vol.15 (1), p.36-36, Article 36

Liehr, Thomas

2022

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Editorial: Co-occurrence of numerical and structural aberration-small supernumerary marker chromosomes and B-chromosomes

Frontiers in genetics, 2024-04, Vol.15, p.1408674-1408674

Liehr, Thomas

2024

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Molecular Cytogenetics in the Era of Chromosomics and Cytogenomic Approaches

Frontiers in genetics, 2021-10, Vol.12, p.720507-720507

Liehr, Thomas

2021

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From Human Cytogenetics to Human Chromosomics

International journal of molecular sciences, 2019-02, Vol.20 (4), p.826

Liehr, Thomas

2019

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Uniparental disomy is a chromosomic disorder in the first place

Molecular cytogenetics, 2022-02, Vol.15 (1), p.5-12, Article 5

Liehr, Thomas

2022

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

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1769, p.79

Liehr, Thomas

2018

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Chromosomal Heteromorphisms and Cancer Susceptibility Revisited

Cells (Basel, Switzerland), 2022-10, Vol.11 (20), p.3239

Liehr, Thomas

2022

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About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI

Molecular cytogenetics, 2021-03, Vol.14 (1), p.20-20, Article 20

Liehr, Thomas

2021

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Cytogenetic contribution to uniparental disomy (UPD)

Molecular cytogenetics, 2010-03, Vol.3 (1), p.8-8

Liehr, Thomas

2010

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

Frontiers in genetics, 2019-11, Vol.10, p.1131-1131

2019

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The Diagnostic, Prognostic, and Therapeutic Potential of Cell-Free DNA with a Special Focus on COVID-19 and Other Viral Infections

International journal of molecular sciences, 2023-09, Vol.24 (18), p.14163

2023

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DNA Copy Number Variations as Markers of Mutagenic Impact

International journal of molecular sciences, 2019-09, Vol.20 (19), p.4723

2019

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Thoughts on the Etiology of Cherubism

Journal of clinical medicine, 2024-04, Vol.13 (7), p.2082

2024

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

International journal of molecular sciences, 2020-07, Vol.21 (13), p.4716

2020

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Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling

Liehr, Thomas

1, 2013

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LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells

Genome Biology, 2018-11, Vol.19 (1), p.189-189, Article 189

2018

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International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts

Cytogenetic and genome research, 2021-01, Vol.161 (5), p.223-224

Liehr, Thomas

2021

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Comparative karyotypic study of fifteen cyprinids (Cyprinidae, Cyprininae) species. An insight into the chromosomal evolution of the tribe Systomini

PloS one, 2024-07, Vol.19 (7), p.e0305828

2024

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Changes in Telomere Length in Leukocytes and Leukemic Cells after Ultrashort Electron Beam Radiation

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6709

2024

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The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system

Psychogeriatrics, 2022-11, Vol.22 (6), p.869-878

2022

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Non-Invasive Prenatal Testing in Germany

Diagnostics (Basel), 2022-11, Vol.12 (11), p.2816

2022

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Repetitive Elements in Humans

Cytogenomics

Non-invasive Prenatal Testing, What Patients Do Not Learn, May Be Due to Lack of Specialist Genetic Training by Gynecologists and Obstetricians?

Cytogenetics and Molecular Cytogenetics

False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests?

Editorial: Co-occurrence of numerical and structural aberration-small supernumerary marker chromosomes and B-chromosomes

Molecular Cytogenetics in the Era of Chromosomics and Cytogenomic Approaches

From Human Cytogenetics to Human Chromosomics

Uniparental disomy is a chromosomic disorder in the first place

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

Chromosomal Heteromorphisms and Cancer Susceptibility Revisited

About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI

Cytogenetic contribution to uniparental disomy (UPD)

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

The Diagnostic, Prognostic, and Therapeutic Potential of Cell-Free DNA with a Special Focus on COVID-19 and Other Viral Infections

DNA Copy Number Variations as Markers of Mutagenic Impact

Thoughts on the Etiology of Cherubism

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

Benign and Pathological Chromosomal Imbalances: Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling

LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells

International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts

Comparative karyotypic study of fifteen cyprinids (Cyprinidae, Cyprininae) species. An insight into the chromosomal evolution of the tribe Systomini

Changes in Telomere Length in Leukocytes and Leukemic Cells after Ultrashort Electron Beam Radiation

The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system

Non-Invasive Prenatal Testing in Germany

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