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Items: 34

1.

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.

D'Amours G, Langlois M, Mathonnet G, Fetni R, Nizard S, Srour M, Tihy F, Phillips MS, Michaud JL, Lemyre E.

BMC Med Genomics. 2014 Dec 24;7:70. doi: 10.1186/s12920-014-0070-0.

2.

Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature.

Choi J, Bouron Dal Soglio D, Fortier A, Fetni R, Mathonnet G, Cournoyer S, Lallier M, Isler M, Beaulieu Bergeron M, Patey N.

Histopathology. 2014 Apr;64(5):731-40. doi: 10.1111/his.12317. Epub 2014 Jan 17. Review. Erratum in: Histopathology. 2014 Apr;64(5):758.

PMID:
24433523
3.

Extraosseous Ewing sarcoma with foci of neuroblastoma-like differentiation associated with EWSR1(Ewing sarcoma breakpoint region 1)/FLI1 translocation without prior chemotherapy.

Vali K, Kokta V, Beaunoyer M, Fetni R, Teira P, Sartelet H.

Hum Pathol. 2012 Oct;43(10):1772-6. doi: 10.1016/j.humpath.2012.03.006. Epub 2012 Jun 14.

PMID:
22703924
4.

Genotype analysis of tumor-initiating cells expressing CD133 in neuroblastoma.

Cournoyer S, Nyalendo C, Addioui A, Belounis A, Beaunoyer M, Aumont A, Teira P, Duval M, Fernandes K, Fetni R, Haddad E, Sartelet H.

Genes Chromosomes Cancer. 2012 Aug;51(8):792-804. doi: 10.1002/gcc.21964. Epub 2012 Apr 18.

PMID:
22514116
5.

A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma.

Rougemont AL, Bouron-Dal Soglio D, Patey-Mariaud de Serre N, Fetni R, Fan L, Barrette S, Fournet JC.

Cancer Genet. 2012 Jan-Feb;205(1-2):55-60. doi: 10.1016/j.cancergen.2012.01.007.

PMID:
22429598
6.

CD133 expression is associated with poor outcome in neuroblastoma via chemoresistance mediated by the AKT pathway.

Sartelet H, Imbriglio T, Nyalendo C, Haddad E, Annabi B, Duval M, Fetni R, Victor K, Alexendrov L, Sinnett D, Fabre M, Vassal G.

Histopathology. 2012 Jun;60(7):1144-55. doi: 10.1111/j.1365-2559.2012.04191.x. Epub 2012 Mar 6.

PMID:
22394107
7.

Activation of the phosphatidylinositol 3'-kinase/AKT pathway in neuroblastoma and its regulation by thioredoxin 1.

Sartelet H, Rougemont AL, Fabre M, Castaing M, Duval M, Fetni R, Michiels S, Beaunoyer M, Vassal G.

Hum Pathol. 2011 Nov;42(11):1727-39. doi: 10.1016/j.humpath.2011.01.019.

PMID:
21641013
8.

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

D'Amours G, Kibar Z, Mathonnet G, Fetni R, Tihy F, Désilets V, Nizard S, Michaud JL, Lemyre E.

Clin Genet. 2012 Feb;81(2):128-41. doi: 10.1111/j.1399-0004.2011.01687.x. Epub 2011 May 16.

PMID:
21496010
9.

Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.

Fortin F, Beaulieu Bergeron M, Fetni R, Lemieux N.

Cytogenet Genome Res. 2009;125(3):176-85. doi: 10.1159/000230002. Epub 2009 Sep 4.

PMID:
19738378
10.

SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification.

Bouron-Dal Soglio D, Rougemont AL, Absi R, Barrette S, Montpetit A, Fetni R, Fournet JC.

Hum Pathol. 2009 Sep;40(9):1347-52. doi: 10.1016/j.humpath.2009.01.021. Epub 2009 May 19.

PMID:
19454362
11.

Allelic methylation bias of the RARB2 tumor suppressor gene promoter in cancer.

Pappas JJ, Toulouse A, Hébert J, Fetni R, Bradley WE.

Genes Chromosomes Cancer. 2008 Nov;47(11):978-93. doi: 10.1002/gcc.20603.

PMID:
18663751
12.

Chondroid cystic malformation of the lung with trisomy 8 mosaicism: a new cystic lung malformation.

Bouron-Dal Soglio D, Rougemont AL, De Buys Roessingh AS, Fetni R, Rypens F, Bouchard S, Montpetit A, Fournet JC.

Am J Surg Pathol. 2008 Jul;32(7):1095-100. doi: 10.1097/PAS.0b013e3181676fe7.

PMID:
18520437
13.

A B-cell lymphoma-associated chromosomal translocation in a progressive transformation of germinal center.

Bouron-Dal Soglio D, Truong F, Fetni R, Hazourli S, Champagne J, Oligny LL, Fournet JC.

Hum Pathol. 2008 Feb;39(2):292-7. doi: 10.1016/j.humpath.2007.08.002.

PMID:
18206497
14.

A complex translocation (6;12;8)(q25;q24.3;q13) in a fibrous hamartoma of infancy.

Rougemont AL, Fetni R, Murthy S, Fournet JC.

Cancer Genet Cytogenet. 2006 Dec;171(2):115-8.

PMID:
17116490
15.

Overexpression of PRDM16 in the presence and absence of the RUNX1/PRDM16 fusion gene in myeloid leukemias.

Hazourli S, Chagnon P, Sauvageau M, Fetni R, Busque L, Hébert J.

Genes Chromosomes Cancer. 2006 Nov;45(11):1072-6. No abstract available.

16.

Prenatal cytogenetic assessment and inv(2)(p11.2q13).

Hysert M, Bruyère H, Côté GB, Dawson AJ, Dolling JA, Fetni R, Hrynchak M, Lavoie J, McGowan-Jordan J, Tihy F, Duncan AM.

Prenat Diagn. 2006 Sep;26(9):810-3.

PMID:
16821252
17.

[Dominant negative activity of mutated p53 proteins].

Dridi W, Krabchi K, Gadji M, Lavoie J, Bronsard M, Fetni R, Drouin R.

Med Sci (Paris). 2006 Mar;22(3):301-7. Review. French.

18.

Isolated central nervous system relapse in patients with chronic myeloid leukemia on imatinib mesylate.

Johnson NA, Fetni R, Caplan SN.

Leuk Lymphoma. 2005 Apr;46(4):629-30. No abstract available.

PMID:
16019496
19.

Frequency and phenotypic consequences of the 3199del6 CFTR mutation in French Canadians.

Ruchon AF, Ryan SR, Fetni R, Rozen R, Scott P.

Genet Med. 2005 Mar;7(3):210-1. No abstract available.

PMID:
15775760
20.

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).

Dubé S, Fetni R, Hazourli S, Champagne M, Lemieux N.

Cancer Genet Cytogenet. 2003 Aug;145(1):54-9.

PMID:
12885463
21.
22.

The neuronal apoptosis inhibitory protein is a direct inhibitor of caspases 3 and 7.

Maier JK, Lahoua Z, Gendron NH, Fetni R, Johnston A, Davoodi J, Rasper D, Roy S, Slack RS, Nicholson DW, MacKenzie AE.

J Neurosci. 2002 Mar 15;22(6):2035-43.

24.

Cyclin-dependent kinases as a therapeutic target for stroke.

Osuga H, Osuga S, Wang F, Fetni R, Hogan MJ, Slack RS, Hakim AM, Ikeda JE, Park DS.

Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10254-9.

25.

DNA replication asynchrony between the paternal and maternal alleles of imprinted genes does not straddle the R/G transition.

Drouin R, Boutouil M, Fetni R, Holmquist GP, Scott P, Richer CL, Lemieux N.

Chromosoma. 1997 Nov;106(6):405-11.

PMID:
9362549
26.
28.

Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation.

Boutouil M, Fetni R, Qu J, Dallaire L, Richer CL, Lemieux N.

Hum Genet. 1996 Sep;98(3):323-7.

PMID:
8707303
29.

Characterization by fluorescence and electron microscopy in situ hybridization of a double Y isochromosome.

Fetni R, Krabchi K, Messier PE, Richer CL, Lemieux N.

Am J Med Genet. 1996 Jun 14;63(3):454-7.

PMID:
8737651
31.

In situ hybridization approach at infragenic level on metaphase chromosomes.

Lemieux N, Malfoy B, Fetni R, Muleris M, Vogt N, Richer CL, Dutrillaux B.

Cytogenet Cell Genet. 1994;66(2):107-12.

PMID:
8287680
32.
33.

Detection of small, single-copy genes on protein-G-banded chromosomes by electron microscopy.

Fetni R, Lemieux N, Malfoy B, Dutrillaux B, Messier PE, Richer CL.

Cytogenet Cell Genet. 1992;60(3-4):187-9.

PMID:
1505213
34.

Simultaneous visualization of chromosome bands and hybridization signal using colloidal-gold labeling in electron microscopy.

Fetni R, Drouin R, Lemieux N, Messier PE, Richer CL.

Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10916-20.

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