Christine E. Seidman

2.7k total citations · 1 hit paper
10 papers, 1.6k citations indexed

About

Christine E. Seidman is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Christine E. Seidman has authored 10 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Christine E. Seidman's work include Cardiomyopathy and Myosin Studies (3 papers), Vascular Anomalies and Treatments (2 papers) and Congenital Heart Disease Studies (2 papers). Christine E. Seidman is often cited by papers focused on Cardiomyopathy and Myosin Studies (3 papers), Vascular Anomalies and Treatments (2 papers) and Congenital Heart Disease Studies (2 papers). Christine E. Seidman collaborates with scholars based in United States, United Kingdom and Canada. Christine E. Seidman's co-authors include Jonathan G. Seidman, David A. Conner, Lynda Robitaille, Joachim P. Schmitt, Georges Nemer, Benoit G. Bruneau, Sophie Jeanne Cécile Caron, Frédéric Charron, Manfred Gessler and Mona Nemer and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Christine E. Seidman

10 papers receiving 1.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

2001 807 citations Benoit G. Bruneau, Georges Nemer et al. Cell profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Christine E. Seidman United States	8	1.0k	354	265	244	244	10	1.6k
Desirée du Sart Australia	26	888 0.9×	130 0.4×	76 0.3×	394 1.6×	53 0.2×	39	2.0k
Mayada Tassabehji United Kingdom	15	1.2k 1.2×	71 0.2×	106 0.4×	58 0.2×	60 0.2×	17	2.2k
Francesca Vitelli Italy	18	1.9k 1.8×	118 0.3×	399 1.5×	166 0.7×	721 3.0×	28	2.3k
Henny H. Lemmink Netherlands	24	1.3k 1.3×	77 0.2×	247 0.9×	707 2.9×	30 0.1×	55	2.4k
Mary Redmond Hutson United States	21	2.2k 2.1×	317 0.9×	562 2.1×	74 0.3×	956 3.9×	29	2.6k
Amy L. Dickson United States	15	1.6k 1.5×	319 0.9×	327 1.2×	117 0.5×	324 1.3×	22	1.9k
Liesbeth van Iperen Netherlands	22	813 0.8×	125 0.4×	111 0.4×	19 0.1×	128 0.5×	29	1.3k
Joel Zupicich United States	6	2.2k 2.1×	696 2.0×	121 0.5×	166 0.7×	256 1.0×	7	3.0k
Cornelia Wiese Germany	11	1.1k 1.1×	338 1.0×	93 0.4×	170 0.7×	111 0.5×	13	1.5k
Tatiana A. Yatskievych United States	23	1.5k 1.5×	113 0.3×	43 0.2×	71 0.3×	82 0.3×	31	1.8k

Countries citing papers authored by Christine E. Seidman

Since Specialization

Citations

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

Fields of papers citing papers by Christine E. Seidman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christine E. Seidman. 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 Christine E. Seidman. The network helps show where Christine E. Seidman may publish in the future.

Co-authorship network of co-authors of Christine E. Seidman

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

All Works

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10 of 10 papers shown

Rai, Archana, Bo Yuan, Karen J. Coveler, et al.. (2025). Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach. The American Journal of Human Genetics. 112(7). 1664–1680. 1 indexed citations

Cirino, Allison L., Neal K. Lakdawala, Barbara McDonough, et al.. (2017). A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients. Circulation Cardiovascular Genetics. 10(5). 59 indexed citations

Haines, Jonathan L., et al.. (2011). Preface. Current Protocols in Human Genetics. 70(1). 1 indexed citations

Bruneau, Benoit G., Georges Nemer, Joachim P. Schmitt, et al.. (2001). A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease. Cell. 106(6). 709–721. 807 indexed citations breakdown →

Fatkin, Diane, Michael E. Christe, Orlando Aristizábal, et al.. (1999). Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene. Journal of Clinical Investigation. 103(1). 147–153. 91 indexed citations

Gao, Wei Dong, N Pérez, Christine E. Seidman, Jonathan G. Seidman, & Eduardo Marbán. (1999). Altered cardiac excitation–contraction coupling in mutant mice with familial hypertrophic cardiomyopathy. Journal of Clinical Investigation. 103(5). 661–666. 47 indexed citations

Robertson, Nahid G., Stefan Heller, Saumil N. Merchant, et al.. (1998). Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. Nature Genetics. 20(3). 299–303. 268 indexed citations

Shovlin, Claire L., Judith M. Hughes, Jenny Scott, Christine E. Seidman, & Jonathan G. Seidman. (1997). Characterization of Endoglin and Identification of Novel Mutations in Hereditary Hemorrhagic Telangiectasia. The American Journal of Human Genetics. 61(1). 68–79. 137 indexed citations

Shovlin, Claire L., J. M. B. Hughes, Edward G. D. Tuddenham, et al.. (1994). A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3. Nature Genetics. 6(2). 205–209. 153 indexed citations

10.

Johnston, Mark, Christine E. Seidman, David Garfinkel, et al.. (1975). Biochemistry and genetics of Klebsiella pneumoniae mutant strains unable to fix N2. Journal of Bacteriology. 121(3). 759–765. 56 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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