Nora Urraca

776 total citations
17 papers, 382 citations indexed

About

Nora Urraca is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Nora Urraca has authored 17 papers receiving a total of 382 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Nora Urraca's work include Genomic variations and chromosomal abnormalities (8 papers), Congenital heart defects research (4 papers) and Obsessive-Compulsive Spectrum Disorders (3 papers). Nora Urraca is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Congenital heart defects research (4 papers) and Obsessive-Compulsive Spectrum Disorders (3 papers). Nora Urraca collaborates with scholars based in United States, Mexico and United Kingdom. Nora Urraca's co-authors include Lawrence T. Reiter, Janine M. LaSalle, Carmen Esmer, N. Carolyn Schanen, Ronald L. Thibert, Victoria E. Brewer, Kathryn McVicar, Humberto Nicolini, Enikö K. Pivnick and Beatríz Camarena and has published in prestigious journals such as Stem Cells, Psychiatry Research and Frontiers in Genetics.

In The Last Decade

Nora Urraca

17 papers receiving 374 citations

Peers

Nora Urraca

GENET

CMN

Tracie C. Rosser United States

Karina Griesi‐Oliveira Brazil

Madeleine Fannemel Norway

Elizabeth Dykens United States

Jean‐Pierre Müh France

Aneek Das Bhowmik India

Claude Cancès France

Marie‐Christine de Blois France

Tiffany Vu United States

J.J.A. Holden Canada

Tracie C. Rosser United States

Nora Urraca

205 ×0.9

GENET

260 ×1.4

86 ×0.8

30 ×0.5

GENET

91 ×2.3

CMN

Citations per year, relative to Nora Urraca Nora Urraca (= 1×) peers Tracie C. Rosser

Countries citing papers authored by Nora Urraca

Since Specialization

Citations

This map shows the geographic impact of Nora Urraca'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 Nora Urraca with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nora Urraca more than expected).

Fields of papers citing papers by Nora Urraca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nora Urraca. 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 Nora Urraca. The network helps show where Nora Urraca may publish in the future.

Co-authorship network of co-authors of Nora Urraca

This figure shows the co-authorship network connecting the top 25 collaborators of Nora Urraca. A scholar is included among the top collaborators of Nora Urraca 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 Nora Urraca. Nora Urraca is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Chandrasekhar, Anjana, Nora Urraca, Andrew M. Gross, et al.. (2023). Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes. American Journal of Medical Genetics Part A. 194(3). e63462–e63462. 2 indexed citations

Urraca, Nora, Kevin A. Hope, T. Grant Belgard, et al.. (2018). Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons. Molecular Autism. 9(1). 6–6. 20 indexed citations

Huang, Eunice Y., Nora Urraca, Brenda Finucane, et al.. (2017). Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses. JMIR Research Protocols. 6(10). e194–e194. 5 indexed citations

Dunaway, Keith W., Sarita Goorha, Nora Urraca, et al.. (2016). Dental Pulp Stem Cells Model Early Life and Imprinted DNA Methylation Patterns. Stem Cells. 35(4). 981–988. 25 indexed citations

Urraca, Nora, Brian J. Potter, Rachel J. Hundley, et al.. (2016). A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism. Frontiers in Genetics. 7. 205–205. 5 indexed citations

Urraca, Nora, Sarita Goorha, Quynh T. Tran, et al.. (2015). Characterization of neurons from immortalized dental pulp stem cells for the study of neurogenetic disorders. Stem Cell Research. 15(3). 722–730. 30 indexed citations

Urraca, Nora, Cezary Skobowiat, Kevin A. Hope, et al.. (2015). Assessment of the Tumorigenic Potential of Spontaneously Immortalized and hTERT-Immortalized Cultured Dental Pulp Stem Cells. Stem Cells Translational Medicine. 4(8). 905–912. 35 indexed citations

Urraca, Nora, Victoria E. Brewer, Enikö K. Pivnick, et al.. (2013). The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature. Autism Research. 6(4). 268–279. 116 indexed citations

Urraca, Nora, et al.. (2011). Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples. Molecular Autism. 2(1). 19–19. 56 indexed citations

10.

Urraca, Nora, Beatríz Camarena, Alejandro Aguilar, et al.. (2011). Association study of DRD3 gene in schizophrenia in Mexican sib-pairs. Psychiatry Research. 190(2-3). 367–368. 4 indexed citations

11.

Urraca, Nora, Lea K. Davis, Edwin H. Cook, N. Carolyn Schanen, & Lawrence T. Reiter. (2010). A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications. Genetic Testing and Molecular Biomarkers. 14(4). 571–576. 8 indexed citations

12.

Romero‐Hidalgo, Sandra, et al.. (2009). Attitudes and Anticipated Reactions to Genetic Testing for Cancer Among Patients in Mexico City. Genetic Testing and Molecular Biomarkers. 13(4). 477–483. 4 indexed citations

13.

Fresán, Ana, Beatríz Camarena, Rogelio Apiquián, et al.. (2007). Association Study of MAO-A and DRD4 Genes in Schizophrenic Patients with Aggressive Behavior. Neuropsychobiology. 55(3-4). 171–175. 30 indexed citations

14.

Urraca, Nora, et al.. (2005). An 8q21 Deletion in a Patient with Comorbid Psychosis and Mental Retardation. CNS Spectrums. 10(11). 864–866. 5 indexed citations

15.

Urraca, Nora, et al.. (2004). μ opioid receptor gene as a candidate for the study of obsessive compulsive disorder with and without tics. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 127B(1). 94–96. 27 indexed citations

16.

Esmer, Carmen, Nora Urraca, Alessandra Carnevale, & Victoria del Castillo. (2003). Patient follow‐up is a major problem at genetics clinics. American Journal of Medical Genetics Part A. 125A(2). 162–166. 8 indexed citations

17.

Nicolini, Humberto, Nora Urraca, Beatríz Camarena, et al.. (2001). Lack of Association of Apolipoprotein E Polymorphism in Obsessive-Compulsive Disorder. CNS Spectrums. 6(12). 978–979, 992. 2 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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