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The prevalence of HLA‐I LOH in Chinese pan‐cancer patients and genomic features of patients harboring HLA‐I LOH

Human mutation, 2021-10, Vol.42 (10), p.1254-1264

2021

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Decreased copy‐neutral loss of heterozygosity in African American colorectal cancers

Genes chromosomes & cancer, 2020-08, Vol.59 (8), p.454-464

2020

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Pediatric acute myeloid leukemia with t(7;21)(p22;q22)

Genes chromosomes & cancer, 2019-08, Vol.58 (8), p.551-557

2019

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Loss of Heterozygosity in the Tumor DNA of De Novo Diagnosed Patients Is Associated with Poor Outcome for B-ALL but Not for T-ALL

Genes, 2022-02, Vol.13 (3), p.398

2022

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Diverse Lineages of Candida albicans Live on Old Oaks

Genetics (Austin), 2019-01, Vol.211 (1), p.277-288

2019

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Loss of Heterozygosity Drives Adaptation in Hybrid Yeast

Molecular biology and evolution, 2017-07, Vol.34 (7), p.1596-1612

2017

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Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications

American journal of human genetics, 2022-08, Vol.109 (8), p.1421-1435

2022

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Genome-wide identification of copy neutral loss of heterozygosity reveals its possible association with spatial positioning of chromosomes

Human molecular genetics, 2023-03, Vol.32 (7), p.1175-1183

2023

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Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis

Human mutation, 2012-04, Vol.33 (4), p.763-776

2012

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Forward and reverse mutations in stages of cancer development

Human genomics, 2018-08, Vol.12 (1), p.40-40, Article 40

2018

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Fitness benefits of loss of heterozygosity in Saccharomyces hybrids

Genome research, 2019-10, Vol.29 (10), p.1685-1692

2019

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Adaptation by Loss of Heterozygosity in Saccharomyces cerevisiae Clones Under Divergent Selection

Genetics (Austin), 2019-10, Vol.213 (2), p.665-683

2019

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Loss of Heterozygosity and Its Importance in Evolution

Journal of molecular evolution, 2023-06, Vol.91 (3), p.369-377

Smukowski Heil, Caiti

2023

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Autosomal dominant genodermatoses in adults being heralded by superimposed skin lesions in children

American journal of medical genetics. Part C, Seminars in medical genetics, 2023-06, Vol.193 (2), p.109-115

Happle, Rudolf

2023

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Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883)

Journal of medical genetics, 2022-03, Vol.59 (3), p.248-252

2022

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Factors that influence bidirectional long-tract homozygosis due to double-strand break repair in Candida albicans

Genetics (Austin), 2021-05, Vol.218 (1)

2021

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Genome analysis and avirulence gene cloning using a high-density RADseq linkage map of the flax rust fungus, Melampsora lini

BMC genomics, 2016-08, Vol.17 (Suppl 7), p.667-667, Article 667

2016

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Both R-loop removal and ribonucleotide excision repair activities of RNase H2 contribute substantially to chromosome stability

DNA repair, 2017-04, Vol.52, p.110-114

2017

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Characterization and clinical relevance of PDGFRA pathway copy number variation gains across human cancers

Molecular genetics and genomics : MGG, 2022-03, Vol.297 (2), p.561-571

2022

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Evolutionary conservation of the clk-1-dependent mechanism of longevity: loss of mclk1 increases cellular fitness and lifespan in mice

Genes & development, 2005-10, Vol.19 (20), p.2424-2434

2005

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Interpopulational and intrapopulational genetic diversity of the endangered Itasenpara bitterling (Acheilognathus longipinnis) with reference to its demographic history

Conservation genetics, 2020-02, Vol.21 (1), p.55-64

2020

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Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy

Genes, 2022-12, Vol.13 (12), p.2356

2022

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Phenotypic Consequences of a Spontaneous Loss of Heterozygosity in a Common Laboratory Strain of Candida albicans

Genetics (Austin), 2016-07, Vol.203 (3), p.1161-1176

2016

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Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution

Genes chromosomes & cancer, 2020-07, Vol.59 (7), p.396-405

2020

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SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

Oncogene, 2015-01, Vol.34 (5), p.631-638

2015

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The prevalence of HLA‐I LOH in Chinese pan‐cancer patients and genomic features of patients harboring HLA‐I LOH

Decreased copy‐neutral loss of heterozygosity in African American colorectal cancers

Pediatric acute myeloid leukemia with t(7;21)(p22;q22)

Loss of Heterozygosity in the Tumor DNA of De Novo Diagnosed Patients Is Associated with Poor Outcome for B-ALL but Not for T-ALL

Diverse Lineages of Candida albicans Live on Old Oaks

Loss of Heterozygosity Drives Adaptation in Hybrid Yeast

Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications

Genome-wide identification of copy neutral loss of heterozygosity reveals its possible association with spatial positioning of chromosomes

Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis

Forward and reverse mutations in stages of cancer development

Fitness benefits of loss of heterozygosity in Saccharomyces hybrids

Adaptation by Loss of Heterozygosity in Saccharomyces cerevisiae Clones Under Divergent Selection

Loss of Heterozygosity and Its Importance in Evolution

Autosomal dominant genodermatoses in adults being heralded by superimposed skin lesions in children

Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883)

Factors that influence bidirectional long-tract homozygosis due to double-strand break repair in Candida albicans

Genome analysis and avirulence gene cloning using a high-density RADseq linkage map of the flax rust fungus, Melampsora lini

Both R-loop removal and ribonucleotide excision repair activities of RNase H2 contribute substantially to chromosome stability

Characterization and clinical relevance of PDGFRA pathway copy number variation gains across human cancers

Evolutionary conservation of the clk-1-dependent mechanism of longevity: loss of mclk1 increases cellular fitness and lifespan in mice

Interpopulational and intrapopulational genetic diversity of the endangered Itasenpara bitterling (Acheilognathus longipinnis) with reference to its demographic history

Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L -Associated Neuropathy

Phenotypic Consequences of a Spontaneous Loss of Heterozygosity in a Common Laboratory Strain of Candida albicans

Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution

SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

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