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Adriano Bonaldi

CV Lattes

Universidade de São Paulo (USP). Instituto de Biociências (IB)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

Bachelor's degree in Biological Sciences (2008), Master's degree in Genetics (2011), and PhD in Genetics (2016), at the Institute of Biosciences, University of São Paulo. Currently a trainee researcher at the Laboratory of Human Genetics, Institute of Biosciences, University of São Paulo. The investigation of genetic and epigenetic causes of human growth disorders has been the focus of his research. Areas of expertise: human genetics, molecular genetics, medical genetics, molecular cytogenetics, epigenetics and genetic counseling. (Source: Lattes Curriculum)

FAPESP support in numbers * Updated January 18, 2020
Total / Available in English
3 / 3 Completed scholarships in Brazil

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Most frequent collaborators in research granted by FAPESP
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Use this Research Supported by FAPESP (BV/FAPESP) channel only to send messages referring to FAPESP-funded scientific projects.





Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (3)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

Data from Web of Science

FONSECA, ANA CAROLINA S.; BONALDI, ADRIANO; FONSECA, SIMONE A. S.; OTTO, PAULO A.; KOK, FERNANDO; BAK, MADS; TOMMERUP, NIELS; VIANNA-MORGANTE, ANGELA M.. The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation. MOLECULAR CYTOGENETICS, v. 8, . Web of Science Citations: 2. (13/01146-9, 13/08028-1, 11/14293-4)

BONALDI, ADRIANO; MAZZEU, JULIANA F.; COSTA, SILVIA S.; HONJO, RACHEL S.; BERTOLA, DEBORA R.; ALBANO, LILIAN M. J.; FURQUIM, ISABEL M.; KIM, CHONG A.; VIANNA-MORGANTE, ANGELA M.. Microduplication of the ICR2 Domain at Chromosome 11p15 and Familial Silver-Russell Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 155A, n. 10, p. 2479-2483, . Web of Science Citations: 31. (98/14254-2, 09/00898-1, 09/03341-8)

FONSECA, ANA CAROLINA S.; BONALDI, ADRIANO; BERTOLA, DEBORA R.; KIM, CHONG A.; OTTO, PAULO A.; VIANNA-MORGANTE, ANGELA M.. The clinical impact of chromosomal rearrangements with breakpoints upstream of the SOX9 gene: two novel de novo balanced translocations associated with acampomelic campomelic dysplasia. BMC MEDICAL GENETICS, v. 14, . Web of Science Citations: 20. (09/03480-8, 11/14293-4, 11/12486-0)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

BONALDI, Adriano. Estudo genético da síndrome de Silver-Russell. 2011. Dissertação (Mestrado) - Instituto de Biociências. Universidade de São Paulo (USP). São Paulo.

BONALDI, Adriano. Investigação de mecanismos genéticos e epigenéticos em distúrbios do crescimento humano. 2016. Tese (Doutorado) – Instituto de Biociências. Universidade de São Paulo (USP). São Paulo.

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