Silvia Morlino

1.4k total citations
42 papers, 871 citations indexed

About

Silvia Morlino is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Silvia Morlino has authored 42 papers receiving a total of 871 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Silvia Morlino's work include Connective tissue disorders research (24 papers), Dermatological and Skeletal Disorders (6 papers) and Congenital heart defects research (5 papers). Silvia Morlino is often cited by papers focused on Connective tissue disorders research (24 papers), Dermatological and Skeletal Disorders (6 papers) and Congenital heart defects research (5 papers). Silvia Morlino collaborates with scholars based in Italy, Lebanon and United States. Silvia Morlino's co-authors include Marco Castori, Paola Grammatico, Filippo Camerota, Claudia Celletti, Marina Colombi, Carlo Blundo, Marco Ritelli, Chiara Dordoni, Marina Venturini and Aldo Morrone and has published in prestigious journals such as Investigative Ophthalmology & Visual Science, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Lara D. Veeken.

In The Last Decade

Silvia Morlino

40 papers receiving 836 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Silvia Morlino Italy	16	622	239	204	138	104	42	871
Guilherme Lopes Yamamoto Brazil	18	469 0.8×	271 1.1×	732 3.6×	59 0.4×	178 1.7×	57	1.3k
Louise C. Wilson United Kingdom	20	638 1.0×	178 0.7×	629 3.1×	117 0.8×	53 0.5×	46	1.2k
Young Bae Sohn South Korea	19	382 0.6×	88 0.4×	293 1.4×	204 1.5×	59 0.6×	93	1.1k
Melissa Lees United Kingdom	20	673 1.1×	154 0.6×	511 2.5×	47 0.3×	33 0.3×	37	1.1k
J. M. Cobben Netherlands	12	388 0.6×	198 0.8×	589 2.9×	59 0.4×	75 0.7×	16	936
Ann Haskins Olney United States	19	716 1.2×	169 0.7×	842 4.1×	63 0.5×	55 0.5×	43	1.4k
Ingrid M.B.H. van de Laar Netherlands	18	329 0.5×	164 0.7×	321 1.6×	59 0.4×	19 0.2×	40	963
Robert Wallerstein United States	17	399 0.6×	140 0.6×	410 2.0×	50 0.4×	32 0.3×	66	924
Bernard N. Chodirker Canada	15	293 0.5×	96 0.4×	280 1.4×	68 0.5×	74 0.7×	44	752
Roberto Lala Italy	18	333 0.5×	153 0.6×	585 2.9×	229 1.7×	147 1.4×	33	1.2k

Countries citing papers authored by Silvia Morlino

Since Specialization

Citations

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

Fields of papers citing papers by Silvia Morlino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Morlino

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

Fusco, Carmela, Silvia Morlino, Lucia Micale, et al.. (2023). Nucleotide substitutions at the p.Gly117 and p.Thr180 mutational hot-spots of SKI alter molecular dynamics and may affect cell cycle. Journal of Human Genetics. 69(1). 53–58. 1 indexed citations

Majore, Silvia, Emanuele Agolini, Lucia Micale, et al.. (2020). Clinical presentation and molecular characterization of a novel patient with variant POC1A ‐ related syndrome. Clinical Genetics. 99(4). 540–546. 9 indexed citations

Micale, Lucia, Silvia Morlino, Emanuele Agolini, et al.. (2020). Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia. Genes. 11(12). 1513–1513. 9 indexed citations

Morlino, Silvia, Annalucia Carbone, Marco Ritelli, et al.. (2019). TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis. Human Mutation. 40(10). 1886–1898. 4 indexed citations

Morlino, Silvia, Viola Alesi, Francesca Romana Lepri, et al.. (2018). LTBP2‐related “Marfan‐like” phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant. American Journal of Medical Genetics Part A. 179(1). 104–112. 15 indexed citations

Morlino, Silvia, Marco Castori, Chiara Dordoni, et al.. (2018). A novel MAP3K7 splice mutation causes cardiospondylocarpofacial syndrome with features of hereditary connective tissue disorder. European Journal of Human Genetics. 26(4). 582–586. 11 indexed citations

Gerbino, Andrea, Irene Bottillo, Serena Milano, et al.. (2017). Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects. Cellular Physiology and Biochemistry. 44(4). 1559–1577. 13 indexed citations

Morlino, Silvia, Chiara Dordoni, Isabella Sperduti, et al.. (2017). Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers–Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part A. 173(4). 914–929. 19 indexed citations

Morlino, Silvia, et al.. (2016). Recognizing and treating Ehlers-Danlos syndrome(s): the need for a multidisciplinary approach. 10(3). 7. 2 indexed citations

10.

Travaglini, Lorena, Emanuele Bellacchio, Adele D’Amico, et al.. (2016). Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia. European Journal of Paediatric Neurology. 21(3). 450–456. 31 indexed citations

11.

Castori, Marco, Chiara Dordoni, Silvia Morlino, et al.. (2015). Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 43–53. 29 indexed citations

12.

Castori, Marco, Silvia Morlino, Giulia Pascolini, Carlo Blundo, & Paola Grammatico. (2015). Gastrointestinal and nutritional issues in joint hypermobility syndrome/ehlers–danlos syndrome, hypermobility type. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 54–75. 64 indexed citations

13.

Castori, Marco, Silvia Morlino, Giulia Ghibellini, et al.. (2015). Connective tissue, Ehlers–Danlos syndrome(s), and head and cervical pain. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(1). 84–96. 36 indexed citations

14.

Castori, Marco, Irene Bottillo, Silvia Morlino, et al.. (2014). A 22-Week-Old Fetus with Nager Syndrome and Congenital Diaphragmatic Hernia due to a Novel <b><i>SF3B4</i></b> Mutation. Molecular Syndromology. 5(5). 241–244. 14 indexed citations

15.

Castori, Marco, Irene Bottillo, Luigi Laino, et al.. (2014). An Additional Patient With 3q27.3 Microdeletion Syndrome. Journal of Child Neurology. 30(4). 500–504. 2 indexed citations

16.

Castori, Marco, Chiara Dordoni, Isabella Sperduti, et al.. (2014). Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees. American Journal of Medical Genetics Part A. 164(12). 3010–3020. 68 indexed citations

17.

Castori, Marco, Silvia Morlino, Marco Ritelli, et al.. (2013). Late diagnosis of lateral meningocele syndrome in a 55‐year‐old woman with symptoms of joint instability and chronic musculoskeletal pain. American Journal of Medical Genetics Part A. 164(2). 528–534. 15 indexed citations

18.

Castori, Marco, Silvia Morlino, Claudia Celletti, et al.. (2013). Re‐writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers–Danlos syndrome, hypermobility type. American Journal of Medical Genetics Part A. 161(12). 2989–3004. 121 indexed citations

19.

Castori, Marco, Silvia Morlino, Chiara Dordoni, et al.. (2012). Gynecologic and obstetric implications of the joint hypermobility syndrome (a.k.a. Ehlers–Danlos syndrome hypermobility type) in 82 Italian patients. American Journal of Medical Genetics Part A. 158A(9). 2176–2182. 73 indexed citations

20.

Pierro, Luisa, et al.. (2006). OCT/SLO versus OCT3 in the Evaluation of Epiretinal Membranes. Investigative Ophthalmology & Visual Science. 47(13). 2639–2639. 2 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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