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Picinelli, Chiara
38  results:
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1

Diagnostic yield and clinical impact of chromosomal microar..:

Cucinotta, Francesca ; Lintas, Carla ; Tomaiuolo, Pasquale...
Molecular Genetics & Genomic Medicine.  11 (2023)  8 - p. , 2023
Link: https://doi.org/10.1002/..
 
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2

RNA sequencing of blood from sex- and age-matched discordan..:

Tomaiuolo, Pasquale ; Piras, Ignazio Stefano ; Sain, Simona Baghai...
Scientific Reports.  13 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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3

Yield of array‐CGH analysis in Tunisian children with autis..:

Chehbani, Fethia ; Tomaiuolo, Pasquale ; Picinelli, Chiara...
Molecular Genetics & Genomic Medicine.  10 (2022)  8 - p. , 2022
Link: https://doi.org/10.1002/..
 
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4

FARP‐1 deletion is associated with lack of response to auti..:

Cucinotta, Francesca ; Ricciardello, Arianna ; Turriziani, Laura...
Molecular Genetics & Genomic Medicine.  8 (2020)  9 - p. , 2020
Link: https://doi.org/10.1002/..
 
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5

Huntingtin geneCAGrepeat size affects autism risk: Family‐b..:

Piras, Ignazio Stefano ; Picinelli, Chiara ; Iennaco, Raffaele...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  183 (2020)  6 - p. 341-351 , 2020
Link: https://doi.org/10.1002/..
 
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6

Appropriateness of array‐CGH in the ADHD clinics: A compara..:

Baccarin, Marco ; Picinelli, Chiara ; Tomaiuolo, Pasquale...
Genes, Brain and Behavior.  19 (2020)  6 - p. , 2020
Link: https://doi.org/10.1111/..
 
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7

Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficienc..:

Castronovo, Paola ; Baccarin, Marco ; Ricciardello, Arianna...
Clinical Genetics.  97 (2019)  1 - p. 125-137 , 2019
Link: https://doi.org/10.1111/..
 
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8

Molecular Etiology Disclosed by Array CGH in Patients With ..:

Crippa, Milena ; Bonati, Maria Teresa ; Calzari, Luciano...
Frontiers in Genetics.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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9

Copy number variation in 19 Italian multiplex families with..:

Lintas, Carla ; Picinelli, Chiara ; Piras, Ignazio Stefano...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  174 (2017)  5 - p. 547-556 , 2017
Link: https://doi.org/10.1002/..
 
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10

Recurrent 15q11.2 BP1‐BP2 microdeletions and microduplicati..:

Picinelli, Chiara ; Lintas, Carla ; Piras, Ignazio Stefano...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  171 (2016)  8 - p. 1088-1098 , 2016
Link: https://doi.org/10.1002/..
 
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11

Characterization of 14 novel deletions underlying Rubinstei..:

Rusconi, Daniela ; Negri, Gloria ; Colapietro, Patrizia...
Human Genetics.  134 (2015)  6 - p. 613-626 , 2015
Link: https://doi.org/10.1007/..
 
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12

Constitutional de novo deletion of the FBXW7 gene in a pati..:

Roversi, Gaia ; Picinelli, Chiara ; Bestetti, Ilaria...
Scientific Reports.  5 (2015)  1 - p. , 2015
Link: https://doi.org/10.1038/..
 
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13

Overall and allele-specific expression of theSMC1Agene in f..:

Parenti, Ilaria ; Rovina, Davide ; Masciadri, Maura...
Epigenetics.  9 (2014)  7 - p. 973-979 , 2014
Link: https://doi.org/10.4161/..
 
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14

New case of trichorinophalangeal syndrome-like phenotype wi..:

Crippa, Milena ; Bestetti, Ilaria ; Perotti, Mario...
BMC Medical Genetics.  15 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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15

Genomic imbalances in patients with a clinical presentation..:

Gervasini, Cristina ; Picinelli, Chiara ; Azzollini, Jacopo...
BMC Medical Genetics.  14 (2013)  1 - p. , 2013
Link: https://doi.org/10.1186/..
 
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