Projects per year
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Dive into the research topics where Rosemarie Fritsch is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Projects
- 1 Finished
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Competencia Parental en Madres de Niños con Sobrepeso y Obesidad
31/08/12 → 30/08/13
Project: Research
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Analysis of REM sleep without atonia in 22q11.2 deletion syndrome determined by domiciliary polysomnography: A cross sectional study
Mauro, J., DIaz, M., Córdova, T., Villanueva, K., Cáceres, T., Bassi, A., Fritsch, R., Repetto, G. M. & Ocampo-Garcés, A., 1 Feb 2022, In: Sleep. 45, 2, zsab300.Research output: Contribution to journal › Article › peer-review
4 Scopus citations -
Functional Dysconnectivity in Ventral Striatocortical Systems in 22q11.2 Deletion Syndrome
Tepper, Á., Cuiza, A., Alliende, L. M., Mena, C., Ramirez-Mahaluf, J. P., Iruretagoyena, B., Ornstein, C., Fritsch, R., Nachar, R., González-Valderrama, A., Undurraga, J., Cruz, J. P., Tejos, C., Fornito, A., Repetto, G. & Crossley, N., 1 Mar 2022, In: Schizophrenia Bulletin. 48, 2, p. 485-494 10 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Abnormal nodal and global network organization in resting state functional MRI from subjects with the 22q11 deletion syndrome
Pelgrim, T. A. D., Bossong, M. G., Cuiza, A., Alliende, L. M., Mena, C., Tepper, A., Ramirez-Mahaluf, J. P., Iruretagoyena, B., Ornstein, C., Fritsch, R., Cruz, J. P., Tejos, C., Repetto, G. & Crossley, N., 3 Nov 2021, In: Scientific Reports. 11, 1, p. 21623 21623.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
International 22q11.2DS Brain and Behavior Consortium & Fritsch, R., Aug 2021, In: Molecular Psychiatry. 26, 8, p. 4496-4510 15 p.Research output: Contribution to journal › Article › peer-review
Open Access55 Scopus citations -
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
International 22q11.2 Brain and Behavior Consortium & Fritsch, R., 2 Jan 2020, In: American Journal of Human Genetics. 106, 1, p. 26-40 15 p.Research output: Contribution to journal › Article › peer-review
Open Access34 Scopus citations
Press/Media
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A Randomized Clinical Trial for Depressed Mothers at Primary Care Level; DMH
2/10/18
1 item of Media coverage
Press/Media