| Year |
Citation |
Score |
| 2020 |
Gadji M, Mathur S, Bélanger B, Jangamreddy JR, Lamoureux J, Tsanaclis AMC, Fortin D, Drouin R, Mai S. Three-Dimensional Nuclear Telomere Profiling as a Biomarker for Recurrence in Oligodendrogliomas: A Pilot Study. International Journal of Molecular Sciences. 21. PMID 33198352 DOI: 10.3390/ijms21228539 |
0.648 |
|
| 2018 |
Samassekou O, Bastien N, Yan J, Mai S, Drouin R. Expression of Genes Associated with Telomere Homeostasis in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability. Methods in Molecular Biology (Clifton, N.J.). 1769: 253-262. PMID 29564829 DOI: 10.1007/978-1-4939-7780-2_16 |
0.731 |
|
| 2018 |
Samassekou O, Bastien N, Yan J, Mai S, Drouin R. Study of Telomere Dysfunction in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability. Methods in Molecular Biology (Clifton, N.J.). 1769: 209-230. PMID 29564827 DOI: 10.1007/978-1-4939-7780-2_14 |
0.745 |
|
| 2016 |
Ayub S, Gadji M, Krabchi K, Côté S, Gekas J, Maranda B, Drouin R. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations. American Journal of Medical Genetics. Part A. 170: 896-907. PMID 26822682 DOI: 10.1002/Ajmg.A.37428 |
0.691 |
|
| 2015 |
Emad A, Lamoureux J, Ouellet A, Drouin R. Rapid Aneuploidy Detection of Chromosomes 13, 18, 21, X and Y Using Quantitative Fluorescent Polymerase Chain Reaction with Few Microdissected Fetal Cells. Fetal Diagnosis and Therapy. 38: 65-76. PMID 25999366 DOI: 10.1159/000365810 |
0.436 |
|
| 2014 |
Samassekou O, Bastien N, Lichtensztejn D, Yan J, Mai S, Drouin R. Different TP53 mutations are associated with specific chromosomal rearrangements, telomere length changes, and remodeling of the nuclear architecture of telomeres. Genes, Chromosomes & Cancer. 53: 934-50. PMID 25059482 DOI: 10.1002/Gcc.22205 |
0.752 |
|
| 2014 |
Emad A, Bouchard EF, Lamoureux J, Ouellet A, Dutta A, Klingbeil U, Drouin R. Validation of automatic scanning of microscope slides in recovering rare cellular events: application for detection of fetal cells in maternal blood. Prenatal Diagnosis. 34: 538-46. PMID 24578229 DOI: 10.1002/Pd.4345 |
0.31 |
|
| 2014 |
Gadji M, Crous-Tsanaclis AM, Mathieu D, Mai S, Fortin D, Drouin R. A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 170-8. PMID 24118308 DOI: 10.1111/Neup.12060 |
0.723 |
|
| 2012 |
Emad A, Ayub S, Samassékou O, Grégoire MC, Gadji M, Ntwari A, Lamoureux J, Hemmings F, Tafas T, Kilpatrick MW, Krabchi K, Drouin R. Efficiency of manual scanning in recovering rare cellular events identified by fluorescence in situ hybridization: simulation of the detection of fetal cells in maternal blood. Journal of Biomedicine & Biotechnology. 2012: 610856. PMID 22505816 DOI: 10.1155/2012/610856 |
0.691 |
|
| 2011 |
Gadji M, Krabchi K, Langis P, Aboura A, Périgny M, Côté S, Ferland M, Drouin R. Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22. American Journal of Medical Genetics. Part A. 155: 430-3. PMID 21271667 DOI: 10.1002/Ajmg.A.33654 |
0.687 |
|
| 2010 |
Samassekou O, Gadji M, Drouin R, Yan J. Sizing the ends: normal length of human telomeres. Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft. 192: 284-91. PMID 20732797 DOI: 10.1016/J.Aanat.2010.07.005 |
0.766 |
|
| 2010 |
Millau JF, Mai S, Bastien N, Drouin R. p53 functions and cell lines: have we learned the lessons from the past? Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 32: 392-400. PMID 20414897 DOI: 10.1002/Bies.200900160 |
0.306 |
|
| 2010 |
Lacoste S, Rochette PJ, Drouin R. [Mapping DNA damage to understand somatic mutagenesis]. MéDecine Sciences : M/S. 26: 193-200. PMID 20188052 DOI: 10.1051/Medsci/2010262193 |
0.319 |
|
| 2010 |
Gadji M, Fortin D, Tsanaclis AM, Garini Y, Katzir N, Wienburg Y, Yan J, Klewes L, Klonisch T, Drouin R, Mai S. Three-dimensional nuclear telomere architecture is associated with differential time to progression and overall survival in glioblastoma patients. Neoplasia (New York, N.Y.). 12: 183-91. PMID 20126476 DOI: 10.1593/Neo.91752 |
0.67 |
|
| 2009 |
Gadji M, Crous AM, Fortin D, Krcek J, Torchia M, Mai S, Drouin R, Klonisch T. EGF receptor inhibitors in the treatment of glioblastoma multiform: old clinical allies and newly emerging therapeutic concepts. European Journal of Pharmacology. 625: 23-30. PMID 19836372 DOI: 10.1016/J.Ejphar.2009.10.010 |
0.636 |
|
| 2009 |
Klonisch T, Drouin R. Fetal-maternal exchange of multipotent stem/progenitor cells: microchimerism in diagnosis and disease. Trends in Molecular Medicine. 15: 510-8. PMID 19828378 DOI: 10.1016/J.Molmed.2009.09.002 |
0.304 |
|
| 2009 |
Gadji M, Fortin D, Tsanaclis AM, Drouin R. Is the 1p/19q deletion a diagnostic marker of oligodendrogliomas? Cancer Genetics and Cytogenetics. 194: 12-22. PMID 19737649 DOI: 10.1016/J.Cancergencyto.2009.05.004 |
0.699 |
|
| 2009 |
Rochette PJ, Lacoste S, Therrien JP, Bastien N, Brash DE, Drouin R. Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA. Mutation Research. 665: 7-13. PMID 19427505 DOI: 10.1016/J.Mrfmmm.2009.02.008 |
0.338 |
|
| 2009 |
Drouin R, Bastien N, Millau JF, Vigneault F, Paradis I. In cellulo DNA analysis (LMPCR footprinting). Methods in Molecular Biology (Clifton, N.J.). 543: 293-336. PMID 19378174 DOI: 10.1007/978-1-60327-015-1_20 |
0.326 |
|
| 2008 |
Gadji M, Krabchi K, Yan J, Drouin R. Application of multi-PRINS to simultaneously identify chromosomes 18, X, and Y in prenatal diagnosis. Methods in Molecular Biology (Clifton, N.J.). 444: 49-58. PMID 18425471 DOI: 10.1007/978-1-59745-066-9_4 |
0.71 |
|
| 2007 |
Lacoste S, Castonguay A, Drouin R. Repair kinetics of specific types of nitroso-induced DNA damage using the comet assay in human cells. Mutation Research. 624: 18-30. PMID 17612576 DOI: 10.1016/J.Mrfmmm.2007.02.030 |
0.335 |
|
| 2007 |
Boily G, Ouellet S, Langlois S, Larivière M, Drouin R, Sinnett D. In vivo footprinting analysis of the Glypican 3 (GPC3) promoter region in neuroblastoma cells. Biochimica Et Biophysica Acta. 1769: 182-93. PMID 17350117 DOI: 10.1016/J.Bbaexp.2007.01.014 |
0.314 |
|
| 2007 |
Drouin R, Dridi W, Samassekou O. DNA polymerases for PCR applications Industrial Enzymes: Structure, Function and Applications. 379-401. DOI: 10.1007/1-4020-5377-0_22 |
0.707 |
|
| 2006 |
Ouellet S, Vigneault F, Lessard M, Leclerc S, Drouin R, Guérin SL. Transcriptional regulation of the cyclin-dependent kinase inhibitor 1A (p21) gene by NFI in proliferating human cells. Nucleic Acids Research. 34: 6472-87. PMID 17130157 DOI: 10.1093/Nar/Gkl861 |
0.309 |
|
| 2006 |
Krabchi K, Gadji M, Yan J, Drouin R. Dual-color PRINS for in situ detection of fetal cells in maternal blood. Methods in Molecular Biology (Clifton, N.J.). 334: 141-9. PMID 16861760 DOI: 10.1385/1-59745-068-5:141 |
0.714 |
|
| 2006 |
Yan J, Gadji M, Krabchi K, Drouin R. New rapid multicolor PRINS protocol. Methods in Molecular Biology (Clifton, N.J.). 334: 3-13. PMID 16861747 DOI: 10.1385/1-59745-068-5:3 |
0.691 |
|
| 2006 |
Dridi W, Krabchi K, Gadji M, Lavoie J, Bronsard M, Fetni R, Drouin R. [Dominant negative activity of mutated p53 proteins]. MéDecine Sciences : M/S. 22: 301-7. PMID 16527213 DOI: 10.1051/Medsci/2006223301 |
0.658 |
|
| 2006 |
Krabchi K, Gadji M, Forest JC, Drouin R. Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies. Clinical Genetics. 69: 145-54. PMID 16433695 DOI: 10.1111/j.1399-0004.2005.00564.x |
0.648 |
|
| 2006 |
Krabchi K, Gadji M, Samassekou O, Grégoire MC, Forest JC, Drouin R. Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques. Prenatal Diagnosis. 26: 28-34. PMID 16374897 DOI: 10.1002/Pd.1325 |
0.74 |
|
| 2005 |
Denarier E, Forghani R, Farhadi HF, Dib S, Dionne N, Friedman HC, Lepage P, Hudson TJ, Drouin R, Peterson A. Functional organization of a Schwann cell enhancer. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 11210-7. PMID 16319321 DOI: 10.1523/Jneurosci.2596-05.2005 |
0.311 |
|
| 2005 |
Rochette PJ, Bastien N, Lavoie J, Guérin SL, Drouin R. SW480, a p53 double-mutant cell line retains proficiency for some p53 functions. Journal of Molecular Biology. 352: 44-57. PMID 16061257 DOI: 10.1016/J.Jmb.2005.06.033 |
0.373 |
|
| 2005 |
Gadji M, Krabchi K, Drouin R. Simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes by using multi-primed in situ labelling technique. Clinical Genetics. 68: 15-22. PMID 15952981 DOI: 10.1111/J.1399-0004.2005.00454.X |
0.706 |
|
| 2005 |
Hanel ML, Lau JC, Paradis I, Drouin R, Wevrick R. Chromatin modification of the human imprinted NDN (necdin) gene detected by in vivo footprinting. Journal of Cellular Biochemistry. 94: 1046-57. PMID 15669020 DOI: 10.1002/Jcb.20365 |
0.333 |
|
| 2005 |
Saba TG, Montpetit A, Verner A, Rioux P, Hudson TJ, Drouin R, Drouin CA. An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. Human Genetics. 116: 167-71. PMID 15668823 DOI: 10.1007/S00439-004-1193-8 |
0.339 |
|
| 2005 |
Lavoie J, Carter R, Drouin R, Lebel M. Increased frequency of multiradial chromosome structures in mouse embryonic fibroblasts lacking functional Werner syndrome protein and poly(ADP-ribose) polymerase-1. Cancer Genetics and Cytogenetics. 156: 134-43. PMID 15642393 DOI: 10.1016/J.Cancergencyto.2004.05.005 |
0.428 |
|
| 2004 |
Yan J, Chen BZ, Bouchard EF, Drouin R. The labeling efficiency of human telomeres is increased by double-strand PRINS. Chromosoma. 113: 204-9. PMID 15349787 DOI: 10.1007/S00412-004-0310-8 |
0.357 |
|
| 2004 |
Lee DF, Drouin R, Pitsikas P, Rainbow AJ. Detection of an involvement of the human mismatch repair genes hMLH1 and hMSH2 in nucleotide excision repair is dependent on UVC fluence to cells. Cancer Research. 64: 3865-70. PMID 15172995 DOI: 10.1158/0008-5472.Can-03-3193 |
0.319 |
|
| 2004 |
Krabchi K, Gadji M, Ferland M, Bronsard M, Jackson L, Forest J, Drouin R. Identification et quantification des cellules foetales aneuploïdes circulant dans le sang maternel par méthodes cytogénétiques moléculaires Annales De Pathologie. 24: 92. DOI: 10.1016/S0242-6498(04)93919-3 |
0.616 |
|
| 2004 |
Gadji M, Krabchi K, Roy S, Côté S, Bonsard M, Périgny M, Langis P, Drouin R. Diagnostic prénatal et caractérisation d’un chromosome 22 en anneau Annales De Pathologie. 24: 90-91. DOI: 10.1016/S0242-6498(04)93916-8 |
0.687 |
|
| 2003 |
Mathonnet G, Leger C, Desnoyers J, Drouin R, Therrien JP, Drobetsky EA. UV wavelength-dependent regulation of transcription-coupled nucleotide excision repair in p53-deficient human cells. Proceedings of the National Academy of Sciences of the United States of America. 100: 7219-24. PMID 12775760 DOI: 10.1073/Pnas.1232161100 |
0.345 |
|
| 2003 |
Rochette PJ, Therrien JP, Drouin R, Perdiz D, Bastien N, Drobetsky EA, Sage E. UVA-induced cyclobutane pyrimidine dimers form predominantly at thymine-thymine dipyrimidines and correlate with the mutation spectrum in rodent cells Nucleic Acids Research. 31: 2786-2794. PMID 12771205 DOI: 10.1093/Nar/Gkg402 |
0.324 |
|
| 2003 |
Dridi W, Fetni R, Lavoie J, Poupon MF, Drouin R. The dominant-negative effect of p53 mutants and p21 induction in tetraploid G1 arrest depends on the type of p53 mutation and the nature of the stimulus. Cancer Genetics and Cytogenetics. 143: 39-49. PMID 12742155 DOI: 10.1016/S0165-4608(02)00837-3 |
0.309 |
|
| 2003 |
Lavoie J, Bronsard M, Lebel M, Drouin R. Mouse telomere analysis using an optimized primed in situ (PRINS) labeling technique. Chromosoma. 111: 438-44. PMID 12707781 DOI: 10.1007/S00412-002-0225-1 |
0.422 |
|
| 2003 |
Lebel M, Lavoie J, Gaudreault I, Bronsard M, Drouin R. Genetic cooperation between the Werner syndrome protein and poly(ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal rearrangements, and cancer in mice. The American Journal of Pathology. 162: 1559-69. PMID 12707040 DOI: 10.1016/S0002-9440(10)64290-3 |
0.337 |
|
| 2003 |
Yan J, Whittom R, Delage R, Drouin R. A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case. Cancer Genetics and Cytogenetics. 140: 138-44. PMID 12645652 DOI: 10.1016/S0165-4608(02)00682-9 |
0.418 |
|
| 2002 |
Dellaire G, Yan J, Little KC, Drouin R, Chartrand P. Evidence that extrachromosomal double-strand break repair can be coupled to the repair of chromosomal double-strand breaks in mammalian cells. Chromosoma. 111: 304-12. PMID 12474059 DOI: 10.1007/S00412-002-0212-6 |
0.408 |
|
| 2002 |
Rochette PJ, Bastien N, McKay BC, Therrien JP, Drobetsky EA, Drouin R. Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair. Oncogene. 21: 5743-52. PMID 12173044 DOI: 10.1038/Sj.Onc.1205641 |
0.344 |
|
| 2001 |
Cloutier JF, Drouin R, Weinfeld M, O'Connor TR, Castonguay A. Characterization and mapping of DNA damage induced by reactive metabolites of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) at nucleotide resolution in human genomic DNA. Journal of Molecular Biology. 313: 539-57. PMID 11676538 DOI: 10.1006/Jmbi.2001.4997 |
0.304 |
|
| 2001 |
Angers M, Cloutier JF, Castonguay A, Drouin R. Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols. Nucleic Acids Research. 29: E83. PMID 11504891 DOI: 10.1093/Nar/29.16.E83 |
0.301 |
|
| 2001 |
Yan J, Zhang XX, Fetni R, Drouin R. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses. A study of 54 cases with hematological disorders Cancer Genetics and Cytogenetics. 125: 30-40. PMID 11297765 DOI: 10.1016/S0165-4608(00)00355-1 |
0.387 |
|
| 2001 |
Yan J, Marceau D, Drouin R. Tetrasomy 8 is associated with a major cellular proliferative advantage and a poor prognosistwo cases of myeloid hematologic disorders and review of the literature Cancer Genetics and Cytogenetics. 125: 14-20. PMID 11297762 DOI: 10.1016/S0165-4608(00)00352-6 |
0.392 |
|
| 2000 |
Yan J, Bronsard M, Drouin R. Creating a new color by omission of 3′ end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique Chromosoma. 109: 565-570. PMID 11305789 DOI: 10.1007/S004120000111 |
0.389 |
|
| 2000 |
Yan J, Guilbault E, Massé J, Bronsard M, DeGrandpré P, Forest JC, Drouin R. Optimization of the fluorescence in situ hybridization (FISH) technique for high detection efficiency of very small proportions of target interphase nuclei Clinical Genetics. 58: 309-318. PMID 11076056 DOI: 10.1034/J.1399-0004.2000.580409.X |
0.356 |
|
| 2000 |
Wang CS, Goulet F, Lavoie J, Drouin RE, Auger F, Champetier S, Germain L, Têtu B. Establishment and characterization of a new cell line derived from a human primary breast carcinoma Cancer Genetics and Cytogenetics. 120: 58-72. PMID 10913678 DOI: 10.1016/S0165-4608(99)00253-8 |
0.346 |
|
| 2000 |
Angers M, Drouin R, Bachvarova M, Paradis I, Marceau F, Bachvarov DR. In vivo protein-DNA interactions at the kinin B1 receptor gene promoter: No modification on interleukin-1 beta or lipopolysaccharide induction Journal of Cellular Biochemistry. 78: 278-296. PMID 10842322 DOI: 10.1002/(Sici)1097-4644(20000801)78:2<278::Aid-Jcb10>3.0.Co;2-F |
0.309 |
|
| 1999 |
Therrien JP, Drouin R, Baril C, Drobetsky EA. Human cells compromised for p53 function exhibit defective global and transcription-coupled nucleotide excision repair, whereas cells compromised for pRb function are defective only in global repair Proceedings of the National Academy of Sciences of the United States of America. 96: 15038-15043. PMID 10611334 DOI: 10.1073/Pnas.96.26.15038 |
0.3 |
|
| 1999 |
Akoum A, Lavoie J, Drouin R, Jolicoeur C, Lemay A, Maheux R, Khandjian EW. Physiological and cytogenetic characterization of immortalized human endometriotic cells containing episomal simian virus 40 DNA. The American Journal of Pathology. 154: 1245-57. PMID 10233862 DOI: 10.1016/S0002-9440(10)65376-X |
0.353 |
|
| 1997 |
Drouin R, Therrien JP. UVB-induced Cyclobutane Pyrimidine Dimer Frequency Correlates with Skin Cancer Mutational Hotspots in p53 Photochemistry and Photobiology. 66: 719-726. PMID 9383997 DOI: 10.1111/J.1751-1097.1997.Tb03213.X |
0.307 |
|
| 1997 |
Drouin R, Boutouil M, Fetni R, Holmquist GP, Scott P, Richer CL, Lemieux N. DNA replication asynchrony between the paternal and maternal alleles of imprinted genes does not straddle the R/G transition Chromosoma. 106: 405-411. PMID 9362549 DOI: 10.1007/S004120050262 |
0.343 |
|
| 1991 |
Fetni R, Drouin R, Lemieux N, Messier PE, Richer CL. Simultaneous visualization of chromosome bands and hybridization signal using colloidal-gold labeling in electron microscopy Proceedings of the National Academy of Sciences of the United States of America. 88: 10916-10920. PMID 1961763 DOI: 10.1073/Pnas.88.23.10916 |
0.367 |
|
| 1989 |
Messier PE, Drouin R, Richer CL. Electron microscopy of gold-labeled human and equine chromosomes Journal of Histochemistry and Cytochemistry. 37: 1443-1447. PMID 2768813 DOI: 10.1177/37.9.2768813 |
0.399 |
|
| 1989 |
Qu J, Dallaire L, Lemieux N, Drouin R, Richer CL. Synchronization of amniotic fluid cells for high resolution cytogenetics Prenatal Diagnosis. 9: 49-56. PMID 2748550 DOI: 10.1002/Pd.1970090107 |
0.349 |
|
| 1987 |
Romagnano A, Drouin R, Richer CL. Idiograms of horse chromosomes at prometaphase, early metaphase, and midmetaphase after R-banding by BrdU incorporation followed by the fluorochrome-photolysis-Giemsa technique Genome / National Research Council Canada = Genome / Conseil National De Recherches Canada. 29: 674-679. PMID 3666451 DOI: 10.1139/G87-113 |
0.359 |
|
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