Babett Heye

497 total citations
7 papers, 365 citations indexed

About

Babett Heye is a scholar working on Genetics, Nutrition and Dietetics and Reproductive Medicine. According to data from OpenAlex, Babett Heye has authored 7 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Nutrition and Dietetics and 3 papers in Reproductive Medicine. Recurrent topics in Babett Heye's work include Hypothalamic control of reproductive hormones (3 papers), Biochemical Analysis and Sensing Techniques (3 papers) and Olfactory and Sensory Function Studies (2 papers). Babett Heye is often cited by papers focused on Hypothalamic control of reproductive hormones (3 papers), Biochemical Analysis and Sensing Techniques (3 papers) and Olfactory and Sensory Function Studies (2 papers). Babett Heye collaborates with scholars based in Germany, Italy and Switzerland. Babett Heye's co-authors include Adrian Danek, Thomas Meitinger, Corinna Menzel, Ida Vogel, Hans‐Hilger Ropers, Niels Tommerup, Vera M. Kalscheuer, Rikke S. Møller, Zeynep Tümer and Maria Hoeltzenbein and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and European Journal of Neuroscience.

In The Last Decade

Babett Heye

7 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Babett Heye Germany 7 206 147 77 61 48 7 365
Beatriz R. Versiani Brazil 10 149 0.7× 126 0.9× 17 0.2× 178 2.9× 11 0.2× 16 335
Elisabeth Gabau Spain 16 463 2.2× 336 2.3× 45 0.6× 37 0.6× 103 2.1× 36 675
Ikuo Tomioka Japan 12 83 0.4× 283 1.9× 101 1.3× 62 1.0× 23 0.5× 23 429
Marzieh Mohseni Iran 13 120 0.6× 259 1.8× 40 0.5× 51 0.8× 27 0.6× 37 470
Ανδρέας Παμπάνος Greece 12 140 0.7× 233 1.6× 32 0.4× 21 0.3× 92 1.9× 28 459
Tiia Reimand Estonia 13 291 1.4× 229 1.6× 20 0.3× 11 0.2× 21 0.4× 41 488
Kil Saeng Chung South Korea 13 135 0.7× 243 1.7× 306 4.0× 189 3.1× 6 0.1× 16 476
D F Smeets Netherlands 10 391 1.9× 296 2.0× 30 0.4× 122 2.0× 47 1.0× 11 478
D Robinson United Kingdom 10 410 2.0× 269 1.8× 31 0.4× 32 0.5× 28 0.6× 14 534
Yu Tao China 11 88 0.4× 454 3.1× 64 0.8× 24 0.4× 53 1.1× 18 557

Countries citing papers authored by Babett Heye

Since Specialization
Citations

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

Fields of papers citing papers by Babett Heye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Babett Heye

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

All Works

7 of 7 papers shown
1.
Møller, Rikke S., Maria Hoeltzenbein, Babett Heye, et al.. (2008). Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly. The American Journal of Human Genetics. 82(5). 1165–1170. 116 indexed citations
2.
Wagenstaller, Janine, Stephanie Spranger, Bettina Lorenz‐Depiereux, et al.. (2007). Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation. The American Journal of Human Genetics. 81(4). 768–779. 93 indexed citations
3.
Panza, Emanuele, Giorgio Gimelli, Mario Passalacqua, et al.. (2007). The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. International Journal of Molecular Medicine. 19(3). 429–35. 13 indexed citations
4.
Schiavi, Elia Di, et al.. (2005). UMODL1/Olfactorin is an extracellular membrane‐bound molecule with a restricted spatial expression in olfactory and vomeronasal neurons. European Journal of Neuroscience. 21(12). 3291–3300. 14 indexed citations
5.
Hudson, Robyn, Matthias Laska, Thomas Berger, et al.. (1994). Olfactory function in patients with hypogonadotropic hypogonadism: an all-or-none phenomenon?. Chemical Senses. 19(1). 57–69. 16 indexed citations
6.
Danek, Adrian, et al.. (1992). Cortically evoked motor responses in patients with Xp22.3‐linked Kallmann's syndrome and in female gene carriers. Annals of Neurology. 31(3). 299–304. 60 indexed citations
7.
Meitinger, Thomas, Babett Heye, Christine Petit, et al.. (1990). Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.. PubMed. 47(4). 664–9. 53 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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