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Lina Ramos

Observed names: L Ramos, L. Ramos, LEANDRA MARIA SOARES RAMOS, LISSIANA ZEFERINO RAMOS, LUANA GOMES RAMOS, Larissa Adriane Corrêa Ramos, Larissa Borges Ramos, Larissa Letícia Andara Ramos, Laudicéia Brito Ramos, Lavínia Barros Ramos, Leandro de Menezes Ramos, Leila Valverde Ramos, Lenir Caldeira da Silva Ramos, Lilian Moreira de Castilho Ramos, Lina Maria Jesus Ferreira Cardoso Ramos, Lucas José dos Santos Ramos, Luciana Rodrigues Ramos, Luciano Osio Ramos, Lucía de Los Ángeles Pimentel Ramos, Luisa Maria Jiménez Ramos, Luisa Natalia Rezende Ramos, Luiz Celson da Silva Ramos, Luiz Henrique Margutti Ramos, Luiz Philippe dos Santos Ramos, Ramos, L., Ramos, Lina, Ramos, Lina Maria Jesus Ferreira Cardoso
ORCID: 0000-0002-2908-7504
Observed ORCID: 0000-0002-2908-7504
OpenAlex ID: A5018625519
Oculo-auriculo-vertebral spectrum: Clinical and molecular analysis of 51 patients
2015 · Ana Beleza-Meireles, Rachel Hart, et al. · European Journal of Medical Genetics · 113
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations
2014 · Charlotte W Ockeloen, Marjolein H Willemsen, et al. · European Journal of Human Genetics · 107
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Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice
2011 · Joe Rainger, Ellen van Beusekom, et al. · PLoS Genetics · 93
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Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene
2015 · Joana B Melo, Alexandra Estevinho, et al. · Molecular Cytogenetics · 55
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IgE levels are negatively correlated with clinical response to ciclosporin in chronic spontaneous urticaria
2018 · L. Santiago, B. Ferreira, et al. · British Journal of Dermatology · 31
Tetra‐amelia and lung hypo/aplasia syndrome: New case report and review
2008 · Sérgio B. Sousa, Raquel Pina, et al. · American Journal of Medical Genetics Part A · 27
Copy number variants prioritization after array-CGH analysis – a cohort of 1000 patients
2015 · Isabel Marques Carreira, Susana Isabel Ferreira, et al. · Molecular Cytogenetics · 23
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Dupilumab for atopic dermatitis: a real-world Portuguese multicenter retrospective study
2022 · T. Torres, M. J. Paiva-Lopes, et al. · Journal of Dermatological Treatment · 20
Phenotyping GABA transaminase deficiency: a case description and literature review
2016 · Pedro Louro, Lina Ramos, et al. · Journal of Inherited Metabolic Disease · 20
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Clinical and Molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 ( FGFR3 ) in Portugal
2009 · MR Almeida, AB Campos‐Xavier, et al. · Clinical Genetics · 20
Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18
2007 · Isabel M. Carreira, Alexandra Mascarenhas, et al. · Journal of Histochemistry & Cytochemistry · 13
Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement
2005 · António Pires, Lina Ramos, et al. · Prenatal Diagnosis · 10
Childhood bullous pemphigoid: report of 2 cases
2014 · L. Ramos, O. Tellechea, et al. · Journal of the European Academy of Dermatology and Venereology · 9
Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism
2013 · Ana Beleza‐Meireles, Eunice Matoso, et al. · American Journal of Medical Genetics Part A · 9
Contact sensitization in pediatric patients with atopic dermatitis: a purpose for a new patch testing serie for the Portuguese population
2022 · J. Costa Carvalho, I.A. Coutinho, et al. · European Annals of Allergy and Clinical Immunology · 8
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Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis
2007 · A. Jardim, J. B. Melo, et al. · Prenatal Diagnosis · 6
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Another source of allergic contact dermatitis to isothiazolinones in children—urgent call for regulation
2019 · F. Morgado, M. Batista, et al. · Journal of the European Academy of Dermatology and Venereology · 5
Accuracy of Prenatal Diagnosis in Elective Termination of Pregnancy: 385 Cases from 2000 to 2007
2010 · Fabiana Ramos, Sofia Maia, et al. · ISRN Obstetrics and Gynecology · 4
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Tremor is a major feature of 9p13 deletion syndrome
2020 · Susana Isabel Ferreira, Giacomo Cinnirella, et al. · American Journal of Medical Genetics Part A · 3
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Hyperglycemia in pediatric age: could it be maturity onset diabetes of the young? Case reports and review of the literature
2019 · Mafalda Cascais, Ester Pereira, et al. · Annals of Pediatric Endocrinology & Metabolism · 3
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Congenital dacryocystocoele with prenatal diagnosis
2016 · Gracinda Nogueira Oliveira, Miguel Branco, et al. · BMJ Case Reports · 3
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Intellectual disability, unusual facial morphology and hand anomalies in sibs
2013 · Sérgio B. Sousa, Margarida Venâncio, et al. · American Journal of Medical Genetics Part A · 3
Dilated fetal bowel as indication for prenatal diagnosis of cystic fibrosis
2010 · Raquel Soares, Paula Neto, et al. · BMJ Case Reports · 3
Relação entre a prática de atividades extracurriculares e o desempenho acadêmico na medicina
2025 · Caio De Moura Torres, Luisa Natalia Rezende Ramos, et al. · Revista Científica da Faculdade de Medicina de Campos · 2
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Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice
2018 · Joe Rainger, Ellen van Beusekom, et al. · PLoS Genetics · 2
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Works count: 62
Citation count: 600
H-index: 11
I10-index: 12
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