Sandra M. Pasternack

1.5k total citations
21 papers, 823 citations indexed

About

Sandra M. Pasternack is a scholar working on Molecular Biology, Cell Biology and Urology. According to data from OpenAlex, Sandra M. Pasternack has authored 21 papers receiving a total of 823 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cell Biology and 8 papers in Urology. Recurrent topics in Sandra M. Pasternack's work include RNA regulation and disease (10 papers), Hair Growth and Disorders (8 papers) and Skin and Cellular Biology Research (8 papers). Sandra M. Pasternack is often cited by papers focused on RNA regulation and disease (10 papers), Hair Growth and Disorders (8 papers) and Skin and Cellular Biology Research (8 papers). Sandra M. Pasternack collaborates with scholars based in Germany, Austria and Spain. Sandra M. Pasternack's co-authors include Regina C. Betz, Markus M. Nöthen, Ivar von Kügelgen, Roland Kruse, Alfredo Ramı́rez, Franz Rüschendorf, Khalid Al Aboud, Young‐Ae Lee, Axel M. Hillmer and Katrin Voß and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Investigative Dermatology.

In The Last Decade

Sandra M. Pasternack

21 papers receiving 810 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra M. Pasternack Germany 14 538 378 240 124 98 21 823
York Kamenisch Germany 15 435 0.8× 119 0.3× 115 0.5× 229 1.8× 84 0.9× 21 765
Tammy‐Claire Troy Canada 15 511 0.9× 166 0.4× 66 0.3× 75 0.6× 60 0.6× 27 841
Takahiro Aoto Japan 8 484 0.9× 145 0.4× 92 0.4× 98 0.8× 80 0.8× 12 697
Peter S. Budd United Kingdom 10 374 0.7× 426 1.1× 61 0.3× 102 0.8× 156 1.6× 18 740
N. Meier Germany 10 256 0.5× 156 0.4× 127 0.5× 83 0.7× 37 0.4× 11 487
Yahav Yosefzon Israel 14 415 0.8× 89 0.2× 48 0.2× 41 0.3× 57 0.6× 19 576
R. Paus Germany 11 198 0.4× 288 0.8× 559 2.3× 417 3.4× 35 0.4× 15 867
Chiung-Ying Chang United States 8 399 0.7× 115 0.3× 56 0.2× 38 0.3× 33 0.3× 10 597
Yonghua Pan China 7 290 0.5× 76 0.2× 78 0.3× 86 0.7× 54 0.6× 16 460
Ka Wai Mok United States 6 238 0.4× 155 0.4× 171 0.7× 76 0.6× 41 0.4× 7 495

Countries citing papers authored by Sandra M. Pasternack

Since Specialization
Citations

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

Fields of papers citing papers by Sandra M. Pasternack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra M. Pasternack. 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 Sandra M. Pasternack. The network helps show where Sandra M. Pasternack may publish in the future.

Co-authorship network of co-authors of Sandra M. Pasternack

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

All Works

20 of 20 papers shown
1.
Redler, Silke, Sandra M. Pasternack, Sabrina Wolf, et al.. (2015). A novelKRT86mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. Clinical and Experimental Dermatology. 40(7). 781–785. 5 indexed citations
2.
3.
Pasternack, Sandra M., Elham Paknia, Hans Christian Hennies, et al.. (2012). Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex. The American Journal of Human Genetics. 92(1). 81–87. 32 indexed citations
4.
Giehl, Kathrin, Gertrud Eckstein, Sandra M. Pasternack, et al.. (2012). Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer. The American Journal of Human Genetics. 91(4). 754–759. 41 indexed citations
5.
Redler, Silke, Felix F. Brockschmidt, Christine Herold, et al.. (2012). Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance. Journal of Investigative Dermatology. 132(9). 2192–2197. 98 indexed citations
6.
Pasternack, Sandra M., Detlef Böckenhauer, Velibor Tasic, et al.. (2012). A Premature Termination Mutation in a Patient with Lowe Syndrome without Congenital Cataracts: Dropping the “O” in OCRL. Klinische Pädiatrie. 225(1). 29–33. 13 indexed citations
7.
Hanneken, S., Arno Rütten, Sibylle Eigelshoven, et al.. (2011). Morbus Galli-Galli. Der Hautarzt. 62(11). 842–851. 13 indexed citations
8.
Pasternack, Sandra M., Britta Fiebig, Nina Ishorst, et al.. (2011). Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay. British Journal of Dermatology. 165(5). 1127–1132. 2 indexed citations
9.
Mauerer, Andreas, Regina C. Betz, Sandra M. Pasternack, Michael Landthaler, & Christian Hafner. (2010). Generalized Solar Lentigines in a Patient with a History of Radon Exposure. Dermatology. 221(3). 206–210. 7 indexed citations
10.
Hanneken, S., Arno Rütten, Sandra M. Pasternack, et al.. (2010). Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. British Journal of Dermatology. 163(1). 197–200. 24 indexed citations
11.
Pasternack, Sandra M., Ivar von Kügelgen, Melanie Müller, et al.. (2009). In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth. Journal of Investigative Dermatology. 129(12). 2772–2776. 27 indexed citations
12.
Pasternack, Sandra M., Sibylle Eigelshoven, Melanie Müller, et al.. (2009). Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair. Archives of Dermatological Research. 301(8). 621–624. 15 indexed citations
13.
Redler, Silke, et al.. (2009). Identification of aU2HRgene mutation in Turkish families with Marie Unna hereditary hypotrichosis. Clinical and Experimental Dermatology. 34(8). e953–e956. 14 indexed citations
14.
Meißner, Thomas, Regina C. Betz, Sandra M. Pasternack, et al.. (2008). Richner–Hanhart Syndrome Detected by Expanded Newborn Screening. Pediatric Dermatology. 25(3). 378–380. 13 indexed citations
15.
Pasternack, Sandra M., Regina C. Betz, F Brandrup, et al.. (2008). Identification of two new mutations in theTATgene in a Danish family with tyrosinaemia type II. British Journal of Dermatology. 160(3). 704–706. 10 indexed citations
16.
Pasternack, Sandra M., Margarita Indelman, Bernd Wollnik, et al.. (2008). A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families. Archives of Dermatological Research. 301(5). 391–393. 18 indexed citations
17.
Pasternack, Sandra M., Ivar von Kügelgen, Khalid Al Aboud, et al.. (2008). G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nature Genetics. 40(3). 329–334. 298 indexed citations
18.
Betz, Regina C., Laura Planko, Sibylle Eigelshoven, et al.. (2006). Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease. The American Journal of Human Genetics. 78(3). 510–519. 145 indexed citations
19.
Pasternack, Sandra M., et al.. (2006). Indirect exclusion of four candidate genes for generalized progressive retinal atrophy in several breeds of dogs. Journal of Negative Results in BioMedicine. 5(1). 19–19. 5 indexed citations
20.
Dekomien, Gabriele, et al.. (2005). Long‐ and short‐haired Weimaraner dogs represent two populations of one breed. Electrophoresis. 26(9). 1668–1672. 5 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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