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L. Montenegro · SciRah

Researcher profile · Semantic Scholar

L. Montenegro

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L. Montenegro — researcher profile on SciRah

h-index: 19
Works: 79
Citations: 1,929

Most-cited papers

Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
A. Abreu, A. Dauber, D. Macedo, S. Noel +17 more
2013New England Journal of Medicine467 citations Open access
Semantic Scholar
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
A. Dauber, Marina Cunha-Silva, D. Macedo, V. Brito +15 more
2017Journal of Clinical Endocrinology and Metabolism176 citations Open access
Semantic Scholar
Growth hormone (GH) pharmacogenetics: influence of GH receptor exon 3 retention or deletion on first-year growth response and final height in patients with severe GH deficiency.
A. Jorge, F. Marchisotti, L. Montenegro, L. Carvalho +2 more
2006Journal of Clinical Endocrinology and Metabolism153 citations Open access
Semantic Scholar
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.
D. Macedo, A. Abreu, A. Reis, L. Montenegro +19 more
2014Journal of Clinical Endocrinology and Metabolism128 citations Open access
Semantic Scholar
Wide spectrum of NR5A1‐related phenotypes in 46,XY and 46,XX individuals
S. Domenice, A. Z. Machado, F. M. Ferreira, B. Ferraz-de-Souza +12 more
2016Birth Defects Research Part C Embryo Today Reviews102 citations Open access
Semantic Scholar
DLK1 Is a Novel Link Between Reproduction and Metabolism.
L. Gomes, Marina Cunha-Silva, Raiane P Crespo, C. Ramos +13 more
2018Journal of Clinical Endocrinology and Metabolism98 citations Open access
Semantic Scholar
Deletion of copies of the gene encoding old yellow enzyme (TcOYE), a NAD(P)H flavin oxidoreductase, associates with in vitro-induced benznidazole resistance in Trypanosoma cruzi.
S. Murta/, M. Krieger, L. Montenegro, F. F. Campos +9 more
2006Molecular and biochemical parasitology (Print)84 citations
Semantic Scholar
New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism.
L. L. Amato, L. Montenegro, A. Lerário, A. Jorge +8 more
2019European Journal of Endocrinology77 citations Open access
Semantic Scholar
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic
D. Bessa, D. Macedo, V. Brito, M. França +11 more
2016Neuroendocrinology66 citations Open access
Semantic Scholar
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies
F. Correa, E. Trarbach, C. Tusset, A. Latronico +13 more
2015Endocrine Connections47 citations Open access
Semantic Scholar
Contribution of clinical and genetic approaches for diagnosing 209 index cases with 46,XY Differences of Sex Development.
N. Gomes, R. Batista, M. Y. Nishi, A. Lerário +14 more
2022Journal of Clinical Endocrinology and Metabolism38 citations Open access
Semantic Scholar
Genotype-phenotype correlations in central precocious puberty caused by MKRN3 mutations.
C. Seraphim, A. Canton, L. Montenegro, M. Piovesan +22 more
2020Journal of Clinical Endocrinology and Metabolism37 citations Open access
Semantic Scholar
Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
L. Montenegro, J. Labarta, M. Piovesan, A. Canton +9 more
2020Journal of Clinical Endocrinology and Metabolism37 citations Open access
Semantic Scholar
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
J. Granadillo, A. Stegmann, Hui Guo, K. Xia +31 more
2020Journal of Medical Genetics31 citations
Semantic Scholar
Rare Variants in the MECP2 Gene in Girls with Central Precocious Puberty
A. Canton, F. Tinano, L. Guasti, L. Montenegro +26 more
2023The Lancet Diabetes and Endocrinology26 citations Open access
Semantic Scholar
Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region
D. Macedo, M. França, L. Montenegro, Marina Cunha-Silva +7 more
2018Neuroendocrinology25 citations Open access
Semantic Scholar
SELAdb: A database of exonic variants in a Brazilian population referred to a quaternary medical center in São Paulo
A. Lerário, D. Mohan, L. Montenegro, Mariana Ferreira de Assis Funari +10 more
2020Clinics21 citations Open access
Semantic Scholar
Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.
A. Canton, A. Krepischi, L. Montenegro, S. Costa +16 more
2020Human Reproduction21 citations
Semantic Scholar
Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty
M. Krstevska-Konstantinova, J. Jovanovska, V. Tasic, L. Montenegro +3 more
2014Journal of Pediatric Endocrinology & Metabolism (JPEM)20 citations
Semantic Scholar
Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort
Priscila S. Barroso, A. Jorge, A. Lerário, L. Montenegro +5 more
2019Neuroendocrinology18 citations
Semantic Scholar
Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency
E. Şimşek, L. Montenegro, Ç. Binay, M. Demiral +2 more
2015Hormone Research in Paediatrics18 citations
Semantic Scholar
The interactive effect of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndrome.
A. F. Braz, E. F. Costalonga, L. Montenegro, E. Trarbach +6 more
2012Journal of Clinical Endocrinology and Metabolism18 citations
Semantic Scholar
High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
Raiane P Crespo, Thais P. Rocha, L. Montenegro, M. Y. Nishi +6 more
2022Journal of the Endocrine Society17 citations Open access
Semantic Scholar
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant.
F. Marchisotti, A. Jorge, L. Montenegro, Karina Berger +3 more
2009Growth Hormone & IGF Research17 citations
Semantic Scholar
Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels.
L. Montenegro, C. Seraphim, F. Tinano, M. Piovesan +12 more
2023European Journal of Endocrinology16 citations Open access
Semantic Scholar
Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development
L. Montenegro, A. Lerário, Miriam Y. Nishi, A. Jorge +1 more
2021Clinics16 citations Open access
Semantic Scholar
Analysis of the insulin‐like growth factor 1 receptor gene in children born small for gestational age: in vitro characterization of a novel mutation (p.Arg511Trp)
A. Leal, L. Montenegro, R. F. Saito, T. C. Ribeiro +4 more
2013Clinical Endocrinology15 citations
Semantic Scholar
Clinical and genetic characterization of familial central precocious puberty.
F. Tinano, A. Canton, L. Montenegro, André Luiz de Castro Leal +8 more
2023Journal of Clinical Endocrinology and Metabolism13 citations
Semantic Scholar
Novel MKRN3 Missense Mutations Associated with Central Precocious Puberty Reveal Distinct Effects on Ubiquitination.
J. C. Magnotto, A. Mancini, Keisha Bird, L. Montenegro +14 more
2023Journal of Clinical Endocrinology and Metabolism13 citations Open access
Semantic Scholar
Low Protein Expression of both ATRX and ZNRF3 as Novel Negative Prognostic Markers of Adult Adrenocortical Carcinoma
V. Brondani, A. M. F. Lacombe, Beatriz Marinho de Paula Mariani, L. Montenegro +9 more
2021International Journal of Molecular Sciences13 citations Open access
Semantic Scholar
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients
L. V. Ferreira, Silvia C. Souza, L. Montenegro, A. Malaquias +3 more
2008Clinical Endocrinology13 citations
Semantic Scholar
High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53
V. Brondani, L. Montenegro, A. M. F. Lacombe, Breno M. Magalhães +13 more
2020Cancers10 citations Open access
Semantic Scholar
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome.
L. Montenegro, L. Silveira, C. Tusset, M. de Castro +4 more
2013Fertility and Sterility10 citations Open access
Semantic Scholar
[Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism].
C. Tusset, E. Trarbach, L. Silveira, Daiane Beneduzzi +2 more
2011Arquivos brasileiros de endocrinologia e metabologia10 citations Open access
Semantic Scholar
Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver-Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11.
L. Montenegro, A. Leal, D. Coutinho, H. Valassi +4 more
2012European Journal of Endocrinology8 citations Open access
Semantic Scholar
The Genetic Etiology is a Relevant Cause of Central Precocious Puberty.
A. Canton, C. Seraphim, L. Montenegro, A. Krepischi +3 more
2024European Journal of Endocrinology7 citations
Semantic Scholar
Brazilian cohort and genes encoding for drug metabolizing enzymes and drug transporters.
V. Kim, T. van der Wal, Miriam Y. Nishi, L. Montenegro +3 more
2020Pharmacogenomics (London)7 citations Open access
Semantic Scholar
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
João L O Madeira, A. Jorge, R. Martin, L. Montenegro +9 more
2016European Journal of Endocrinology7 citations
Semantic Scholar
[Mutations in insulin-like growth factor receptor 1 gene (IGF1R) resulting in intrauterine and postnatal growth retardation].
André Luiz de Castro Leal, A. Canton, L. Montenegro, D. Coutinho +2 more
2011Arquivos brasileiros de endocrinologia e metabologia7 citations Open access
Semantic Scholar
[Phenotype variability in Noonan syndrome patients with and without PTPN11 mutation].
L. V. Ferreira, Sílvia C. A. L. Souza, L. Montenegro, I. J. Arnhold +5 more
2007Arquivos brasileiros de endocrinologia e metabologia5 citations
Semantic Scholar
Effects of Type 1 Insulin-Like Growth Factor Receptor Silencing in a Human Adrenocortical Cell Line
T. C. Ribeiro, A. Jorge, L. Montenegro, M. Almeida +4 more
2016Hormone and Metabolic Research4 citations
Semantic Scholar
Mutational analysis of TAC and TACR3 in idiopathic central precocious puberty.
M. Krstevska-Konstantinova, V. Tasic, L. Montenegro, Donco Dervisov +3 more
2014PRILOZI4 citations
Semantic Scholar
Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series
A. Faria, L. Montenegro, A. Jorge, Regina Matsunaga Martin +14 more
2025Archives of Endocrinology and Metabolism3 citations Open access
Semantic Scholar
Targeted massively parallel sequencing panel to diagnose genetic endocrine disorders in a tertiary hospital
A. Narcizo, Lais C. Cardoso, A. F. Benedetti, A. Jorge +7 more
2022Clinics2 citations Open access
Semantic Scholar
8151 The Genetic Etiology Is a Relevant Cause of Central Precocious Puberty
Ana Pinheiro Machado Canton, C. Seraphim, L. Montenegro, Ana Cristina Krepsichi +3 more
2024Journal of the Endocrine Society1 citations Open access
Semantic Scholar
Role of the Mevalonate Pathway in Adrenocortical Tumorigenesis
H. Lima-Valassi, A. Lerário, L. Montenegro, M. Fragoso +3 more
2020Hormone and Metabolic Research1 citations
Semantic Scholar
OR17-5 Clinical and Genetic Features of Constitutional Delay of Growth and Puberty
Priscila Sales Barroso, A. Lerário, L. Montenegro, Gabriela A. Vasques +5 more
2019Journal of the Endocrine Society1 citations Open access
Semantic Scholar
SUN-035 Performance of Mutation Pathogenicity Prediction Tools on Missense Variants Associated with 46XY Disorders of Sex Development
L. Montenegro, A. Lerário, M. Nishi, B. Mendonça
2019Journal of the Endocrine Society1 citations Open access
Semantic Scholar
Clinical and Genetic Features of Central Precocious Puberty Associated with Complex Phenotypes
A. Canton, V. Brito, L. Montenegro, C. Ramos +6 more
20181 citations
Semantic Scholar
Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort
L. Silveira, M. Teles, A. Abreu, L. Montenegro +11 more
20111 citations
Semantic Scholar

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A. Latronico×28
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D. Macedo — researcher profile on SciRah

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