A. Apessos

发表

Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders

C. Rodeck, P. Abou-Sleiman, J. Harper, 2002, Prenatal diagnosis.

Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

P. Abou-Sleiman, J. Harper, A. Apessos, 2001, Prenatal diagnosis.

Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome.

P. Abou-Sleiman, J. Harper, A. Apessos, 2002, Molecular human reproduction.

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

C. Markopoulos, A. Apessos, G. Nasioulas, 2019, BMC Cancer.

Molecular predictive markers in tumors of the gastrointestinal tract

A. Apessos, G. Nasioulas, V. Metaxa-Mariatou, 2016, World journal of gastrointestinal oncology.

KRAS, NRAS and BRAF mutations in Greek and Romanian patients with colorectal cancer: a cohort study

G. Aravantinos, H. Kalofonos, A. Croitoru, 2014, BMJ Open.

Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center.

C. Markopoulos, A. Apessos, G. Nasioulas, 2018, Cancer genetics.

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

C. Markopoulos, A. Apessos, S. Kampouri, 2019, BMC Cancer.

Breast Cancer Genetics

A. Apessos, G. Nasioulas, 2021, Breast Cancer Essentials.

Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR

A. Apessos, A. Divane, L. Florentin, 2002, Prenatal diagnosis.

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

K. Kyriacou, D. Yannoukakos, A. Hadjisavvas, 2004, BMC Cancer.

First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)

P. Abou-Sleiman, J. Harper, A. Apessos, 2002, Prenatal diagnosis.

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

N. Agnantis, G. Fountzilas, A. Apessos, 2005, BMC Cancer.

Different intrafamilial clinical presentation of FMF mutation carriers.

V. Kyriakopoulou, A. Apessos, G. Nasioulas, 2008, Genetic testing.

hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients

N. Agnantis, G. Fountzilas, A. Apessos, 2005, British Journal of Cancer.

Determination of EGFR and KRAS mutational status in Greek non-small-cell lung cancer patients

G. Aravantinos, M. Gaga, A. Apessos, 2015, Oncology letters.

Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis

S. Bione, T. Venesio, G. Ranzani, 2007, Genetics in Medicine.

Inherited cancer predisposition syndromes in Greece.

A. Apessos, P. Kosmidis, J. Triantafillidis, 2008, Anticancer research.

Culture of primary epithelial adenoma cells from familial adenomatous polyposis patients.

F. Fostira, D. Yannoukakos, A. Pintzas, 2008, Anticancer research.