Katherina Walz

2.5k total citations
59 papers, 1.7k citations indexed

About

Katherina Walz is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Katherina Walz has authored 59 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 35 papers in Genetics and 7 papers in Sensory Systems. Recurrent topics in Katherina Walz's work include Genomic variations and chromosomal abnormalities (24 papers), Congenital heart defects research (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Katherina Walz is often cited by papers focused on Genomic variations and chromosomal abnormalities (24 papers), Congenital heart defects research (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Katherina Walz collaborates with scholars based in United States, Chile and Argentina. Katherina Walz's co-authors include James R. Lupski, Juan I. Young, Paulina Carmona-Mora, Weimin Bi, Jiong Yan, Jéssica Molina, César P. Canales, Clemer Abad, Lorraine Potocki and Allan Bradley and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Katherina Walz

57 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katherina Walz United States 26 1.1k 965 193 146 134 59 1.7k
Aldamaria Puliti Italy 22 1.1k 1.0× 536 0.6× 57 0.3× 47 0.3× 109 0.8× 62 2.2k
Mirella Bruttini Italy 22 1.0k 1.0× 777 0.8× 289 1.5× 36 0.2× 34 0.3× 40 1.6k
Alix Weaver United States 5 825 0.8× 837 0.9× 109 0.6× 181 1.2× 47 0.4× 6 1.7k
Kimia Kahrizi Iran 30 1.8k 1.7× 835 0.9× 162 0.8× 68 0.5× 826 6.2× 141 3.0k
Dorien Lugtenberg Netherlands 18 1.0k 1.0× 920 1.0× 209 1.1× 97 0.7× 16 0.1× 34 1.6k
Arjan P.M. de Brouwer Netherlands 30 1.6k 1.5× 923 1.0× 155 0.8× 60 0.4× 267 2.0× 77 2.4k
Gretel Beck United States 8 837 0.8× 362 0.4× 108 0.6× 173 1.2× 117 0.9× 8 1.4k
Arnold Munnich France 25 1.6k 1.5× 580 0.6× 155 0.8× 61 0.4× 49 0.4× 55 2.3k
Fiorella Gurrieri Italy 27 1.4k 1.3× 1.3k 1.3× 290 1.5× 83 0.6× 16 0.1× 88 2.4k
Francesca Ariani Italy 29 1.3k 1.2× 1.6k 1.7× 581 3.0× 111 0.8× 9 0.1× 70 2.4k

Countries citing papers authored by Katherina Walz

Since Specialization
Citations

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

Fields of papers citing papers by Katherina Walz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katherina Walz

This figure shows the co-authorship network connecting the top 25 collaborators of Katherina Walz. A scholar is included among the top collaborators of Katherina Walz 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 Katherina Walz. Katherina Walz 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.
Rebelo, Adriana, Clemer Abad, Maike F. Dohrn, et al.. (2024). SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain. 147(9). 3131–3143. 5 indexed citations
2.
Ramzan, Memoona, Stephanie Bivona, Romina Armando, et al.. (2024). Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss. SHILAP Revista de lepidopterología. 5(4). 2400040–2400040.
3.
Ramzan, Memoona, Clemer Abad, Shengru Guo, et al.. (2024). Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2. European Journal of Human Genetics. 32(6). 639–646. 2 indexed citations
4.
Abad, Clemer, María Gabriela Otero, Anthony J. Griswold, et al.. (2024). Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning. Translational Psychiatry. 14(1). 33–33. 3 indexed citations
5.
Myers, Héctor F., Alecia M. Fair, Fernando Villalta, et al.. (2021). Transdisciplinary Perspectives on Precision Medicine. Health Equity. 5(1). 288–298. 1 indexed citations
6.
Li, Chong, Güney Bademci, Oscar Diaz‐Horta, et al.. (2019). Dysfunction of GRAP , encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss. Proceedings of the National Academy of Sciences. 116(4). 1347–1352. 12 indexed citations
7.
Droguett, Alejandra, Paola Krall, M. Eugenia Burgos, et al.. (2014). Tubular Overexpression of Gremlin Induces Renal Damage Susceptibility in Mice. PLoS ONE. 9(7). e101879–e101879. 30 indexed citations
8.
Canales, César P., Paola Krall, Miryam A. Fragoso, et al.. (2014). Characterization of a Trpc6 Transgenic Mouse Associated with Early Onset FSGS. British Journal of Medicine and Medical Research. 5(10). 1198–1212. 7 indexed citations
9.
Walz, Katherina, Paul M. Neilsen, Joseph Foster, et al.. (2014). Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome. Human Genetics. 134(2). 181–190. 40 indexed citations
10.
Carmona-Mora, Paulina, César P. Canales, Lei Cao, et al.. (2012). RAI1 Transcription Factor Activity Is Impaired in Mutants Associated with Smith-Magenis Syndrome. PLoS ONE. 7(9). e45155–e45155. 28 indexed citations
11.
Lacaria, Melanie, Pradip Saha, Lorraine Potocki, et al.. (2012). A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men. PLoS Genetics. 8(5). e1002713–e1002713. 36 indexed citations
12.
Kerr, Bredford, et al.. (2011). Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes. European Journal of Human Genetics. 20(1). 69–76. 44 indexed citations
13.
Kerr, Bredford, et al.. (2010). Unconventional Transcriptional Response to Environmental Enrichment in a Mouse Model of Rett Syndrome. PLoS ONE. 5(7). e11534–e11534. 45 indexed citations
14.
Carmona-Mora, Paulina, Jéssica Molina, Carlos López Encina, & Katherina Walz. (2009). Mouse Models of Genomic Syndromes as Tools for Understanding the Basis of Complex Traits: An Example with the Smith-Magenis and the Potocki-Lupski Syndromes. Current Genomics. 10(4). 259–268. 11 indexed citations
15.
Walz, Katherina, Richard Paylor, Jiong Yan, Weimin Bi, & James R. Lupski. (2006). Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2). Journal of Clinical Investigation. 116(11). 3035–3041. 54 indexed citations
16.
Bi, Weimin, Gulam Mustafa Saifi, Christine J. Shaw, et al.. (2004). Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome. Human Genetics. 115(6). 515–524. 81 indexed citations
17.
Walz, Katherina. (2003). Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2). Human Molecular Genetics. 13(4). 367–378. 60 indexed citations
18.
19.
Biondi, Ricardo M., Katherina Walz, Olaf‐Georg Issinger, Matthias Engel, & Susana Passeron. (1996). Discrimination between Acid and Alkali-Labile Phosphorylated Residues on Immobilon: Phosphorylation Studies of Nucleoside Diphosphate Kinase. Analytical Biochemistry. 242(2). 165–171. 14 indexed citations
20.
Walz, Katherina, et al.. (1980). Morphology of fallopian tubes removed from a patient after failure of clip sterilization. Archives of Gynecology and Obstetrics. 230(2). 123–135. 1 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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