Carlo Sidore
Overview
Explore the profile of Carlo Sidore including associated specialties, affiliations and a list of published articles.
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56
Citations
9953
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Recent Articles
1.
Steri M, Orru V, Sidore C, Mulas A, Pitzalis M, Busonero F, et al.
Immunology
. 2025 Jan;
174(4):462-469.
PMID: 39835539
The TYK2:p.Pro1104Ala (rs34536443) hypomorph variant has been associated with protection against numerous autoimmune disorders. Thus, its mechanism of action becomes of great interest. Here, consistent with the participation of activated...
2.
Crouch D, Inshaw J, Robertson C, Ng E, Zhang J, Chen W, et al.
Genet Epidemiol
. 2025 Jan;
49(1):e22608.
PMID: 39749473
Biological datasets often consist of thousands or millions of variables, e.g. genetic variants or biomarkers, and when sample sizes are large it is common to find many associated with an...
3.
Kosmicki J, Marcketta A, Sharma D, Di Gioia S, Batista S, Yang X, et al.
Nat Genet
. 2024 Aug;
56(8):1592-1596.
PMID: 39103650
Coronavirus disease 2019 (COVID-19) and influenza are respiratory illnesses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses, respectively. Both diseases share symptoms and clinical risk...
4.
Sterenborg R, Steinbrenner I, Li Y, Bujnis M, Naito T, Marouli E, et al.
Nat Commun
. 2024 Jan;
15(1):888.
PMID: 38291025
To date only a fraction of the genetic footprint of thyroid function has been clarified. We report a genome-wide association study meta-analysis of thyroid function in up to 271,040 individuals...
5.
Graham S, Clarke S, Wu K, Kanoni S, Zajac G, Ramdas S, et al.
Nature
. 2023 May;
618(7965):E19-E20.
PMID: 37237109
No abstract available.
6.
Zajac G, Gagliano Taliun S, Sidore C, Graham S, Asvold B, Brumpton B, et al.
Genet Epidemiol
. 2023 Feb;
47(3):231-248.
PMID: 36739617
Linkage analysis, a class of methods for detecting co-segregation of genomic segments and traits in families, was used to map disease-causing genes for decades before genotyping arrays and dense SNP...
7.
Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, et al.
Nature
. 2022 Oct;
610(7933):704-712.
PMID: 36224396
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes. Here, using...
8.
Marongiu M, Perez-Mejias G, Orru V, Steri M, Sidore C, Diaz-Quintana A, et al.
Hum Mol Genet
. 2022 Sep;
32(5):790-797.
PMID: 36136759
Few genome-wide association studies (GWAS) analyzing genetic regulation of morphological traits of white blood cells have been reported. We carried out a GWAS of 12 morphological traits in 869 individuals...
9.
Richardson T, Crouch D, Power G, Morales-Berstein F, Hazelwood E, Fang S, et al.
Nat Commun
. 2022 Apr;
13(1):2337.
PMID: 35484151
The rising prevalence of childhood obesity has been postulated as an explanation for the increasing rate of individuals diagnosed with type 1 diabetes (T1D). In this study, we use Mendelian...
10.
Graham S, Clarke S, Wu K, Kanoni S, Zajac G, Ramdas S, et al.
Nature
. 2021 Dec;
600(7890):675-679.
PMID: 34887591
Increased blood lipid levels are heritable risk factors of cardiovascular disease with varied prevalence worldwide owing to different dietary patterns and medication use. Despite advances in prevention and treatment, in...