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Marcella Devoto

Showing results (11-20 of 122) with videos related to

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Human Heredity|October 16, 2007
Estimates of genetic and environmental contribution to 43 quantitative traits support sharing of a homogeneous environment in an isolated population from South Tyrol, ItalyFabio Marroni, Daniela Grazio, Cristian Pattaro, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 8, 2010
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellumFrancesca Lantieri, Joseph T Glessner, Hakon Hakonarson, et al.
BMC Proceedings|December 19, 2009
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association studyFrancesca Lantieri, Min A Jhun, Jungsun Park, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Quantile-specific confounding: correction for subtle population stratification via quantile regressionChen Wang, Marco Masala, Edoardo Fiorillo, et al.
Inflammatory Bowel Diseases|October 13, 2017
Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel DiseaseMáire A Conrad, Noor Dawany, Kathleen E Sullivan, et al.
Genetics|July 21, 2025
Quantile-specific confounding: correction for subtle population stratification via quantile regressionChen Wang, Marco Masala, Edoardo Fiorillo, et al.
Investigative Ophthalmology & Visual Science|June 28, 2005
Identification of a novel locus on 2q for autosomal dominant high-grade myopiaPrasuna C Paluru, Sudha Nallasamy, Marcella Devoto, et al.
Human Mutation|January 12, 2005
A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expressionPaola Griseri, Tiziana Bachetti, Francesca Puppo, et al.
Human Heredity|July 8, 2011
Genome-wide linkage analysis to identify genetic modifiers of ALK mutation penetrance in familial neuroblastomaMarcella Devoto, Claudia Specchia, Marci Laudenslager, et al.
Clinical Immunology (Orlando, Fla.)|May 25, 2022
Clinical and laboratory predictors of monogenic very early onset inflammatory bowel diseaseJudith Kelsen, Noor Dawany, Maire Conrad, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
Human Heredity|October 16, 2007
Estimates of genetic and environmental contribution to 43 quantitative traits support sharing of a homogeneous environment in an isolated population from South Tyrol, ItalyFabio Marroni, Daniela Grazio, Cristian Pattaro, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 8, 2010
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellumFrancesca Lantieri, Joseph T Glessner, Hakon Hakonarson, et al.
BMC Proceedings|December 19, 2009
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association studyFrancesca Lantieri, Min A Jhun, Jungsun Park, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Quantile-specific confounding: correction for subtle population stratification via quantile regressionChen Wang, Marco Masala, Edoardo Fiorillo, et al.
Inflammatory Bowel Diseases|October 13, 2017
Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel DiseaseMáire A Conrad, Noor Dawany, Kathleen E Sullivan, et al.
Genetics|July 21, 2025
Quantile-specific confounding: correction for subtle population stratification via quantile regressionChen Wang, Marco Masala, Edoardo Fiorillo, et al.
Investigative Ophthalmology & Visual Science|June 28, 2005
Identification of a novel locus on 2q for autosomal dominant high-grade myopiaPrasuna C Paluru, Sudha Nallasamy, Marcella Devoto, et al.
Human Mutation|January 12, 2005
A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expressionPaola Griseri, Tiziana Bachetti, Francesca Puppo, et al.
Human Heredity|July 8, 2011
Genome-wide linkage analysis to identify genetic modifiers of ALK mutation penetrance in familial neuroblastomaMarcella Devoto, Claudia Specchia, Marci Laudenslager, et al.
Clinical Immunology (Orlando, Fla.)|May 25, 2022
Clinical and laboratory predictors of monogenic very early onset inflammatory bowel diseaseJudith Kelsen, Noor Dawany, Maire Conrad, et al.
Pageof 13