Beatriz R. Versiani

481 total citations
16 papers, 335 citations indexed

About

Beatriz R. Versiani is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Beatriz R. Versiani has authored 16 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Reproductive Medicine. Recurrent topics in Beatriz R. Versiani's work include Hypothalamic control of reproductive hormones (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (3 papers). Beatriz R. Versiani is often cited by papers focused on Hypothalamic control of reproductive hormones (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (3 papers). Beatriz R. Versiani collaborates with scholars based in Brazil, United States and Netherlands. Beatriz R. Versiani's co-authors include Margaret de Castro, Ericka Barbosa Trarbach, Ana Cláudia Latronico, Berenice B. Mendonça, Heraldo Mendes Garmes, Elaine Maria Frade Costa, Maria Tereza Matias Baptista, Marcel Koenigkam Santos, Ana Paula Abreu and Paula Rejane Beserra Diniz and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Fertility and Sterility and Journal of the Neurological Sciences.

In The Last Decade

Beatriz R. Versiani

16 papers receiving 321 citations

Peers

Beatriz R. Versiani

GENET

Alexandre Moerman France

Eeva‐Maria Laitinen Finland

Blandine Esteva France

L Korniszewski Poland

Marzieh Mohseni Iran

B D Weintraub United States

Ανδρέας Παμπάνος Greece

Naoko Tsukamoto Japan

Robert F. Payette United States

Alenka Hodžić Slovenia

Alexandre Moerman France

Beatriz R. Versiani

247 ×1.4

152 ×1.0

GENET

186 ×1.5

15 ×0.4

60 ×1.8

GENET

Citations per year, relative to Beatriz R. Versiani Beatriz R. Versiani (= 1×) peers Alexandre Moerman

Countries citing papers authored by Beatriz R. Versiani

Since Specialization

Citations

This map shows the geographic impact of Beatriz R. Versiani's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Beatriz R. Versiani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beatriz R. Versiani more than expected).

Fields of papers citing papers by Beatriz R. Versiani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beatriz R. Versiani. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Beatriz R. Versiani. The network helps show where Beatriz R. Versiani may publish in the future.

Co-authorship network of co-authors of Beatriz R. Versiani

This figure shows the co-authorship network connecting the top 25 collaborators of Beatriz R. Versiani. A scholar is included among the top collaborators of Beatriz R. Versiani based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Beatriz R. Versiani. Beatriz R. Versiani is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Versiani, Beatriz R., et al.. (2025). SMAD4 Pathogenic Variants in Seven New Brazilian Individuals With Myhre Syndrome Including a New Family. American Journal of Medical Genetics Part A. 197(5). e63984–e63984. 1 indexed citations

Versiani, Beatriz R., et al.. (2022). ZDHHC9 X‐linked intellectual disability: Clinical and molecular characterization. American Journal of Medical Genetics Part A. 191(2). 599–604. 5 indexed citations

Moretti, Patricia, et al.. (2019). Defining the Critical Region for Intellectual Disability and Brain Malformations in 6q27 Microdeletions. Molecular Syndromology. 10(4). 202–208. 7 indexed citations

Shen, Jun, Beatriz R. Versiani, Robert Pogue, et al.. (2018). Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing. Hearing Research. 370. 181–188. 7 indexed citations

Versiani, Beatriz R., et al.. (2017). Expanding the spectrum of TBL1XR1 deletion: Report of a patient with brain and cardiac malformations. European Journal of Medical Genetics. 61(1). 29–33. 13 indexed citations

Varela, Patrícia, Beatriz R. Versiani, Érika L. Freitas, et al.. (2015). Partial 1q Duplications and Associated Phenotype. Molecular Syndromology. 6(6). 297–303. 11 indexed citations

Montenegro, Luciana Ribeiro, Letícia Ferreira Gontijo Silveira, Cíntia Tusset, et al.. (2013). Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome. Fertility and Sterility. 100(3). 854–859. 9 indexed citations

Santos, Marcel Koenigkam, Antônio Carlos Santos, Beatriz R. Versiani, et al.. (2011). Quantitative Magnetic Resonance Imaging Evaluation of the Olfactory System in Kallmann Syndrome: Correlation with a Clinical Smell Test. Neuroendocrinology. 94(3). 209–217. 38 indexed citations

Leite, André Ferreira, et al.. (2011). Craniofacial and Dental Features in Kabuki Syndrome Patients. The Cleft Palate-Craniofacial Journal. 50(4). 440–447. 6 indexed citations

10.

Santos, Marcel Koenigkam, Margaret de Castro, Beatriz R. Versiani, Paula Rejane Beserra Diniz, & Antônio Carlos dos Santos. (2010). Kallmann syndrome and mirror movements: White matter quantitative evaluation with magnetic resonance imaging. Journal of the Neurological Sciences. 292(1-2). 40–44. 10 indexed citations

11.

Santos, Marcel Koenigkam, Antônio Carlos dos Santos, Beatriz R. Versiani, et al.. (2008). Whole-Brain Voxel-Based Morphometry in Kallmann Syndrome Associated with Mirror Movements. American Journal of Neuroradiology. 29(9). 1799–1804. 13 indexed citations

12.

Abreu, Ana Paula, Ericka Barbosa Trarbach, Margaret de Castro, et al.. (2008). Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome. The Journal of Clinical Endocrinology & Metabolism. 93(10). 4113–4118. 90 indexed citations

13.

Trarbach, Ericka Barbosa, Elaine Maria Frade Costa, Beatriz R. Versiani, et al.. (2006). Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia. The Journal of Clinical Endocrinology & Metabolism. 91(10). 4006–4012. 82 indexed citations

14.

Versiani, Beatriz R., Ericka Barbosa Trarbach, Marcel Koenigkam Santos, et al.. (2006). Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism. Clinical Endocrinology. 66(2). 173–179. 21 indexed citations

15.

Kokitsu‐Nakata, Nancy Mizue, et al.. (2004). Encephalocraniocutaneous lipomatosis: report on a brazilian girl. Arquivos de Ciências da Saúde. 11(3). 192–194. 1 indexed citations

16.

Versiani, Beatriz R., et al.. (2003). Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes. Clinical Dysmorphology. 13(1). 1–5. 21 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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