Lutz Priebe

2.0k total citations
13 papers, 373 citations indexed

About

Lutz Priebe is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Lutz Priebe has authored 13 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Psychiatry and Mental health. Recurrent topics in Lutz Priebe's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (3 papers). Lutz Priebe is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (3 papers). Lutz Priebe collaborates with scholars based in Germany, United States and Switzerland. Lutz Priebe's co-authors include Sven Cichon, Markus M. Nöthen, Per Hoffmann, Lena Backlund, Louise Frisén, Marquis P. Vawter, Sophie Erhardt, Urban Ösby, Lil Träskman‐Bendz and Mikael Landén and has published in prestigious journals such as PLoS ONE, Brain Research and Molecular Psychiatry.

In The Last Decade

Lutz Priebe

13 papers receiving 368 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lutz Priebe Germany	11	170	159	95	89	55	13	373
Claudia Hanses Germany	5	287 1.7×	195 1.2×	55 0.6×	90 1.0×	70 1.3×	6	508
Jingyuan Zhao China	10	67 0.4×	69 0.4×	96 1.0×	105 1.2×	39 0.7×	16	292
Yusuke Wakabayashi Japan	7	60 0.4×	130 0.8×	65 0.7×	24 0.3×	101 1.8×	16	343
Jue Ji China	12	148 0.9×	177 1.1×	41 0.4×	89 1.0×	9 0.2×	27	378
Christin Weissleder Australia	10	46 0.3×	84 0.5×	159 1.7×	60 0.7×	69 1.3×	17	332
Joel Wood United States	9	175 1.0×	148 0.9×	41 0.4×	142 1.6×	12 0.2×	12	388
Ashwini Rajasekaran India	8	39 0.2×	134 0.8×	93 1.0×	37 0.4×	29 0.5×	14	329
Michael P. Geaghan Australia	10	101 0.6×	211 1.3×	48 0.5×	33 0.4×	19 0.3×	15	378
Roshni Thakkar United States	4	100 0.6×	87 0.5×	17 0.2×	20 0.2×	43 0.8×	6	306
Xiaoxia Li United States	7	61 0.4×	137 0.9×	61 0.6×	88 1.0×	32 0.6×	11	323

Countries citing papers authored by Lutz Priebe

Since Specialization

Citations

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

Fields of papers citing papers by Lutz Priebe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lutz Priebe

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

All Works

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13 of 13 papers shown

Sharma, Amit, Felix Schreiner, Lutz Priebe, et al.. (2015). DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations. Clinical Epigenetics. 7(1). 76–76. 58 indexed citations

Hammer, Christian, Franziska Degenhardt, Lutz Priebe, et al.. (2014). A common microdeletion affecting a hippocampus‐ and amygdala‐specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar Disorders. 16(7). 764–768. 2 indexed citations

Haß, Johanna, Esther Walton, Holger Kirsten, et al.. (2013). A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLoS ONE. 8(6). e64872–e64872. 20 indexed citations

Lavebratt, Catharina, Sven J. G. Olsson, Lena Backlund, et al.. (2013). The KMO allele encoding Arg452 is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression. Molecular Psychiatry. 19(3). 334–341. 90 indexed citations

Pernhorst, Katharina, Karen M. J. van Loo, Marec von Lehe, et al.. (2013). Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue. Brain Research. 1499. 136–144. 12 indexed citations

Pernhorst, Katharina, Rainer Surges, Pitt Niehusmann, et al.. (2013). Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampi. Neurobiology of Disease. 60. 115–125. 16 indexed citations

Priebe, Lutz, Franziska Degenhardt, Jana Strohmaier, et al.. (2013). Copy Number Variants in German Patients with Schizophrenia. PLoS ONE. 8(7). e64035–e64035. 16 indexed citations

Degenhardt, Franziska, Lutz Priebe, Jana Strohmaier, et al.. (2012). No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatric Genetics. 23(1). 45–46. 5 indexed citations

Jamra, Rami Abou, Sigrun Wohlfart, Markus Zweier, et al.. (2011). Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity. European Journal of Human Genetics. 19(11). 1161–1166. 63 indexed citations

10.

Mühleisen, Thomas W., F. Buket Basmanav, Andreas J. Forstner, et al.. (2011). Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. Schizophrenia Research. 127(1-3). 35–40. 11 indexed citations

11.

Schramm, Charlotte, Markus Draaken, Enrika Bartels, et al.. (2010). Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature. European Journal of Pediatrics. 170(6). 741–746. 15 indexed citations

12.

Grigoroiu‐Serbânescu, Maria, Carmen C. Diaconu, Stefan Herms, et al.. (2008). Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population. Psychiatric Genetics. 18(5). 240–247. 22 indexed citations

13.

Schulze, E, Gunter Scharer, Lutz Priebe, et al.. (1995). Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylase. Endocrine Research. 21(1-2). 359–364. 43 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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