Patrick Nitschké

1.3k total citations
7 papers, 296 citations indexed

About

Patrick Nitschké is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Patrick Nitschké has authored 7 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Patrick Nitschké's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (3 papers) and RNA regulation and disease (2 papers). Patrick Nitschké is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (3 papers) and RNA regulation and disease (2 papers). Patrick Nitschké collaborates with scholars based in France. Patrick Nitschké's co-authors include Nathalie Boddaert, Arnold Münnich, Christine Bôle‐Feysot, Agnès Rötig, Valérie Serre, Pascale de Lonlay, Florence Habarou, Chris Ottolenghi, Asma Smahi and Philippe Guigue and has published in prestigious journals such as The American Journal of Human Genetics, Human Reproduction and European Journal of Endocrinology.

In The Last Decade

Patrick Nitschké

6 papers receiving 292 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 5 200 72 69 42 31 7 296
Elisa Rahikkala Finland 9 163 0.8× 61 0.8× 81 1.2× 18 0.4× 20 0.6× 38 269
Malavika Hebbar India 9 207 1.0× 39 0.5× 70 1.0× 15 0.4× 12 0.4× 19 290
Aisha Al‐Shamsi United Arab Emirates 13 268 1.3× 107 1.5× 176 2.6× 14 0.3× 30 1.0× 29 466
Mervi Kuronen Finland 8 261 1.3× 54 0.8× 52 0.8× 21 0.5× 15 0.5× 10 456
Muriel Asheuer France 8 245 1.2× 65 0.9× 23 0.3× 69 1.6× 17 0.5× 8 349
Anthony S. Castanza United States 5 410 2.0× 121 1.7× 46 0.7× 18 0.4× 42 1.4× 5 534
Magalie Barth France 12 274 1.4× 171 2.4× 35 0.5× 13 0.3× 22 0.7× 32 378
Birgit Haberberger Germany 5 432 2.2× 243 3.4× 64 0.9× 21 0.5× 42 1.4× 5 504
Sali M.K. Farhan Canada 12 221 1.1× 17 0.2× 79 1.1× 32 0.8× 19 0.6× 33 368
Hiroko Shimbo Japan 12 192 1.0× 101 1.4× 73 1.1× 10 0.2× 17 0.5× 33 315

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

7 of 7 papers shown
1.
Siquier-Pernet, Karine, Pauline Marzin, Christine Bôle‐Feysot, et al.. (2024). LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy. Human Genetics and Genomics Advances. 6(1). 100372–100372.
2.
Mayeur, Anne, Nicolas Cagnard, Mohammed Zarhrate, et al.. (2023). A shared pattern of altered gene expression in human embryos affected by mitochondrial diseases. Human Reproduction. 38(5). 992–1002. 3 indexed citations
3.
Stoupa, Athanasia, Dulanjalee Kariyawasam, Christine Bôle‐Feysot, et al.. (2020). First case of fetal goitrous hypothyroidism due to SLC5A5/NIS mutations. European Journal of Endocrinology. 183(5). K1–K5. 11 indexed citations
4.
Babdor, Joël, Michaël Dussiot, Nicolas Goudin, et al.. (2018). Impaired Transferrin Receptor Palmitoylation and Recycling in Neurodegeneration with Brain Iron Accumulation. The American Journal of Human Genetics. 102(2). 266–277. 71 indexed citations
5.
Boutron, Audrey, Florence Habarou, Christine Barnérias, et al.. (2013). Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. Orphanet Journal of Rare Diseases. 8(1). 192–192. 69 indexed citations
6.
Ali, Gowher, Pascale de Lonlay, Patrick Nitschké, et al.. (2012). Mutation in PNPT1 , which Encodes a Polyribonucleotide Nucleotidyltransferase, Impairs RNA Import into Mitochondria and Causes Respiratory-Chain Deficiency. The American Journal of Human Genetics. 91(5). 912–918. 69 indexed citations
7.
Rio, Marlène, Jean-Marc Plaza, Philippe Guigue, et al.. (2009). Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation. The American Journal of Human Genetics. 85(6). 903–908. 73 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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2026