Isabella Wimplinger

598 total citations
6 papers, 381 citations indexed

About

Isabella Wimplinger is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Isabella Wimplinger has authored 6 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cell Biology. Recurrent topics in Isabella Wimplinger's work include Ocular Disorders and Treatments (3 papers), melanin and skin pigmentation (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Isabella Wimplinger is often cited by papers focused on Ocular Disorders and Treatments (3 papers), melanin and skin pigmentation (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Isabella Wimplinger collaborates with scholars based in Germany, United States and Italy. Isabella Wimplinger's co-authors include Kerstin Kutsche, Juliane Najm, Victor V. Chizhikov, Susan L. Christian, Lawrence Charnas, Gökhan Uyanık, Jyotsna Sudi, Ulrike Orth, Denise Horn and Jeffrey A. Golden and has published in prestigious journals such as Nature Genetics, Neurology and The FASEB Journal.

In The Last Decade

Isabella Wimplinger

6 papers receiving 363 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Isabella Wimplinger Germany	6	226	178	102	61	34	6	381
Damir Musaev United States	12	359 1.6×	100 0.6×	105 1.0×	46 0.8×	31 0.9×	14	499
Carissa Adams United States	2	171 0.8×	124 0.7×	39 0.4×	32 0.5×	29 0.9×	3	275
Stéphanie Valence France	11	217 1.0×	114 0.6×	158 1.5×	123 2.0×	64 1.9×	22	407
Linda Manwaring United States	8	136 0.6×	175 1.0×	75 0.7×	31 0.5×	17 0.5×	15	374
Jane Juusola United States	13	218 1.0×	192 1.1×	28 0.3×	33 0.5×	34 1.0×	22	390
Emma Bedoukian United States	13	238 1.1×	119 0.7×	30 0.3×	17 0.3×	29 0.9×	31	375
Frédéric Tran Mau‐Them France	11	238 1.1×	167 0.9×	33 0.3×	32 0.5×	36 1.1×	30	397
Saadet Mercimek‐Andrews Canada	13	276 1.2×	226 1.3×	102 1.0×	95 1.6×	77 2.3×	52	623
Junehawk Lee South Korea	9	371 1.6×	221 1.2×	31 0.3×	34 0.6×	44 1.3×	20	569
Arivudainambi Ramalingam United States	9	219 1.0×	128 0.7×	32 0.3×	29 0.5×	12 0.4×	13	361

Countries citing papers authored by Isabella Wimplinger

Since Specialization

Citations

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

Fields of papers citing papers by Isabella Wimplinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabella Wimplinger

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

All Works

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6 of 6 papers shown

1.

Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations

2.

Huellner, Martin W., Sonja Schrepfer, Michael Weyand, et al.. (2008). Inhibition of aldehyde dehydrogenase type 2 attenuates vasodilatory action of nitroglycerin in human veins. The FASEB Journal. 22(7). 2561–2568. 20 indexed citations

3.

Wimplinger, Isabella, et al.. (2007). Mother and daughter with a terminal Xp deletion: Implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. European Journal of Medical Genetics. 50(6). 421–431. 29 indexed citations

4.

Jung, Hae Hyuk, et al.. (2007). Phenotypes of female adrenoleukodystrophy. Neurology. 68(12). 960–961. 20 indexed citations

5.

Wimplinger, Isabella, Gary M. Shaw, & Kerstin Kutsche. (2007). HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?. PubMed. 13. 1475–82. 29 indexed citations

6.

Wimplinger, Isabella, Manuela Morleo, Georg Rosenberger, et al.. (2006). Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome. The American Journal of Human Genetics. 79(5). 878–889. 81 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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