Manuela Pendziwiat

3.8k total citations
21 papers, 379 citations indexed

About

Manuela Pendziwiat is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Manuela Pendziwiat has authored 21 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in Manuela Pendziwiat's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (7 papers) and Epilepsy research and treatment (6 papers). Manuela Pendziwiat is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (7 papers) and Epilepsy research and treatment (6 papers). Manuela Pendziwiat collaborates with scholars based in Germany, United States and Israel. Manuela Pendziwiat's co-authors include Gregor Kuhlenbäumer, Ingo Helbig, Zaid Afawi, Xiaobo Bai, Jonathan R. Bowen, Silke Appenzeller, Kaifeng Zhou, Elias T. Spiliotis, Charles V. Sindelar and Amos D. Korczyn and has published in prestigious journals such as The Journal of Cell Biology, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

Manuela Pendziwiat

21 papers receiving 376 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Pendziwiat Germany 12 204 103 73 71 70 21 379
Giulia Massaro United Kingdom 10 189 0.9× 86 0.8× 80 1.1× 29 0.4× 83 1.2× 17 391
Takuya Hiraide Japan 12 271 1.3× 185 1.8× 56 0.8× 26 0.4× 82 1.2× 34 441
Bouchra Ouled Amar Bencheikh Canada 9 105 0.5× 79 0.8× 80 1.1× 22 0.3× 65 0.9× 13 307
Kazushi Miya Japan 11 204 1.0× 94 0.9× 31 0.4× 48 0.7× 138 2.0× 20 500
Tatsuyuki Ohto Japan 11 312 1.5× 63 0.6× 184 2.5× 27 0.4× 52 0.7× 38 507
Romina Inès Cervigni Italy 8 181 0.9× 55 0.5× 196 2.7× 44 0.6× 51 0.7× 8 323
Akiko Takizawa Japan 13 437 2.1× 315 3.1× 47 0.6× 59 0.8× 131 1.9× 33 804
Kyoungin Cho United States 12 265 1.3× 36 0.3× 98 1.3× 21 0.3× 31 0.4× 19 393
Gianluca Verlengia Italy 12 255 1.3× 175 1.7× 22 0.3× 32 0.5× 118 1.7× 16 446
Emmanuelle Ranza Switzerland 12 137 0.7× 103 1.0× 19 0.3× 30 0.4× 36 0.5× 22 295

Countries citing papers authored by Manuela Pendziwiat

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Pendziwiat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Pendziwiat

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Pendziwiat. A scholar is included among the top collaborators of Manuela Pendziwiat 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 Manuela Pendziwiat. Manuela Pendziwiat 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.
Schröder, Katja, Sebastian Heinzel, Annika Kluge, et al.. (2025). Evaluation of an antibody panel for alpha-synuclein detection in FFPE rectal biopsies in Parkinson’s disease. IBRO Neuroscience Reports. 19. 844–853. 1 indexed citations
2.
Pendziwiat, Manuela, et al.. (2023). KCNC2 variants of uncertain significance are also associated to various forms of epilepsy. Frontiers in Neurology. 14. 1212079–1212079. 2 indexed citations
3.
Hammer, Michael F., Medhane Cumbay, Manuela Pendziwiat, et al.. (2022). Whole exome sequencing and co‐expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus. Epilepsia. 63(8). 1970–1980. 4 indexed citations
4.
Pendziwiat, Manuela, Tatjana Bierhals, Himanshu Goel, et al.. (2022). Modulating effects of FGF12 variants on NaV1.2 and NaV1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case series. EBioMedicine. 83. 104234–104234. 19 indexed citations
5.
Saffari, Afshin, Thomas Bast, Knut Brockmann, et al.. (2022). Efficacy, Tolerability, and Retention of Antiseizure Medications in PRRT2 -Associated Infantile Epilepsy. Neurology Genetics. 8(5). e200020–e200020. 8 indexed citations
6.
Bayat, Allan, Manuela Pendziwiat, Ewa Obersztyn, et al.. (2021). Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures. Frontiers in Genetics. 12. 663643–663643. 7 indexed citations
7.
Shalash, Ali, Thomas W. Rösler, Mohamed Salama, et al.. (2021). Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasia. Neurogenetics. 22(2). 143–147. 3 indexed citations
8.
Ganesan, Shiva, David Lewis‐Smith, Manuela Pendziwiat, et al.. (2020). Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies. The American Journal of Human Genetics. 107(4). 683–697. 22 indexed citations
9.
Helbig, Ingo, Giulia Barcia, Manuela Pendziwiat, et al.. (2020). Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome. Annals of Clinical and Translational Neurology. 7(8). 1429–1435. 16 indexed citations
10.
Canavati, Christina, Karl Martin Klein, Zaid Afawi, et al.. (2019). Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL3 pathogenic variants in familial focal epilepsy with variable foci. Epilepsia. 60(6). e67–e73. 13 indexed citations
11.
Neubauer, Katharina, et al.. (2018). Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study. Cytoskeleton. 76(1). 131–136. 11 indexed citations
12.
Klein, Karl Martin, Manuela Pendziwiat, Anda Eilam, et al.. (2017). The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizures. Journal of Neurology. 264(7). 1421–1425. 19 indexed citations
13.
Knaus, Alexej, Tomonari Awaya, Ingo Helbig, et al.. (2016). Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome. Human Mutation. 37(8). 737–744. 35 indexed citations
14.
Benninger, Felix, Zaid Afawi, Amos D. Korczyn, et al.. (2016). Seizures as presenting and prominent symptom in chorea‐acanthocytosis with c.2343del VPS13A gene mutation. Epilepsia. 57(4). 549–556. 13 indexed citations
15.
Klein, Karl Martin, Manuela Pendziwiat, Rony Cohen, et al.. (2015). Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. Journal of Neurology. 263(1). 11–16. 7 indexed citations
16.
Hopfner, Franziska, Giovanni Stévanin, Stefanie H. Müller, et al.. (2015). The impact of rare variants in FUS in essential tremor. Movement Disorders. 30(5). 721–724. 7 indexed citations
17.
Appenzeller, Silke, Wolfgang Völker, Inken Lorenzen, et al.. (2014). Differential aggregation properties of alpha-synuclein isoforms. Neurobiology of Aging. 35(8). 1913–1919. 33 indexed citations
18.
Bai, Xiaobo, Jonathan R. Bowen, Kaifeng Zhou, et al.. (2013). Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules. The Journal of Cell Biology. 203(6). 895–905. 87 indexed citations
19.
Goldberg‐Stern, Hadassa, Sharon Aharoni, Zaid Afawi, et al.. (2013). Broad Phenotypic Heterogeneity due to a Novel SCN1A Mutation in a Family With Genetic Epilepsy With Febrile Seizures Plus. Journal of Child Neurology. 29(2). 221–226. 40 indexed citations
20.
Appenzeller, Silke, Anja Schirmacher, Hartmut Halfter, et al.. (2010). Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene. The American Journal of Human Genetics. 86(1). 83–87. 23 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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