Heide Seidel

1.2k total citations
24 papers, 337 citations indexed

About

Heide Seidel is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Heide Seidel has authored 24 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Heide Seidel's work include Genomic variations and chromosomal abnormalities (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Connective tissue disorders research (4 papers). Heide Seidel is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Connective tissue disorders research (4 papers). Heide Seidel collaborates with scholars based in Germany, Australia and Austria. Heide Seidel's co-authors include H. Zankl, Thomas Meitinger, Simone Schuffenhauer, K. D. Zang, Tim M. Strom, Kerstin Kutsche, Janine Wagenstaller, Jan Murken, Martin Zenker and Maja Hempel and has published in prestigious journals such as The Lancet, Gene and Human Mutation.

In The Last Decade

Heide Seidel

23 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heide Seidel Germany 14 192 182 48 45 42 24 337
Clara S. Moore United States 12 219 1.1× 209 1.1× 47 1.0× 32 0.7× 16 0.4× 13 407
Pietro Sirleto Italy 12 137 0.7× 221 1.2× 20 0.4× 30 0.7× 28 0.7× 25 399
Ken L. Jones United States 6 96 0.5× 154 0.8× 22 0.5× 38 0.8× 28 0.7× 7 284
Eugene W. Taylor United States 9 189 1.0× 159 0.9× 28 0.6× 30 0.7× 42 1.0× 17 335
Natália D. Linhares Brazil 10 102 0.5× 168 0.9× 27 0.6× 21 0.5× 89 2.1× 21 350
Alina Khromykh United States 10 164 0.9× 202 1.1× 9 0.2× 42 0.9× 30 0.7× 13 367
Milena Simioni Brazil 9 195 1.0× 125 0.7× 10 0.2× 20 0.4× 14 0.3× 26 272
Philip N. Mowrey United States 11 232 1.2× 162 0.9× 24 0.5× 38 0.8× 7 0.2× 22 436
Angeline Lai Singapore 10 133 0.7× 152 0.8× 12 0.3× 67 1.5× 17 0.4× 31 349
Katherine Neas New Zealand 12 103 0.5× 214 1.2× 158 3.3× 26 0.6× 50 1.2× 22 430

Countries citing papers authored by Heide Seidel

Since Specialization
Citations

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

Fields of papers citing papers by Heide Seidel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heide Seidel

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

All Works

20 of 20 papers shown
1.
Westphal, Dominik S., Elisa Mastantuono, Heide Seidel, et al.. (2022). There is more to it than just congenital heart defects – The phenotypic spectrum of TAB2-related syndrome. Gene. 814. 146167–146167. 2 indexed citations
2.
Meierhofer, Christian, Alfred Hager, Andreas Kühn, et al.. (2019). Long-term outcomes of childhood onset Noonan compared to sarcomere hypertrophic cardiomyopathy. Cardiovascular Diagnosis and Therapy. 9(S2). S299–S309. 18 indexed citations
3.
Seidel, Heide, Claudia Pujol, Christian Meierhofer, et al.. (2019). Hemostatic abnormalities in adult patients with Marfan syndrome. Cardiovascular Diagnosis and Therapy. 9(S2). S209–S220. 7 indexed citations
4.
Backer, Julie De, Yskert Von Kodolitsch, Kerstin Kutsche, et al.. (2019). Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome. Journal of Clinical Medicine. 8(12). 2079–2079. 16 indexed citations
5.
Umair, Muhammad, Heide Seidel, Asmat Ullah, et al.. (2017). Ellis–van Creveld syndrome and profound deafness resulted by sequence variants in the EVC / EVC2 and TMC1 genes. Journal of Genetics. 96(6). 1005–1014. 20 indexed citations
6.
Cleuziou, Julie, Jelena Pabst von Ohain, Christian Meierhofer, et al.. (2017). Clinical long-term outcome of septal myectomy for obstructive hypertrophic cardiomyopathy in infants. European Journal of Cardio-Thoracic Surgery. 53(3). 538–544. 16 indexed citations
7.
Wendorff, Heiko, Jaroslav Pelisek, Alexander Zimmermann, et al.. (2013). Early venous manifestation of Ehlers–Danlos syndrome Type IV through a novel mutation in COL3A1. Cardiovascular Pathology. 22(6). 488–492. 4 indexed citations
8.
Lorenz, Sybille, et al.. (2012). Two cases with severe lethal course of Costello syndrome associated with HRAS p.G12C and p.G12D. European Journal of Medical Genetics. 55(11). 615–619. 24 indexed citations
9.
Hempel, Maja, et al.. (2009). Microdeletion syndrome 16p11.2‐p12.2: Clinical and molecular characterization. American Journal of Medical Genetics Part A. 149A(10). 2106–2112. 40 indexed citations
10.
Frank, Valeska, Nadina Ortiz Brüchle, Suzanna G.M. Frints, et al.. (2007). Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome. Human Mutation. 28(6). 638–639. 17 indexed citations
11.
Seidel, Heide & Ortrud K. Steinlein. (2007). Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean fever. European Journal of Pediatrics. 167(7). 827–828. 1 indexed citations
12.
Kaemmerer, Harald, Erwin Oechslin, Heide Seidel, et al.. (2005). Marfan syndrome: what internists and pediatric or adult cardiologists need to know. Expert Review of Cardiovascular Therapy. 3(5). 891–909. 10 indexed citations
13.
Holinski‐Feder, Elke, Astrid Golla, Imma Rost, et al.. (1996). Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). American Journal of Medical Genetics. 64(1). 125–130. 18 indexed citations
14.
Schuffenhauer, Simone, et al.. (1995). DiGeorge syndrome and partial monosomy 10p: case report and review.. PubMed. 38(3). 162–7. 23 indexed citations
15.
Steinbach, Peter, Gholamali Tariverdian, Ingo Kennerknecht, et al.. (1993). Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families. Human Genetics. 92(5). 491–498. 12 indexed citations
16.
Schuffenhauer, Simone, et al.. (1992). De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10‐year‐old boy. Clinical Genetics. 42(5). 246–250. 12 indexed citations
17.
Weber, Bernhard H. F., W. Schempp, Ulrike Orth, Heide Seidel, & Andreas Gal. (1987). A Y/5 translocation in a 45,X male with cri du chat syndrome. Human Genetics. 77(2). 145–150. 15 indexed citations
18.
Seidel, Heide, et al.. (1981). 45, X Constitution in a H‐Y antigen positive boy with partial monosomy 5p. Clinical Genetics. 19(4). 290–297. 9 indexed citations
19.
Zankl, H., Heide Seidel, & K. D. Zang. (1975). SEX-CHROMOSOME LOSS IN HUMAN TUMOURS. The Lancet. 305(7900). 221–221. 11 indexed citations
20.
Zankl, H., et al.. (1975). Cytological and cytogenetical studies on brain tumors. V. Preferential loss of sex chromosomes in human meningiomas.. PubMed. 27(2). 119–28. 16 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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