Marco Zucchelli

2.8k total citations
37 papers, 1.3k citations indexed

About

Marco Zucchelli is a scholar working on Molecular Biology, Genetics and Computer Vision and Pattern Recognition. According to data from OpenAlex, Marco Zucchelli has authored 37 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Computer Vision and Pattern Recognition. Recurrent topics in Marco Zucchelli's work include Advanced Vision and Imaging (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Optical measurement and interference techniques (6 papers). Marco Zucchelli is often cited by papers focused on Advanced Vision and Imaging (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Optical measurement and interference techniques (6 papers). Marco Zucchelli collaborates with scholars based in Sweden, Finland and United Kingdom. Marco Zucchelli's co-authors include Juha Kere, Outi Hovatta, Mauro D’Amato, Cecilia M. Lindgren, Myriam Peyrard‐Janvid, Pu Zhang, Fredwell Hambiliki, Lev Levkov, Heidi Anthoni and Markus M. Nöthen and has published in prestigious journals such as Gastroenterology, PLoS ONE and Environmental Health Perspectives.

In The Last Decade

Marco Zucchelli

37 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marco Zucchelli Sweden	20	430	373	284	195	134	37	1.3k
Holger Kirsten Germany	24	381 0.9×	371 1.0×	307 1.1×	152 0.8×	203 1.5×	99	1.4k
Dominique Brémond‐Gignac France	28	389 0.9×	278 0.7×	186 0.7×	75 0.4×	295 2.2×	207	2.5k
John P. Kemp United Kingdom	26	592 1.4×	871 2.3×	33 0.1×	66 0.3×	165 1.2×	47	2.0k
Rose Tobias Canada	15	303 0.7×	523 1.4×	62 0.2×	79 0.4×	77 0.6×	19	979
David Mellits United States	10	93 0.2×	58 0.2×	267 0.9×	108 0.6×	236 1.8×	11	1.4k
W. O. C. M. Cookson United Kingdom	14	503 1.2×	742 2.0×	30 0.1×	344 1.8×	63 0.5×	25	2.2k
Beth Wilmot United States	22	711 1.7×	319 0.9×	16 0.1×	123 0.6×	227 1.7×	70	2.0k
J. L. Black Australia	19	162 0.4×	50 0.1×	72 0.3×	35 0.2×	159 1.2×	50	1.0k
R. R. Greb Germany	12	174 0.4×	146 0.4×	33 0.1×	118 0.6×	83 0.6×	19	934
Drake D. Duane United States	16	157 0.4×	36 0.1×	144 0.5×	79 0.4×	94 0.7×	40	2.1k

Countries citing papers authored by Marco Zucchelli

Since Specialization

Citations

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

Fields of papers citing papers by Marco Zucchelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Zucchelli

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Zucchelli. A scholar is included among the top collaborators of Marco Zucchelli 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 Marco Zucchelli. Marco Zucchelli 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

Zucchelli, Marco, Susanne Ström, Frida Holm, et al.. (2012). In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period. Stem Cells and Development. 21(18). 3363–3371. 5 indexed citations

Camilleri, Michael, Paula Carlson, Sanna McKinzie, et al.. (2011). Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis. Neurogastroenterology & Motility. 23(10). 935–935. 38 indexed citations

Grad, Iwona, Youssef Hibaoui, Marisa Jaconi, et al.. (2011). NANOG priming before full reprogramming may generate germ cell tumours. European Cells and Materials. 22. 258–274. 21 indexed citations

Hellquist, Anna, Marco Zucchelli, Sari Koskenmies, et al.. (2011). Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population. Lara D. Veeken. 51(1). 87–92. 46 indexed citations

Hovatta, Outi, Marisa Jaconi, Virpi Töhönen, et al.. (2010). A Teratocarcinoma-Like Human Embryonic Stem Cell (hESC) Line and Four hESC Lines Reveal Potentially Oncogenic Genomic Changes. PLoS ONE. 5(4). e10263–e10263. 39 indexed citations

D’Amato, Mauro, Marco Zucchelli, Maria Seddighzadeh, et al.. (2010). Analysis of Neuropeptide S Receptor Gene (NPSR1) Polymorphism in Rheumatoid Arthritis. PLoS ONE. 5(2). e9315–e9315. 30 indexed citations

Camilleri, Michael, Paula Carlson, Alan R. Zinsmeister, et al.. (2009). Neuropeptide S Receptor Induces Neuropeptide Expression and Associates With Intermediate Phenotypes of Functional Gastrointestinal Disorders. Gastroenterology. 138(1). 98–107.e4. 48 indexed citations

Zhang, Pu, Marco Zucchelli, Sara Bruce, et al.. (2009). Transcriptome Profiling of Human Pre-Implantation Development. PLoS ONE. 4(11). e7844–e7844. 87 indexed citations

Hellquist, Anna, Tiina M. Järvinen, Sari Koskenmies, et al.. (2009). Evidence for Genetic Association and Interaction Between the TYK2 and IRF5 Genes in Systemic Lupus Erythematosus. The Journal of Rheumatology. 36(8). 1631–1638. 60 indexed citations

10.

Zhang, Pu, Marco Zucchelli, Fredwell Hambiliki, et al.. (2008). Expression Analysis of the NLRP Gene Family Suggests a Role in Human Preimplantation Development. PLoS ONE. 3(7). e2755–e2755. 117 indexed citations

11.

Melén, Erik, Fredrik Nyberg, Cecilia M. Lindgren, et al.. (2008). Interactions between Glutathione S- Transferase P1, Tumor Necrosis Factor, and Traffic-Related Air Pollution for Development of Childhood Allergic Disease. Environmental Health Perspectives. 116(8). 1077–1084. 108 indexed citations

12.

Kainu, Kati, Katja Kivinen, Marco Zucchelli, et al.. (2008). Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families. Experimental Dermatology. 18(2). 109–115. 34 indexed citations

13.

Pegelow, Marie, Myriam Peyrard‐Janvid, Marco Zucchelli, et al.. (2008). Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes. European Journal of Orthodontics. 30(2). 169–175. 37 indexed citations

14.

Hannelius, Ulf, et al.. (2007). Large-Scale Zygosity Testing Using Single Nucleotide Polymorphisms. Twin Research and Human Genetics. 10(4). 604–625. 99 indexed citations

15.

Anthoni, Heidi, Marco Zucchelli, Hans Matsson, et al.. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics. 16(6). 667–677. 91 indexed citations

16.

Schumacher, Julia, Inke R. Koenig, Marco Zucchelli, et al.. (2005). Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia. American Journal of Medical Genetics. 114–114. 2 indexed citations

17.

Holmkvist, Johan, Peter Almgren, Hemang Parikh, et al.. (2005). Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes. European Journal of Human Genetics. 13(7). 849–855. 6 indexed citations

18.

Schumacher, Johannes, Heidi Anthoni, Inke R. König, et al.. (2005). Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia. The American Journal of Human Genetics. 78(1). 52–62. 180 indexed citations

19.

Peyrard‐Janvid, Myriam, Heidi Anthoni, Marco Zucchelli, et al.. (2004). Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene. Human Genetics. 114(5). 510–516. 22 indexed citations

20.

Zucchelli, Marco, José Santos-Victor, & Henrik I. Christensen. (2002). Multiple Plane Segmentation Using Optical Flow. 29.1–29.10. 21 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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