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On the Traceability of Commercial Saffron Samples Using 1H-NMR and FT-IR Metabolomics
Author / Creator:Consonni, Roberto ; Ordoudi, Stella ; Cagliani, Laura ; Tsiangali, Maria ; Tsimidou, Maria
Publisher:Switzerland: MDPI AG
Journal title:Molecules (Basel, Switzerland), 2016-02, Vol.21 (3), p.286-286
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Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene
Author / Creator:Cagliani, R. ; Fumagalli, M. ; Biasin, M. ; Piacentini, L. ; Riva, S. ; Pozzoli, U. ; Bonaglia, M. C. ; Bresolin, N. ; Clerici, M. ; Sironi, Manuela
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Human genetics, 2010-12, Vol.128 (6), p.577-588
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A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis
Author / Creator:Cagliani, R ; Guerini, F R ; Fumagalli, M ; Riva, S ; Agliardi, C ; Galimberti, D ; Pozzoli, U ; Goris, A ; Dubois, B ; Fenoglio, C ; ni, D ; Sanna, S ; Zara, I ; Pitzalis, M ; Zoledziewska, M ; Cucca, F ; Marini, F ; Comi, G P ; Scarpini, E ; Bresolin, N ; Clerici, M ; Sironi, M
Publisher:Oxford: Oxford University Press
Journal title:Molecular biology and evolution, 2012-06, Vol.29 (6), p.1599-1613
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Classroom Based Intensive Toilet Training for Children with Autism Spectrum Disorder
Author / Creator:Cagliani, Rachel R. ; Snyder, Sara Kathryn ; White, Emily N.
Publisher:New York: Springer US
Journal title:Journal of autism and developmental disorders, 2021-12, Vol.51 (12), p.4436-4446
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An evolutionary history of the selectin gene cluster in humans
Author / Creator:Fumagalli, M ; Fracassetti, M ; Cagliani, R ; Forni, D ; Pozzoli, U ; Comi, G P ; Marini, F ; Bresolin, N ; Clerici, M ; Sironi, M
Publisher:England: Springer Nature B.V
Journal title:Heredity, 2012-08, Vol.109 (2), p.117-126
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Augmentative and Alternative Communication and Speech Production for Individuals with ASD: A Systematic Review
Author / Creator:White, Emily N. ; Ayres, Kevin M. ; Snyder, Sara K. ; Cagliani, Rachel R. ; Ledford, Jennifer R.
Publisher:New York: Springer US
Journal title:Journal of autism and developmental disorders, 2021-11, Vol.51 (11), p.4199-4212
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A population genetics study of the Familial Mediterranean Fever gene: evidence of balancing selection under an overdominance regime
Author / Creator:Fumagalli, M ; Cagliani, R ; Pozzoli, U ; Riva, S ; Comi, G P ; Menozzi, G ; Bresolin, N ; Sironi, M
Publisher:London: Nature Publishing Group UK
Journal title:Genes and immunity, 2009-12, Vol.10 (8), p.678-686
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Effect of Task Sequence and Preference on On-Task Behavior
Author / Creator:Warren, Tiffani ; Cagliani, Rachel R. ; Whiteside, Erinn ; Ayres, Kevin M.
Publisher:New York: Springer
Journal title:Journal of behavioral education, 2021-03, Vol.30 (1), p.112-129
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Picture Exchange Communication System and Delay to Reinforcement
Author / Creator:Cagliani, Rachel R. ; Ayres, Kevin M. ; Whiteside, Erinn ; Ringdahl, Joel E.
Publisher:New York: Springer US
Journal title:Journal of developmental and physical disabilities, 2017-12, Vol.29 (6), p.925-939
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The Effect of Delay to Reinforcement and Response Effort on Response Variability for Individuals with Autism Spectrum Disorder
Author / Creator:Cagliani, Rachel R. ; Ayres, Kevin M. ; Ringdahl, Joel E. ; Whiteside, Erinn
Publisher:New York: Springer US
Journal title:Journal of developmental and physical disabilities, 2019-02, Vol.31 (1), p.55-71
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A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype
Author / Creator:Sironi, M. ; Corti, S. ; Locatelli, F. ; Cagliani, R. ; Comi, G.P.
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-03, Vol.17 (3), p.239-239
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Erratum: A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype
Author / Creator:Sironi, M. ; Corti, S. ; Locatelli, F. ; Cagliani, R. ; Comi, G.P.
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-12, Vol.18 (6), p.552-552
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Population Genetics of IFIH1: Ancient Population Structure, Local Selection, and Implications for Susceptibility to Type 1 Diabetes
Author / Creator:Fumagalli, Matteo ; Cagliani, Rachele ; Riva, Stefania ; Pozzoli, Uberto ; Biasin, Mara ; Piacentini, Luca ; Comi, Giacomo P ; Bresolin, Nereo ; Clerici, Mario ; Sironi, Manuela
Publisher:Oxford: Oxford University Press
Journal title:Molecular biology and evolution, 2010-11, Vol.27 (11), p.2555-2566
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An Evolutionary Analysis of RAC2 Identifies Haplotypes Associated with Human Autoimmune Diseases
Author / Creator:Sironi, Manuela ; Franca Rosa Guerini ; Agliardi, Cristina ; Biasin, Mara ; Cagliani, Rachele ; Fumagalli, Matteo ; Caputo, Domenico ; Cassinotti, Andrea ; Ardizzone, Sandro ; Zanzottera, Milena ; Bolognesi, Elisabetta ; Riva, Stefania ; Kanari, Yasuyoshi ; Miyazawa, Masaaki ; Clerici, Mario
Publisher:Oxford: Oxford University Press
Journal title:Molecular biology and evolution, 2011-12, Vol.28 (12), p.3319-3329
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Polymorphisms in the CPB2 Gene Are Maintained by Balancing Selection and Result in Haplotype-Preferential Splicing of Exon 7
Author / Creator:Cagliani, Rachele ; Fumagalli, Matteo ; Riva, Stefania ; Pozzoli, Uberto ; Fracassetti, Marco ; Bresolin, Nereo ; Comi, Giacomo P ; Sironi, Manuela
Publisher:Oxford: Oxford University Press
Journal title:Molecular biology and evolution, 2010-08, Vol.27 (8), p.1945-1954
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Long-term balancing selection maintains trans-specific polymorphisms in the human TRIMS gene
Author / Creator:CAGLIANI, R ; FUMAGALLI, M ; BIASIN, M ; PIACENTINI, L ; RIVA, S ; POZZOLI, U ; BONAGLIA, M. C ; BRESOLIN, N ; CLERICI, M ; SIRONI, Manuela
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2010, Vol.128 (6), p.577-588
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Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot
Author / Creator:Sironi, Manuela ; Pozzoli, Uberto ; Cagliani, Rachele ; Giorda, Roberto ; Comi, Giacomo P. ; Bardoni, Alessandra ; Menozzi, Giorgia ; Bresolin, Nereo
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2003-03, Vol.112 (3), p.272-288
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An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype
Author / Creator:Cagliani, Rachele ; Sironi, Manuela ; Ciafaloni, Emma ; Bardoni, Alessandra ; Fortunato, Francesco ; Prelle, Alessandro ; Serafini, Massimo ; Bresolin, Nereo ; Comi, Giacomo P.
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2004-06, Vol.115 (1), p.13-18
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Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms
Author / Creator:Sironi, Manuela ; Pozzoli, Uberto ; Cagliani, Rachele ; Comi, Giacomo P. ; Bardoni, Alessandra ; Bresolin, Nereo
Publisher:Germany
Journal title:Human genetics, 2001-07, Vol.109 (1), p.73-84
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On the Traceability of Commercial Saffron Samples Using 1H-NMR and FT-IR Metabolomics

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Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene

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A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis

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Classroom Based Intensive Toilet Training for Children with Autism Spectrum Disorder

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An evolutionary history of the selectin gene cluster in humans

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Augmentative and Alternative Communication and Speech Production for Individuals with ASD: A Systematic Review

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A population genetics study of the Familial Mediterranean Fever gene: evidence of balancing selection under an overdominance regime

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Effect of Task Sequence and Preference on On-Task Behavior

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Picture Exchange Communication System and Delay to Reinforcement

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The Effect of Delay to Reinforcement and Response Effort on Response Variability for Individuals with Autism Spectrum Disorder

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A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype

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Erratum: A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype

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Population Genetics of IFIH1: Ancient Population Structure, Local Selection, and Implications for Susceptibility to Type 1 Diabetes

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An Evolutionary Analysis of RAC2 Identifies Haplotypes Associated with Human Autoimmune Diseases

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Polymorphisms in the CPB2 Gene Are Maintained by Balancing Selection and Result in Haplotype-Preferential Splicing of Exon 7

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Long-term balancing selection maintains trans-specific polymorphisms in the human TRIMS gene

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Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot

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An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype

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Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms

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