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D. Horovitz · SciRah

Researcher profile · Semantic Scholar

D. Horovitz

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D. Horovitz — researcher profile on SciRah

h-index: 12
Works: 39
Citations: 1,983

Most-cited papers

Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015.
L. Schuler-faccini, E. Ribeiro, Ian M. L. Feitosa, D. Horovitz +11 more
2016MMWR. Morbidity and mortality weekly report932 citations Open access
Semantic Scholar
Zika Virus Infection in Pregnant Women in Rio de Janeiro
P. Brasil, J. Pereira, M. E. Moreira, R. M. Ribeiro Nogueira +29 more
2016New England Journal of Medicine416 citations Open access
Semantic Scholar
The phenotypic spectrum of congenital Zika syndrome
M. Del Campo, Ian M. L. Feitosa, E. Ribeiro, D. Horovitz +22 more
2017American Journal of Medical Genetics. Part A190 citations Open access
Semantic Scholar
Genetic services and testing in Brazil
D. Horovitz, V. E. de Faria Ferraz, Sulamis Dain, A. Marques-de-Faria
2013Journal of Community Genetics98 citations Open access
Semantic Scholar
[Birth defects and health strategies in Brazil: an overview].
D. Horovitz, J. Llerena, Ruben Araujo de Mattos
2005Cadernos de Saúde Pública78 citations
Semantic Scholar
Genetics and genomics in Brazil: a promising future
M. Passos-Bueno, D. Bertola, D. Horovitz, V. E. de Faria Ferraz +1 more
2014Molecular Genetics & Genomic Medicine57 citations Open access
Semantic Scholar
Birth defects in Brazil and health care: proposals for public policies in clinical genetics
D. Horovitz, mAriA HeleNA cAbrAl De AlmeiDA cArDoso, J. Llerena, Ruben Araujo de Mattos
200643 citations Open access
Semantic Scholar
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN)
T. Félix, B. D. de Oliveira, Milena Artifon, I. Carvalho +55 more
2022Orphanet Journal of Rare Diseases41 citations Open access
Semantic Scholar
Birth defects and health strategies in Brazil: an overview
D. Horovitz, J. Llerena, Ruben Araujo de Mattos
200520 citations Open access
Semantic Scholar
[Complex care, high cost, and loss of income: frequent issues for families of children and adolescents with rare health conditions].
M. Pinto, A. Madureira, Letícia Baptista de Paula Barros, M. Nascimento +7 more
2019Cadernos de Saúde Pública19 citations Open access
Semantic Scholar
Medical Genetics in Brazil in the 21st Century: A Thriving Specialty and Its Incorporation in Public Health Policies
D. Horovitz, T. Félix, V. E. de Faria Ferraz
2024Genes17 citations Open access
Semantic Scholar
Cranial bone collapse in microcephalic infants prenatally exposed to Zika virus infection
D. Horovitz, Marcos Vinicius da Silva Pone, S. Pone, T. S. Salles +1 more
201617 citations Open access
Semantic Scholar
Building a National Policy for Rare Disease in Brazil
T. Félix, B. D. de Oliveira, D. Horovitz
2024Journal of Community Genetics9 citations Open access
Semantic Scholar
When rarity is an asset: political activism for the rights of persons with rare diseases in the Brazilian Unified National Health System.
M. C. N. Moreira, M. Nascimento, D. Horovitz, Antília Januária Martins +1 more
2018Cadernos de Saúde Pública6 citations Open access
Semantic Scholar
Identification of a founder effect involving n.197C>T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients
M. E. Gomes, Fernanda de Souza Gomes Kehdy, Fernanda Saloum de Neves-Manta, D. Horovitz +6 more
2024Scientific Reports5 citations Open access
Semantic Scholar
Identification of relevant International Classification of Functioning Disability and Health (ICF) categories in patients with 22q11.2 Deletion Syndrome: a Delphi exercise.
Ana Paula Carvalho Corrêa, C. T. M. Ribeiro, D. Horovitz, L. Ribeiro
2020International Symposium on Cooperative Database Systems for Advanced Applications5 citations Open access
Semantic Scholar
Conceptions on genetics in a group of college students
P. Correia, P. Vitiello, mAriA HeleNA cAbrAl De AlmeiDA cArDoso, D. Horovitz
2012Journal of Community Genetics5 citations Open access
Semantic Scholar
Genetic services and testing in Brazil
D. Horovitz, V. E. de Faria Ferraz, Sulamis Dain, A. Marques-de-Faria
2012Journal of Community Genetics5 citations Open access
Semantic Scholar
Medical Genetic Services in the State of Rio de Janeiro, Brazil
D. Horovitz, Ruben Araujo de Mattos, J. Llerena
2004Public Health Genomics4 citations
Semantic Scholar
The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis
Luiza M. Neves, Márcia Pinto, Olivia A Zin, Daniela P Cunha +14 more
2024Journal of Community Genetics3 citations Open access
Semantic Scholar
Venous anomalies in hypoplastic posterior fossa: unsolved questions
T. Protzenko, A. Bellas, C. Ribeiro, S. Maria de Carvalho Gonzalez +1 more
2021Child's Nervous System3 citations
Semantic Scholar
[Contradictions of public health policies geared to rare disorders: the example of the Osteogenesis Imperfecta Treatment Program in the Brazilian Unified Health System (SUS)].
Maria Angélica de Faria Domingues de Lima, D. Horovitz
2014Ciência & Saúde Coletiva3 citations
Semantic Scholar
Hyperargininaemia: A late-diagnosed Brazilian case with increased urinary excretion of homocystine
R. E. Simoni, C. P. D. de Oliveira, M. J. Braga, C. D. de Menezes +6 more
1997Journal of Inherited Metabolic Disease3 citations
Semantic Scholar
Genotype–Phenotype Correlations of Nance–Horan Syndrome in Male and Female Carriers of a Novel Variant
Olivia A Zin, Luiza M. Neves, F. Motta, Daltro C Junior +11 more
2025Genes1 citations
Semantic Scholar
Living with alveolar capillary dysplasia with misalignment of the pulmonary veins—case report
R. Cohen, F. Sztajnbok, Evanice Lima de Marca, V. Capelozzi +6 more
2024Pediatric Pulmonology1 citations Open access
Semantic Scholar
The 22q11.2 Deletion Syndrome from A Biopsychosocial Perspective: A Series of Cases with an ICF-Based Approach
A. P. C. Cabral, D. Horovitz, Lidiane Nogueira Santos, A. O. de Carvalho +4 more
2024Children1 citations Open access
Semantic Scholar
Spinal cord occupation ratio (SCOR) and its application in the diagnosis of cervical spinal cord compression in Mucopolysaccharidoses
Julia Valeriano de Almeida, A. Barth, Alessandra A. P. Costa, D. Horovitz
2022Journal of Inborn Errors of Metabolism and Screening1 citations Open access
Semantic Scholar
Description of Functioning in Children and Adolescents with Mucopolysaccharidosis - Case series
Aline Mota Fleming, C. T. M. Ribeiro, D. Horovitz, L. Ribeiro +1 more
2020Journal of Inborn Errors of Metabolism and Screening1 citations Open access
Semantic Scholar
Erratum to: Genetic services and testing in Brazil
D. Horovitz, V. E. de Faria Ferraz, Sulamis Dain, A. Marques-de-Faria
2013Journal of Community Genetics1 citations Open access
Semantic Scholar
Five-year outcomes of next-generation sequencing implementation at a Brazilian public health system reference centre for rare diseases
N. C. Rabelo, M. E. Gomes, Isabel Kodama Correa de Moraes, B. B. Abdala +10 more
2026Frontiers in Genetics0 citations Open access
Semantic Scholar
Clinical Utility of NGS-Based Diagnosis in Primary Ciliary Dyskinesia: Experience from a Brazilian Pediatric Cohort at a Reference Center for Rare Diseases
P. F. B. M. Costa, Danielle de Freitas F M Fins, Isabelle de Oliveira Moraes, T. Folescu +10 more
2026Genes0 citations Open access
Semantic Scholar
Clinical and Genetic Spectrum of ATP1A3-Related Disorders
Victor Rebelo Procaci, Raphael Pinheiro Camurugy da Hora, Anna Maria Gomes, T. Silva +32 more
2026Neurology: Genetics0 citations Open access
Semantic Scholar
Cyanosis in Childhood: A Clue to Hepatopulmonary Syndrome Due to Portosystemic Shunt
R. Cohen, M. Valladares, M. de Fátima Leite, C. Ribeiro +2 more
2025Pediatric Pulmonology0 citations Open access
Semantic Scholar
The 22q11.2 deletion syndrome from a biopsychosocial perspective: an ICF-based approach
A. P. C. Cabral, D. Horovitz, L. N. dos Santos, A. O. de Carvalho +4 more
2024medRxiv0 citations Open access
Semantic Scholar
Networks in Rare Diseases
Maria Angélica de Faria Domingues de Lima, A. C. B. Gilbert, D. Horovitz
20200 citations
Semantic Scholar
The Practice of Medical Genetics in Brazil
D. Horovitz, A. Marques-de-Faria, V. E. de Faria Ferraz
20120 citations
Semantic Scholar
Conceptions on genetics in a group of college students
P. Correia, P. Vitiello, mAriA HeleNA cAbrAl De AlmeiDA cArDoso, D. Horovitz
2012Journal of Community Genetics0 citations Open access
Semantic Scholar
Erratum to: Genetic services and testing in Brazil
D. Horovitz, V. E. de Faria Ferraz, Sulamis Dain, A. Marques-de-Faria
2012Journal of Community Genetics0 citations Open access
Semantic Scholar
[Birth defects in Brazil and health care: proposals for public policies in clinical genetics].
D. Horovitz, mAriA HeleNA cAbrAl De AlmeiDA cArDoso, J. Llerena, Ruben Araujo de Mattos
2006Cadernos de Saúde Pública0 citations
Semantic Scholar

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