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Michael J. Schertzer

Extension of Cell Life-Span and Telomere Length in Animals Cloned from Senescent Somatic Cells
2000 · Robert P. Lanza, Jose B. Cibelli, et al. · Science · 465
Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNA
2002 · Iris Cheung, Michael Schertzer, et al. · Nature Genetics · 274
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability
2013 · Tangui Le Guen, Laurent Jullien, et al. · Human Molecular Genetics · 202
Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal–Hreidarsson syndrome
2013 · Zhong Deng, Galina Glousker, et al. · Proceedings of the National Academy of Sciences · 171
Endogenous Retroviruses Provide the Primary Polyadenylation Signal for Two New Human Genes (HHLA2 and HHLA3)
1999 · Dixie L. Mager, D.Garvin Hunter, et al. · Genomics · 142
Genome-wide Control of Heterochromatin Replication by the Telomere Capping Protein TRF2
2018 · Aaron Mendez-Bermudez, Liudmyla Lototska, et al. · Molecular Cell · 78
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SLX4 interacts with RTEL1 to prevent transcription-mediated DNA replication perturbations
2020 · A. Takedachi, E. Despras, et al. · Nature Structural & Molecular Biology · 62
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors
1992 · James Tomfohrde, Stephen Wood, et al. · Genomics · 62
Inverted tandem duplication generates a duplication deficiency of chromosome 8p
1987 · F. J. Dill, M. Schertzer, et al. · Clinical Genetics · 59
Genomic Organization, Expression, and Chromosome Location of the Human SNAIL Gene (SNAI1) and a Related Processed Pseudogene (SNAI1P)
1999 · William A. Paznekas, Kazuki Okajima, et al. · Genomics · 54
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HumanSLUGGene Organization, Expression, and Chromosome Map Location on 8q
1998 · Michael E Cohen, Mingfei Yin, et al. · Genomics · 46
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A Polymorphic Complex Dinucleotide Repeat at the Telomeric D8S7 Locus
1992 · Stephen Wood, Michael Schertzer · Human Heredity · 45
Characterization of a human chromosome 8 cosmid library constructed from flow-sorted chromosomes
2008 · S. Wood, M. Schertzer, et al. · Cytogenetics and Cell Genetics · 44
The C‐terminal extension of human RTEL1, mutated in Hoyeraal‐Hreidarsson syndrome, contains Harmonin‐N‐like domains
2013 · Guilhem Faure, Patrick Revy, et al. · Proteins Structure Function and Bioinformatics · 40
Human regulator of telomere elongation helicase 1 (RTEL1) is required for the nuclear and cytoplasmic trafficking of pre-U2 RNA
2015 · Michael Schertzer, Karina Jouravleva, et al. · Nucleic Acids Research · 27
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Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene
1993 · Stephen Wood, Michael Schertzer, et al. · Human Genetics · 19
Mapping of the Pulmonary Surfactant SP5 (SFTP2) Locus to 8p21 and Characterization of a Microsatellite Repeat Marker That Shows Frequent Loss of Heterozygosity in Human Carcinomas
1994 · Stephen Wood, M.Lisa Yaremko, et al. · Genomics · 15
Identification of the human neuronal nicotinic cholinergic α2 receptor locus, (CHRNA2), within an 8p21 mapped locus, by sequence homology with rat DNA
1995 · Stephen Wood, Michael Schertzer, et al. · Somatic Cell and Molecular Genetics · 11
Sequence identity locates CEBPD and FGFR1 to mapped human loci within proximal 8p
2008 · S. Wood, M. Schertzer, et al. · Cytogenetics and Cell Genetics · 10
Linkage mapping of the D8S133 locus to chromosome 8p using a highly informative, polymorphic, complex dinucleotide repeat
1992 · Stephen Wood, Michael Schertzer · Genomics · 10
DNA damage–induced EMT controlled by the PARP-dependent chromatin remodeler ALC1 promotes DNA repair efficiency through RAD51 in tumor cells
2024 · Fatemeh Rajabi, Rebecca Smith, et al. · Molecular Biology of the Cell · 9
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Human RTEL1 Interacts with KPNB1 (Importin β) and NUP153 and Connects Nuclear Import to Nuclear Envelope Stability in S-Phase
2023 · Michael Schertzer, Laurent Jullien, et al. · Cells · 5
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Analysis of CA repeat polymorphisms places three human gene loci on the 8p linkage map
2008 · R. Bruskiewich, T. Everson, et al. · Cytogenetics and Cell Genetics · 5
A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus
1997 · R. Bruskiewich, M. Schertzer, et al. · Genome · 2
Author Correction: SLX4 interacts with RTEL1 to prevent transcription-mediated DNA replication perturbations
2020 · A. Takedachi, E. Despras, et al. · Nature Structural & Molecular Biology · 1
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Works count: 44
Citation count: 1,861
H-index: 16
I10-index: 20
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