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Fingerprint Dive into the research topics where Maria Clara Bonaglia is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 45 Similar Profiles
Chromosomes Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Genes Medicine & Life Sciences
Genomic Segmental Duplications Medicine & Life Sciences
Haploinsufficiency Medicine & Life Sciences
Trisomy Medicine & Life Sciences
Agenesis of Corpus Callosum Medicine & Life Sciences

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Research Output 1996 2019

  • 2345 Citations
  • 29 h-Index
  • 72 Article
  • 1 Chapter
3 Citations (Scopus)

Role of mycotoxins in the pathobiology of autism: A first evidence

De Santis, B., Brera, C., Mezzelani, A., Soricelli, S., Ciceri, F., Moretti, G., Debegnach, F., Bonaglia, M. C., Villa, L., Molteni, M. & Raggi, M. E., 2019, In : Nutritional Neuroscience. 22, 2, p. 132-144 13 p.

Research output: Contribution to journalArticle

Mycotoxins
Autistic Disorder
Siblings
Gliotoxin
Urine

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Kurtas, N. E., Xumerle, L., Leonardelli, L., Delledonne, M., Brusco, A., Chrzanowska, K., Schinzel, A., Larizza, D., Guerneri, S., Natacci, F., Bonaglia, M. C., Reho, P., Manolakos, E., Mattina, T., Soli, F., Provenzano, A., Al-Rikabi, A. H., Errichiello, E., Nazaryan-Petersen, L., Giglio, S. & 3 others, Tommerup, N., Liehr, T. & Zuffardi, O., 2019, In : Human Mutation. 40, 2, p. 193-200

Research output: Contribution to journalArticle

Chromosomes, Human, 1-3
Trisomy
Genetic Markers
Chromosomes
Mothers

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Kurtas, N. E., Xumerle, L., Leonardelli, L., Delledonne, M., Brusco, A., Chrzanowska, K., Schinzel, A., Larizza, D., Guerneri, S., Natacci, F., Bonaglia, M. C., Reho, P., Manolakos, E., Mattina, T., Soli, F., Provenzano, A., Al-Rikabi, A. H., Errichiello, E., Nazaryan-Petersen, L., Giglio, S. & 3 others, Tommerup, N., Liehr, T. & Zuffardi, O., Feb 2019, In : Human Mutation. 40, 2, p. 193-200 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, 1-3
Trisomy
Genetic Markers
Chromosomes
Mothers

Small supernumerary marker chromosomes: A legacy of trisomy rescue?

Kurtas, N. E., Xumerle, L., Leonardelli, L., Delledonne, M., Brusco, A., Chrzanowska, K., Schinzel, A., Larizza, D., Guerneri, S., Natacci, F., Bonaglia, M. C., Reho, P., Manolakos, E., Mattina, T., Soli, F., Provenzano, A., Al-Rikabi, A. H., Errichiello, E., Nazaryan-Petersen, L., Giglio, S. & 3 others, Tommerup, N., Liehr, T. & Zuffardi, O., 2019, In : Human Mutation. 40, 2, p. 193-200 8 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Chromothripsis and ring chromosome 22: A paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

Kurtas, N., Arrigoni, F., Errichiello, E., Zucca, C., Maghini, C., D'Angelo, M. G., Beri, S., Giorda, R., Bertuzzo, S., Delledonne, M., Xumerle, L., Rossato, M., Zuffardi, O. & Bonaglia, M. C., Apr 1 2018, In : Journal of Medical Genetics. 55, 4, p. 269-277 9 p.

Research output: Contribution to journalArticle

Ring Chromosomes
Exome
Haploinsufficiency
Exanthema
Alu Elements