Veronica I. Lagos

669 total citations
9 papers, 493 citations indexed

About

Veronica I. Lagos is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Veronica I. Lagos has authored 9 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Veronica I. Lagos's work include BRCA gene mutations in cancer (8 papers), Prenatal Screening and Diagnostics (2 papers) and DNA Repair Mechanisms (2 papers). Veronica I. Lagos is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Prenatal Screening and Diagnostics (2 papers) and DNA Repair Mechanisms (2 papers). Veronica I. Lagos collaborates with scholars based in United States and Spain. Veronica I. Lagos's co-authors include Jeffrey N. Weitzel, Kathleen R. Blazer, Charité Ricker, Katrina Lowstuter, Josef Herzog, Melanie R. Palomares, Deborah J. MacDonald, Susan L. Neuhausen, Rebecca A. Nelson and Colleen McGuire and has published in prestigious journals such as JAMA, Critical Care and Annals of Surgical Oncology.

In The Last Decade

Veronica I. Lagos

9 papers receiving 463 citations

Peers

Countries citing papers authored by Veronica I. Lagos

Since Specialization

Citations

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

Fields of papers citing papers by Veronica I. Lagos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veronica I. Lagos. 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 Veronica I. Lagos. The network helps show where Veronica I. Lagos may publish in the future.

Co-authorship network of co-authors of Veronica I. Lagos

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Prognostic value of cell-free plasma DNA in patients with cardiac arrest outside the hospital: an observational cohort study 2010 ·Critical Care ·Francisco Arnalich, Marta Menéndez, Veronica I. Lagos, (unknown), (unknown), Rosa Codoceo, Juan José Vázquez, Eduardo López‐Collazo, Carmen Montiel	31
2	Evolving perspectives on genetic discrimination in health insurance among health care providers 2009 ·Familial Cancer ·(unknown), Katrina Lowstuter, Kimberly C. Banks, Veronica I. Lagos, (unknown), Jeffrey N. Weitzel	17
3	Contralateral Risk-Reducing Mastectomy in Young Breast Cancer Patients with and without Genetic Cancer Risk Assessment 2008 ·Annals of Surgical Oncology ·L. Phuong, Veronica I. Lagos, Melanie R. Palomares, Jeffrey N. Weitzel	7
4	Social‐cognitive aspects of underserved Latinas preparing to undergo genetic cancer risk assessment for hereditary breast and ovarian cancer 2008 ·Psycho-Oncology ·Veronica I. Lagos, Martin A. Perez, Charité Ricker, Kathleen R. Blazer, (unknown), Nancy Feldman, (unknown), Jeffrey N. Weitzel	41
5	Limited Family Structure and BRCA Gene Mutation Status in Single Cases of Breast Cancer 2007 ·JAMA ·Jeffrey N. Weitzel, Veronica I. Lagos, Carey A. Cullinane, (unknown), Julie O. Culver, Kathleen R. Blazer, Melanie R. Palomares, Katrina Lowstuter, Deborah J. MacDonald	128
6	Evidence for Common Ancestral Origin of a Recurring BRCA1 Genomic Rearrangement Identified in High-Risk Hispanic Families 2007 ·Cancer Epidemiology Biomarkers & Prevention ·Jeffrey N. Weitzel, Veronica I. Lagos, Josef Herzog, Thaddeus Judkins, Brant C. Hendrickson, (unknown), Charité Ricker, Katrina Lowstuter, Kathleen R. Blazer, Gail E. Tomlinson, (unknown)	72
7	Impact of genetic cancer risk assessment on cancer screening and prevention behaviors in an underserved predominantly Latina population. 2006 ·Cancer Epidemiology and Prevention Biomarkers ·Jeffrey N. Weitzel, Veronica I. Lagos, (unknown), Charité Ricker, (unknown), Nancy Feldman, (unknown), Martin A. Perez	1
8	If We Build It … Will They Come? – Establishing a Cancer Genetics Services Clinic for an Underserved Predominantly Latina Cohort 2006 ·Journal of Genetic Counseling ·Charité Ricker, Veronica I. Lagos, Nancy Feldman, (unknown), (unknown), (unknown), Kelly Gonzalez, Melanie R. Palomares, Kathleen R. Blazer, Katrina Lowstuter, Deborah J. MacDonald, Jeffrey N. Weitzel	56
9	Prevalence of BRCA Mutations and Founder Effect in High-Risk Hispanic Families 2005 ·Cancer Epidemiology Biomarkers & Prevention ·Jeffrey N. Weitzel, Veronica I. Lagos, Kathleen R. Blazer, Rebecca A. Nelson, Charité Ricker, Josef Herzog, Colleen McGuire, Susan L. Neuhausen	140

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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