Katja Kloth

789 total citations
18 papers, 238 citations indexed

About

Katja Kloth is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Katja Kloth has authored 18 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Katja Kloth's work include Genomics and Rare Diseases (6 papers), Congenital heart defects research (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). Katja Kloth is often cited by papers focused on Genomics and Rare Diseases (6 papers), Congenital heart defects research (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). Katja Kloth collaborates with scholars based in Germany, United States and Austria. Katja Kloth's co-authors include Maja Hempel, Jonas Denecke, Davor Lessel, Jessika Johannsen, René Santer, Christian Kubisch, Kerstin Kutsche, Frederike L. Harms, Fanny Kortüm and Annette Bley and has published in prestigious journals such as Journal of Neurochemistry, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Katja Kloth

18 papers receiving 237 citations

Peers

Katja Kloth

GENET

SURGE

CMN

Yukiko Kuroda Japan

Juliette Piard France

Eda Ütine Türkiye

Aida Telegrafi United States

Yumi Enomoto Japan

Suzana Ezquina Brazil

Fernando Santos‐Simarro Spain

Ana Medeira Portugal

Marije Meuwissen Belgium

Kelly E. Jackson United States

Yukiko Kuroda Japan

Katja Kloth

127 ×1.0

178 ×1.6

GENET

25 ×0.8

27 ×1.0

SURGE

11 ×0.5

CMN

Citations per year, relative to Katja Kloth Katja Kloth (= 1×) peers Yukiko Kuroda

Countries citing papers authored by Katja Kloth

Since Specialization

Citations

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

Fields of papers citing papers by Katja Kloth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katja Kloth

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

All Works

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18 of 18 papers shown

Kloth, Katja, Bernarda Lozić, Mariëtte J.V. Hoffer, et al.. (2021). ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants. Neurogenetics. 22(4). 263–269. 14 indexed citations

Ven, Amelie T. van der, Jessika Johannsen, Fanny Kortüm, et al.. (2021). Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort. Clinical Genetics. 100(6). 766–770. 8 indexed citations

Kloth, Katja, Denise Obrecht, Dominik Sturm, et al.. (2021). Defining the Spectrum, Treatment and Outcome of Patients With Genetically Confirmed Gorlin Syndrome From the HIT-MED Cohort. Frontiers in Oncology. 11. 756025–756025. 2 indexed citations

Blohm, Martin, Fanny Kortüm, Tatjana Bierhals, et al.. (2021). Whole-Exome Sequencing in Critically Ill Neonates and Infants: Diagnostic Yield and Predictability of Monogenic Diagnosis. Neonatology. 118(4). 454–461. 18 indexed citations

Kloth, Katja, Luitgard Graul‐Neumann, Katharina Hermann, et al.. (2021). More evidence on TRIO missense mutations in the spectrin repeat domain causing severe developmental delay and recognizable facial dysmorphism with macrocephaly. Neurogenetics. 22(3). 221–224. 3 indexed citations

Kloth, Katja, Axel Neu, Isabella Rau, et al.. (2021). Severe congenital contractural arachnodactyly caused by biallelic pathogenic variants in FBN2. European Journal of Medical Genetics. 64(3). 104161–104161. 5 indexed citations

Reinshagen, Konrad, et al.. (2021). The Epidemiology behind Pectus Excavatum: Clinical Study and Review of the Literature. European Journal of Pediatric Surgery. 32(4). 316–320. 8 indexed citations

Kloth, Katja, et al.. (2020). Mucopolysaccharidosis type I due to maternal uniparental disomy of chromosome 4 with partial isodisomy of 4p16.3p15.2. Molecular Genetics and Metabolism Reports. 25. 100660–100660. 2 indexed citations

Nia, Fatemeh Hassani, et al.. (2020). Truncating mutations in SHANK3 associated with global developmental delay interfere with nuclear β‐catenin signaling. Journal of Neurochemistry. 155(3). 250–263. 19 indexed citations

10.

Kloth, Katja, Doris Steinemann, Brigitte Pabst, et al.. (2019). 16p13.11 microdeletion uncovers loss‐of‐function of a MYH11 missense variant in a patient with megacystis‐microcolon‐intestinal‐hypoperistalsis syndrome. Clinical Genetics. 96(1). 85–90. 20 indexed citations

11.

Kloth, Katja, Matthis Synofzik, Christoph Kernstock, et al.. (2019). Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports. BMC Medical Genetics. 20(1). 62–62. 9 indexed citations

12.

Kloth, Katja, Tatjana Bierhals, Jessika Johannsen, et al.. (2019). Biallelic variants in SMAD6 are associated with a complex cardiovascular phenotype. Human Genetics. 138(6). 625–634. 11 indexed citations

13.

Johannsen, Jessika, Konstantinos Tsiakas, Katja Kloth, et al.. (2019). Exome Sequencing in Children. Deutsches Ärzteblatt international. 21 indexed citations

14.

Johannsen, Jessika, Tatjana Bierhals, Philipp Deindl, et al.. (2019). Excessive Seizure Clusters in an Otherwise Well-Controlled Epilepsy as a Possible Hallmark of Untreated Vitamin B6-Responsive Epilepsy due to a Homozygous PLPBP Missense Variant. Journal of Pediatric Genetics. 8(4). 222–225. 8 indexed citations

15.

Li, Jun, Martina Koch, Katja Kloth, et al.. (2018). Dual antibody induction and de novo use of everolimus enable low-dose tacrolimus with early corticosteroid withdrawal in simultaneous pancreas-kidney transplantation. Transplant Immunology. 50. 26–33. 4 indexed citations

16.

Jensen, Hanne, Jennifer J. Johnston, Emilio Di Maria, et al.. (2018). Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome. The American Journal of Human Genetics. 103(6). 976–983. 18 indexed citations

17.

Harms, Frederike L., Katja Kloth, Annette Bley, et al.. (2018). Activating Mutations in PAK1, Encoding p21-Activated Kinase 1, Cause a Neurodevelopmental Disorder. The American Journal of Human Genetics. 103(4). 579–591. 47 indexed citations

18.

Kloth, Katja, Jonas Denecke, Maja Hempel, et al.. (2017). First de novo ANK3 nonsense mutation in a boy with intellectual disability, speech impairment and autistic features. European Journal of Medical Genetics. 60(9). 494–498. 21 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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