Monica Mottes

3.2k total citations
91 papers, 1.9k citations indexed

About

Monica Mottes is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Monica Mottes has authored 91 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 38 papers in Genetics and 23 papers in Rheumatology. Recurrent topics in Monica Mottes's work include Connective tissue disorders research (35 papers), Bone and Dental Protein Studies (15 papers) and Bone health and treatments (11 papers). Monica Mottes is often cited by papers focused on Connective tissue disorders research (35 papers), Bone and Dental Protein Studies (15 papers) and Bone health and treatments (11 papers). Monica Mottes collaborates with scholars based in Italy, United States and Germany. Monica Mottes's co-authors include Luca Dalle Carbonare, Maria Teresa Valenti, Maurizia Valli, Franco Antoniazzi, Antonella Sangalli, Michela Deiana, Samuele Cheri, V. Sgaramella, Giuseppe Cetta and Giuseppe Attardi and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Monica Mottes

89 papers receiving 1.8k citations

Peers

Monica Mottes

GENET

RHEUM

ONCOL

Lee Ann Garrett‐Sinha United States

Claudine Blin‐Wakkach France

Mary Ann Weis United States

Susan Millard Australia

Takako Hattori Japan

Paul R. Odgren United States

Qingxia Wei Canada

Aditi Mukherjee United States

Hideo Orimo Japan

Shigeyuki Kon Japan

Lee Ann Garrett‐Sinha United States

Monica Mottes

1.1k ×1.5

334 ×0.5

GENET

285 ×0.7

RHEUM

511 ×1.4

ONCOL

319 ×1.1

Citations per year, relative to Monica Mottes Monica Mottes (= 1×) peers Lee Ann Garrett‐Sinha

Countries citing papers authored by Monica Mottes

Since Specialization

Citations

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

Fields of papers citing papers by Monica Mottes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monica Mottes

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

Carbonare, Luca Dalle, et al.. (2023). Modulation of miR-146b Expression during Aging and the Impact of Physical Activity on Its Expression and Chondrogenic Progenitors. International Journal of Molecular Sciences. 24(17). 13163–13163. 1 indexed citations

Deiana, Michela, Luca Dalle Carbonare, Samuele Cheri, et al.. (2020). A Potential Role of RUNX2- RUNT Domain in Modulating the Expression of Genes Involved in Bone Metastases: An In Vitro Study with Melanoma Cells. Cells. 9(3). 751–751. 6 indexed citations

Besio, Roberta, Laura Leoni, Lina Cipolla, et al.. (2019). Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate. Disease Models & Mechanisms. 12(6). 52 indexed citations

Lanzafame, Massimiliano, et al.. (2019). Relationship Between Vertebral Fractures, Bone Mineral Density, and Osteometabolic Profile in HIV and Hepatitis B and C-Infected Patients Treated With ART. Frontiers in Endocrinology. 10. 302–302. 9 indexed citations

Valenti, Maria Teresa, Monica Mottes, Samuele Cheri, et al.. (2018). Runx2 overexpression compromises bone quality in acromegalic patients. Endocrine Related Cancer. 25(3). 269–277. 21 indexed citations

Kaneko, Hiroshi, Hiroshi Kitoh, Tohru Matsuura, et al.. (2011). Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8. Human Genetics. 130(5). 671–683. 7 indexed citations

Valli, Maurizia, Aileen M. Barnes, Simona Viglio, et al.. (2011). Deficiency of CRTAP in non‐lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. Clinical Genetics. 82(5). 453–459. 23 indexed citations

Monti, Elena, et al.. (2010). Current and emerging treatments for the management of osteogenesis imperfecta. SHILAP Revista de lepidopterología. 21 indexed citations

Romanelli, Maria Grazia, et al.. (2008). Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5′ flanking region. Genomics. 93(3). 227–234. 20 indexed citations

10.

Origa, Raffaella, Elisa Fiumana, Maria Rita Gamberini, et al.. (2005). Osteoporosis in β‐Thalassemia: Clinical and Genetic Aspects. Annals of the New York Academy of Sciences. 1054(1). 451–456. 38 indexed citations

11.

Parentin, Fulvio, et al.. (2001). Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a case. Graefe s Archive for Clinical and Experimental Ophthalmology. 239(4). 316–319. 16 indexed citations

12.

Antoniazzi, Franco, et al.. (2000). Osteogenesis Imperfecta. Pediatric Drugs. 2(6). 465–488. 65 indexed citations

13.

Пигнатти, П. Ф., et al.. (1999). A novel intragenic polymorphism within the COL1A1 locus which can be detected byTaqI restriction of amplified genomic DNA. Molecular and Cellular Probes. 13(3). 243–245.

14.

Zolezzi, Francesca, Maurizia Valli, Massimo Clementi, et al.. (1997). Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variability. American Journal of Medical Genetics. 71(3). 366–370. 14 indexed citations

15.

Dyne, Katharine M., Maurizia Valli, Antonella Forlino, et al.. (1996). Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. American Journal of Medical Genetics. 63(1). 161–166. 15 indexed citations

16.

Cohen-Solal, L, Francesca Zolezzi, Pier Franco Pignatti, & Monica Mottes. (1996). Intrafamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in theCOL1A1gene. Molecular and Cellular Probes. 10(3). 219–225. 11 indexed citations

17.

Zolezzi, Francesca, Antonella Forlino, Monica Mottes, et al.. (1995). A 931 + 2T → C transition in one COL1A2 allele causes exon 16 skipping in PROα2(I) mRNA and produces moderately severe OI. Human Mutation. 6(3). 268–271. 4 indexed citations

18.

Gomez‐Lira, Macarena, et al.. (1995). A common ? hexosaminidase gene mutation in adult Sandhoff disease patients. Human Genetics. 96(4). 417–22. 28 indexed citations

19.

Mottes, Monica, Antonella Sangalli, Maurizia Valli, et al.. (1994). A base substitution at IVS-19 3?-end splice junction causes exon 20 skipping in pro?2(I) collagen mRNA and produces mild osteogenesis imperfecta. Human Genetics. 93(6). 681–7. 13 indexed citations

20.

Mottes, Monica, Antonella Sangalli, Maurizia Valli, et al.. (1992). Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine ?1(I) 901 substitution in a type-I collagen gene. Human Genetics. 89(5). 480–4. 24 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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