Sara Loddo

1.1k total citations
39 papers, 639 citations indexed

About

Sara Loddo is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sara Loddo has authored 39 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sara Loddo's work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (9 papers). Sara Loddo is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (9 papers). Sara Loddo collaborates with scholars based in Italy, United States and France. Sara Loddo's co-authors include Antonio Novelli, Laura Bernardini, Agatino Battaglia, Viola Alesi, Tiziana Filippi, Bruno Dallapiccola, Anna Capalbo, Viola Doccini, John C. Carey and M. Cristina Digilio and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Gene.

In The Last Decade

Sara Loddo

39 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sara Loddo Italy 13 402 277 123 73 59 39 639
Anna Capalbo Italy 16 389 1.0× 244 0.9× 112 0.9× 59 0.8× 77 1.3× 29 579
Chantal Missirian France 16 418 1.0× 404 1.5× 100 0.8× 64 0.9× 36 0.6× 39 720
Fanny Kortüm Germany 15 313 0.8× 285 1.0× 48 0.4× 52 0.7× 22 0.4× 29 558
Joanna Wiszniewska United States 12 360 0.9× 348 1.3× 106 0.9× 36 0.5× 67 1.1× 22 607
Tiziana Filippi Italy 9 374 0.9× 207 0.7× 157 1.3× 67 0.9× 71 1.2× 10 539
Maureen Holvoet Belgium 15 435 1.1× 338 1.2× 64 0.5× 64 0.9× 86 1.5× 33 607
Gerarda Cappuccio Italy 15 287 0.7× 348 1.3× 55 0.4× 33 0.5× 28 0.5× 59 611
Katharina Steindl Switzerland 18 323 0.8× 411 1.5× 49 0.4× 23 0.3× 23 0.4× 50 698
Shino Shimada Japan 15 318 0.8× 315 1.1× 62 0.5× 35 0.5× 45 0.8× 36 545
Alisha Wilkens United States 13 255 0.6× 239 0.9× 104 0.8× 26 0.4× 67 1.1× 20 438

Countries citing papers authored by Sara Loddo

Since Specialization
Citations

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

Fields of papers citing papers by Sara Loddo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Loddo

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Loddo. A scholar is included among the top collaborators of Sara Loddo 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 Sara Loddo. Sara Loddo 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.
Alesi, Viola, Silvia Genovese, Silvia Di Tommaso, et al.. (2024). Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency. Human Genomics. 18(1). 29–29. 1 indexed citations
2.
3.
Alesi, Viola, Silvia Genovese, Francesca Romana Lepri, et al.. (2023). Deep Intronic LINE-1 Insertions in NF1: Expanding the Spectrum of Neurofibromatosis Type 1-Associated Rearrangements. Biomolecules. 13(5). 725–725. 3 indexed citations
4.
Baban, Anwar, Viola Alesi, Silvia Genovese, et al.. (2022). Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients. Journal of Cardiovascular Development and Disease. 9(10). 332–332. 4 indexed citations
5.
Alesi, Viola, Maria Lisa Dentici, Silvia Genovese, et al.. (2021). Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis. International Journal of Molecular Sciences. 22(2). 750–750. 1 indexed citations
6.
Dentici, Maria Lisa, Sara Loddo, Luigi Laino, et al.. (2021). Congenital heart defects in the recurrent 2q13 deletion syndrome. European Journal of Medical Genetics. 65(1). 104381–104381. 12 indexed citations
7.
Inzaghi, Elena, Annalisa Deodati, Sara Loddo, et al.. (2021). Prevalence of copy number variants (CNVs) and rhGH treatment efficacy in an Italian cohort of children born small for gestational age (SGA) with persistent short stature associated with a complex clinical phenotype. Journal of Endocrinological Investigation. 45(1). 79–87. 3 indexed citations
8.
Brasch‐Andersen, Charlotte, Helen Cox, Michael Parker, et al.. (2020). A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis. Clinical Genetics. 97(6). 927–932. 2 indexed citations
9.
Amati, Francesca, Andrea Latini, Vito Luigi Colona, et al.. (2020). Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients. Heliyon. 6(10). e05143–e05143. 22 indexed citations
10.
Bonati, Maria Teresa, Chiara Castronovo, M. Crippa, et al.. (2019). 9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression. Neurogenetics. 20(3). 145–154. 11 indexed citations
11.
Loddo, Sara, Viola Alesi, Silvia Genovese, et al.. (2018). First Report of Low-Rate Mosaicism for 20q11.21q12 Deletion and Delineation of the Associated Disorder. Cytogenetic and Genome Research. 156(2). 87–94. 2 indexed citations
12.
Alesi, Viola, et al.. (2017). Reassessment of the 12q15 deletion syndrome critical region. European Journal of Medical Genetics. 60(4). 220–223. 9 indexed citations
13.
Alesi, Viola, Silvia Genovese, Sara Loddo, et al.. (2017). Interstitial 10q21.1q23.31 Duplication due to Meiotic Recombination of a Paternal Balanced Complex Rearrangement: Cytogenetic and Molecular Characterization. Cytogenetic and Genome Research. 151(4). 179–185. 2 indexed citations
14.
15.
Farhan, Sali M.K., John F. Robinson, Adam D. McIntyre, et al.. (2014). A Novel LIPE Nonsense Mutation Found Using Exome Sequencing in Siblings With Late-Onset Familial Partial Lipodystrophy. Canadian Journal of Cardiology. 30(12). 1649–1654. 59 indexed citations
16.
Battaglia, Agatino, Viola Doccini, Laura Bernardini, et al.. (2013). Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features. European Journal of Paediatric Neurology. 17(6). 589–599. 147 indexed citations
17.
Ferraris, Alessandro, Laura Bernardini, Ginevra Zanni, et al.. (2013). Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. Orphanet Journal of Rare Diseases. 8(1). 75–75. 25 indexed citations
18.
Grossi, Armando, Ginevra Zanni, Antonio Novelli, et al.. (2012). Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p. Gene. 515(2). 439–443. 11 indexed citations
19.
Briguglio, Marilena, Lorenzo Pinelli, Lucio Giordano, et al.. (2011). Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients. Orphanet Journal of Rare Diseases. 6(1). 36–36. 31 indexed citations
20.
Bernardini, Laura, Viola Alesi, Sara Loddo, et al.. (2009). High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?. European Journal of Human Genetics. 18(2). 178–185. 44 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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