Davor Lessel

7.9k total citations
44 papers, 733 citations indexed

About

Davor Lessel is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Davor Lessel has authored 44 papers receiving a total of 733 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 17 papers in Genetics and 5 papers in Surgery. Recurrent topics in Davor Lessel's work include RNA Research and Splicing (13 papers), Nuclear Structure and Function (9 papers) and DNA Repair Mechanisms (8 papers). Davor Lessel is often cited by papers focused on RNA Research and Splicing (13 papers), Nuclear Structure and Function (9 papers) and DNA Repair Mechanisms (8 papers). Davor Lessel collaborates with scholars based in Germany, United States and Austria. Davor Lessel's co-authors include Christian Kubisch, Maja Hempel, Kristijan Ramadan, Jonas Denecke, Nina Kaczmarek, Junko Oshima, Hanspeter Naegeli, Katja Kloth, Fuki M. Hisama and George M. Martin and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and Brain.

In The Last Decade

Davor Lessel

43 papers receiving 728 citations

Peers

Davor Lessel

GENET

ONCOL

PRM

Ortal Barel Israel

Bryn D. Webb United States

Pelin Özlem Şimşek‐Kiper Türkiye

Soo‐Mi Park United Kingdom

Nisha Patel Saudi Arabia

Romi Biswas United States

Marjon A. van Slegtenhorst Netherlands

Maria Lisa Dentici Italy

Boris Keren France

Sharon Lin United States

Ortal Barel Israel

Davor Lessel

450 ×0.9

247 ×1.4

GENET

73 ×0.8

ONCOL

38 ×0.5

PRM

58 ×0.8

Citations per year, relative to Davor Lessel Davor Lessel (= 1×) peers Ortal Barel

Countries citing papers authored by Davor Lessel

Since Specialization

Citations

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

Fields of papers citing papers by Davor Lessel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davor Lessel

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

All Works

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20 of 20 papers shown

Ven, Amelie T. van der, Maja Hempel, Chris G. Kruse, et al.. (2025). Homozygous DBX1 Nonsense Variant in a Case of Atypical Congenital Central Hypoventilation. Neurology Genetics. 11(5). e200302–e200302.

Leitinger, Markus, Gudrun Kalss, Julia Höfler, et al.. (2024). Multiple intracerebral hematomas during SEEG recording and intradural hemorrhage after spinal tap: A case report prompting more research on collagen IV gene mutation and oral nicotine consumption as risk factors. Epilepsia Open. 10(1). 329–335. 1 indexed citations

Seidel, Christoph, et al.. (2023). Further Association of Germline CHEK2 Loss-of-Function Variants with Testicular Germ Cell Tumors. Journal of Clinical Medicine. 12(22). 7065–7065. 1 indexed citations

Dahimène, Shehrazade, Davor Lessel, Kjara S Pilch, et al.. (2022). Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy. Brain. 145(8). 2721–2729. 29 indexed citations

Reuter, Miriam S., Michael Zech, Maja Hempel, et al.. (2022). Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies. European Journal of Human Genetics. 30(5). 611–618. 3 indexed citations

Nasrallah, Mona, et al.. (2022). Werner syndrome in a Lebanese family. American Journal of Medical Genetics Part A. 188(5). 1630–1634. 1 indexed citations

Gamulin, Marija, et al.. (2022). Comprehensive Clinical and Genetic Analysis of CHEK2 in Croatian Men with Prostate Cancer. Genes. 13(11). 1955–1955. 2 indexed citations

Sailer, Verena, Davor Lessel, Jutta Kirfel, et al.. (2022). Aggressive variants of prostate cancer: underlying mechanisms of neuroendocrine transdifferentiation. Journal of Experimental & Clinical Cancer Research. 41(1). 46–46. 67 indexed citations

Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations

10.

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

11.

Lessel, Davor, et al.. (2021). A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A‐related pathologies. American Journal of Medical Genetics Part A. 188(1). 216–223. 6 indexed citations

12.

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

13.

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

14.

Lüttgen, Sabine, Sigrid Fuchs, Holger Thiele, et al.. (2020). Two novel cases further expand the phenotype of TOR1AIP1-associated nuclear envelopathies. Human Genetics. 139(4). 483–498. 12 indexed citations

15.

Halder, Swagata, Ignacio Torrecilla, Martin D. Burkhalter, et al.. (2019). SPRTN protease and checkpoint kinase 1 cross-activation loop safeguards DNA replication. Nature Communications. 10(1). 3142–3142. 35 indexed citations

16.

Lessel, Davor & Christian Kubisch. (2019). Hereditary Syndromes With Signs of Premature Aging. Deutsches Ärzteblatt international. 116(29-30). 489–496. 19 indexed citations

17.

Engel, Nils W., Simon Schliffke, Ulrich Schüller, et al.. (2019). Fatal Myelotoxicity Following Palliative Chemotherapy With Cisplatin and Gemcitabine in a Patient With Stage IV Cholangiocarcinoma Linked to Post Mortem Diagnosis of Fanconi Anemia. Frontiers in Oncology. 9. 420–420. 8 indexed citations

18.

Lessel, Davor, Ayse Bilge Ozel, Susan Campbell, et al.. (2018). Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations. Human Genetics. 137(11-12). 921–939. 16 indexed citations

19.

Gunjača, Ivana, Miroslav Radman, Veselin Škrabić, et al.. (2018). Genome-wide association analysis suggests novel loci for Hashimoto’s thyroiditis. Journal of Endocrinological Investigation. 42(5). 567–576. 19 indexed citations

20.

Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 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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