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Patricia Maciel - Publications

Affiliations: 
University of Minho School of Medicine 
Area:
Genetics, Neuroscience, Neurogenetics, Movement Disorders, Neurodegeneration, Ataxias, Polyglutamine diseases, Neurodevelopmental disorders, autism, intellectual disability
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4 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Da Silva JD, Costa MD, Almeida B, Lopes F, Maciel P, Teixeira-Castro A. Case Report: A Novel Mutation Causes Global Developmental Delay With Intellectual Disability and Behavioral Disorders. Frontiers in Neurology. 12: 735549. PMID 34646230 DOI: 10.3389/fneur.2021.735549  0.336
2020 Seabra CM, Aneichyk T, Erdin S, Tai DJC, De Esch CEF, Razaz P, An Y, Manavalan P, Ragavendran A, Stortchevoi A, Abad C, Young JI, Maciel P, Talkowski ME, Gusella JF. Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons. Molecular Autism. 11: 45. PMID 32503625 DOI: 10.1186/S13229-020-00354-1  0.371
2017 Seabra CM, Szoko N, Erdin S, Ragavendran A, Stortchevoi A, Maciel P, Lundberg K, Schlatzer D, Smith J, Talkowski ME, Gusella JF, Natowicz MR. A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings. American Journal of Medical Genetics. Part A. PMID 28691782 DOI: 10.1002/Ajmg.A.38327  0.383
2007 Coutinho AM, Oliveira G, Katz C, Feng J, Yan J, Yang C, Marques C, Ataíde A, Miguel TS, Borges L, Almeida J, Correia C, Currais A, Bento C, Mota-Vieira L, ... ... Maciel P, et al. MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 475-83. PMID 17427193 DOI: 10.1002/Ajmg.B.30490  0.32
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