Pertesi, M: search on Z-Library

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1

High prevalence of BRCA1 founder mutations in Greek breast/ovarian families

Konstantopoulou, I, Tsitlaidou, M, Fostira, F, Pertesi, M, Stavropoulou, A-V, Triantafyllidou, O, Tsotra, E, Tsiftsoglou, AP, Tsionou, C, Droufakou, S, Dimitrakakis, C, Fountzilas, G, Yannoukakos, D

Journal:

Clinical Genetics

Year:

2014

Language:

english

File:

PDF, 650 KB

english, 2014

2

G1738R is aBRCA1founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history

Theodore Anagnostopoulos, Maroulio Pertesi, Irene Konstantopoulou, Sofia Armaou, Smaragda Kamakari, George Nasioulas, Athanassios Athanasiou, Alex Dobrovic, Mary-Anne Young, David Goldgar, George Foun

Journal:

Breast Cancer Research and Treatment

Year:

2008

Language:

english

File:

PDF, 345 KB

english, 2008

3

Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek population

M Pertesi, I Konstantopoulou, D Yannoukakos

Journal:

Clinical Genetics

Year:

2011

Language:

english

File:

PDF, 637 KB

english, 2011

4

Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases

Armaou, S, Pertesi, M, Fostira, F, Thodi, G, Athanasopoulos, P S, Kamakari, S, Athanasiou, A, Gogas, H, Yannoukakos, D, Fountzilas, G

Journal:

British Journal of Cancer

Year:

2009

Language:

english

File:

PDF, 118 KB

english, 2009

5

Prevalence ofBRCA1mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study

Florentia Fostira, Marianthi Tsitlaidou, Christos Papadimitriou, Maroulio Pertesi, Eleni Timotheadou, Alexandra V. Stavropoulou, Stavros Glentis, Evangelos Bournakis, Mattheos Bobos, Dimitrios Pectasi

Journal:

Breast Cancer Research and Treatment

Year:

2012

Language:

english

File:

PDF, 328 KB

english, 2012

6

Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

D.J. Park, F. Lesueur, T. Nguyen-Dumont, M. Pertesi, F. Odefrey, F. Hammet, S.L. Neuhausen, E.M. John, I.L. Andrulis, M.B. Terry, M. Daly, S. Buys, F. Le Calvez-Kelm, A. Lonie, B.J. Pope, H. Tsimiklis

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 457 KB

english, 2012

7

Identification of new breast cancer predisposition genes via whole exome sequencing

MC Southey, DJ Park, F Lesueur, F Odefrey, T Nguyen-Dumont, F Hammet, SL Neuhausen, EM John, IL Andrulis, G Chenevix-Trench, L Baglietto, F Le Calvez-Kelm, M Pertesi, A Lonie, B Pope, O Sinilnikova, H

Journal:

Hereditary Cancer in Clinical Practice

Year:

2012

Language:

english

File:

PDF, 79 KB

english, 2012

8

Contribution of ATM and FOXE1 ( TTF2 ) to risk of papillary thyroid carcinoma in Belarusian children exposed to radiation

Damiola, Francesca, Byrnes, Graham, Moissonnier, Monika, Pertesi, Maroulio, Deltour, Isabelle, Fillon, Aurélie, Le Calvez-Kelm, Florence, Tenet, Vanessa, McKay-Chopin, Sandrine, McKay, James D., Malak

Journal:

International Journal of Cancer

Year:

2014

Language:

english

File:

PDF, 258 KB

english, 2014

9

Efficient skyline query processing in SpatialHadoop

Pertesis, Dimitris, Doulkeridis, Christos

Journal:

Information Systems

Year:

2014

Language:

english

File:

PDF, 745 KB

english, 2014

10

Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population

Pereda, Celia M, Lesueur, Fabienne, Pertesi, Maroulio, Robinot, Nivonirina, Lence-Anta, Juan J, Turcios, Silvia, Velasco, Milagros, Chappe, Mae, Infante, Idalmis, Bustillo, Marlene, García, Anabel, Cl

Journal:

Year:

2015

Language:

english

File:

PDF, 396 KB

english, 2015

11

Prevalence of BRCA1 Mutations in Familial and Sporadic Greek Ovarian Cancer Cases

Stavropoulou, Alexandra V., Fostira, Florentia, Pertesi, Maroulio, Tsitlaidou, Marianthi, Voutsinas, Gerassimos E., Triantafyllidou, Olga, Bamias, Aristotelis, Dimopoulos, Meletios A., Timotheadou, El

Journal:

Year:

2013

Language:

english

File:

PDF, 245 KB

english, 2013

12

Multigene testing of moderate-risk genes: be mindful of the missense

Young, E L, Feng, B J, Stark, A W, Damiola, F, Durand, G, Forey, N, Francy, T C, Gammon, A, Kohlmann, W K, Kaphingst, K A, McKay-Chopin, S, Nguyen-Dumont, T, Oliver, J, Paquette, A M, Pertesi, M, Robi

Journal:

Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 905 KB

english, 2016

13

Rare key functional domain missense substitutions inMRE11A,RAD50, andNBNcontribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

Damiola, Francesca, Pertesi, Maroulio, Oliver, Javier, Le Calvez-Kelm, Florence, Voegele, Catherine, Young, Erin L, Robinot, Nivonirina, Forey, Nathalie, Durand, Geoffroy, Vallée, Maxime P, Tao, Kayok

Journal:

Breast Cancer Research

Year:

2014

Language:

english

File:

PDF, 486 KB

english, 2014

14

Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

Apostolou, Paraskevi, Pertesi, Maroulio, Aleporou-Marinou, Vassiliki, Dimitrakakis, Constantine, Papadimitriou, Christos, Razis, Evangelia, Christodoulou, Christos, Fountzilas, George, Yannoukakos, Dr

Journal:

Clinical Genetics

Year:

2016

Language:

english

File:

PDF, 1.30 MB

english, 2016

15

Common Variants at 9q22.33, 14q13.3, and ATM Loci, and Risk of Differentiated Thyroid Cancer in the French Polynesian Population

Maillard, Stéphane, Damiola, Francesca, Clero, Enora, Pertesi, Maroulio, Robinot, Nivonirina, Rachédi, Frédérique, Boissin, Jean-Louis, Sebbag, Joseph, Shan, Larrys, Bost-Bezeaud, Frédérique, Petitdid

Journal:

Year:

2015

Language:

english

File:

PDF, 189 KB

english, 2015

16

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

Pertesi, Maroulio, Vallée, Maxime, Wei, Xiaomu, Revuelta, Maria V., Galia, Perrine, Demangel, Delphine, Oliver, Javier, Foll, Matthieu, Chen, Siwei, Perrial, Emeline, Garderet, Laurent, Corre, Jill, L

Journal:

Year:

2019

File:

PDF, 1.42 MB

2019

17

Essential genes shape cancer genomes through linear limitation of homozygous deletions

Pertesi, Maroulio, Ekdahl, Ludvig, Palm, Angelica, Johnsson, Ellinor, Järvstråt, Linnea, Wihlborg, Anna-Karin, Nilsson, Björn

Journal:

Communications Biology

Year:

2019

Language:

english

File:

PDF, 962 KB

english, 2019

18

Menopause, cognition and dementia – A review

Pertesi, S, Coughlan, G, Puthusseryppady, V, Morris, E, Hornberger, M

Journal:

Post Reproductive Health

Year:

2019

Language:

english

File:

PDF, 291 KB

english, 2019

19

Menopause, cognition and dementia – A review

Pertesi, S, Coughlan, G, Puthusseryppady, V, Morris, E, Hornberger, M

Journal:

Post Reproductive Health

Year:

2019

File:

PDF, 291 KB

2019

20

S100A6 is a critical regulator of hematopoietic stem cells

Grahn, Tan Hooi Min, Niroula, Abhishek, VÃ©gvÃ¡ri, Ãkos, Oburoglu, Leal, Pertesi, Maroulio, Warsi, Sarah, Safi, Fatemeh, Miharada, Natsumi, Garcia, Sandra C., Siva, Kavitha, Liu, Yang, RÃ¶rby, Emma,

Journal:

Year:

2020

File:

PDF, 3.50 MB

2020

21

Adult Education and International Organizations (UNESCO): Contemporary Policies and Strategies

Panagiotopoulos, George, Pertesi, Katerina, Karanikola, Zoe

Journal:

International Journal of Learning and Development

Year:

2018

File:

PDF, 164 KB

2018

22

Correction: S100A6 is a critical regulator of hematopoietic stem cells

Grahn, Tan Hooi Min, Niroula, Abhishek, VÃ©gvÃ¡ri, Ãkos, Oburoglu, Leal, Pertesi, Maroulio, Warsi, Sarah, Safi, Fatemeh, Miharada, Natsumi, Capellera-Garcia, Sandra, Siva, Kavitha, Liu, Yang, RÃ¶rby,

Journal:

Year:

2020

File:

PDF, 431 KB

2020

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