| Year |
Citation |
Score |
| 2020 |
Douma Z, Dallel M, Bahia W, Ben Salem A, Hachani Ben Ali F, Almawi WY, Lautier C, Haydar S, Grigorescu F, Mahjoub T. Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia. Gene. 144560. PMID 32169631 DOI: 10.1016/j.gene.2020.144560 |
0.395 |
|
| 2019 |
Haydar S, Grigorescu F, Vintilă M, Cogne Y, Lautier C, Tutuncu Y, Brun JF, Robine JM, Pugeat M, Normand C, Poucheret P, Gheorghiu ML, Georgescu C, Badiu C, Băculescu N, et al. Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation. Plos One. 14: e0214122. PMID 30913280 DOI: 10.1371/journal.pone.0214122 |
0.378 |
|
| 2019 |
HAYDAR S, LAUTIER C, GRIGORESCU F. 1702-P: Fine-Scale Haplotype Mapping of PPM1K Gene Reveals New Genetic Markers for the Study of Insulin Resistance at Clinical Scale Diabetes. 68: 1702-P. DOI: 10.2337/Db19-1702-P |
0.479 |
|
| 2018 |
HAYDAR S, GRIGORESCU F, LAUTIER C, NORMAND C, HADI JC, VINTILA M, GHEORGHIU M, FOUNTAS A, TSATSOULIS A, COPOLA A, LAURO D, YLLI D, YLLI A, BRUGNARA L, HANZU F, et al. Association of ATF5 Gene with Metabolic Syndrome and Insulin Resistance in Mediterranean Populations Diabetes. 67: 2410-PUB. DOI: 10.2337/Db18-2410-Pub |
0.493 |
|
| 2018 |
Douma Z, Haydar S, Dallel M, Ben Salem A, Ben Lamine L, Sellami N, Hadi J, Hachani Ben Ali F, Lautier C, Pugeat M, Mahjoub T, Grigorescu F. L’amélioration du signal d’association du gène LHCGR au syndrome des ovaires polykystiques par une étude comparative de deux populations française et tunisienne Annales D'Endocrinologie. 79: 253. DOI: 10.1016/j.ando.2018.06.165 |
0.347 |
|
| 2017 |
Kefi R, Hechmi M, Dallali H, Elouej S, Jmel H, Halima YB, Nagara M, Chargui M, Fadhel SB, Romdhane S, Kamoun I, Turki Z, Abid A, Bahri S, Bahlous A, ... ... Grigorescu F, et al. Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population. Annales D'Endocrinologie. PMID 28624160 DOI: 10.1016/J.Ando.2017.01.005 |
0.472 |
|
| 2017 |
Ilie M, Haydar S, Baculescu N, Vintila M, Gheorghiu M, Lautier C, Normand C, Poiana C, Badiu C, Pugeat M, Grigorescu F. Les gènes intervenant dans l’homéostasie du zinc sont impliqués dans les altérations cliniques et biologiques du syndrome des ovaires polykystiques Annales D'Endocrinologie. 78: 239. DOI: 10.1016/j.ando.2017.07.255 |
0.344 |
|
| 2016 |
Auguštin DH, Šarac J, Novokmet N, Khusnutdinova E, Litvinov S, Haydar S, Lautier C, Normand C, Attaoua R, Vintila M, Bosch-Comas A, Jares P, Gomis R, Missoni S, Marjanović D, ... Grigorescu F, et al. Diversity of Y-chromosomal and mtDNA Markers Included in Mediscope Chip within Two Albanian Subpopulations from Croatia and Kosovo: Preliminary Data. Collegium Antropologicum. 40: 195-8. PMID 29139639 |
0.669 |
|
| 2016 |
Elouej S, Rejeb I, Attaoua R, Nagara M, Sallem OK, Kamoun I, Chargui M, Jamoussi H, Turki Z, Abid A, Slama CB, Bahri S, Romdhane HB, Abdelhak S, Kefi R, ... Grigorescu F, et al. Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population. Endocrine Research. 1-10. PMID 26905813 DOI: 10.3109/07435800.2016.1141945 |
0.743 |
|
| 2016 |
Elouej S, Belfki-Benali H, Nagara M, Lasram K, Attaoua R, Sallem OK, Kamoun I, Chargui M, Romdhane L, Jamoussi H, Turki Z, Abid A, Ben Slama C, Bahri S, Abdelhak S, ... Grigorescu F, et al. Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome. Metabolic Syndrome and Related Disorders. 14: 121-8. PMID 26741700 DOI: 10.1089/Met.2015.0090 |
0.756 |
|
| 2016 |
Elouej S, Nagara M, Attaoua R, Sallem OK, Rejeb I, Hsouna S, Lasram K, Halim NB, Chargui M, Jamoussi H, Turki Z, Kamoun I, Belfki-Benali H, Abid A, Slama CB, ... ... Grigorescu F, et al. Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population. Journal of Diabetes and Its Complications. 30: 206-11. PMID 26700404 DOI: 10.1016/J.Jdiacomp.2015.11.013 |
0.762 |
|
| 2016 |
Ajina M, Kacem O, Salem AB, Sallem A, Poucheret P, Vintila M, Grigorescu F, Mahjoub T, Saad A. PP-013 - Common polymorphisms of calpin-10 and the risk of polycystic ovary syndrome in a Tunisian population Reproductive Biomedicine Online. 32: S7. DOI: 10.1016/S1472-6483(16)30148-1 |
0.44 |
|
| 2016 |
Elouej S, Belfki-Benali H, Nagara M, Attaoua R, Sallem O, Kamoun I, Chargui M, Romdhane L, Jamoussi H, Turki Z, Abid A, Ben Slama C, Bahri S, Abdelhak S, Grigorescu F, et al. CO-13: Association du gène FTO au syndrome métabolique ou à ses composantes chez la population tunisienne Diabetes & Metabolism. 42: A4. DOI: 10.1016/S1262-3636(16)30031-3 |
0.769 |
|
| 2015 |
Attaoua R, Boeckler N, Radian S, Ait El Mkadem S, Poucheret P, Latapie V, Gheorghiu M, Fica S, Vintila M, Normand C, Coculescu M, Grigorescu F. Dense mapping of the region of insulin gene VNTR in polycystic ovary syndrome in a population of women from Central Europe. Endokrynologia Polska. 66: 198-206. PMID 26136127 DOI: 10.5603/Ep.2015.0026 |
0.736 |
|
| 2015 |
Ben Salem A, Attaoua R, Mtiraoui N, Meddeb S, Kacem O, Ajina M, Souissi M, Poucheret P, Normand C, Mahjoub T, Grigorescu F. Haplotyping strategy highlights the specificity of FTO gene association with polycystic ovary syndrome in Tunisian women population. Gene. 565: 166-70. PMID 25498334 DOI: 10.1016/J.Gene.2014.12.004 |
0.767 |
|
| 2015 |
Elouej S, Nagara M, Attaoua R, Sallem OK, Rejeb I, Hsouna S, Lasram K, Halim NB, Chargui M, Jamoussi H, Turki Z, Kamoun I, Belfki-Benali H, Abid A, Slama CB, ... ... Grigorescu F, et al. Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population Journal of Diabetes and Its Complications. DOI: 10.1016/j.jdiacomp.2015.11.013 |
0.741 |
|
| 2015 |
Haydar S, Attaoua R, Baculescu N, Coculescu M, Vintila M, Ben Salem A, Normand C, Grigorescu F. Association du gène isovaleryl-CoA dehydrogenase (IVD) avec les altérations métaboliques dans le syndrome des ovaires polykystiques permet une meilleure compréhension du rôle des aminoacides branchés dans l’insulinorésistance Annales D'Endocrinologie. 76: 348. DOI: 10.1016/j.ando.2015.07.155 |
0.739 |
|
| 2014 |
Ben Salem A, Attaoua R, Mtiraoui N, Belkahla S, Ezzidi I, Ajina M, Souissi M, Poucheret P, Vintila M, Grigorescu F, Mahjoub T. Common polymorphisms of calpain-10 and the risk of polycystic ovary syndrome in Tunisian population: a case-control study. Molecular Biology Reports. 41: 6569-74. PMID 24993116 DOI: 10.1007/S11033-014-3540-8 |
0.768 |
|
| 2014 |
Ben Salem A, Attaoua R, Ajina M, Suissi M, Mahjoub T, Grigorescu F. P135 Association du gène FTO à l’obésité dans le SOPK dans une population de femmes de Tunisie via un marquage génétique informatif sur les populations africaines pour une meilleure compréhension de l’association génétique aux maladies métaboliques complexes Diabetes & Metabolism. 40: A61. DOI: 10.1016/S1262-3636(14)72427-9 |
0.77 |
|
| 2014 |
Attaoua R, Grigorescu F, Baculescu N, Ben Salem A, Fakih D, Poucheret P, Radian S, Normand C, Coculescu M. P130 Le gène DUSP9 (dual specificity phosphatase 9) s’associe à l’obésité et à la forme la plus sévère du syndrome des ovaires polykystiques avec Acanthosis nigricans Diabetes & Metabolism. 40: A60. DOI: 10.1016/S1262-3636(14)72422-X |
0.77 |
|
| 2014 |
Douaibia L, Attaoua R, Makrelouf M, Otmane A, Boukli A, Zenati A, Grigorescu F. O34 Association des gènes FTO et CRP au syndrome métabolique (SMet) ou à ses composantes dans la population d’Algérie dans la perspective des études du programme MEDIGENE dans la Méditerranée Diabetes & Metabolism. 40: A9. DOI: 10.1016/S1262-3636(14)72208-6 |
0.745 |
|
| 2013 |
Attaoua R, Huguin A, Poucheret P, Baculescu N, Radian S, Coculescu M, Grigorescu F. PO31 Cartographie génétique dense du locus FTO indique l’association du gène au syndrome des ovaires polykystiques Diabetes & Metabolism. 39: A28. DOI: 10.1016/S1262-3636(13)71727-0 |
0.779 |
|
| 2012 |
Wojciechowski P, Lipowska A, Rys P, Ewens KG, Franks S, Tan S, Lerchbaum E, Vcelak J, Attaoua R, Straczkowski M, Azziz R, Barber TM, Hinney A, Obermayer-Pietsch B, Lukasova P, ... ... Grigorescu F, et al. Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome: a systematic review and meta-analysis. Diabetologia. 55: 2636-45. PMID 22801903 DOI: 10.1007/S00125-012-2638-6 |
0.754 |
|
| 2012 |
Pouplard C, Cornillet-Lefebvre P, Attaoua R, Leroux D, Lecocq-Lafon C, Rollin J, Grigorescu F, Nguyen P, Gruel Y. Interleukin-10 promoter microsatellite polymorphisms influence the immune response to heparin and the risk of heparin-induced thrombocytopenia. Thrombosis Research. 129: 465-9. PMID 22239992 DOI: 10.1182/Blood.V116.21.3682.3682 |
0.717 |
|
| 2010 |
Hanzu FA, Radian S, Attaoua R, Ait-El-Mkadem S, Fica S, Gheorghiu M, Coculescu M, Grigorescu F. Association of insulin receptor genetic variants with polycystic ovary syndrome in a population of women from Central Europe. Fertility and Sterility. 94: 2389-92. PMID 20493471 DOI: 10.1016/J.Fertnstert.2010.04.029 |
0.782 |
|
| 2010 |
Ait El Mkadem S, Bannwarth S, Attaoua R, Grigorescu F, Dubois N, Mutz S, Chafino B, Vialettes B, Paquis-Flucklinger V. O11 La cartographie des SNP du gène WFS1 révèle son rôle dans le diabète de type 2 associé à une surdité neurosensorielle dans la population française Diabetes & Metabolism. 36: A3. DOI: 10.1016/S1262-3636(10)70015-X |
0.755 |
|
| 2009 |
Attaoua R, Ait El Mkadem S, Lautier C, Kaouache S, Renard E, Brun JF, Fedou C, Gris JC, Bringer J, Grigorescu F. Association of the FTO gene with obesity and the metabolic syndrome is independent of the IRS-2 gene in the female population of Southern France. Diabetes & Metabolism. 35: 476-83. PMID 19818665 DOI: 10.1016/J.Diabet.2009.07.002 |
0.734 |
|
| 2008 |
Attaoua R, Ait El Mkadem S, Radian S, Fica S, Hanzu F, Albu A, Gheorghiu M, Coculescu M, Grigorescu F. FTO gene associates to metabolic syndrome in women with polycystic ovary syndrome. Biochemical and Biophysical Research Communications. 373: 230-4. PMID 18572014 DOI: 10.1016/J.Bbrc.2008.06.039 |
0.769 |
|
| 2008 |
Attaoua R, Ait El Mkadem S, Radian S, Hanzu F, Fica S, Coculesu M, Grigorescu F. O101 Découverte de l’association du gène FTO avec le SOPK et la résistance à l’insuline dans une population d’Europe Centrale Diabetes & Metabolism. 34: H42. DOI: 10.1016/S1262-3636(08)72911-2 |
0.759 |
|
| 2008 |
Ait El Mkadem S, Attaoua R, Poucheret P, Brichard S, Grigorescu F. O16 Effet protecteur de l’adiponectine contre le diabète expérimental chez la souris transgénique Diabetes & Metabolism. 34: H13-H14. DOI: 10.1016/S1262-3636(08)72826-X |
0.722 |
|
| 2003 |
Lautier C, El Mkadem SA, Renard E, Brun JF, Gris JC, Bringer J, Grigorescu F. Complex haplotypes of IRS2 gene are associated with severe obesity and reveal heterogeneity in the effect of Gly1057Asp mutation. Human Genetics. 113: 34-43. PMID 12687350 DOI: 10.1007/S00439-003-0935-3 |
0.426 |
|
| 2002 |
Van Maldergem L, Magré J, Khallouf TE, Gedde-Dahl T, Delépine M, Trygstad O, Seemanova E, Stephenson T, Albott CS, Bonnici F, Panz VR, Medina JL, Bogalho P, Huet F, Savasta S, ... ... Grigorescu F, et al. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. Journal of Medical Genetics. 39: 722-33. PMID 12362029 DOI: 10.1136/Jmg.39.10.722 |
0.327 |
|
| 2001 |
El Mkadem SA, Lautier C, Macari F, Molinari N, Lefèbvre P, Renard E, Gris JC, Cros G, Daurès JP, Bringer J, White MF, Grigorescu F. Role of allelic variants Gly972Arg of IRS-1 and Gly1057Asp of IRS-2 in moderate-to-severe insulin resistance of women with polycystic ovary syndrome. Diabetes. 50: 2164-8. PMID 11522686 DOI: 10.2337/Diabetes.50.9.2164 |
0.362 |
|
| 2001 |
Magré J, Delépine M, Khallouf E, Gedde-Dahl T, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, ... ... Grigorescu F, et al. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nature Genetics. 28: 365-70. PMID 11479539 DOI: 10.1038/Ng585 |
0.306 |
|
| 2000 |
Rasmussen SK, Lautier C, Hansen L, Echwald SM, Hansen T, Ekstrøm CT, Urhammer SA, Borch-Johnsen K, Grigorescu F, Smith RJ, Pedersen O. Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus Journal of Clinical Endocrinology and Metabolism. 85: 1606-1610. PMID 10770205 DOI: 10.1210/Jcem.85.4.6494 |
0.364 |
|
| 2000 |
Grigorescu F, Lautier C, Mkadem SAE, Macari F, Brun J, Gris J, Guttierez J, Cros G, Mercier J, Bringer J, Jaffiol C. Gly1057Asp allelic variant of IRS-2 gene has synergistic effect with Gly972Arg variant of IRS-1 on insulin secretion in obesity and NIDDM Diabetes Research and Clinical Practice. 50: 226. DOI: 10.1016/S0168-8227(00)82228-7 |
0.401 |
|
| 1999 |
Macari F, Lautier C, Girardet A, Dadoun F, Darmon P, Dutour A, Renard E, Bouvagnet P, Claustres M, Oliver C, Grigorescu F. Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family. Human Genetics. 103: 658-61. PMID 9921899 DOI: 10.1007/S004390050887 |
0.418 |
|
| 1997 |
Rouard M, Macari F, Bouix O, Lautier C, Brun JF, Lefebvre P, Renard E, Bringer J, Jaffiol C, Grigorescu F. Identification of two novel insulin receptor mutations, Asp59Gly and Leu62Pro, in type A syndrome of extreme insulin resistance. Biochemical and Biophysical Research Communications. 234: 764-8. PMID 9175790 DOI: 10.1006/Bbrc.1997.6695 |
0.323 |
|
| 1994 |
Moller DE, Cohen O, Yamaguchi Y, Assiz R, Grigorescu F, Eberle A, Morrow LA, Moses AC, Flier JS. Prevalence of mutations in the insulin receptor gene in subjects with features of the type A syndrome of insulin resistance. Diabetes. 43: 247-55. PMID 8288049 DOI: 10.2337/Diab.43.2.247 |
0.392 |
|
| 1993 |
Bringer J, Lefebvre P, Boulet F, Grigorescu F, Renard E, Hedon B, Orsetti A, Jaffiol C. Body composition and regional fat distribution in polycystic ovarian syndrome. Relationship to hormonal and metabolic profiles. Annals of the New York Academy of Sciences. 687: 115-23. PMID 8323166 DOI: 10.1111/J.1749-6632.1993.Tb43860.X |
0.334 |
|
| 1987 |
Grigorescu F, Herzberg V, King G, Meistas M, Elders J, Frazer T, Kahn CR. Defects in insulin binding and autophosphorylation of erythrocyte insulin receptors in patients with syndromes of severe insulin resistance and their parents. The Journal of Clinical Endocrinology and Metabolism. 64: 549-56. PMID 3029156 DOI: 10.1210/Jcem-64-3-549 |
0.306 |
|
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