alexa Achatz MIW | OMICS International
ISSN: 2161-1041

Hereditary Genetics: Current Research
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Achatz MIW

Department of Oncogenetics,
AC Camargo Cancer Center,
São Paulo, Brazil
Biography

I was born in the city of Rio de Janeiro and realized my education in São Paulo. I graduated from the Faculty of Medicine of the ABC Foundation, concludes the Masters in Oncology by Fundação Antonio Prudente / AC Camargo Hospital and IARC / International Agency for Research on Cancer, IARC (WHO / OMS) and a doctorate in Science from the School of Medicine University of Sao Paulo.

Currently, I am Advisor of graduate Antonio Prudente Foundation / Hospital AC Camargo, Head of Molecular Oncogenetics Laboratory and Director of the Department of Oncogenetics the AC Camargo Hospital, department in which, along with my team, study the profile of numerous syndromes predisposing hereditary cancer as Li-Fraumeni syndrome (TP53 R337H mutation and) and Breast Cancer and Ovarian Syndrome Hereditary.

Research Interest

Study the profile of numerous syndromes predisposing hereditary cancer as Li-Fraumeni syndrome (TP53 R337H mutation and) and Breast Cancer and Ovarian Syndrome Hereditary.

Publications

Low Frequency of Germline TERT and MITF Mutations in Brazilian Melanoma- Prone Patients

Pramio DT, Aguiar T, Araujo ESSD, Moredo LF, Sá BCSD, Achatz MIW, Duprat JP, Rosenberg C, Carraro MD and Krepischi ACV

Short Communication: Hereditary Genet 2014, 3: 135

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