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Paula Rendeiro

Observed names: P Rendeiro, P. Rendeiro, PAULA RENDEIRO, Rendeiro, Paula, Rendeiro,Paula
OpenAlex ID: A5086782624
Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals
2015 · Melissa Hill, Jo-Ann Johnson, et al. · European Journal of Human Genetics · 113
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Instability of mRNA expression signatures of drug transporters in chronic myeloid leukemia patients resistant to imatinib
2012 · MARTA GROMICHO, MARTA MAGALHÃES, et al. · Oncology Reports · 41
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The rs5743836 polymorphism in TLR9 confers a population-based increased risk of non-Hodgkin lymphoma
2011 · A Carvalho, C Cunha, et al. · Genes and Immunity · 41
DNA damage response in imatinib resistant chronic myeloid leukemia K562 cells
2012 · Joana Dinis, Vânia Silva, et al. · Leukemia & lymphoma/Leukemia and lymphoma · 16
The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review
2019 · Fátima Lopes, Fátima Torres, et al. · Frontiers in Genetics · 12
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Cat eye syndrome and growth hormone deficiency with pituitary anomalies: A case report and review of the literature
2013 · Cláudia Melo, Susana Gama-de-Sousa, et al. · Gene · 12
Genomic imbalances defining novel intellectual disability associated loci
2019 · Fátima Lopes, Fátima Torres, et al. · Orphanet Journal of Rare Diseases · 6
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The contribution of 7q33 copy number variations for intellectual disability
2017 · Fátima Lopes, Fátima Torres, et al. · Neurogenetics · 5
Single-Test Parallel Assessment of Multiple Genetic Disorders
2011 · Purificação Tavares, Luís Dias, et al. · Personalized Medicine · 5
Comparison between CVS and early amniocentesis
1998 · P. Tavares, A. Tavares, et al. · Prenatal Diagnosis · 5
Portugal: The practice of medical genetics in Portugal
2001 · Jorge M Saraiva, Maximina R Pinto, et al. · Genetics in Medicine · 3
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Assessment of telomere length in the combined pulmonary fibrosis and emphysema syndrome
2014 · Ana Verónica Cardoso, Patrícia Caetano Mota, et al. · European Respiratory Journal · 1
Seudohipoparatiroidismo tipo Ia. Una mutación original
2010 · M. Reis Oliveira, A. Oliveira Bandeira, et al. · Anales de Pediatría · 1
Koolen-de Vries syndrome – National Case Series with clinical and molecular characterization
2019 · Marta P. Soares, Márcia T. Rodrigues, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
A case report of de novo 11q triplication, duplication, and segmental area of absence of heterozygosity in an infant with dysmorphic features, failure to thrive, and developmental delay.
2019 · Mohammed Almannai, Walaa Althunayyan, et al. · Journal of Biochemical and Clinical Genetics
Síndrome de Turner: diagnóstico tardio na adolescência
2014 · Torres, Teresa, Lopes, Susana, et al. · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
The Clinical Laboratory Genetics profession in Portugal
2013 · Lina Ramos, Paula Jorge, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
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Type 2 diabetes risk alleles frequencies in the Portuguese population
2013 · Duarte Pignatelli, Aida Palmeiro, et al. · Endocrine Abstracts
Microarray for skeletal dysplasias: thanatophoric dysplasia diagnosed in utero using microarray technology
2012 · C. Guerra, P. Rendeiro, et al. · Ultrasound in Obstetrics and Gynecology
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Works count: 23
Citation count: 261
H-index: 6
I10-index: 6
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