Luisa Mackenroth

723 total citations
15 papers, 245 citations indexed

About

Luisa Mackenroth is a scholar working on Molecular Biology, Genetics and Biophysics. According to data from OpenAlex, Luisa Mackenroth has authored 15 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 2 papers in Biophysics. Recurrent topics in Luisa Mackenroth's work include Genomic variations and chromosomal abnormalities (5 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (3 papers). Luisa Mackenroth is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (3 papers). Luisa Mackenroth collaborates with scholars based in Germany, Austria and Lithuania. Luisa Mackenroth's co-authors include Andreas Rump, Jens Schallner, Bernd Wollnik, Evelin Schröck, Jörg Striessnig, Filippo Beleggia, Alexandra Pinggera, Nataliya Di Donato, Andreas Tzschach and Karl Hackmann and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Analytical and Bioanalytical Chemistry.

In The Last Decade

Luisa Mackenroth

15 papers receiving 243 citations

Peers

Luisa Mackenroth

GENET

CMN

CCM

Valeria Y. Vasileva Russia

Emma M. Lessieur United States

Sirisha Achanta United States

Fılız Hazan Türkiye

Alejandro Mata‐Daboin United States

Majdi Nagara Tunisia

Julie A. Jurgens United States

Anastasia V. Sudarikova Russia

Elena McBeath United States

Ok‐Hwa Kim South Korea

Valeria Y. Vasileva Russia

Luisa Mackenroth

187 ×1.3

40 ×0.3

GENET

29 ×1.0

CMN

28 ×1.0

CCM

12 ×0.5

Citations per year, relative to Luisa Mackenroth Luisa Mackenroth (= 1×) peers Valeria Y. Vasileva

Countries citing papers authored by Luisa Mackenroth

Since Specialization

Citations

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

Fields of papers citing papers by Luisa Mackenroth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Mackenroth

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

All Works

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15 of 15 papers shown

Gieldon, Laura, Luisa Mackenroth, Anne‐Karin Kahlert, et al.. (2018). Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE. 13(8). e0201041–e0201041. 29 indexed citations

Gieldon, Laura, Luisa Mackenroth, Andreas Rump, et al.. (2017). Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 173(9). 2545–2550. 12 indexed citations

Becker, Kerstin, Luisa Mackenroth, Andreas Rump, et al.. (2017). Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study. Archives of Gynecology and Obstetrics. 295(5). 1227–1238. 16 indexed citations

Pinggera, Alexandra, Luisa Mackenroth, Andreas Rump, et al.. (2017). New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy. Human Molecular Genetics. 26(15). 2923–2932. 74 indexed citations

Kahlert, Anne‐Karin, Luisa Mackenroth, Joseph Porrmann, et al.. (2017). Pierpont syndrome: report of a new patient. Clinical Dysmorphology. 26(4). 205–208. 13 indexed citations

Sadowski, Carolin E., Kerstin Becker, Luisa Mackenroth, et al.. (2017). BRCA1/2 missense mutations and the value of in-silico analyses. European Journal of Medical Genetics. 60(11). 572–577. 5 indexed citations

Hackmann, Karl, Anne‐Karin Kahlert, Luisa Mackenroth, et al.. (2016). Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH. Breast Cancer Research and Treatment. 159(3). 585–590. 12 indexed citations

Mackenroth, Luisa, Björn Fischer‐Zirnsak, Johannes Egerer, et al.. (2016). An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A. 170(4). 1080–1085. 15 indexed citations

Brenner, Sebastian, Meinolf Suttorp, Gabriele Hahn, et al.. (2016). Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure. Neuropediatrics. 47(3). 182–186. 8 indexed citations

10.

Mackenroth, Luisa, Andreas Rump, Peter Lorenz, Evelin Schröck, & Andreas Tzschach. (2016). Novel ADAMTSL2-mutations in a patient with geleophysic dysplasia type I. Clinical Dysmorphology. 25(3). 106–109. 4 indexed citations

11.

Mackenroth, Luisa, et al.. (2016). Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disability. American Journal of Medical Genetics Part A. 170(9). 2394–2399. 4 indexed citations

12.

Faust, Ulrike, Marc Sturm, Karl Hackmann, et al.. (2015). HBOC multi-gene panel testing: comparison of two sequencing centers. Breast Cancer Research and Treatment. 152(1). 129–136. 35 indexed citations

13.

Mackenroth, Luisa, Karl Hackmann, Jens Schallner, et al.. (2015). 6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalities. American Journal of Medical Genetics Part A. 167(11). 2800–2807. 2 indexed citations

14.

Uckermann, Ortrud, Roberta Galli, Luisa Mackenroth, et al.. (2014). Optical Biochemical Imaging: Potential New Applications in Neuro-Oncology. Journal für Kardiologie (Krause & Pachernegg GmbH). 4(1). 20–26. 5 indexed citations

15.

Steiner, Gerald, Luisa Mackenroth, Kathrin Geiger, et al.. (2012). Label-free differentiation of human pituitary adenomas by FT-IR spectroscopic imaging. Analytical and Bioanalytical Chemistry. 403(3). 727–735. 11 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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