Heidi Thiese

2.4k total citations
4 papers, 113 citations indexed

About

Heidi Thiese is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Heidi Thiese has authored 4 papers receiving a total of 113 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Heidi Thiese's work include Genomics and Rare Diseases (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Heidi Thiese is often cited by papers focused on Genomics and Rare Diseases (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Heidi Thiese collaborates with scholars based in United States and Canada. Heidi Thiese's co-authors include Kathleen A. Leppig, Jill A. Rosenfeld, Beth S. Torchia, Lisa G. Shaffer, Anne M. Bandholz, Blake C. Ballif, Sarah Dyack, Bassem A. Bejjani, Christine Erdie-Lalena and Urvashi Surti and has published in prestigious journals such as Genetics in Medicine, Clinical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Heidi Thiese

4 papers receiving 98 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Heidi Thiese United States	4	92	66	11	9	7	4	113
Lila Allou France	6	89 1.0×	87 1.3×	12 1.1×	9 1.0×	3 0.4×	7	151
Petra F. de Vries Netherlands	5	86 0.9×	98 1.5×	7 0.6×	16 1.8×	4 0.6×	5	173
Candace Muss United States	3	114 1.2×	58 0.9×	29 2.6×	13 1.4×	8 1.1×	3	149
Jessica Sebastian United States	6	92 1.0×	64 1.0×	13 1.2×	21 2.3×	5 0.7×	11	146
Alfonso Caro‐Llopis Spain	7	132 1.4×	102 1.5×	16 1.5×	16 1.8×	7 1.0×	14	190
Chieko Chijiwa Canada	6	110 1.2×	89 1.3×	11 1.0×	15 1.7×	5 0.7×	9	147
Eva Maria Christina Schwaibold Germany	7	57 0.6×	66 1.0×	7 0.6×	31 3.4×	10 1.4×	11	124
Liliana Fernández United States	6	87 0.9×	49 0.7×	10 0.9×	41 4.6×	7 1.0×	8	151
Gwenaël Nadeau France	4	82 0.9×	48 0.7×	12 1.1×	17 1.9×	4 0.6×	6	120
Stefanie Beck‐Woedl Germany	7	68 0.7×	67 1.0×	14 1.3×	6 0.7×	7 1.0×	10	118

Countries citing papers authored by Heidi Thiese

Since Specialization

Citations

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

Fields of papers citing papers by Heidi Thiese

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi Thiese

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

All Works

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4 of 4 papers shown

1.

Leppig, Kathleen A., Heidi Thiese, David Carrel, et al.. (2016). Building a family network from genetic testing. Molecular Genetics & Genomic Medicine. 5(2). 122–129. 5 indexed citations

2.

Chowdhury, Shimul, Anne M. Bandholz, Sandhya Parkash, et al.. (2013). Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients. American Journal of Medical Genetics Part A. 164(1). 62–69. 33 indexed citations

3.

Alliman, Sarah, Justine Coppinger, Janet Marcadier, et al.. (2010). Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2. Clinical Genetics. 78(2). 162–168. 20 indexed citations

4.

Rosenfeld, Jill A., Kathleen A. Leppig, Blake C. Ballif, et al.. (2009). Genotype–phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations. Genetics in Medicine. 11(11). 797–805. 55 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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