Patrick Nitschké

17.2k total citations
78 papers, 3.7k citations indexed

About

Patrick Nitschké is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Patrick Nitschké has authored 78 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 36 papers in Genetics and 15 papers in Immunology. Recurrent topics in Patrick Nitschké's work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Immune Cell Function and Interaction (8 papers). Patrick Nitschké is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Immune Cell Function and Interaction (8 papers). Patrick Nitschké collaborates with scholars based in France, United States and United Kingdom. Patrick Nitschké's co-authors include Christine Bôle‐Feysot, Capucine Pïcard, Alain Fischer, Arnold Münnich, Isabelle Callebaut, Frédéric Rieux‐Laucat, Geneviève de Saint Basile, Laurence Colleaux, Jean‐Laurent Casanova and Avinash Abhyankar and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Patrick Nitschké

74 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick Nitschké France 33 1.9k 1.1k 1.0k 348 322 78 3.7k
Carol A. Wise United States 35 2.7k 1.4× 1.6k 1.4× 1.2k 1.2× 571 1.6× 130 0.4× 85 5.7k
Alessandra Biffi Italy 33 2.0k 1.0× 474 0.4× 907 0.9× 358 1.0× 121 0.4× 134 3.8k
Gudrun Nürnberg Germany 44 2.9k 1.5× 524 0.5× 1.6k 1.6× 335 1.0× 144 0.4× 93 5.1k
Domenico Lazzaro Italy 24 2.1k 1.1× 797 0.7× 862 0.9× 299 0.9× 75 0.2× 37 4.3k
Ralf Dressel Germany 32 2.5k 1.3× 1.0k 0.9× 440 0.4× 289 0.8× 72 0.2× 107 4.1k
Valérie Ferreira Netherlands 22 3.4k 1.7× 685 0.6× 749 0.7× 267 0.8× 98 0.3× 30 5.0k
Patrick Salmon Switzerland 32 2.2k 1.1× 853 0.8× 1.0k 1.0× 81 0.2× 158 0.5× 60 3.9k
Erik A. Sistermans Netherlands 37 2.9k 1.5× 395 0.4× 2.7k 2.7× 137 0.4× 199 0.6× 123 5.6k
Udo Baron Germany 27 2.7k 1.4× 3.4k 3.0× 1.5k 1.5× 259 0.7× 132 0.4× 44 6.8k
Akihiro Kume Japan 34 2.2k 1.1× 844 0.8× 1.5k 1.4× 131 0.4× 172 0.5× 135 4.1k

Countries citing papers authored by Patrick Nitschké

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Nitschké

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Nitschké

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick Nitschké. A scholar is included among the top collaborators of Patrick Nitschké 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 Patrick Nitschké. Patrick Nitschké 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.
Assan, Florence, et al.. (2024). 280 ADAR1 mutations drive an interferon type I dependent psoriasis subtype. Journal of Investigative Dermatology. 144(12). S277–S277.
2.
Dorval, Guillaume, Gérald Le Gac, Vincent Morinière, et al.. (2024). Targeted RNAseq from patients’ urinary cells to validate pathogenic noncoding variants in autosomal dominant polycystic kidney disease genes: a proof of concept. Kidney International. 106(3). 532–535. 1 indexed citations
3.
Kornobis, Étienne, Frédéric Torès, Patrick Nitschké, et al.. (2022). Complex regulation of Gephyrin splicing is a determinant of inhibitory postsynaptic diversity. Nature Communications. 13(1). 3507–3507. 13 indexed citations
4.
Silvente, Francisco Requena, et al.. (2021). CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients. Nucleic Acids Research. 49(W1). W93–W103. 16 indexed citations
5.
Stoupa, Athanasia, Dulanjalee Kariyawasam, Gabor Szinnai, et al.. (2021). High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis. Frontiers in Endocrinology. 11. 545339–545339. 17 indexed citations
6.
Duchatelet, Sabine, Christian Osterburg, S. Mallet, et al.. (2019). A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia. Journal of Investigative Dermatology. 140(5). 1103–1106.e4. 2 indexed citations
7.
Duchatelet, Sabine, Lynn M. Boyden, Akemi Ishida‐Yamamoto, et al.. (2018). Mutations in PERP Cause Dominant and Recessive Keratoderma. Journal of Investigative Dermatology. 139(2). 380–390. 21 indexed citations
8.
Cavallin, Mara, Marie Hully, Nathalie Boddaert, et al.. (2018). TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly. European Journal of Medical Genetics. 61(12). 729–732. 7 indexed citations
9.
McInerney‐Leo, Aideen, Carine Le Goff, Paul Leo, et al.. (2016). Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia. Queensland's institutional digital repository (The University of Queensland). 3 indexed citations
10.
Lévy, E, Marie‐Claude Stolzenberg, Julie Bruneau, et al.. (2016). LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis. Clinical Immunology. 168. 88–93. 40 indexed citations
11.
Gougèlet, Angélique, Chiara Sartor, Laura Bachelot, et al.. (2015). Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations. Gut. 65(6). 1024–1034. 52 indexed citations
12.
Thévenon, Julien, Caroline Michot, Christine Bole, et al.. (2015). RPL10 mutation segregating in a family with X‐linked syndromic Intellectual Disability. American Journal of Medical Genetics Part A. 167(8). 1908–1912. 22 indexed citations
13.
Guen, Tangui Le, Fabien Touzot, Isabelle André‐Schmutz, et al.. (2015). An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation. Journal of Allergy and Clinical Immunology. 136(6). 1619–1626.e5. 54 indexed citations
14.
Bui, Catherine, Céline Huber, Beyhan Tüysüz, et al.. (2014). XYLT1 Mutations in Desbuquois Dysplasia Type 2. The American Journal of Human Genetics. 94(3). 405–414. 81 indexed citations
15.
Guen, Tangui Le, Fabien Touzot, Michael Schertzer, et al.. (2013). Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability. Human Molecular Genetics. 22(16). 3239–3249. 122 indexed citations
16.
Moshous, Despina, Emmanuel Martin, Wassila Carpentier, et al.. (2013). Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation. Journal of Allergy and Clinical Immunology. 131(6). 1594–1603.e9. 103 indexed citations
17.
Huber, Céline, Eissa Faqeih, Deborah Bartholdi, et al.. (2012). Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia. The American Journal of Human Genetics. 92(1). 144–149. 41 indexed citations
18.
Michot, Caroline, Carine Le Goff, Alice Goldenberg, et al.. (2012). Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis. The American Journal of Human Genetics. 90(4). 740–745. 84 indexed citations
19.
Côte, Marjorie, Mickaël Ménager, Nizar Mahlaoui, et al.. (2009). Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells. Journal of Clinical Investigation. 119(12). 3765–3773. 247 indexed citations
20.
Aude, Jean-Christophe, et al.. (1998). Evolution of Genes, Evolution of Species: The Case of Aminoacyl-tRNA Synthetases. Molecular Biology and Evolution. 15(11). 1548–1561. 40 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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