Gloria Zender

707 total citations
11 papers, 461 citations indexed

About

Gloria Zender is a scholar working on Molecular Biology, Epidemiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Gloria Zender has authored 11 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Epidemiology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Gloria Zender's work include Congenital heart defects research (8 papers), Congenital Heart Disease Studies (6 papers) and Cardiac Valve Diseases and Treatments (2 papers). Gloria Zender is often cited by papers focused on Congenital heart defects research (8 papers), Congenital Heart Disease Studies (6 papers) and Cardiac Valve Diseases and Treatments (2 papers). Gloria Zender collaborates with scholars based in United States, Tunisia and Russia. Gloria Zender's co-authors include Kim L. McBride, Sara Fitzgerald‐Butt, John W. Belmont, Vidu Garg, J.A. Towbin, Sarah Cole, Stephanie LaHaye, Elizabeth Bonachea, Peter White and Sheng‐Wei Chang and has published in prestigious journals such as Circulation, Kidney International and Human Molecular Genetics.

In The Last Decade

Gloria Zender

11 papers receiving 455 citations

Peers

Countries citing papers authored by Gloria Zender

Since Specialization

Citations

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

Fields of papers citing papers by Gloria Zender

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gloria Zender

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	17O Schwann cell transduction and PMP22 target engagement in non-human primates supports translation of RNAi-based gene therapy for CMT1A 2024 ·Neuromuscular Disorders ·Lindsay M. Wallace, (unknown), (unknown), (unknown), Gloria Zender, Murat Bayazıt, (unknown), Kleopas A. Kleopa, (unknown)	1
2	Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery 2022 ·PLoS Genetics ·David Gordon, David Cunningham, Gloria Zender, Patrick J. Lawrence, (unknown), Hui Lin, Sara Fitzgerald‐Butt, Katherine Myers, (unknown), Donald J. Corsmeier, (unknown), Harkness Kuck, Saranga Wijeratne, (unknown), Benjamin Kelly, Vidu Garg, Peter White, Kim L. McBride	15
3	Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy 2020 ·PLoS Genetics ·Sathiyanarayanan Manivannan, (unknown), (unknown), David Gordon, Gloria Zender, Zhe Han, Sara Fitzgerald‐Butt, Peter White, Kim L. McBride, Maher Kharrat, Vidu Garg	19
4	Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease 2016 ·Circulation Cardiovascular Genetics ·Stephanie LaHaye, (unknown), Madhumita Basu, Jessica Bowman, Sara Fitzgerald‐Butt, Gloria Zender, Kevin Bosse, Kim L. McBride, Peter White, Vidu Garg	62
5	Abstract 12295: Utilization of Whole-Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease 2015 ·Circulation ·Stephanie LaHaye, (unknown), Jessica Bowman, Sara Fitzgerald‐Butt, Gloria Zender, Kevin Bosse, Kim L. McBride, Peter White, Vidu Garg	1
6	Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve 2014 ·BMC Medical Genomics ·Elizabeth Bonachea, Gloria Zender, Peter White, (unknown), David L. Newsom, Sara Fitzgerald‐Butt, Vidu Garg, Kim L. McBride	43
7	Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve 2014 ·Pediatric Research ·Elizabeth Bonachea, Sheng‐Wei Chang, Gloria Zender, Stephanie LaHaye, Sara Fitzgerald‐Butt, Kim L. McBride, Vidu Garg	69
8	Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects 2011 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Kim L. McBride, Gloria Zender, Sara Fitzgerald‐Butt, (unknown), Susan Fernbach, Gladys Zapata, Mark Lewin, Jeffrey A. Towbin, John W. Belmont	34
9	Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruption 2010 ·Kidney International ·Brian Becknell, Gloria Zender, (unknown), Peter B. Baker, Kim L. McBride, Wentian Luo, David S. Hains, Dorin‐Bogdan Borza, Andrew L. Schwaderer	14
10	Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome) 2009 ·European Journal of Human Genetics ·Kim L. McBride, Gloria Zender, Sara Fitzgerald‐Butt, Daniel Koehler, (unknown), Susan Fernbach, Kwanghyuk Lee, Jeffrey A. Towbin, Suzanne M. Leal, John W. Belmont	54
11	NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling 2008 ·Human Molecular Genetics ·Kim L. McBride, (unknown), Gloria Zender, Sara Fitzgerald‐Butt, J.A. Towbin, John W. Belmont, Sarah Cole	149

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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