Doriana Misceo

3.2k total citations
52 papers, 1.4k citations indexed

About

Doriana Misceo is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Doriana Misceo has authored 52 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 34 papers in Molecular Biology and 17 papers in Plant Science. Recurrent topics in Doriana Misceo's work include Genomic variations and chromosomal abnormalities (23 papers), Chromosomal and Genetic Variations (17 papers) and Genomics and Chromatin Dynamics (10 papers). Doriana Misceo is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Chromosomal and Genetic Variations (17 papers) and Genomics and Chromatin Dynamics (10 papers). Doriana Misceo collaborates with scholars based in Norway, Italy and United States. Doriana Misceo's co-authors include Mariano Rocchi, Nicoletta Archidiacono, Eirik Frengen, Evan E. Eichler, Maria Francesca Cardone, Tuva Barøy, Asbjørn Holmgren, Mario Ventura, Madeleine Fannemel and Petter Strømme and has published in prestigious journals such as PLoS ONE, Brain and Genome Research.

In The Last Decade

Doriana Misceo

50 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Doriana Misceo Norway 21 957 720 628 109 105 52 1.4k
Andrew S. McCallion United States 25 1.7k 1.8× 698 1.0× 168 0.3× 173 1.6× 32 0.3× 48 2.5k
Gretel Beck United States 8 837 0.9× 362 0.5× 173 0.3× 166 1.5× 117 1.1× 8 1.4k
Anne W. Kerrebrock United States 12 1.2k 1.3× 273 0.4× 283 0.5× 209 1.9× 30 0.3× 13 1.5k
Jon Schoorlemmer Spain 17 1.3k 1.3× 391 0.5× 67 0.1× 194 1.8× 54 0.5× 33 1.5k
Flávio S. J. de Souza Argentina 17 651 0.7× 200 0.3× 269 0.4× 192 1.8× 16 0.2× 28 1.3k
Sarah Baxendale United Kingdom 22 834 0.9× 273 0.4× 109 0.2× 307 2.8× 114 1.1× 38 1.3k
Nicholas F. Tsinoremas United States 19 756 0.8× 153 0.2× 275 0.4× 185 1.7× 19 0.2× 35 1.3k
Diana Mitter Germany 15 572 0.6× 390 0.5× 50 0.1× 138 1.3× 121 1.2× 28 923
Adriano Flora Italy 17 855 0.9× 209 0.3× 58 0.1× 180 1.7× 134 1.3× 20 1.2k
Hiroko Fujita Japan 15 383 0.4× 288 0.4× 113 0.2× 316 2.9× 248 2.4× 59 1.1k

Countries citing papers authored by Doriana Misceo

Since Specialization
Citations

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

Fields of papers citing papers by Doriana Misceo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Doriana Misceo

This figure shows the co-authorship network connecting the top 25 collaborators of Doriana Misceo. A scholar is included among the top collaborators of Doriana Misceo 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 Doriana Misceo. Doriana Misceo 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.
Misceo, Doriana, et al.. (2024). Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome. Genes. 15(4). 500–500. 6 indexed citations
2.
Gunnes, Gjermund, Asbjørn Holmgren, Janne E. Reseland, et al.. (2019). STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone. Cell Calcium. 85. 102110–102110. 10 indexed citations
3.
Barøy, Tuva, Madeleine Fannemel, Doriana Misceo, et al.. (2015). A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms. Molecular Cytogenetics. 8(1). 31 indexed citations
4.
Pedurupillay, Christeen Ramane J., Tuva Barøy, Asbjørn Holmgren, et al.. (2015). Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B. American Journal of Medical Genetics Part A. 167(3). 657–663. 11 indexed citations
5.
Koht, Jeanette, Gia Tuong Tran, Doriana Misceo, et al.. (2014). Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions. PLoS ONE. 9(1). e86340–e86340. 43 indexed citations
6.
Andreescu, Nicoleta, et al.. (2014). A de novo 2.3Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl. Gene. 539(1). 168–172. 18 indexed citations
7.
Pedurupillay, Christeen Ramane J., et al.. (2013). Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay. Gene. 533(1). 403–410. 7 indexed citations
8.
Barøy, Tuva, et al.. (2013). Hyperphagia, Mild Developmental Delay But Apparently No Structural Brain Anomalies in a Boy Without SOX3 Expression. American Journal of Medical Genetics Part A. 161(5). 1137–1142. 9 indexed citations
9.
Misceo, Doriana, et al.. (2013). A balanced de novo inv(7)(p14.3q22.3) disrupting PDE1C and ATXN7L1 in a 14-year old developmentally delayed boy. European Journal of Medical Genetics. 56(7). 361–364. 4 indexed citations
10.
11.
Selmer, Kaja Kristine, Gregor D. Gilfillan, Petter Strømme, et al.. (2011). A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions. European Journal of Human Genetics. 20(1). 58–63. 21 indexed citations
12.
Misceo, Doriana, Karen Helene Ørstavik, Helle Lybæk, et al.. (2009). Inheritance of a terminal 7.1 Mb 18p deletion flanked by a 2.3 Mb duplication from a physically normal mother. American Journal of Medical Genetics Part A. 149A(12). 2877–2881. 4 indexed citations
13.
Barøy, Tuva, Doriana Misceo, & Eirik Frengen. (2008). Strukturell variasjon i genomet bidrar til variasjon i egenskaper. Tidsskrift for Den Norske Laegeforening.
14.
Misceo, Doriana, Oronzo Capozzi, Roberta Roberto, et al.. (2008). Tracking the complex flow of chromosome rearrangements from the Hominoidea Ancestor to extant Hylobates and Nomascus Gibbons by high-resolution synteny mapping. Genome Research. 18(9). 1530–1537. 35 indexed citations
15.
Stanyon, Roscoe, Mariano Rocchi, Oronzo Capozzi, et al.. (2008). Primate chromosome evolution: Ancestral karyotypes, marker order and neocentromeres. Chromosome Research. 16(1). 17–39. 90 indexed citations
16.
Cardone, Maria Francesca, Doriana Misceo, Roberta Roberto, et al.. (2007). Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini. Genomics. 90(1). 35–43. 23 indexed citations
17.
She, Xinwei, Ge Liu, Mario Ventura, et al.. (2006). A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. Genome Research. 16(5). 576–583. 72 indexed citations
18.
Misceo, Doriana, et al.. (2003). Human chromosome 16 conservation in primates. Chromosome Research. 11(4). 323–326. 8 indexed citations
19.
Bailey, Jeffrey A., Luigi Viggiano, Doriana Misceo, et al.. (2002). Human-Specific Duplication and Mosaic Transcripts: The Recent Paralogous Structure of Chromosome 22. The American Journal of Human Genetics. 70(1). 83–100. 123 indexed citations
20.
Eichler, Evan E., Matthew E. Johnson, Can Alkan, et al.. (2001). Divergent Origins and Concerted Expansion of Two Segmental Duplications on Chromosome 16. Journal of Heredity. 92(6). 462–468. 19 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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