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Mobile Elements: Drivers of Genome Evolution

Science (American Association for the Advancement of Science), 2004-03, Vol.303 (5664), p.1626-1632

Kazazian, Haig H.

2004

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A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells

Nature biotechnology, 2021-01, Vol.39 (1), p.47-55

2021

Volltextzugriff (PDF)

High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes

Genome research, 2010-09, Vol.20 (9), p.1262

2010

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LINE-1 expression and retrotransposition in Barrett’s esophagus and esophageal carcinoma

Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (35), p.E4894-E4900

2015

Volltextzugriff (PDF)

Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition

Nucleic acids research, 2013-08, Vol.41 (15), p.7401

2013

Volltextzugriff (PDF)

A Long, Fulfilling Career in Human Genetics

Annual review of genomics and human genetics, 2021-01, Vol.22 (1), p.27-53

Kazazian, Haig H

2021

Volltextzugriff (PDF)

Fifty years in human genetics—a career retrospective

The FASEB journal, 2017-09, Vol.31 (9), p.3712-3718

Kazazian, Haig H.

2017

Volltextzugriff (PDF)

Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans

Genome research, 2011-06, Vol.21 (6), p.985

2011

Volltextzugriff (PDF)

Extensive somatic L1 retrotransposition in colorectal tumors

Genome research, 2012-12, Vol.22 (12), p.2328

2012

Volltextzugriff (PDF)

L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism

Genes & development, 2009-06, Vol.23 (11), p.1303-1312

2009

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Progress in understanding the biology of the human mutagen LINE-1

Human mutation, 2007-06, Vol.28 (6), p.527-539

2007

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Aicardi-Goutières syndrome protein TREX1 suppresses L1 and maintains genome integrity through exonuclease-independent ORF1p depletion

Nucleic acids research, 2017-05, Vol.45 (8), p.4619

2017

Volltextzugriff (PDF)

Many LINE1 elements contribute to the transcriptome of human somatic cells

Genome biology, 2009-01, Vol.10 (9), p.R100-R100, Article R100

2009

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Somatically Acquired LINE-1 Insertions in Normal Esophagus Undergo Clonal Expansion in Esophageal Squamous Cell Carcinoma

Human mutation, 2016-09, Vol.37 (9), p.942-954

2016

Volltextzugriff (PDF)

Mobile elements in the human genome: implications for disease

Genome medicine, 2012-02, Vol.4 (2), p.12-12, Article 12

2012

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Hot L1s Account for the Bulk of Retrotransposition in the Human Population

Proceedings of the National Academy of Sciences - PNAS, 2003-04, Vol.100 (9), p.5280-5285

2003

Volltextzugriff (PDF)

Heritable L1 retrotransposition in the mouse primordial germline and early embryo

Genome research, 2017-08, Vol.27 (8), p.1395

2017

Volltextzugriff (PDF)

LINE-1 ORF1 Protein Localizes in Stress Granules with Other RNA-Binding Proteins, Including Components of RNA Interference RNA-Induced Silencing Complex

Molecular and Cellular Biology, 2007-09, Vol.27 (18), p.6469-6483

2007

Volltextzugriff (PDF)

Reflections on the history of genetic medicine at Johns Hopkins University

American journal of medical genetics. Part A, 2021-11, Vol.185 (11), p.3224-3229

2021

Volltextzugriff (PDF)

Widespread somatic L1 retrotransposition occurs early during gastrointestinal cancer evolution

Genome research, 2015-10, Vol.25 (10), p.1536

2015

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L1 Retrotransposition in Nondividing and Primary Human Somatic Cells

Proceedings of the National Academy of Sciences - PNAS, 2006-05, Vol.103 (21), p.8036-8041

2006

Volltextzugriff (PDF)

Long Interspersed Element Sequencing (L1-Seq): A Method to Identify Somatic LINE-1 Insertions in the Human Genome

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1400, p.79

2016

Volltextzugriff (PDF)

Exon Shuffling by L1 Retrotransposition

Science (American Association for the Advancement of Science), 1999-03, Vol.283 (5407), p.1530-1534

1999

Volltextzugriff (PDF)

25 Years of Human Mutation

Human mutation, 2016-06, Vol.37 (6), p.503-504

2016

Volltextzugriff (PDF)

A New Spin on Digenic Inheritance: Retrotransposition in Rotor Syndrome

Human mutation, 2015-03, Vol.36 (3), p.v-v

Kazazian Jr, Haig H.

2015

Volltextzugriff (PDF)

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Mobile Elements: Drivers of Genome Evolution

A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells

High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes

LINE-1 expression and retrotransposition in Barrett’s esophagus and esophageal carcinoma

Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition

A Long, Fulfilling Career in Human Genetics

Fifty years in human genetics—a career retrospective

Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans

Extensive somatic L1 retrotransposition in colorectal tumors

L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism

Progress in understanding the biology of the human mutagen LINE-1

Aicardi-Goutières syndrome protein TREX1 suppresses L1 and maintains genome integrity through exonuclease-independent ORF1p depletion

Many LINE1 elements contribute to the transcriptome of human somatic cells

Somatically Acquired LINE-1 Insertions in Normal Esophagus Undergo Clonal Expansion in Esophageal Squamous Cell Carcinoma

Mobile elements in the human genome: implications for disease

Hot L1s Account for the Bulk of Retrotransposition in the Human Population

Heritable L1 retrotransposition in the mouse primordial germline and early embryo

LINE-1 ORF1 Protein Localizes in Stress Granules with Other RNA-Binding Proteins, Including Components of RNA Interference RNA-Induced Silencing Complex

Reflections on the history of genetic medicine at Johns Hopkins University

Widespread somatic L1 retrotransposition occurs early during gastrointestinal cancer evolution

L1 Retrotransposition in Nondividing and Primary Human Somatic Cells

Long Interspersed Element Sequencing (L1-Seq): A Method to Identify Somatic LINE-1 Insertions in the Human Genome

Exon Shuffling by L1 Retrotransposition

25 Years of Human Mutation

A New Spin on Digenic Inheritance: Retrotransposition in Rotor Syndrome

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