Janine Wagenstaller

1.7k total citations
9 papers, 842 citations indexed

About

Janine Wagenstaller is a scholar working on Genetics, Nephrology and Rheumatology. According to data from OpenAlex, Janine Wagenstaller has authored 9 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Nephrology and 3 papers in Rheumatology. Recurrent topics in Janine Wagenstaller's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (3 papers). Janine Wagenstaller is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Chromosomal and Genetic Variations (3 papers). Janine Wagenstaller collaborates with scholars based in Germany, Poland and Austria. Janine Wagenstaller's co-authors include Tim M. Strom, Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Feliciano J. Ramos, Murat Bastepe, Miikka Vikkula, Francis H. Glorieux, Stéphanie Kaiser, C Loris and José L. Olivares and has published in prestigious journals such as Nature Genetics, Brain and The American Journal of Human Genetics.

In The Last Decade

Janine Wagenstaller

8 papers receiving 808 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janine Wagenstaller Germany 7 502 419 283 191 167 9 842
Roz D. Lasker United States 10 433 0.9× 264 0.6× 326 1.2× 37 0.2× 106 0.6× 11 790
A. Miyauchi Japan 15 117 0.2× 57 0.1× 352 1.2× 82 0.4× 64 0.4× 26 611
Eva M. Pastor‐Arroyo Switzerland 12 182 0.4× 112 0.3× 156 0.6× 16 0.1× 79 0.5× 15 456
Xue Jun Fu Japan 16 147 0.3× 147 0.4× 434 1.5× 22 0.1× 59 0.4× 22 661
Gundula Leschik Germany 9 65 0.1× 234 0.6× 380 1.3× 123 0.6× 16 0.1× 11 608
Emilia Ballarè Italy 13 70 0.1× 213 0.5× 347 1.2× 61 0.3× 17 0.1× 14 757
A.M.H. Suiker Belgium 10 40 0.1× 195 0.5× 363 1.3× 45 0.2× 36 0.2× 10 787
Claudia Mischung Germany 6 58 0.1× 119 0.3× 234 0.8× 133 0.7× 11 0.1× 6 565
Vassos Neocleous Cyprus 15 103 0.2× 261 0.6× 444 1.6× 28 0.1× 13 0.1× 61 728
Velibor Tasic Germany 10 89 0.2× 114 0.3× 383 1.4× 37 0.2× 25 0.1× 14 620

Countries citing papers authored by Janine Wagenstaller

Since Specialization
Citations

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

Fields of papers citing papers by Janine Wagenstaller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janine Wagenstaller

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

All Works

9 of 9 papers shown
1.
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
2.
Zirn, Birgit, Maja Hempel, Andreas Hahn, et al.. (2008). Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype. American Journal of Medical Genetics Part A. 146A(22). 2960–2965. 6 indexed citations
3.
Stögmann, Elisabeth, Shadi Tawil, Janine Wagenstaller, et al.. (2008). A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. Neurogenetics. 10(1). 73–77. 28 indexed citations
4.
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
5.
Asmus, Friedrich, L. E. Hjermind, E. Dupont, et al.. (2007). Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype. Brain. 130(10). 2736–2745. 34 indexed citations
6.
Lorenz‐Depiereux, Bettina, Anna Benet‐Pagès, Gertrud Eckstein, et al.. (2006). Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3. The American Journal of Human Genetics. 78(2). 193–201. 252 indexed citations
7.
Bastepe, Murat, Bettina Lorenz‐Depiereux, Michella Ghassibe‐Sabbagh, et al.. (2006). An autosomal recessive hypophosphatemic disorder caused by homozygous mutations in dentin matrix protein 1 (DMP1).. Journal of Bone and Mineral Research. 21.
8.
Lorenz‐Depiereux, Bettina, Murat Bastepe, Anna Benet‐Pagès, et al.. (2006). DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nature Genetics. 38(11). 1248–1250. 373 indexed citations
9.
Langer, Sabine, Jochen B. Geigl, Janine Wagenstaller, et al.. (2006). Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy. American Journal of Medical Genetics Part A. 140A(7). 764–768. 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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