Andreas Hehr

1.2k total citations
12 papers, 747 citations indexed

About

Andreas Hehr is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Andreas Hehr has authored 12 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Andreas Hehr's work include Cleft Lip and Palate Research (4 papers), Craniofacial Disorders and Treatments (3 papers) and Receptor Mechanisms and Signaling (3 papers). Andreas Hehr is often cited by papers focused on Cleft Lip and Palate Research (4 papers), Craniofacial Disorders and Treatments (3 papers) and Receptor Mechanisms and Signaling (3 papers). Andreas Hehr collaborates with scholars based in Germany, United States and Switzerland. Andreas Hehr's co-authors include Maximilian Muenke, Nathaniel H. Robin, Paul Rutland, H. Wolfgang Losken, Sue Malcolm, William Reardon, Robin M. Winter, Louise J. Pulleyn, Albert Schinzel and Elaine H. Zackai and has published in prestigious journals such as Nature Genetics, International Journal of Molecular Sciences and Annals of the New York Academy of Sciences.

In The Last Decade

Andreas Hehr

12 papers receiving 725 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andreas Hehr Germany	6	568	490	56	45	38	12	747
Farooq Ahmad Pakistan	12	227 0.4×	272 0.6×	25 0.4×	34 0.8×	54 1.4×	38	421
Emma Hobson United Kingdom	9	256 0.5×	213 0.4×	40 0.7×	40 0.9×	42 1.1×	24	405
Miriam Aza‐Carmona Spain	11	345 0.6×	303 0.6×	20 0.4×	30 0.7×	23 0.6×	26	488
Satoshi Ishikiriyama Japan	10	283 0.5×	289 0.6×	20 0.4×	128 2.8×	23 0.6×	21	472
Fernanda Sarquis Jehee Brazil	13	521 0.9×	393 0.8×	52 0.9×	72 1.6×	15 0.4×	26	691
A Baxová Czechia	10	246 0.4×	243 0.5×	39 0.7×	23 0.5×	33 0.9×	40	416
Martha Kalff-Suske Germany	10	159 0.3×	312 0.6×	27 0.5×	27 0.6×	12 0.3×	15	475
Nina Bögershausen Germany	11	234 0.4×	280 0.6×	28 0.5×	13 0.3×	16 0.4×	13	444
Josephine Wincent Sweden	12	214 0.4×	243 0.5×	51 0.9×	66 1.5×	11 0.3×	19	467
Anna Sowińska‐Seidler Poland	13	237 0.4×	254 0.5×	22 0.4×	74 1.6×	34 0.9×	38	409

Countries citing papers authored by Andreas Hehr

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Hehr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Hehr

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

All Works

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12 of 12 papers shown

Hintze, Stefan, et al.. (2021). Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 22(16). 8607–8607. 8 indexed citations

Hehr, Andreas, et al.. (2016). Präimplantationsdiagnostik – methodische Aspekte. Medizinische Genetik. 28(3). 332–341. 2 indexed citations

Hehr, Andreas, et al.. (2014). Präimplantationsdiagnostik. Medizinische Genetik. 26(4). 417–426. 1 indexed citations

Hehr, Andreas, et al.. (2011). Präimplantationsdiagnostik für monogen vererbte Erkrankungen. Medizinische Genetik. 23(4). 469–478. 1 indexed citations

Hehr, Ute, Daniel Pineda‐Alvarez, Goekhan Uyanik, et al.. (2010). Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly. Human Genetics. 127(5). 555–561. 33 indexed citations

Hehr, Andreas, Burkhardt Seifert, Ute Hehr, & M. Bals‐Pratsch. (2009). Polar Body Diagnosis for Monogenic Disorders in Regensburg. Journal für Kardiologie (Krause & Pachernegg GmbH). 6(1). 27–31. 2 indexed citations

Hehr, Ute, et al.. (2004). Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation. European Journal of Pediatrics. 163(7). 347–52. 40 indexed citations

Hieble, J. Paul, et al.. (1998). Molecular basis for the stereoselective interactions of catecholamines with alpha-adrenoceptors.. PubMed. 41. 225–8. 4 indexed citations

Hehr, Andreas, et al.. (1997). Ser<sup>16</sup><sup>5</sup> of Transmembrane Helix IV Is Not Involved in the Interaction of Catecholamines with the Alpha-2a-Adrenoceptor. Pharmacology. 55(1). 18–24. 5 indexed citations

10.

Hehr, Andreas, George Feldman, Nathaniel H. Robin, et al.. (1995). Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome. Human Molecular Genetics. 4(3). 323–328. 184 indexed citations

11.

Muenke, Maximilian, Andreas Hehr, Nathaniel H. Robin, et al.. (1994). A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome. Nature Genetics. 8(3). 269–274. 466 indexed citations

12.

Gläser, Christiane, et al.. (1994). The Importance of the α₂MR/LRP for Human Genetics. Annals of the New York Academy of Sciences. 737(1). 447–450. 1 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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