Advanced search
Start date
Betweenand

Vera Lúcia Gil da Silva Lopes

CV Lattes GoogleMyCitations ResearcherID ORCID


Universidade Estadual de Campinas (UNICAMP). Faculdade de Ciências Médicas (FCM)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

graduate at Medicina from Universidade Estadual de Campinas (1990), master's at Genetics from Universidade Estadual de Campinas (1995) and ph.d. at Genetics from Universidade Estadual de Campinas (1997). Has experience in Genetics, acting on the following subjects: genética clínica, anomalias craniofaciais, dismorfologia, aconselhamento genético and genética molecular. (Source: Lattes Curriculum)

Articles published in other media outlets (2 total):
Jornal do Sudoeste : Tecnologia a favor da população com anomalias craniofaciais (23/Sep/2019)
Inova Unicamp: Tecnologia a favor da população com anomalias craniofaciais (20/Sep/2019)
Research grants
Scholarships in Brazil
FAPESP support in numbers * Updated June 12, 2021
Total / Available in English
Most frequent collaborators in research granted by FAPESP
Contact researcher

Use this Research Supported by FAPESP (BV/FAPESP) channel only to send messages referring to FAPESP-funded scientific projects.


 

 

 

 

Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (35)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

Publications35
Citations145
Cit./Article4.1
Data from Web of Science

ZAMARIOLLI, MALU; BURSSED, BRUNA; MOYSES-OLIVEIRA, MARIANA; COLOVATI, MILENY; BELLUCCO, FERNANDA TEIXEIRA DA SILVA; DOS SANTOS, LEONARDO CAIRES; ALVAREZ PEREZ, ANA BEATRIZ; BRAGAGNOLO, SILVIA; MELARAGNO, MARIA ISABEL. Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanisms. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, . Web of Science Citations: 0. (11/23794-7, 14/11572-8)

CRUZ, PEDRO R. S.; ANANINA, GALINA; GIL-DA-SILVA-LOPES, VERA LUCIA; SIMIONI, MILENA; MENAA, FARID; BEZERRA, MARCOS A. C.; DOMINGOS, IGOR F.; ARAUJO, ADERSON S.; PELLEGRINO, RENATA; HAKONARSON, HAKON; et al. Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. SCIENTIFIC REPORTS, v. 9, . Web of Science Citations: 1. (12/06438-5, 08/57441-0, 15/13152-9, 08/10596-0, 14/00984-3)

SGARDIOLI, ILARIA CRISTINA; MONTEIRO, FABIOLA PAOLI; FANTI, PAULO; PAIVA VIEIRA, TARSIS; GIL-DA-SILVA-LOPES, VERA LUCIA. Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health. ORPHANET JOURNAL OF RARE DISEASES, v. 14, . Web of Science Citations: 2. (12/51799-6)

MOLCK, MIRIAM COELHO; SIMIONI, MILENA; VIEIRA, TARSIS PAIVA; MONTEIRO, FABIOLA PAOLI; GIL-DA-SILVA-LOPES, VERA L.. A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4. MOLECULAR SYNDROMOLOGY, v. 8, n. 3, p. 161-167, . Web of Science Citations: 0. (09/08756-1, 12/51799-6, 08/10596-0, 11/23794-7)

MOLCK, MIRIAM COELHO; SIMIONI, MILENA; VIEIRA, TARSIS PAIVA; SGARDIOLI, ILARIA CRISTINA; MONTEIRO, FABIOLA PAOLI; SOUZA, JOSIANE; FETT-CONTE, AGNES CRISTINA; FELIX, TEMIS MARIA; MONLLEO, ISABELLA LOPES; GIL-DA-SILVA-LOPES, VERA LUCIA. Genomic imbalances in syndromic congenital heart disease. Jornal de Pediatria, v. 93, n. 5, p. 497-507, . Web of Science Citations: 6. (11/23794-7, 09/08756-1, 08/10596-0)

DE ARAUJO, TANIA KAWASAKI; LUSTOSA-MENDES, ELAINE; DOS SANTOS, ANA P.; MOLCK, MIRIAM COELHO; VOLPE-AQUINO, ROBERTA MAZZARIOL; GIL-DA-SILVA-LOPES, VERA L.. ADULT Phenotype and rs16864880 in the TP63 Gene: Two New Cases and Review of the Literature. MOLECULAR SYNDROMOLOGY, v. 8, n. 4, p. 201-205, . Web of Science Citations: 0. (11/23794-7)

MOLCK, MIRIAM COELHO; VIEIRA, TARSIS PAIVA; SIMIONI, MILENA; SGARDIOLI, ILARIA CRISTINA; DOS SANTOS, ANA PAULA; XAVIER, ANA CAROLINA; GIL-DA-SILVA-LOPES, VERA LUCIA. Distal 22q11.2 Microduplication Combined With Typical 22q11.2 Proximal Deletion: A Case Report. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 167, n. 1, p. 215-220, . Web of Science Citations: 3. (11/23794-7, 09/08756-1, 08/10596-0)

SGARDIOLI, ILARIA CRISTINA; SIMIONI, MILENA; VIGUETTI-CAMPOS, NILMA LUCIA; PROTA, JOANA ROSA; GIL-DA-SILVA-LOPES, VERA LUCIA. A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion. Gene, v. 523, n. 2, p. 192-194, . Web of Science Citations: 4. (08/10596-0)

MONTEIRO, FABOLA P.; VIEIRA, TARSIS P.; SGARDIOLI, ILARIA C.; MOLCK, MIRIAM C.; DAMIANO, ANA PAULA; SOUZA, JOSIANE; MONLLEO, ISABELLA L.; FONTES, MARSHALL I. B.; FETT-CONTE, AGNES C.; FELIX, TEMIS M.; et al. Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature. EUROPEAN JOURNAL OF PEDIATRICS, v. 172, n. 7, p. 927-945, . Web of Science Citations: 34.

LUSTOSA-MENDES, ELAINE; DOS SANTOS, ANA PAULA; VIGUETTI-CAMPOS, NILMA LUCIA; VIEIRA, TARSIS PAIVA; GIL-DA-SILVA-LOPES, VERA LUCIA. A Boy With Partial dup(18q)/del(18p) Due to a Maternal Pericentric Inversion: Genotype-Phenotype Correlation and Risk of Recombinant Chromosomes Based on Systematic Review of the Literature. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 173, n. 1, p. 143-150, . Web of Science Citations: 5. (12/51799-6)

SPINELI-SILVA, SAMIRA; BISPO, LUCIANA M.; GIL-DA-SILVA-LOPES, VERA L.; VIEIRA, TARSIS P.. Distal deletion at 22q11.2 as differential diagnosis in Craniofacial Microsomia: Case report and literature review. EUROPEAN JOURNAL OF MEDICAL GENETICS, v. 61, n. 5, p. 262-268, . Web of Science Citations: 5. (12/51799-6)

MOLCK, MIRIAM C.; MONTEIRO, FABIOLA P.; SIMIONI, MILENA; GIL-DA-SILVA-LOPES, VERA L.. 8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome. JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, v. 36, n. 7, p. 544-548, . Web of Science Citations: 3. (11/23794-7, 09/08756-1, 08/10596-0)

FONTES, MARSHALL I. B.; SANTOS, ANA P.; MOLCK, MIRIAM C.; SIMIONI, MILENA; NASCIMENTO, DIOGO L. L.; ANDRADE, ANA K. M.; ROSENBERG, CARLA; KREPISCHI, ANA C. V.; APPENZELLER, SIMONE; MONLLEO, ISABELLA L.; et al. Genotype-Phenotype Correlation of 16p13.3 Terminal Duplication and 22q13.33 Deletion: Natural History of a Patient and Review of the Literature. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 170, n. 3, p. 766-772, . Web of Science Citations: 3. (13/08028-1, 12/51799-6, 12/10071-0, 09/00898-1)

DE SOUZA, LAIARA CRISTINA; SGARDIOLI, ILARIA CRISTINA; GIL-DA-SILVA-LOPES, VERA LUCIA; VIEIRA, TARSIS PAIVA. A recognizable phenotype related to 19p13.12 microdeletion. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 176, n. 8, p. 1753-1759, . Web of Science Citations: 1. (12/51799-6)

SGARDIOLI, ILARIA C.; COPELLI, MATHEUS DE MELLO; MONTEIRO, FABIOLA P.; DOS SANTOS, ANA P.; MENDES, ELAINE LUSTOSA; VIEIRA, TARSIS PAIVA; GIL-DA-SILVA-LOPES, VERA L.. Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases. MOLECULAR SYNDROMOLOGY, v. 8, n. 5, p. 244-252, . Web of Science Citations: 2. (12/51799-6)

VOLPE-AQUINO, ROBERTA M.; MONLLEO, ISABELLA L.; LUSTOSA-MENDES, ELAINE; MORA, AMANDA F.; FETT-CONTE, AGNES C.; FELIX, TEMIS M.; XAVIER, ANA C.; TONOCCHI, RITA; RIBEIRO, ERLANE M.; PEREIRA, RUI; et al. CranFlow: An Application for Record-Taking and Management Through the Brazilian Database on Craniofacial Anomalies. BIRTH DEFECTS RESEARCH, v. 110, n. 1, p. 72-80, . Web of Science Citations: 2. (12/51799-6)

SIMIONI, MILENA; MONLLEO, ISABELLA LOPES; COSTA DE QUEIROZ, CAMILA M.; PEIXOTO GAZZANEO, ILANNA FRAGOSO; LIMA DO NASCIMENTO, DIOGO L.; DE OMENA FILHO, REINALDO LUNA; DA CRUZ PIVETA, CRISTIANE SANTOS; DE MELLO, MARICILDA PALANDI; GIL-DA-SILVA-LOPES, VERA L.. A Cytogenomic Approach in a Case of Syndromic XY Gonadal Dysgenesis. SEXUAL DEVELOPMENT, v. 10, n. 1, p. 23-27, . Web of Science Citations: 0. (11/23794-7)

BARBOSA, FERNANDA BUENO; SIMIONI, MILENA; VIEIRA WIEZEL, CLAUDIA EMILIA; TORRES, FABIO ROSSI; MOLCK, MIRIAM COELHO; BONILLA, MELVIN M.; DE ARAUJO, TABIA KAWASAKI; DONADI, EDUARDO ANTONIO; GIL-DA-SILVA-LOPES, VERA LUCIA; LEMOS, BERNARDO; et al. Copy number variation in the susceptibility to systemic lupus erythematosus. PLoS One, v. 13, n. 11, . Web of Science Citations: 4. (13/17062-9, 11/23794-7, 16/10306-8)

MOLCK, MIRIAM COELHO; SIMIONI, MILENA; VIEIRA, TARSIS PAIVA; MONTEIRO, FABIOLA PAOLI; GIL-DA-SILVA-LOPES, VERA L.. A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome. MOLECULAR SYNDROMOLOGY, v. 9, n. 4, p. 197-204, . Web of Science Citations: 0. (09/08756-1, 12/51799-6, 08/10596-0, 11/23794-7)

VIEIRA, TARSIS P.; MONTEIRO, FABIOLA P.; SGARDIOLI, ILARIA C.; SOUZA, JOSIANE; FETT-CONTE, AGNES C.; MONLLEO, ISABELLA L.; FONTES, MARSHALL B.; FELIX, TEMIS M.; LEAL, GABRIELA F.; RIBEIRO, ERLANE MARQUES; et al. Clinical Features in Patients With 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities. CLEFT PALATE-CRANIOFACIAL JOURNAL, v. 52, n. 4, p. 411-416, . Web of Science Citations: 5. (09/08756-1)

SIMIONI, MILENA; ARAUJO, TANIA KAWASAKI; MONLLEO, ISABELLA LOPES; MAURER-MORELLI, CLAUDIA VIANNA; GIL-DA-SILVA-LOPES, VERA LUCIA. Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation. JOURNAL OF HUMAN GENETICS, v. 60, n. 1, p. 17-25, . Web of Science Citations: 13. (08/10596-0)

SIMIONI, MILENA; STEINER, CARLOS EDUARDO; GIL-DA-SILVA-LOPES, VERA LUCIA. De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case. Gene, v. 573, n. 1, p. 166-170, . Web of Science Citations: 4. (12/10071-0, 11/23794-7)

SIMIONI, MILENA; VIEIRA, TARSIS PAIVA; SGARDIOLI, ILARIA CRISTINA; FREITAS, ERIKA LOPES; ROSENBERG, CARLA; MAURER-MORELLI, CLAUDIA VIANNA; LOPES-CENDES, ISCIA; FETT-CONTE, AGNES CRISTINA; GIL-DA-SILVA-LOPES, VERA LUCIA. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 158A, n. 11, p. 2905-2910, . Web of Science Citations: 9. (08/10596-0, 09/00898-1)

BARROS FONTES, MARSHALL ITALO; ALMEIDA, LANUSIA NUNES; REIS JUNIOR, GILBERTO DE OLIVEIRA; VIEIRA FILHO, JOSE IVAM; DOS SANTOS, KATHLEEN MOURA; DOS ANJOS, FILIPE SILVEIRA; MAIA DE ANDRADE, ANA KAROLINA; GAELZER PORCIUNCULA, CARLOS GUILHERME; DE OLIVEIRA, MICHELLINE COSTA; PEREIRA, RUI MANOEL; et al. Local Strategies to Address Health Needs of Individuals With Orofacial Clefts in Alagoas, Brazil. CLEFT PALATE-CRANIOFACIAL JOURNAL, v. 50, n. 4, p. 424-431, . Web of Science Citations: 2.

FREITAS, ERIKA L.; GRIBBLE, SUSAN M.; SIMIONI, MILENA; VIEIRA, TARSIS P.; SILVA-GRECCO, ROSEANE L.; BALARIN, MARLY A. S.; PRIGMORE, ELENA; KREPISCHI-SANTOS, ANA C.; ROSENBERG, CARLA; SZUHAI, KAROLY; et al. Maternally Inherited Partial Monosomy 9p (pter -> p24.1) and Partial Trisomy 20p (pter -> p12.1) Characterized by Microarray Comparative Genomic Hybridization. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 155A, n. 11, p. 2754-2761, . Web of Science Citations: 9. (05/03480-7)

SIMIONI, M.; FREITAS, E. LOPES; VIEIRA, T. PAIVA; LOPES-CENDES, I.; GIL-DA-SILVA-LOPES, V. LUCIA. Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism. JOURNAL OF APPLIED GENETICS, v. 51, n. 2, p. 219-221, . Web of Science Citations: 1. (05/03480-7)

DE SOUZA, L. C.; DOS SANTOS, A. P.; SGARDIOLI, I. C.; VIGUETTI-CAMPOS, N. L.; MARQUES PROTA, J. R.; DE OLIVEIRA-SOBRINHO, R. P.; VIEIRA, T. P.; GIL-DA-SILVA-LOPES, V. L.. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances. JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, v. 63, n. 11, p. 1379-1389, . Web of Science Citations: 0. (12/51799-6)

SGARDIOLI, ILARIA C.; LUSTOSA-MENDES, ELAINE; DOS SANTOS, ANA P.; VIEIRA, TARSIS P.; GIL-DA-SILVA-LOPES, VERA L.. A Rare Case of Concomitant Deletions in 15q11.2 and 19p13.3. Cytogenetic and Genome Research, v. 156, n. 2, p. 80-86, . Web of Science Citations: 0. (12/51799-6)

GIL-DA-SILVA-LOPES, VERA LUCIA; BARROS FONTES, MARSHALL ITALO; DOS SANTOS, ANA PAULA; APPENZELLER, SIMONE; FETT-CONTE, AGNES CRISTINA; CANO FRANCISQUETTI, MARINA CRISTINE; MONLLEO, ISABELLA LOPES. Syndromic Oral Clefts: Challenges of Genetic Assessment in Brazil and Suggestions to Improve Health Policies. PUBLIC HEALTH GENOMICS, v. 22, n. 1-2, p. 69-75, . Web of Science Citations: 0. (12/51799-6)

SGARDIOLI, ILARIA C.; VIEIRA, TARSIS P.; SIMIONI, MILENA; MONTEIRO, FABIOLA P.; GIL-DA-SILVA-LOPES, VERA L.. 22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening. JOURNAL OF PEDIATRIC GENETICS, v. 4, n. 1, p. 17-22, . Web of Science Citations: 2. (09/08756-1)

SGARDIOLI, ILARIA C.; VIEIRA, TARSIS P.; SIMIONI, MILENA; MONTEIRO, FABIOLA P.; GIL-DA-SILVA-LOPES, VERA L.. 22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening. JOURNAL OF PEDIATRIC GENETICS, v. 4, n. 1, p. 17-22, . Web of Science Citations: 2. (09/08756-1)

BARBOSA, FERNANDA B.; CAGNIN, NATALIA F.; SIMIONI, MILENA; FARIAS, ALLYSSON A.; TORRES, FABIO R.; MOLCK, MIRIAM C.; ARAUJO, TANIA K.; GIL-DA-SILVA-LOPES, VERA L.; DONADI, EDUARDO A.; SIMOES, AGUINALDO L.. Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome-wide Human Array. ANNALS OF HUMAN GENETICS, v. 81, n. 6, p. 225-233, . Web of Science Citations: 8. (13/17062-9, 11/23794-7)

SGARDIOLI, ILARIA CRISTINA; COPELLI, MATHEUS DE MELO; LUSTOSA-MENDES, ELAINE; VIEIRA, TARSIS PAIVA; GIL-DA-SILVA-LOPES, VERA LUCIA. Pure 21q22.3 deletion identified in a patient with mild phenotypic features. CONGENITAL ANOMALIES, v. 58, n. 5, p. 178-180, . Web of Science Citations: 0. (12/51799-6)

SIMIONI, MILENA; ARTIGUENAVE, FRANCOIS; MEYER, VINCENT; SGARDIOLI, ILARIA C.; VIGUETTI-CAMPOS, NILMA L.; MONLLEO, ISABELLA LOPES; MACIEL-GUERRA, ANDREA T.; STEINER, CARLOS E.; GIL-DA-SILVA-LOPES, VERA L.. Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes. MOLECULAR SYNDROMOLOGY, v. 8, n. 4, p. 187-194, . Web of Science Citations: 1. (12/10071-0, 11/23794-7)

MIRIAM COELHO MOLCK; MILENA SIMIONI; TÁRSIS PAIVA VIEIRA; ILÁRIA CRISTINA SGARDIOLI; FABÍOLA PAOLI MONTEIRO; JOSIANE SOUZA; AGNES CRISTINA FETT-CONTE; TÊMIS MARIA FÉLIX; ISABELLA LOPES MONLLÉO; VERA LÚCIA GIL-DA-SILVA-LOPES. Genomic imbalances in syndromic congenital heart disease,. Jornal de Pediatria, v. 93, n. 5, p. -, . (09/08756-1, 08/10596-0, 11/23794-7)

GIL-DA-SILVA-LOPES, VERA LUCIA; MONLLEO, ISABELLA LOPES. Risk factors and the prevention of oral clefts. Brazilian Oral Research, v. 28, n. 1, . Web of Science Citations: 11.

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

CARVALHO, Milena Simioni de. Investigação da região 22q11.2 em defeitos de linha media facial com hipertelorismo. Dissertação (Mestrado) -  Faculdade de Ciências Médicas.  Universidade Estadual de Campinas (UNICAMP).  (05/03555-7

MEIRELLES, Ana Paula Arduino. Aspectos fonoaudiologicos da sindrome de Saethre-Chotzen. Dissertação (Mestrado) -  Faculdade de Ciencias Medicas.  Universidade Estadual de Campinas (UNICAMP).  (05/01284-6

Please report errors in researcher information by writing to: cdi@fapesp.br.
X

Report errors in this page


Error details: