Get started
Author

Mirlene Cecília Soares Pinho Cernach

Observed names: Cernach, Mirlene Cecilia Soares Pinho, M. C. S. P. Cernach, M. Cernach, M.C. Cernach, M.C.S. Cernach, M.C.S.P. Cernach, Mirlene C. Cernach, Mirlene C. S. P. Cernach, Mirlene C. Soares Pinho Cernach, Mirlene C.P. Cernach, Mirlene C.S.P. Cernach, Mirlene Cecilia S.P. Cernach, Mirlene Cecilia Soares Pinho Cernach, Mirlene Cecília Cernach, Mirlene Cecília S. Pinho Cernach, Mirlene Cecília Soares P. Cernach, Mirlene Cernach
ORCID: 0000-0002-9093-4370
Observed ORCID: 0000-0002-9093-4370
OpenAlex ID: A5035649074
Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015
2016 · Lavinia Schuler-Faccini, Erlane M. Ribeiro, et al. · MMWR Morbidity and Mortality Weekly Report · 1,071
PDF
The phenotypic spectrum of congenital Zika syndrome
2017 · Miguel del Campo, Ian M. L. Feitosa, et al. · American Journal of Medical Genetics Part A · 215
Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015
2016 · Lavinia Schuler-Faccini, Erlane M. Ribeiro, et al. · MMWR Morbidity and Mortality Weekly Report · 72
A Complex Chromosome Rearrangement Involving Four Chromosomes, Nine Breakpoints and a Cryptic 0.6-Mb Deletion in a Boy with Cerebellar Hypoplasia and Defects in Skull Ossification
2013 · R.S. Guilherme, M.C.S.P. Cernach, et al. · Cytogenetic and Genome Research · 40
Wide Clinical Variability in Cat Eye Syndrome Patients: Four Non-Related Patients and Three Patients from the Same Family
2012 · S.I. Belangero, A.N.X. Pacanaro, et al. · Cytogenetic and Genome Research · 39
Investigating 22q11.2 Deletion and Other Chromosomal Aberrations in Fetuses With Heart Defects Detected by Prenatal Echocardiography
2010 · Fernanda Teixeira da Silva Bellucco, Sintia Iole Nogueira Belangero, et al. · Pediatric Cardiology · 27
PDF
Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum
2008 · Sintia Iole Nogueira, April M. Hacker, et al. · European Journal of Medical Genetics · 21
Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome
2022 · Sarah R. Poll, Renan Martin, et al. · PLoS Genetics · 18
PDF
A utilização da Internet na notificação dos defeitos congênitos na Declaração de Nascido Vivo em quatro maternidades públicas do Município de São Paulo, Brasil
2010 · Pablo Domingos Rodrigues de Nicola, Mirlene Cecília Soares Pinho Cernach, et al. · Cadernos de Saúde Pública · 18
PDF
Interaction between physical exercise and APOE gene polymorphism on cognitive function in older people
2020 · M.E.S. Colovati, I.P. Novais, et al. · Brazilian Journal of Medical and Biological Research · 17
PDF
Novel mutations in the TBX5 gene in patients with Holt-Oram Syndrome
2010 · Marianna P.R. Porto, Naja Vergani, et al. · Genetics and Molecular Biology · 16
PDF
Deleção 22q11.2 em pacientes com defeito cardíaco conotruncal e fenótipo da síndrome da deleção 22q11.2
2009 · Sintia Iole Nogueira Belangero, Fernanda T.S. Bellucco, et al. · Arquivos Brasileiros de Cardiologia · 16
PDF
Gomez–López–Hernández syndrome: A case report with clinical and molecular evaluation and literature review
2020 · Eduardo Perrone, Vânia D'Almeida, et al. · American Journal of Medical Genetics Part A · 15
Finlay–Marks (SEN) syndrome: A sporadic case and the delineation of the syndrome
2006 · Nara Lygia de Macena Sobreira, Décio Brunoni, et al. · American Journal of Medical Genetics Part A · 14
Evaluation of a Protocol for Postmortem Examination of Stillbirths and Neonatal Deaths with Congenital Anomalies
2004 · Mirlene C.S.P. Cernach, Francy R.S. Patrício, et al. · Pediatric and Developmental Pathology · 13
Assessment of 22q11.2 copy number variations in a sample of Brazilian schizophrenia patients
2011 · Denise M. Christofolini, Fernanda T. Bellucco, et al. · Schizophrenia Research · 12
A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: A case report with clinical and molecular review
2021 · Manuella Galvão de Oliveira, Célia Tengan, et al. · European Journal of Medical Genetics · 9
Anomalias Congénitas Identificadas ao Nascimento em Recém-Nascidos de Mulheres Adolescentes
2015 · Leandro Valim dos Reis, Edward Araujo Júnior, et al. · Acta Médica Portuguesa · 9
Isodicentric X chromosome and mosaicism: Report on two cases of 45,X/46,X,idic(Xq)/47,X,idic(Xq),idic(Xq) and review of the literature
1993 · Maria Isabel Melaragno, Laila M. A. Fakih, et al. · American Journal of Medical Genetics · 9
Clinical, molecular, and pathological findings in a Neu–Laxova syndrome stillborn: A Brazilian case report
2020 · Thiago R. Cavole, Eduardo Perrone, et al. · American Journal of Medical Genetics Part A · 8
Interrupção do arco aórtico tipo B em uma paciente com síndrome de olho de gato
2009 · Sintia Iole Nogueira Belangero, Fernanda Teixeira da Silva Bellucco, et al. · Arquivos Brasileiros de Cardiologia · 7
PDF
Diphallia associated with malformation of hindgut derivatives
1989 · M.C.S.P. Cernach, H. Hayashi, et al. · Urology · 7
Association between genetic polymorphisms and osteoarthritis development. Overview of systematic reviews
2022 · Amanda Almeida Brisola, Mileny Esbravatti Stephano Colovati, et al. · International Journal of Rheumatic Diseases · 3
Pseudoaminopterin syndrome: Clinical report with new characteristics
2009 · N. Sobreira, M. Cernach, et al. · American Journal of Medical Genetics Part A · 3
Complex toe syndactyly with characteristic facial phenotype: A new syndrome?
2008 · Nara Lygia Macena Sobreira, Mirlene Cecilia S.P. Cernach, et al. · American Journal of Medical Genetics Part A · 3
Works count: 42
Citation count: 1,690
H-index: 14
I10-index: 16
Year
Topic
Type