Jill D. Siegfried

2.2k total citations
16 papers, 1.6k citations indexed

About

Jill D. Siegfried is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Jill D. Siegfried has authored 16 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cardiology and Cardiovascular Medicine, 7 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Jill D. Siegfried's work include Cardiomyopathy and Myosin Studies (13 papers), Cardiovascular Effects of Exercise (8 papers) and Viral Infections and Immunology Research (7 papers). Jill D. Siegfried is often cited by papers focused on Cardiomyopathy and Myosin Studies (13 papers), Cardiovascular Effects of Exercise (8 papers) and Viral Infections and Immunology Research (7 papers). Jill D. Siegfried collaborates with scholars based in United States. Jill D. Siegfried's co-authors include Ray E. Hershberger, Ana Morales, Duanxiang Li, Nadine Norton, Jorge Gonzalez‐Quintana, Jason Cowan, Evadnie Rampersaud, Eden R. Martin, Mark Hofmeyer and Ran Li and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Journal of the American College of Cardiology.

In The Last Decade

Jill D. Siegfried

16 papers receiving 1.6k citations

Peers

Jill D. Siegfried

CCM

GENET

SURGE

EPIDE

Michael Gramlich Germany

Melanie Care Canada

Koshiro Monzen Japan

Grazyna Czernuszewicz United States

Cornelis J. Boogerd Netherlands

Ying‐Jia Xu China

Hanying Chen China

Xing‐Biao Qiu China

Jiaxiang Qu United States

Cathy J. Hatcher United States

Michael Gramlich Germany

Jill D. Siegfried

1.1k ×0.9

CCM

773 ×1.0

58 ×0.3

GENET

116 ×0.7

SURGE

125 ×2.0

EPIDE

Citations per year, relative to Jill D. Siegfried Jill D. Siegfried (= 1×) peers Michael Gramlich

Countries citing papers authored by Jill D. Siegfried

Since Specialization

Citations

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

Fields of papers citing papers by Jill D. Siegfried

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jill D. Siegfried. 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 Jill D. Siegfried. The network helps show where Jill D. Siegfried may publish in the future.

Co-authorship network of co-authors of Jill D. Siegfried

This figure shows the co-authorship network connecting the top 25 collaborators of Jill D. Siegfried. A scholar is included among the top collaborators of Jill D. Siegfried 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 Jill D. Siegfried. Jill D. Siegfried 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

Gau, Chia‐Ling, Holly LaDuca, Hong Lu, et al.. (2014). Abstract 14: Identification of probands with multiple mutations in cancer susceptibility genes using a multigene panel approach. Cancer Research. 74(23_Supplement). 14–14. 2 indexed citations

Siegfried, Jill D., Mark Hofmeyer, Evadnie Rampersaud, et al.. (2013). Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy. Journal of Cardiac Failure. 19(4). 233–239. 39 indexed citations

Siegfried, Jill D., Ana Morales, Jessica D. Kushner, et al.. (2012). Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project. Journal of Genetic Counseling. 22(2). 164–174. 10 indexed citations

Norton, Nadine, Jill D. Siegfried, Duanxiang Li, & Ray E. Hershberger. (2011). Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy. Clinical and Translational Science. 4(5). 351–352. 12 indexed citations

Hershberger, Ray E. & Jill D. Siegfried. (2011). Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy. Journal of the American College of Cardiology. 57(16). 1641–1649. 228 indexed citations

Norton, Nadine, Duanxiang Li, Mark J. Rieder, et al.. (2011). Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy. The American Journal of Human Genetics. 88(3). 273–282. 262 indexed citations

Pinto, José R., Jill D. Siegfried, Michelle S. Parvatiyar, et al.. (2011). Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy. Journal of Biological Chemistry. 286(39). 34404–34412. 48 indexed citations

Rampersaud, Evadnie, Jill D. Siegfried, Nadine Norton, et al.. (2011). Rare variant mutations identified in pediatric patients with dilated cardiomyopathy. Progress in Pediatric Cardiology. 31(1). 39–47. 51 indexed citations

Hershberger, Ray E., Ana Morales, & Jill D. Siegfried. (2010). Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals. Genetics in Medicine. 12(11). 655–667. 199 indexed citations

10.

Li, Duanxiang, Ana Morales, Jorge Gonzalez‐Quintana, et al.. (2010). Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy. Clinical and Translational Science. 3(3). 90–97. 143 indexed citations

11.

Morales, Ana, José R. Pinto, Jill D. Siegfried, et al.. (2010). Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T Mutation. Clinical and Translational Science. 3(5). 219–226. 9 indexed citations

12.

Hershberger, Ray E., Nadine Norton, Ana Morales, et al.. (2010). Coding Sequence Rare Variants Identified in MYBPC3 , MYH6 , TPM1 , TNNC1 , and TNNI3 From 312 Patients With Familial or Idiopathic Dilated Cardiomyopathy. Circulation Cardiovascular Genetics. 3(2). 155–161. 186 indexed citations

13.

Painter, Thomas, Ran Li, Jill D. Siegfried, et al.. (2010). Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy. Circulation. 121(20). 2176–2182. 147 indexed citations

14.

Shah, Payal D., Mark Rosen, Jill E. Stopfer, et al.. (2009). Prospective study of breast MRI in BRCA1 and BRCA2 mutation carriers: effect of mutation status on cancer incidence. Breast Cancer Research and Treatment. 118(3). 539–546. 26 indexed citations

15.

Hershberger, Ray E., Jason Cowan, Ana Morales, & Jill D. Siegfried. (2009). Progress With Genetic Cardiomyopathies. Circulation Heart Failure. 2(3). 253–261. 147 indexed citations

16.

Palma, Maurizia Dalla, Susan M. Domchek, Jill E. Stopfer, et al.. (2008). The Relative Contribution of Point Mutations and Genomic Rearrangements in BRCA1 and BRCA2 in High-Risk Breast Cancer Families. Cancer Research. 68(17). 7006–7014. 82 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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