| Year |
Citation |
Score |
| 2011 |
Beaulieu Bergeron M, Brochu P, Lemyre E, Lemieux N. Correlation of intercentromeric distance, mosaicism, and sexual phenotype: molecular localization of breakpoints in isodicentric Y chromosomes. American Journal of Medical Genetics. Part A. 155: 2705-12. PMID 21964771 DOI: 10.1002/Ajmg.A.34260 |
0.52 |
|
| 2011 |
Beaulieu Bergeron M, Lemieux N, Brochu P. Undifferentiated gonadal tissue, Y chromosome instability, and tumors in XY gonadal dysgenesis. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 14: 445-59. PMID 21692598 DOI: 10.2350/11-01-0960-Oa.1 |
0.46 |
|
| 2011 |
Beaulieu Bergeron M, Lemyre E, Lemieux N. Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development. Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation. 5: 1-6. PMID 21088380 DOI: 10.1159/000321995 |
0.515 |
|
| 2010 |
Fortin F, Anghel T, Brochu P, Lemieux N. Optimizing urothelial cell preparation for the human urinary micronucleus assay. Toxicology in Vitro : An International Journal Published in Association With Bibra. 24: 1821-7. PMID 20580813 DOI: 10.1016/J.Tiv.2010.05.011 |
0.684 |
|
| 2010 |
Beaulieu Bergeron M, Soglio DB, Maietta A, Fournet JC, Blumenkrantz M, Brochu P, Lemieux N. Coexistence of a choriocarcinoma and a gonadoblastoma in the gonad of a 46,XY female: a single nucleotide polymorphism array analysis. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 13: 66-71. PMID 19425818 DOI: 10.2350/09-02-0606-Cr.1 |
0.464 |
|
| 2009 |
Fortin F, Beaulieu Bergeron M, Fetni R, Lemieux N. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities. Cytogenetic and Genome Research. 125: 176-85. PMID 19738378 DOI: 10.1159/000230002 |
0.727 |
|
| 2009 |
Labuda M, Lemieux N, Tihy F, Prinster C, Glorieux FH. Human 25-hydroxyvitamin D 24-hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D-deficient rickets Journal of Bone and Mineral Research. 8: 1397-1406. PMID 8266831 DOI: 10.1002/Jbmr.5650081114 |
0.424 |
|
| 2006 |
DesGroseilliers M, Fortin F, Lafrenière AM, Brochu P, Lemyre E, Lemieux N. Dynamic increase of a 45,X cell line in a patient with multicentric ring Y chromosomes. Cytogenetic and Genome Research. 115: 90-3. PMID 16974088 DOI: 10.1159/000094805 |
0.736 |
|
| 2006 |
DesGroseilliers M, Beaulieu Bergeron M, Brochu P, Lemyre E, Lemieux N. Phenotypic variability in isodicentric Y patients: study of nine cases. Clinical Genetics. 70: 145-50. PMID 16879197 DOI: 10.1111/J.1399-0004.2006.00654.X |
0.472 |
|
| 2006 |
Beaulieu Bergeron M, Tran-Thanh D, Fournet JC, Lemyre E, Lemieux N, Bouron-Dal Soglio D. Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetus. American Journal of Medical Genetics. Part A. 140: 1768-72. PMID 16835917 DOI: 10.1002/Ajmg.A.31338 |
0.438 |
|
| 2006 |
Depault F, Cojocaru M, Fortin F, Chakrabarti S, Lemieux N. Genotoxic effects of chromium(VI) and cadmium(II) in human blood lymphocytes using the electron microscopy in situ end-labeling (EM-ISEL) assay. Toxicology in Vitro : An International Journal Published in Association With Bibra. 20: 513-8. PMID 16278061 DOI: 10.1016/J.Tiv.2005.09.003 |
0.692 |
|
| 2006 |
DesGroseilliers M, Fortin F, Lemyre E, Lemieux N. Complex mosaicism in sex reversed SRY+ male twins. Cytogenetic and Genome Research. 112: 176-9. PMID 16276109 DOI: 10.1159/000087532 |
0.704 |
|
| 2005 |
M'Bemba-Meka P, Lemieux N, Chakrabarti SK. Nickel compound-induced DNA single-strand breaks in chromosomal and nuclear chromatin in human blood lymphocytes in vitro: role of oxidative stress and intracellular calcium. Mutation Research. 586: 124-37. PMID 16099703 DOI: 10.1016/J.Mrgentox.2005.06.001 |
0.422 |
|
| 2003 |
Dubé S, Fetni R, Hazourli S, Champagne M, Lemieux N. Rearrangement of the MLL gene and a region proximal to the RARalpha gene in a case of acute myelocytic leukemia M5 with a t(11;17)(q23;q21). Cancer Genetics and Cytogenetics. 145: 54-9. PMID 12885463 DOI: 10.1016/S0165-4608(03)00056-6 |
0.385 |
|
| 2002 |
DesGroseilliers M, Lemyre E, Dallaire L, Lemieux N. Tetrasomy Y by structural rearrangement: clinical report. American Journal of Medical Genetics. 111: 401-4. PMID 12210299 DOI: 10.1002/Ajmg.10591 |
0.545 |
|
| 2001 |
Bonvouloir N, Lemieux N, Crine P, Boileau G, DesGroseillers L. Molecular cloning, tissue distribution, and chromosomal localization of MMEL2, a gene coding for a novel human member of the neutral endopeptidase-24.11 family Dna and Cell Biology. 20: 493-498. PMID 11560781 DOI: 10.1089/104454901316976127 |
0.313 |
|
| 2000 |
Tihy F, Lemyre E, Dallaire L, Lemieux N. Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p. American Journal of Medical Genetics. 91: 383-6. PMID 10767003 DOI: 10.1002/(Sici)1096-8628(20000424)91:5<383::Aid-Ajmg12>3.0.Co;2-G |
0.473 |
|
| 1999 |
Tihy F, Lemyre E, Lemieux N, Dallaire L. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype. American Journal of Medical Genetics. 87: 302-5. PMID 10588834 DOI: 10.1002/(Sici)1096-8628(19991203)87:4<302::Aid-Ajmg4>3.0.Co;2-D |
0.418 |
|
| 1999 |
Bossolasco M, Lebel M, Lemieux N, Mes-Masson AM. The human TDE gene homologue: localization to 20q13.1-13.3 and variable expression in human tumor cell lines and tissue. Molecular Carcinogenesis. 26: 189-200. PMID 10559794 DOI: 10.1002/(Sici)1098-2744(199911)26:3<189::Aid-Mc8>3.0.Co;2-T |
0.356 |
|
| 1999 |
Milot J, Michaud J, Lemieux N, Allaire G, Gagnon MM. Persistent hyperplastic primary vitreous with retinal tumor in tuberous sclerosis: report of a case including tumoral immunohistochemistry and cytogenetic analyses. Ophthalmology. 106: 630-4. PMID 10080226 DOI: 10.1016/S0161-6420(99)90128-8 |
0.352 |
|
| 1999 |
Fetni R, Scott P, Tihy F, Richer C, Lemieux N. Increased Resolution Of In Situ Hybridization Signal By Electron Microscopy : A Comparison With Fluorescence Microscopy Genome. 42: 1001-1007. DOI: 10.1139/G99-071 |
0.347 |
|
| 1998 |
Tihy F, Scott P, Russo P, Champagne M, Tabet JC, Lemieux N. Cytogenetic analysis of a parachordoma. Cancer Genetics and Cytogenetics. 105: 14-9. PMID 9689924 DOI: 10.1016/S0165-4608(97)00481-0 |
0.498 |
|
| 1998 |
Lemyre E, Lemieux N, Décarie JC, Lambert M. Del(14)(q22.1q23.2) in a patient with anophthalmia and pituitary hypoplasia. American Journal of Medical Genetics. 77: 162-5. PMID 9605291 DOI: 10.1002/(Sici)1096-8628(19980501)77:2<162::Aid-Ajmg10>3.0.Co;2-L |
0.416 |
|
| 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 |
0.389 |
|
| 1997 |
Fetni R, Richer CL, Malfoy B, Dutrillaux B, Lemieux N. Cytologic characterization of two distinct alpha satellite DNA domains on human chromosome 7, using double-labeling hybridizations in fluorescence and electron microscopy on a melanoma cell line. Cancer Genetics and Cytogenetics. 96: 17-22. PMID 9209464 DOI: 10.1016/S0165-4608(96)00282-8 |
0.495 |
|
| 1997 |
Kos CH, Tihy F, Murer H, Lemieux N, Tenenhouse HS. Comparative mapping of Na+-phosphate cotransporter genes, NPT1 and NPT2, in human and rabbit. Cytogenetics and Cell Genetics. 75: 22-4. PMID 8995482 DOI: 10.1159/000134449 |
0.491 |
|
| 1996 |
Fetni R, Drouin R, Richer CL, Lemieux N. Complementary replication R- and G-band patterns induced by cell blocking at the R-band/G-band transition, a possible regulatory checkpoint within the S phase of the cell cycle Cytogenetics and Cell Genetics. 75: 172-179. PMID 9040787 DOI: 10.1159/000134472 |
0.308 |
|
| 1996 |
DesGroseillers L, Lemieux N. Localization of a human double-stranded RNA-binding protein gene (STAU) to band 20q13.1 by fluorescence in situ hybridization Genomics. 36: 527-529. PMID 8884277 DOI: 10.1006/Geno.1996.0499 |
0.369 |
|
| 1996 |
Sévigny G, Lemieux N, Steyaert A, Bibor-Hardy V. Structure of the gene coding for the mouse TRiC-P5 subunit of the cytosolic chaperonin TRiC. Genomics. 31: 107-110. PMID 8808286 DOI: 10.1006/Geno.1996.0015 |
0.328 |
|
| 1996 |
Lemieux N, Apiou F, Vogt N, Malfoy B, Dutrillaux B. Structural heterogeneity of hsr(11) in the MDA-MB-134 mammary carcinoma cell line. Cancer Genetics and Cytogenetics. 90: 75-79. PMID 8780752 DOI: 10.1016/0165-4608(96)00061-1 |
0.505 |
|
| 1996 |
Fetni R, Krabchi K, Messier P, Richer C, Lemieux N. Characterization by fluorescence and electron microscopy in situ hybridization of a double Y isochromosome American Journal of Medical Genetics. 63: 454-457. PMID 8737651 DOI: 10.1002/(Sici)1096-8628(19960614)63:3<454::Aid-Ajmg7>3.0.Co;2-R |
0.542 |
|
| 1996 |
Boutouil M, Fetni R, Qu J, Dallaire L, Richer C, Lemieux N. Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation. Human Genetics. 98: 323-327. PMID 8707303 DOI: 10.1007/S004390050216 |
0.496 |
|
| 1996 |
Tihy F, Lemieux N, Lombard M, Dutrillaux B. Comparative RB1 gene mapping in Homo sapiens, Pithecia pithecia, Macaca sylvana, and Cercopithecus aethiops tantalus Cytogenetic and Genome Research. 72: 9-11. PMID 8565644 DOI: 10.1159/000134151 |
0.473 |
|
| 1995 |
Lemieux N, Zhang XX, Dufort D, Nepveu A. Assignment of the human homologue of the Drosophila Cut homeobox gene (CUTL1) to band 7q22 by fluorescence in situ hybridization. Genomics. 24: 191-3. PMID 7896281 DOI: 10.1006/Geno.1994.1603 |
0.406 |
|
| 1995 |
Lebeau J, Gerbault-Seureau M, Lemieux N, Apiou F, Calvo F, Berthon P, Goubin G, Dutrillaux B. Loss of chromosome 3p arm differentiating tumorigenic from non-tumorigenic cells derived from the same SV40-transformed human mammary epithelial cells. International Journal of Cancer. 60: 244-8. PMID 7829223 DOI: 10.1002/Ijc.2910600219 |
0.476 |
|
| 1994 |
Kos CH, Tihy F, Econs MJ, Murer H, Lemieux N, Tenenhouse HS. Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35. Genomics. 19: 176-7. PMID 8188224 DOI: 10.1006/Geno.1994.1034 |
0.308 |
|
| 1994 |
Tihy F, Vogt N, Recan D, Malfoy B, Coquet M, Serville F, Fontan D, Guillard J, Kaplan J, Dutrillaux B, Lemieux N. Skewed inactivation of an X chromosome deleted at thé dystrophin gène in an asymptomatic mother and her affected daughter Human Genetics. 93: 563-567. PMID 8168835 DOI: 10.1007/Bf00202824 |
0.53 |
|
| 1994 |
Sevigny G, Joly EC, Bibor-Hardy V, Lemieux N. Assignment of the human homologue of the mTRiC-P5 gene (TRIC5) to band 1q23 by fluorescence in situ hybridization Genomics. 22: 634-636. PMID 8001976 DOI: 10.1006/Geno.1994.1438 |
0.447 |
|
| 1993 |
Lemieux N, Malfoy B, Forrest GL. Human Carbonyl Reductase (CBR) Localized to Band 21q22.1 by High-Resolution Fluorescence in Situ Hybridization Displays Gene Dosage Effects in Trisomy 21 Cells Genomics. 15: 169-172. PMID 8432528 DOI: 10.1006/Geno.1993.1024 |
0.4 |
|
| 1992 |
Fetni R, Lemieux N, Malfoy B, Dutrillaux B, Messier P-, Richer C-. Detection of small, single-copy genes on protein-G-banded chromosomes by electron microscopy. Cytogenetic and Genome Research. 60: 187-189. PMID 1505213 DOI: 10.1159/000133332 |
0.435 |
|
| 1992 |
Hoffschir F, Ricoul M, Lemieux N, Estrade S, Cassingena R, Dutrillaux B. Jumping translocations originate clonal rearrangements in SV40-transformed human fibroblasts. International Journal of Cancer. 52: 130-6. PMID 1323537 DOI: 10.1002/ijc.2910520123 |
0.36 |
|
| 1992 |
Lemieux N, Malfoy B, Fetni R, Muleris M, Vogt N, Richer CL, Dutrillaux B. Metaphase chromosome structure: An in situ hybridization approach at infragenic level Cancer Genetics and Cytogenetics. 63: 105. DOI: 10.1016/0165-4608(92)90393-M |
0.431 |
|
| 1991 |
DROUIN R, LEMIEUX N, RICHER C‐. High‐resolution R‐banding at the 1250‐band level: III. Comparative analysis of morphologic and dynamic R‐band patterns (RHG and RBG) Hereditas. 114: 65-77. PMID 2071451 DOI: 10.1111/J.1601-5223.1991.Tb00554.X |
0.367 |
|
| 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 |
0.438 |
|
| 1991 |
Drouin R, Lemieux N, Richer CL. Chromosome condensation from prophase to late metaphase: Relationship to chromosome bands and their replication time Cytogenetic and Genome Research. 57: 91-99. PMID 1914528 DOI: 10.1159/000133121 |
0.41 |
|
| 1991 |
Kokalj-Vokac N, Saint-Ruf C, Lefrançois D, Viegas-Péquignot E, Lemieux N, Malfoy B, Dutrillaux B. A t(X;15)(q23;q25) with Xq reactivation in a lymphoblastoid cell line from Fanconi anemia. Cytogenetic and Genome Research. 57: 11-15. PMID 1855386 DOI: 10.1159/000133103 |
0.442 |
|
| 1990 |
Lemieux N, Messier PE, Drouin R, Jacob JL, Milot J, Richer CL. Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma Cancer Genetics and Cytogenetics. 48: 265-269. PMID 2397457 DOI: 10.1016/0165-4608(90)90130-3 |
0.424 |
|
| 1990 |
Lemieux N, Drouin R, Richer CL. High-resolution dynamic and morphological G-bandings (GBG and GTG): a comparative study Human Genetics. 85: 261-266. PMID 2394443 DOI: 10.1007/Bf00206742 |
0.301 |
|
| 1990 |
Lemieux N, Richer C. Chromosome evolution and high-resolution analysis of leucocytes, bone marrow, and tumor cells of retinoblastoma patients. American Journal of Medical Genetics. 36: 456-462. PMID 2389803 DOI: 10.1002/Ajmg.1320360417 |
0.422 |
|
| 1990 |
Drouin R, Lemieux N, Richer CL. Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution Chromosoma. 99: 273-280. PMID 2209226 DOI: 10.1007/Bf01731703 |
0.422 |
|
| 1989 |
Lemieux N, Milot J, Barsoum-Homsy M, Michaud J, Leung TK, Richer CL. First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13. Cancer Genetics and Cytogenetics. 43: 73-8. PMID 2790775 DOI: 10.1016/0165-4608(89)90129-5 |
0.495 |
|
| 1989 |
Lemieux N, Richer C. Synchronization of cultured retinoblastoma cells for high-resolution chromosomes showing up to 1000 bands. Cancer Genetics and Cytogenetics. 40: 55-63. PMID 2758401 DOI: 10.1016/0165-4608(89)90145-3 |
0.451 |
|
| 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 |
0.42 |
|
| 1989 |
Richer CL, Bleau G, Chapdelaine A, Murer-Orlando M, Lemieux N, Cadotte M. A man with isochromosome Xq Klinefelter syndrome with lack of height increase and normal androgenization American Journal of Medical Genetics. 32: 42-44. PMID 2705482 DOI: 10.1002/Ajmg.1320320110 |
0.335 |
|
| 1987 |
Lemieux N, Richer CL, Jean P. Combined myeloid cell synchronization and chromosome G-banding by bromodeoxyuridine. Cancer Genetics and Cytogenetics. 28: 229-36. PMID 2441850 DOI: 10.1016/0165-4608(87)90208-1 |
0.363 |
|
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