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Lusine Nazaryan‐Petersen

Observed names: Lusine Nazaryan-Petersen, Nazaryan-Petersen, Lusine
ORCID: 0000-0002-4807-6827
Observed ORCID: 0000-0002-4807-6827
OpenAlex ID: A5046933198
A germline chromothripsis event stably segregating in 11 individuals through three generations
2015 · Birgitte Bertelsen, Lusine Nazaryan-Petersen, et al. · Genetics in Medicine · 99
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Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination
2016 · Lusine Nazaryan-Petersen, Birgitte Bertelsen, et al. · Human Mutation · 60
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Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes
2018 · Christina Halgren, Nete M. Nielsen, et al. · The American Journal of Human Genetics · 47
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Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023 · Daniel G. Calame, Tianyu Guo, et al. · The American Journal of Human Genetics · 43
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Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
2018 · Lusine Nazaryan-Petersen, Jesper Eisfeldt, et al. · PLoS Genetics · 39
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Small supernumerary marker chromosomes: A legacy of trisomy rescue?
2018 · Nehir Edibe Kurtas, Luciano Xumerle, et al. · Human Mutation · 39
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Chromothripsis and DNA Repair Disorders
2020 · Lusine Nazaryan-Petersen, Victoria Alexandra Bjerregaard, et al. · Journal of Clinical Medicine · 35
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Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly
2018 · Zuzana Slamova, Lusine Nazaryan-Petersen, et al. · Human Mutation · 24
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Added Value of Reanalysis of Whole Exome- and Whole Genome Sequencing Data From Patients Suspected of Primary Immune Deficiency Using an Extended Gene Panel and Structural Variation Calling
2022 · Sara Bohnstedt Mørup, Lusine Nazaryan-Petersen, et al. · Frontiers in Immunology · 21
Haploinsufficiency of ARHGAP42 is associated with hypertension
2019 · Amanda S. Fjorder, Malene B. Rasmussen, et al. · European Journal of Human Genetics · 17
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Chromothripsis and Human Genetic Disease
2016 · Lusine Nazaryan‐Petersen, Niels Tommerup · Encyclopedia of Life Sciences · 11
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorder
2024 · Nour Elkhateeb, Renarta Crookes, et al. · Genetics in Medicine · 8
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Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients
2022 · Nanna Dahl Rendtorff, Helena Gásdal Karstensen, et al. · Scientific Reports · 8
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Multigenic truncation of the semaphorin–plexin pathway by a germline chromothriptic rearrangement associated with Moebius syndrome
2019 · Lusine Nazaryan‐Petersen, Inês R. Oliveira, et al. · Human Mutation · 8
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A novel DOCK2 variant in siblings with severe combined immunodeficiency
2022 · Maria Anna Bruusgaard‐Mouritsen, Tania Masmas, et al. · Scandinavian Journal of Immunology · 2
Monoallelic variation in DHX9 , the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023 · Daniel G. Calame, Tianyu Guo, et al. · medRxiv
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Whole genome characterization of array defined clustered CNVs reveals two distinct complex rearrangement subclasses generated through either non-homologous repair or template switching
2018 · Lusine Nazaryan‐Petersen, Jesper Eisfeldt, et al. · European Journal of Human Genetics
Whole genome characterization of array defined clustered CNVs reveals two distinct complex rearrangement subclasses generated through either non homologous repair or template switching
2017 · Jesper Eisfeldt, Lusine Nazaryan‐Petersen, et al. · Molecular Cytogenetics
Works count: 19
Citation count: 462
H-index: 11
I10-index: 11
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